name	term_id	term_name	term_namespace	term_distance
MESH:C	MESH:C	Diseases	root	0
MESH:D013568	MESH:D013568	Pathological Conditions, Signs and Symptoms	CTD_diseases	1
MESH:D014777	MESH:D014777	Virus Diseases	CTD_diseases	1
MESH:D014947	MESH:D014947	Wounds and Injuries	CTD_diseases	1
MESH:D017437	MESH:D017437	Skin and Connective Tissue Diseases	CTD_diseases	1
MESH:D052801	MESH:D052801	Male Urogenital Diseases	CTD_diseases	1
MESH:D064419	MESH:D064419	Chemically-Induced Disorders	CTD_diseases	1
MESH:D000820	MESH:D000820	Animal Diseases	CTD_diseases	1
MESH:D001423	MESH:D001423	Bacterial Infections and Mycoses	CTD_diseases	1
MESH:D001523	MESH:D001523	Mental Disorders	CTD_diseases	1
MESH:D002318	MESH:D002318	Cardiovascular Diseases	CTD_diseases	1
MESH:D004066	MESH:D004066	Digestive System Diseases	CTD_diseases	1
MESH:D004700	MESH:D004700	Endocrine System Diseases	CTD_diseases	1
MESH:D005128	MESH:D005128	Eye Diseases	CTD_diseases	1
MESH:D005261	MESH:D005261	Female Urogenital Diseases and Pregnancy Complications	CTD_diseases	1
MESH:D006425	MESH:D006425	Hemic and Lymphatic Diseases	CTD_diseases	1
MESH:D007154	MESH:D007154	Immune System Diseases	CTD_diseases	1
MESH:D007280	MESH:D007280	Disorders of Environmental Origin	CTD_diseases	1
MESH:D009057	MESH:D009057	Stomatognathic Diseases	CTD_diseases	1
MESH:D009140	MESH:D009140	Musculoskeletal Diseases	CTD_diseases	1
MESH:D009358	MESH:D009358	Congenital, Hereditary, and Neonatal Diseases and Abnormalities	CTD_diseases	1
MESH:D009369	MESH:D009369	Neoplasms	CTD_diseases	1
MESH:D009422	MESH:D009422	Nervous System Diseases	CTD_diseases	1
MESH:D009750	MESH:D009750	Nutritional and Metabolic Diseases	CTD_diseases	1
MESH:D009784	MESH:D009784	Occupational Diseases	CTD_diseases	1
MESH:D010038	MESH:D010038	Otorhinolaryngologic Diseases	CTD_diseases	1
MESH:D010272	MESH:D010272	Parasitic Diseases	CTD_diseases	1
MESH:D012140	MESH:D012140	Respiratory Tract Diseases	CTD_diseases	1
MESH:C567425	MESH:C567425	Alopecia, Neurologic Defects, and Endocrinopathy Syndrome	CTD_diseases	2
MESH:C567648	MESH:C567648	Exudative Vitreoretinopathy 5	CTD_diseases	2
MESH:C567716	MESH:C567716	Cutis Laxa With Severe Pulmonary, Gastrointestinal, And Urinary Abnormalities	CTD_diseases	2
MESH:C579754	MESH:C579754	abc disease	CTD_diseases	2
MESH:D000007	MESH:D000007	Abdominal Injuries	CTD_diseases	2
MESH:D000013	MESH:D000013	Congenital Abnormalities	CTD_diseases	2
MESH:D000034	MESH:D000034	Abortion, Veterinary	CTD_diseases	2
MESH:D000187	MESH:D000187	Actinobacillosis	CTD_diseases	2
MESH:D000275	MESH:D000275	Adjustment Disorders	CTD_diseases	2
MESH:D000307	MESH:D000307	Adrenal Gland Diseases	CTD_diseases	2
MESH:D000382	MESH:D000382	Agricultural Workers' Diseases	CTD_diseases	2
MESH:D000453	MESH:D000453	Aleutian Mink Disease	CTD_diseases	2
MESH:D000673	MESH:D000673	Amputation, Traumatic	CTD_diseases	2
MESH:D000694	MESH:D000694	Anal Gland Neoplasms	CTD_diseases	2
MESH:D000712	MESH:D000712	Anaplasmosis	CTD_diseases	2
MESH:D001008	MESH:D001008	Anxiety Disorders	CTD_diseases	2
MESH:D001068	MESH:D001068	Eating Disorders	CTD_diseases	2
MESH:D001102	MESH:D001102	Arbovirus Infections	CTD_diseases	2
MESH:D001134	MESH:D001134	Arm Injuries	CTD_diseases	2
MESH:D001237	MESH:D001237	Asphyxia	CTD_diseases	2
MESH:D001248	MESH:D001248	Asthenopia	CTD_diseases	2
MESH:D001265	MESH:D001265	Athletic Injuries	CTD_diseases	2
MESH:D001327	MESH:D001327	Autoimmune Diseases	CTD_diseases	2
MESH:D001342	MESH:D001342	Autonomic Nervous System Diseases	CTD_diseases	2
MESH:D001424	MESH:D001424	Bacterial Infections	CTD_diseases	2
MESH:D001469	MESH:D001469	Barotrauma	CTD_diseases	2
MESH:D001660	MESH:D001660	Biliary Tract Diseases	CTD_diseases	2
MESH:D001715	MESH:D001715	Bird Diseases	CTD_diseases	2
MESH:D001716	MESH:D001716	Bird Fancier's Lung	CTD_diseases	2
MESH:D001720	MESH:D001720	Birth Injuries	CTD_diseases	2
MESH:D001733	MESH:D001733	Bites and Stings	CTD_diseases	2
MESH:D001787	MESH:D001787	Blood Group Incompatibility	CTD_diseases	2
MESH:D001847	MESH:D001847	Bone Diseases	CTD_diseases	2
MESH:D001849	MESH:D001849	Bone Diseases, Endocrine	CTD_diseases	2
MESH:D001890	MESH:D001890	Borna Disease	CTD_diseases	2
MESH:D001922	MESH:D001922	Brain Abscess	CTD_diseases	2
MESH:D001982	MESH:D001982	Bronchial Diseases	CTD_diseases	2
MESH:D001990	MESH:D001990	Bronchiolitis, Viral	CTD_diseases	2
MESH:D002056	MESH:D002056	Burns	CTD_diseases	2
MESH:D002357	MESH:D002357	Cartilage Diseases	CTD_diseases	2
MESH:D002371	MESH:D002371	Cat Diseases	CTD_diseases	2
MESH:D002418	MESH:D002418	Cattle Diseases	CTD_diseases	2
MESH:D002493	MESH:D002493	Central Nervous System Diseases	CTD_diseases	2
MESH:D002494	MESH:D002494	Central Nervous System Infections	CTD_diseases	2
MESH:D002925	MESH:D002925	Ciliary Motility Disorders	CTD_diseases	2
MESH:D003229	MESH:D003229	Conjunctival Diseases	CTD_diseases	2
MESH:D003240	MESH:D003240	Connective Tissue Diseases	CTD_diseases	2
MESH:D003288	MESH:D003288	Contusions	CTD_diseases	2
MESH:D003316	MESH:D003316	Corneal Diseases	CTD_diseases	2
MESH:D003389	MESH:D003389	Cranial Nerve Diseases	CTD_diseases	2
MESH:D003560	MESH:D003560	Cysts	CTD_diseases	2
MESH:D003711	MESH:D003711	Demyelinating Diseases	CTD_diseases	2
MESH:D003920	MESH:D003920	Diabetes Mellitus	CTD_diseases	2
MESH:D004065	MESH:D004065	Digestive System Abnormalities	CTD_diseases	2
MESH:D004067	MESH:D004067	Digestive System Neoplasms	CTD_diseases	2
MESH:D004195	MESH:D004195	Disease Models, Animal	CTD_diseases	2
MESH:D004204	MESH:D004204	Dislocations	CTD_diseases	2
MESH:D004213	MESH:D004213	Dissociative Disorders	CTD_diseases	2
MESH:D004266	MESH:D004266	DNA Virus Infections	CTD_diseases	2
MESH:D004283	MESH:D004283	Dog Diseases	CTD_diseases	2
MESH:D004332	MESH:D004332	Drowning	CTD_diseases	2
MESH:D004392	MESH:D004392	Dwarfism	CTD_diseases	2
MESH:D004427	MESH:D004427	Ear Diseases	CTD_diseases	2
MESH:D004556	MESH:D004556	Electric Injuries	CTD_diseases	2
MESH:D004701	MESH:D004701	Endocrine Gland Neoplasms	CTD_diseases	2
MESH:D004767	MESH:D004767	Enterotoxemia	CTD_diseases	2
MESH:D004889	MESH:D004889	Erysipelothrix Infections	CTD_diseases	2
MESH:D004939	MESH:D004939	Esophageal Perforation	CTD_diseases	2
MESH:D005119	MESH:D005119	Extravasation of Diagnostic and Therapeutic Materials	CTD_diseases	2
MESH:D005124	MESH:D005124	Eye Abnormalities	CTD_diseases	2
MESH:D005130	MESH:D005130	Eye Hemorrhage	CTD_diseases	2
MESH:D005131	MESH:D005131	Eye Injuries	CTD_diseases	2
MESH:D005132	MESH:D005132	Eye Manifestations	CTD_diseases	2
MESH:D005134	MESH:D005134	Eye Neoplasms	CTD_diseases	2
MESH:D005141	MESH:D005141	Eyelid Diseases	CTD_diseases	2
MESH:D005162	MESH:D005162	Factitious Disorders	CTD_diseases	2
MESH:D005208	MESH:D005208	Fasciitis	CTD_diseases	2
MESH:D005315	MESH:D005315	Fetal Diseases	CTD_diseases	2
MESH:D005393	MESH:D005393	Fish Diseases	CTD_diseases	2
MESH:D005530	MESH:D005530	Foot Deformities	CTD_diseases	2
MESH:D005534	MESH:D005534	Foot Diseases	CTD_diseases	2
MESH:D005535	MESH:D005535	Foot Rot	CTD_diseases	2
MESH:D005536	MESH:D005536	Foot-and-Mouth Disease	CTD_diseases	2
MESH:D005547	MESH:D005547	Foreign Bodies	CTD_diseases	2
MESH:D005627	MESH:D005627	Frostbite	CTD_diseases	2
MESH:D005767	MESH:D005767	Gastrointestinal Diseases	CTD_diseases	2
MESH:D005832	MESH:D005832	Genital Diseases, Male	CTD_diseases	2
MESH:D006058	MESH:D006058	Gonadal Disorders	CTD_diseases	2
MESH:D006086	MESH:D006086	Graft vs Host Disease	CTD_diseases	2
MESH:D006222	MESH:D006222	Hamartoma	CTD_diseases	2
MESH:D006226	MESH:D006226	Hand Deformities	CTD_diseases	2
MESH:D006230	MESH:D006230	Hand Injuries	CTD_diseases	2
MESH:D006259	MESH:D006259	Craniocerebral Trauma	CTD_diseases	2
MESH:D006331	MESH:D006331	Heart Diseases	CTD_diseases	2
MESH:D006357	MESH:D006357	Heartwater Disease	CTD_diseases	2
MESH:D006373	MESH:D006373	Helminthiasis	CTD_diseases	2
MESH:D006402	MESH:D006402	Hematologic Diseases	CTD_diseases	2
MESH:D006520	MESH:D006520	Hepatitis, Animal	CTD_diseases	2
MESH:D006524	MESH:D006524	Hepatitis, Viral, Animal	CTD_diseases	2
MESH:D006525	MESH:D006525	Hepatitis, Viral, Human	CTD_diseases	2
MESH:D006610	MESH:D006610	High Pressure Neurological Syndrome	CTD_diseases	2
MESH:D006734	MESH:D006734	Horse Diseases	CTD_diseases	2
MESH:D006967	MESH:D006967	Hypersensitivity	CTD_diseases	2
MESH:D007153	MESH:D007153	Immunologic Deficiency Syndromes	CTD_diseases	2
MESH:D007160	MESH:D007160	Immunoproliferative Disorders	CTD_diseases	2
MESH:D007174	MESH:D007174	Impulse Control Disorders	CTD_diseases	2
MESH:D007222	MESH:D007222	Inert Gas Narcosis	CTD_diseases	2
MESH:D007232	MESH:D007232	Infant, Newborn, Diseases	CTD_diseases	2
MESH:D007239	MESH:D007239	Infection	CTD_diseases	2
MESH:D007411	MESH:D007411	Intestinal Diseases, Parasitic	CTD_diseases	2
MESH:D007571	MESH:D007571	Jaw Diseases	CTD_diseases	2
MESH:D007592	MESH:D007592	Joint Diseases	CTD_diseases	2
MESH:D007639	MESH:D007639	Keratoconjunctivitis, Infectious	CTD_diseases	2
MESH:D007757	MESH:D007757	Laboratory Infection	CTD_diseases	2
MESH:D007766	MESH:D007766	Lacrimal Apparatus Diseases	CTD_diseases	2
MESH:D007794	MESH:D007794	Lameness, Animal	CTD_diseases	2
MESH:D007818	MESH:D007818	Laryngeal Diseases	CTD_diseases	2
MESH:D007869	MESH:D007869	Leg Injuries	CTD_diseases	2
MESH:D007905	MESH:D007905	Lens Diseases	CTD_diseases	2
MESH:D008107	MESH:D008107	Liver Diseases	CTD_diseases	2
MESH:D008109	MESH:D008109	Liver Diseases, Parasitic	CTD_diseases	2
MESH:D008171	MESH:D008171	Lung Diseases	CTD_diseases	2
MESH:D008174	MESH:D008174	Lung Diseases, Parasitic	CTD_diseases	2
MESH:D008206	MESH:D008206	Lymphatic Diseases	CTD_diseases	2
MESH:D008587	MESH:D008587	Meningitis, Viral	CTD_diseases	2
MESH:D008659	MESH:D008659	Metabolic Diseases	CTD_diseases	2
MESH:D009059	MESH:D009059	Mouth Diseases	CTD_diseases	2
MESH:D009104	MESH:D009104	Multiple Trauma	CTD_diseases	2
MESH:D009135	MESH:D009135	Muscular Diseases	CTD_diseases	2
MESH:D009137	MESH:D009137	Muscular Dystrophy, Animal	CTD_diseases	2
MESH:D009139	MESH:D009139	Musculoskeletal Abnormalities	CTD_diseases	2
MESH:D009181	MESH:D009181	Mycoses	CTD_diseases	2
MESH:D009234	MESH:D009234	Myxomatosis, Infectious	CTD_diseases	2
MESH:D009370	MESH:D009370	Neoplasms by Histologic Type	CTD_diseases	2
MESH:D009371	MESH:D009371	Neoplasms by Site	CTD_diseases	2
MESH:D009374	MESH:D009374	Neoplasms, Experimental	CTD_diseases	2
MESH:D009376	MESH:D009376	Neoplasms, Hormone-Dependent	CTD_diseases	2
MESH:D009378	MESH:D009378	Neoplasms, Multiple Primary	CTD_diseases	2
MESH:D009381	MESH:D009381	Neoplasms, Radiation-Induced	CTD_diseases	2
MESH:D009385	MESH:D009385	Neoplastic Processes	CTD_diseases	2
MESH:D009386	MESH:D009386	Neoplastic Syndromes, Hereditary	CTD_diseases	2
MESH:D009421	MESH:D009421	Nervous System Malformations	CTD_diseases	2
MESH:D009423	MESH:D009423	Nervous System Neoplasms	CTD_diseases	2
MESH:D009461	MESH:D009461	Neurologic Manifestations	CTD_diseases	2
MESH:D009468	MESH:D009468	Neuromuscular Diseases	CTD_diseases	2
MESH:D009497	MESH:D009497	Neurotic Disorders	CTD_diseases	2
MESH:D009668	MESH:D009668	Nose Diseases	CTD_diseases	2
MESH:D009748	MESH:D009748	Nutrition Disorders	CTD_diseases	2
MESH:D009783	MESH:D009783	Dermatitis, Occupational	CTD_diseases	2
MESH:D009798	MESH:D009798	Ocular Hypertension	CTD_diseases	2
MESH:D009894	MESH:D009894	Opportunistic Infections	CTD_diseases	2
MESH:D009901	MESH:D009901	Optic Nerve Diseases	CTD_diseases	2
MESH:D009916	MESH:D009916	Orbital Diseases	CTD_diseases	2
MESH:D010039	MESH:D010039	Otorhinolaryngologic Neoplasms	CTD_diseases	2
MESH:D010182	MESH:D010182	Pancreatic Diseases	CTD_diseases	2
MESH:D010257	MESH:D010257	Paraneoplastic Syndromes	CTD_diseases	2
MESH:D010273	MESH:D010273	Parasitic Diseases, Animal	CTD_diseases	2
MESH:D010279	MESH:D010279	Parathyroid Diseases	CTD_diseases	2
MESH:D010283	MESH:D010283	Paratuberculosis	CTD_diseases	2
MESH:D010319	MESH:D010319	Parturient Paresis	CTD_diseases	2
MESH:D010335	MESH:D010335	Pathologic Processes	CTD_diseases	2
MESH:D010532	MESH:D010532	Peritoneal Diseases	CTD_diseases	2
MESH:D010554	MESH:D010554	Personality Disorders	CTD_diseases	2
MESH:D010608	MESH:D010608	Pharyngeal Diseases	CTD_diseases	2
MESH:D010900	MESH:D010900	Pituitary Diseases	CTD_diseases	2
MESH:D010995	MESH:D010995	Pleural Diseases	CTD_diseases	2
MESH:D011002	MESH:D011002	Pleuropneumonia, Contagious	CTD_diseases	2
MESH:D011009	MESH:D011009	Pneumoconiosis	CTD_diseases	2
MESH:D011024	MESH:D011024	Pneumonia, Viral	CTD_diseases	2
MESH:D011041	MESH:D011041	Poisoning	CTD_diseases	2
MESH:D011230	MESH:D011230	Precancerous Conditions	CTD_diseases	2
MESH:D011248	MESH:D011248	Pregnancy Complications	CTD_diseases	2
MESH:D011249	MESH:D011249	Pregnancy Complications, Cardiovascular	CTD_diseases	2
MESH:D011252	MESH:D011252	Pregnancy Complications, Neoplastic	CTD_diseases	2
MESH:D011528	MESH:D011528	Protozoan Infections	CTD_diseases	2
MESH:D011557	MESH:D011557	Pseudorabies	CTD_diseases	2
MESH:D011681	MESH:D011681	Pupil Disorders	CTD_diseases	2
MESH:D011696	MESH:D011696	Purpura, Thrombocytopenic	CTD_diseases	2
MESH:D011832	MESH:D011832	Radiation Injuries	CTD_diseases	2
MESH:D012030	MESH:D012030	Refractive Errors	CTD_diseases	2
MESH:D012120	MESH:D012120	Respiration Disorders	CTD_diseases	2
MESH:D012130	MESH:D012130	Respiratory Hypersensitivity	CTD_diseases	2
MESH:D012141	MESH:D012141	Respiratory Tract Infections	CTD_diseases	2
MESH:D012142	MESH:D012142	Respiratory Tract Neoplasms	CTD_diseases	2
MESH:D012148	MESH:D012148	Restless Legs Syndrome	CTD_diseases	2
MESH:D012164	MESH:D012164	Retinal Diseases	CTD_diseases	2
MESH:D012188	MESH:D012188	Retropneumoperitoneum	CTD_diseases	2
MESH:D012216	MESH:D012216	Rheumatic Diseases	CTD_diseases	2
MESH:D012301	MESH:D012301	Rinderpest	CTD_diseases	2
MESH:D012327	MESH:D012327	RNA Virus Infections	CTD_diseases	2
MESH:D012376	MESH:D012376	Rodent Diseases	CTD_diseases	2
MESH:D012421	MESH:D012421	Rupture	CTD_diseases	2
MESH:D012481	MESH:D012481	Salmonella Infections, Animal	CTD_diseases	2
MESH:D012652	MESH:D012652	Self Mutilation	CTD_diseases	2
MESH:D012749	MESH:D012749	Sexually Transmitted Diseases	CTD_diseases	2
MESH:D012757	MESH:D012757	Sheep Diseases	CTD_diseases	2
MESH:D012774	MESH:D012774	Shock, Traumatic	CTD_diseases	2
MESH:D012816	MESH:D012816	Signs and Symptoms	CTD_diseases	2
MESH:D012871	MESH:D012871	Skin Diseases	CTD_diseases	2
MESH:C535530	MESH:C535530	Interferon gamma, receptor 1, deficiency	CTD_diseases	2
MESH:C535736	MESH:C535736	Encephalocraniocutaneous lipomatosis	CTD_diseases	2
MESH:C535780	MESH:C535780	Spondylocarpotarsal synostosis	CTD_diseases	2
MESH:C535809	MESH:C535809	Mollica Pavone Antener syndrome	CTD_diseases	2
MESH:C535875	MESH:C535875	Roy Maroteaux Kremp syndrome	CTD_diseases	2
MESH:C535908	MESH:C535908	Marcus Gunn phenomenon	CTD_diseases	2
MESH:C535984	MESH:C535984	Congenital bilateral aplasia of vas deferens	CTD_diseases	2
MESH:C536062	MESH:C536062	Hernandez Fragoso syndrome	CTD_diseases	2
MESH:C536897	MESH:C536897	Tang Hsi Ryu syndrome	CTD_diseases	2
MESH:C536984	MESH:C536984	MORM syndrome	CTD_diseases	2
MESH:C537254	MESH:C537254	Hemorrhagic shock and encephalopathy syndrome	CTD_diseases	2
MESH:C537335	MESH:C537335	Siegler Brewer Carey syndrome	CTD_diseases	2
MESH:C537394	MESH:C537394	Neuronal intestinal pseudoobstruction	CTD_diseases	2
MESH:C537849	MESH:C537849	Norrie disease	CTD_diseases	2
MESH:C537851	MESH:C537851	Novak syndrome	CTD_diseases	2
MESH:C562707	MESH:C562707	ACTH Deficiency, Isolated	CTD_diseases	2
MESH:C563413	MESH:C563413	Hydrocephalus, Skeletal Anomalies, and Mental Disturbance	CTD_diseases	2
MESH:C563423	MESH:C563423	Proprotein Convertase 1 3 Deficiency	CTD_diseases	2
MESH:C563515	MESH:C563515	Neutrophil Chemotactic Response	CTD_diseases	2
MESH:C563517	MESH:C563517	Neuropathy, Hereditary Sensorimotor, with Upper Motor Neuron, Visual Pathway and Autonomic Disturban	CTD_diseases	2
MESH:C563734	MESH:C563734	Chromosome 18 Pericentric Inversion	CTD_diseases	2
MESH:C564066	MESH:C564066	Radiation Sensitivity of Natural Killer Activity	CTD_diseases	2
MESH:C564505	MESH:C564505	Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders	CTD_diseases	2
MESH:C564678	MESH:C564678	Spongiform Encephalopathy with Neuropsychiatric Features	CTD_diseases	2
MESH:C564839	MESH:C564839	Retinohepatoendocrinologic Syndrome	CTD_diseases	2
MESH:C564878	MESH:C564878	Polyglucosan Body Disease, Adult Form	CTD_diseases	2
MESH:C564954	MESH:C564954	Neurologic Disease, Infantile Multisystem, with Osseous Fragility	CTD_diseases	2
MESH:C565001	MESH:C565001	Fragile Site 16p12	CTD_diseases	2
MESH:C565371	MESH:C565371	Monocyte Chemotactic Disorder	CTD_diseases	2
MESH:C565425	MESH:C565425	Macrosomia Adiposa Congenita	CTD_diseases	2
MESH:C565433	MESH:C565433	Lymphoblastic Transformation, Inhibition of	CTD_diseases	2
MESH:C565768	MESH:C565768	Alpha-Methylacyl-CoA Racemase Deficiency	CTD_diseases	2
MESH:C565786	MESH:C565786	Myoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders	CTD_diseases	2
MESH:C565822	MESH:C565822	Congenital Cataracts, Facial Dysmorphism, And Neuropathy	CTD_diseases	2
MESH:C565848	MESH:C565848	Chromosomal Instability with Tissue-Specific Radiosensitivity	CTD_diseases	2
MESH:C565852	MESH:C565852	Chondroitin-6-Sulfaturia, Defective Cellular Immunity, Nephrotic Syndrome	CTD_diseases	2
MESH:C566619	MESH:C566619	Exudative Vitreoretinopathy 4	CTD_diseases	2
MESH:C566918	MESH:C566918	Renal Tubular Acidosis, Distal, With Nephrocalcinosis, Short Stature, Mental Retardation, And Distin	CTD_diseases	2
MESH:C566945	MESH:C566945	Trifunctional Protein Deficiency With Myopathy And Neuropathy	CTD_diseases	2
MESH:C567210	MESH:C567210	Endocrine-Cerebroosteodysplasia	CTD_diseases	2
MESH:D012876	MESH:D012876	Skin Diseases, Parasitic	CTD_diseases	2
MESH:D012893	MESH:D012893	Sleep Disorders	CTD_diseases	2
MESH:D012897	MESH:D012897	Slow Virus Diseases	CTD_diseases	2
MESH:D013001	MESH:D013001	Somatoform Disorders	CTD_diseases	2
MESH:D013119	MESH:D013119	Spinal Cord Injuries	CTD_diseases	2
MESH:D013124	MESH:D013124	Spinal Injuries	CTD_diseases	2
MESH:D013180	MESH:D013180	Sprains and Strains	CTD_diseases	2
MESH:D013231	MESH:D013231	Steatitis	CTD_diseases	2
MESH:D013553	MESH:D013553	Swine Diseases	CTD_diseases	2
MESH:D013705	MESH:D013705	Temporomandibular Joint Disorders	CTD_diseases	2
MESH:D013708	MESH:D013708	Tendon Injuries	CTD_diseases	2
MESH:D013716	MESH:D013716	Tennis Elbow	CTD_diseases	2
MESH:D013896	MESH:D013896	Thoracic Diseases	CTD_diseases	2
MESH:D013898	MESH:D013898	Thoracic Injuries	CTD_diseases	2
MESH:D013959	MESH:D013959	Thyroid Diseases	CTD_diseases	2
MESH:D014076	MESH:D014076	Tooth Diseases	CTD_diseases	2
MESH:D014133	MESH:D014133	Tracheal Diseases	CTD_diseases	2
MESH:D014383	MESH:D014383	Tuberculosis, Endocrine	CTD_diseases	2
MESH:D014401	MESH:D014401	Tuberculosis, Urogenital	CTD_diseases	2
MESH:D014412	MESH:D014412	Tumor Virus Infections	CTD_diseases	2
MESH:D014564	MESH:D014564	Urogenital Abnormalities	CTD_diseases	2
MESH:D014565	MESH:D014565	Urogenital Neoplasms	CTD_diseases	2
MESH:D014570	MESH:D014570	Urologic Diseases	CTD_diseases	2
MESH:D014603	MESH:D014603	Uveal Diseases	CTD_diseases	2
MESH:D014652	MESH:D014652	Vascular Diseases	CTD_diseases	2
MESH:D014685	MESH:D014685	Venereal Tumors, Veterinary	CTD_diseases	2
MESH:D014766	MESH:D014766	Viremia	CTD_diseases	2
MESH:D014786	MESH:D014786	Vision Disorders	CTD_diseases	2
MESH:D014946	MESH:D014946	Wound Infection	CTD_diseases	2
MESH:D014949	MESH:D014949	Wounds, Nonpenetrating	CTD_diseases	2
MESH:D014950	MESH:D014950	Wounds, Penetrating	CTD_diseases	2
MESH:D015047	MESH:D015047	Zoonoses	CTD_diseases	2
MESH:D015422	MESH:D015422	Scleral Diseases	CTD_diseases	2
MESH:D015432	MESH:D015432	Glomerulonephritis, Membranoproliferative	CTD_diseases	2
MESH:D015511	MESH:D015511	Goat Diseases	CTD_diseases	2
MESH:D015597	MESH:D015597	Pregnancy Complications, Parasitic	CTD_diseases	2
MESH:D015619	MESH:D015619	Respiratory System Abnormalities	CTD_diseases	2
MESH:D015673	MESH:D015673	Fatigue Syndrome, Chronic	CTD_diseases	2
MESH:D015674	MESH:D015674	Mammary Neoplasms, Animal	CTD_diseases	2
MESH:D015769	MESH:D015769	Granuloma, Respiratory Tract	CTD_diseases	2
MESH:D015785	MESH:D015785	Eye Diseases, Hereditary	CTD_diseases	2
MESH:D015814	MESH:D015814	Ocular Hypotension	CTD_diseases	2
MESH:D015817	MESH:D015817	Eye Infections	CTD_diseases	2
MESH:D015822	MESH:D015822	Eye Infections, Parasitic	CTD_diseases	2
MESH:D015828	MESH:D015828	Eye Infections, Viral	CTD_diseases	2
MESH:D015835	MESH:D015835	Ocular Motility Disorders	CTD_diseases	2
MESH:D016154	MESH:D016154	Digestive System Fistula	CTD_diseases	2
MESH:D016156	MESH:D016156	Respiratory Tract Fistula	CTD_diseases	2
MESH:D016609	MESH:D016609	Neoplasms, Second Primary	CTD_diseases	2
MESH:D016884	MESH:D016884	Polyendocrinopathies, Autoimmune	CTD_diseases	2
MESH:D017169	MESH:D017169	Neoplasms, Post-Traumatic	CTD_diseases	2
MESH:D017193	MESH:D017193	Skin Diseases, Viral	CTD_diseases	2
MESH:D017695	MESH:D017695	Soft Tissue Injuries	CTD_diseases	2
MESH:D018058	MESH:D018058	Tympanic Membrane Perforation	CTD_diseases	2
MESH:D018376	MESH:D018376	Cardiovascular Abnormalities	CTD_diseases	2
MESH:D018419	MESH:D018419	Primate Diseases	CTD_diseases	2
MESH:D018512	MESH:D018512	Parasitemia	CTD_diseases	2
MESH:D018630	MESH:D018630	Vitreoretinopathy, Proliferative	CTD_diseases	2
MESH:D018640	MESH:D018640	Stomatognathic System Abnormalities	CTD_diseases	2
MESH:D018677	MESH:D018677	Tooth Injuries	CTD_diseases	2
MESH:D018792	MESH:D018792	Encephalitis, Viral	CTD_diseases	2
MESH:D018876	MESH:D018876	Environmental Illness	CTD_diseases	2
MESH:D018882	MESH:D018882	Heat Stress Disorders	CTD_diseases	2
MESH:D018923	MESH:D018923	Persian Gulf Syndrome	CTD_diseases	2
MESH:D019567	MESH:D019567	Back Injuries	CTD_diseases	2
MESH:D019636	MESH:D019636	Neurodegenerative Diseases	CTD_diseases	2
MESH:D019838	MESH:D019838	Neck Injuries	CTD_diseases	2
MESH:D019952	MESH:D019952	Mental Disorders Diagnosed in Childhood	CTD_diseases	2
MESH:D019964	MESH:D019964	Mood Disorders	CTD_diseases	2
MESH:D019965	MESH:D019965	Delirium, Dementia, Amnestic, Cognitive Disorders	CTD_diseases	2
MESH:D019966	MESH:D019966	Substance-Related Disorders	CTD_diseases	2
MESH:D019967	MESH:D019967	Schizophrenia and Disorders with Psychotic Features	CTD_diseases	2
MESH:D019968	MESH:D019968	Sexual and Gender Disorders	CTD_diseases	2
MESH:D020178	MESH:D020178	Sleep Disorders, Circadian Rhythm	CTD_diseases	2
MESH:D020196	MESH:D020196	Trauma, Nervous System	CTD_diseases	2
MESH:D020255	MESH:D020255	Vitreous Detachment	CTD_diseases	2
MESH:D020258	MESH:D020258	Neurotoxicity Syndromes	CTD_diseases	2
MESH:D020274	MESH:D020274	Autoimmune Diseases of the Nervous System	CTD_diseases	2
MESH:D020752	MESH:D020752	Neurocutaneous Syndromes	CTD_diseases	2
MESH:D020763	MESH:D020763	Pathological Conditions, Anatomical	CTD_diseases	2
MESH:D020805	MESH:D020805	Central Nervous System Viral Diseases	CTD_diseases	2
MESH:D020807	MESH:D020807	Central Nervous System Parasitic Infections	CTD_diseases	2
MESH:D021081	MESH:D021081	Chronobiology Disorders	CTD_diseases	2
MESH:D022125	MESH:D022125	Lacerations	CTD_diseases	2
MESH:D025981	MESH:D025981	Hip Injuries	CTD_diseases	2
MESH:D029021	MESH:D029021	Peste-des-Petits-Ruminants	CTD_diseases	2
MESH:D030342	MESH:D030342	Genetic Diseases, Inborn	CTD_diseases	2
MESH:D034081	MESH:D034081	Wasting Disease, Chronic	CTD_diseases	2
MESH:D047489	MESH:D047489	Preconception Injuries	CTD_diseases	2
MESH:D050723	MESH:D050723	Fractures, Bone	CTD_diseases	2
MESH:D050724	MESH:D050724	Fractures, Cartilage	CTD_diseases	2
MESH:D050738	MESH:D050738	Mesomycetozoea Infections	CTD_diseases	2
MESH:D052776	MESH:D052776	Female Urogenital Diseases	CTD_diseases	2
MESH:D053421	MESH:D053421	Hand-Arm Vibration Syndrome	CTD_diseases	2
MESH:D053489	MESH:D053489	Mink Viral Enteritis	CTD_diseases	2
MESH:D053821	MESH:D053821	Cardiovascular Infections	CTD_diseases	2
MESH:D054019	MESH:D054019	Immune Reconstitution Inflammatory Syndrome	CTD_diseases	2
MESH:D054243	MESH:D054243	Vesicular Stomatitis	CTD_diseases	2
MESH:D055952	MESH:D055952	Cogan Syndrome	CTD_diseases	2
MESH:D056886	MESH:D056886	Contrecoup Injury	CTD_diseases	2
MESH:D057772	MESH:D057772	Vascular System Injuries	CTD_diseases	2
MESH:D058066	MESH:D058066	Digital Dermatitis	CTD_diseases	2
MESH:D058968	MESH:D058968	Pythiosis	CTD_diseases	2
MESH:D059366	MESH:D059366	Asthma, Occupational	CTD_diseases	2
MESH:D059952	MESH:D059952	Pelvic Floor Disorders	CTD_diseases	2
MESH:D060051	MESH:D060051	Occupational Injuries	CTD_diseases	2
MESH:D060085	MESH:D060085	Coinfection	CTD_diseases	2
MESH:D061270	MESH:D061270	Nasal Septal Perforation	CTD_diseases	2
MESH:D064420	MESH:D064420	Drug-Related Side Effects and Adverse Reactions	CTD_diseases	2
OMIM:146820	OMIM:146820	IMMUNE RESPONSE TO SYNTHETIC POLYPEPTIDE--IRGAT	CTD_diseases	2
OMIM:146850	OMIM:146850	IMMUNE SUPPRESSION	CTD_diseases	2
OMIM:211750	OMIM:211750	C SYNDROME	CTD_diseases	2
OMIM:600955	OMIM:600955	PROPROTEIN CONVERTASE 1/3 DEFICIENCY	CTD_diseases	2
MESH:D012874	MESH:D012874	Skin Diseases, Infectious	CTD_diseases	3
MESH:D012875	MESH:D012875	Skin Diseases, Metabolic	CTD_diseases	3
MESH:D012877	MESH:D012877	Skin Manifestations	CTD_diseases	3
MESH:D012878	MESH:D012878	Skin Neoplasms	CTD_diseases	3
MESH:D012883	MESH:D012883	Skin Ulcer	CTD_diseases	3
MESH:D012887	MESH:D012887	Skull Fractures	CTD_diseases	3
MESH:D012983	MESH:D012983	Soft Tissue Neoplasms	CTD_diseases	3
MESH:D013086	MESH:D013086	Spermatic Cord Torsion	CTD_diseases	3
MESH:D013088	MESH:D013088	Spermatocele	CTD_diseases	3
MESH:D013118	MESH:D013118	Spinal Cord Diseases	CTD_diseases	3
MESH:D013122	MESH:D013122	Spinal Diseases	CTD_diseases	3
MESH:D013145	MESH:D013145	Spirochaetales Infections	CTD_diseases	3
MESH:D013158	MESH:D013158	Splenic Diseases	CTD_diseases	3
MESH:D013159	MESH:D013159	Splenic Infarction	CTD_diseases	3
MESH:D013160	MESH:D013160	Splenic Neoplasms	CTD_diseases	3
MESH:D013161	MESH:D013161	Splenic Rupture	CTD_diseases	3
MESH:D013272	MESH:D013272	Stomach Diseases	CTD_diseases	3
MESH:D013275	MESH:D013275	Stomach Rupture	CTD_diseases	3
MESH:D013280	MESH:D013280	Stomatitis	CTD_diseases	3
MESH:D013319	MESH:D013319	Strongyle Infections, Equine	CTD_diseases	3
MESH:D013344	MESH:D013344	Subacute Sclerosing Panencephalitis	CTD_diseases	3
MESH:D013375	MESH:D013375	Substance Withdrawal Syndrome	CTD_diseases	3
MESH:D013436	MESH:D013436	Sulfhemoglobinemia	CTD_diseases	3
MESH:D013471	MESH:D013471	Sunburn	CTD_diseases	3
MESH:D013479	MESH:D013479	Superior Vena Cava Syndrome	CTD_diseases	3
MESH:D013492	MESH:D013492	Suppuration	CTD_diseases	3
MESH:D013540	MESH:D013540	Swayback	CTD_diseases	3
MESH:D013543	MESH:D013543	Sweat Gland Diseases	CTD_diseases	3
MESH:D013547	MESH:D013547	Sweating, Gustatory	CTD_diseases	3
MESH:D013554	MESH:D013554	Swine Erysipelas	CTD_diseases	3
MESH:D013555	MESH:D013555	Swine Vesicular Disease	CTD_diseases	3
MESH:D013585	MESH:D013585	Synovitis	CTD_diseases	3
MESH:D013590	MESH:D013590	Syphilis, Congenital	CTD_diseases	3
MESH:D013684	MESH:D013684	Telangiectasis	CTD_diseases	3
MESH:D013733	MESH:D013733	Testicular Diseases	CTD_diseases	3
MESH:D013796	MESH:D013796	Thanatophoric Dysplasia	CTD_diseases	3
MESH:D013801	MESH:D013801	Theileriasis	CTD_diseases	3
MESH:D013899	MESH:D013899	Thoracic Neoplasms	CTD_diseases	3
MESH:D013901	MESH:D013901	Thoracic Outlet Syndrome	CTD_diseases	3
MESH:D013952	MESH:D013952	Thymus Hyperplasia	CTD_diseases	3
MESH:D013953	MESH:D013953	Thymus Neoplasms	CTD_diseases	3
MESH:D013964	MESH:D013964	Thyroid Neoplasms	CTD_diseases	3
MESH:D013966	MESH:D013966	Thyroiditis	CTD_diseases	3
MESH:D013967	MESH:D013967	Thyroiditis, Autoimmune	CTD_diseases	3
MESH:D013971	MESH:D013971	Thyrotoxicosis	CTD_diseases	3
MESH:D013978	MESH:D013978	Tibial Fractures	CTD_diseases	3
MESH:D013981	MESH:D013981	Tic Disorders	CTD_diseases	3
MESH:D014029	MESH:D014029	Tobacco Use Disorder	CTD_diseases	3
MESH:D014036	MESH:D014036	Togaviridae Infections	CTD_diseases	3
MESH:D014060	MESH:D014060	Tongue Diseases	CTD_diseases	3
MESH:D014071	MESH:D014071	Tooth Abnormalities	CTD_diseases	3
MESH:D014075	MESH:D014075	Tooth Discoloration	CTD_diseases	3
MESH:D014079	MESH:D014079	Tooth Eruption, Ectopic	CTD_diseases	3
MESH:D014091	MESH:D014091	Tooth Resorption	CTD_diseases	3
MESH:D014095	MESH:D014095	Tooth, Impacted	CTD_diseases	3
MESH:D014097	MESH:D014097	Tooth, Unerupted	CTD_diseases	3
MESH:D014098	MESH:D014098	Toothache	CTD_diseases	3
MESH:D014102	MESH:D014102	Torsion Abnormality	CTD_diseases	3
MESH:D014115	MESH:D014115	Toxemia	CTD_diseases	3
MESH:D014125	MESH:D014125	Toxoplasmosis, Congenital	CTD_diseases	3
MESH:D014134	MESH:D014134	Tracheal Neoplasms	CTD_diseases	3
MESH:D014135	MESH:D014135	Tracheal Stenosis	CTD_diseases	3
MESH:D014136	MESH:D014136	Tracheitis	CTD_diseases	3
MESH:D014137	MESH:D014137	Tracheobronchomegaly	CTD_diseases	3
MESH:D014138	MESH:D014138	Tracheoesophageal Fistula	CTD_diseases	3
MESH:D014141	MESH:D014141	Trachoma	CTD_diseases	3
MESH:D014201	MESH:D014201	Trematode Infections	CTD_diseases	3
MESH:D014245	MESH:D014245	Trichomonas Infections	CTD_diseases	3
MESH:D014256	MESH:D014256	Trichotillomania	CTD_diseases	3
MESH:D014354	MESH:D014354	Trypanosomiasis, Bovine	CTD_diseases	3
MESH:D014379	MESH:D014379	Tuberculosis, Avian	CTD_diseases	3
MESH:D014380	MESH:D014380	Tuberculosis, Bovine	CTD_diseases	3
MESH:D014385	MESH:D014385	Tuberculosis, Gastrointestinal	CTD_diseases	3
MESH:D014386	MESH:D014386	Tuberculosis, Hepatic	CTD_diseases	3
MESH:D014387	MESH:D014387	Tuberculosis, Laryngeal	CTD_diseases	3
MESH:D014388	MESH:D014388	Tuberculosis, Lymph Node	CTD_diseases	3
MESH:D014389	MESH:D014389	Tuberculosis, Male Genital	CTD_diseases	3
MESH:D014393	MESH:D014393	Tuberculosis, Oral	CTD_diseases	3
MESH:D014396	MESH:D014396	Tuberculosis, Pleural	CTD_diseases	3
MESH:D014397	MESH:D014397	Tuberculosis, Pulmonary	CTD_diseases	3
MESH:D014402	MESH:D014402	Tuberous Sclerosis	CTD_diseases	3
MESH:D014456	MESH:D014456	Ulcer	CTD_diseases	3
MESH:D014458	MESH:D014458	Ulna Fractures	CTD_diseases	3
MESH:D014552	MESH:D014552	Urinary Tract Infections	CTD_diseases	3
MESH:D014597	MESH:D014597	Uterine Rupture	CTD_diseases	3
MESH:D014604	MESH:D014604	Uveal Neoplasms	CTD_diseases	3
MESH:D014605	MESH:D014605	Uveitis	CTD_diseases	3
MESH:D014646	MESH:D014646	Varicocele	CTD_diseases	3
MESH:D014648	MESH:D014648	Varicose Veins	CTD_diseases	3
MESH:D014657	MESH:D014657	Vasculitis	CTD_diseases	3
MESH:D014681	MESH:D014681	Velopharyngeal Insufficiency	CTD_diseases	3
MESH:D014689	MESH:D014689	Venous Insufficiency	CTD_diseases	3
MESH:D014694	MESH:D014694	Ventricular Outflow Obstruction	CTD_diseases	3
MESH:D014720	MESH:D014720	Vesicular Exanthema of Swine	CTD_diseases	3
MESH:D014770	MESH:D014770	Virilism	CTD_diseases	3
MESH:D014782	MESH:D014782	Visceral Prolapse	CTD_diseases	3
MESH:D014826	MESH:D014826	Vocal Cord Paralysis	CTD_diseases	3
MESH:D014832	MESH:D014832	Voice Disorders	CTD_diseases	3
MESH:D014869	MESH:D014869	Water Intoxication	CTD_diseases	3
MESH:D014883	MESH:D014883	Water-Electrolyte Imbalance	CTD_diseases	3
MESH:D014898	MESH:D014898	Werner Syndrome	CTD_diseases	3
MESH:D014911	MESH:D014911	Whiplash Injuries	CTD_diseases	3
MESH:D014912	MESH:D014912	White Muscle Disease	CTD_diseases	3
MESH:D014923	MESH:D014923	Wiskott-Aldrich Syndrome	CTD_diseases	3
MESH:D014924	MESH:D014924	Wissler's Syndrome	CTD_diseases	3
MESH:D014948	MESH:D014948	Wounds, Gunshot	CTD_diseases	3
MESH:D014951	MESH:D014951	Wounds, Stab	CTD_diseases	3
MESH:D014954	MESH:D014954	Wrist Injuries	CTD_diseases	3
MESH:D014972	MESH:D014972	Xanthogranuloma, Juvenile	CTD_diseases	3
MESH:D014983	MESH:D014983	Xeroderma Pigmentosum	CTD_diseases	3
MESH:D014985	MESH:D014985	Xerophthalmia	CTD_diseases	3
MESH:D015004	MESH:D015004	Yellow Fever	CTD_diseases	3
MESH:D015168	MESH:D015168	Lightning Injuries	CTD_diseases	3
MESH:D015211	MESH:D015211	Zellweger Syndrome	CTD_diseases	3
MESH:D015223	MESH:D015223	Wolman Disease	CTD_diseases	3
MESH:D015231	MESH:D015231	Sexually Transmitted Diseases, Bacterial	CTD_diseases	3
MESH:D015352	MESH:D015352	Dry Eye Syndromes	CTD_diseases	3
MESH:D015356	MESH:D015356	Retinal Artery Occlusion	CTD_diseases	3
MESH:D015362	MESH:D015362	Child Nutrition Disorders	CTD_diseases	3
MESH:D015423	MESH:D015423	Scleritis	CTD_diseases	3
MESH:D015427	MESH:D015427	Reperfusion Injury	CTD_diseases	3
MESH:D015433	MESH:D015433	Glomerulonephritis, Membranous	CTD_diseases	3
MESH:D015434	MESH:D015434	Panniculitis	CTD_diseases	3
MESH:D015436	MESH:D015436	Panniculitis, Peritoneal	CTD_diseases	3
MESH:D015508	MESH:D015508	Nasal Obstruction	CTD_diseases	3
MESH:D015576	MESH:D015576	Hyperostosis	CTD_diseases	3
MESH:D015614	MESH:D015614	Histiocytosis	CTD_diseases	3
MESH:D015615	MESH:D015615	Cystic Adenomatoid Malformation of Lung, Congenital	CTD_diseases	3
MESH:D015620	MESH:D015620	Histiocytic Disorders, Malignant	CTD_diseases	3
MESH:D015624	MESH:D015624	Lambert-Eaton Myasthenic Syndrome	CTD_diseases	3
MESH:D015651	MESH:D015651	Mycotoxicosis	CTD_diseases	3
MESH:D015658	MESH:D015658	HIV Infections	CTD_diseases	3
MESH:D015715	MESH:D015715	Corneal Edema	CTD_diseases	3
MESH:D015775	MESH:D015775	Fractures, Stress	CTD_diseases	3
MESH:D015792	MESH:D015792	Retinal Dysplasia	CTD_diseases	3
MESH:D015807	MESH:D015807	Eye Injuries, Penetrating	CTD_diseases	3
MESH:D015818	MESH:D015818	Eye Infections, Bacterial	CTD_diseases	3
MESH:D015819	MESH:D015819	Substance Abuse, Intravenous	CTD_diseases	3
MESH:D015821	MESH:D015821	Eye Infections, Fungal	CTD_diseases	3
MESH:D015838	MESH:D015838	Chondromatosis, Synovial	CTD_diseases	3
MESH:D015840	MESH:D015840	Oculomotor Nerve Diseases	CTD_diseases	3
MESH:D015841	MESH:D015841	Enophthalmos	CTD_diseases	3
MESH:D015858	MESH:D015858	Anisometropia	CTD_diseases	3
MESH:D015861	MESH:D015861	Retinal Neovascularization	CTD_diseases	3
MESH:D015862	MESH:D015862	Choroid Diseases	CTD_diseases	3
MESH:D016097	MESH:D016097	Simian Acquired Immunodeficiency Syndrome	CTD_diseases	3
MESH:D016103	MESH:D016103	Spinal Fractures	CTD_diseases	3
MESH:D016104	MESH:D016104	Oligohydramnios	CTD_diseases	3
MESH:D016155	MESH:D016155	Oral Fistula	CTD_diseases	3
MESH:D016157	MESH:D016157	Vascular Fistula	CTD_diseases	3
MESH:D016181	MESH:D016181	Feline Acquired Immunodeficiency Syndrome	CTD_diseases	3
MESH:D016182	MESH:D016182	Visna	CTD_diseases	3
MESH:D016183	MESH:D016183	Murine Acquired Immunodeficiency Syndrome	CTD_diseases	3
MESH:D016262	MESH:D016262	Postpoliomyelitis Syndrome	CTD_diseases	3
MESH:D016388	MESH:D016388	Tooth Loss	CTD_diseases	3
MESH:D016459	MESH:D016459	Prosthesis-Related Infections	CTD_diseases	3
MESH:D016469	MESH:D016469	Fungemia	CTD_diseases	3
MESH:D016470	MESH:D016470	Bacteremia	CTD_diseases	3
MESH:D016472	MESH:D016472	Motor Neuron Disease	CTD_diseases	3
MESH:D016489	MESH:D016489	Head Injuries, Closed	CTD_diseases	3
MESH:D016491	MESH:D016491	Peripheral Vascular Diseases	CTD_diseases	3
MESH:D016510	MESH:D016510	Corneal Neovascularization	CTD_diseases	3
MESH:D016511	MESH:D016511	Severe Combined Immunodeficiency	CTD_diseases	3
MESH:D016512	MESH:D016512	Ankle Injuries	CTD_diseases	3
MESH:D016534	MESH:D016534	Cardiac Output, High	CTD_diseases	3
MESH:D016535	MESH:D016535	Bronchial Hyperreactivity	CTD_diseases	3
MESH:D016553	MESH:D016553	Purpura, Thrombocytopenic, Idiopathic	CTD_diseases	3
MESH:D016569	MESH:D016569	Blepharophimosis	CTD_diseases	3
MESH:D016582	MESH:D016582	Leukemia, Feline	CTD_diseases	3
MESH:D016583	MESH:D016583	Enzootic Bovine Leukosis	CTD_diseases	3
MESH:D016584	MESH:D016584	Panic Disorder	CTD_diseases	3
MESH:D016585	MESH:D016585	Vaginosis, Bacterial	CTD_diseases	3
MESH:D016640	MESH:D016640	Diabetes, Gestational	CTD_diseases	3
MESH:D016643	MESH:D016643	Encephalopathy, Bovine Spongiform	CTD_diseases	3
MESH:D016697	MESH:D016697	Herpes Zoster Oticus	CTD_diseases	3
MESH:D016710	MESH:D016710	Yin Deficiency	CTD_diseases	3
MESH:D016711	MESH:D016711	Yang Deficiency	CTD_diseases	3
MESH:D016720	MESH:D016720	Pneumocystis Infections	CTD_diseases	3
MESH:D016724	MESH:D016724	Empyema, Pleural	CTD_diseases	3
MESH:D016726	MESH:D016726	Plasma Cell Granuloma, Pulmonary	CTD_diseases	3
MESH:D016727	MESH:D016727	Orbital Pseudotumor	CTD_diseases	3
MESH:D016736	MESH:D016736	Antiphospholipid Syndrome	CTD_diseases	3
MESH:D016738	MESH:D016738	Alagille Syndrome	CTD_diseases	3
MESH:D016750	MESH:D016750	Stiff-Person Syndrome	CTD_diseases	3
MESH:D016751	MESH:D016751	Hepatitis E	CTD_diseases	3
MESH:D016766	MESH:D016766	Feline Infectious Peritonitis	CTD_diseases	3
MESH:D016769	MESH:D016769	Embolism and Thrombosis	CTD_diseases	3
MESH:D016770	MESH:D016770	Ciliophora Infections	CTD_diseases	3
MESH:D016881	MESH:D016881	Microsporidiosis	CTD_diseases	3
MESH:D016888	MESH:D016888	Angiodysplasia	CTD_diseases	3
MESH:D016905	MESH:D016905	Gram-Negative Bacterial Infections	CTD_diseases	3
MESH:D016908	MESH:D016908	Gram-Positive Bacterial Infections	CTD_diseases	3
MESH:D016916	MESH:D016916	Joint Deformities, Acquired	CTD_diseases	3
MESH:D017001	MESH:D017001	Tooth Demineralization	CTD_diseases	3
MESH:D017042	MESH:D017042	Phenylketonuria, Maternal	CTD_diseases	3
MESH:D017043	MESH:D017043	Chalazion	CTD_diseases	3
MESH:D017044	MESH:D017044	Polycystic Kidney, Autosomal Recessive	CTD_diseases	3
MESH:D017074	MESH:D017074	Common Variable Immunodeficiency	CTD_diseases	3
MESH:D017091	MESH:D017091	Colitis, Ischemic	CTD_diseases	3
MESH:D017094	MESH:D017094	Porphyrias, Hepatic	CTD_diseases	3
MESH:D017096	MESH:D017096	Prion Diseases	CTD_diseases	3
MESH:D017109	MESH:D017109	Akathisia, Drug-Induced	CTD_diseases	3
MESH:D017192	MESH:D017192	Skin Diseases, Bacterial	CTD_diseases	3
MESH:D017202	MESH:D017202	Myocardial Ischemia	CTD_diseases	3
MESH:D017250	MESH:D017250	Caliciviridae Infections	CTD_diseases	3
MESH:D017282	MESH:D017282	Tick-Borne Diseases	CTD_diseases	3
MESH:D017436	MESH:D017436	Kallmann Syndrome	CTD_diseases	3
MESH:D017441	MESH:D017441	Necrobiotic Disorders	CTD_diseases	3
MESH:D017443	MESH:D017443	Skin Diseases, Eczematous	CTD_diseases	3
MESH:D017444	MESH:D017444	Skin Diseases, Papulosquamous	CTD_diseases	3
MESH:D017445	MESH:D017445	Skin Diseases, Vascular	CTD_diseases	3
MESH:D017486	MESH:D017486	Acneiform Eruptions	CTD_diseases	3
MESH:D017520	MESH:D017520	Mucinoses	CTD_diseases	3
MESH:D017562	MESH:D017562	Postcholecystectomy Syndrome	CTD_diseases	3
MESH:D017563	MESH:D017563	Lung Diseases, Interstitial	CTD_diseases	3
MESH:D017564	MESH:D017564	Radiation Pneumonitis	CTD_diseases	3
MESH:D017573	MESH:D017573	Focal Epithelial Hyperplasia	CTD_diseases	3
MESH:D017577	MESH:D017577	Cutaneous Fistula	CTD_diseases	3
MESH:D017590	MESH:D017590	Myelinolysis, Central Pontine	CTD_diseases	3
MESH:D017676	MESH:D017676	Lichen Planus, Oral	CTD_diseases	3
MESH:D017714	MESH:D017714	Community-Acquired Infections	CTD_diseases	3
MESH:D017759	MESH:D017759	Fractures, Malunited	CTD_diseases	3
MESH:D017760	MESH:D017760	Bone Malalignment	CTD_diseases	3
MESH:D018173	MESH:D018173	Circoviridae Infections	CTD_diseases	3
MESH:D018175	MESH:D018175	Birnaviridae Infections	CTD_diseases	3
MESH:D018178	MESH:D018178	Flaviviridae Infections	CTD_diseases	3
MESH:D018190	MESH:D018190	Lymphatic Vessel Tumors	CTD_diseases	3
MESH:D018193	MESH:D018193	Neoplasms, Complex and Mixed	CTD_diseases	3
MESH:D018204	MESH:D018204	Neoplasms, Connective and Soft Tissue	CTD_diseases	3
MESH:D018309	MESH:D018309	Neoplasms, Gonadal Tissue	CTD_diseases	3
MESH:D018326	MESH:D018326	Nevi and Melanomas	CTD_diseases	3
MESH:D018347	MESH:D018347	Hepadnaviridae Infections	CTD_diseases	3
MESH:D018370	MESH:D018370	Leukocyte-Adhesion Deficiency Syndrome	CTD_diseases	3
MESH:D018409	MESH:D018409	Foot Injuries	CTD_diseases	3
MESH:D018410	MESH:D018410	Pneumonia, Bacterial	CTD_diseases	3
MESH:D018420	MESH:D018420	Ape Diseases	CTD_diseases	3
MESH:D018424	MESH:D018424	Cholesteatoma, Middle Ear	CTD_diseases	3
MESH:D018460	MESH:D018460	Fractures, Comminuted	CTD_diseases	3
MESH:D018461	MESH:D018461	Soft Tissue Infections	CTD_diseases	3
MESH:D018701	MESH:D018701	Mononegavirales Infections	CTD_diseases	3
MESH:D018754	MESH:D018754	Ventricular Dysfunction	CTD_diseases	3
MESH:D018771	MESH:D018771	Arthralgia	CTD_diseases	3
MESH:D018805	MESH:D018805	Sepsis	CTD_diseases	3
MESH:D018827	MESH:D018827	Carcinoma, Lewis Lung	CTD_diseases	3
MESH:D018883	MESH:D018883	Heat Stroke	CTD_diseases	3
MESH:D018908	MESH:D018908	Muscle Weakness	CTD_diseases	3
MESH:D018917	MESH:D018917	Optic Neuropathy, Ischemic	CTD_diseases	3
MESH:D018934	MESH:D018934	Fournier Gangrene	CTD_diseases	3
MESH:D019043	MESH:D019043	Vascular Neoplasms	CTD_diseases	3
MESH:D019115	MESH:D019115	Fasciitis, Necrotizing	CTD_diseases	3
MESH:D019189	MESH:D019189	Iron Metabolism Disorders	CTD_diseases	3
MESH:D019226	MESH:D019226	Oral Ulcer	CTD_diseases	3
MESH:D019282	MESH:D019282	Wasting Syndrome	CTD_diseases	3
MESH:D019310	MESH:D019310	Pseudolymphoma	CTD_diseases	3
MESH:D019315	MESH:D019315	Retrobulbar Hemorrhage	CTD_diseases	3
MESH:D019318	MESH:D019318	Porcine Reproductive and Respiratory Syndrome	CTD_diseases	3
MESH:D019337	MESH:D019337	Hematologic Neoplasms	CTD_diseases	3
MESH:D019350	MESH:D019350	Astroviridae Infections	CTD_diseases	3
MESH:D019534	MESH:D019534	Shoulder Impingement Syndrome	CTD_diseases	3
MESH:D019559	MESH:D019559	Capillary Leak Syndrome	CTD_diseases	3
MESH:D019568	MESH:D019568	Lung, Hyperlucent	CTD_diseases	3
MESH:D019569	MESH:D019569	Hemifacial Spasm	CTD_diseases	3
MESH:D019572	MESH:D019572	Retinal Neoplasms	CTD_diseases	3
MESH:D019578	MESH:D019578	Multiple System Atrophy	CTD_diseases	3
MESH:D019584	MESH:D019584	Hot Flashes	CTD_diseases	3
MESH:D019588	MESH:D019588	Aging, Premature	CTD_diseases	3
MESH:D019591	MESH:D019591	Pseudophakia	CTD_diseases	3
MESH:D019693	MESH:D019693	Hepatitis, Autoimmune	CTD_diseases	3
MESH:D019773	MESH:D019773	Epiretinal Membrane	CTD_diseases	3
MESH:D019851	MESH:D019851	Thrombophilia	CTD_diseases	3
MESH:D019867	MESH:D019867	Anti-Glomerular Basement Membrane Disease	CTD_diseases	3
MESH:D019896	MESH:D019896	alpha 1-Antitrypsin Deficiency	CTD_diseases	3
MESH:D019956	MESH:D019956	Stereotypic Movement Disorder	CTD_diseases	3
MESH:D019957	MESH:D019957	Motor Skills Disorders	CTD_diseases	3
MESH:D019958	MESH:D019958	Attention Deficit and Disruptive Behavior Disorders	CTD_diseases	3
MESH:D019959	MESH:D019959	Feeding and Eating Disorders of Childhood	CTD_diseases	3
MESH:D019960	MESH:D019960	Elimination Disorders	CTD_diseases	3
MESH:D019962	MESH:D019962	Reactive Attachment Disorder	CTD_diseases	3
MESH:D019969	MESH:D019969	Amphetamine-Related Disorders	CTD_diseases	3
MESH:D019970	MESH:D019970	Cocaine-Related Disorders	CTD_diseases	3
MESH:D019973	MESH:D019973	Alcohol-Related Disorders	CTD_diseases	3
MESH:D020018	MESH:D020018	Sexual Dysfunctions, Psychological	CTD_diseases	3
MESH:D020065	MESH:D020065	Hepatopulmonary Syndrome	CTD_diseases	3
MESH:D020096	MESH:D020096	Zygomycosis	CTD_diseases	3
MESH:D020141	MESH:D020141	Hemostatic Disorders	CTD_diseases	3
MESH:D020149	MESH:D020149	Manganese Poisoning	CTD_diseases	3
MESH:D020150	MESH:D020150	Chorea Gravidarum	CTD_diseases	3
MESH:D020179	MESH:D020179	Jet Lag Syndrome	CTD_diseases	3
MESH:D020197	MESH:D020197	Head Injuries, Penetrating	CTD_diseases	3
MESH:D020209	MESH:D020209	Cranial Nerve Injuries	CTD_diseases	3
MESH:D020211	MESH:D020211	Autonomic Dysreflexia	CTD_diseases	3
MESH:D020214	MESH:D020214	Cerebrovascular Trauma	CTD_diseases	3
MESH:D020230	MESH:D020230	Serotonin Syndrome	CTD_diseases	3
MESH:D020254	MESH:D020254	Tooth Ankylosis	CTD_diseases	3
MESH:D020257	MESH:D020257	Ventricular Remodeling	CTD_diseases	3
MESH:D020261	MESH:D020261	Arsenic Poisoning	CTD_diseases	3
MESH:D020271	MESH:D020271	Heredodegenerative Disorders, Nervous System	CTD_diseases	3
MESH:D020278	MESH:D020278	Demyelinating Autoimmune Diseases, CNS	CTD_diseases	3
MESH:D020279	MESH:D020279	Hereditary Central Nervous System Demyelinating Diseases	CTD_diseases	3
MESH:D020294	MESH:D020294	Myasthenic Syndromes, Congenital	CTD_diseases	3
MESH:D020314	MESH:D020314	Central Nervous System Fungal Infections	CTD_diseases	3
MESH:D020315	MESH:D020315	Latex Hypersensitivity	CTD_diseases	3
MESH:D020330	MESH:D020330	Bell Palsy	CTD_diseases	3
MESH:D020331	MESH:D020331	Mobius Syndrome	CTD_diseases	3
MESH:D020347	MESH:D020347	Lithiasis	CTD_diseases	3
MESH:D020361	MESH:D020361	Paraneoplastic Syndromes, Nervous System	CTD_diseases	3
MESH:D020386	MESH:D020386	Isaacs Syndrome	CTD_diseases	3
MESH:D020417	MESH:D020417	Nystagmus, Congenital	CTD_diseases	3
MESH:D020421	MESH:D020421	Vagus Nerve Diseases	CTD_diseases	3
MESH:D020431	MESH:D020431	Olfactory Nerve Diseases	CTD_diseases	3
MESH:D020432	MESH:D020432	Trochlear Nerve Diseases	CTD_diseases	3
MESH:D020433	MESH:D020433	Trigeminal Nerve Diseases	CTD_diseases	3
MESH:D020434	MESH:D020434	Abducens Nerve Diseases	CTD_diseases	3
MESH:D020435	MESH:D020435	Glossopharyngeal Nerve Diseases	CTD_diseases	3
MESH:D020436	MESH:D020436	Accessory Nerve Diseases	CTD_diseases	3
MESH:D020437	MESH:D020437	Hypoglossal Nerve Diseases	CTD_diseases	3
MESH:D020511	MESH:D020511	Neuromuscular Junction Diseases	CTD_diseases	3
MESH:D020518	MESH:D020518	Focal Nodular Hyperplasia	CTD_diseases	3
MESH:D020758	MESH:D020758	Spinal Cord Vascular Diseases	CTD_diseases	3
MESH:D020806	MESH:D020806	Central Nervous System Bacterial Infections	CTD_diseases	3
MESH:D020808	MESH:D020808	Central Nervous System Protozoal Infections	CTD_diseases	3
MESH:D020857	MESH:D020857	Hallux Limitus	CTD_diseases	3
MESH:D020859	MESH:D020859	Hallux Rigidus	CTD_diseases	3
MESH:D020896	MESH:D020896	Hypovolemia	CTD_diseases	3
MESH:D020918	MESH:D020918	Complex Regional Pain Syndromes	CTD_diseases	3
MESH:D020924	MESH:D020924	Urological Manifestations	CTD_diseases	3
MESH:D020936	MESH:D020936	Epilepsy, Benign Neonatal	CTD_diseases	3
MESH:D020961	MESH:D020961	Lewy Body Disease	CTD_diseases	3
MESH:D020966	MESH:D020966	Muscular Disorders, Atrophic	CTD_diseases	3
MESH:D020969	MESH:D020969	Disease Attributes	CTD_diseases	3
MESH:D022124	MESH:D022124	Hyperammonemia	CTD_diseases	3
MESH:D023341	MESH:D023341	Chills	CTD_diseases	3
MESH:D024741	MESH:D024741	Cardiomyopathy, Hypertrophic, Familial	CTD_diseases	3
MESH:D024801	MESH:D024801	Tauopathies	CTD_diseases	3
MESH:D024821	MESH:D024821	Metabolic Syndrome X	CTD_diseases	3
MESH:D025063	MESH:D025063	Chromosome Disorders	CTD_diseases	3
MESH:D025861	MESH:D025861	Blood Coagulation Disorders, Inherited	CTD_diseases	3
MESH:D027601	MESH:D027601	Polyomavirus Infections	CTD_diseases	3
MESH:D028361	MESH:D028361	Mitochondrial Diseases	CTD_diseases	3
MESH:D029502	MESH:D029502	Anemia, Hypoplastic, Congenital	CTD_diseases	3
MESH:D030243	MESH:D030243	Hemorrhagic Syndrome, Bovine	CTD_diseases	3
MESH:D030341	MESH:D030341	Nidovirales Infections	CTD_diseases	3
MESH:D030361	MESH:D030361	Papillomavirus Infections	CTD_diseases	3
MESH:D031221	MESH:D031221	Knee Dislocation	CTD_diseases	3
MESH:D031222	MESH:D031222	Patellar Dislocation	CTD_diseases	3
MESH:D031300	MESH:D031300	Retinal Vasculitis	CTD_diseases	3
MESH:D031845	MESH:D031845	Hajdu-Cheney Syndrome	CTD_diseases	3
MESH:D031941	MESH:D031941	Hemorrhagic Septicemia, Viral	CTD_diseases	3
MESH:D033461	MESH:D033461	Hyperuricemia	CTD_diseases	3
MESH:D034161	MESH:D034161	Pelvic Infection	CTD_diseases	3
MESH:D034321	MESH:D034321	Hyperamylasemia	CTD_diseases	3
MESH:D036981	MESH:D036981	Fasciitis, Plantar	CTD_diseases	3
MESH:D037061	MESH:D037061	Metatarsalgia	CTD_diseases	3
MESH:D037801	MESH:D037801	Hammer Toe Syndrome	CTD_diseases	3
MESH:D040181	MESH:D040181	Genetic Diseases, X-Linked	CTD_diseases	3
MESH:D040921	MESH:D040921	Stress Disorders, Traumatic	CTD_diseases	3
MESH:D042822	MESH:D042822	Genomic Instability	CTD_diseases	3
MESH:D044148	MESH:D044148	Lymphatic Abnormalities	CTD_diseases	3
MESH:D044342	MESH:D044342	Malnutrition	CTD_diseases	3
MESH:D044343	MESH:D044343	Overnutrition	CTD_diseases	3
MESH:D044882	MESH:D044882	Glucose Metabolism Disorders	CTD_diseases	3
MESH:D044903	MESH:D044903	Congenital Hyperinsulinism	CTD_diseases	3
MESH:D045262	MESH:D045262	Reticulocytosis	CTD_diseases	3
MESH:D045729	MESH:D045729	Pneumonia of Swine, Mycoplasmal	CTD_diseases	3
MESH:D045908	MESH:D045908	Monkeypox	CTD_diseases	3
MESH:D046110	MESH:D046110	Hypertension, Pregnancy-Induced	CTD_diseases	3
MESH:D046548	MESH:D046548	Pubic Symphysis Diastasis	CTD_diseases	3
MESH:D046589	MESH:D046589	CADASIL	CTD_diseases	3
MESH:D046788	MESH:D046788	Patellofemoral Pain Syndrome	CTD_diseases	3
MESH:D048090	MESH:D048090	Bovine Respiratory Disease Complex	CTD_diseases	3
MESH:D048550	MESH:D048550	Hepatic Insufficiency	CTD_diseases	3
MESH:D048968	MESH:D048968	Morning Sickness	CTD_diseases	3
MESH:D049188	MESH:D049188	Prenatal Injuries	CTD_diseases	3
MESH:D049248	MESH:D049248	Decapitation	CTD_diseases	3
MESH:D049292	MESH:D049292	Leukoaraiosis	CTD_diseases	3
MESH:D049914	MESH:D049914	DNA Repair-Deficiency Disorders	CTD_diseases	3
MESH:D050010	MESH:D050010	Hyperthyroxinemia, Familial Dysalbuminemic	CTD_diseases	3
MESH:D050033	MESH:D050033	Thyroid Dysgenesis	CTD_diseases	3
MESH:D050072	MESH:D050072	White Heifer Disease	CTD_diseases	3
MESH:D050174	MESH:D050174	Genetic Diseases, Y-Linked	CTD_diseases	3
MESH:D050488	MESH:D050488	Hallux Varus	CTD_diseases	3
MESH:D050815	MESH:D050815	Fractures, Compression	CTD_diseases	3
MESH:D051261	MESH:D051261	Granulomatosis, Orofacial	CTD_diseases	3
MESH:D051346	MESH:D051346	Mobility Limitation	CTD_diseases	3
MESH:D051516	MESH:D051516	Hemospermia	CTD_diseases	3
MESH:D051556	MESH:D051556	Hyperbilirubinemia, Neonatal	CTD_diseases	3
MESH:D051799	MESH:D051799	Delayed Graft Function	CTD_diseases	3
MESH:D052016	MESH:D052016	Mucositis	CTD_diseases	3
MESH:D052018	MESH:D052018	Bulimia Nervosa	CTD_diseases	3
MESH:D052159	MESH:D052159	Frasier Syndrome	CTD_diseases	3
MESH:D052256	MESH:D052256	Tendinopathy	CTD_diseases	3
MESH:D052439	MESH:D052439	Lipid Metabolism Disorders	CTD_diseases	3
MESH:D052879	MESH:D052879	Subacute Combined Degeneration	CTD_diseases	3
MESH:D053099	MESH:D053099	Azotemia	CTD_diseases	3
MESH:D053120	MESH:D053120	Respiratory Aspiration	CTD_diseases	3
MESH:D053306	MESH:D053306	Hyper-IgM Immunodeficiency Syndrome	CTD_diseases	3
MESH:D053447	MESH:D053447	Channelopathies	CTD_diseases	3
MESH:D053570	MESH:D053570	Porcine Postweaning Multisystemic Wasting Syndrome	CTD_diseases	3
MESH:D053589	MESH:D053589	Nuchal Cord	CTD_diseases	3
MESH:D053716	MESH:D053716	Female Athlete Triad Syndrome	CTD_diseases	3
MESH:D053840	MESH:D053840	Brugada Syndrome	CTD_diseases	3
MESH:D054098	MESH:D054098	Thrombocytopenia, Neonatal Alloimmune	CTD_diseases	3
MESH:D054179	MESH:D054179	Angioedemas, Hereditary	CTD_diseases	3
MESH:D054219	MESH:D054219	Neoplasms, Plasma Cell	CTD_diseases	3
MESH:D054319	MESH:D054319	Marchiafava-Bignami Disease	CTD_diseases	3
MESH:D054508	MESH:D054508	Acute Radiation Syndrome	CTD_diseases	3
MESH:D054517	MESH:D054517	Orbital Cellulitis	CTD_diseases	3
MESH:D054969	MESH:D054969	Primary Dysautonomias	CTD_diseases	3
MESH:D054975	MESH:D054975	Pallister-Hall Syndrome	CTD_diseases	3
MESH:D054989	MESH:D054989	Nephrogenic Fibrosing Dermopathy	CTD_diseases	3
MESH:D055034	MESH:D055034	Osteochondrosis	CTD_diseases	3
MESH:D055089	MESH:D055089	Tracheobronchomalacia	CTD_diseases	3
MESH:D055092	MESH:D055092	Laryngomalacia	CTD_diseases	3
MESH:D055370	MESH:D055370	Lung Injury	CTD_diseases	3
MESH:D055499	MESH:D055499	Catheter-Related Infections	CTD_diseases	3
MESH:D055535	MESH:D055535	Morgellons Disease	CTD_diseases	3
MESH:D055622	MESH:D055622	Orbital Myositis	CTD_diseases	3
MESH:D055623	MESH:D055623	Keratosis, Actinic	CTD_diseases	3
MESH:D055761	MESH:D055761	Reticuloendotheliosis, Avian	CTD_diseases	3
MESH:D055947	MESH:D055947	Loeys-Dietz Syndrome	CTD_diseases	3
MESH:D055954	MESH:D055954	Corneal Endothelial Cell Loss	CTD_diseases	3
MESH:D055955	MESH:D055955	Susac Syndrome	CTD_diseases	3
MESH:D056146	MESH:D056146	Corpse Dismemberment	CTD_diseases	3
MESH:D056151	MESH:D056151	Airway Remodeling	CTD_diseases	3
MESH:D056304	MESH:D056304	Genu Valgum	CTD_diseases	3
MESH:D056305	MESH:D056305	Genu Varum	CTD_diseases	3
MESH:D056486	MESH:D056486	Drug-Induced Liver Injury	CTD_diseases	3
MESH:D056586	MESH:D056586	Acute Chest Syndrome	CTD_diseases	3
MESH:D056627	MESH:D056627	Peritoneal Fibrosis	CTD_diseases	3
MESH:D056648	MESH:D056648	Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis	CTD_diseases	3
MESH:D056660	MESH:D056660	Hereditary Autoinflammatory Diseases	CTD_diseases	3
MESH:D056684	MESH:D056684	Yellow Nail Syndrome	CTD_diseases	3
MESH:D056685	MESH:D056685	Costello Syndrome	CTD_diseases	3
MESH:D056731	MESH:D056731	Donohue Syndrome	CTD_diseases	3
MESH:D056735	MESH:D056735	Autoimmune Lymphoproliferative Syndrome	CTD_diseases	3
MESH:D056833	MESH:D056833	Central Serous Chorioretinopathy	CTD_diseases	3
MESH:D056846	MESH:D056846	Weill-Marchesani Syndrome	CTD_diseases	3
MESH:D056912	MESH:D056912	Binge-Eating Disorder	CTD_diseases	3
MESH:D056986	MESH:D056986	Euglenozoa Infections	CTD_diseases	3
MESH:D056987	MESH:D056987	Vasoplegia	CTD_diseases	3
MESH:D057045	MESH:D057045	Laryngopharyngeal Reflux	CTD_diseases	3
MESH:D057068	MESH:D057068	Periprosthetic Fractures	CTD_diseases	3
MESH:D057072	MESH:D057072	Intra-Articular Fractures	CTD_diseases	3
MESH:D057085	MESH:D057085	Tooth Wear	CTD_diseases	3
MESH:D057088	MESH:D057088	Anetoderma	CTD_diseases	3
MESH:D057108	MESH:D057108	Corneal Wavefront Aberration	CTD_diseases	3
MESH:D057112	MESH:D057112	Corneal Perforation	CTD_diseases	3
MESH:D057129	MESH:D057129	Iridocorneal Endothelial Syndrome	CTD_diseases	3
MESH:D057130	MESH:D057130	Leber Congenital Amaurosis	CTD_diseases	3
MESH:D057165	MESH:D057165	Proteostasis Deficiencies	CTD_diseases	3
MESH:D057177	MESH:D057177	TDP-43 Proteinopathies	CTD_diseases	3
MESH:D057215	MESH:D057215	Body Dysmorphic Disorders	CTD_diseases	3
MESH:D057667	MESH:D057667	Conducted Energy Weapon Injuries	CTD_diseases	3
MESH:D057831	MESH:D057831	Lemierre Syndrome	CTD_diseases	3
MESH:D057873	MESH:D057873	Peri-Implantitis	CTD_diseases	3
MESH:D057925	MESH:D057925	Femoracetabular Impingement	CTD_diseases	3
MESH:D058088	MESH:D058088	Sarcoglycanopathies	CTD_diseases	3
MESH:D058225	MESH:D058225	Plaque, Amyloid	CTD_diseases	3
MESH:D058226	MESH:D058226	Plaque, Atherosclerotic	CTD_diseases	3
MESH:D058246	MESH:D058246	Prehypertension	CTD_diseases	3
MESH:D058426	MESH:D058426	Neointima	CTD_diseases	3
MESH:D058437	MESH:D058437	Hypertensive Retinopathy	CTD_diseases	3
MESH:D058456	MESH:D058456	Retinal Telangiectasis	CTD_diseases	3
MESH:D058457	MESH:D058457	Trichiasis	CTD_diseases	3
MESH:D058496	MESH:D058496	Smith-Magenis Syndrome	CTD_diseases	3
MESH:D058540	MESH:D058540	Aicardi Syndrome	CTD_diseases	3
MESH:D058545	MESH:D058545	Inhalant Abuse	CTD_diseases	3
MESH:D058568	MESH:D058568	Necrolytic Migratory Erythema	CTD_diseases	3
MESH:D058606	MESH:D058606	Accessory Atrioventricular Bundle	CTD_diseases	3
MESH:D058631	MESH:D058631	Pycnodysostosis	CTD_diseases	3
MESH:D058739	MESH:D058739	Aberrant Crypt Foci	CTD_diseases	3
MESH:D058747	MESH:D058747	CHARGE Syndrome	CTD_diseases	3
MESH:D058866	MESH:D058866	Osteoporotic Fractures	CTD_diseases	3
MESH:D058923	MESH:D058923	Medial Tibial Stress Syndrome	CTD_diseases	3
MESH:D059246	MESH:D059246	Tachypnea	CTD_diseases	3
MESH:D059249	MESH:D059249	Otomycosis	CTD_diseases	3
MESH:D059266	MESH:D059266	Bisphosphonate-Associated Osteonecrosis of the Jaw	CTD_diseases	3
MESH:D059348	MESH:D059348	Peripheral Nerve Injuries	CTD_diseases	3
MESH:D059369	MESH:D059369	Pott Puffy Tumor	CTD_diseases	3
MESH:D059407	MESH:D059407	Pinguecula	CTD_diseases	3
MESH:D059413	MESH:D059413	Intraabdominal Infections	CTD_diseases	3
MESH:D059525	MESH:D059525	Supraglottitis	CTD_diseases	3
MESH:D059545	MESH:D059545	Paraneoplastic Syndromes, Ocular	CTD_diseases	3
MESH:D059606	MESH:D059606	Polydipsia	CTD_diseases	3
MESH:D059608	MESH:D059608	Laryngocele	CTD_diseases	3
MESH:D060437	MESH:D060437	Artificial Lens Implant Migration	CTD_diseases	3
MESH:D060446	MESH:D060446	Phaeohyphomycosis	CTD_diseases	3
MESH:D060486	MESH:D060486	Ophthalmoplegic Migraine	CTD_diseases	3
MESH:D060586	MESH:D060586	Trichosporonosis	CTD_diseases	3
MESH:D060605	MESH:D060605	Hyalohyphomycosis	CTD_diseases	3
MESH:D060737	MESH:D060737	Reproductive Tract Infections	CTD_diseases	3
MESH:D060906	MESH:D060906	Coxa Valga	CTD_diseases	3
MESH:D061085	MESH:D061085	Agenesis of Corpus Callosum	CTD_diseases	3
MESH:D061224	MESH:D061224	Laryngeal Nerve Injuries	CTD_diseases	3
MESH:D062025	MESH:D062025	Organophosphate Poisoning	CTD_diseases	3
MESH:D062027	MESH:D062027	Linear IgA Bullous Dermatosis	CTD_diseases	3
MESH:D062706	MESH:D062706	Prodromal Symptoms	CTD_diseases	3
MESH:D062787	MESH:D062787	Drug Overdose	CTD_diseases	3
MESH:D063130	MESH:D063130	Maternal Death	CTD_diseases	3
MESH:D063192	MESH:D063192	Pregnancy, Heterotopic	CTD_diseases	3
MESH:D063371	MESH:D063371	Myringosclerosis	CTD_diseases	3
MESH:D063726	MESH:D063726	Delusional Parasitosis	CTD_diseases	3
MESH:D064250	MESH:D064250	Hypertriglyceridemic Waist	CTD_diseases	3
MESH:D064386	MESH:D064386	Ankle Fractures	CTD_diseases	3
MESH:D064706	MESH:D064706	Vocal Cord Dysfunction	CTD_diseases	3
MESH:D064752	MESH:D064752	Atrial Remodeling	CTD_diseases	3
MESH:D064793	MESH:D064793	Teratogenesis	CTD_diseases	3
MESH:D064806	MESH:D064806	Dysbiosis	CTD_diseases	3
MESH:D064807	MESH:D064807	Anticholinergic Syndrome	CTD_diseases	3
OMIM:184460	OMIM:184460	STAPES ANKYLOSIS WITH BROAD THUMB AND TOES	CTD_diseases	3
OMIM:193200	OMIM:193200	VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6	CTD_diseases	3
OMIM:208540	OMIM:208540	RENAL-HEPATIC-PANCREATIC DYSPLASIA 1	CTD_diseases	3
OMIM:216950	OMIM:216950	COMPLEMENT COMPONENT C1r/C1s DEFICIENCY	CTD_diseases	3
OMIM:217000	OMIM:217000	COMPLEMENT COMPONENT 2 DEFICIENCY	CTD_diseases	3
OMIM:256600	OMIM:256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A	CTD_diseases	3
OMIM:312550	OMIM:312550	RETINAL DYSPLASIA, PRIMARY	CTD_diseases	3
OMIM:601696	OMIM:601696	NOVELTY SEEKING PERSONALITY TRAIT	CTD_diseases	3
OMIM:606579	OMIM:606579	VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1	CTD_diseases	3
OMIM:606770	OMIM:606770	ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 2	CTD_diseases	3
OMIM:606771	OMIM:606771	ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 3	CTD_diseases	3
OMIM:607426	OMIM:607426	COENZYME Q10 DEFICIENCY, PRIMARY, 1	CTD_diseases	3
OMIM:607836	OMIM:607836	AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 1	CTD_diseases	3
OMIM:608033	OMIM:608033	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3	CTD_diseases	3
OMIM:608391	OMIM:608391	AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 2	CTD_diseases	3
OMIM:608392	OMIM:608392	AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 3	CTD_diseases	3
OMIM:608447	OMIM:608447	CAROTID INTIMAL MEDIAL THICKNESS 2	CTD_diseases	3
OMIM:608852	OMIM:608852	PULMONARY FUNCTION	CTD_diseases	3
OMIM:609400	OMIM:609400	AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 4	CTD_diseases	3
OMIM:609981	OMIM:609981	NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT	CTD_diseases	3
OMIM:610217	OMIM:610217	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B	CTD_diseases	3
OMIM:611040	OMIM:611040	MICROPHTHALMIA, ISOLATED 5	CTD_diseases	3
OMIM:611809	OMIM:611809	BESTROPHINOPATHY, AUTOSOMAL RECESSIVE	CTD_diseases	3
OMIM:611812	OMIM:611812	46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS	CTD_diseases	3
OMIM:612306	OMIM:612306	THYROID-STIMULATING HORMONE LEVEL QUANTITATIVE TRAIT LOCUS 1	CTD_diseases	3
OMIM:612852	OMIM:612852	OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS	CTD_diseases	3
OMIM:613385	OMIM:613385	AUTOIMMUNE DISEASE, SYNDROMIC MULTISYSTEM	CTD_diseases	3
OMIM:613700	OMIM:613700	SUPERNUMERARY DER(22)t(8	CTD_diseases	3
OMIM:614187	OMIM:614187	HYPERTELORISM, PREAURICULAR SINUS, PUNCTAL PITS, AND DEAFNESS	CTD_diseases	3
MESH:C531698	MESH:C531698	Intestinal helminthiasis	CTD_diseases	3
MESH:C531729	MESH:C531729	Autoimmune limbic encephalitis	CTD_diseases	3
MESH:C535283	MESH:C535283	Rambaud Galian syndrome	CTD_diseases	3
MESH:C535286	MESH:C535286	Ramos Arroyo Clark syndrome	CTD_diseases	3
MESH:C535299	MESH:C535299	Autoimmune progesterone dermatitis	CTD_diseases	3
MESH:C535376	MESH:C535376	Dermoids of cornea	CTD_diseases	3
MESH:C535391	MESH:C535391	Asrar Facharzt Haque syndrome	CTD_diseases	3
MESH:C535440	MESH:C535440	Bietti Crystalline Dystrophy	CTD_diseases	3
MESH:C535441	MESH:C535441	Bifid nose	CTD_diseases	3
MESH:C535520	MESH:C535520	Renal cysts and diabetes syndrome	CTD_diseases	3
MESH:C535538	MESH:C535538	Iris hypoplasia and glaucoma	CTD_diseases	3
MESH:C535547	MESH:C535547	Kantaputra Gorlin syndrome	CTD_diseases	3
MESH:C535565	MESH:C535565	Absent breasts and nipples	CTD_diseases	3
MESH:C535600	MESH:C535600	dopamine beta hydroxylase deficiency	CTD_diseases	3
MESH:C535610	MESH:C535610	Akesson syndrome	CTD_diseases	3
MESH:C535617	MESH:C535617	Al Gazali Sabrinathan Nair syndrome	CTD_diseases	3
MESH:C535625	MESH:C535625	Hamano Tsukamoto syndrome	CTD_diseases	3
MESH:C535634	MESH:C535634	Harlequin syndrome	CTD_diseases	3
MESH:C535645	MESH:C535645	Gardner-Diamond syndrome	CTD_diseases	3
MESH:C535684	MESH:C535684	Ring dermoid of cornea	CTD_diseases	3
MESH:C535724	MESH:C535724	Dwarfism stiff joint ocular abnormalities	CTD_diseases	3
MESH:C535768	MESH:C535768	Daentl Towsend Siegel syndrome	CTD_diseases	3
MESH:C535782	MESH:C535782	Spondyloenchondrodysplasia	CTD_diseases	3
MESH:C535784	MESH:C535784	Spondyloepimetaphyseal dysplasia with multiple dislocations	CTD_diseases	3
MESH:C535802	MESH:C535802	Sprengel deformity	CTD_diseases	3
MESH:C535814	MESH:C535814	Neurosarcoidosis	CTD_diseases	3
MESH:C535817	MESH:C535817	Pruritic urticarial papules plaques of pregnancy	CTD_diseases	3
MESH:C535839	MESH:C535839	Pancreatic lipomatosis duodenal stenosis	CTD_diseases	3
MESH:C535854	MESH:C535854	Heavy Metal Toxicity	CTD_diseases	3
MESH:C535866	MESH:C535866	Roifman syndrome	CTD_diseases	3
MESH:C535880	MESH:C535880	Johanson Blizzard syndrome	CTD_diseases	3
MESH:C535894	MESH:C535894	Lichtenstein syndrome	CTD_diseases	3
MESH:C535910	MESH:C535910	Marden-Walker syndrome	CTD_diseases	3
MESH:C535915	MESH:C535915	Cartilage hair hypoplasia like syndrome	CTD_diseases	3
MESH:C535916	MESH:C535916	Cartilage-hair hypoplasia	CTD_diseases	3
MESH:C535929	MESH:C535929	Chitty Hall Webb syndrome	CTD_diseases	3
MESH:C535932	MESH:C535932	Intrahepatic Cholestasis of Pregnancy	CTD_diseases	3
MESH:C535988	MESH:C535988	Davenport Donlan syndrome	CTD_diseases	3
MESH:C536003	MESH:C536003	Accessory pancreas	CTD_diseases	3
MESH:C536004	MESH:C536004	Familial apoceruloplasmin deficiency	CTD_diseases	3
MESH:C536030	MESH:C536030	MASS syndrome	CTD_diseases	3
MESH:C536054	MESH:C536054	Whyte Murphy syndrome	CTD_diseases	3
MESH:C536131	MESH:C536131	Meckel syndrome type 2	CTD_diseases	3
MESH:C536132	MESH:C536132	Meckel syndrome type 3	CTD_diseases	3
MESH:C536133	MESH:C536133	Meckel syndrome type 1	CTD_diseases	3
MESH:C536135	MESH:C536135	Median cleft lip, corpus callosum, lipoma, and skin polyps	CTD_diseases	3
MESH:C536143	MESH:C536143	Neuhauser syndrome	CTD_diseases	3
MESH:C536178	MESH:C536178	Feigenbaum Bergeron Richardson syndrome	CTD_diseases	3
MESH:C536181	MESH:C536181	Ectodermal dysplasia, hypohidrotic, with immune deficiency	CTD_diseases	3
MESH:C536183	MESH:C536183	Ectodermal dysplasia/ skin fragility syndrome	CTD_diseases	3
MESH:C536202	MESH:C536202	Elastosis perforans serpiginosa	CTD_diseases	3
MESH:C536204	MESH:C536204	Elliott Ludman Teebi syndrome	CTD_diseases	3
MESH:C536223	MESH:C536223	Cushing's symphalangism	CTD_diseases	3
MESH:C536229	MESH:C536229	Cyprus facial neuromusculoskeletal syndrome	CTD_diseases	3
MESH:C536265	MESH:C536265	Radiation induced brachial plexopathy	CTD_diseases	3
MESH:C536275	MESH:C536275	Idiopathic basal ganglia calcification 1	CTD_diseases	3
MESH:C536281	MESH:C536281	Idiopathic pulmonary hemosiderosis	CTD_diseases	3
MESH:C536286	MESH:C536286	Immotile cilia syndrome, due to defective radial spokes	CTD_diseases	3
MESH:C536287	MESH:C536287	Immotile cilia syndrome, due to excessively long cilia	CTD_diseases	3
MESH:C536288	MESH:C536288	Thymic aplasia	CTD_diseases	3
MESH:C536289	MESH:C536289	Immunodeficiency without anhidrotic ectodermal dysplasia	CTD_diseases	3
MESH:C536311	MESH:C536311	Patterson Stevenson syndrome	CTD_diseases	3
MESH:C536317	MESH:C536317	PEHO syndrome	CTD_diseases	3
MESH:C536323	MESH:C536323	Pointer syndrome	CTD_diseases	3
MESH:C536330	MESH:C536330	Polycystic liver disease	CTD_diseases	3
MESH:C536344	MESH:C536344	Vertebral fusion posterior lumbosacral blepharoptosis	CTD_diseases	3
MESH:C536376	MESH:C536376	Annular pancreas	CTD_diseases	3
MESH:C536383	MESH:C536383	Eyebrows duplication of, with stretchable skin and syndactyly	CTD_diseases	3
MESH:C536384	MESH:C536384	FACES syndrome	CTD_diseases	3
MESH:C536385	MESH:C536385	Facial ectodermal dysplasia	CTD_diseases	3
MESH:C536420	MESH:C536420	Primrose syndrome	CTD_diseases	3
MESH:C536429	MESH:C536429	Cloverleaf skull micromelia thoracic dysplasia	CTD_diseases	3
MESH:C536430	MESH:C536430	COACH syndrome	CTD_diseases	3
MESH:C536440	MESH:C536440	Corneal hypesthesia, familial	CTD_diseases	3
MESH:C536452	MESH:C536452	Crane-Heise syndrome	CTD_diseases	3
MESH:C536473	MESH:C536473	Upton Young syndrome	CTD_diseases	3
MESH:C536482	MESH:C536482	Hereditary renal agenesis	CTD_diseases	3
MESH:C536499	MESH:C536499	Tetra-amelia with pulmonary hypoplasia	CTD_diseases	3
MESH:C536523	MESH:C536523	Vagina, absence of	CTD_diseases	3
MESH:C536550	MESH:C536550	Tricho-dento-osseous syndrome 1	CTD_diseases	3
MESH:C536576	MESH:C536576	Bork Stender Schmidt syndrome	CTD_diseases	3
MESH:C536577	MESH:C536577	Borrone Di Rocco Crovato syndrome	CTD_diseases	3
MESH:C536629	MESH:C536629	Schimke immunoosseous dysplasia	CTD_diseases	3
MESH:C536635	MESH:C536635	Schlegelberger Grote syndrome	CTD_diseases	3
MESH:C536649	MESH:C536649	Penis agenesis	CTD_diseases	3
MESH:C536654	MESH:C536654	Phosphoenolpyruvate carboxykinase deficiency	CTD_diseases	3
MESH:C536697	MESH:C536697	WHIM syndrome	CTD_diseases	3
MESH:C536714	MESH:C536714	Yorifuji Okuno syndrome	CTD_diseases	3
MESH:C536780	MESH:C536780	T cell immunodeficiency primary	CTD_diseases	3
MESH:C536818	MESH:C536818	Giant mammary hamartoma	CTD_diseases	3
MESH:C536855	MESH:C536855	Fanconi like syndrome	CTD_diseases	3
MESH:C536903	MESH:C536903	Thumb deformity	CTD_diseases	3
MESH:C536908	MESH:C536908	Thyrocerebral-retinal syndrome	CTD_diseases	3
MESH:C536977	MESH:C536977	Tracheobronchopathia osteoplastica	CTD_diseases	3
MESH:C536983	MESH:C536983	Morillo-Cucci Passarge syndrome	CTD_diseases	3
MESH:C536988	MESH:C536988	Motor neuropathy peripheral with dysautonomia	CTD_diseases	3
MESH:C537005	MESH:C537005	Complement component 5 deficiency	CTD_diseases	3
MESH:C537010	MESH:C537010	Kashani Strom Utley syndrome	CTD_diseases	3
MESH:C537019	MESH:C537019	Kennerknecht Vogel syndrome	CTD_diseases	3
MESH:C537025	MESH:C537025	Kotzot-Richter syndrome	CTD_diseases	3
MESH:C537032	MESH:C537032	Laryngo onycho cutaneous syndrome	CTD_diseases	3
MESH:C537065	MESH:C537065	FLOTCH syndrome	CTD_diseases	3
MESH:C537066	MESH:C537066	Flynn Aird syndrome	CTD_diseases	3
MESH:C537071	MESH:C537071	Follicular hamartoma alopecia cystic fibrosis	CTD_diseases	3
MESH:C537083	MESH:C537083	Boylan Dew Greco syndrome	CTD_diseases	3
MESH:C537086	MESH:C537086	Brachydactylous dwarfism Mseleni type	CTD_diseases	3
MESH:C537118	MESH:C537118	Leri pleonosteosis	CTD_diseases	3
MESH:C537137	MESH:C537137	Orstavik Lindemann Solberg syndrome	CTD_diseases	3
MESH:C537158	MESH:C537158	Hypothalamic hamartomas	CTD_diseases	3
MESH:C537159	MESH:C537159	Hypotonia, congenital nystagmus, ataxia and abnormal auditory brainstem response	CTD_diseases	3
MESH:C537163	MESH:C537163	Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcal infections	CTD_diseases	3
MESH:C537226	MESH:C537226	Saito Kuba Tsuruta syndrome	CTD_diseases	3
MESH:C537255	MESH:C537255	Hennekam lymphangiectasia lymphedema syndrome	CTD_diseases	3
MESH:C537257	MESH:C537257	Hepatic venoocclusive disease with immunodeficiency	CTD_diseases	3
MESH:C537302	MESH:C537302	Griscelli syndrome type 2	CTD_diseases	3
MESH:C537305	MESH:C537305	Groll Hirschowitz syndrome	CTD_diseases	3
MESH:C537327	MESH:C537327	SHORT syndrome	CTD_diseases	3
MESH:C537347	MESH:C537347	Mesenteric vascular disease	CTD_diseases	3
MESH:C537362	MESH:C537362	Immunodeficiency syndrome, variable	CTD_diseases	3
MESH:C537371	MESH:C537371	Mullerian aplasia	CTD_diseases	3
MESH:C537395	MESH:C537395	Neuronal intranuclear inclusion disease	CTD_diseases	3
MESH:C537431	MESH:C537431	Arnold Stickler Bourne syndrome	CTD_diseases	3
MESH:C537438	MESH:C537438	Arrhinia	CTD_diseases	3
MESH:C537488	MESH:C537488	Stern Lubinsky Durrie syndrome	CTD_diseases	3
MESH:C537492	MESH:C537492	Stickler syndrome, type 1	CTD_diseases	3
MESH:C537493	MESH:C537493	Stickler syndrome, type 2	CTD_diseases	3
MESH:C537494	MESH:C537494	Stickler syndrome, type 3	CTD_diseases	3
MESH:C537517	MESH:C537517	Plexosarcoma	CTD_diseases	3
MESH:C537523	MESH:C537523	Sclerosing bone dysplasia mental retardation	CTD_diseases	3
MESH:C537554	MESH:C537554	Microgastria limb reduction defect	CTD_diseases	3
MESH:C537575	MESH:C537575	Michelin tire baby syndrome	CTD_diseases	3
MESH:C537603	MESH:C537603	Short stature and locking fingers	CTD_diseases	3
MESH:C537618	MESH:C537618	Krauss Herman Holmes syndrome	CTD_diseases	3
MESH:C537620	MESH:C537620	Growth mental deficiency syndrome of Myhre	CTD_diseases	3
MESH:C537679	MESH:C537679	GEMSS syndrome	CTD_diseases	3
MESH:C537682	MESH:C537682	Geniospasm	CTD_diseases	3
MESH:C537705	MESH:C537705	Kabuki syndrome	CTD_diseases	3
MESH:C537721	MESH:C537721	Macroepiphyseal dysplasia, McAlister Coe type	CTD_diseases	3
MESH:C537725	MESH:C537725	Lung agenesis	CTD_diseases	3
MESH:C537727	MESH:C537727	Lymphangiectasia, pulmonary, congenital	CTD_diseases	3
MESH:C537737	MESH:C537737	Oculomelic amyoplasia	CTD_diseases	3
MESH:C537768	MESH:C537768	Anophthalmia with pulmonary hypoplasia	CTD_diseases	3
MESH:C537772	MESH:C537772	Anotia	CTD_diseases	3
MESH:C537799	MESH:C537799	Gerodermia osteodysplastica	CTD_diseases	3
MESH:C537829	MESH:C537829	Macrophagic myofasciitis	CTD_diseases	3
MESH:C537869	MESH:C537869	Laplane Fontaine Lagardere syndrome	CTD_diseases	3
MESH:C537872	MESH:C537872	Larsen like syndrome, lethal type	CTD_diseases	3
MESH:C537873	MESH:C537873	Larsen syndrome, dominant type	CTD_diseases	3
MESH:C537874	MESH:C537874	Larsen syndrome, recessive type	CTD_diseases	3
MESH:C537875	MESH:C537875	Laryngeal cleft	CTD_diseases	3
MESH:C537889	MESH:C537889	Pfeiffer Palm Teller syndrome	CTD_diseases	3
MESH:C537908	MESH:C537908	Barber Say syndrome	CTD_diseases	3
MESH:C537939	MESH:C537939	Boudhina Yedes Khiari syndrome	CTD_diseases	3
MESH:C537957	MESH:C537957	Acute fatty liver of pregnancy	CTD_diseases	3
MESH:C537965	MESH:C537965	CAMFAK syndrome	CTD_diseases	3
MESH:C538015	MESH:C538015	Ectodermal dysplasia adrenal cyst	CTD_diseases	3
MESH:C538074	MESH:C538074	Curly hair-ankyloblepharon-nail dysplasia syndrome	CTD_diseases	3
MESH:C538109	MESH:C538109	Pancreas agenesis, dorsal	CTD_diseases	3
MESH:C538131	MESH:C538131	Lachiewicz Sibley syndrome	CTD_diseases	3
MESH:C538132	MESH:C538132	Lacrimoauriculodentodigital syndrome	CTD_diseases	3
MESH:C538157	MESH:C538157	Synovitis granulomatous with uveitis and cranial neuropathies	CTD_diseases	3
MESH:C538196	MESH:C538196	Atlanto-Axial Fusion	CTD_diseases	3
MESH:C538206	MESH:C538206	Deal Barratt Dillon syndrome	CTD_diseases	3
MESH:C538220	MESH:C538220	Dermatoleukodystrophy	CTD_diseases	3
MESH:C538270	MESH:C538270	Auriculo-condylar syndrome	CTD_diseases	3
MESH:C538272	MESH:C538272	Ausems Wittebol-Post Hennekam syndrome	CTD_diseases	3
MESH:C538287	MESH:C538287	Cataract microcornea syndrome	CTD_diseases	3
MESH:C538325	MESH:C538325	Ho Kaufman Mcalister syndrome	CTD_diseases	3
MESH:C538344	MESH:C538344	Navajo neurohepatopathy	CTD_diseases	3
MESH:C538399	MESH:C538399	NEMO mutation with immunodeficiency	CTD_diseases	3
MESH:C538458	MESH:C538458	Rapidly progressive glomerulonephritis with pulmonary hemorrhage	CTD_diseases	3
MESH:C548016	MESH:C548016	Hypermanganesemia with Dystonia Polycythemia and Cirrhosis	CTD_diseases	3
MESH:C562378	MESH:C562378	Hepatic Fibrosis, Congenital	CTD_diseases	3
MESH:C562384	MESH:C562384	Branchial Cleft Anomalies	CTD_diseases	3
MESH:C562390	MESH:C562390	Humoral Hypercalcemia Of Malignancy	CTD_diseases	3
MESH:C562400	MESH:C562400	Hyperpigmentation of Eyelids	CTD_diseases	3
MESH:C562405	MESH:C562405	Pulmonary Alveolar Microlithiasis	CTD_diseases	3
MESH:C562407	MESH:C562407	Aplasia of Lacrimal and Salivary Glands	CTD_diseases	3
MESH:C567287	MESH:C567287	Ciliary Dyskinesia, Primary, 10	CTD_diseases	3
MESH:C567307	MESH:C567307	Complement Component 6 Deficiency	CTD_diseases	3
MESH:C567320	MESH:C567320	Bone Fragility with Contractures, Arterial Rupture, and Deafness	CTD_diseases	3
MESH:C567379	MESH:C567379	MYD88 Deficiency	CTD_diseases	3
MESH:C567401	MESH:C567401	Cerebroretinal Microangiopathy with Calcifications and Cysts	CTD_diseases	3
MESH:C567411	MESH:C567411	Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant	CTD_diseases	3
MESH:C567453	MESH:C567453	Riddle Syndrome	CTD_diseases	3
MESH:C567457	MESH:C567457	Immunodeficiency, Gonadal Dysgenesis, And Pulmonary Fibrosis	CTD_diseases	3
MESH:C567517	MESH:C567517	Sex Reversal, Female, With Dysgenesis Of Kidneys, Adrenals, And Lungs	CTD_diseases	3
MESH:C567518	MESH:C567518	Bestrophinopathy	CTD_diseases	3
MESH:C567567	MESH:C567567	Hypoglossia With Situs Inversus	CTD_diseases	3
MESH:C567568	MESH:C567568	Hypoglossia, Isolated	CTD_diseases	3
MESH:C567641	MESH:C567641	Roifman-Chitayat Syndrome	CTD_diseases	3
MESH:C567713	MESH:C567713	Ciliary Dyskinesia, Primary, 13	CTD_diseases	3
MESH:C567763	MESH:C567763	Capillary Malformation Of The Lower Lip, Lymphatic Malformation Of Face And Neck, Asymmetry Of Face 	CTD_diseases	3
MESH:C571911	MESH:C571911	Gastrointestinal anthrax	CTD_diseases	3
MESH:C572568	MESH:C572568	Complement Factor I Deficiency	CTD_diseases	3
MESH:C580013	MESH:C580013	Congenital Hepatic Fibrosis	CTD_diseases	3
MESH:C580083	MESH:C580083	Familial Exudative Vitreoretinopathy	CTD_diseases	3
MESH:C580199	MESH:C580199	Inherited Thyroxine-Binding Globulin Deficiency	CTD_diseases	3
MESH:D000008	MESH:D000008	Abdominal Neoplasms	CTD_diseases	3
MESH:D000014	MESH:D000014	Abnormalities, Drug-Induced	CTD_diseases	3
MESH:D000015	MESH:D000015	Abnormalities, Multiple	CTD_diseases	3
MESH:D000016	MESH:D000016	Abnormalities, Radiation-Induced	CTD_diseases	3
MESH:D000022	MESH:D000022	Abortion, Spontaneous	CTD_diseases	3
MESH:D000051	MESH:D000051	Acantholysis	CTD_diseases	3
MESH:D000137	MESH:D000137	Acid-Base Imbalance	CTD_diseases	3
MESH:D000160	MESH:D000160	Vestibulocochlear Nerve Diseases	CTD_diseases	3
MESH:D000163	MESH:D000163	Acquired Immunodeficiency Syndrome	CTD_diseases	3
MESH:D000224	MESH:D000224	Addison Disease	CTD_diseases	3
MESH:D000257	MESH:D000257	Adenoviridae Infections	CTD_diseases	3
MESH:D000270	MESH:D000270	Adie Syndrome	CTD_diseases	3
MESH:D000303	MESH:D000303	Adrenal Cortex Diseases	CTD_diseases	3
MESH:D000308	MESH:D000308	Adrenocortical Hyperfunction	CTD_diseases	3
MESH:D000309	MESH:D000309	Adrenal Insufficiency	CTD_diseases	3
MESH:D000310	MESH:D000310	Adrenal Gland Neoplasms	CTD_diseases	3
MESH:D000312	MESH:D000312	Adrenal Hyperplasia, Congenital	CTD_diseases	3
MESH:D000341	MESH:D000341	Affective Disorders, Psychotic	CTD_diseases	3
MESH:D000355	MESH:D000355	African Horse Sickness	CTD_diseases	3
MESH:D000357	MESH:D000357	African Swine Fever	CTD_diseases	3
MESH:D000361	MESH:D000361	Agammaglobulinemia	CTD_diseases	3
MESH:D000379	MESH:D000379	Agoraphobia	CTD_diseases	3
MESH:D000386	MESH:D000386	AIDS-Related Complex	CTD_diseases	3
MESH:D000505	MESH:D000505	Alopecia	CTD_diseases	3
MESH:D000532	MESH:D000532	Altitude Sickness	CTD_diseases	3
MESH:D000562	MESH:D000562	Amebiasis	CTD_diseases	3
MESH:D000647	MESH:D000647	Amnesia	CTD_diseases	3
MESH:D000652	MESH:D000652	Amniotic Band Syndrome	CTD_diseases	3
MESH:D000699	MESH:D000699	Pain Insensitivity, Congenital	CTD_diseases	3
MESH:D000740	MESH:D000740	Anemia	CTD_diseases	3
MESH:D000744	MESH:D000744	Anemia, Hemolytic, Autoimmune	CTD_diseases	3
MESH:D000745	MESH:D000745	Anemia, Hemolytic, Congenital	CTD_diseases	3
MESH:D000751	MESH:D000751	Anemia, Neonatal	CTD_diseases	3
MESH:D000783	MESH:D000783	Aneurysm	CTD_diseases	3
MESH:D000785	MESH:D000785	Aneurysm, Infected	CTD_diseases	3
MESH:D000793	MESH:D000793	Angioid Streaks	CTD_diseases	3
MESH:D000796	MESH:D000796	Angiolymphoid Hyperplasia with Eosinophilia	CTD_diseases	3
MESH:D000798	MESH:D000798	Angiomatosis	CTD_diseases	3
MESH:D000799	MESH:D000799	Angioedema	CTD_diseases	3
MESH:D000839	MESH:D000839	Aniseikonia	CTD_diseases	3
MESH:D000844	MESH:D000844	Ankylosis	CTD_diseases	3
MESH:D000856	MESH:D000856	Anorexia Nervosa	CTD_diseases	3
MESH:D000987	MESH:D000987	Antisocial Personality Disorder	CTD_diseases	3
MESH:D001010	MESH:D001010	Anxiety, Separation	CTD_diseases	3
MESH:D001018	MESH:D001018	Aortic Diseases	CTD_diseases	3
MESH:D001019	MESH:D001019	Aortic Rupture	CTD_diseases	3
MESH:D001035	MESH:D001035	Aphakia	CTD_diseases	3
MESH:D001049	MESH:D001049	Apnea	CTD_diseases	3
MESH:D001117	MESH:D001117	Arenaviridae Infections	CTD_diseases	3
MESH:D001129	MESH:D001129	Argyria	CTD_diseases	3
MESH:D001145	MESH:D001145	Arrhythmias, Cardiac	CTD_diseases	3
MESH:D001157	MESH:D001157	Arterial Occlusive Diseases	CTD_diseases	3
MESH:D001165	MESH:D001165	Arteriovenous Malformations	CTD_diseases	3
MESH:D001167	MESH:D001167	Arteritis	CTD_diseases	3
MESH:D001168	MESH:D001168	Arthritis	CTD_diseases	3
MESH:D001170	MESH:D001170	Arthritis, Infectious	CTD_diseases	3
MESH:D001171	MESH:D001171	Arthritis, Juvenile	CTD_diseases	3
MESH:D001172	MESH:D001172	Arthritis, Rheumatoid	CTD_diseases	3
MESH:D001176	MESH:D001176	Arthrogryposis	CTD_diseases	3
MESH:D001177	MESH:D001177	Arthropathy, Neurogenic	CTD_diseases	3
MESH:D001201	MESH:D001201	Ascites	CTD_diseases	3
MESH:D001238	MESH:D001238	Asphyxia Neonatorum	CTD_diseases	3
MESH:D001247	MESH:D001247	Asthenia	CTD_diseases	3
MESH:D001249	MESH:D001249	Asthma	CTD_diseases	3
MESH:D001251	MESH:D001251	Astigmatism	CTD_diseases	3
MESH:D001260	MESH:D001260	Ataxia Telangiectasia	CTD_diseases	3
MESH:D001261	MESH:D001261	Pulmonary Atelectasis	CTD_diseases	3
MESH:D001284	MESH:D001284	Atrophy	CTD_diseases	3
MESH:D001353	MESH:D001353	Avian Leukosis	CTD_diseases	3
MESH:D001357	MESH:D001357	Sarcoma, Avian	CTD_diseases	3
MESH:D001404	MESH:D001404	Babesiosis	CTD_diseases	3
MESH:D001528	MESH:D001528	Behcet Syndrome	CTD_diseases	3
MESH:D001630	MESH:D001630	Bezoars	CTD_diseases	3
MESH:D001649	MESH:D001649	Bile Duct Diseases	CTD_diseases	3
MESH:D001655	MESH:D001655	Bile Reflux	CTD_diseases	3
MESH:D001661	MESH:D001661	Biliary Tract Neoplasms	CTD_diseases	3
MESH:D001753	MESH:D001753	Blast Injuries	CTD_diseases	3
MESH:D001759	MESH:D001759	Blastomycosis	CTD_diseases	3
MESH:D001762	MESH:D001762	Blepharitis	CTD_diseases	3
MESH:D001763	MESH:D001763	Blepharoptosis	CTD_diseases	3
MESH:D001764	MESH:D001764	Blepharospasm	CTD_diseases	3
MESH:D001768	MESH:D001768	Blister	CTD_diseases	3
MESH:D001778	MESH:D001778	Blood Coagulation Disorders	CTD_diseases	3
MESH:D001791	MESH:D001791	Blood Platelet Disorders	CTD_diseases	3
MESH:D001796	MESH:D001796	Blood Protein Disorders	CTD_diseases	3
MESH:D001819	MESH:D001819	Bluetongue	CTD_diseases	3
MESH:D001832	MESH:D001832	Body Temperature Changes	CTD_diseases	3
MESH:D001835	MESH:D001835	Body Weight	CTD_diseases	3
MESH:D001845	MESH:D001845	Bone Cysts	CTD_diseases	3
MESH:D001848	MESH:D001848	Bone Diseases, Developmental	CTD_diseases	3
MESH:D001850	MESH:D001850	Bone Diseases, Infectious	CTD_diseases	3
MESH:D001851	MESH:D001851	Bone Diseases, Metabolic	CTD_diseases	3
MESH:D001855	MESH:D001855	Bone Marrow Diseases	CTD_diseases	3
MESH:D001859	MESH:D001859	Bone Neoplasms	CTD_diseases	3
MESH:D001862	MESH:D001862	Bone Resorption	CTD_diseases	3
MESH:D001882	MESH:D001882	Border Disease	CTD_diseases	3
MESH:D001883	MESH:D001883	Borderline Personality Disorder	CTD_diseases	3
MESH:D001912	MESH:D001912	Bovine Virus Diarrhea-Mucosal Disease	CTD_diseases	3
MESH:D001924	MESH:D001924	Brain Concussion	CTD_diseases	3
MESH:D001927	MESH:D001927	Brain Diseases	CTD_diseases	3
MESH:D001928	MESH:D001928	Brain Diseases, Metabolic	CTD_diseases	3
MESH:D001941	MESH:D001941	Breast Diseases	CTD_diseases	3
MESH:D001943	MESH:D001943	Breast Neoplasms	CTD_diseases	3
MESH:D001983	MESH:D001983	Bronchial Fistula	CTD_diseases	3
MESH:D001984	MESH:D001984	Bronchial Neoplasms	CTD_diseases	3
MESH:D001986	MESH:D001986	Bronchial Spasm	CTD_diseases	3
MESH:D001987	MESH:D001987	Bronchiectasis	CTD_diseases	3
MESH:D001991	MESH:D001991	Bronchitis	CTD_diseases	3
MESH:D001994	MESH:D001994	Bronchogenic Cyst	CTD_diseases	3
MESH:D001996	MESH:D001996	Bronchopneumonia	CTD_diseases	3
MESH:D002007	MESH:D002007	Brucellosis, Bovine	CTD_diseases	3
MESH:D002012	MESH:D002012	Bruxism	CTD_diseases	3
MESH:D002044	MESH:D002044	Bunyaviridae Infections	CTD_diseases	3
MESH:D002054	MESH:D002054	Burning Mouth Syndrome	CTD_diseases	3
MESH:D002057	MESH:D002057	Burns, Chemical	CTD_diseases	3
MESH:D002058	MESH:D002058	Burns, Electric	CTD_diseases	3
MESH:D002059	MESH:D002059	Burns, Inhalation	CTD_diseases	3
MESH:D002062	MESH:D002062	Bursitis	CTD_diseases	3
MESH:D002105	MESH:D002105	Cadmium Poisoning	CTD_diseases	3
MESH:D002128	MESH:D002128	Calcium Metabolism Disorders	CTD_diseases	3
MESH:D002137	MESH:D002137	Calculi	CTD_diseases	3
MESH:D002177	MESH:D002177	Candidiasis	CTD_diseases	3
MESH:D002180	MESH:D002180	Candidiasis, Oral	CTD_diseases	3
MESH:D002189	MESH:D002189	Marijuana Abuse	CTD_diseases	3
MESH:D002194	MESH:D002194	Capgras Syndrome	CTD_diseases	3
MESH:D002252	MESH:D002252	Carbon Tetrachloride Poisoning	CTD_diseases	3
MESH:D002275	MESH:D002275	Carcinoid Heart Disease	CTD_diseases	3
MESH:D002279	MESH:D002279	Carcinoma 256, Walker	CTD_diseases	3
MESH:D002284	MESH:D002284	Carcinoma, Brown-Pearce	CTD_diseases	3
MESH:D002286	MESH:D002286	Carcinoma, Ehrlich Tumor	CTD_diseases	3
MESH:D002287	MESH:D002287	Carcinoma, Krebs 2	CTD_diseases	3
MESH:D002303	MESH:D002303	Cardiac Output, Low	CTD_diseases	3
MESH:D002305	MESH:D002305	Cardiac Tamponade	CTD_diseases	3
MESH:D002386	MESH:D002386	Cataract	CTD_diseases	3
MESH:D002481	MESH:D002481	Cellulitis	CTD_diseases	3
MESH:D002561	MESH:D002561	Cerebrovascular Disorders	CTD_diseases	3
MESH:D002578	MESH:D002578	Uterine Cervical Dysplasia	CTD_diseases	3
MESH:D002590	MESH:D002590	Cestode Infections	CTD_diseases	3
MESH:D002636	MESH:D002636	Cherubism	CTD_diseases	3
MESH:D002639	MESH:D002639	Cheyne-Stokes Respiration	CTD_diseases	3
MESH:D002647	MESH:D002647	Chilblains	CTD_diseases	3
MESH:D002653	MESH:D002653	Child Behavior Disorders	CTD_diseases	3
MESH:D002658	MESH:D002658	Developmental Disabilities	CTD_diseases	3
MESH:D002659	MESH:D002659	Child Development Disorders, Pervasive	CTD_diseases	3
MESH:D002754	MESH:D002754	Choanal Atresia	CTD_diseases	3
MESH:D002769	MESH:D002769	Cholelithiasis	CTD_diseases	3
MESH:D002780	MESH:D002780	Cholestasis, Intrahepatic	CTD_diseases	3
MESH:D002828	MESH:D002828	Choristoma	CTD_diseases	3
MESH:D002869	MESH:D002869	Chromosome Aberrations	CTD_diseases	3
MESH:D002915	MESH:D002915	Chylous Ascites	CTD_diseases	3
MESH:D002916	MESH:D002916	Chylothorax	CTD_diseases	3
MESH:D003047	MESH:D003047	Coccidioidomycosis	CTD_diseases	3
MESH:D003048	MESH:D003048	Coccidiosis	CTD_diseases	3
MESH:D003072	MESH:D003072	Cognition Disorders	CTD_diseases	3
MESH:D003074	MESH:D003074	Solitary Pulmonary Nodule	CTD_diseases	3
MESH:D003095	MESH:D003095	Collagen Diseases	CTD_diseases	3
MESH:D003141	MESH:D003141	Communicable Diseases	CTD_diseases	3
MESH:D003147	MESH:D003147	Communication Disorders	CTD_diseases	3
MESH:D003161	MESH:D003161	Compartment Syndromes	CTD_diseases	3
MESH:D003193	MESH:D003193	Compulsive Personality Disorder	CTD_diseases	3
MESH:D003230	MESH:D003230	Conjunctival Neoplasms	CTD_diseases	3
MESH:D003231	MESH:D003231	Conjunctivitis	CTD_diseases	3
MESH:D003244	MESH:D003244	Consciousness Disorders	CTD_diseases	3
MESH:D003251	MESH:D003251	Constriction, Pathologic	CTD_diseases	3
MESH:D003286	MESH:D003286	Contracture	CTD_diseases	3
MESH:D003291	MESH:D003291	Conversion Disorder	CTD_diseases	3
MESH:D003317	MESH:D003317	Corneal Dystrophies, Hereditary	CTD_diseases	3
MESH:D003318	MESH:D003318	Corneal Opacity	CTD_diseases	3
MESH:D003371	MESH:D003371	Cough	CTD_diseases	3
MESH:D003390	MESH:D003390	Cranial Nerve Neoplasms	CTD_diseases	3
MESH:D003428	MESH:D003428	Cross Infection	CTD_diseases	3
MESH:D003453	MESH:D003453	Cryptococcosis	CTD_diseases	3
MESH:D003483	MESH:D003483	Cutis Laxa	CTD_diseases	3
MESH:D003490	MESH:D003490	Cyanosis	CTD_diseases	3
MESH:D003550	MESH:D003550	Cystic Fibrosis	CTD_diseases	3
MESH:D003607	MESH:D003607	Dacryocystitis	CTD_diseases	3
MESH:D003643	MESH:D003643	Death	CTD_diseases	3
MESH:D003665	MESH:D003665	Decompression Sickness	CTD_diseases	3
MESH:D003680	MESH:D003680	Deglutition Disorders	CTD_diseases	3
MESH:D003681	MESH:D003681	Dehydration	CTD_diseases	3
MESH:D003693	MESH:D003693	Delirium	CTD_diseases	3
MESH:D003699	MESH:D003699	Hepatitis D	CTD_diseases	3
MESH:D003704	MESH:D003704	Dementia	CTD_diseases	3
MESH:D003715	MESH:D003715	Dengue	CTD_diseases	3
MESH:D003741	MESH:D003741	Dental Deposits	CTD_diseases	3
MESH:D003763	MESH:D003763	Dental Leakage	CTD_diseases	3
MESH:D003788	MESH:D003788	Dental Pulp Diseases	CTD_diseases	3
MESH:D003807	MESH:D003807	Dentin Sensitivity	CTD_diseases	3
MESH:D003859	MESH:D003859	Dependent Personality Disorder	CTD_diseases	3
MESH:D003866	MESH:D003866	Depressive Disorder	CTD_diseases	3
MESH:D003872	MESH:D003872	Dermatitis	CTD_diseases	3
MESH:D003874	MESH:D003874	Dermatitis Herpetiformis	CTD_diseases	3
MESH:D003881	MESH:D003881	Dermatomycoses	CTD_diseases	3
MESH:D003882	MESH:D003882	Dermatomyositis	CTD_diseases	3
MESH:D003922	MESH:D003922	Diabetes Mellitus, Type 1	CTD_diseases	3
MESH:D003925	MESH:D003925	Diabetic Angiopathies	CTD_diseases	3
MESH:D003930	MESH:D003930	Diabetic Retinopathy	CTD_diseases	3
MESH:D003966	MESH:D003966	Camurati-Engelmann Syndrome	CTD_diseases	3
MESH:D004030	MESH:D004030	Dientamoebiasis	CTD_diseases	3
MESH:D004108	MESH:D004108	Dilatation, Pathologic	CTD_diseases	3
MESH:D004194	MESH:D004194	Disease	CTD_diseases	3
MESH:D004216	MESH:D004216	Distemper	CTD_diseases	3
MESH:D004240	MESH:D004240	Diverticulum	CTD_diseases	3
MESH:D004342	MESH:D004342	Drug Hypersensitivity	CTD_diseases	3
MESH:D004368	MESH:D004368	Dry Socket	CTD_diseases	3
MESH:D004387	MESH:D004387	Dupuytren Contracture	CTD_diseases	3
MESH:D004406	MESH:D004406	Dysgammaglobulinemia	CTD_diseases	3
MESH:D004409	MESH:D004409	Dyskinesia, Drug-Induced	CTD_diseases	3
MESH:D004411	MESH:D004411	Dyslexia, Acquired	CTD_diseases	3
MESH:D004417	MESH:D004417	Dyspnea	CTD_diseases	3
MESH:D004426	MESH:D004426	Ear Deformities, Acquired	CTD_diseases	3
MESH:D004428	MESH:D004428	Ear Neoplasms	CTD_diseases	3
MESH:D004433	MESH:D004433	Earache	CTD_diseases	3
MESH:D004474	MESH:D004474	Ecthyma, Contagious	CTD_diseases	3
MESH:D004482	MESH:D004482	Ectromelia, Infectious	CTD_diseases	3
MESH:D004483	MESH:D004483	Ectropion	CTD_diseases	3
MESH:D004487	MESH:D004487	Edema	CTD_diseases	3
MESH:D004488	MESH:D004488	Edema Disease of Swine	CTD_diseases	3
MESH:D004646	MESH:D004646	Emphysema	CTD_diseases	3
MESH:D004671	MESH:D004671	Encephalitis, Arbovirus	CTD_diseases	3
MESH:D004679	MESH:D004679	Encephalomyelitis	CTD_diseases	3
MESH:D004682	MESH:D004682	Encephalomyelitis, Enzootic Porcine	CTD_diseases	3
MESH:D004683	MESH:D004683	Encephalomyelitis, Equine	CTD_diseases	3
MESH:D004696	MESH:D004696	Endocarditis	CTD_diseases	3
MESH:D004697	MESH:D004697	Endocarditis, Bacterial	CTD_diseases	3
MESH:D004774	MESH:D004774	Entropion	CTD_diseases	3
MESH:D004803	MESH:D004803	Eosinophilic Granuloma	CTD_diseases	3
MESH:D004810	MESH:D004810	Ephemeral Fever	CTD_diseases	3
MESH:D004818	MESH:D004818	Epidermitis, Exudative, of Swine	CTD_diseases	3
MESH:D004823	MESH:D004823	Epididymitis	CTD_diseases	3
MESH:D004839	MESH:D004839	Epiphyses, Slipped	CTD_diseases	3
MESH:D004844	MESH:D004844	Epistaxis	CTD_diseases	3
MESH:D004859	MESH:D004859	Equine Infectious Anemia	CTD_diseases	3
MESH:D004881	MESH:D004881	Ergotism	CTD_diseases	3
MESH:D004890	MESH:D004890	Erythema	CTD_diseases	3
MESH:D004899	MESH:D004899	Erythroblastosis, Fetal	CTD_diseases	3
MESH:D004919	MESH:D004919	Erythroplasia	CTD_diseases	3
MESH:D004935	MESH:D004935	Esophageal Diseases	CTD_diseases	3
MESH:D005067	MESH:D005067	Euthyroid Sick Syndromes	CTD_diseases	3
MESH:D005076	MESH:D005076	Exanthema	CTD_diseases	3
MESH:D005094	MESH:D005094	Exophthalmos	CTD_diseases	3
MESH:D005126	MESH:D005126	Eye Burns	CTD_diseases	3
MESH:D005129	MESH:D005129	Eye Foreign Bodies	CTD_diseases	3
MESH:D005142	MESH:D005142	Eyelid Neoplasms	CTD_diseases	3
MESH:D005146	MESH:D005146	Facial Asymmetry	CTD_diseases	3
MESH:D005148	MESH:D005148	Facial Dermatoses	CTD_diseases	3
MESH:D005150	MESH:D005150	Facial Hemiatrophy	CTD_diseases	3
MESH:D005155	MESH:D005155	Facial Nerve Diseases	CTD_diseases	3
MESH:D005156	MESH:D005156	Facial Neuralgia	CTD_diseases	3
MESH:D005158	MESH:D005158	Facial Paralysis	CTD_diseases	3
MESH:D005183	MESH:D005183	Failure to Thrive	CTD_diseases	3
MESH:D005203	MESH:D005203	Farmer's Lung	CTD_diseases	3
MESH:D005221	MESH:D005221	Fatigue	CTD_diseases	3
MESH:D005234	MESH:D005234	Fatty Liver	CTD_diseases	3
MESH:D005254	MESH:D005254	Feline Panleukopenia	CTD_diseases	3
MESH:D005262	MESH:D005262	Feminization	CTD_diseases	3
MESH:D005264	MESH:D005264	Femoral Fractures	CTD_diseases	3
MESH:D005313	MESH:D005313	Fetal Death	CTD_diseases	3
MESH:D005316	MESH:D005316	Fetal Distress	CTD_diseases	3
MESH:D005355	MESH:D005355	Fibrosis	CTD_diseases	3
MESH:D005383	MESH:D005383	Finger Injuries	CTD_diseases	3
MESH:D005391	MESH:D005391	Firesetting Behavior	CTD_diseases	3
MESH:D005402	MESH:D005402	Fistula	CTD_diseases	3
MESH:D005409	MESH:D005409	Flail Chest	CTD_diseases	3
MESH:D005413	MESH:D005413	Flatfoot	CTD_diseases	3
MESH:D005458	MESH:D005458	Fluoride Poisoning	CTD_diseases	3
MESH:D005483	MESH:D005483	Flushing	CTD_diseases	3
MESH:D005490	MESH:D005490	Focal Infection	CTD_diseases	3
MESH:D005491	MESH:D005491	Focal Infection, Dental	CTD_diseases	3
MESH:D005517	MESH:D005517	Foodborne Diseases	CTD_diseases	3
MESH:D005531	MESH:D005531	Foot Deformities, Acquired	CTD_diseases	3
MESH:D005532	MESH:D005532	Foot Deformities, Congenital	CTD_diseases	3
MESH:D005543	MESH:D005543	Forearm Injuries	CTD_diseases	3
MESH:D005548	MESH:D005548	Foreign-Body Migration	CTD_diseases	3
MESH:D005549	MESH:D005549	Foreign-Body Reaction	CTD_diseases	3
MESH:D005585	MESH:D005585	Influenza in Birds	CTD_diseases	3
MESH:D005586	MESH:D005586	Fowlpox	CTD_diseases	3
MESH:D005596	MESH:D005596	Fractures, Closed	CTD_diseases	3
MESH:D005597	MESH:D005597	Fractures, Open	CTD_diseases	3
MESH:D005598	MESH:D005598	Fractures, Spontaneous	CTD_diseases	3
MESH:D005599	MESH:D005599	Fractures, Ununited	CTD_diseases	3
MESH:D005611	MESH:D005611	Freemartinism	CTD_diseases	3
MESH:D005667	MESH:D005667	Furunculosis	CTD_diseases	3
MESH:D005705	MESH:D005705	Gallbladder Diseases	CTD_diseases	3
MESH:D005715	MESH:D005715	Gambling	CTD_diseases	3
MESH:D005739	MESH:D005739	Gas Poisoning	CTD_diseases	3
MESH:D005759	MESH:D005759	Gastroenteritis	CTD_diseases	3
MESH:D005761	MESH:D005761	Gastroenteritis, Transmissible, of Swine	CTD_diseases	3
MESH:D005770	MESH:D005770	Gastrointestinal Neoplasms	CTD_diseases	3
MESH:D005831	MESH:D005831	Genital Diseases, Female	CTD_diseases	3
MESH:D005834	MESH:D005834	Genital Neoplasms, Male	CTD_diseases	3
MESH:D005847	MESH:D005847	Geotrichosis	CTD_diseases	3
MESH:D005873	MESH:D005873	Giardiasis	CTD_diseases	3
MESH:D005892	MESH:D005892	Gingivitis, Necrotizing Ulcerative	CTD_diseases	3
MESH:D005896	MESH:D005896	Glanders	CTD_diseases	3
MESH:D005901	MESH:D005901	Glaucoma	CTD_diseases	3
MESH:D005911	MESH:D005911	Gliosis	CTD_diseases	3
MESH:D005922	MESH:D005922	Glomerulonephritis, IGA	CTD_diseases	3
MESH:D006042	MESH:D006042	Goiter	CTD_diseases	3
MESH:D006099	MESH:D006099	Granuloma	CTD_diseases	3
MESH:D006101	MESH:D006101	Granuloma, Giant Cell	CTD_diseases	3
MESH:D006102	MESH:D006102	Granuloma, Laryngeal	CTD_diseases	3
MESH:D006103	MESH:D006103	Granuloma, Lethal Midline	CTD_diseases	3
MESH:D006111	MESH:D006111	Graves Disease	CTD_diseases	3
MESH:D006130	MESH:D006130	Growth Disorders	CTD_diseases	3
MESH:D006201	MESH:D006201	Hair Diseases	CTD_diseases	3
MESH:D006215	MESH:D006215	Hallux Valgus	CTD_diseases	3
MESH:D006223	MESH:D006223	Hamartoma Syndrome, Multiple	CTD_diseases	3
MESH:D006227	MESH:D006227	Hand Deformities, Acquired	CTD_diseases	3
MESH:D006228	MESH:D006228	Hand Deformities, Congenital	CTD_diseases	3
MESH:D006229	MESH:D006229	Hand Dermatoses	CTD_diseases	3
MESH:D006258	MESH:D006258	Head and Neck Neoplasms	CTD_diseases	3
MESH:D006311	MESH:D006311	Hearing Disorders	CTD_diseases	3
MESH:D006322	MESH:D006322	Heart Aneurysm	CTD_diseases	3
MESH:D006323	MESH:D006323	Heart Arrest	CTD_diseases	3
MESH:D006330	MESH:D006330	Heart Defects, Congenital	CTD_diseases	3
MESH:D006332	MESH:D006332	Cardiomegaly	CTD_diseases	3
MESH:D006333	MESH:D006333	Heart Failure	CTD_diseases	3
MESH:D006335	MESH:D006335	Heart Injuries	CTD_diseases	3
MESH:D006337	MESH:D006337	Heart Murmurs	CTD_diseases	3
MESH:D006338	MESH:D006338	Heart Neoplasms	CTD_diseases	3
MESH:D006341	MESH:D006341	Heart Rupture	CTD_diseases	3
MESH:D006349	MESH:D006349	Heart Valve Diseases	CTD_diseases	3
MESH:D006359	MESH:D006359	Heat Exhaustion	CTD_diseases	3
MESH:D006374	MESH:D006374	Helminthiasis, Animal	CTD_diseases	3
MESH:D006395	MESH:D006395	Hemarthrosis	CTD_diseases	3
MESH:D006398	MESH:D006398	Hematocele	CTD_diseases	3
MESH:D006453	MESH:D006453	Hemoglobinopathies	CTD_diseases	3
MESH:D006461	MESH:D006461	Hemolysis	CTD_diseases	3
MESH:D006465	MESH:D006465	Hemoperitoneum	CTD_diseases	3
MESH:D006468	MESH:D006468	Hemopneumothorax	CTD_diseases	3
MESH:D006469	MESH:D006469	Hemoptysis	CTD_diseases	3
MESH:D006470	MESH:D006470	Hemorrhage	CTD_diseases	3
MESH:D006471	MESH:D006471	Gastrointestinal Hemorrhage	CTD_diseases	3
MESH:D006472	MESH:D006472	Oral Hemorrhage	CTD_diseases	3
MESH:D006474	MESH:D006474	Hemorrhagic Disorders	CTD_diseases	3
MESH:D006475	MESH:D006475	Vitamin K Deficiency Bleeding	CTD_diseases	3
MESH:D006482	MESH:D006482	Hemorrhagic Fevers, Viral	CTD_diseases	3
MESH:D006484	MESH:D006484	Hemorrhoids	CTD_diseases	3
MESH:D006491	MESH:D006491	Hemothorax	CTD_diseases	3
MESH:D006502	MESH:D006502	Budd-Chiari Syndrome	CTD_diseases	3
MESH:D006504	MESH:D006504	Hepatic Veno-Occlusive Disease	CTD_diseases	3
MESH:D006505	MESH:D006505	Hepatitis	CTD_diseases	3
MESH:D006522	MESH:D006522	Hepatitis, Infectious Canine	CTD_diseases	3
MESH:D006527	MESH:D006527	Hepatolenticular Degeneration	CTD_diseases	3
MESH:D006529	MESH:D006529	Hepatomegaly	CTD_diseases	3
MESH:D006530	MESH:D006530	Hepatorenal Syndrome	CTD_diseases	3
MESH:D006547	MESH:D006547	Hernia	CTD_diseases	3
MESH:D006549	MESH:D006549	Hernia, Diaphragmatic, Traumatic	CTD_diseases	3
MESH:D006554	MESH:D006554	Hernia, Umbilical	CTD_diseases	3
MESH:D006558	MESH:D006558	Herpes Genitalis	CTD_diseases	3
MESH:D006559	MESH:D006559	Pemphigoid Gestationis	CTD_diseases	3
MESH:D006566	MESH:D006566	Herpesviridae Infections	CTD_diseases	3
MESH:D006617	MESH:D006617	Hip Dislocation	CTD_diseases	3
MESH:D006619	MESH:D006619	Hip Dysplasia, Canine	CTD_diseases	3
MESH:D006620	MESH:D006620	Hip Fractures	CTD_diseases	3
MESH:D006660	MESH:D006660	Histoplasmosis	CTD_diseases	3
MESH:D006677	MESH:D006677	Histrionic Personality Disorder	CTD_diseases	3
MESH:D006685	MESH:D006685	Hoarseness	CTD_diseases	3
MESH:D006691	MESH:D006691	Classical Swine Fever	CTD_diseases	3
MESH:D006712	MESH:D006712	Homocystinuria	CTD_diseases	3
MESH:D006726	MESH:D006726	Hordeolum	CTD_diseases	3
MESH:D006732	MESH:D006732	Horner Syndrome	CTD_diseases	3
MESH:D006800	MESH:D006800	Deltaretrovirus Infections	CTD_diseases	3
MESH:D006810	MESH:D006810	Humeral Fractures	CTD_diseases	3
MESH:D006831	MESH:D006831	Polyhydramnios	CTD_diseases	3
MESH:D006833	MESH:D006833	Hydrarthrosis	CTD_diseases	3
MESH:D006848	MESH:D006848	Testicular Hydrocele	CTD_diseases	3
MESH:D006871	MESH:D006871	Hydrophthalmos	CTD_diseases	3
MESH:D006872	MESH:D006872	Hydropneumothorax	CTD_diseases	3
MESH:D006876	MESH:D006876	Hydrothorax	CTD_diseases	3
MESH:D006932	MESH:D006932	Hyperbilirubinemia	CTD_diseases	3
MESH:D006936	MESH:D006936	Hypercementosis	CTD_diseases	3
MESH:D006940	MESH:D006940	Hyperemia	CTD_diseases	3
MESH:D006942	MESH:D006942	Hypergammaglobulinemia	CTD_diseases	3
MESH:D006956	MESH:D006956	Hyperopia	CTD_diseases	3
MESH:D006958	MESH:D006958	Hyperostosis, Cortical, Congenital	CTD_diseases	3
MESH:D006961	MESH:D006961	Hyperparathyroidism	CTD_diseases	3
MESH:D006965	MESH:D006965	Hyperplasia	CTD_diseases	3
MESH:D006968	MESH:D006968	Hypersensitivity, Delayed	CTD_diseases	3
MESH:D006969	MESH:D006969	Hypersensitivity, Immediate	CTD_diseases	3
MESH:D006973	MESH:D006973	Hypertension	CTD_diseases	3
MESH:D006975	MESH:D006975	Hypertension, Portal	CTD_diseases	3
MESH:D006976	MESH:D006976	Hypertension, Pulmonary	CTD_diseases	3
MESH:D006980	MESH:D006980	Hyperthyroidism	CTD_diseases	3
MESH:D006981	MESH:D006981	Hyperthyroxinemia	CTD_diseases	3
MESH:D006984	MESH:D006984	Hypertrophy	CTD_diseases	3
MESH:D006985	MESH:D006985	Hyperventilation	CTD_diseases	3
MESH:D006986	MESH:D006986	Hypervitaminosis A	CTD_diseases	3
MESH:D006998	MESH:D006998	Hypochondriasis	CTD_diseases	3
MESH:D007006	MESH:D007006	Hypogonadism	CTD_diseases	3
MESH:D007011	MESH:D007011	Hypoparathyroidism	CTD_diseases	3
MESH:D007022	MESH:D007022	Hypotension	CTD_diseases	3
MESH:D007037	MESH:D007037	Hypothyroidism	CTD_diseases	3
MESH:D007057	MESH:D007057	Ichthyosis	CTD_diseases	3
MESH:D007105	MESH:D007105	Immune Complex Diseases	CTD_diseases	3
MESH:D007228	MESH:D007228	Infant Nutrition Disorders	CTD_diseases	3
MESH:D007235	MESH:D007235	Infant, Premature, Diseases	CTD_diseases	3
MESH:D007241	MESH:D007241	Infectious Bovine Rhinotracheitis	CTD_diseases	3
MESH:D007246	MESH:D007246	Infertility	CTD_diseases	3
MESH:D007249	MESH:D007249	Inflammation	CTD_diseases	3
MESH:D007383	MESH:D007383	Intermittent Claudication	CTD_diseases	3
MESH:D007410	MESH:D007410	Intestinal Diseases	CTD_diseases	3
MESH:D007431	MESH:D007431	Intraoperative Complications	CTD_diseases	3
MESH:D007499	MESH:D007499	Iris Diseases	CTD_diseases	3
MESH:D007511	MESH:D007511	Ischemia	CTD_diseases	3
MESH:D007569	MESH:D007569	Jaw Abnormalities	CTD_diseases	3
MESH:D007570	MESH:D007570	Jaw Cysts	CTD_diseases	3
MESH:D007573	MESH:D007573	Jaw Neoplasms	CTD_diseases	3
MESH:D007575	MESH:D007575	Jaw, Edentulous	CTD_diseases	3
MESH:D007593	MESH:D007593	Joint Instability	CTD_diseases	3
MESH:D007594	MESH:D007594	Joint Loose Bodies	CTD_diseases	3
MESH:D007619	MESH:D007619	Kartagener Syndrome	CTD_diseases	3
MESH:D007634	MESH:D007634	Keratitis	CTD_diseases	3
MESH:D007636	MESH:D007636	Keratoacanthoma	CTD_diseases	3
MESH:D007640	MESH:D007640	Keratoconus	CTD_diseases	3
MESH:D007642	MESH:D007642	Keratosis	CTD_diseases	3
MESH:D007718	MESH:D007718	Knee Injuries	CTD_diseases	3
MESH:D007744	MESH:D007744	Obstetric Labor Complications	CTD_diseases	3
MESH:D007759	MESH:D007759	Labyrinth Diseases	CTD_diseases	3
MESH:D007767	MESH:D007767	Lacrimal Duct Obstruction	CTD_diseases	3
MESH:D007819	MESH:D007819	Laryngeal Edema	CTD_diseases	3
MESH:D007822	MESH:D007822	Laryngeal Neoplasms	CTD_diseases	3
MESH:D007827	MESH:D007827	Laryngitis	CTD_diseases	3
MESH:D007829	MESH:D007829	Laryngostenosis	CTD_diseases	3
MESH:D007855	MESH:D007855	Lead Poisoning	CTD_diseases	3
MESH:D007859	MESH:D007859	Learning Disorders	CTD_diseases	3
MESH:D007868	MESH:D007868	Leg Dermatoses	CTD_diseases	3
MESH:D007870	MESH:D007870	Leg Length Inequality	CTD_diseases	3
MESH:D007906	MESH:D007906	Lens Subluxation	CTD_diseases	3
MESH:D007938	MESH:D007938	Leukemia	CTD_diseases	3
MESH:D007942	MESH:D007942	Leukemia, Experimental	CTD_diseases	3
MESH:D007953	MESH:D007953	Leukemia, Radiation-Induced	CTD_diseases	3
MESH:D007960	MESH:D007960	Leukocyte Disorders	CTD_diseases	3
MESH:D007964	MESH:D007964	Leukocytosis	CTD_diseases	3
MESH:D007967	MESH:D007967	Leukoedema, Oral	CTD_diseases	3
MESH:D007968	MESH:D007968	Leukoencephalopathy, Progressive Multifocal	CTD_diseases	3
MESH:D007971	MESH:D007971	Leukoplakia	CTD_diseases	3
MESH:D008047	MESH:D008047	Lip Diseases	CTD_diseases	3
MESH:D008068	MESH:D008068	Lipomatosis	CTD_diseases	3
MESH:D008100	MESH:D008100	Liver Abscess	CTD_diseases	3
MESH:D008103	MESH:D008103	Liver Cirrhosis	CTD_diseases	3
MESH:D008108	MESH:D008108	Liver Diseases, Alcoholic	CTD_diseases	3
MESH:D008113	MESH:D008113	Liver Neoplasms	CTD_diseases	3
MESH:D008114	MESH:D008114	Liver Neoplasms, Experimental	CTD_diseases	3
MESH:D008146	MESH:D008146	Louping Ill	CTD_diseases	3
MESH:D008158	MESH:D008158	Ludwig's Angina	CTD_diseases	3
MESH:D008166	MESH:D008166	Lumpy Skin Disease	CTD_diseases	3
MESH:D008169	MESH:D008169	Lung Abscess	CTD_diseases	3
MESH:D008172	MESH:D008172	Lung Diseases, Fungal	CTD_diseases	3
MESH:D008173	MESH:D008173	Lung Diseases, Obstructive	CTD_diseases	3
MESH:D008175	MESH:D008175	Lung Neoplasms	CTD_diseases	3
MESH:D008178	MESH:D008178	Lupus Erythematosus, Cutaneous	CTD_diseases	3
MESH:D008180	MESH:D008180	Lupus Erythematosus, Systemic	CTD_diseases	3
MESH:D008199	MESH:D008199	Lymphadenitis	CTD_diseases	3
MESH:D008200	MESH:D008200	Lymphangiectasis	CTD_diseases	3
MESH:D008205	MESH:D008205	Lymphangitis	CTD_diseases	3
MESH:D008209	MESH:D008209	Lymphedema	CTD_diseases	3
MESH:D008210	MESH:D008210	Lymphocele	CTD_diseases	3
MESH:D008223	MESH:D008223	Lymphoma	CTD_diseases	3
MESH:D008230	MESH:D008230	Lymphomatoid Granulomatosis	CTD_diseases	3
MESH:D008231	MESH:D008231	Lymphopenia	CTD_diseases	3
MESH:D008232	MESH:D008232	Lymphoproliferative Disorders	CTD_diseases	3
MESH:D008286	MESH:D008286	Malabsorption Syndromes	CTD_diseases	3
MESH:D008287	MESH:D008287	Malacoplakia	CTD_diseases	3
MESH:D008288	MESH:D008288	Malaria	CTD_diseases	3
MESH:D008289	MESH:D008289	Malaria, Avian	CTD_diseases	3
MESH:D008304	MESH:D008304	Malignant Catarrh	CTD_diseases	3
MESH:D008310	MESH:D008310	Malocclusion	CTD_diseases	3
MESH:D008325	MESH:D008325	Mammary Neoplasms, Experimental	CTD_diseases	3
MESH:D008336	MESH:D008336	Mandibular Diseases	CTD_diseases	3
MESH:D008380	MESH:D008380	Marek Disease	CTD_diseases	3
MESH:D008382	MESH:D008382	Marfan Syndrome	CTD_diseases	3
MESH:D008414	MESH:D008414	Mastitis, Bovine	CTD_diseases	3
MESH:D008415	MESH:D008415	Mastocytosis	CTD_diseases	3
MESH:D008439	MESH:D008439	Maxillary Diseases	CTD_diseases	3
MESH:D008471	MESH:D008471	Meconium Aspiration Syndrome	CTD_diseases	3
MESH:D008477	MESH:D008477	Mediastinal Diseases	CTD_diseases	3
MESH:D008546	MESH:D008546	Melanoma, Experimental	CTD_diseases	3
MESH:D008556	MESH:D008556	Melkersson-Rosenthal Syndrome	CTD_diseases	3
MESH:D008581	MESH:D008581	Meningitis	CTD_diseases	3
MESH:D008599	MESH:D008599	Menstruation Disturbances	CTD_diseases	3
MESH:D008607	MESH:D008607	Intellectual Disability	CTD_diseases	3
MESH:D008630	MESH:D008630	Mercury Poisoning	CTD_diseases	3
MESH:D008640	MESH:D008640	Mesenteric Lymphadenitis	CTD_diseases	3
MESH:D008641	MESH:D008641	Mesenteric Vascular Occlusion	CTD_diseases	3
MESH:D008661	MESH:D008661	Metabolism, Inborn Errors	CTD_diseases	3
MESH:D008679	MESH:D008679	Metaplasia	CTD_diseases	3
MESH:D008708	MESH:D008708	Methemoglobinemia	CTD_diseases	3
MESH:D008947	MESH:D008947	Mixed Connective Tissue Disease	CTD_diseases	3
MESH:D008992	MESH:D008992	Monkey Diseases	CTD_diseases	3
MESH:D009008	MESH:D009008	Abnormalities, Severe Teratoid	CTD_diseases	3
MESH:D009041	MESH:D009041	Motion Sickness	CTD_diseases	3
MESH:D009050	MESH:D009050	Fluorosis, Dental	CTD_diseases	3
MESH:D009056	MESH:D009056	Mouth Abnormalities	CTD_diseases	3
MESH:D009058	MESH:D009058	Mouth Breathing	CTD_diseases	3
MESH:D009062	MESH:D009062	Mouth Neoplasms	CTD_diseases	3
MESH:D009066	MESH:D009066	Mouth, Edentulous	CTD_diseases	3
MESH:D009069	MESH:D009069	Movement Disorders	CTD_diseases	3
MESH:D009080	MESH:D009080	Mucocutaneous Lymph Node Syndrome	CTD_diseases	3
MESH:D009105	MESH:D009105	Multiple Personality Disorder	CTD_diseases	3
MESH:D009110	MESH:D009110	Munchausen Syndrome	CTD_diseases	3
MESH:D009134	MESH:D009134	Muscular Atrophy, Spinal	CTD_diseases	3
MESH:D009136	MESH:D009136	Muscular Dystrophies	CTD_diseases	3
MESH:D009155	MESH:D009155	Mutism	CTD_diseases	3
MESH:D009202	MESH:D009202	Cardiomyopathies	CTD_diseases	3
MESH:D009216	MESH:D009216	Myopia	CTD_diseases	3
MESH:D009260	MESH:D009260	Nail Diseases	CTD_diseases	3
MESH:D009261	MESH:D009261	Nail-Patella Syndrome	CTD_diseases	3
MESH:D009264	MESH:D009264	Nails, Malformed	CTD_diseases	3
MESH:D009265	MESH:D009265	Nairobi Sheep Disease	CTD_diseases	3
MESH:D009293	MESH:D009293	Opioid-Related Disorders	CTD_diseases	3
MESH:D009298	MESH:D009298	Nasal Polyps	CTD_diseases	3
MESH:D009302	MESH:D009302	Nasopharyngeal Diseases	CTD_diseases	3
MESH:D009336	MESH:D009336	Necrosis	CTD_diseases	3
MESH:D009349	MESH:D009349	Nematode Infections	CTD_diseases	3
MESH:D009357	MESH:D009357	Neonatal Abstinence Syndrome	CTD_diseases	3
MESH:D009372	MESH:D009372	Neoplasms, Connective Tissue	CTD_diseases	3
MESH:D009373	MESH:D009373	Neoplasms, Germ Cell and Embryonal	CTD_diseases	3
MESH:D009375	MESH:D009375	Neoplasms, Glandular and Epithelial	CTD_diseases	3
MESH:D009377	MESH:D009377	Multiple Endocrine Neoplasia	CTD_diseases	3
MESH:D009380	MESH:D009380	Neoplasms, Nerve Tissue	CTD_diseases	3
MESH:D009383	MESH:D009383	Neoplasms, Vascular Tissue	CTD_diseases	3
MESH:D009384	MESH:D009384	Paraneoplastic Endocrine Syndromes	CTD_diseases	3
MESH:D009410	MESH:D009410	Nerve Degeneration	CTD_diseases	3
MESH:D009440	MESH:D009440	Neurasthenia	CTD_diseases	3
MESH:D009449	MESH:D009449	Neurocirculatory Asthenia	CTD_diseases	3
MESH:D009521	MESH:D009521	Newcastle Disease	CTD_diseases	3
MESH:D009625	MESH:D009625	Noma	CTD_diseases	3
MESH:D009634	MESH:D009634	Noonan Syndrome	CTD_diseases	3
MESH:D009667	MESH:D009667	Nose Deformities, Acquired	CTD_diseases	3
MESH:D009669	MESH:D009669	Nose Neoplasms	CTD_diseases	3
MESH:D009771	MESH:D009771	Obsessive-Compulsive Disorder	CTD_diseases	3
MESH:D009794	MESH:D009794	Ochronosis	CTD_diseases	3
MESH:D009808	MESH:D009808	Odontogenic Tumors	CTD_diseases	3
MESH:D009849	MESH:D009849	Olivopontocerebellar Atrophies	CTD_diseases	3
MESH:D009878	MESH:D009878	Ophthalmia Neonatorum	CTD_diseases	3
MESH:D009879	MESH:D009879	Ophthalmia, Sympathetic	CTD_diseases	3
MESH:D009912	MESH:D009912	Oral Manifestations	CTD_diseases	3
MESH:D009914	MESH:D009914	Oral Submucous Fibrosis	CTD_diseases	3
MESH:D009918	MESH:D009918	Orbital Neoplasms	CTD_diseases	3
MESH:D009976	MESH:D009976	Orthomyxoviridae Infections	CTD_diseases	3
MESH:D009999	MESH:D009999	Ossification, Heterotopic	CTD_diseases	3
MESH:D010000	MESH:D010000	Osteitis	CTD_diseases	3
MESH:D010001	MESH:D010001	Osteitis Deformans	CTD_diseases	3
MESH:D010004	MESH:D010004	Osteoarthropathy, Primary Hypertrophic	CTD_diseases	3
MESH:D010005	MESH:D010005	Osteoarthropathy, Secondary Hypertrophic	CTD_diseases	3
MESH:D010007	MESH:D010007	Osteochondritis	CTD_diseases	3
MESH:D010013	MESH:D010013	Osteogenesis Imperfecta	CTD_diseases	3
MESH:D010020	MESH:D010020	Osteonecrosis	CTD_diseases	3
MESH:D010023	MESH:D010023	Osteopoikilosis	CTD_diseases	3
MESH:D010025	MESH:D010025	Osteoradionecrosis	CTD_diseases	3
MESH:D010031	MESH:D010031	Otitis	CTD_diseases	3
MESH:D010040	MESH:D010040	Otosclerosis	CTD_diseases	3
MESH:D010049	MESH:D010049	Ovarian Diseases	CTD_diseases	3
MESH:D010146	MESH:D010146	Pain	CTD_diseases	3
MESH:D010181	MESH:D010181	Pancreatic Cyst	CTD_diseases	3
MESH:D010185	MESH:D010185	Pancreatic Fistula	CTD_diseases	3
MESH:D010188	MESH:D010188	Exocrine Pancreatic Insufficiency	CTD_diseases	3
MESH:D010190	MESH:D010190	Pancreatic Neoplasms	CTD_diseases	3
MESH:D010195	MESH:D010195	Pancreatitis	CTD_diseases	3
MESH:D010198	MESH:D010198	Pancytopenia	CTD_diseases	3
MESH:D010217	MESH:D010217	Phlebotomus Fever	CTD_diseases	3
MESH:D010229	MESH:D010229	Paracoccidioidomycosis	CTD_diseases	3
MESH:D010254	MESH:D010254	Paranasal Sinus Diseases	CTD_diseases	3
MESH:D010259	MESH:D010259	Paranoid Disorders	CTD_diseases	3
MESH:D010260	MESH:D010260	Paranoid Personality Disorder	CTD_diseases	3
MESH:D010265	MESH:D010265	Paraproteinemias	CTD_diseases	3
MESH:D010282	MESH:D010282	Parathyroid Neoplasms	CTD_diseases	3
MESH:D010300	MESH:D010300	Parkinson Disease	CTD_diseases	3
MESH:D010322	MESH:D010322	Parvoviridae Infections	CTD_diseases	3
MESH:D010324	MESH:D010324	Passive-Aggressive Personality Disorder	CTD_diseases	3
MESH:D010381	MESH:D010381	Pelger-Huet Anomaly	CTD_diseases	3
MESH:D010382	MESH:D010382	Peliosis Hepatis	CTD_diseases	3
MESH:D010386	MESH:D010386	Pelvic Neoplasms	CTD_diseases	3
MESH:D010390	MESH:D010390	Pemphigoid, Benign Mucous Membrane	CTD_diseases	3
MESH:D010391	MESH:D010391	Pemphigoid, Bullous	CTD_diseases	3
MESH:D010392	MESH:D010392	Pemphigus	CTD_diseases	3
MESH:D010409	MESH:D010409	Penile Diseases	CTD_diseases	3
MESH:D010411	MESH:D010411	Penile Induration	CTD_diseases	3
MESH:D010437	MESH:D010437	Peptic Ulcer	CTD_diseases	3
MESH:D010483	MESH:D010483	Periapical Diseases	CTD_diseases	3
MESH:D010490	MESH:D010490	Pericardial Effusion	CTD_diseases	3
MESH:D010493	MESH:D010493	Pericarditis	CTD_diseases	3
MESH:D010510	MESH:D010510	Periodontal Diseases	CTD_diseases	3
MESH:D010523	MESH:D010523	Peripheral Nervous System Diseases	CTD_diseases	3
MESH:D010534	MESH:D010534	Peritoneal Neoplasms	CTD_diseases	3
MESH:D010538	MESH:D010538	Peritonitis	CTD_diseases	3
MESH:D010547	MESH:D010547	Persistent Fetal Circulation Syndrome	CTD_diseases	3
MESH:D010585	MESH:D010585	Phagocyte Bactericidal Dysfunction	CTD_diseases	3
MESH:D010610	MESH:D010610	Pharyngeal Neoplasms	CTD_diseases	3
MESH:D010612	MESH:D010612	Pharyngitis	CTD_diseases	3
MESH:D010623	MESH:D010623	Phencyclidine Abuse	CTD_diseases	3
MESH:D010698	MESH:D010698	Phobic Disorders	CTD_diseases	3
MESH:D010760	MESH:D010760	Phosphorus Metabolism Disorders	CTD_diseases	3
MESH:D010787	MESH:D010787	Photosensitivity Disorders	CTD_diseases	3
MESH:D010842	MESH:D010842	Pica	CTD_diseases	3
MESH:D010850	MESH:D010850	Picornaviridae Infections	CTD_diseases	3
MESH:D010854	MESH:D010854	Piedra	CTD_diseases	3
MESH:D010859	MESH:D010859	Pigmentation Disorders	CTD_diseases	3
MESH:D010922	MESH:D010922	Placenta Diseases	CTD_diseases	3
MESH:D010939	MESH:D010939	Plant Poisoning	CTD_diseases	3
MESH:D010996	MESH:D010996	Pleural Effusion	CTD_diseases	3
MESH:D010997	MESH:D010997	Pleural Neoplasms	CTD_diseases	3
MESH:D010998	MESH:D010998	Pleurisy	CTD_diseases	3
MESH:D011007	MESH:D011007	Pneumocephalus	CTD_diseases	3
MESH:D011014	MESH:D011014	Pneumonia	CTD_diseases	3
MESH:D011021	MESH:D011021	Pneumonia, Progressive Interstitial, of Sheep	CTD_diseases	3
MESH:D011026	MESH:D011026	Pneumopericardium	CTD_diseases	3
MESH:D011027	MESH:D011027	Pneumoperitoneum	CTD_diseases	3
MESH:D011030	MESH:D011030	Pneumothorax	CTD_diseases	3
MESH:D011038	MESH:D011038	Rothmund-Thomson Syndrome	CTD_diseases	3
MESH:D011051	MESH:D011051	Poliomyelitis	CTD_diseases	3
MESH:D011086	MESH:D011086	Polycythemia	CTD_diseases	3
MESH:D011127	MESH:D011127	Polyps	CTD_diseases	3
MESH:D011129	MESH:D011129	Polyradiculoneuropathy	CTD_diseases	3
MESH:D011164	MESH:D011164	Porphyrias	CTD_diseases	3
MESH:D011183	MESH:D011183	Postoperative Complications	CTD_diseases	3
MESH:D011185	MESH:D011185	Postpericardiotomy Syndrome	CTD_diseases	3
MESH:D011201	MESH:D011201	Poultry Diseases	CTD_diseases	3
MESH:D011213	MESH:D011213	Poxviridae Infections	CTD_diseases	3
MESH:D011250	MESH:D011250	Pregnancy Complications, Hematologic	CTD_diseases	3
MESH:D011251	MESH:D011251	Pregnancy Complications, Infectious	CTD_diseases	3
MESH:D011254	MESH:D011254	Pregnancy in Diabetics	CTD_diseases	3
MESH:D011271	MESH:D011271	Pregnancy, Ectopic	CTD_diseases	3
MESH:D011273	MESH:D011273	Pregnancy, Prolonged	CTD_diseases	3
MESH:D011289	MESH:D011289	Preleukemia	CTD_diseases	3
MESH:D011305	MESH:D011305	Presbyopia	CTD_diseases	3
MESH:D011391	MESH:D011391	Prolapse	CTD_diseases	3
MESH:D011469	MESH:D011469	Prostatic Diseases	CTD_diseases	3
MESH:D011529	MESH:D011529	Protozoan Infections, Animal	CTD_diseases	3
MESH:D011536	MESH:D011536	Prurigo	CTD_diseases	3
MESH:D011537	MESH:D011537	Pruritus	CTD_diseases	3
MESH:D011561	MESH:D011561	Pseudoxanthoma Elasticum	CTD_diseases	3
MESH:D011605	MESH:D011605	Psychoses, Substance-Induced	CTD_diseases	3
MESH:D011618	MESH:D011618	Psychotic Disorders	CTD_diseases	3
MESH:D011625	MESH:D011625	Pterygium	CTD_diseases	3
MESH:D011628	MESH:D011628	Puberty, Delayed	CTD_diseases	3
MESH:D011629	MESH:D011629	Puberty, Precocious	CTD_diseases	3
MESH:D011644	MESH:D011644	Puerperal Disorders	CTD_diseases	3
MESH:D011648	MESH:D011648	Pulmonary Adenomatosis, Ovine	CTD_diseases	3
MESH:D011649	MESH:D011649	Pulmonary Alveolar Proteinosis	CTD_diseases	3
MESH:D011654	MESH:D011654	Pulmonary Edema	CTD_diseases	3
MESH:D011655	MESH:D011655	Pulmonary Embolism	CTD_diseases	3
MESH:D011657	MESH:D011657	Pulmonary Eosinophilia	CTD_diseases	3
MESH:D011658	MESH:D011658	Pulmonary Fibrosis	CTD_diseases	3
MESH:D011660	MESH:D011660	Pulmonary Heart Disease	CTD_diseases	3
MESH:D011668	MESH:D011668	Pulmonary Veno-Occlusive Disease	CTD_diseases	3
MESH:D011711	MESH:D011711	Pyoderma	CTD_diseases	3
MESH:D011833	MESH:D011833	Radiation Injuries, Experimental	CTD_diseases	3
MESH:D011855	MESH:D011855	Radiodermatitis	CTD_diseases	3
MESH:D011885	MESH:D011885	Radius Fractures	CTD_diseases	3
MESH:D011900	MESH:D011900	Ranula	CTD_diseases	3
MESH:D012088	MESH:D012088	Reoviridae Infections	CTD_diseases	3
MESH:D012090	MESH:D012090	Cumulative Trauma Disorders	CTD_diseases	3
MESH:D012127	MESH:D012127	Respiratory Distress Syndrome, Newborn	CTD_diseases	3
MESH:D012128	MESH:D012128	Respiratory Distress Syndrome, Adult	CTD_diseases	3
MESH:D012131	MESH:D012131	Respiratory Insufficiency	CTD_diseases	3
MESH:D012162	MESH:D012162	Retinal Degeneration	CTD_diseases	3
MESH:D012163	MESH:D012163	Retinal Detachment	CTD_diseases	3
MESH:D012166	MESH:D012166	Retinal Hemorrhage	CTD_diseases	3
MESH:D012167	MESH:D012167	Retinal Perforations	CTD_diseases	3
MESH:D012170	MESH:D012170	Retinal Vein Occlusion	CTD_diseases	3
MESH:D012173	MESH:D012173	Retinitis	CTD_diseases	3
MESH:D012178	MESH:D012178	Retinopathy of Prematurity	CTD_diseases	3
MESH:D012181	MESH:D012181	Retrocochlear Diseases	CTD_diseases	3
MESH:D012192	MESH:D012192	Retroviridae Infections	CTD_diseases	3
MESH:D012214	MESH:D012214	Rheumatic Heart Disease	CTD_diseases	3
MESH:D012220	MESH:D012220	Rhinitis	CTD_diseases	3
MESH:D012226	MESH:D012226	Rhinoscleroma	CTD_diseases	3
MESH:D012227	MESH:D012227	Rhinosporidiosis	CTD_diseases	3
MESH:D012253	MESH:D012253	Rib Fractures	CTD_diseases	3
MESH:D012295	MESH:D012295	Rift Valley Fever	CTD_diseases	3
MESH:D012393	MESH:D012393	Rosacea	CTD_diseases	3
MESH:D012422	MESH:D012422	Rupture, Spontaneous	CTD_diseases	3
MESH:D012466	MESH:D012466	Salivary Gland Diseases	CTD_diseases	3
MESH:D012513	MESH:D012513	Sarcoma, Experimental	CTD_diseases	3
MESH:D012536	MESH:D012536	Scalp Dermatoses	CTD_diseases	3
MESH:D012557	MESH:D012557	Schizoid Personality Disorder	CTD_diseases	3
MESH:D012559	MESH:D012559	Schizophrenia	CTD_diseases	3
MESH:D012561	MESH:D012561	Schizophrenia, Childhood	CTD_diseases	3
MESH:D012569	MESH:D012569	Schizotypal Personality Disorder	CTD_diseases	3
MESH:D012587	MESH:D012587	Scimitar Syndrome	CTD_diseases	3
MESH:D012592	MESH:D012592	Scleredema Adultorum	CTD_diseases	3
MESH:D012593	MESH:D012593	Sclerema Neonatorum	CTD_diseases	3
MESH:D012594	MESH:D012594	Scleroderma, Localized	CTD_diseases	3
MESH:D012595	MESH:D012595	Scleroderma, Systemic	CTD_diseases	3
MESH:D012598	MESH:D012598	Sclerosis	CTD_diseases	3
MESH:D012608	MESH:D012608	Scrapie	CTD_diseases	3
MESH:D012625	MESH:D012625	Sebaceous Gland Diseases	CTD_diseases	3
MESH:D012734	MESH:D012734	Disorders of Sex Development	CTD_diseases	3
MESH:D012735	MESH:D012735	Sexual Dysfunction, Physiological	CTD_diseases	3
MESH:D012769	MESH:D012769	Shock	CTD_diseases	3
MESH:D012783	MESH:D012783	Shoulder Dislocation	CTD_diseases	3
MESH:D012784	MESH:D012784	Shoulder Fractures	CTD_diseases	3
MESH:D012791	MESH:D012791	Shy-Drager Syndrome	CTD_diseases	3
MESH:D012817	MESH:D012817	Signs and Symptoms, Digestive	CTD_diseases	3
MESH:D012818	MESH:D012818	Signs and Symptoms, Respiratory	CTD_diseases	3
MESH:D012832	MESH:D012832	Silo Filler's Disease	CTD_diseases	3
MESH:D012857	MESH:D012857	Situs Inversus	CTD_diseases	3
MESH:D012868	MESH:D012868	Skin Abnormalities	CTD_diseases	3
MESH:D012872	MESH:D012872	Skin Diseases, Vesiculobullous	CTD_diseases	3
MESH:D012873	MESH:D012873	Skin Diseases, Genetic	CTD_diseases	3
MESH:C562470	MESH:C562470	Interstitial Pneumonitis, Desquamative, Familial	CTD_diseases	3
MESH:C562487	MESH:C562487	Eosinophilic Fasciitis	CTD_diseases	3
MESH:C562564	MESH:C562564	Gallbladder, Agenesis Of	CTD_diseases	3
MESH:C562581	MESH:C562581	Hypercalcemia, Idiopathic, of Infancy	CTD_diseases	3
MESH:C562672	MESH:C562672	Hyperglycinemia, Transient Neonatal	CTD_diseases	3
MESH:C562682	MESH:C562682	Methionine Malabsorption Syndrome	CTD_diseases	3
MESH:C562708	MESH:C562708	Prolactin Deficiency, Isolated	CTD_diseases	3
MESH:C562711	MESH:C562711	Adrenocortical Hypofunction, Chronic Primary Congenital	CTD_diseases	3
MESH:C562717	MESH:C562717	Rh Deficiency Syndrome	CTD_diseases	3
MESH:C562719	MESH:C562719	Tn Syndrome	CTD_diseases	3
MESH:C562733	MESH:C562733	Fundus Albipunctatus	CTD_diseases	3
MESH:C562738	MESH:C562738	Histiocytosis, Familial Lipochrome	CTD_diseases	3
MESH:C562751	MESH:C562751	Epistaxis, Hereditary	CTD_diseases	3
MESH:C562753	MESH:C562753	Nasal Bones, Absence of	CTD_diseases	3
MESH:C562757	MESH:C562757	Ciliary Discoordination Due To Random Ciliary Orientation	CTD_diseases	3
MESH:C562780	MESH:C562780	Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked	CTD_diseases	3
MESH:C562827	MESH:C562827	Alacrima	CTD_diseases	3
MESH:C562856	MESH:C562856	Cerebral Palsy, Ataxic, Autosomal Recessive	CTD_diseases	3
MESH:C562872	MESH:C562872	Tuftsin Deficiency	CTD_diseases	3
MESH:C562909	MESH:C562909	Pseudoatrophoderma Colli	CTD_diseases	3
MESH:C562992	MESH:C562992	Pulmonary Hypoplasia, Primary	CTD_diseases	3
MESH:C563024	MESH:C563024	Spastic Pseudosclerosis	CTD_diseases	3
MESH:C563028	MESH:C563028	Splenic Hypoplasia	CTD_diseases	3
MESH:C563156	MESH:C563156	Brunner Syndrome	CTD_diseases	3
MESH:C563163	MESH:C563163	Stridor, Congenital	CTD_diseases	3
MESH:C563219	MESH:C563219	Fascial Dystrophy, Congenital	CTD_diseases	3
MESH:C563237	MESH:C563237	Cystic Disease Of Lung	CTD_diseases	3
MESH:C563255	MESH:C563255	Microspherophakia	CTD_diseases	3
MESH:C563311	MESH:C563311	Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, NK Cell-Pos	CTD_diseases	3
MESH:C563322	MESH:C563322	Diabetes Mellitus, Transient Neonatal, 1	CTD_diseases	3
MESH:C563345	MESH:C563345	Myelodysplasia, Immunodeficiency, Facial Dysmorphism, Short Stature, and Psychomotor Delay	CTD_diseases	3
MESH:C563375	MESH:C563375	Hyperparathyroidism, Neonatal Severe Primary	CTD_diseases	3
MESH:C563457	MESH:C563457	Microtia-Anotia	CTD_diseases	3
MESH:C563462	MESH:C563462	Carnitine Palmitoyltransferase II Deficiency, Infantile	CTD_diseases	3
MESH:C563463	MESH:C563463	Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal	CTD_diseases	3
MESH:C563483	MESH:C563483	Osteosclerosis with Ichthyosis and Fractures	CTD_diseases	3
MESH:C563487	MESH:C563487	Osteogenesis Imperfecta with Opalescent Teeth, Blue Sclerae and Wormian Bones, but Without Fractures	CTD_diseases	3
MESH:C563533	MESH:C563533	Nasal Alar Collapse, Bilateral	CTD_diseases	3
MESH:C563583	MESH:C563583	Microcephaly with Chorioretinopathy, Autosomal Dominant	CTD_diseases	3
MESH:C563621	MESH:C563621	Lip, Hamartomatous	CTD_diseases	3
MESH:C563636	MESH:C563636	Laryngeal Web, Familial	CTD_diseases	3
MESH:C563637	MESH:C563637	Larynx, Congenital Partial Atresia of	CTD_diseases	3
MESH:C563639	MESH:C563639	Cutis Laxa-Marfanoid Syndrome	CTD_diseases	3
MESH:C563662	MESH:C563662	Invasive Pneumococcal Disease, Recurrent Isolated, 1	CTD_diseases	3
MESH:C563663	MESH:C563663	Immunodeficiency due to Defect in MAPBP-Interacting Protein	CTD_diseases	3
MESH:C563672	MESH:C563672	Diabetes Mellitus, Transient Neonatal, 2	CTD_diseases	3
MESH:C563691	MESH:C563691	Alpha/Beta T-Cell Lymphopenia with Gamma/Delta T-Cell Expansion, Severe Cytomegalovirus Infection, a	CTD_diseases	3
MESH:C563745	MESH:C563745	B-Cell Immunodeficiency, Distal Limb Anomalies, And Urogenital Malformations	CTD_diseases	3
MESH:C563824	MESH:C563824	CD8 Deficiency, Familial	CTD_diseases	3
MESH:C563876	MESH:C563876	AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency	CTD_diseases	3
MESH:C563886	MESH:C563886	Ciliary Dyskinesia, Primary, 5	CTD_diseases	3
MESH:C563914	MESH:C563914	Larsen-Like Syndrome	CTD_diseases	3
MESH:C563937	MESH:C563937	Arterial Dissection with Lentiginosis	CTD_diseases	3
MESH:C563939	MESH:C563939	Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction	CTD_diseases	3
MESH:C563949	MESH:C563949	Enteropathy, Familial, with Villous Edema and Immunoglobulin G2 Deficiency	CTD_diseases	3
MESH:C563984	MESH:C563984	Atrial Standstill	CTD_diseases	3
MESH:C564004	MESH:C564004	Macrocytosis, Familial	CTD_diseases	3
MESH:C564022	MESH:C564022	Cyclic Vomiting Syndrome with Neuromuscular Disease	CTD_diseases	3
MESH:C564075	MESH:C564075	Properdin Deficiency, Type II	CTD_diseases	3
MESH:C564076	MESH:C564076	Properdin Deficiency, Type III	CTD_diseases	3
MESH:C564120	MESH:C564120	Immunodeficiency, X-Linked, with Deficiency of 115,000 Dalton Surface Glycoprotein	CTD_diseases	3
MESH:C564131	MESH:C564131	Kappa-Chain Deficiency	CTD_diseases	3
MESH:C564135	MESH:C564135	Immunodeficiency with Defective Leukocyte and Lymphocyte Function and with Response to Histamine-1 A	CTD_diseases	3
MESH:C564136	MESH:C564136	Immune Deficiency, Familial Variable	CTD_diseases	3
MESH:C564144	MESH:C564144	Hypoplasia of Teeth Roots	CTD_diseases	3
MESH:C564185	MESH:C564185	Hip Dysplasia, Beukes Type	CTD_diseases	3
MESH:C564245	MESH:C564245	Platelet Glycoprotein IV Deficiency	CTD_diseases	3
MESH:C564275	MESH:C564275	Neutrophil Immunodeficiency Syndrome	CTD_diseases	3
MESH:C564298	MESH:C564298	Bile and Pancreatic Ducts, Complete Absence of	CTD_diseases	3
MESH:C564303	MESH:C564303	Thai Symphalangism Syndrome	CTD_diseases	3
MESH:C564307	MESH:C564307	Combined Immunodeficiency with Autoimmunity and Spondylometaphyseal Dysplasia	CTD_diseases	3
MESH:C564315	MESH:C564315	Caudal Duplication Anomaly	CTD_diseases	3
MESH:C564320	MESH:C564320	Neutropenia, Nonimmune Chronic Idiopathic, Adult	CTD_diseases	3
MESH:C564321	MESH:C564321	Aural Atresia, Congenital	CTD_diseases	3
MESH:C564323	MESH:C564323	Neuroticism	CTD_diseases	3
MESH:C564352	MESH:C564352	IRAK4 Deficiency	CTD_diseases	3
MESH:C564392	MESH:C564392	Bothnia Retinal Dystrophy	CTD_diseases	3
MESH:C564468	MESH:C564468	Invasive Pneumococcal Disease, Recurrent Isolated, 2	CTD_diseases	3
MESH:C564519	MESH:C564519	Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ea	CTD_diseases	3
MESH:C564538	MESH:C564538	Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema	CTD_diseases	3
MESH:C564620	MESH:C564620	Laryngeal Atresia, Encephalocele, and Limb Deformities	CTD_diseases	3
MESH:C564694	MESH:C564694	LIG4 Syndrome	CTD_diseases	3
MESH:C564750	MESH:C564750	Vascular Hyalinosis	CTD_diseases	3
MESH:C564770	MESH:C564770	Thumb Agenesis, Short Stature, And Immunodeficiency	CTD_diseases	3
MESH:C564805	MESH:C564805	Spinal Muscular Atrophy, Type I, with Congenital Bone Fractures	CTD_diseases	3
MESH:C564833	MESH:C564833	Rh-Null, Regulator Type	CTD_diseases	3
MESH:C564853	MESH:C564853	Renal and Mullerian Duct Hypoplasia	CTD_diseases	3
MESH:C564888	MESH:C564888	Glycogen Storage Disease of Heart, Lethal Congenital	CTD_diseases	3
MESH:C564908	MESH:C564908	Pancreatic Agenesis, Congenital	CTD_diseases	3
MESH:C565011	MESH:C565011	Fibula, Recurrent Dislocation of Head of	CTD_diseases	3
MESH:C565027	MESH:C565027	Complement Factor D Deficiency	CTD_diseases	3
MESH:C565051	MESH:C565051	Epiblepharon of Upper Lid	CTD_diseases	3
MESH:C565099	MESH:C565099	Diarrhea, Glucose-Stimulated Secretory, with Common Variable Immunodeficiency	CTD_diseases	3
MESH:C565114	MESH:C565114	Failure of Tooth Eruption, Primary	CTD_diseases	3
MESH:C565138	MESH:C565138	Cryptophthalmos, Unilateral or Bilateral, Isolated	CTD_diseases	3
MESH:C565140	MESH:C565140	Cryptotia, Familial	CTD_diseases	3
MESH:C565141	MESH:C565141	Cryoglobulinemia, Familial Mixed	CTD_diseases	3
MESH:C565152	MESH:C565152	Corticosteroid-Binding Globulin Deficiency	CTD_diseases	3
MESH:C565153	MESH:C565153	Coronary Artery Dissection, Spontaneous	CTD_diseases	3
MESH:C565158	MESH:C565158	Cornea Plana 1	CTD_diseases	3
MESH:C565161	MESH:C565161	Coracoclavicular Joint, Anomalous	CTD_diseases	3
MESH:C565165	MESH:C565165	C9 Deficiency	CTD_diseases	3
MESH:C565166	MESH:C565166	C9 Deficiency with Dermatomyositis	CTD_diseases	3
MESH:C565167	MESH:C565167	Complement Component 4a Deficiency	CTD_diseases	3
MESH:C565168	MESH:C565168	Complement Component 4, Partial Deficiency Of	CTD_diseases	3
MESH:C565169	MESH:C565169	Complement Component 3 Deficiency, Autosomal Recessive	CTD_diseases	3
MESH:C565170	MESH:C565170	Complement Component C1s Deficiency	CTD_diseases	3
MESH:C565177	MESH:C565177	Stickler Syndrome, Autosomal Recessive, COL9A1-Related	CTD_diseases	3
MESH:C565179	MESH:C565179	Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia	CTD_diseases	3
MESH:C565209	MESH:C565209	Sclerocornea	CTD_diseases	3
MESH:C565226	MESH:C565226	Hamartoma, Precalcaneal Congenital Fibrolipomatous	CTD_diseases	3
MESH:C565232	MESH:C565232	Interleukin 2 Receptor, Alpha, Deficiency of	CTD_diseases	3
MESH:C565248	MESH:C565248	Mental Retardation, Short Stature, Facial Anomalies, and Joint Dislocations	CTD_diseases	3
MESH:C565253	MESH:C565253	Developmental Delay, Epilepsy, and Neonatal Diabetes	CTD_diseases	3
MESH:C565262	MESH:C565262	Myopathy, Distal 2	CTD_diseases	3
MESH:C565272	MESH:C565272	Liver Fibrocystic Disease and Polydactyly	CTD_diseases	3
MESH:C565284	MESH:C565284	Basaloid Follicular Hamartoma Syndrome, Generalized, Autosomal Dominant	CTD_diseases	3
MESH:C565326	MESH:C565326	Radiation Sensitivity Chromosome Instability Syndrome, Autosomal Dominant	CTD_diseases	3
MESH:C565360	MESH:C565360	MASP2 Deficiency	CTD_diseases	3
MESH:C565379	MESH:C565379	Microcephaly with Chorioretinopathy, Autosomal Recessive	CTD_diseases	3
MESH:C565427	MESH:C565427	Lymphopenic Hypergammaglobulinemia, Antibody Deficiency, Autoimmune Hemolytic Anemia, and Glomerulon	CTD_diseases	3
MESH:C565428	MESH:C565428	Lymphokine Deficiency	CTD_diseases	3
MESH:C565430	MESH:C565430	Lymphoid System Deterioration, Progressive	CTD_diseases	3
MESH:C565431	MESH:C565431	Lymphoblastic Transformation, Intrinsic Defect in	CTD_diseases	3
MESH:C565465	MESH:C565465	Inosine Phosphorylase Deficiency, Immune Defect Due To	CTD_diseases	3
MESH:C565468	MESH:C565468	Immunodeficiency, Partial Combined, with Absence of HLA Determinants and Beta-2-Microglobulin from L	CTD_diseases	3
MESH:C565469	MESH:C565469	Immune Deficiency Disease	CTD_diseases	3
MESH:C565484	MESH:C565484	Hypoglycemia, Neonatal, Simulating Foetopathia Diabetica	CTD_diseases	3
MESH:C565485	MESH:C565485	Glycogen Storage Disease 0, Liver	CTD_diseases	3
MESH:C565530	MESH:C565530	Grouped Pigmentation of the Macula	CTD_diseases	3
MESH:C565540	MESH:C565540	GSD IV, Nonprogressive Hepatic	CTD_diseases	3
MESH:C565541	MESH:C565541	GSD IV, Neuromuscular Form, Fatal Perinatal	CTD_diseases	3
MESH:C565542	MESH:C565542	GSD IV, Neuromuscular Form, Congenital	CTD_diseases	3
MESH:C565543	MESH:C565543	GSD IV, Neuromuscular Form, Childhood	CTD_diseases	3
MESH:C565544	MESH:C565544	GSD IV, Neuromuscular Form, Adult, with Isolated Myopathy	CTD_diseases	3
MESH:C565564	MESH:C565564	Fleck Retina, Familial Benign	CTD_diseases	3
MESH:C565604	MESH:C565604	Ectodermal Dysplasia, Hypohidrotic, with Hypothyroidism and Ciliary Dyskinesia	CTD_diseases	3
MESH:C565633	MESH:C565633	Retinal Nonattachment, Nonsyndromic Congenital	CTD_diseases	3
MESH:C565660	MESH:C565660	Cyanosis and Hepatic Disease	CTD_diseases	3
MESH:C565672	MESH:C565672	Cranial Nerves, Recurrent Paresis Of	CTD_diseases	3
MESH:C565673	MESH:C565673	Cranial Nerves, Congenital Paresis Of	CTD_diseases	3
MESH:C565677	MESH:C565677	Cornea Plana 2	CTD_diseases	3
MESH:C565684	MESH:C565684	Combined Inflammatory and Immunologic Defect	CTD_diseases	3
MESH:C565712	MESH:C565712	Immunodeficiency due to Defect in CD3-Zeta	CTD_diseases	3
MESH:C565730	MESH:C565730	Diabetes Mellitus, Congenital Autoimmune	CTD_diseases	3
MESH:C565765	MESH:C565765	Hypoglobulinemia and Absent B Cells	CTD_diseases	3
MESH:C565891	MESH:C565891	Calcification of Joints and Arteries	CTD_diseases	3
MESH:C565958	MESH:C565958	Amyloidosis of Gingiva and Conjunctiva, with Mental Retardation	CTD_diseases	3
MESH:C565963	MESH:C565963	Alpha-2-Deficient Collagen Disease	CTD_diseases	3
MESH:C565993	MESH:C565993	Vulvovaginitis, Allergic Seminal	CTD_diseases	3
MESH:C566007	MESH:C566007	Vasculopathy, Retinal, With Cerebral Leukodystrophy	CTD_diseases	3
MESH:C566008	MESH:C566008	Vasculitis, Lymphocytic, Nodular	CTD_diseases	3
MESH:C566018	MESH:C566018	Twinning due to Superfetation	CTD_diseases	3
MESH:C566022	MESH:C566022	Trochlea of the Humerus, Aplasia of	CTD_diseases	3
MESH:C566079	MESH:C566079	Cd4+ Lymphocyte Deficiency	CTD_diseases	3
MESH:C566080	MESH:C566080	T-Cell OKT4 Deficiency	CTD_diseases	3
MESH:C566082	MESH:C566082	Immunodeficiency due to Defect in CD3-Epsilon	CTD_diseases	3
MESH:C566083	MESH:C566083	Immunodeficiency due to Defect in CD3-Gamma	CTD_diseases	3
MESH:C566123	MESH:C566123	Cirrhosis, Familial	CTD_diseases	3
MESH:C566223	MESH:C566223	Blepharochalasis, Superior	CTD_diseases	3
MESH:C566275	MESH:C566275	Antibody Deficiency due to Defect in CD19	CTD_diseases	3
MESH:C566304	MESH:C566304	alpha-2-Macroglobulin Deficiency	CTD_diseases	3
MESH:C566307	MESH:C566307	Alacrima, Congenital	CTD_diseases	3
MESH:C566310	MESH:C566310	Adenosine Triphosphate, Elevated, Of Erythrocytes	CTD_diseases	3
MESH:C566343	MESH:C566343	Hereditary Myopathy with Early Respiratory Failure	CTD_diseases	3
MESH:C566347	MESH:C566347	Eccrine Syringofibroadenomatosis with Eyelid Abnormalities	CTD_diseases	3
MESH:C566362	MESH:C566362	Tracheobronchial Stenosis, Congenital	CTD_diseases	3
MESH:C566375	MESH:C566375	Expansile Bone Lesions	CTD_diseases	3
MESH:C566379	MESH:C566379	Laryngotracheal Stenosis, Progressive, with Short Stature and Arthropathy	CTD_diseases	3
MESH:C566384	MESH:C566384	Hyperthyroidism, Familial Gestational	CTD_diseases	3
MESH:C566417	MESH:C566417	Endotoxin Hyporesponsiveness	CTD_diseases	3
MESH:C566443	MESH:C566443	Complement Component 7 Deficiency	CTD_diseases	3
MESH:C566454	MESH:C566454	Thyroid Hormone Metabolism, Abnormal	CTD_diseases	3
MESH:C566492	MESH:C566492	Natural Killer Cell Deficiency, Familial Isolated	CTD_diseases	3
MESH:C566514	MESH:C566514	Skeletal Dysplasia And Progressive Central Nervous System Degeneration, Lethal	CTD_diseases	3
MESH:C566533	MESH:C566533	Macrophthalmia, Colobomatous, with Microcornea	CTD_diseases	3
MESH:C566692	MESH:C566692	Sclerocornea, Autosomal Dominant	CTD_diseases	3
MESH:C566703	MESH:C566703	Lacrimal Puncta, Absence of	CTD_diseases	3
MESH:C566708	MESH:C566708	Rhiny	CTD_diseases	3
MESH:C566720	MESH:C566720	Retinal Aplasia	CTD_diseases	3
MESH:C566776	MESH:C566776	Polyposis, Intestinal, With Multiple Exostoses	CTD_diseases	3
MESH:C566816	MESH:C566816	Patella, Familial Recurrent Dislocation Of	CTD_diseases	3
MESH:C566821	MESH:C566821	Parotidomegaly, Hereditary Bilateral	CTD_diseases	3
MESH:C566836	MESH:C566836	Pancytopenia and Occlusive Vascular Disease	CTD_diseases	3
MESH:C566895	MESH:C566895	Gangliosidosis, Generalized GM1, Type I, with Cardiac Involvement	CTD_diseases	3
MESH:C566904	MESH:C566904	Preauricular Tag, Isolated, Autosomal Dominant, 1	CTD_diseases	3
MESH:C566988	MESH:C566988	Hypertelorism, Severe, With Midface Prominence, Myopia, Mental Retardation, And Bone Fragility	CTD_diseases	3
MESH:C567049	MESH:C567049	Pulmonary Alveolar Proteinosis, Acquired	CTD_diseases	3
MESH:C567057	MESH:C567057	Ciliary Dyskinesia, Primary, 6	CTD_diseases	3
MESH:C567137	MESH:C567137	Ciliary Dyskinesia With Transposition Of Ciliary Microtubules	CTD_diseases	3
MESH:C567200	MESH:C567200	Immunodeficiency, Hypogammaglobulinemia, and Reduced B Cells	CTD_diseases	3
MESH:C567209	MESH:C567209	Mental Retardation, Joint Hypermobility, And Skin Laxity, With Or Without Metabolic Abnormalities	CTD_diseases	3
MESH:C567211	MESH:C567211	Ciliary Dyskinesia, Primary, 12	CTD_diseases	3
MESH:C567212	MESH:C567212	Ciliary Dyskinesia, Primary, 11	CTD_diseases	3
MESH:C562467	MESH:C562467	Lymphedema, Hereditary, II	CTD_diseases	4
MESH:C562477	MESH:C562477	Halothane Hepatitis	CTD_diseases	4
MESH:C562478	MESH:C562478	Hypogammaglobulinemia, X-Linked	CTD_diseases	4
MESH:C562483	MESH:C562483	Granulosis Rubra Nasi	CTD_diseases	4
MESH:C562485	MESH:C562485	Pili Torti	CTD_diseases	4
MESH:C562486	MESH:C562486	Perifolliculitis Capitis Abscedens Et Suffodiens, Familial	CTD_diseases	4
MESH:C562489	MESH:C562489	Lymphoid Interstitial Pneumonia	CTD_diseases	4
MESH:C562490	MESH:C562490	Cardiac Conduction Defect	CTD_diseases	4
MESH:C562492	MESH:C562492	Robinow Syndrome, Autosomal Dominant	CTD_diseases	4
MESH:C562509	MESH:C562509	Popliteal Pterygium Syndrome	CTD_diseases	4
MESH:C562515	MESH:C562515	Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects	CTD_diseases	4
MESH:C562524	MESH:C562524	Fibrochondrogenesis	CTD_diseases	4
MESH:C562543	MESH:C562543	German Syndrome	CTD_diseases	4
MESH:C562551	MESH:C562551	Dyskeratosis, Hereditary Benign Intraepithelial	CTD_diseases	4
MESH:C562557	MESH:C562557	Polythelia, Familial	CTD_diseases	4
MESH:C562565	MESH:C562565	Uterine Anomalies	CTD_diseases	4
MESH:C562568	MESH:C562568	Cerebellar Hypoplasia	CTD_diseases	4
MESH:C562576	MESH:C562576	Diarrhea 3, Secretory Sodium, Congenital	CTD_diseases	4
MESH:C562577	MESH:C562577	Cirrhosis, Cryptogenic	CTD_diseases	4
MESH:C562580	MESH:C562580	Cirrhosis, Familial, with Pulmonary Hypertension	CTD_diseases	4
MESH:C562584	MESH:C562584	Xanthinuria, Type I	CTD_diseases	4
MESH:C562629	MESH:C562629	Hemolytic Anemia, Congenital, with Emphysema and Cutis Laxa	CTD_diseases	4
MESH:C562642	MESH:C562642	Amyloidosis, Primary Cutaneous	CTD_diseases	4
MESH:C562643	MESH:C562643	Amyloidosis IX	CTD_diseases	4
MESH:C562644	MESH:C562644	Amyloidosis, Cutaneous Bullous	CTD_diseases	4
MESH:C562645	MESH:C562645	Acid Phosphatase Deficiency	CTD_diseases	4
MESH:C562649	MESH:C562649	Enterokinase Deficiency	CTD_diseases	4
MESH:C562651	MESH:C562651	Ethanolaminosis	CTD_diseases	4
MESH:C562654	MESH:C562654	Hypokalemia, Familial	CTD_diseases	4
MESH:C562657	MESH:C562657	Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency	CTD_diseases	4
MESH:C562663	MESH:C562663	BADS Syndrome	CTD_diseases	4
MESH:C562664	MESH:C562664	Aland Island Eye Disease	CTD_diseases	4
MESH:C562700	MESH:C562700	Pupillary Membrane, Persistence Of	CTD_diseases	4
MESH:C562721	MESH:C562721	Lazy Leukocyte Syndrome	CTD_diseases	4
MESH:C562723	MESH:C562723	Hyperheparinemia	CTD_diseases	4
MESH:C562725	MESH:C562725	Prekallikrein Deficiency	CTD_diseases	4
MESH:C562735	MESH:C562735	Osseous Heteroplasia, Progressive	CTD_diseases	4
MESH:C562736	MESH:C562736	Nevus, Epidermal	CTD_diseases	4
MESH:C562769	MESH:C562769	Thyroid Dyshormonogenesis 3	CTD_diseases	4
MESH:C562771	MESH:C562771	Thyroid Dyshormonogenesis 5	CTD_diseases	4
MESH:C562782	MESH:C562782	Hypoparathyroidism, X-Linked	CTD_diseases	4
MESH:C562783	MESH:C562783	Hypercalciuric Hypocalcemia, Familial	CTD_diseases	4
MESH:C562785	MESH:C562785	Idiopathic Hypogonadotropic Hypogonadism	CTD_diseases	4
MESH:C562787	MESH:C562787	Precocious Puberty, Central	CTD_diseases	4
MESH:C562798	MESH:C562798	Transcobalamin I Deficiency	CTD_diseases	4
MESH:C562801	MESH:C562801	3-Methylglutaconic Aciduria, Type I	CTD_diseases	4
MESH:C562803	MESH:C562803	Beta-Hydroxyisobutyryl CoA Deacylase Deficiency	CTD_diseases	4
MESH:C562815	MESH:C562815	Dihydropyrimidinase Deficiency	CTD_diseases	4
MESH:C562824	MESH:C562824	Poikiloderma, Hereditary Sclerosing	CTD_diseases	4
MESH:C562829	MESH:C562829	Megalocornea	CTD_diseases	4
MESH:C562838	MESH:C562838	Comedones, Familial Dyskeratotic	CTD_diseases	4
MESH:C562841	MESH:C562841	Ovarian Germ Cell Cancer	CTD_diseases	4
MESH:C562864	MESH:C562864	Myeloperoxidase Deficiency	CTD_diseases	4
MESH:C562866	MESH:C562866	Thromboxane Synthetase Deficiency	CTD_diseases	4
MESH:C562873	MESH:C562873	Specific Granule Deficiency	CTD_diseases	4
MESH:C562901	MESH:C562901	Nephrolithiasis, X-Linked Recessive, with Renal Failure	CTD_diseases	4
MESH:C562907	MESH:C562907	Twenty-Nail Dystrophy	CTD_diseases	4
MESH:C562908	MESH:C562908	Telangiectasia, Hereditary Benign	CTD_diseases	4
MESH:C562912	MESH:C562912	Rudiger Syndrome	CTD_diseases	4
MESH:C562924	MESH:C562924	dowling-degos disease	CTD_diseases	4
MESH:C562925	MESH:C562925	Collagenoma, Familial Cutaneous	CTD_diseases	4
MESH:C562938	MESH:C562938	Metachondromatosis	CTD_diseases	4
MESH:C562949	MESH:C562949	Adducted Thumbs Syndrome	CTD_diseases	4
MESH:C562968	MESH:C562968	Spondyloepimetaphyseal Dysplasia With Joint Laxity	CTD_diseases	4
MESH:C562988	MESH:C562988	Pseudomonilethrix	CTD_diseases	4
MESH:C562989	MESH:C562989	Amastia	CTD_diseases	4
MESH:C562993	MESH:C562993	Book Syndrome	CTD_diseases	4
MESH:C562998	MESH:C562998	Telangiectasia, Generalized Essential	CTD_diseases	4
MESH:C563002	MESH:C563002	Opticocochleodentate Degeneration	CTD_diseases	4
MESH:C563010	MESH:C563010	Neutrophilia, Hereditary	CTD_diseases	4
MESH:C563014	MESH:C563014	Facial Hemihypertrophy	CTD_diseases	4
MESH:C563016	MESH:C563016	Pseudofolliculitis Barbae	CTD_diseases	4
MESH:C563023	MESH:C563023	Alpha-Thalassemia Myelodysplasia Syndrome	CTD_diseases	4
MESH:C563034	MESH:C563034	Basal Laminar Drusen	CTD_diseases	4
MESH:C563037	MESH:C563037	Arthritis, Sacroiliac	CTD_diseases	4
MESH:C563039	MESH:C563039	Coumarin Resistance	CTD_diseases	4
MESH:C563051	MESH:C563051	Edinburgh Malformation Syndrome	CTD_diseases	4
MESH:C563052	MESH:C563052	Digitorenocerebral Syndrome	CTD_diseases	4
MESH:C563065	MESH:C563065	Bullous Dystrophy, Hereditary Macular Type	CTD_diseases	4
MESH:C563067	MESH:C563067	Hypospadias-Mental Retardation Syndrome	CTD_diseases	4
MESH:C563086	MESH:C563086	Ataxia-Microcephaly-Cataract Syndrome	CTD_diseases	4
MESH:C563095	MESH:C563095	Mental Retardation, Buenos Aires Type	CTD_diseases	4
MESH:C563110	MESH:C563110	Proud Syndrome	CTD_diseases	4
MESH:C563111	MESH:C563111	Absent Eyebrows and Eyelashes with Mental Retardation	CTD_diseases	4
MESH:C563117	MESH:C563117	Rosselli-Gulienetti Syndrome	CTD_diseases	4
MESH:C563119	MESH:C563119	Sao Paulo MCA/MR Syndrome	CTD_diseases	4
MESH:C563120	MESH:C563120	Scott Syndrome	CTD_diseases	4
MESH:C563124	MESH:C563124	Spondylometaphyseal Dysplasia, X-Linked	CTD_diseases	4
MESH:C563127	MESH:C563127	Corpus Callosum, Agenesis of, with Facial Anomalies and Robin Sequence	CTD_diseases	4
MESH:C563134	MESH:C563134	Spinocerebellar Ataxia, X-Linked 1	CTD_diseases	4
MESH:C563154	MESH:C563154	Brooks-Wisniewski-Brown Syndrome	CTD_diseases	4
MESH:C563160	MESH:C563160	Oculodentodigital Dysplasia	CTD_diseases	4
MESH:C563168	MESH:C563168	Askin Tumor	CTD_diseases	4
MESH:C563171	MESH:C563171	Methemoglobin Reductase Deficiency	CTD_diseases	4
MESH:C563178	MESH:C563178	Aortic Valve Disease	CTD_diseases	4
MESH:C563195	MESH:C563195	Chondrosarcoma, Extraskeletal Myxoid	CTD_diseases	4
MESH:C563210	MESH:C563210	Beta-Ureidopropionase Deficiency	CTD_diseases	4
MESH:C563215	MESH:C563215	Genochondromatosis	CTD_diseases	4
MESH:C563221	MESH:C563221	Mydriasis, Congenital	CTD_diseases	4
MESH:C563233	MESH:C563233	Myelocerebellar Disorder	CTD_diseases	4
MESH:C563236	MESH:C563236	Testicular Germ Cell Tumor	CTD_diseases	4
MESH:C563238	MESH:C563238	Parathyroid Glands, Agenesis Of	CTD_diseases	4
MESH:C563247	MESH:C563247	Muscular Dystrophy, Cardiac Type	CTD_diseases	4
MESH:C563249	MESH:C563249	Carnitine Acetyltransferase Deficiency	CTD_diseases	4
MESH:C563261	MESH:C563261	Renal Adysplasia	CTD_diseases	4
MESH:C563273	MESH:C563273	Hyperparathyroidism 2	CTD_diseases	4
MESH:C563276	MESH:C563276	Osteofibrous Dysplasia	CTD_diseases	4
MESH:C563287	MESH:C563287	Prepapillary Vascular Loops	CTD_diseases	4
MESH:C563290	MESH:C563290	Dyssegmental Dysplasia with Glaucoma	CTD_diseases	4
MESH:C563294	MESH:C563294	Cataract, Congenital, Cerulean Type, 2	CTD_diseases	4
MESH:C563296	MESH:C563296	Microcephaly, Retinitis Pigmentosa, and Sutural Cataract	CTD_diseases	4
MESH:C563309	MESH:C563309	Facial Palsy, Congenital, Unilateral Or Bilateral	CTD_diseases	4
MESH:C563315	MESH:C563315	Dislocation of Hip, Congenital, with Hyperextensibility of Fingers and Facial Dysmorphism	CTD_diseases	4
MESH:C563319	MESH:C563319	Myopathy, Myofibrillar, Desmin-Related	CTD_diseases	4
MESH:C563324	MESH:C563324	Platelet Disorder, Familial, with Associated Myeloid Malignancy	CTD_diseases	4
MESH:C563333	MESH:C563333	Cataract, Age-Related Nuclear	CTD_diseases	4
MESH:C563342	MESH:C563342	Mental Retardation, Microcephaly, Epilepsy, And Coarse Face	CTD_diseases	4
MESH:C563346	MESH:C563346	Martinez-Frias Syndrome	CTD_diseases	4
MESH:C563349	MESH:C563349	Atrophia Maculosa Varioliformis Cutis, Familial	CTD_diseases	4
MESH:C563358	MESH:C563358	Pulmonary Arterial Hypertension, Hereditary Hemorrhagic Telangiectasia-Related	CTD_diseases	4
MESH:C563370	MESH:C563370	Alopecia-Mental Retardation Syndrome with Convulsions and Hypergonadotropic Hypogonadism	CTD_diseases	4
MESH:C563378	MESH:C563378	Muscular Dystrophy, Congenital, with Severe Central Nervous System Atrophy and Absence of Large Myel	CTD_diseases	4
MESH:C563380	MESH:C563380	Diaphragmatic Defects, Limb Deficiencies, and Ossification Defects Of Skull	CTD_diseases	4
MESH:C563382	MESH:C563382	Trisomy 18-Like Syndrome	CTD_diseases	4
MESH:C563383	MESH:C563383	Lissencephaly Type III and Bone Dysplasia	CTD_diseases	4
MESH:C563390	MESH:C563390	Cataracts, Congenital, with Sensorineural Deafness, Down Syndrome-Like Facial Appearance, Short Stat	CTD_diseases	4
MESH:C563394	MESH:C563394	Aplasia Cutis Congenita, High Myopia, and Cone-Rod Dysfunction	CTD_diseases	4
MESH:C563402	MESH:C563402	Ichthyosis-Mental Retardation Syndrome with Large Keratohyalin Granules in the Skin	CTD_diseases	4
MESH:C563403	MESH:C563403	Tibia, Absence or Hypoplasia of, with Polydactyly, Retrocerebellar Arachnoid Cyst, and Other Anomali	CTD_diseases	4
MESH:C563407	MESH:C563407	Portal Vein, Cavernous Transformation Of	CTD_diseases	4
MESH:C563420	MESH:C563420	Epiphyseal Dysplasia, Multiple, with Myopathy	CTD_diseases	4
MESH:C563424	MESH:C563424	Diabetes Mellitus, Permanent Neonatal, With Neurologic Features	CTD_diseases	4
MESH:C563426	MESH:C563426	Cataract, Pulverulent	CTD_diseases	4
MESH:C563429	MESH:C563429	Agonadism, XY, with Mental Retardation, Short Stature, Retarded Bone Age, and Multiple Extragenital 	CTD_diseases	4
MESH:C563430	MESH:C563430	Enamel Hypoplasia, Cataracts, and Aqueductal Stenosis	CTD_diseases	4
MESH:C563435	MESH:C563435	Cataract, Congenital Zonular, with Sutural Opacities	CTD_diseases	4
MESH:C563453	MESH:C563453	Proximal Myopathy with Focal Depletion of Mitochondria	CTD_diseases	4
MESH:C563461	MESH:C563461	Carnitine Palmitoyltransferase II Deficiency, Late-Onset	CTD_diseases	4
MESH:C563466	MESH:C563466	UV-Sensitive Syndrome	CTD_diseases	4
MESH:C563470	MESH:C563470	Setting-Sun Phenomenon, Familial Benign	CTD_diseases	4
MESH:C563472	MESH:C563472	Spondyloepiphyseal Dysplasia with Atlantoaxial Instability	CTD_diseases	4
MESH:C563476	MESH:C563476	Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia	CTD_diseases	4
MESH:C563478	MESH:C563478	Osteochondrodysplasia, Rhizomelic, with Callosal Agenesis, Thrombocytopenia, Hydrocephalus, and Hype	CTD_diseases	4
MESH:C563482	MESH:C563482	Otodental Dysplasia	CTD_diseases	4
MESH:C563484	MESH:C563484	Osteopoikilosis, Isolated	CTD_diseases	4
MESH:C563492	MESH:C563492	Optic Nerve Hypoplasia, Bilateral	CTD_diseases	4
MESH:C563493	MESH:C563493	Optic Nerve Aplasia, Bilateral	CTD_diseases	4
MESH:C563497	MESH:C563497	Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant	CTD_diseases	4
MESH:C563501	MESH:C563501	Ophthalmomandibulomelic Dysplasia	CTD_diseases	4
MESH:C563503	MESH:C563503	Onycholysis, Partial, with Scleronychia	CTD_diseases	4
MESH:C563506	MESH:C563506	Onychogryposis, Pedal, with Keratosis Plantaris and Coarse Hair	CTD_diseases	4
MESH:C563512	MESH:C563512	Noduli Cutanei, Multiple, with Urinary Tract Abnormalities	CTD_diseases	4
MESH:C563514	MESH:C563514	Hypertension Resistant to Conventional Therapy	CTD_diseases	4
MESH:C563516	MESH:C563516	Neuropathy, with Paraprotein in Serum, Cerebrospinal Fluid and Urine	CTD_diseases	4
MESH:C563519	MESH:C563519	Ganglioneuromatosis of the Alimentary Tract	CTD_diseases	4
MESH:C563527	MESH:C563527	Retinal Degeneration, Autosomal Recessive, Clumped Pigment Type	CTD_diseases	4
MESH:C563541	MESH:C563541	Myopia 2	CTD_diseases	4
MESH:C563553	MESH:C563553	Muscular Hypoplasia, Congenital Universal, of Krabbe	CTD_diseases	4
MESH:C563575	MESH:C563575	Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1	CTD_diseases	4
MESH:C563576	MESH:C563576	Progressive External Ophthalmoplegia With Hypogonadism	CTD_diseases	4
MESH:C563578	MESH:C563578	Myopathy, Cataract, Hypogonadism Syndrome	CTD_diseases	4
MESH:C563580	MESH:C563580	Tauopathy and Respiratory Failure	CTD_diseases	4
MESH:C563581	MESH:C563581	Microphthalmia, Isolated, With Corectopia	CTD_diseases	4
MESH:C563582	MESH:C563582	Microphthalmia, Isolated, with Cataract 1	CTD_diseases	4
MESH:C563591	MESH:C563591	Mental and Growth Retardation with Amblyopia	CTD_diseases	4
MESH:C563592	MESH:C563592	Membranous Cranial Ossification, Delayed	CTD_diseases	4
MESH:C563596	MESH:C563596	Melanoma, Malignant Familial Intraocular	CTD_diseases	4
MESH:C563598	MESH:C563598	Median-Ulnar Nerve Communications	CTD_diseases	4
MESH:C563599	MESH:C563599	Maxillofacial Dysostosis	CTD_diseases	4
MESH:C563600	MESH:C563600	Masticatory Muscles, Hypertrophy of	CTD_diseases	4
MESH:C563601	MESH:C563601	Mannose 6-Phosphate Receptor Recognition Defect, Lebanese Type	CTD_diseases	4
MESH:C563602	MESH:C563602	Mannose-Binding Protein Deficiency	CTD_diseases	4
MESH:C563603	MESH:C563603	Cataract, Polymorphic and Lamellar	CTD_diseases	4
MESH:C563604	MESH:C563604	Cataract, Cortical Pulverulent, Late-Onset	CTD_diseases	4
MESH:C563612	MESH:C563612	Lymphedema and Cerebral Arteriovenous Anomaly	CTD_diseases	4
MESH:C563613	MESH:C563613	Lumbar Stenosis, Familial	CTD_diseases	4
MESH:C563625	MESH:C563625	Levator-Medial Rectus Synkinesis	CTD_diseases	4
MESH:C563626	MESH:C563626	Leukocyte Nuclear Appendages, Hereditary Prevalence of	CTD_diseases	4
MESH:C563633	MESH:C563633	Lattice Degeneration of Retina Leading to Retinal Detachment	CTD_diseases	4
MESH:C563641	MESH:C563641	Lactate Dehydrogenase B Deficiency	CTD_diseases	4
MESH:C563649	MESH:C563649	Keratoconus 1	CTD_diseases	4
MESH:C563650	MESH:C563650	Keratitis Fugax Hereditaria	CTD_diseases	4
MESH:C563653	MESH:C563653	Kallikrein, Decreased Urinary Activity of	CTD_diseases	4
MESH:C563658	MESH:C563658	Polyosteolysis-Hyperostosis Syndrome	CTD_diseases	4
MESH:C563665	MESH:C563665	Mitochondrial Phosphate Carrier Deficiency	CTD_diseases	4
MESH:C563670	MESH:C563670	Aneurysm, Intracranial Berry, 5	CTD_diseases	4
MESH:C563681	MESH:C563681	Aicardi-Goutieres Syndrome 4	CTD_diseases	4
MESH:C563683	MESH:C563683	Aicardi-Goutieres Syndrome 3	CTD_diseases	4
MESH:C563686	MESH:C563686	Gallbladder Disease 3	CTD_diseases	4
MESH:C563687	MESH:C563687	Gallbladder Disease 2	CTD_diseases	4
MESH:C563693	MESH:C563693	Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria	CTD_diseases	4
MESH:C563695	MESH:C563695	Photoparoxysmal Response 3	CTD_diseases	4
MESH:C563698	MESH:C563698	Mitochondrial DNA Depletion Syndrome, Myopathic Form	CTD_diseases	4
MESH:C563701	MESH:C563701	Omphalocele, Diaphragmatic Hernia, And Radial Ray Defects	CTD_diseases	4
MESH:C563703	MESH:C563703	Drug Metabolism, Poor, CYP2C19-Related	CTD_diseases	4
MESH:C563704	MESH:C563704	Proguanil, Poor Metabolism of	CTD_diseases	4
MESH:C563709	MESH:C563709	Stickler Syndrome, Type I, Nonsyndromic Ocular	CTD_diseases	4
MESH:C563710	MESH:C563710	Rhegmatogenous Retinal Detachment, Autosomal Dominant	CTD_diseases	4
MESH:C563728	MESH:C563728	Cataract, Congenital Nuclear, Autosomal Recessive 1	CTD_diseases	4
MESH:C563730	MESH:C563730	Epidermolysis Bullosa Simplex with Migratory Circinate Erythema	CTD_diseases	4
MESH:C563752	MESH:C563752	Keratoconus 4	CTD_diseases	4
MESH:C563758	MESH:C563758	Myopia 10	CTD_diseases	4
MESH:C563759	MESH:C563759	Myopia 9	CTD_diseases	4
MESH:C563760	MESH:C563760	Myopia 8	CTD_diseases	4
MESH:C563761	MESH:C563761	Myopia 7	CTD_diseases	4
MESH:C563774	MESH:C563774	Foveal Hypoplasia and Anterior Segment Dysgenesis	CTD_diseases	4
MESH:C563776	MESH:C563776	Glucocorticoid Deficiency 3	CTD_diseases	4
MESH:C563780	MESH:C563780	Branchiogenic-Deafness Syndrome	CTD_diseases	4
MESH:C563783	MESH:C563783	Striatal Degeneration, Autosomal Dominant	CTD_diseases	4
MESH:C563786	MESH:C563786	Hyperthyroidism, Nonautoimmune	CTD_diseases	4
MESH:C563789	MESH:C563789	Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung 	CTD_diseases	4
MESH:C563797	MESH:C563797	Combined Oxidative Phosphorylation Deficiency 1	CTD_diseases	4
MESH:C563805	MESH:C563805	Nephrotic Syndrome, Congenital, with or without Ocular Abnormalities	CTD_diseases	4
MESH:C563806	MESH:C563806	Skeletal Dysplasia, Rhizomelic, with Retinitis Pigmentosa	CTD_diseases	4
MESH:C563810	MESH:C563810	Mental Retardation with Optic Atrophy, Facial Dysmorphism, Microcephaly, and Short Stature	CTD_diseases	4
MESH:C563812	MESH:C563812	Cataract, Age-Related Cortical, 1	CTD_diseases	4
MESH:C563814	MESH:C563814	Marfanoid Habitus with Situs Inversus	CTD_diseases	4
MESH:C563819	MESH:C563819	Cataract, Congenital, Cerulean Type, 3	CTD_diseases	4
MESH:C563827	MESH:C563827	Keratoconus 2	CTD_diseases	4
MESH:C563830	MESH:C563830	Myasthenic Syndrome, Congenital, Associated with Facial Dysmorphism	CTD_diseases	4
MESH:C563835	MESH:C563835	Drug Metabolism, Poor, CYP2D6-Related	CTD_diseases	4
MESH:C563840	MESH:C563840	Cryohydrocytosis, Stomatin-Deficient, with Mental Retardation, Seizures, Cataracts, and Massive Hepa	CTD_diseases	4
MESH:C563848	MESH:C563848	Alpha-B Crystallinopathy	CTD_diseases	4
MESH:C563849	MESH:C563849	Alpha-B Crystallinopathy with Cataract	CTD_diseases	4
MESH:C563852	MESH:C563852	Leukoencephalopathy, Arthritis, Colitis, and Hypogammaglobulinema	CTD_diseases	4
MESH:C563858	MESH:C563858	Otosclerosis 5	CTD_diseases	4
MESH:C563867	MESH:C563867	Insulin-Like Growth Factor I Deficiency	CTD_diseases	4
MESH:C563896	MESH:C563896	Midface Hypoplasia, Obesity, Developmental Delay, and Neonatal Hypotonia	CTD_diseases	4
MESH:C563897	MESH:C563897	Hypertension, Diastolic, Resistance to	CTD_diseases	4
MESH:C563900	MESH:C563900	Keratoconus 3	CTD_diseases	4
MESH:C563904	MESH:C563904	Cerebrofrontofacial Syndrome	CTD_diseases	4
MESH:C563918	MESH:C563918	Erythrocytosis, Familial, 2	CTD_diseases	4
MESH:C563922	MESH:C563922	Myopia 5	CTD_diseases	4
MESH:C563935	MESH:C563935	Hemolytic Anemia, Lethal Congenital Nonspherocytic, with Genital and Other Abnormalities	CTD_diseases	4
MESH:C563936	MESH:C563936	Cleft Palate, Cardiac Defect, Genital Anomalies, and Ectrodactyly	CTD_diseases	4
MESH:C563938	MESH:C563938	Obesity, Hyperphagia, and Developmental Delay	CTD_diseases	4
MESH:C563941	MESH:C563941	Pectus Excavatum, Macrocephaly, Short Stature, Dysplastic Nails	CTD_diseases	4
MESH:C563951	MESH:C563951	Parotid Salivary Glands, Polycystic Disease of	CTD_diseases	4
MESH:C563952	MESH:C563952	Succinic Acidemia	CTD_diseases	4
MESH:C563954	MESH:C563954	Motor Neuron Disease with Dementia and Ophthalmoplegia	CTD_diseases	4
MESH:C563983	MESH:C563983	Nanophthalmos 1	CTD_diseases	4
MESH:C563985	MESH:C563985	Melanoma-Pancreatic Cancer Syndrome	CTD_diseases	4
MESH:C563990	MESH:C563990	Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy	CTD_diseases	4
MESH:C563994	MESH:C563994	Atrioventricular Septal Defect with Blepharophimosis and Anal and Radial Defects	CTD_diseases	4
MESH:C564015	MESH:C564015	Parkinson Disease, Mitochondrial	CTD_diseases	4
MESH:C564020	MESH:C564020	Ataxia and Polyneuropathy, Adult-Onset	CTD_diseases	4
MESH:C564024	MESH:C564024	Hypomagnesemia, Hypertension, and Hypercholesterolemia, Mitochondrial	CTD_diseases	4
MESH:C564029	MESH:C564029	Hairy Ears, Y-Linked	CTD_diseases	4
MESH:C564030	MESH:C564030	Spermatogenic Failure, Nonobstructive, Y-Linked	CTD_diseases	4
MESH:C564034	MESH:C564034	Hodgkin Disease, Y-Linked Pseudoautosomal	CTD_diseases	4
MESH:C564035	MESH:C564035	Retinitis Pigmentosa, Y-Linked	CTD_diseases	4
MESH:C564040	MESH:C564040	Widow's Peak Syndrome	CTD_diseases	4
MESH:C564041	MESH:C564041	Von Willebrand Disease, X-Linked Form	CTD_diseases	4
MESH:C564042	MESH:C564042	Vesicoureteral Reflux, X-Linked	CTD_diseases	4
MESH:C564048	MESH:C564048	Dystonia 3, Torsion, X-Linked	CTD_diseases	4
MESH:C564049	MESH:C564049	Thyroxine-Binding Globulin Deficiency	CTD_diseases	4
MESH:C564050	MESH:C564050	Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis	CTD_diseases	4
MESH:C564052	MESH:C564052	Thrombocytopenia 1	CTD_diseases	4
MESH:C564053	MESH:C564053	Thrombocytopenia, X-Linked, Intermittent	CTD_diseases	4
MESH:C564054	MESH:C564054	Midline Defects, X-Linked	CTD_diseases	4
MESH:C564056	MESH:C564056	Split-Hand Foot Malformation 2	CTD_diseases	4
MESH:C564065	MESH:C564065	Retinitis Pigmentosa 6	CTD_diseases	4
MESH:C564072	MESH:C564072	Multiple Pterygium Syndrome, X-Linked	CTD_diseases	4
MESH:C564087	MESH:C564087	Ophthalmoplegia, External, and Myopia	CTD_diseases	4
MESH:C564090	MESH:C564090	Neuropathy, Hereditary Sensory, X-Linked	CTD_diseases	4
MESH:C564091	MESH:C564091	Myopia 1	CTD_diseases	4
MESH:C564092	MESH:C564092	Bornholm Eye Disease	CTD_diseases	4
MESH:C564093	MESH:C564093	Myopathy, X-Linked, with Excessive Autophagy	CTD_diseases	4
MESH:C564095	MESH:C564095	Muscular Dystrophy, Progressive Pectorodorsal	CTD_diseases	4
MESH:C564098	MESH:C564098	Modifier, X-Linked, for Neurofunctional Defects	CTD_diseases	4
MESH:C564101	MESH:C564101	Mental Retardation, Skeletal Dysplasia, and Abducens Palsy	CTD_diseases	4
MESH:C564106	MESH:C564106	Mental Retardation, X-Linked, Syndromic 12	CTD_diseases	4
MESH:C564108	MESH:C564108	Major Affective Disorder 2	CTD_diseases	4
MESH:C564110	MESH:C564110	Macular Dystrophy, X-Linked	CTD_diseases	4
MESH:C564112	MESH:C564112	Leukemia, Acute, X-Linked	CTD_diseases	4
MESH:C564114	MESH:C564114	Leigh Syndrome, X-Linked	CTD_diseases	4
MESH:C564115	MESH:C564115	Corpus Callosum, Partial Agenesis of, X-Linked	CTD_diseases	4
MESH:C564122	MESH:C564122	Hyperthyroxinemia due to Decreased Peripheral Conversion of T4	CTD_diseases	4
MESH:C564127	MESH:C564127	Inosine Triphosphatase Deficiency	CTD_diseases	4
MESH:C564145	MESH:C564145	Hypophosphatemic Bone Disease	CTD_diseases	4
MESH:C564146	MESH:C564146	Odontohypophosphatasia	CTD_diseases	4
MESH:C564148	MESH:C564148	Hypoparathyroidism, Autosomal Recessive	CTD_diseases	4
MESH:C564152	MESH:C564152	Hypertrophia Musculorum Vera	CTD_diseases	4
MESH:C564154	MESH:C564154	Thyroid Hormone Resistance, Selective Pituitary	CTD_diseases	4
MESH:C564157	MESH:C564157	Hypertaurinuric Cardiomyopathy	CTD_diseases	4
MESH:C564168	MESH:C564168	Hyperostosis Cranialis Interna	CTD_diseases	4
MESH:C564183	MESH:C564183	Histiocytic Dermatoarthritis	CTD_diseases	4
MESH:C564186	MESH:C564186	Histiocytosis, Progressive Mucinous	CTD_diseases	4
MESH:C564192	MESH:C564192	Methemoglobinemia, Beta-Globin Type	CTD_diseases	4
MESH:C564194	MESH:C564194	Methemoglobinemia, Alpha-Globin Type	CTD_diseases	4
MESH:C564199	MESH:C564199	Hemifacial Hyperplasia With Strabismus	CTD_diseases	4
MESH:C564200	MESH:C564200	Heme Oxygenase 1 Deficiency	CTD_diseases	4
MESH:C564206	MESH:C564206	Achromatopsia 4	CTD_diseases	4
MESH:C564209	MESH:C564209	Graying of Hair, Precocious	CTD_diseases	4
MESH:C564214	MESH:C564214	Goniodysgenesis-Mental Retardation-Short Stature Syndrome	CTD_diseases	4
MESH:C564215	MESH:C564215	Glyoxalase II Deficiency	CTD_diseases	4
MESH:C564221	MESH:C564221	Glucocorticoid Receptor Deficiency	CTD_diseases	4
MESH:C564229	MESH:C564229	Globulin Anomaly involving Beta (2A)-Globulin	CTD_diseases	4
MESH:C564232	MESH:C564232	Glaucoma and Sleep Apnea	CTD_diseases	4
MESH:C564243	MESH:C564243	Prolonged Electroretinal Response Suppression	CTD_diseases	4
MESH:C564244	MESH:C564244	Vater-Like Defects with Pulmonary Hypertension, Laryngeal Webs, and Growth Deficiency	CTD_diseases	4
MESH:C564253	MESH:C564253	Myopathy, Myosin Storage	CTD_diseases	4
MESH:C564263	MESH:C564263	Craniosynostosis with Ocular Abnormalities and Hallucal Defects	CTD_diseases	4
MESH:C564264	MESH:C564264	Growth Failure, Microcephaly, Mental Retardation, Cataracts, Large Joint Contractures, Osteoporosis,	CTD_diseases	4
MESH:C564267	MESH:C564267	Mandibulofacial Dysostosis with Ptosis, Autosomal Dominant	CTD_diseases	4
MESH:C564268	MESH:C564268	Otosclerosis 3	CTD_diseases	4
MESH:C564271	MESH:C564271	Craniofacial Abnormalities, Cataracts, Congenital Heart Disease, Sacral Neural Tube Defects, and Gro	CTD_diseases	4
MESH:C564283	MESH:C564283	Lipodystrophy, Generalized, with Mental Retardation, Deafness, Short Stature, and Slender Bones	CTD_diseases	4
MESH:C564309	MESH:C564309	Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa of Siemens-like	CTD_diseases	4
MESH:C564327	MESH:C564327	Hypotrichosis-Lymphedema-Telangiectasia Syndrome	CTD_diseases	4
MESH:C564332	MESH:C564332	Craniolenticulosutural Dysplasia	CTD_diseases	4
MESH:C564334	MESH:C564334	Acrocapitofemoral Dysplasia	CTD_diseases	4
MESH:C564353	MESH:C564353	Cataract, Congenital, with Mental Impairment and Dentate Gyrus Atrophy	CTD_diseases	4
MESH:C564354	MESH:C564354	Dystonia 13, Torsion	CTD_diseases	4
MESH:C564359	MESH:C564359	Skin Fragility-Woolly Hair Syndrome	CTD_diseases	4
MESH:C564361	MESH:C564361	Candidiasis, Familial, 3	CTD_diseases	4
MESH:C564365	MESH:C564365	Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis	CTD_diseases	4
MESH:C564382	MESH:C564382	Secretory Diarrhea, Myopathy, and Deafness	CTD_diseases	4
MESH:C564384	MESH:C564384	Toenail Dystrophy, Isolated	CTD_diseases	4
MESH:C564395	MESH:C564395	Spinocerebellar Ataxia with Epilepsy	CTD_diseases	4
MESH:C564403	MESH:C564403	Coenzyme Q10 Deficiency	CTD_diseases	4
MESH:C564406	MESH:C564406	Hypogonadism, Male, With Mental Retardation And Skeletal Anomalies	CTD_diseases	4
MESH:C564407	MESH:C564407	Hydrocephalus With Cerebellar Agenesis	CTD_diseases	4
MESH:C564408	MESH:C564408	Hydrocephalus, X-Linked, with Congenital Idiopathic Intestinal Pseudoobstruction	CTD_diseases	4
MESH:C564421	MESH:C564421	Liver Glycogenosis, X-Linked, Type II	CTD_diseases	4
MESH:C564422	MESH:C564422	Glutamyl Ribose-5-Phosphate Storage Disease	CTD_diseases	4
MESH:C564423	MESH:C564423	Membranoproliferative Glomerulonephritis, X-Linked	CTD_diseases	4
MESH:C564424	MESH:C564424	Genitourinary Tract Anomalies	CTD_diseases	4
MESH:C564425	MESH:C564425	Fingerprint Body Myopathy	CTD_diseases	4
MESH:C564427	MESH:C564427	Faciogenital Dysplasia with Attention Deficit-Hyperactivity Disorder	CTD_diseases	4
MESH:C564428	MESH:C564428	Exudative Vitreoretinopathy, Familial, X-Linked Recessive	CTD_diseases	4
MESH:C564429	MESH:C564429	Anemia, X-Linked, without Thrombocytopenia	CTD_diseases	4
MESH:C564430	MESH:C564430	Epidermodysplasia Verruciformis, X-Linked	CTD_diseases	4
MESH:C564432	MESH:C564432	Deafness, High-Frequency Sensorineural, X-Linked	CTD_diseases	4
MESH:C564433	MESH:C564433	Deafness, X-Linked 1	CTD_diseases	4
MESH:C564435	MESH:C564435	Deafness-Hypogonadism Syndrome	CTD_diseases	4
MESH:C564438	MESH:C564438	Cone-Rod Dystrophy, X-Linked, Type 1	CTD_diseases	4
MESH:C564439	MESH:C564439	Cone Dystrophy, X-Linked, 1	CTD_diseases	4
MESH:C564442	MESH:C564442	Cleft Palate with Ankyloglossia	CTD_diseases	4
MESH:C564452	MESH:C564452	Microphthalmia, Isolated, with Cataract 3	CTD_diseases	4
MESH:C564459	MESH:C564459	Spina Bifida, X-Linked	CTD_diseases	4
MESH:C564461	MESH:C564461	Pigmentary Disorder, Reticulate, with Systemic Manifestations	CTD_diseases	4
MESH:C564467	MESH:C564467	Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked	CTD_diseases	4
MESH:C564469	MESH:C564469	Lymphoproliferative Syndrome, X-Linked, 2	CTD_diseases	4
MESH:C564472	MESH:C564472	Deafness, X-Linked 5	CTD_diseases	4
MESH:C564473	MESH:C564473	Myopia 13	CTD_diseases	4
MESH:C564474	MESH:C564474	Hyperekplexia and Epilepsy	CTD_diseases	4
MESH:C564475	MESH:C564475	Retinitis Pigmentosa 34	CTD_diseases	4
MESH:C564478	MESH:C564478	Nystagmus 5, Infantile Periodic Alternating	CTD_diseases	4
MESH:C564479	MESH:C564479	Short Stature, Idiopathic, X-Linked	CTD_diseases	4
MESH:C564480	MESH:C564480	Fg Syndrome 5	CTD_diseases	4
MESH:C564485	MESH:C564485	Glycogen Storage Disease, Type IXD	CTD_diseases	4
MESH:C564486	MESH:C564486	Parkinson Disease 12	CTD_diseases	4
MESH:C564487	MESH:C564487	Dent Disease 2	CTD_diseases	4
MESH:C564491	MESH:C564491	Nephrogenic Syndrome of Inappropriate Antidiuresis	CTD_diseases	4
MESH:C564492	MESH:C564492	Heterotopia, Periventricular, Ehlers-Danlos Variant	CTD_diseases	4
MESH:C564495	MESH:C564495	Martin-Probst Deafness-Mental Retardation Syndrome	CTD_diseases	4
MESH:C564498	MESH:C564498	Premature Ovarian Failure 2a	CTD_diseases	4
MESH:C564499	MESH:C564499	Ovarian Dysgenesis 2	CTD_diseases	4
MESH:C564506	MESH:C564506	Spinal Muscular Atrophy, Distal, X-Linked 3	CTD_diseases	4
MESH:C564507	MESH:C564507	Cone-Rod Dystrophy, X-Linked, 3	CTD_diseases	4
MESH:C564508	MESH:C564508	Contiguous Abcd1/Dxs1375e Deletion Syndrome	CTD_diseases	4
MESH:C564520	MESH:C564520	Retinitis Pigmentosa 3	CTD_diseases	4
MESH:C564523	MESH:C564523	Radial Ray Deficiency, X-Linked	CTD_diseases	4
MESH:C564525	MESH:C564525	Dyserythropoietic Anemia with Thrombocytopenia	CTD_diseases	4
MESH:C564526	MESH:C564526	Macrothrombocytopenia, X-Linked	CTD_diseases	4
MESH:C564527	MESH:C564527	Mental Retardation, X-Linked, with Short Stature	CTD_diseases	4
MESH:C564531	MESH:C564531	Microphthalmia, Isolated, with Coloboma 1	CTD_diseases	4
MESH:C564532	MESH:C564532	Thrombocytosis, Familial X-Linked	CTD_diseases	4
MESH:C564539	MESH:C564539	Neutropenia, Severe Congenital, X-Linked	CTD_diseases	4
MESH:C564543	MESH:C564543	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, And Genital An	CTD_diseases	4
MESH:C564544	MESH:C564544	Uruguay Faciocardiomusculoskeletal Syndrome	CTD_diseases	4
MESH:C564553	MESH:C564553	Ptosis, Hereditary Congenital 2	CTD_diseases	4
MESH:C564554	MESH:C564554	Terminal Osseous Dysplasia and Pigmentary Defects	CTD_diseases	4
MESH:C564559	MESH:C564559	Testicular Germ Cell Tumor 1	CTD_diseases	4
MESH:C564561	MESH:C564561	Myotubular Myopathy with Abnormal Genital Development	CTD_diseases	4
MESH:C564563	MESH:C564563	Lissencephaly, X-Linked, 2	CTD_diseases	4
MESH:C564565	MESH:C564565	Episodic Muscle Weakness, X-Linked	CTD_diseases	4
MESH:C564567	MESH:C564567	Simpson-Golabi-Behmel Syndrome, Type 2	CTD_diseases	4
MESH:C564568	MESH:C564568	Adrenal Hypoplasia, Congenital, with Precocious Puberty	CTD_diseases	4
MESH:C564570	MESH:C564570	Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis	CTD_diseases	4
MESH:C564572	MESH:C564572	X Inactivation, Familial Skewed, 2	CTD_diseases	4
MESH:C564574	MESH:C564574	Arthrogryposis, X-Linked, Type V	CTD_diseases	4
MESH:C564577	MESH:C564577	Glucocorticoid Deficiency 2	CTD_diseases	4
MESH:C564596	MESH:C564596	Cataract, Nuclear Progressive	CTD_diseases	4
MESH:C564606	MESH:C564606	Anonychia, Total, with Microcephaly	CTD_diseases	4
MESH:C564611	MESH:C564611	Multiple Congenital Anomalies Syndrome with Cloverleaf Skull	CTD_diseases	4
MESH:C564619	MESH:C564619	Cataract, Sutural, with Punctate and Cerulean Opacities	CTD_diseases	4
MESH:C564654	MESH:C564654	Cree Mental Retardation Syndrome	CTD_diseases	4
MESH:C564655	MESH:C564655	Cardioneuromyopathy with Hyaline Masses and Nemaline Rods	CTD_diseases	4
MESH:C564658	MESH:C564658	Peripheral Arterial Occlusive Disease 1	CTD_diseases	4
MESH:C564660	MESH:C564660	MOMES Syndrome	CTD_diseases	4
MESH:C564661	MESH:C564661	Abducens Palsy	CTD_diseases	4
MESH:C564669	MESH:C564669	Lipodystrophy with Congenital Cataracts and Neurodegeneration	CTD_diseases	4
MESH:C564700	MESH:C564700	Craniosynostosis Syndrome, Autosomal Recessive	CTD_diseases	4
MESH:C564701	MESH:C564701	Homozygous 11p15-p14 Deletion Syndrome	CTD_diseases	4
MESH:C564708	MESH:C564708	Huntington Disease-Like 2	CTD_diseases	4
MESH:C564710	MESH:C564710	Hypotonia-Cystinuria Syndrome	CTD_diseases	4
MESH:C564714	MESH:C564714	Spondyloepimetaphyseal Dysplasia, X-Linked	CTD_diseases	4
MESH:C564715	MESH:C564715	Epilepsy, Female-Restricted, with Mental Retardation	CTD_diseases	4
MESH:C564716	MESH:C564716	X Inactivation, Familial Skewed, 1	CTD_diseases	4
MESH:C564717	MESH:C564717	Cone-Rod Dystrophy, X-Linked, 2	CTD_diseases	4
MESH:C564721	MESH:C564721	Cardiomyopathy, Dilated, 3A	CTD_diseases	4
MESH:C564723	MESH:C564723	Deafness, X-Linked 4	CTD_diseases	4
MESH:C564724	MESH:C564724	Mental Retardation with Psychosis, Pyramidal Signs, and Macroorchidism	CTD_diseases	4
MESH:C564725	MESH:C564725	Heterotopia, Periventricular Nodular, with Frontometaphyseal Dysplasia	CTD_diseases	4
MESH:C564727	MESH:C564727	Deafness, X-Linked 3	CTD_diseases	4
MESH:C564735	MESH:C564735	Woolly Hair, Autosomal Recessive	CTD_diseases	4
MESH:C564739	MESH:C564739	Vitiligo, Progressive, with Mental Retardation and Urethral Duplication	CTD_diseases	4
MESH:C564751	MESH:C564751	VACTERL Association With Hydrocephalus	CTD_diseases	4
MESH:C564757	MESH:C564757	Ulnar Hypoplasia with Mental Retardation	CTD_diseases	4
MESH:C564760	MESH:C564760	Trichoodontoonychial Dysplasia	CTD_diseases	4
MESH:C564768	MESH:C564768	Thymic Aplasia with Fetal Death	CTD_diseases	4
MESH:C564769	MESH:C564769	Thumb, Hypoplastic, with Choroid Coloboma, Poorly Developed Antihelix, and Deafness	CTD_diseases	4
MESH:C564777	MESH:C564777	Male Germ Cell Tumor	CTD_diseases	4
MESH:C564791	MESH:C564791	Cold-Induced Sweating Syndrome 1	CTD_diseases	4
MESH:C564799	MESH:C564799	Spondylocostal Dysostosis with Anal Atresia and Urogenital Anomalies	CTD_diseases	4
MESH:C564809	MESH:C564809	Spastic Paresis, Glaucoma, and Mental Retardation	CTD_diseases	4
MESH:C564816	MESH:C564816	Insulin-Like Growth Factor I, Resistance To	CTD_diseases	4
MESH:C564817	MESH:C564817	Insulin-Like Growth Factor I, Resistance to, due to Increased Binding Protein	CTD_diseases	4
MESH:C564818	MESH:C564818	Peeling Skin Syndrome	CTD_diseases	4
MESH:C564835	MESH:C564835	Enhanced S-Cone Syndrome	CTD_diseases	4
MESH:C564841	MESH:C564841	Retinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism	CTD_diseases	4
MESH:C564847	MESH:C564847	Retinal Degeneration and Epilepsy	CTD_diseases	4
MESH:C564848	MESH:C564848	Respiratory Underresponsiveness to Hypoxia and Hypercapnia	CTD_diseases	4
MESH:C564849	MESH:C564849	Renal, Genital, and Middle Ear Anomalies	CTD_diseases	4
MESH:C564856	MESH:C564856	Radioulnar Synostosis, Unilateral, with Developmental Retardation and Hypotonia	CTD_diseases	4
MESH:C564861	MESH:C564861	Pygmy	CTD_diseases	4
MESH:C564862	MESH:C564862	Pulmonary Hypertension, Primary, Autosomal Recessive	CTD_diseases	4
MESH:C564863	MESH:C564863	Pulmonary Bullae Causing Pneumothorax	CTD_diseases	4
MESH:C564866	MESH:C564866	Acrootoocular Syndrome	CTD_diseases	4
MESH:C564873	MESH:C564873	Prenatal Bowing	CTD_diseases	4
MESH:C564874	MESH:C564874	Popliteal Pterygium Syndrome, Lethal Type	CTD_diseases	4
MESH:C564876	MESH:C564876	Polyhydramnios, Chronic Idiopathic	CTD_diseases	4
MESH:C564881	MESH:C564881	Polycystic Kidney Disease, Potter Type I, with Microbrachycephaly, Hypertelorism, and Brachymelia	CTD_diseases	4
MESH:C564882	MESH:C564882	Polycystic Kidney, Cataract, and Congenital Blindness	CTD_diseases	4
MESH:C564884	MESH:C564884	Platelet Prostacyclin Receptor Defect	CTD_diseases	4
MESH:C564885	MESH:C564885	Plasma Clot Retraction Factor, Deficiency of	CTD_diseases	4
MESH:C564890	MESH:C564890	Phosphoenolpyruvate Carboxykinase Deficiency, Mitochondrial	CTD_diseases	4
MESH:C564893	MESH:C564893	Presentey Anomaly	CTD_diseases	4
MESH:C564894	MESH:C564894	Peripheral Neuropathy, Ataxia, Focal Necrotizing Encephalopathy, and Spongy Degeneration of Brain	CTD_diseases	4
MESH:C564895	MESH:C564895	Pericardial Effusion, Chronic	CTD_diseases	4
MESH:C564899	MESH:C564899	Pelger-Huet-Like Anomaly and Episodic Fever with Abdominal Pain	CTD_diseases	4
MESH:C564905	MESH:C564905	Parana Hard Skin Syndrome	CTD_diseases	4
MESH:C564907	MESH:C564907	Pancreatic Insufficiency, Combined Exocrine	CTD_diseases	4
MESH:C564912	MESH:C564912	Otoonychoperoneal Syndrome	CTD_diseases	4
MESH:C564925	MESH:C564925	Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria	CTD_diseases	4
MESH:C564927	MESH:C564927	Ophthalmoplegia Totalis with Ptosis and Miosis	CTD_diseases	4
MESH:C564934	MESH:C564934	Oculotrichodysplasia	CTD_diseases	4
MESH:C564935	MESH:C564935	Oculopalatocerebral Syndrome	CTD_diseases	4
MESH:C564942	MESH:C564942	Neutrophil Actin Dysfunction	CTD_diseases	4
MESH:C564945	MESH:C564945	Neuropathy, Painful	CTD_diseases	4
MESH:C564946	MESH:C564946	Neuropathy, Hereditary Sensory, Atypical	CTD_diseases	4
MESH:C564970	MESH:C564970	Myopathy, Hyaline Body, Autosomal Recessive	CTD_diseases	4
MESH:C564971	MESH:C564971	Myopathy with Giant Abnormal Mitochondria	CTD_diseases	4
MESH:C564972	MESH:C564972	Myopathy with Lactic Acidosis, Hereditary	CTD_diseases	4
MESH:C564973	MESH:C564973	Myopathy due to Malate-Aspartate Shuttle Defect	CTD_diseases	4
MESH:C564974	MESH:C564974	Myopathy, Granulovacuolar Lobular, with Electrical Myotonia	CTD_diseases	4
MESH:C565005	MESH:C565005	Foveal Hypoplasia, Isolated	CTD_diseases	4
MESH:C565006	MESH:C565006	Foveal Hypoplasia with Anterior Segment Anomalies	CTD_diseases	4
MESH:C565007	MESH:C565007	Fourth Cranial Nerve Palsy, Familial Congenital	CTD_diseases	4
MESH:C565008	MESH:C565008	Focal Epithelial Hyperplasia of the Oral Mucosa	CTD_diseases	4
MESH:C565010	MESH:C565010	Fingerprints, Absence of	CTD_diseases	4
MESH:C565017	MESH:C565017	Fibrinolytic Defect	CTD_diseases	4
MESH:C565026	MESH:C565026	Factor V Excess with Spontaneous Thrombosis	CTD_diseases	4
MESH:C565032	MESH:C565032	Extrasystoles, Multiform Ventricular, with Short Stature, Hyperpigmentation and Microcephaly	CTD_diseases	4
MESH:C565041	MESH:C565041	Erythema Palmare Hereditarium	CTD_diseases	4
MESH:C565043	MESH:C565043	Arene Oxide Detoxification Defect	CTD_diseases	4
MESH:C565044	MESH:C565044	Diphenylhydantoin, Defect in Hydroxylation of	CTD_diseases	4
MESH:C565046	MESH:C565046	Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness	CTD_diseases	4
MESH:C565063	MESH:C565063	Edema, Familial Idiopathic, Prepubertal	CTD_diseases	4
MESH:C565076	MESH:C565076	Dysplasia Epiphysealis Hemimelica with Chondromas and Osteochondromas	CTD_diseases	4
MESH:C565077	MESH:C565077	Diffuse Lewy Body Disease with Gaze Palsy	CTD_diseases	4
MESH:C565080	MESH:C565080	Dyschondrosteosis and Nephritis	CTD_diseases	4
MESH:C565084	MESH:C565084	Plantar Fibromatosis, Familial	CTD_diseases	4
MESH:C565088	MESH:C565088	Drusen, Radial, Autosomal Dominant	CTD_diseases	4
MESH:C565089	MESH:C565089	Doughnut Lesions of Skull, Familial	CTD_diseases	4
MESH:C565090	MESH:C565090	Double Nail for Fifth Toe	CTD_diseases	4
MESH:C565094	MESH:C565094	Disproportionate Short Stature with Ptosis and Valvular Heart Lesions	CTD_diseases	4
MESH:C565103	MESH:C565103	Dermoodontodysplasia	CTD_diseases	4
MESH:C565109	MESH:C565109	Dermal Ridges, Patternless	CTD_diseases	4
MESH:C565110	MESH:C565110	Dermal Ridges, Nelson Syndrome	CTD_diseases	4
MESH:C565112	MESH:C565112	Deoxyribose-5-Phosphate Aldolase Deficiency	CTD_diseases	4
MESH:C565115	MESH:C565115	Dementia/Parkinsonism With Non-Alzheimer Amyloid Plaques	CTD_diseases	4
MESH:C565117	MESH:C565117	Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy	CTD_diseases	4
MESH:C565123	MESH:C565123	Deafness, Conductive Stapedial, with Ear Malformation and Facial Palsy	CTD_diseases	4
MESH:C565127	MESH:C565127	Phenacetin O-Deethylase, Deficiency of	CTD_diseases	4
MESH:C565128	MESH:C565128	Mitochondrial Complex III Deficiency	CTD_diseases	4
MESH:C565129	MESH:C565129	Cutis Gyrata Syndrome of Beare And Stevenson	CTD_diseases	4
MESH:C565130	MESH:C565130	Cataract, Progressive Polymorphic Cortical	CTD_diseases	4
MESH:C565131	MESH:C565131	Cataract, Punctate, Progressive Juvenile-Onset	CTD_diseases	4
MESH:C565132	MESH:C565132	Cataract, Variable Zonular Pulverulent	CTD_diseases	4
MESH:C565133	MESH:C565133	Cataract, Coppock-Like	CTD_diseases	4
MESH:C565134	MESH:C565134	Cataract, Posterior Polar, 2	CTD_diseases	4
MESH:C565135	MESH:C565135	Cataract, Zonular Central Nuclear	CTD_diseases	4
MESH:C565136	MESH:C565136	Cataract, Autosomal Recessive Congenital 1	CTD_diseases	4
MESH:C565137	MESH:C565137	Cataract, Autosomal Dominant Nuclear	CTD_diseases	4
MESH:C565148	MESH:C565148	Coxoauricular Syndrome	CTD_diseases	4
MESH:C565150	MESH:C565150	Polydysspondyly	CTD_diseases	4
MESH:C565160	MESH:C565160	Delayed Cranial Ossification due to CBFB Haploinsufficiency	CTD_diseases	4
MESH:C565172	MESH:C565172	Colonic Varices without Portal Hypertension	CTD_diseases	4
MESH:C565184	MESH:C565184	Cerebrooculofacioskeletal Syndrome 4	CTD_diseases	4
MESH:C565185	MESH:C565185	Cerebrooculofacioskeletal Syndrome 2	CTD_diseases	4
MESH:C565192	MESH:C565192	Neutral Lipid Storage Disease with Myopathy	CTD_diseases	4
MESH:C565202	MESH:C565202	Myopia 14	CTD_diseases	4
MESH:C565217	MESH:C565217	Seborrhea-Like Dermatitis with Psoriasiform Elements	CTD_diseases	4
MESH:C565221	MESH:C565221	Erythrocytosis, Familial, 3	CTD_diseases	4
MESH:C565222	MESH:C565222	Vasculitis, Lymphocytic, Cutaneous Small Vessel	CTD_diseases	4
MESH:C565240	MESH:C565240	Paget Disease Of Bone 4	CTD_diseases	4
MESH:C565246	MESH:C565246	Mental Retardation, Microcephaly, Growth Retardation, Joint Contractures, and Facial Dysmorphism	CTD_diseases	4
MESH:C565255	MESH:C565255	Genitopatellar Syndrome	CTD_diseases	4
MESH:C565273	MESH:C565273	Arthropathy, Erosive	CTD_diseases	4
MESH:C565275	MESH:C565275	Bleeding Disorder, East Texas Type	CTD_diseases	4
MESH:C565282	MESH:C565282	Baby Rattle Pelvis Dysplasia	CTD_diseases	4
MESH:C565285	MESH:C565285	Spondyloocular Syndrome, Autosomal Recessive	CTD_diseases	4
MESH:C565295	MESH:C565295	Gonadal Dysgenesis, Hypergonadotropic, XX Type, Short Stature, and Recurrent Metabolic Acidosis	CTD_diseases	4
MESH:C565297	MESH:C565297	Exudative Vitreoretinopathy 3	CTD_diseases	4
MESH:C565298	MESH:C565298	Cataract, Autosomal Recessive, Early-Onset, Pulverulent	CTD_diseases	4
MESH:C565299	MESH:C565299	Anisomastia	CTD_diseases	4
MESH:C565301	MESH:C565301	Cataract, Central Saccular, With Sutural Opacities	CTD_diseases	4
MESH:C565302	MESH:C565302	Otosclerosis 2	CTD_diseases	4
MESH:C565304	MESH:C565304	Multiple Mitochondrial Dysfunctions Syndrome	CTD_diseases	4
MESH:C565306	MESH:C565306	Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness	CTD_diseases	4
MESH:C565308	MESH:C565308	Cerebellar Ataxia and Hypergonadotropic Hypogonadism	CTD_diseases	4
MESH:C565309	MESH:C565309	Late-Onset Retinal Degeneration	CTD_diseases	4
MESH:C565331	MESH:C565331	Fibromatosis, Gingival, with Hypertrichosis and Mental Retardation	CTD_diseases	4
MESH:C565335	MESH:C565335	Paragangliomas 3	CTD_diseases	4
MESH:C565340	MESH:C565340	Frontoocular Syndrome	CTD_diseases	4
MESH:C565358	MESH:C565358	Growth Deficiency and Mental Retardation with Facial Dysmorphism	CTD_diseases	4
MESH:C565359	MESH:C565359	Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy	CTD_diseases	4
MESH:C565370	MESH:C565370	Monosomy 7 of Bone Marrow	CTD_diseases	4
MESH:C565375	MESH:C565375	Mitochondrial Complex II Deficiency	CTD_diseases	4
MESH:C565393	MESH:C565393	3-Methylglutaconic Aciduria Type IV	CTD_diseases	4
MESH:C565394	MESH:C565394	Methylcobalamin Deficiency, CblG Type	CTD_diseases	4
MESH:C565404	MESH:C565404	Mesomelic Limb Shortening and Bowing	CTD_diseases	4
MESH:C565405	MESH:C565405	Mesangial Sclerosis, Diffuse Renal, with Ocular Abnormalities	CTD_diseases	4
MESH:C565421	MESH:C565421	Malocclusion and Short Stature	CTD_diseases	4
MESH:C565423	MESH:C565423	Hypomagnesemia 5, Renal, with Ocular Involvement	CTD_diseases	4
MESH:C565432	MESH:C565432	Lymphedema, Congenital Recessive	CTD_diseases	4
MESH:C565439	MESH:C565439	Leukotriene C4 Synthase Deficiency	CTD_diseases	4
MESH:C565440	MESH:C565440	Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis	CTD_diseases	4
MESH:C565442	MESH:C565442	Leg, Absence Deformity of, with Congenital Cataract	CTD_diseases	4
MESH:C565446	MESH:C565446	Lactic Aciduria due to D-Lactic Acid	CTD_diseases	4
MESH:C565449	MESH:C565449	Erythrocyte Lactate Transporter Defect	CTD_diseases	4
MESH:C565453	MESH:C565453	Ketoadipicaciduria	CTD_diseases	4
MESH:C565455	MESH:C565455	Keratoconus Posticus Circumscriptus with Associated Malformations	CTD_diseases	4
MESH:C565456	MESH:C565456	Keratoconus And Congenital Hip Dysplasia	CTD_diseases	4
MESH:C565460	MESH:C565460	Jejunal Atresia with Microcephaly and Ocular Anomalies	CTD_diseases	4
MESH:C565461	MESH:C565461	Intrinsic Factor and R Binder, Combined Congenital Deficiency of	CTD_diseases	4
MESH:C565462	MESH:C565462	Iris Coloboma with Ptosis, Hypertelorism, and Mental Retardation	CTD_diseases	4
MESH:C565467	MESH:C565467	Indifference to Pain, Congenital, Autosomal Recessive	CTD_diseases	4
MESH:C565475	MESH:C565475	Hypouricemia, Hypercalcinuria, and Decreased Bone Density	CTD_diseases	4
MESH:C565476	MESH:C565476	Hypoproteinemia, Hypercatabolic	CTD_diseases	4
MESH:C565478	MESH:C565478	Hypophosphatemia, Renal, with Intracerebral Calcifications	CTD_diseases	4
MESH:C565481	MESH:C565481	Hypohidrosis aith Abnormal Palmar Dermal Ridges	CTD_diseases	4
MESH:C565482	MESH:C565482	Hypogonadism with Low-Grade Mental Deficiency and Microcephaly	CTD_diseases	4
MESH:C565486	MESH:C565486	L-Gulonolactone Oxidase, Nonfunctional	CTD_diseases	4
MESH:C565489	MESH:C565489	Hyperuricemia, Infantile, with Abnormal Behavior and Normal Hypoxanthine Guanine Phosphoribosyltrans	CTD_diseases	4
MESH:C565490	MESH:C565490	Hypertrophic Neuropathy And Cataract	CTD_diseases	4
MESH:C565495	MESH:C565495	Hyperphosphatasia with Mental Retardation	CTD_diseases	4
MESH:C565497	MESH:C565497	Hyperopia, High	CTD_diseases	4
MESH:C565498	MESH:C565498	Hypermetabolism due to Defect in Mitochondria	CTD_diseases	4
MESH:C565524	MESH:C565524	Hemihyperplasia, Isolated	CTD_diseases	4
MESH:C565528	MESH:C565528	Growth Retardation, Small and Puffy Hands and Feet, and Eczema	CTD_diseases	4
MESH:C565529	MESH:C565529	Growth Factors, Combined Defect of	CTD_diseases	4
MESH:C565536	MESH:C565536	Gonadal Dysgenesis, XY Type, with Associated Anomalies	CTD_diseases	4
MESH:C565538	MESH:C565538	Glycoprotein Storage Disease	CTD_diseases	4
MESH:C565547	MESH:C565547	Glaucoma 3, Primary Congenital, A	CTD_diseases	4
MESH:C565562	MESH:C565562	Fraser-Like Syndrome	CTD_diseases	4
MESH:C565579	MESH:C565579	Facial Dysmorphism with Multiple Malformations	CTD_diseases	4
MESH:C565584	MESH:C565584	Epithelial Squamous Dysplasia, Keratinizing Desquamative, of Urinary Tract	CTD_diseases	4
MESH:C565585	MESH:C565585	Epiphyseal Dysplasia of Femoral Head, Myopia, and Deafness	CTD_diseases	4
MESH:C565591	MESH:C565591	Endothelial Dystrophy, Congenital Hereditary, with Nail Hypoplasia	CTD_diseases	4
MESH:C565594	MESH:C565594	Encephalopathy with Intracranial Calcification, Growth Hormone Deficiency, Microcephaly, and Retinal	CTD_diseases	4
MESH:C565596	MESH:C565596	Encephalopathy, Axonal, with Necrotizing Myopathy, Cardiomyopathy, and Cataracts	CTD_diseases	4
MESH:C565600	MESH:C565600	Ehlers-Danlos Syndrome with Platelet Dysfunction from Fibronectin Abnormality	CTD_diseases	4
MESH:C565618	MESH:C565618	DK Phocomelia Syndrome	CTD_diseases	4
MESH:C565619	MESH:C565619	Diverticulosis of Bowel, Hernia, and Retinal Detachment	CTD_diseases	4
MESH:C565620	MESH:C565620	Diverticulosis, Small Intestinal	CTD_diseases	4
MESH:C565627	MESH:C565627	Trichohepatoenteric Syndrome	CTD_diseases	4
MESH:C565634	MESH:C565634	Gliosis, Familial Progressive Subcortical	CTD_diseases	4
MESH:C565645	MESH:C565645	Deafness, Cochlear, with Myopia and Intellectual Impairment	CTD_diseases	4
MESH:C565658	MESH:C565658	Cystic Fibrosis with Helicobacter Pylori Gastritis, Megaloblastic Anemia, and Subnormal Mentality	CTD_diseases	4
MESH:C565661	MESH:C565661	Cutis Verticis Gyrata and Mental Deficiency	CTD_diseases	4
MESH:C565664	MESH:C565664	Craniosynostosis-Mental Retardation Syndrome of Lin and Gettig	CTD_diseases	4
MESH:C565681	MESH:C565681	Terminal Transverse Defects of Arm	CTD_diseases	4
MESH:C565682	MESH:C565682	Amputation, Congenital	CTD_diseases	4
MESH:C565687	MESH:C565687	Collagenosis, Familial Reactive Perforating	CTD_diseases	4
MESH:C565690	MESH:C565690	Combined Oxidative Phosphorylation Deficiency 4	CTD_diseases	4
MESH:C565693	MESH:C565693	Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and Sex Reversal	CTD_diseases	4
MESH:C565699	MESH:C565699	NBIA2B	CTD_diseases	4
MESH:C565703	MESH:C565703	Cataract, Pulverulent, Juvenile-Onset	CTD_diseases	4
MESH:C565706	MESH:C565706	3-Methylglutaconic Aciduria, Type V	CTD_diseases	4
MESH:C565722	MESH:C565722	Encephalopathy, Spastic Tetraparesis, and Hypogonadism	CTD_diseases	4
MESH:C565725	MESH:C565725	Cataract, Congenital Nuclear, Autosomal Recessive 2	CTD_diseases	4
MESH:C565726	MESH:C565726	Proopiomelanocortin Deficiency	CTD_diseases	4
MESH:C565733	MESH:C565733	Wolfram Syndrome 2	CTD_diseases	4
MESH:C565734	MESH:C565734	Cortical Defects, Wormian Bones, and Dentinogenesis Imperfecta	CTD_diseases	4
MESH:C565735	MESH:C565735	Becker Nevus Syndrome	CTD_diseases	4
MESH:C565741	MESH:C565741	Retinal Dystrophy, Early Onset Severe	CTD_diseases	4
MESH:C565742	MESH:C565742	Hyaluronan Metabolism, Defect in	CTD_diseases	4
MESH:C565755	MESH:C565755	Growth and Developmental Retardation, Ocular Ptosis, Cardiac Defect, and Anal Atresia	CTD_diseases	4
MESH:C565761	MESH:C565761	Charcot-Marie-Tooth Neuropathy, Type 4B2, with Early-Onset Glaucoma	CTD_diseases	4
MESH:C565767	MESH:C565767	VDAC Deficiency	CTD_diseases	4
MESH:C565796	MESH:C565796	Anemia, Congenital Hypoplastic, with Multiple Congenital Anomalies/Mental Retardation Syndrome	CTD_diseases	4
MESH:C565815	MESH:C565815	Cataract, Autosomal Dominant	CTD_diseases	4
MESH:C565817	MESH:C565817	Hirschsprung Disease with Heart Defects, Laryngeal Anomalies, and Preaxial Polydactyly	CTD_diseases	4
MESH:C565820	MESH:C565820	Poikiloderma with Neutropenia	CTD_diseases	4
MESH:C565826	MESH:C565826	Vohwinkel Syndrome, Variant Form	CTD_diseases	4
MESH:C565842	MESH:C565842	Brittle Bone Disorder	CTD_diseases	4
MESH:C565846	MESH:C565846	Copper Toxicosis, Idiopathic	CTD_diseases	4
MESH:C565847	MESH:C565847	Circumvallate Placenta Syndrome	CTD_diseases	4
MESH:C565850	MESH:C565850	Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism	CTD_diseases	4
MESH:C565856	MESH:C565856	Cholestasis with Gallstone, Ataxia, and Visual Disturbance	CTD_diseases	4
MESH:C565862	MESH:C565862	Cerebrofaciothoracic Dysplasia	CTD_diseases	4
MESH:C565863	MESH:C565863	Cerebrocortical Degeneration of Infancy	CTD_diseases	4
MESH:C565870	MESH:C565870	Cerebellar Ataxia and Hypogonadotropic Hypogonadism	CTD_diseases	4
MESH:C565876	MESH:C565876	Microphthalmia, Isolated, with Cataract 2	CTD_diseases	4
MESH:C565881	MESH:C565881	Cardiomyopathy Associated With Myopathy And Sudden Death	CTD_diseases	4
MESH:C565882	MESH:C565882	Cardiac Valvular Defect, Developmental	CTD_diseases	4
MESH:C565884	MESH:C565884	Cardiac Lipidosis, Familial	CTD_diseases	4
MESH:C565893	MESH:C565893	Brachymetapody-Anodontia-Hypotrichosis-Albinoidism	CTD_diseases	4
MESH:C565896	MESH:C565896	Bone Dysplasia, Lethal, Holmgren Type	CTD_diseases	4
MESH:C565923	MESH:C565923	Aural Atresia, Multiple Congenital Anomalies, and Mental Retardation	CTD_diseases	4
MESH:C565924	MESH:C565924	Atrichia with Papular Lesions	CTD_diseases	4
MESH:C565928	MESH:C565928	Atherosclerosis, Premature, with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degen	CTD_diseases	4
MESH:C565932	MESH:C565932	Ataxia, Deafness, and Cardiomyopathy	CTD_diseases	4
MESH:C565942	MESH:C565942	Arterial Tortuosity Syndrome	CTD_diseases	4
MESH:C565945	MESH:C565945	Aplasia of Extensor Muscles of Fingers, Unilateral, with Generalized Polyneuropathy	CTD_diseases	4
MESH:C565947	MESH:C565947	Antithrombin, Familial Hemorrhagic Diathesis due to	CTD_diseases	4
MESH:C565948	MESH:C565948	Microphthalmia, Syndromic 3	CTD_diseases	4
MESH:C565949	MESH:C565949	Optic Nerve Hypoplasia and Abnormalities of the Central Nervous System	CTD_diseases	4
MESH:C565959	MESH:C565959	Amobarbital, Deficient N-Hydroxylation of	CTD_diseases	4
MESH:C565971	MESH:C565971	Adrenocortical Unresponsiveness To Acth With Postreceptor Defect	CTD_diseases	4
MESH:C565974	MESH:C565974	Familial Glucocorticoid Deficiency 1	CTD_diseases	4
MESH:C565976	MESH:C565976	Adrenal Hypoplasia, Congenital, With Absent Pituitary Luteinizing Hormone	CTD_diseases	4
MESH:C565999	MESH:C565999	Platelet Receptor for Collagen, Deficiency of	CTD_diseases	4
MESH:C566004	MESH:C566004	Venular Insufficiency, Systemic	CTD_diseases	4
MESH:C566012	MESH:C566012	Ureter, Bifid Or Double	CTD_diseases	4
MESH:C566014	MESH:C566014	Undritz Anomaly	CTD_diseases	4
MESH:C566032	MESH:C566032	Trichodysplasia-Xeroderma	CTD_diseases	4
MESH:C566033	MESH:C566033	Trichorhinophalangeal Syndrome, Type III	CTD_diseases	4
MESH:C566034	MESH:C566034	Trichoepitheliomas, Multiple Desmoplastic	CTD_diseases	4
MESH:C566045	MESH:C566045	Tibial Torsion, Bilateral Medial	CTD_diseases	4
MESH:C566049	MESH:C566049	Thyrotropin-Releasing Hormone Resistance, Generalized	CTD_diseases	4
MESH:C566053	MESH:C566053	Thumbs, Stiff, With Brachydactyly Type A1 And Developmental Delay	CTD_diseases	4
MESH:C566055	MESH:C566055	Bleeding Disorder due to Defective Thromboxane A2 Receptor	CTD_diseases	4
MESH:C566057	MESH:C566057	Thrombophilia due to Thrombomodulin Defect	CTD_diseases	4
MESH:C566067	MESH:C566067	Forebrain Defects	CTD_diseases	4
MESH:C566087	MESH:C566087	Synovial Chondromatosis, Familial, with Dwarfism	CTD_diseases	4
MESH:C566089	MESH:C566089	Synostosis of Talus and Calcaneus with Short Stature	CTD_diseases	4
MESH:C566099	MESH:C566099	Symphalangism, Distal	CTD_diseases	4
MESH:C566101	MESH:C566101	Symphalangism of Toes	CTD_diseases	4
MESH:C566102	MESH:C566102	Sulfhemoglobinemia, Congenital	CTD_diseases	4
MESH:C566108	MESH:C566108	Stormorken Syndrome	CTD_diseases	4
MESH:C566109	MESH:C566109	Storm Syndrome	CTD_diseases	4
MESH:C566110	MESH:C566110	Stomatocytosis II	CTD_diseases	4
MESH:C566111	MESH:C566111	Stomatocytosis I	CTD_diseases	4
MESH:C566112	MESH:C566112	Stiff Skin Syndrome	CTD_diseases	4
MESH:C566124	MESH:C566124	Choroidal Osteoma, Bilateral	CTD_diseases	4
MESH:C566125	MESH:C566125	Chromate Resistance	CTD_diseases	4
MESH:C566130	MESH:C566130	Adrenal Insufficiency, Congenital	CTD_diseases	4
MESH:C566131	MESH:C566131	Adrenal Insufficiency, Congenital, With 46,Xy Sex Reversal	CTD_diseases	4
MESH:C566132	MESH:C566132	Chlorpropamide-Alcohol Flushing	CTD_diseases	4
MESH:C566140	MESH:C566140	Cervical Vertebral Dysplasia	CTD_diseases	4
MESH:C566151	MESH:C566151	Celiac Artery Stenosis from Compression by Median Arcuate Ligament of Diaphragm	CTD_diseases	4
MESH:C566153	MESH:C566153	Hyperkeratotic Cutaneous Capillary-Venous Malformations Associated With Cerebral Capillary Malformat	CTD_diseases	4
MESH:C566156	MESH:C566156	Cataract, Nuclear Total	CTD_diseases	4
MESH:C566157	MESH:C566157	Cataract, Nuclear Diffuse Nonprogressive	CTD_diseases	4
MESH:C566158	MESH:C566158	Cataract, Zonular Pulverulent 1	CTD_diseases	4
MESH:C566160	MESH:C566160	Cataract, Floriform	CTD_diseases	4
MESH:C566161	MESH:C566161	Cataract, Crystalline Coralliform	CTD_diseases	4
MESH:C566162	MESH:C566162	Cataract, Crystalline Aculeiform	CTD_diseases	4
MESH:C566173	MESH:C566173	Monocyte Esterase Deficiency	CTD_diseases	4
MESH:C566176	MESH:C566176	Car Factor Deficiency	CTD_diseases	4
MESH:C566179	MESH:C566179	Cancer, Familial, with In Vitro Radioresistance	CTD_diseases	4
MESH:C566182	MESH:C566182	Calcific Aortic Disease with Immunologic Abnormalities, Familial	CTD_diseases	4
MESH:C566186	MESH:C566186	Cardiac Conduction Defect, Nonprogressive	CTD_diseases	4
MESH:C566214	MESH:C566214	Adult i Blood Group with Congenital Cataract	CTD_diseases	4
MESH:C566234	MESH:C566234	Axenfeld-Rieger Anomaly with Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, and Skele	CTD_diseases	4
MESH:C566236	MESH:C566236	Sveinsson Chorioretinal Atrophy	CTD_diseases	4
MESH:C566248	MESH:C566248	Asymmetric Short Stature Syndrome	CTD_diseases	4
MESH:C566250	MESH:C566250	Aryl Hydrocarbon Hydroxylase Inducibility	CTD_diseases	4
MESH:C566272	MESH:C566272	Townes-Brocks-Branchiootorenal-Like Syndrome	CTD_diseases	4
MESH:C566277	MESH:C566277	Anonychia-Ectrodactyly	CTD_diseases	4
MESH:C566278	MESH:C566278	Anonychia with Flexural Pigmentation	CTD_diseases	4
MESH:C566280	MESH:C566280	Aniridia, Microcornea, And Spontaneously Reabsorbed Cataract	CTD_diseases	4
MESH:C566287	MESH:C566287	Anal Sphincter Myopathy, Internal	CTD_diseases	4
MESH:C566295	MESH:C566295	Amastia, Bilateral, With Ureteral Triplication And Dysmorphism	CTD_diseases	4
MESH:C566300	MESH:C566300	alpha-Fetoprotein Deficiency	CTD_diseases	4
MESH:C566322	MESH:C566322	Acroleukopathy, Symmetric	CTD_diseases	4
MESH:C566323	MESH:C566323	Acrokeratoderma, Hereditary Papulotranslucent	CTD_diseases	4
MESH:C566351	MESH:C566351	Atrial Septal Defect, Secundum, with Various Cardiac and Noncardiac Defects	CTD_diseases	4
MESH:C566360	MESH:C566360	Follicular Atrophoderma, Perioral Pigmented, with Milia and Epidermoid Cysts	CTD_diseases	4
MESH:C566367	MESH:C566367	Light Fixation Seizure Syndrome	CTD_diseases	4
MESH:C566368	MESH:C566368	Dyserythropoiesis, Congenital, with Internuclear Chromatin Bridges and Ultrastructurally Normal Eryt	CTD_diseases	4
MESH:C566376	MESH:C566376	Tsukahara Syndrome	CTD_diseases	4
MESH:C566397	MESH:C566397	Myopia 3	CTD_diseases	4
MESH:C566408	MESH:C566408	Dislocated Elbows, Bowed Tibias, Scoliosis, Deafness, Cataract, Microcephaly, And Mental Retardation	CTD_diseases	4
MESH:C566440	MESH:C566440	Microphthalmia, Syndromic 6	CTD_diseases	4
MESH:C566448	MESH:C566448	Microphthalmia, Cataracts, and Iris Abnormalities	CTD_diseases	4
MESH:C566458	MESH:C566458	Trichilemmal Cyst 1	CTD_diseases	4
MESH:C566469	MESH:C566469	Pigmented Nodular Adrenocortical Disease, Primary, 1	CTD_diseases	4
MESH:C566472	MESH:C566472	Pigmented Nodular Adrenocortical Disease, Primary, 2	CTD_diseases	4
MESH:C566474	MESH:C566474	Night Blindness, Congenital Stationary, Autosomal Dominant 1	CTD_diseases	4
MESH:C566475	MESH:C566475	Night Blindness, Congenital Stationary, Autosomal Dominant 3	CTD_diseases	4
MESH:C566476	MESH:C566476	Chromosome 17q21.31 Deletion Syndrome	CTD_diseases	4
MESH:C566478	MESH:C566478	Testicular Microlithiasis	CTD_diseases	4
MESH:C566480	MESH:C566480	Microphthalmia, Isolated, with Cataract 4	CTD_diseases	4
MESH:C566481	MESH:C566481	Cataract, Lamellar 2	CTD_diseases	4
MESH:C566489	MESH:C566489	Myopia 12	CTD_diseases	4
MESH:C566490	MESH:C566490	Myopia 11	CTD_diseases	4
MESH:C566504	MESH:C566504	Short QT Syndrome 3	CTD_diseases	4
MESH:C566505	MESH:C566505	Short QT Syndrome 2	CTD_diseases	4
MESH:C566506	MESH:C566506	Short QT Syndrome 1	CTD_diseases	4
MESH:C566508	MESH:C566508	Fibrosis of Extraocular Muscles, Congenital, with Synergistic Divergence	CTD_diseases	4
MESH:C566515	MESH:C566515	Spondyloepiphyseal Dysplasia With Coronal Craniosynostosis, Cataracts, Cleft Palate, And Mental Reta	CTD_diseases	4
MESH:C566519	MESH:C566519	Emphysema, Congenital, With Deafness, Penoscrotal Web, And Mental Retardation	CTD_diseases	4
MESH:C566521	MESH:C566521	Brachydactyly, Intraventricular Septal Defect, And Deafness	CTD_diseases	4
MESH:C566522	MESH:C566522	Craniomicromelic Syndrome	CTD_diseases	4
MESH:C566529	MESH:C566529	Arterial Occlusive Disease, Progressive, with Hypertension, Heart Defects, Bone Fragility, and Brach	CTD_diseases	4
MESH:C566543	MESH:C566543	Creases, Infra-Auricular Cutaneous, with Tall Stature and Advanced Bone Age	CTD_diseases	4
MESH:C566544	MESH:C566544	Short Stature, Auditory Canal Atresia, Mandibular Hypoplasia, Skeletal Abnormalities	CTD_diseases	4
MESH:C566555	MESH:C566555	Desmosterolosis	CTD_diseases	4
MESH:C566559	MESH:C566559	Plantar Lipomatosis, Unusual Facies, and Developmental Delay	CTD_diseases	4
MESH:C566560	MESH:C566560	Sensorineural Hearing Loss, Retinal Pigment Epithelium Lesions, Discolored Teeth	CTD_diseases	4
MESH:C566566	MESH:C566566	Medium Chain 3-Ketoacyl-CoA Thiolase Deficiency	CTD_diseases	4
MESH:C566587	MESH:C566587	Fibrosis Of Extraocular Muscles, Congenital, 2	CTD_diseases	4
MESH:C566588	MESH:C566588	Broad Terminal Phalanges, Familial	CTD_diseases	4
MESH:C566600	MESH:C566600	Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma	CTD_diseases	4
MESH:C566608	MESH:C566608	Cataract, Zonular Pulverulent 3	CTD_diseases	4
MESH:C566638	MESH:C566638	Superior Transverse Scapular Ligament, Calcification Of, Familial	CTD_diseases	4
MESH:C566646	MESH:C566646	Paragangliomas 2	CTD_diseases	4
MESH:C566650	MESH:C566650	Glaucoma Iridogoniodysplasia, Familial	CTD_diseases	4
MESH:C566651	MESH:C566651	Iris Pigment Epithelium Anomalies	CTD_diseases	4
MESH:C566659	MESH:C566659	Spondyloepiphyseal Dysplasia, Myopia, And Sensorineural Deafness	CTD_diseases	4
MESH:C566662	MESH:C566662	Split-Hand With Obstructive Uropathy, Spina Bifida, And Diaphragmatic Defects	CTD_diseases	4
MESH:C566669	MESH:C566669	Spinocerebellar Ataxia With Rigidity And Peripheral Neuropathy	CTD_diseases	4
MESH:C566687	MESH:C566687	Skeletal Dysplasia With Delayed Epiphyseal And Carpal Bone Ossification	CTD_diseases	4
MESH:C566690	MESH:C566690	Sinus Node Disease and Myopia	CTD_diseases	4
MESH:C566695	MESH:C566695	Scapuloperoneal Syndrome, Neurogenic, Kaeser Type	CTD_diseases	4
MESH:C566711	MESH:C566711	Retinol-Binding Protein Deficiency	CTD_diseases	4
MESH:C566717	MESH:C566717	Retinal Nonattachment And Falciform Detachment	CTD_diseases	4
MESH:C566719	MESH:C566719	Retinal Cone Dystrophy 1	CTD_diseases	4
MESH:C566725	MESH:C566725	Ragweed Sensitivity	CTD_diseases	4
MESH:C566728	MESH:C566728	Radial Heads, Posterior Dislocation Of	CTD_diseases	4
MESH:C566731	MESH:C566731	Pupil, Egg-Shaped	CTD_diseases	4
MESH:C566736	MESH:C566736	Ptosis, Strabismus, And Ectopic Pupils	CTD_diseases	4
MESH:C566737	MESH:C566737	Ptosis, Hereditary Congenital 1	CTD_diseases	4
MESH:C566738	MESH:C566738	Pterygium, Antecubital	CTD_diseases	4
MESH:C566740	MESH:C566740	Pterygium Of Conjunctiva And Cornea	CTD_diseases	4
MESH:C566741	MESH:C566741	Pterygium Colli, Isolated	CTD_diseases	4
MESH:C566748	MESH:C566748	Pseudoglaucoma	CTD_diseases	4
MESH:C566750	MESH:C566750	Acholinesterasemia	CTD_diseases	4
MESH:C566751	MESH:C566751	Butyrylcholinesterase Deficiency, Fluoride-Resistant, Japanese Type	CTD_diseases	4
MESH:C566753	MESH:C566753	Pseudoarthrogryposis	CTD_diseases	4
MESH:C566755	MESH:C566755	Hyperprothrombinemia	CTD_diseases	4
MESH:C566757	MESH:C566757	Pronation-Supination Of The Forearm, Impairment Of	CTD_diseases	4
MESH:C566759	MESH:C566759	Primary Release Disorder Of Platelets	CTD_diseases	4
MESH:C566775	MESH:C566775	Polyposis Of Gastric Fundus Without Polyposis Coli	CTD_diseases	4
MESH:C566780	MESH:C566780	Actinic Prurigo	CTD_diseases	4
MESH:C566781	MESH:C566781	Juvenile Spring Eruption of Ears	CTD_diseases	4
MESH:C566793	MESH:C566793	Pectoralis Muscle, Absence of	CTD_diseases	4
MESH:C566795	MESH:C566795	Pneumothorax, Primary Spontaneous	CTD_diseases	4
MESH:C566796	MESH:C566796	Platelet Signal Processing Defect	CTD_diseases	4
MESH:C566798	MESH:C566798	Platelet Factor 3 Deficiency	CTD_diseases	4
MESH:C566799	MESH:C566799	Platelet Disorder, Undefined	CTD_diseases	4
MESH:C566800	MESH:C566800	Platelet Aggregation, Spontaneous	CTD_diseases	4
MESH:C566801	MESH:C566801	Pigmented Paravenous Chorioretinal Atrophy	CTD_diseases	4
MESH:C566803	MESH:C566803	6-Phosphogluconolactonase Deficiency	CTD_diseases	4
MESH:C566806	MESH:C566806	Phlebectasia Of Lips	CTD_diseases	4
MESH:C566808	MESH:C566808	Phagocytosis, Plasma-Related Defect in	CTD_diseases	4
MESH:C566811	MESH:C566811	Pelvis-Shoulder Dysplasia	CTD_diseases	4
MESH:C566815	MESH:C566815	Char syndrome	CTD_diseases	4
MESH:C566817	MESH:C566817	Paroxysmal Tonic Upgaze, Benign Childhood, With Ataxia	CTD_diseases	4
MESH:C566832	MESH:C566832	Papillomatosis, Familial Cutaneous	CTD_diseases	4
MESH:C566834	MESH:C566834	Panic Disorder with Bladder Conditions	CTD_diseases	4
MESH:C566835	MESH:C566835	Panic Disorder with Joint Laxity	CTD_diseases	4
MESH:C566852	MESH:C566852	Hypothyroidism, Congenital, Nongoitrous, 2	CTD_diseases	4
MESH:C566861	MESH:C566861	Cataract, Microcephaly, Arthrogryposis, Kyphosis Syndrome	CTD_diseases	4
MESH:C566869	MESH:C566869	Night Blindness, Congenital Stationary, Autosomal Dominant 2	CTD_diseases	4
MESH:C566880	MESH:C566880	Tachycardia, Hypertension, Microphthalmia, And Hyperglycinuria	CTD_diseases	4
MESH:C566882	MESH:C566882	Surfactant Metabolism Dysfunction, Pulmonary, 1	CTD_diseases	4
MESH:C566884	MESH:C566884	Microphthalmia With Hyperopia, Retinal Degeneration, Macrophakia, And Dental Anomalies	CTD_diseases	4
MESH:C566896	MESH:C566896	Myopathy, Congenital, With Excess Of Muscle Spindles	CTD_diseases	4
MESH:C566897	MESH:C566897	Plasminogen Deficiency, Type I	CTD_diseases	4
MESH:C566898	MESH:C566898	Peripapillary Atrophy, Beta Type	CTD_diseases	4
MESH:C566900	MESH:C566900	Primary Lateral Sclerosis, Adult, 1	CTD_diseases	4
MESH:C566909	MESH:C566909	Cataract, Autosomal Dominant, Multiple Types 1	CTD_diseases	4
MESH:C566913	MESH:C566913	Otosclerosis 7	CTD_diseases	4
MESH:C566914	MESH:C566914	Otosclerosis 4	CTD_diseases	4
MESH:C566915	MESH:C566915	Meckel Syndrome, Type 5	CTD_diseases	4
MESH:C566916	MESH:C566916	Joubert Syndrome 7	CTD_diseases	4
MESH:C566923	MESH:C566923	Cataract, Congenital Nuclear, Autosomal Recessive 3	CTD_diseases	4
MESH:C566924	MESH:C566924	Cavitary Optic Disc Anomalies	CTD_diseases	4
MESH:C566934	MESH:C566934	Corticosteroid-Binding Globulin, Elevated	CTD_diseases	4
MESH:C566936	MESH:C566936	Gallbladder Disease 4	CTD_diseases	4
MESH:C566955	MESH:C566955	Cataract, Cortical, Juvenile-Onset	CTD_diseases	4
MESH:C566966	MESH:C566966	Persistent Hyperplastic Primary Vitreous, Autosomal Recessive	CTD_diseases	4
MESH:C566970	MESH:C566970	Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing 	CTD_diseases	4
MESH:C566980	MESH:C566980	Mental Retardation, Fra12a Type	CTD_diseases	4
MESH:C566985	MESH:C566985	Microphthalmia, Syndromic 10	CTD_diseases	4
MESH:C566989	MESH:C566989	Short Stature, Mental Retardation, Callosal Agenesis, Heminasal Hypoplasia, Microphthalmia, And Atyp	CTD_diseases	4
MESH:C566996	MESH:C566996	Cardiac Arrhythmia, Ankyrin-B-Related	CTD_diseases	4
MESH:C566997	MESH:C566997	Aplasia Cutis Congenita, Congenital Heart Defect, And Frontonasal Cysts	CTD_diseases	4
MESH:C567006	MESH:C567006	Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of	CTD_diseases	4
MESH:C567009	MESH:C567009	Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation	CTD_diseases	4
MESH:C567020	MESH:C567020	Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy	CTD_diseases	4
MESH:C567038	MESH:C567038	Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation	CTD_diseases	4
MESH:C567046	MESH:C567046	Surfactant Metabolism Dysfunction, Pulmonary, 3	CTD_diseases	4
MESH:C567048	MESH:C567048	Surfactant Metabolism Dysfunction, Pulmonary, 2	CTD_diseases	4
MESH:C567060	MESH:C567060	Tooth Agenesis, Selective, X-Linked, 1	CTD_diseases	4
MESH:C567065	MESH:C567065	Leukoencephalopathy With Metaphyseal Chondrodysplasia	CTD_diseases	4
MESH:C567067	MESH:C567067	Phosphoglycerate Kinase 1 Deficiency	CTD_diseases	4
MESH:C567068	MESH:C567068	Atypical Mycobacteriosis, Familial, X-Linked 2	CTD_diseases	4
MESH:C567070	MESH:C567070	Atypical Mycobacteriosis, Familial, X-Linked 1	CTD_diseases	4
MESH:C567080	MESH:C567080	Warfarin Sensitivity	CTD_diseases	4
MESH:C567086	MESH:C567086	Erythrocytosis, Familial, 4	CTD_diseases	4
MESH:C567091	MESH:C567091	Skin/Hair/Eye Pigmentation, Variation In, 9	CTD_diseases	4
MESH:C567093	MESH:C567093	Short Stature, Facial Dysmorphism, Severe Brachydactyly, and Syndactyly	CTD_diseases	4
MESH:C567096	MESH:C567096	Skin/Hair/Eye Pigmentation, Variation In, 8	CTD_diseases	4
MESH:C567100	MESH:C567100	Mucolipidosis II Alpha Beta	CTD_diseases	4
MESH:C567102	MESH:C567102	Methemoglobinemia Type IV	CTD_diseases	4
MESH:C567108	MESH:C567108	Hypogonadism and Testicular Atrophy	CTD_diseases	4
MESH:C567109	MESH:C567109	Hypergonadotropic Hypogonadism And Partial Alopecia	CTD_diseases	4
MESH:C567116	MESH:C567116	Kininogen Deficiency, High Molecular Weight and Low Molecular Weight	CTD_diseases	4
MESH:C567119	MESH:C567119	Skin/Hair/Eye Pigmentation, Variation In, 5	CTD_diseases	4
MESH:C567126	MESH:C567126	Combined Oxidative Phosphorylation Deficiency 5	CTD_diseases	4
MESH:C567129	MESH:C567129	Myopathy, Early-Onset, with Fatal Cardiomyopathy	CTD_diseases	4
MESH:C567139	MESH:C567139	Skin/Hair/Eye Pigmentation, Variation In, 6	CTD_diseases	4
MESH:C567155	MESH:C567155	Skin/Hair/Eye Pigmentation, Variation In, 7	CTD_diseases	4
MESH:C567166	MESH:C567166	Leukodystrophy, Hypomyelinating, 5	CTD_diseases	4
MESH:C567168	MESH:C567168	Leydig Cell Adenoma, Somatic, with Male-Limited Precocious Puberty	CTD_diseases	4
MESH:C567173	MESH:C567173	NF1 Microduplication Syndrome	CTD_diseases	4
MESH:C567184	MESH:C567184	Chromosome 3q29 Deletion Syndrome	CTD_diseases	4
MESH:C567188	MESH:C567188	Lymphedema-Distichiasis Syndrome with Renal Disease and Diabetes Mellitus	CTD_diseases	4
MESH:C567192	MESH:C567192	Arginine:Glycine Amidinotransferase Deficiency	CTD_diseases	4
MESH:C567193	MESH:C567193	Myopia 15	CTD_diseases	4
MESH:C567194	MESH:C567194	Dyschromatosis Universalis Hereditaria 2	CTD_diseases	4
MESH:C567195	MESH:C567195	Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis	CTD_diseases	4
MESH:C567196	MESH:C567196	Kahrizi Syndrome	CTD_diseases	4
MESH:C567203	MESH:C567203	Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract	CTD_diseases	4
MESH:C567224	MESH:C567224	Chromosome 22q11.2 Microduplication Syndrome	CTD_diseases	4
MESH:C567232	MESH:C567232	Chromosome 15q26-Qter Deletion Syndrome	CTD_diseases	4
MESH:C567239	MESH:C567239	Chromosome 6pter-P24 Deletion Syndrome	CTD_diseases	4
MESH:C567258	MESH:C567258	Hypoadiponectinemia	CTD_diseases	4
MESH:C567259	MESH:C567259	Myopia 16	CTD_diseases	4
MESH:C567273	MESH:C567273	Dyschromatosis Universalis Hereditaria 1	CTD_diseases	4
MESH:C567274	MESH:C567274	Deafness, Congenital, and Onychodystrophy, Autosomal Dominant	CTD_diseases	4
MESH:C531613	MESH:C531613	Amoebiasis due to Entamoeba histolytica	CTD_diseases	4
MESH:C531614	MESH:C531614	Amniotic Band Sequence	CTD_diseases	4
MESH:C531622	MESH:C531622	Familial antiphospholipid syndrome	CTD_diseases	4
MESH:C531639	MESH:C531639	Stomatodynia	CTD_diseases	4
MESH:C531654	MESH:C531654	Congenital chylous ascites	CTD_diseases	4
MESH:C531720	MESH:C531720	Noninflammatory corneal thinning	CTD_diseases	4
MESH:C531736	MESH:C531736	Acute malaria	CTD_diseases	4
MESH:C531754	MESH:C531754	Ridges-off-the-end syndrome	CTD_diseases	4
MESH:C531760	MESH:C531760	Oro-facial gangrene	CTD_diseases	4
MESH:C531762	MESH:C531762	Alkaptonuric ochronosis	CTD_diseases	4
MESH:C531821	MESH:C531821	Stenotrophomonas maltophilia bacteremia	CTD_diseases	4
MESH:C535270	MESH:C535270	Premature aging, Okamoto type	CTD_diseases	4
MESH:C535275	MESH:C535275	Primary amebic meningoencephalitis	CTD_diseases	4
MESH:C535281	MESH:C535281	Radius absent anogenital anomalies	CTD_diseases	4
MESH:C535282	MESH:C535282	Raine syndrome	CTD_diseases	4
MESH:C535285	MESH:C535285	Ramon Syndrome	CTD_diseases	4
MESH:C535291	MESH:C535291	Rasmussen subacute encephalitis	CTD_diseases	4
MESH:C535293	MESH:C535293	Reactive angioendotheliomatosis	CTD_diseases	4
MESH:C535295	MESH:C535295	Reardon Wilson Cavanagh syndrome	CTD_diseases	4
MESH:C535296	MESH:C535296	Recombinant chromosome 8 syndrome	CTD_diseases	4
MESH:C535297	MESH:C535297	Recurrent respiratory papillomatosis	CTD_diseases	4
MESH:C535298	MESH:C535298	Red cell phospholipid defect with hemolysis	CTD_diseases	4
MESH:C535310	MESH:C535310	3-Hydroxyacyl-CoA Dehydrogenase Deficiency	CTD_diseases	4
MESH:C535311	MESH:C535311	Costeff optic atrophy syndrome	CTD_diseases	4
MESH:C535313	MESH:C535313	3C syndrome	CTD_diseases	4
MESH:C535315	MESH:C535315	4-hydroxyphenylacetic aciduria	CTD_diseases	4
MESH:C535321	MESH:C535321	5-Nucleotidase syndrome	CTD_diseases	4
MESH:C535326	MESH:C535326	Holt-Oram syndrome	CTD_diseases	4
MESH:C535327	MESH:C535327	Holzgreve Wagner Rehder syndrome	CTD_diseases	4
MESH:C535329	MESH:C535329	Hooft disease	CTD_diseases	4
MESH:C535330	MESH:C535330	Aagenaes syndrome	CTD_diseases	4
MESH:C535331	MESH:C535331	Aarskog Syndrome	CTD_diseases	4
MESH:C535332	MESH:C535332	Aase Smith syndrome	CTD_diseases	4
MESH:C535336	MESH:C535336	Cataract, alopecia, sclerodactyly	CTD_diseases	4
MESH:C535337	MESH:C535337	Cataract, autosomal recessive congenital 2	CTD_diseases	4
MESH:C535338	MESH:C535338	Cataract, congenital, with microcornea or slight microphthalmia	CTD_diseases	4
MESH:C535339	MESH:C535339	Cataract, posterior polar, 1	CTD_diseases	4
MESH:C535340	MESH:C535340	Cataract, posterior polar, 5	CTD_diseases	4
MESH:C535342	MESH:C535342	Cataract, zonular	CTD_diseases	4
MESH:C535343	MESH:C535343	Cataract, posterior polar, 3	CTD_diseases	4
MESH:C535344	MESH:C535344	Cataract, posterior polar, 4	CTD_diseases	4
MESH:C535345	MESH:C535345	Cataracts, ataxia, short stature, and mental retardation	CTD_diseases	4
MESH:C535346	MESH:C535346	Catatrichy	CTD_diseases	4
MESH:C535352	MESH:C535352	Cerebellar degeneration, subacute	CTD_diseases	4
MESH:C535358	MESH:C535358	Choroidal dystrophy central areolar	CTD_diseases	4
MESH:C535362	MESH:C535362	Chromosome 1p36 Deletion Syndrome	CTD_diseases	4
MESH:C535373	MESH:C535373	Dermatoosteolysis Kirghizian type	CTD_diseases	4
MESH:C535374	MESH:C535374	Dermatopathia pigmentosa reticularis	CTD_diseases	4
MESH:C535380	MESH:C535380	Arthrogryposis multiplex congenita, distal, X-linked	CTD_diseases	4
MESH:C535387	MESH:C535387	Arthropathy, progressive pseudorheumatoid, of childhood	CTD_diseases	4
MESH:C535388	MESH:C535388	Arts syndrome	CTD_diseases	4
MESH:C535397	MESH:C535397	Athabaskan brainstem dysgenesis	CTD_diseases	4
MESH:C535406	MESH:C535406	Game Friedman Paradice syndrome	CTD_diseases	4
MESH:C535422	MESH:C535422	Charcot-Marie-Tooth disease, Type 4B2, with early-onset glaucoma	CTD_diseases	4
MESH:C535427	MESH:C535427	Ben Ari Shuper Mimouni syndrome	CTD_diseases	4
MESH:C535428	MESH:C535428	Benign essential blepharospasm	CTD_diseases	4
MESH:C535432	MESH:C535432	Berk-Tabatznik syndrome	CTD_diseases	4
MESH:C535437	MESH:C535437	Bhaskar Jagannathan syndrome	CTD_diseases	4
MESH:C535439	MESH:C535439	Biemond syndrome type 2	CTD_diseases	4
MESH:C535448	MESH:C535448	Bird headed dwarfism Montreal type	CTD_diseases	4
MESH:C535449	MESH:C535449	Deletion 13q syndrome, partial	CTD_diseases	4
MESH:C535458	MESH:C535458	Chudley-Rozdilsky syndrome	CTD_diseases	4
MESH:C535461	MESH:C535461	Chylothorax, congenital	CTD_diseases	4
MESH:C535465	MESH:C535465	Contractures ectodermal dysplasia cleft lip palate	CTD_diseases	4
MESH:C535468	MESH:C535468	Copper deficiency, familial benign	CTD_diseases	4
MESH:C535471	MESH:C535471	Cornea guttata with anterior polar cataract	CTD_diseases	4
MESH:C535481	MESH:C535481	Fraser Jequier Chen syndrome	CTD_diseases	4
MESH:C535484	MESH:C535484	13q deletion syndrome	CTD_diseases	4
MESH:C535486	MESH:C535486	Chromosome 13q-mosaicism	CTD_diseases	4
MESH:C535492	MESH:C535492	Epidermolysis bullosa, late-onset localized junctional, with mental retardation	CTD_diseases	4
MESH:C535497	MESH:C535497	Epilepsy telangiectasia	CTD_diseases	4
MESH:C535515	MESH:C535515	Red skin pigment anomaly of New Guinea	CTD_diseases	4
MESH:C535516	MESH:C535516	Reed's syndrome	CTD_diseases	4
MESH:C535517	MESH:C535517	Refsum disease with increased pipecolic acidemia	CTD_diseases	4
MESH:C535519	MESH:C535519	Reginato Schiapachasse syndrome	CTD_diseases	4
MESH:C535528	MESH:C535528	Infundibulopelvic dysgenesis	CTD_diseases	4
MESH:C535532	MESH:C535532	Congenital idiopathic intestinal pseudoobstruction	CTD_diseases	4
MESH:C535534	MESH:C535534	Iridogoniodysgenesis and skeletal anomalies	CTD_diseases	4
MESH:C535535	MESH:C535535	Iridogoniodysgenesis type1	CTD_diseases	4
MESH:C535536	MESH:C535536	Iridogoniodysgenesis, dominant type	CTD_diseases	4
MESH:C535537	MESH:C535537	Iris dysplasia hypertelorism deafness	CTD_diseases	4
MESH:C535539	MESH:C535539	Irons Bhan syndrome	CTD_diseases	4
MESH:C535540	MESH:C535540	Ischiopatellar dysplasia	CTD_diseases	4
MESH:C535542	MESH:C535542	Isotretinoin embryopathy like syndrome	CTD_diseases	4
MESH:C535544	MESH:C535544	Oculootoradial syndrome	CTD_diseases	4
MESH:C535552	MESH:C535552	Abdominal chemodectomas with cutaneous angiolipomas	CTD_diseases	4
MESH:C535555	MESH:C535555	Aberrant subclavian artery	CTD_diseases	4
MESH:C535557	MESH:C535557	Ablepharon macrostomia syndrome	CTD_diseases	4
MESH:C535559	MESH:C535559	Abruzzo Erickson syndrome	CTD_diseases	4
MESH:C535561	MESH:C535561	Congenital absence of gluteal muscles	CTD_diseases	4
MESH:C535566	MESH:C535566	Absent corpus callosum cataract immunodeficiency	CTD_diseases	4
MESH:C535567	MESH:C535567	Absent duct of Santorini	CTD_diseases	4
MESH:C535568	MESH:C535568	Absent patella	CTD_diseases	4
MESH:C535569	MESH:C535569	Abuse dwarfism syndrome	CTD_diseases	4
MESH:C535571	MESH:C535571	Cantu Sanchez-Corona Fragoso syndrome	CTD_diseases	4
MESH:C535572	MESH:C535572	Cantu syndrome	CTD_diseases	4
MESH:C535573	MESH:C535573	Capillary leak syndrome with monoclonal gammopathy	CTD_diseases	4
MESH:C535575	MESH:C535575	Carcinoma, squamous cell of head and neck	CTD_diseases	4
MESH:C535576	MESH:C535576	Cardiac valvular dysplasia, X-linked	CTD_diseases	4
MESH:C535579	MESH:C535579	Cardiofaciocutaneous syndrome	CTD_diseases	4
MESH:C535580	MESH:C535580	Najjar syndrome	CTD_diseases	4
MESH:C535581	MESH:C535581	Cardiomyopathy dilated with Woolly hair and keratoderma	CTD_diseases	4
MESH:C535582	MESH:C535582	Cardiomyopathy hypogonadism collagenoma syndrome	CTD_diseases	4
MESH:C535584	MESH:C535584	Cardiomyopathy, infantile histiocytoid	CTD_diseases	4
MESH:C535586	MESH:C535586	Carnevale syndrome	CTD_diseases	4
MESH:C535589	MESH:C535589	Carnitine palmitoyl transferase 2 deficiency	CTD_diseases	4
MESH:C535603	MESH:C535603	Drachtman Weinblatt Sitarz syndrome	CTD_diseases	4
MESH:C535607	MESH:C535607	Aicardi-Goutieres syndrome	CTD_diseases	4
MESH:C535608	MESH:C535608	Aicardi-Goutieres syndrome 5	CTD_diseases	4
MESH:C535611	MESH:C535611	Aksu von Stockhausen syndrome	CTD_diseases	4
MESH:C535613	MESH:C535613	Al Gazali Aziz Salem syndrome	CTD_diseases	4
MESH:C535615	MESH:C535615	Al Gazali Hirschsprung syndrome	CTD_diseases	4
MESH:C535616	MESH:C535616	Al Gazali Khidr Prem Chandran syndrome	CTD_diseases	4
MESH:C535618	MESH:C535618	Hairy elbows	CTD_diseases	4
MESH:C535620	MESH:C535620	Hairy palms and soles	CTD_diseases	4
MESH:C535622	MESH:C535622	Halal syndrome	CTD_diseases	4
MESH:C535623	MESH:C535623	Hall Riggs mental retardation syndrome	CTD_diseases	4
MESH:C535627	MESH:C535627	Hand foot uterus syndrome	CTD_diseases	4
MESH:C535629	MESH:C535629	Hanhart syndrome	CTD_diseases	4
MESH:C535635	MESH:C535635	Harrod Doman Keele syndrome	CTD_diseases	4
MESH:C535638	MESH:C535638	Frenkel Russe syndrome	CTD_diseases	4
MESH:C535639	MESH:C535639	Frias syndrome	CTD_diseases	4
MESH:C535640	MESH:C535640	Fried Goldberg Mundel syndrome	CTD_diseases	4
MESH:C535642	MESH:C535642	Growth retardation, Alopecia, Pseudoanodontia and Optic atrophy	CTD_diseases	4
MESH:C535643	MESH:C535643	Gardner Morrisson Abbot syndrome	CTD_diseases	4
MESH:C535647	MESH:C535647	Gas bloat syndrome	CTD_diseases	4
MESH:C535651	MESH:C535651	Gastrocutaneous syndrome	CTD_diseases	4
MESH:C535652	MESH:C535652	Bellini Chiumello Rimoldi syndrome	CTD_diseases	4
MESH:C535654	MESH:C535654	Rosenthal-Kloepfer syndrome	CTD_diseases	4
MESH:C535656	MESH:C535656	Acromegaloid features, overgrowth, cleft palate, and hernia	CTD_diseases	4
MESH:C535661	MESH:C535661	Acromesomelic dysplasia, Maroteaux type	CTD_diseases	4
MESH:C535662	MESH:C535662	Acromicric dysplasia	CTD_diseases	4
MESH:C535665	MESH:C535665	Acrorenal mandibular syndrome	CTD_diseases	4
MESH:C535666	MESH:C535666	Acrorenal syndrome recessive	CTD_diseases	4
MESH:C535668	MESH:C535668	Adrenocorticotropic hormone deficiency	CTD_diseases	4
MESH:C535670	MESH:C535670	Accutane embryopathy	CTD_diseases	4
MESH:C535672	MESH:C535672	Acute cholinergic dysautonomia	CTD_diseases	4
MESH:C535674	MESH:C535674	Richards-Rundle syndrome	CTD_diseases	4
MESH:C535679	MESH:C535679	Axenfeld-Rieger syndrome	CTD_diseases	4
MESH:C535680	MESH:C535680	Rieger syndrome 2	CTD_diseases	4
MESH:C535686	MESH:C535686	Rippling muscle disease, 1	CTD_diseases	4
MESH:C535689	MESH:C535689	Laurin-Sandrow syndrome	CTD_diseases	4
MESH:C535693	MESH:C535693	Male pseudohermaphroditism/mental retardation syndrome, Verloes type	CTD_diseases	4
MESH:C535702	MESH:C535702	Malonic aciduria	CTD_diseases	4
MESH:C535703	MESH:C535703	Malouf syndrome	CTD_diseases	4
MESH:C535704	MESH:C535704	Malpuech facial clefting syndrome	CTD_diseases	4
MESH:C535708	MESH:C535708	Manouvrier syndrome	CTD_diseases	4
MESH:C535713	MESH:C535713	Opitz Reynolds Fitzgerald syndrome	CTD_diseases	4
MESH:C535718	MESH:C535718	Dubowitz syndrome	CTD_diseases	4
MESH:C535719	MESH:C535719	Duker Weiss Siber syndrome	CTD_diseases	4
MESH:C535723	MESH:C535723	Subungual exostoses	CTD_diseases	4
MESH:C535726	MESH:C535726	Dyggve-Melchior-Clausen syndrome	CTD_diseases	4
MESH:C535728	MESH:C535728	Dysautonomia like disorder	CTD_diseases	4
MESH:C535729	MESH:C535729	Dyschromatosis symmetrica hereditaria 1	CTD_diseases	4
MESH:C535730	MESH:C535730	Dyschromatosis universalis hereditaria	CTD_diseases	4
MESH:C535733	MESH:C535733	Emanuel syndrome	CTD_diseases	4
MESH:C535738	MESH:C535738	Erythrokeratodermia with ataxia	CTD_diseases	4
MESH:C535752	MESH:C535752	Congenital disorder of glycosylation type 2A	CTD_diseases	4
MESH:C535763	MESH:C535763	Euhidrotic ectodermal dysplasia	CTD_diseases	4
MESH:C535769	MESH:C535769	Dahlberg Borer Newcomer syndrome	CTD_diseases	4
MESH:C535770	MESH:C535770	Daish Hardman Lamont syndrome	CTD_diseases	4
MESH:C535774	MESH:C535774	Piepkorn Karp Hickok syndrome	CTD_diseases	4
MESH:C535779	MESH:C535779	Spondylocamptodactyly	CTD_diseases	4
MESH:C535787	MESH:C535787	Spondyloepiphyseal dysplasia tarda, Toledo type	CTD_diseases	4
MESH:C535790	MESH:C535790	Spondylohypoplasia, arthrogryposis and popliteal pterygium	CTD_diseases	4
MESH:C535793	MESH:C535793	Spondylometaphyseal dysplasia, 'corner fracture' type	CTD_diseases	4
MESH:C535801	MESH:C535801	Spranger Schinzel Myers syndrome	CTD_diseases	4
MESH:C535806	MESH:C535806	Moebius axonal neuropathy hypogonadism	CTD_diseases	4
MESH:C535812	MESH:C535812	Macrosomia obesity macrocephaly ocular abnormalities	CTD_diseases	4
MESH:C535821	MESH:C535821	Pseudoainhum	CTD_diseases	4
MESH:C535823	MESH:C535823	Pseudoaminopterin syndrome	CTD_diseases	4
MESH:C535824	MESH:C535824	Pseudoangiomatous stromal hyperplasia	CTD_diseases	4
MESH:C535831	MESH:C535831	Pterygium colli mental retardation digital anomalies	CTD_diseases	4
MESH:C535832	MESH:C535832	Pulmonary alveolar proteinosis, congenital	CTD_diseases	4
MESH:C535833	MESH:C535833	Pulmonary edema of mountaineers	CTD_diseases	4
MESH:C535841	MESH:C535841	Hashimoto's encephalitis	CTD_diseases	4
MESH:C535842	MESH:C535842	Thyroiditis, Chronic	CTD_diseases	4
MESH:C535844	MESH:C535844	Haspeslagh Fryns Muelenaere syndrome	CTD_diseases	4
MESH:C535847	MESH:C535847	Hay-Wells syndrome	CTD_diseases	4
MESH:C535850	MESH:C535850	Heart defects limb shortening	CTD_diseases	4
MESH:C535855	MESH:C535855	Hydrocephalus, endocardial fibroelastosis, and cataracts	CTD_diseases	4
MESH:C535856	MESH:C535856	Hecht Scott syndrome	CTD_diseases	4
MESH:C535857	MESH:C535857	Hecht syndrome	CTD_diseases	4
MESH:C535860	MESH:C535860	Hemangioma, capillary infantile	CTD_diseases	4
MESH:C535861	MESH:C535861	Hemangiomatosis, familial pulmonary capillary	CTD_diseases	4
MESH:C535862	MESH:C535862	Hemifacial myohyperplasia	CTD_diseases	4
MESH:C535865	MESH:C535865	Rodrigues blindness	CTD_diseases	4
MESH:C535870	MESH:C535870	Rombo syndrome	CTD_diseases	4
MESH:C535871	MESH:C535871	Rommen Mueller Sybert syndrome	CTD_diseases	4
MESH:C535874	MESH:C535874	Rowley-Rosenberg syndrome	CTD_diseases	4
MESH:C535876	MESH:C535876	Rozin Hertz Goodman syndrome	CTD_diseases	4
MESH:C535877	MESH:C535877	Rubinstein Taybi like syndrome	CTD_diseases	4
MESH:C535878	MESH:C535878	Rud Syndrome	CTD_diseases	4
MESH:C535882	MESH:C535882	Johnson neuroectodermal syndrome	CTD_diseases	4
MESH:C535883	MESH:C535883	Johnston Aarons Schelley syndrome	CTD_diseases	4
MESH:C535887	MESH:C535887	Leukocyte adhesion deficiency type 1	CTD_diseases	4
MESH:C535888	MESH:C535888	Leukoencephalopathy, arthritis, colitis, and hypogammaglobulinemia	CTD_diseases	4
MESH:C535889	MESH:C535889	Leukonychia totalis	CTD_diseases	4
MESH:C535891	MESH:C535891	Familial popliteal pterygium syndrome	CTD_diseases	4
MESH:C535905	MESH:C535905	Lipoatrophy with diabetes, hepatic steatosis, cardiomyopathy, and leukomelanodermic papules	CTD_diseases	4
MESH:C535909	MESH:C535909	Marden Walker like syndrome	CTD_diseases	4
MESH:C535913	MESH:C535913	Marinesco-Sjogren-like syndrome (MSLS)	CTD_diseases	4
MESH:C535914	MESH:C535914	Mononen Karnes Senac syndrome	CTD_diseases	4
MESH:C535917	MESH:C535917	Cartwright Nelson Fryns syndrome	CTD_diseases	4
MESH:C535918	MESH:C535918	Schmid-Fraccaro syndrome	CTD_diseases	4
MESH:C535922	MESH:C535922	Chemke Oliver Mallek syndrome	CTD_diseases	4
MESH:C535924	MESH:C535924	Chilblain lupus	CTD_diseases	4
MESH:C535927	MESH:C535927	Chitayat Moore Del Bigio syndrome	CTD_diseases	4
MESH:C535928	MESH:C535928	Chitty Hall Baraitser syndrome	CTD_diseases	4
MESH:C535941	MESH:C535941	Chondrodysplasia punctata, brachytelephalangic	CTD_diseases	4
MESH:C535943	MESH:C535943	Desbuquois syndrome	CTD_diseases	4
MESH:C535944	MESH:C535944	Desmoid disease, hereditary	CTD_diseases	4
MESH:C535947	MESH:C535947	Devriendt syndrome	CTD_diseases	4
MESH:C535953	MESH:C535953	Eosinophilic pustular folliculitis	CTD_diseases	4
MESH:C535954	MESH:C535954	Eosinophilic synovitis	CTD_diseases	4
MESH:C535963	MESH:C535963	Cole Carpenter syndrome	CTD_diseases	4
MESH:C535973	MESH:C535973	Colpocephaly	CTD_diseases	4
MESH:C535975	MESH:C535975	Cone dystrophy, x-linked, with tapetal-like sheen	CTD_diseases	4
MESH:C535977	MESH:C535977	Congenital absence of the sternocleidomastoid muscle	CTD_diseases	4
MESH:C535981	MESH:C535981	Congenital alopecia X-linked	CTD_diseases	4
MESH:C535985	MESH:C535985	Dandy-walker malformation with mental retardation, macrocephaly, myopia, and brachytelephalangy	CTD_diseases	4
MESH:C535990	MESH:C535990	De Barsy syndrome	CTD_diseases	4
MESH:C535991	MESH:C535991	De Hauwere Leroy Adriaenssens syndrome	CTD_diseases	4
MESH:C535992	MESH:C535992	De Sanctis-Cacchione syndrome	CTD_diseases	4
MESH:C535993	MESH:C535993	Deafness conductive ptosis skeletal anomalies	CTD_diseases	4
MESH:C535994	MESH:C535994	Deafness enamel hypoplasia nail defects	CTD_diseases	4
MESH:C535995	MESH:C535995	Deafness hyperuricemia neurologic ataxia	CTD_diseases	4
MESH:C535996	MESH:C535996	Deafness nephritis ano rectal malformation	CTD_diseases	4
MESH:C536001	MESH:C536001	Accessory deep peroneal nerve	CTD_diseases	4
MESH:C536002	MESH:C536002	Accessory navicular bone	CTD_diseases	4
MESH:C536006	MESH:C536006	Acetylcarnitine deficiency	CTD_diseases	4
MESH:C536008	MESH:C536008	Achalasia Addisonianism Alacrimia syndrome	CTD_diseases	4
MESH:C536012	MESH:C536012	Achard syndrome	CTD_diseases	4
MESH:C536013	MESH:C536013	Achard-Thiers syndrome	CTD_diseases	4
MESH:C536022	MESH:C536022	Marles Greenberg Persaud syndrome	CTD_diseases	4
MESH:C536025	MESH:C536025	Marshall syndrome	CTD_diseases	4
MESH:C536026	MESH:C536026	Marshall-Smith syndrome	CTD_diseases	4
MESH:C536027	MESH:C536027	Martinez Monasterio Pinheiro syndrome	CTD_diseases	4
MESH:C536028	MESH:C536028	Martsolf syndrome	CTD_diseases	4
MESH:C536029	MESH:C536029	MASA (Mental Retardation, Aphasia, Shuffling Gait, Adducted Thumbs) Syndrome	CTD_diseases	4
MESH:C536052	MESH:C536052	Osteolysis syndrome recessive	CTD_diseases	4
MESH:C536061	MESH:C536061	Osteopoikilosis and dacryocystitis	CTD_diseases	4
MESH:C536064	MESH:C536064	Osteosclerosis with ichthyosis and premature ovarian failure	CTD_diseases	4
MESH:C536067	MESH:C536067	Hordnes Engebretsen Knudtson syndrome	CTD_diseases	4
MESH:C536069	MESH:C536069	Human spumaretrovirus infection	CTD_diseases	4
MESH:C536072	MESH:C536072	Hunter-McAlpine syndrome	CTD_diseases	4
MESH:C536074	MESH:C536074	Hutterite cerebroosteonephrodysplasia syndrome	CTD_diseases	4
MESH:C536075	MESH:C536075	Hyaloideoretinal degeneration of Wagner	CTD_diseases	4
MESH:C536078	MESH:C536078	Hydrocephalus, X-linked	CTD_diseases	4
MESH:C536093	MESH:C536093	Myelocytic leukemia-like syndrome, familial, chronic	CTD_diseases	4
MESH:C536100	MESH:C536100	Myopathic carnitine deficiency	CTD_diseases	4
MESH:C536102	MESH:C536102	Myopathy, congenital nonprogressive with Moebius and Robin sequences	CTD_diseases	4
MESH:C536105	MESH:C536105	Myopia 6	CTD_diseases	4
MESH:C536106	MESH:C536106	Myostatin-related muscle hypertrophy	CTD_diseases	4
MESH:C536107	MESH:C536107	N acetyltransferase deficiency	CTD_diseases	4
MESH:C536108	MESH:C536108	N syndrome	CTD_diseases	4
MESH:C536110	MESH:C536110	Nablus mask-like facial syndrome	CTD_diseases	4
MESH:C536121	MESH:C536121	Night blindness skeletal anomalies unusual facies	CTD_diseases	4
MESH:C536122	MESH:C536122	Night blindness, congenital stationary	CTD_diseases	4
MESH:C536124	MESH:C536124	Noble Bass Sherman syndrome	CTD_diseases	4
MESH:C536136	MESH:C536136	Mediastinal Fibrosis	CTD_diseases	4
MESH:C536138	MESH:C536138	Megacystis microcolon intestinal hypoperistalsis syndrome	CTD_diseases	4
MESH:C536139	MESH:C536139	Megaduodenum	CTD_diseases	4
MESH:C536141	MESH:C536141	Megalencephalic leukoencephalopathy with subcortical cysts	CTD_diseases	4
MESH:C536142	MESH:C536142	Megalencephaly cutis marmorata telangiectatica congenita	CTD_diseases	4
MESH:C536145	MESH:C536145	Megarbane syndrome	CTD_diseases	4
MESH:C536146	MESH:C536146	Mehes syndrome	CTD_diseases	4
MESH:C536147	MESH:C536147	Mehta Lewis Patton syndrome	CTD_diseases	4
MESH:C536148	MESH:C536148	Meier Blumberg Imahorn syndrome	CTD_diseases	4
MESH:C536149	MESH:C536149	Melanoma astrocytoma syndrome	CTD_diseases	4
MESH:C536150	MESH:C536150	Keratoacanthoma familial	CTD_diseases	4
MESH:C536151	MESH:C536151	Keratoconus posticus circumscriptus	CTD_diseases	4
MESH:C536153	MESH:C536153	Keratoderma palmoplantar spastic paralysis	CTD_diseases	4
MESH:C536155	MESH:C536155	Keratolytic winter erythema	CTD_diseases	4
MESH:C536158	MESH:C536158	Keratosis follicularis dwarfism cerebral atrophy	CTD_diseases	4
MESH:C536159	MESH:C536159	Keratosis Follicularis Spinulosa Decalvans, X-Linked	CTD_diseases	4
MESH:C536166	MESH:C536166	Keshan disease	CTD_diseases	4
MESH:C536167	MESH:C536167	Keutel syndrome	CTD_diseases	4
MESH:C536168	MESH:C536168	Keratitis, Ichthyosis, and Deafness (KID) Syndrome	CTD_diseases	4
MESH:C536169	MESH:C536169	Diaphyseal medullary stenosis with malignant fibrous histiocytoma	CTD_diseases	4
MESH:C536176	MESH:C536176	Dimauro disease	CTD_diseases	4
MESH:C536177	MESH:C536177	Dincsoy Salih Patel syndrome	CTD_diseases	4
MESH:C536179	MESH:C536179	Feingold Trainer syndrome	CTD_diseases	4
MESH:C536187	MESH:C536187	Ectrodactyly cardiopathy dysmorphism	CTD_diseases	4
MESH:C536188	MESH:C536188	Blepharo-cheilo-dontic syndrome	CTD_diseases	4
MESH:C536197	MESH:C536197	Ehlers-Danlos syndrome type 5	CTD_diseases	4
MESH:C536203	MESH:C536203	Elejalde Disease	CTD_diseases	4
MESH:C536205	MESH:C536205	Ellis Yale Winter syndrome	CTD_diseases	4
MESH:C536208	MESH:C536208	Clark-Baraitser syndrome	CTD_diseases	4
MESH:C536210	MESH:C536210	Congenital chloride diarrhea	CTD_diseases	4
MESH:C536216	MESH:C536216	Crome syndrome	CTD_diseases	4
MESH:C536217	MESH:C536217	Crumpled helices and small mouth	CTD_diseases	4
MESH:C536219	MESH:C536219	Cryptomicrotia brachydactyly syndrome	CTD_diseases	4
MESH:C536220	MESH:C536220	Curly hair-acral keratoderma-caries syndrome	CTD_diseases	4
MESH:C536221	MESH:C536221	Currarino triad	CTD_diseases	4
MESH:C536224	MESH:C536224	Cutaneous photosensitivity and colitis, lethal	CTD_diseases	4
MESH:C536226	MESH:C536226	Cutis marmorata telangiectatica congenita	CTD_diseases	4
MESH:C536230	MESH:C536230	Cystic medial necrosis of aorta	CTD_diseases	4
MESH:C536232	MESH:C536232	Blepharophimosis syndrome Ohdo type	CTD_diseases	4
MESH:C536233	MESH:C536233	Blepharophimosis syndrome type 1	CTD_diseases	4
MESH:C536234	MESH:C536234	Blepharophimosis syndrome type 2	CTD_diseases	4
MESH:C536235	MESH:C536235	Blepharophimosis with ptosis, syndactyly, and short stature	CTD_diseases	4
MESH:C536236	MESH:C536236	Blepharoptosis myopia ectopia lentis	CTD_diseases	4
MESH:C536237	MESH:C536237	Blount disease	CTD_diseases	4
MESH:C536239	MESH:C536239	Blue diaper syndrome	CTD_diseases	4
MESH:C536240	MESH:C536240	Blue rubber bleb nevus syndrome	CTD_diseases	4
MESH:C536242	MESH:C536242	Brachymorphism-onychodysplasia-dysphalangism syndrome	CTD_diseases	4
MESH:C536243	MESH:C536243	Non-lissencephalic cortical dysplasia	CTD_diseases	4
MESH:C536259	MESH:C536259	Qazi Markouizos syndrome	CTD_diseases	4
MESH:C536261	MESH:C536261	Radial defect Robin sequence	CTD_diseases	4
MESH:C536262	MESH:C536262	Radial hypoplasia, triphalangeal thumbs and hypospadias	CTD_diseases	4
MESH:C536263	MESH:C536263	Radial ray hypoplasia choanal atresia	CTD_diseases	4
MESH:C536264	MESH:C536264	Radiation induced angiosarcoma of the breast	CTD_diseases	4
MESH:C536266	MESH:C536266	Radiation induced meningioma	CTD_diseases	4
MESH:C536268	MESH:C536268	Radio-ulnar synostosis type 1	CTD_diseases	4
MESH:C536269	MESH:C536269	Radio-ulnar synostosis type 2	CTD_diseases	4
MESH:C536270	MESH:C536270	Radioulnar synostosis retinal pigment abnormalities	CTD_diseases	4
MESH:C536271	MESH:C536271	Ichthyosis prematurity syndrome	CTD_diseases	4
MESH:C536282	MESH:C536282	Pulmonary arterial hypertension	CTD_diseases	4
MESH:C536283	MESH:C536283	Idiopathic subglottic tracheal stenosis	CTD_diseases	4
MESH:C536292	MESH:C536292	Jorgenson Lenz syndrome	CTD_diseases	4
MESH:C536293	MESH:C536293	Joubert syndrome 1	CTD_diseases	4
MESH:C536294	MESH:C536294	Joubert syndrome 2	CTD_diseases	4
MESH:C536295	MESH:C536295	Joubert syndrome 3	CTD_diseases	4
MESH:C536296	MESH:C536296	Joubert syndrome 4	CTD_diseases	4
MESH:C536299	MESH:C536299	Partington Anderson syndrome	CTD_diseases	4
MESH:C536305	MESH:C536305	Patau syndrome	CTD_diseases	4
MESH:C536306	MESH:C536306	Patel Bixler syndrome	CTD_diseases	4
MESH:C536310	MESH:C536310	Patterson pseudoleprechaunism syndrome	CTD_diseases	4
MESH:C536313	MESH:C536313	Pavone Fiumara Rizzo syndrome	CTD_diseases	4
MESH:C536316	MESH:C536316	Peeling skin syndrome, acral type	CTD_diseases	4
MESH:C536321	MESH:C536321	Poikiloderma of Kindler	CTD_diseases	4
MESH:C536331	MESH:C536331	Polydactyly myopia syndrome	CTD_diseases	4
MESH:C536347	MESH:C536347	Vibratory angioedema	CTD_diseases	4
MESH:C536349	MESH:C536349	Viljoen Kallis Voges syndrome	CTD_diseases	4
MESH:C536351	MESH:C536351	Visceral Steatosis, Congenital	CTD_diseases	4
MESH:C536352	MESH:C536352	Vitreoretinochoroidopathy	CTD_diseases	4
MESH:C536353	MESH:C536353	VLCAD deficiency	CTD_diseases	4
MESH:C536358	MESH:C536358	Anemia, sideroblastic spinocerebellar ataxia	CTD_diseases	4
MESH:C536359	MESH:C536359	Anencephaly and spina bifida X-linked	CTD_diseases	4
MESH:C536361	MESH:C536361	Angel shaped phalangoepiphyseal dysplasia	CTD_diseases	4
MESH:C536365	MESH:C536365	Angioma serpiginosum, autosomal dominant	CTD_diseases	4
MESH:C536366	MESH:C536366	Angioma serpiginosum, X-linked	CTD_diseases	4
MESH:C536367	MESH:C536367	Angiomatosis, diffuse corticomeningeal, of Divry and Van Bogaert	CTD_diseases	4
MESH:C536373	MESH:C536373	Ankyloblepharon filiforme adnatum cleft palate	CTD_diseases	4
MESH:C536375	MESH:C536375	Abnormal fusion of dental cementum with alveolar bone	CTD_diseases	4
MESH:C536377	MESH:C536377	Anonychia congenita	CTD_diseases	4
MESH:C536378	MESH:C536378	Anonychia onychodystrophy	CTD_diseases	4
MESH:C536379	MESH:C536379	Anonychia-onychodystrophy with brachydactyly type B and ectrodactyly	CTD_diseases	4
MESH:C536382	MESH:C536382	Exudative vitreoretinopathy 1	CTD_diseases	4
MESH:C536387	MESH:C536387	Facio thoraco genital syndrome	CTD_diseases	4
MESH:C536390	MESH:C536390	Donnai-Barrow syndrome	CTD_diseases	4
MESH:C536395	MESH:C536395	Neonatal herpes	CTD_diseases	4
MESH:C536397	MESH:C536397	Neonatal Systemic lupus erythematosus	CTD_diseases	4
MESH:C536401	MESH:C536401	Nephropathy deafness hyperparathyroidism	CTD_diseases	4
MESH:C536402	MESH:C536402	Nephrosis deafness urinary tract digital malformation	CTD_diseases	4
MESH:C536403	MESH:C536403	Nephrotic syndrome ocular anomalies	CTD_diseases	4
MESH:C536405	MESH:C536405	Neu Laxova syndrome	CTD_diseases	4
MESH:C536410	MESH:C536410	Neural tube defects X-linked	CTD_diseases	4
MESH:C536416	MESH:C536416	Primary lateral sclerosis juvenile	CTD_diseases	4
MESH:C536422	MESH:C536422	Progeria short stature pigmented nevi	CTD_diseases	4
MESH:C536424	MESH:C536424	Progressive hearing loss stapes fixation	CTD_diseases	4
MESH:C536426	MESH:C536426	Cleft palate X-linked	CTD_diseases	4
MESH:C536427	MESH:C536427	Cleft palate, midfacial hypoplasia, triangular facies, and sensorineural hearing loss	CTD_diseases	4
MESH:C536432	MESH:C536432	Cochleosaccular degeneration of the inner ear and progressive cataracts	CTD_diseases	4
MESH:C536434	MESH:C536434	CODAS syndrome	CTD_diseases	4
MESH:C536435	MESH:C536435	Coffin syndrome 1	CTD_diseases	4
MESH:C536436	MESH:C536436	Coffin-Siris syndrome	CTD_diseases	4
MESH:C536438	MESH:C536438	Cohen syndrome	CTD_diseases	4
MESH:C536446	MESH:C536446	Corpus callosum agenesis neuronopathy	CTD_diseases	4
MESH:C536448	MESH:C536448	Costocoracoid ligament congenitally short	CTD_diseases	4
MESH:C536449	MESH:C536449	Cote Katsantoni syndrome	CTD_diseases	4
MESH:C536453	MESH:C536453	Craniofacial deafness hand syndrome	CTD_diseases	4
MESH:C536457	MESH:C536457	Vohwinkel syndrome	CTD_diseases	4
MESH:C536476	MESH:C536476	Urban Schosser Spohn syndrome	CTD_diseases	4
MESH:C536477	MESH:C536477	Urethral obstruction sequence	CTD_diseases	4
MESH:C536478	MESH:C536478	Urioste Martinez-Frias syndrome	CTD_diseases	4
MESH:C536480	MESH:C536480	Urofacial syndrome	CTD_diseases	4
MESH:C536481	MESH:C536481	Urogenital adysplasia	CTD_diseases	4
MESH:C536483	MESH:C536483	Uropathy distal obstructive polydactyly	CTD_diseases	4
MESH:C536496	MESH:C536496	Tetra amelia with ectodermal dysplasia and lacrimal duct abnormalities	CTD_diseases	4
MESH:C536497	MESH:C536497	X-linked tetra-amelia	CTD_diseases	4
MESH:C536500	MESH:C536500	Tetraamelia multiple malformations	CTD_diseases	4
MESH:C536501	MESH:C536501	Tetralogy of fallot and glaucoma	CTD_diseases	4
MESH:C536503	MESH:C536503	Thakker Donnai syndrome	CTD_diseases	4
MESH:C536509	MESH:C536509	Theodor Hertz Goodman syndrome	CTD_diseases	4
MESH:C536512	MESH:C536512	Thiopurine S methyltranferase deficiency	CTD_diseases	4
MESH:C536513	MESH:C536513	Thomas Jewett Raines syndrome	CTD_diseases	4
MESH:C536514	MESH:C536514	Thomas syndrome	CTD_diseases	4
MESH:C536515	MESH:C536515	Thompson Baraitser syndrome	CTD_diseases	4
MESH:C536517	MESH:C536517	Thoracolaryngopelvic dysplasia	CTD_diseases	4
MESH:C536519	MESH:C536519	Thrombocytopenia chromosome breakage	CTD_diseases	4
MESH:C536520	MESH:C536520	VACTERL association with hydrocephaly, X-linked	CTD_diseases	4
MESH:C536522	MESH:C536522	Vacuolar myopathy	CTD_diseases	4
MESH:C536525	MESH:C536525	Valproic acid antenatal infection	CTD_diseases	4
MESH:C536526	MESH:C536526	Van Bogaert-Hozay syndrome	CTD_diseases	4
MESH:C536528	MESH:C536528	Van der Woude syndrome	CTD_diseases	4
MESH:C536529	MESH:C536529	Van der Woude syndrome 2	CTD_diseases	4
MESH:C536530	MESH:C536530	Van Maldergem Wetzburger Verloes syndrome	CTD_diseases	4
MESH:C536533	MESH:C536533	Vasquez Hurst Sotos syndrome	CTD_diseases	4
MESH:C536536	MESH:C536536	Velofacioskeletal syndrome	CTD_diseases	4
MESH:C536541	MESH:C536541	Verloove-Vanhorick Brubakk syndrome	CTD_diseases	4
MESH:C536543	MESH:C536543	Vertebral body fusion overgrowth	CTD_diseases	4
MESH:C536544	MESH:C536544	Treft Sanborn Carey syndrome	CTD_diseases	4
MESH:C536549	MESH:C536549	Tricho-dento-osseous syndrome	CTD_diseases	4
MESH:C536552	MESH:C536552	Trichoepithelioma multiple familial	CTD_diseases	4
MESH:C536553	MESH:C536553	Trichofolliculoma	CTD_diseases	4
MESH:C536554	MESH:C536554	Oliver-McFarlane syndrome	CTD_diseases	4
MESH:C536558	MESH:C536558	Trichostasis spinulosa	CTD_diseases	4
MESH:C536560	MESH:C536560	Triglyceride storage disease with impaired long-chain fatty acid oxidation	CTD_diseases	4
MESH:C536561	MESH:C536561	Trimethylaminuria	CTD_diseases	4
MESH:C536564	MESH:C536564	Triphalangeal thumbs brachyectrodactyly	CTD_diseases	4
MESH:C536566	MESH:C536566	Walbaum Titran Durieux Crepin syndrome	CTD_diseases	4
MESH:C536567	MESH:C536567	Waldmann disease	CTD_diseases	4
MESH:C536571	MESH:C536571	Boerhaave syndrome	CTD_diseases	4
MESH:C536575	MESH:C536575	Borjeson-Forssman-Lehmann syndrome	CTD_diseases	4
MESH:C536580	MESH:C536580	Chromosome 18 deletion syndrome	CTD_diseases	4
MESH:C536608	MESH:C536608	Fallot complex with severe mental and growth retardation	CTD_diseases	4
MESH:C536609	MESH:C536609	Familial capillaro-venous leptomeningeal angiomatosis	CTD_diseases	4
MESH:C536611	MESH:C536611	Familial cylindromatosis	CTD_diseases	4
MESH:C536619	MESH:C536619	Say Field Coldwell syndrome	CTD_diseases	4
MESH:C536620	MESH:C536620	Say Meyer syndrome	CTD_diseases	4
MESH:C536621	MESH:C536621	Say syndrome	CTD_diseases	4
MESH:C536623	MESH:C536623	Scalp ear nipple syndrome	CTD_diseases	4
MESH:C536625	MESH:C536625	SCARF syndrome	CTD_diseases	4
MESH:C536626	MESH:C536626	Schaap Taylor Baraitser syndrome	CTD_diseases	4
MESH:C536627	MESH:C536627	Schaefer Stein Oshman syndrome	CTD_diseases	4
MESH:C536630	MESH:C536630	Schimke X-linked mental retardation syndrome	CTD_diseases	4
MESH:C536632	MESH:C536632	Schinzel-Giedion syndrome	CTD_diseases	4
MESH:C536633	MESH:C536633	Schisis association	CTD_diseases	4
MESH:C536634	MESH:C536634	Schizotaxia	CTD_diseases	4
MESH:C536638	MESH:C536638	Scholte syndrome	CTD_diseases	4
MESH:C536639	MESH:C536639	Schrander-Stumpel Theunissen Hulsmans syndrome	CTD_diseases	4
MESH:C536641	MESH:C536641	Schwannomatosis	CTD_diseases	4
MESH:C536642	MESH:C536642	Spastic paraplegia 15, autosomal recessive	CTD_diseases	4
MESH:C536643	MESH:C536643	Spastic paraplegia 16, X-linked	CTD_diseases	4
MESH:C536646	MESH:C536646	Pena Shokeir syndrome Type 2	CTD_diseases	4
MESH:C536650	MESH:C536650	Penoscrotal transposition	CTD_diseases	4
MESH:C536658	MESH:C536658	Perisylvian syndrome	CTD_diseases	4
MESH:C536666	MESH:C536666	Situs inversus totalis with cystic dysplasia of kidneys and pancreas	CTD_diseases	4
MESH:C536671	MESH:C536671	Sketetal dysplasia coarse facies mental retardation	CTD_diseases	4
MESH:C536672	MESH:C536672	Slavotinek Pike Mills Hurst syndrome	CTD_diseases	4
MESH:C536673	MESH:C536673	Slti Salem syndrome	CTD_diseases	4
MESH:C536677	MESH:C536677	Snowflake vitreoretinal degeneration	CTD_diseases	4
MESH:C536679	MESH:C536679	Sohval Soffer syndrome	CTD_diseases	4
MESH:C536680	MESH:C536680	Sonoda syndrome	CTD_diseases	4
MESH:C536681	MESH:C536681	Warburg Sjo Fledelius syndrome	CTD_diseases	4
MESH:C536682	MESH:C536682	Warburton Anyane Yeboa syndrome	CTD_diseases	4
MESH:C536683	MESH:C536683	Warfarin syndrome	CTD_diseases	4
MESH:C536687	MESH:C536687	Weaver syndrome	CTD_diseases	4
MESH:C536688	MESH:C536688	Weinstein Kliman Scully syndrome	CTD_diseases	4
MESH:C536691	MESH:C536691	Wellesley Carmen French syndrome	CTD_diseases	4
MESH:C536692	MESH:C536692	Wells Jankovic syndrome	CTD_diseases	4
MESH:C536695	MESH:C536695	Weyers acrofacial dysostosis	CTD_diseases	4
MESH:C536696	MESH:C536696	Weyers ulnar ray/oligodactyly syndrome	CTD_diseases	4
MESH:C536700	MESH:C536700	White forelock with malformations	CTD_diseases	4
MESH:C536701	MESH:C536701	Curatolo Cilio Pessagno syndrome	CTD_diseases	4
MESH:C536702	MESH:C536702	White platelet syndrome	CTD_diseases	4
MESH:C536703	MESH:C536703	Wieacker syndrome	CTD_diseases	4
MESH:C536704	MESH:C536704	Wiedemann Grosse Dibbern syndrome	CTD_diseases	4
MESH:C536705	MESH:C536705	Wiedemann Oldigs Oppermann syndrome	CTD_diseases	4
MESH:C536709	MESH:C536709	Winchester syndrome	CTD_diseases	4
MESH:C536712	MESH:C536712	Winter Harding Hyde syndrome	CTD_diseases	4
MESH:C536713	MESH:C536713	Yim Ebbin syndrome	CTD_diseases	4
MESH:C536715	MESH:C536715	Young Hughes syndrome	CTD_diseases	4
MESH:C536717	MESH:C536717	Young Simpson syndrome	CTD_diseases	4
MESH:C536718	MESH:C536718	Young Syndrome	CTD_diseases	4
MESH:C536721	MESH:C536721	Zadik Barak Levin syndrome	CTD_diseases	4
MESH:C536724	MESH:C536724	Zerres Rietschel Majewski syndrome	CTD_diseases	4
MESH:C536725	MESH:C536725	Zimmerman Laband syndrome	CTD_diseases	4
MESH:C536727	MESH:C536727	Zonular cataract and nystagmus	CTD_diseases	4
MESH:C536728	MESH:C536728	Zori Stalker Williams syndrome	CTD_diseases	4
MESH:C536730	MESH:C536730	Zuska's Disease	CTD_diseases	4
MESH:C536735	MESH:C536735	Winter Shortland Temple syndrome	CTD_diseases	4
MESH:C536736	MESH:C536736	Witkop syndrome	CTD_diseases	4
MESH:C536737	MESH:C536737	Wittwer syndrome	CTD_diseases	4
MESH:C536742	MESH:C536742	Woodhouse Sakati syndrome	CTD_diseases	4
MESH:C536745	MESH:C536745	Woolly hair, congenital	CTD_diseases	4
MESH:C536746	MESH:C536746	Woolly hair, hypotrichosis, everted lower lip and outstanding ears	CTD_diseases	4
MESH:C536751	MESH:C536751	WT limb blood syndrome	CTD_diseases	4
MESH:C536757	MESH:C536757	X-linked adrenal hypoplasia congenita	CTD_diseases	4
MESH:C536761	MESH:C536761	X-linked sideroblastic anemia	CTD_diseases	4
MESH:C536767	MESH:C536767	XK aprosencephaly	CTD_diseases	4
MESH:C536771	MESH:C536771	Yemenite deaf-blind hypopigmentation syndrome	CTD_diseases	4
MESH:C536777	MESH:C536777	Systemic candidiasis	CTD_diseases	4
MESH:C536778	MESH:C536778	Systemic carnitine deficiency	CTD_diseases	4
MESH:C536781	MESH:C536781	T-cell immunodeficiency, congenital alopecia and nail dystrophy	CTD_diseases	4
MESH:C536789	MESH:C536789	Craniosynostosis, anal anomalies, and porokeratosis	CTD_diseases	4
MESH:C536796	MESH:C536796	Trisomy 22 mosaicism syndrome	CTD_diseases	4
MESH:C536798	MESH:C536798	Chromosome 22, monosome mosaic	CTD_diseases	4
MESH:C536801	MESH:C536801	Telomeric 22q13 Monosomy Syndrome	CTD_diseases	4
MESH:C536803	MESH:C536803	Chromosome 3 duplication syndrome	CTD_diseases	4
MESH:C536817	MESH:C536817	Al-Gazali Syndrome	CTD_diseases	4
MESH:C536819	MESH:C536819	Giant pigmented hairy nevus	CTD_diseases	4
MESH:C536820	MESH:C536820	Giedion syndrome	CTD_diseases	4
MESH:C536821	MESH:C536821	Gigantomastia	CTD_diseases	4
MESH:C536824	MESH:C536824	Glaucoma 3, primary infantile, B	CTD_diseases	4
MESH:C536825	MESH:C536825	Glomerulonephritis sparse hair telangiectases	CTD_diseases	4
MESH:C536837	MESH:C536837	Glyceraldehyde-3-phosphate dehydrogenase deficiency	CTD_diseases	4
MESH:C536841	MESH:C536841	Familial encephalopathy with neuroserpin inclusion bodies	CTD_diseases	4
MESH:C536842	MESH:C536842	Polycythemia, primary familial and congenital	CTD_diseases	4
MESH:C536845	MESH:C536845	Familial hypersecretion of adrenal androgens	CTD_diseases	4
MESH:C536847	MESH:C536847	Familial multiple trichodiscomas	CTD_diseases	4
MESH:C536850	MESH:C536850	Familial porencephaly	CTD_diseases	4
MESH:C536857	MESH:C536857	Spastic paraplegia 2, X-linked	CTD_diseases	4
MESH:C536859	MESH:C536859	Spastic paraplegia 23	CTD_diseases	4
MESH:C536868	MESH:C536868	Spastic paraplegia 9, autosomal dominant	CTD_diseases	4
MESH:C536874	MESH:C536874	Spastic paraplegia with precocious puberty	CTD_diseases	4
MESH:C536878	MESH:C536878	Spinal intradural arachnoid cysts	CTD_diseases	4
MESH:C536885	MESH:C536885	Kleiner Holmes syndrome	CTD_diseases	4
MESH:C536894	MESH:C536894	Talo-patello-scaphoid osteolysis, synovitis, and short fourth metacarpals	CTD_diseases	4
MESH:C536896	MESH:C536896	Tamari Goodman syndrome	CTD_diseases	4
MESH:C536898	MESH:C536898	Thrombocytopenia Robin sequence	CTD_diseases	4
MESH:C536900	MESH:C536900	Thrombomodulin anomalies, familial	CTD_diseases	4
MESH:C536904	MESH:C536904	Thumb deformity, alopecia, pigmentation anomaly	CTD_diseases	4
MESH:C536905	MESH:C536905	Thymic epithelial tumor	CTD_diseases	4
MESH:C536916	MESH:C536916	Thyroid hormone plasma membrane transport defect	CTD_diseases	4
MESH:C536920	MESH:C536920	Tight skin contracture syndrome, lethal	CTD_diseases	4
MESH:C536922	MESH:C536922	Tubulointerstitial nephritis and uveitis	CTD_diseases	4
MESH:C536923	MESH:C536923	Tucker syndrome	CTD_diseases	4
MESH:C536924	MESH:C536924	Tufted angioma	CTD_diseases	4
MESH:C536925	MESH:C536925	Tukel syndrome	CTD_diseases	4
MESH:C536927	MESH:C536927	Tunglang Savage Bellman syndrome	CTD_diseases	4
MESH:C536928	MESH:C536928	Turcot syndrome	CTD_diseases	4
MESH:C536934	MESH:C536934	Ulna hypoplasia with mental retardation	CTD_diseases	4
MESH:C536937	MESH:C536937	Ulnar-mammary syndrome	CTD_diseases	4
MESH:C536938	MESH:C536938	Umbilical cord ulceration and intestinal atresia	CTD_diseases	4
MESH:C536939	MESH:C536939	Uncombable hair syndrome	CTD_diseases	4
MESH:C536948	MESH:C536948	Teebi Kaurah syndrome	CTD_diseases	4
MESH:C536950	MESH:C536950	Teebi Shaltout syndrome	CTD_diseases	4
MESH:C536951	MESH:C536951	Teebi syndrome	CTD_diseases	4
MESH:C536952	MESH:C536952	Teeth noneruption of with maxillary hypoplasia and genu valgum	CTD_diseases	4
MESH:C536953	MESH:C536953	Tel Hashomer camptodactyly syndrome	CTD_diseases	4
MESH:C536955	MESH:C536955	Telfer Sugar Jaeger syndrome	CTD_diseases	4
MESH:C536957	MESH:C536957	Temporomandibular ankylosis	CTD_diseases	4
MESH:C536960	MESH:C536960	Hapnes Boman Skeie syndrome	CTD_diseases	4
MESH:C536961	MESH:C536961	Familial Testotoxicosis	CTD_diseases	4
MESH:C536964	MESH:C536964	Tollner Horst Manzke syndrome	CTD_diseases	4
MESH:C536967	MESH:C536967	Tonoki syndrome	CTD_diseases	4
MESH:C536969	MESH:C536969	Torsion dystonia with onset in infancy	CTD_diseases	4
MESH:C536970	MESH:C536970	Torticollis keloids cryptorchidism renal dysplasia	CTD_diseases	4
MESH:C536972	MESH:C536972	Torulopsis	CTD_diseases	4
MESH:C536974	MESH:C536974	Townes-Brocks syndrome	CTD_diseases	4
MESH:C536975	MESH:C536975	Tracheal agenesis	CTD_diseases	4
MESH:C536987	MESH:C536987	Mosaic variegated aneuploidy syndrome	CTD_diseases	4
MESH:C536989	MESH:C536989	Mousa Al din Al Nassar syndrome	CTD_diseases	4
MESH:C536997	MESH:C536997	Le Marec Bracq Picaud syndrome	CTD_diseases	4
MESH:C537000	MESH:C537000	Ledderhose disease	CTD_diseases	4
MESH:C537001	MESH:C537001	Left-sided gallbladder	CTD_diseases	4
MESH:C537008	MESH:C537008	Kapur Toriello syndrome	CTD_diseases	4
MESH:C537009	MESH:C537009	Karandikar Maria Kamble syndrome	CTD_diseases	4
MESH:C537011	MESH:C537011	Kasznica Carlson Coppedge syndrome	CTD_diseases	4
MESH:C537012	MESH:C537012	Katsantoni Papadakou Lagoyanni syndrome	CTD_diseases	4
MESH:C537013	MESH:C537013	Kaufman oculocerebrofacial syndrome	CTD_diseases	4
MESH:C537015	MESH:C537015	KBG syndrome	CTD_diseases	4
MESH:C537022	MESH:C537022	Keratitis, hereditary	CTD_diseases	4
MESH:C537024	MESH:C537024	Kosztolanyi syndrome	CTD_diseases	4
MESH:C537026	MESH:C537026	Lipodermatosclerosis	CTD_diseases	4
MESH:C537036	MESH:C537036	Lopes Gorlin syndrome	CTD_diseases	4
MESH:C537037	MESH:C537037	Lowry Maclean syndrome	CTD_diseases	4
MESH:C537038	MESH:C537038	Lowry Wood syndrome	CTD_diseases	4
MESH:C537039	MESH:C537039	Lubani Al Saleh Teebi syndrome	CTD_diseases	4
MESH:C537048	MESH:C537048	Allanson Pantzar McLeod syndrome	CTD_diseases	4
MESH:C537049	MESH:C537049	Aloi Tomasini Isaia syndrome	CTD_diseases	4
MESH:C537053	MESH:C537053	Alopecia hypogonadism extrapyramidal disorder	CTD_diseases	4
MESH:C537056	MESH:C537056	Alopecia universalis onychodystrophy vitiligo	CTD_diseases	4
MESH:C537059	MESH:C537059	Flat umbilicus familial	CTD_diseases	4
MESH:C537060	MESH:C537060	Flaujeac factor deficiency	CTD_diseases	4
MESH:C537062	MESH:C537062	Floating-harbor syndrome	CTD_diseases	4
MESH:C537067	MESH:C537067	Focal cortical dysplasia of Taylor	CTD_diseases	4
MESH:C537076	MESH:C537076	Faye-Petersen Ward Carey syndrome	CTD_diseases	4
MESH:C537082	MESH:C537082	Weismann Netter syndrome	CTD_diseases	4
MESH:C537084	MESH:C537084	Brachioskeletogenital syndrome	CTD_diseases	4
MESH:C537087	MESH:C537087	Brachydactyly preaxial with hallux varus and thumb abduction	CTD_diseases	4
MESH:C537091	MESH:C537091	Brachydactyly type A5 nail dysplasia	CTD_diseases	4
MESH:C537095	MESH:C537095	Brachydactyly with hypertension	CTD_diseases	4
MESH:C537096	MESH:C537096	Brachymesomelia renal syndrome	CTD_diseases	4
MESH:C537102	MESH:C537102	Branchial arch syndrome X-linked	CTD_diseases	4
MESH:C537115	MESH:C537115	Lenz Majewski hyperostotic dwarfism	CTD_diseases	4
MESH:C537119	MESH:C537119	Leri-Weil syndrome	CTD_diseases	4
MESH:C537121	MESH:C537121	Short stature syndrome, Brussels type	CTD_diseases	4
MESH:C537125	MESH:C537125	Optic atrophy, X-linked	CTD_diseases	4
MESH:C537128	MESH:C537128	Optic atrophy and cataract, autosomal dominant	CTD_diseases	4
MESH:C537138	MESH:C537138	Oslam syndrome	CTD_diseases	4
MESH:C537144	MESH:C537144	Osteoarthropathy of fingers familial	CTD_diseases	4
MESH:C537149	MESH:C537149	Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked	CTD_diseases	4
MESH:C537155	MESH:C537155	Hypomelia mullerian duct anomalies	CTD_diseases	4
MESH:C537156	MESH:C537156	Hypoparathyroidism familial isolated	CTD_diseases	4
MESH:C537157	MESH:C537157	Hypoparathyroidism-retardation-dysmorphism syndrome	CTD_diseases	4
MESH:C537164	MESH:C537164	Panostotic fibrous dysplasia	CTD_diseases	4
MESH:C537169	MESH:C537169	Papular urticaria	CTD_diseases	4
MESH:C537171	MESH:C537171	Paraquat lung	CTD_diseases	4
MESH:C537179	MESH:C537179	Parkinsonism, early onset with mental retardation	CTD_diseases	4
MESH:C537185	MESH:C537185	Pierson syndrome	CTD_diseases	4
MESH:C537186	MESH:C537186	Pigmented purpuric eruption	CTD_diseases	4
MESH:C537187	MESH:C537187	Pili annulati	CTD_diseases	4
MESH:C537188	MESH:C537188	Pili multigemini	CTD_diseases	4
MESH:C537193	MESH:C537193	Saal Bulas syndrome	CTD_diseases	4
MESH:C537207	MESH:C537207	Kniest dysplasia	CTD_diseases	4
MESH:C537208	MESH:C537208	Kniest like dysplasia lethal	CTD_diseases	4
MESH:C537209	MESH:C537209	Knobloch syndrome	CTD_diseases	4
MESH:C537210	MESH:C537210	Knuckle pads, leuconychia and sensorineural deafness	CTD_diseases	4
MESH:C537211	MESH:C537211	Kocher-Debre-Semelaigne syndrome	CTD_diseases	4
MESH:C537219	MESH:C537219	Sackey Sakati Aur syndrome	CTD_diseases	4
MESH:C537221	MESH:C537221	Sacral defect and anterior sacral meningocele	CTD_diseases	4
MESH:C537223	MESH:C537223	Sacral meningocele conotruncal heart defects	CTD_diseases	4
MESH:C537224	MESH:C537224	Sacral plexopathy	CTD_diseases	4
MESH:C537225	MESH:C537225	Sacrococcygeal dysgenesis association	CTD_diseases	4
MESH:C537231	MESH:C537231	Samson Viljoen syndrome	CTD_diseases	4
MESH:C537232	MESH:C537232	Sanderson Fraser syndrome	CTD_diseases	4
MESH:C537233	MESH:C537233	Sandhaus Ben-Ami syndrome	CTD_diseases	4
MESH:C537236	MESH:C537236	Sarcosinemia	CTD_diseases	4
MESH:C537238	MESH:C537238	Melhem Fahl syndrome	CTD_diseases	4
MESH:C537241	MESH:C537241	Properdin deficiency, X-linked	CTD_diseases	4
MESH:C537244	MESH:C537244	Prostatic malacoplakia associated with prostatic abscess	CTD_diseases	4
MESH:C537260	MESH:C537260	Hereditary koilonychia	CTD_diseases	4
MESH:C537266	MESH:C537266	Landy Donnai syndrome	CTD_diseases	4
MESH:C537267	MESH:C537267	Langer mesomelic dysplasia	CTD_diseases	4
MESH:C537269	MESH:C537269	Forney Robinson Pascoe syndrome	CTD_diseases	4
MESH:C537270	MESH:C537270	Fountain syndrome	CTD_diseases	4
MESH:C537274	MESH:C537274	Ter Haar syndrome	CTD_diseases	4
MESH:C537282	MESH:C537282	Goldstein Hutt syndrome	CTD_diseases	4
MESH:C537284	MESH:C537284	GOMBO syndrome	CTD_diseases	4
MESH:C537285	MESH:C537285	Gomez Lopez Hernandez syndrome	CTD_diseases	4
MESH:C537289	MESH:C537289	Gorlin Bushkell Jensen syndrome	CTD_diseases	4
MESH:C537290	MESH:C537290	Gorlin Chaudhry Moss syndrome	CTD_diseases	4
MESH:C537291	MESH:C537291	Gracile bone dysplasia	CTD_diseases	4
MESH:C537293	MESH:C537293	Grant syndrome	CTD_diseases	4
MESH:C537294	MESH:C537294	Granulomas, congenital cerebral	CTD_diseases	4
MESH:C537298	MESH:C537298	Autosomal recessive nonsyndromic congenital nuclear cataract	CTD_diseases	4
MESH:C537301	MESH:C537301	Griscelli syndrome type 1	CTD_diseases	4
MESH:C537303	MESH:C537303	Griscelli syndrome type 3	CTD_diseases	4
MESH:C537315	MESH:C537315	Spinocerebellar ataxia, X-linked, 3	CTD_diseases	4
MESH:C537321	MESH:C537321	Microcephalic primordial dwarfism Toriello type	CTD_diseases	4
MESH:C537322	MESH:C537322	Microcephaly albinism digital anomalies syndrome	CTD_diseases	4
MESH:C537325	MESH:C537325	Microcephaly cervical spine fusion anomalies	CTD_diseases	4
MESH:C537329	MESH:C537329	Shprintzen omphalocele syndrome	CTD_diseases	4
MESH:C537330	MESH:C537330	Shwachman syndrome	CTD_diseases	4
MESH:C537336	MESH:C537336	Silengo Lerone Pelizza syndrome	CTD_diseases	4
MESH:C537340	MESH:C537340	Simpson-Golabi-Behmel syndrome	CTD_diseases	4
MESH:C537341	MESH:C537341	Singh Chhaparwal Dhanda syndrome	CTD_diseases	4
MESH:C537343	MESH:C537343	Singleton Merten syndrome	CTD_diseases	4
MESH:C537345	MESH:C537345	Sitosterolemia	CTD_diseases	4
MESH:C537346	MESH:C537346	Mesangial sclerosis, diffuse	CTD_diseases	4
MESH:C537348	MESH:C537348	Mesomelia-synostoses syndrome	CTD_diseases	4
MESH:C537357	MESH:C537357	Methylenetetrahydrofolate reductase deficiency	CTD_diseases	4
MESH:C537364	MESH:C537364	Jagell Holmgren Hofer syndrome	CTD_diseases	4
MESH:C537365	MESH:C537365	Ichthyosis and male hypogonadism	CTD_diseases	4
MESH:C537370	MESH:C537370	Muller Barth Menger syndrome	CTD_diseases	4
MESH:C537377	MESH:C537377	Multiple pterygium syndrome	CTD_diseases	4
MESH:C537385	MESH:C537385	Muscular dystrophy, congenital, infantile with cataract and hypogonadism	CTD_diseases	4
MESH:C537388	MESH:C537388	Neurofaciodigitorenal syndrome	CTD_diseases	4
MESH:C537398	MESH:C537398	Pili torti developmental delay neurological abnormalities	CTD_diseases	4
MESH:C537399	MESH:C537399	Pili torti onychodysplasia	CTD_diseases	4
MESH:C537400	MESH:C537400	Pilotto syndrome	CTD_diseases	4
MESH:C537402	MESH:C537402	Pinheiro Freire-Maia Miranda syndrome	CTD_diseases	4
MESH:C537409	MESH:C537409	Bruton type agammaglobulinemia	CTD_diseases	4
MESH:C537412	MESH:C537412	Burnett Schwartz Berberian syndrome	CTD_diseases	4
MESH:C537413	MESH:C537413	Burning mouth syndrome- Type 3	CTD_diseases	4
MESH:C537415	MESH:C537415	Buschke-Ollendorff syndrome	CTD_diseases	4
MESH:C537417	MESH:C537417	Butyrylcholinesterase deficiency	CTD_diseases	4
MESH:C537424	MESH:C537424	Arachnodactyly ataxia cataract aminoaciduria mental retardation	CTD_diseases	4
MESH:C537425	MESH:C537425	Glutamate formiminotransferase deficiency	CTD_diseases	4
MESH:C537436	MESH:C537436	Aromatase deficiency	CTD_diseases	4
MESH:C537442	MESH:C537442	Arthrogryposis epileptic seizures migrational brain disorder	CTD_diseases	4
MESH:C537443	MESH:C537443	Meningioma, familial	CTD_diseases	4
MESH:C537444	MESH:C537444	Mental retardation Mietens Weber type	CTD_diseases	4
MESH:C537451	MESH:C537451	MEHMO syndrome	CTD_diseases	4
MESH:C537452	MESH:C537452	Mental retardation, keratoconus, febrile seizures, and sinoatrial block	CTD_diseases	4
MESH:C537457	MESH:C537457	Mental retardation-hypotonic facies syndrome, x-linked, 1	CTD_diseases	4
MESH:C537462	MESH:C537462	Microphthalmia and mental deficiency	CTD_diseases	4
MESH:C537463	MESH:C537463	Microphthalmia associated with colobomatous cyst	CTD_diseases	4
MESH:C537465	MESH:C537465	Microphthalmia, syndromic 2	CTD_diseases	4
MESH:C537466	MESH:C537466	Microphthalmia, syndromic 7	CTD_diseases	4
MESH:C537468	MESH:C537468	Microspherophakia with hernia	CTD_diseases	4
MESH:C537473	MESH:C537473	Milner Khallouf Gibson syndrome	CTD_diseases	4
MESH:C537475	MESH:C537475	Mitochondrial complex I deficiency	CTD_diseases	4
MESH:C537476	MESH:C537476	Mitochondrial myopathy with lactic acidosis	CTD_diseases	4
MESH:C537478	MESH:C537478	Mitral valve prolapse, familial, X-linked	CTD_diseases	4
MESH:C537487	MESH:C537487	Steatocystoma multiplex with natal teeth	CTD_diseases	4
MESH:C537489	MESH:C537489	Sternal cleft	CTD_diseases	4
MESH:C537496	MESH:C537496	Stoelinga de Koomen Davis syndrome	CTD_diseases	4
MESH:C537498	MESH:C537498	Stoll Levy Francfort syndrome	CTD_diseases	4
MESH:C537503	MESH:C537503	Subcutaneous panniculitis-like T-cell lymphoma	CTD_diseases	4
MESH:C537506	MESH:C537506	Kozlowski Brown Hardwick syndrome	CTD_diseases	4
MESH:C537509	MESH:C537509	Kozlowski Rafinski Klicharska syndrome	CTD_diseases	4
MESH:C537511	MESH:C537511	Piussan Lenaerts Mathieu syndrome	CTD_diseases	4
MESH:C537518	MESH:C537518	Podder-Tolmie syndrome	CTD_diseases	4
MESH:C537519	MESH:C537519	Schwartz-Lelek syndrome	CTD_diseases	4
MESH:C537521	MESH:C537521	Scleroatonic muscular dystrophy	CTD_diseases	4
MESH:C537524	MESH:C537524	Sclerosing lymphocytic lobulitis	CTD_diseases	4
MESH:C537525	MESH:C537525	Sclerosteosis	CTD_diseases	4
MESH:C537526	MESH:C537526	Sclerotylosis	CTD_diseases	4
MESH:C537528	MESH:C537528	Scott Bryant Graham syndrome	CTD_diseases	4
MESH:C537529	MESH:C537529	Seaver Cassidy syndrome	CTD_diseases	4
MESH:C537530	MESH:C537530	Sebaceous gland hyperplasia, familial presenile	CTD_diseases	4
MESH:C537532	MESH:C537532	Seckel like syndrome type Buebel	CTD_diseases	4
MESH:C537536	MESH:C537536	Seemanova Lesny syndrome	CTD_diseases	4
MESH:C537539	MESH:C537539	Microcephaly microcornea syndrome Seemanova type	CTD_diseases	4
MESH:C537540	MESH:C537540	Microcephaly seizures genital hypoplasia	CTD_diseases	4
MESH:C537544	MESH:C537544	Microcephaly seizures mental retardation heart disorders	CTD_diseases	4
MESH:C537547	MESH:C537547	Microcephaly, corpus callosum dysgenesis and cleft lip-palate	CTD_diseases	4
MESH:C537552	MESH:C537552	Microcornea, glaucoma, and absent frontal sinuses	CTD_diseases	4
MESH:C537553	MESH:C537553	Microdontia hypodontia short stature	CTD_diseases	4
MESH:C537558	MESH:C537558	Osteogenesis imperfecta congenita, microcephaly, and cataracts	CTD_diseases	4
MESH:C537560	MESH:C537560	Jacobs syndrome	CTD_diseases	4
MESH:C537561	MESH:C537561	Jaffer Beighton syndrome	CTD_diseases	4
MESH:C537562	MESH:C537562	Jamaican vomiting sickness	CTD_diseases	4
MESH:C537565	MESH:C537565	Jarcho-Levin syndrome	CTD_diseases	4
MESH:C537569	MESH:C537569	Jequier Kozlowski skeletal dysplasia	CTD_diseases	4
MESH:C537572	MESH:C537572	Jeune syndrome situs inversus	CTD_diseases	4
MESH:C537573	MESH:C537573	Methylmalonyl-Coenzyme A mutase deficiency	CTD_diseases	4
MESH:C537574	MESH:C537574	Meyenburg-Altherr-Uehlinger syndrome	CTD_diseases	4
MESH:C537576	MESH:C537576	Michels Caskey syndrome	CTD_diseases	4
MESH:C537579	MESH:C537579	Sener syndrome	CTD_diseases	4
MESH:C537584	MESH:C537584	Seow Najjar syndrome	CTD_diseases	4
MESH:C537587	MESH:C537587	Sertoli cell-only syndrome, Y-linked	CTD_diseases	4
MESH:C537595	MESH:C537595	Sharma Kapoor Ramji syndrome	CTD_diseases	4
MESH:C537609	MESH:C537609	Rhizomelic dysplasia Patterson Lowry type	CTD_diseases	4
MESH:C537610	MESH:C537610	Rhizomelic dysplasia, scoliosis, and retinitis pigmentosa	CTD_diseases	4
MESH:C537611	MESH:C537611	Rhizomelic syndrome	CTD_diseases	4
MESH:C537614	MESH:C537614	Kozlowski Warren Fisher syndrome	CTD_diseases	4
MESH:C537615	MESH:C537615	Kozlowski-Krajewska syndrome	CTD_diseases	4
MESH:C537616	MESH:C537616	Krasnow Qazi syndrome	CTD_diseases	4
MESH:C537617	MESH:C537617	Krause-Kivlin syndrome	CTD_diseases	4
MESH:C537619	MESH:C537619	Krieble Bixler syndrome	CTD_diseases	4
MESH:C537621	MESH:C537621	Grubben de Cock Borghgraef syndrome	CTD_diseases	4
MESH:C537622	MESH:C537622	Guanidinoacetate methyltransferase deficiency	CTD_diseases	4
MESH:C537625	MESH:C537625	Gurrieri Sammito Bellussi syndrome	CTD_diseases	4
MESH:C537628	MESH:C537628	Hair defect with photosensitivity and mental retardation	CTD_diseases	4
MESH:C537632	MESH:C537632	Bixler Christian Gorlin syndrome	CTD_diseases	4
MESH:C537633	MESH:C537633	Bjornstad syndrome	CTD_diseases	4
MESH:C537635	MESH:C537635	Partial Trisomy 3q Syndrome	CTD_diseases	4
MESH:C537636	MESH:C537636	Ring chromosome 4 syndrome	CTD_diseases	4
MESH:C537639	MESH:C537639	Chromosome 4q- Syndrome	CTD_diseases	4
MESH:C537641	MESH:C537641	Chromosome 4, 4q Terminal Deletion Syndrome	CTD_diseases	4
MESH:C537643	MESH:C537643	Duplication 4p Syndrome	CTD_diseases	4
MESH:C537659	MESH:C537659	Basan syndrome	CTD_diseases	4
MESH:C537660	MESH:C537660	Basaran Yilmaz syndrome	CTD_diseases	4
MESH:C537661	MESH:C537661	Bassoe syndrome	CTD_diseases	4
MESH:C537662	MESH:C537662	Battaglia Neri syndrome	CTD_diseases	4
MESH:C537663	MESH:C537663	Bazex-Dupre-Christol syndrome	CTD_diseases	4
MESH:C537664	MESH:C537664	Bazopoulou Kyrkanidou syndrome	CTD_diseases	4
MESH:C537676	MESH:C537676	Gay Feinmesser Cohen syndrome	CTD_diseases	4
MESH:C537680	MESH:C537680	Genee-Wiedemann syndrome	CTD_diseases	4
MESH:C537685	MESH:C537685	Genu valgum, st Helena familial	CTD_diseases	4
MESH:C537688	MESH:C537688	Joubert syndrome 5	CTD_diseases	4
MESH:C537689	MESH:C537689	Joubert syndrome 6	CTD_diseases	4
MESH:C537692	MESH:C537692	Judge Misch Wright syndrome	CTD_diseases	4
MESH:C537694	MESH:C537694	Jung Wolff Back Stahl syndrome	CTD_diseases	4
MESH:C537696	MESH:C537696	Juvenile gout	CTD_diseases	4
MESH:C537701	MESH:C537701	Hyperostosis corticalis deformans juvenilis	CTD_diseases	4
MESH:C537702	MESH:C537702	Juvenile polyposis syndrome	CTD_diseases	4
MESH:C537703	MESH:C537703	Juvenile systemic scleroderma	CTD_diseases	4
MESH:C537706	MESH:C537706	Kaler Garrity Stern syndrome	CTD_diseases	4
MESH:C537707	MESH:C537707	Kallikrein hypertension	CTD_diseases	4
MESH:C537710	MESH:C537710	Lymphedema distichiasis syndrome	CTD_diseases	4
MESH:C537711	MESH:C537711	Lymphedema, microcephaly and chorioretinopathy syndrome	CTD_diseases	4
MESH:C537718	MESH:C537718	Volcke Soekarman syndrome	CTD_diseases	4
MESH:C537722	MESH:C537722	Macrogyria, pseudobulbar palsy and mental retardation	CTD_diseases	4
MESH:C537726	MESH:C537726	Lutz Richner Landolt syndrome	CTD_diseases	4
MESH:C537733	MESH:C537733	Oculodentoosseous dysplasia recessive	CTD_diseases	4
MESH:C537736	MESH:C537736	Oculomaxillofacial dysostosis	CTD_diseases	4
MESH:C537738	MESH:C537738	Oculopalatoskeletal syndrome	CTD_diseases	4
MESH:C537739	MESH:C537739	Oculorenocerebellar syndrome	CTD_diseases	4
MESH:C537741	MESH:C537741	Odontomicronychial dysplasia	CTD_diseases	4
MESH:C537746	MESH:C537746	Omodysplasia type 1	CTD_diseases	4
MESH:C537748	MESH:C537748	Omphalocele exstrophy imperforate anus	CTD_diseases	4
MESH:C537749	MESH:C537749	Onat syndrome	CTD_diseases	4
MESH:C537752	MESH:C537752	Onychotrichodysplasia and neutropenia	CTD_diseases	4
MESH:C537754	MESH:C537754	Renal dysplasia - limb defects syndrome	CTD_diseases	4
MESH:C537756	MESH:C537756	Renal hepatic pancreatic dysplasia Dandy Walker cyst	CTD_diseases	4
MESH:C537763	MESH:C537763	Chromosome 6 ring syndrome	CTD_diseases	4
MESH:C537773	MESH:C537773	Ansell Bywaters Elderking syndrome	CTD_diseases	4
MESH:C537774	MESH:C537774	Anterior polar cataract 2	CTD_diseases	4
MESH:C537775	MESH:C537775	Anterior segment mesenchymal dysgenesis	CTD_diseases	4
MESH:C537777	MESH:C537777	Anti-plasmin deficiency, congenital	CTD_diseases	4
MESH:C537779	MESH:C537779	Antithrombin deficiency type 2	CTD_diseases	4
MESH:C537786	MESH:C537786	Aphakia, congenital primary	CTD_diseases	4
MESH:C537787	MESH:C537787	Aphalangia syndactyly microcephaly	CTD_diseases	4
MESH:C537789	MESH:C537789	Axenfeld-Rieger anomaly with cardiac defects and sensorineural hearing loss	CTD_diseases	4
MESH:C537790	MESH:C537790	Axial mesodermal dysplasia spectrum	CTD_diseases	4
MESH:C537796	MESH:C537796	Bagatelle Cassidy syndrome	CTD_diseases	4
MESH:C537797	MESH:C537797	Bahemuka Brown syndrome	CTD_diseases	4
MESH:C537798	MESH:C537798	Fetal trimethadione syndrome	CTD_diseases	4
MESH:C537803	MESH:C537803	Ghose Sachdev Kumar syndrome	CTD_diseases	4
MESH:C537804	MESH:C537804	Chromosome 10q duplication syndrome	CTD_diseases	4
MESH:C537810	MESH:C537810	6q+ Syndrome, Partial	CTD_diseases	4
MESH:C537813	MESH:C537813	Chromosome 7 ring syndrome	CTD_diseases	4
MESH:C537818	MESH:C537818	7p2 monosomy syndrome	CTD_diseases	4
MESH:C537830	MESH:C537830	Macrosomia with lethal microphthalmia	CTD_diseases	4
MESH:C537836	MESH:C537836	Macules hereditary congenital hypopigmented and hyperpigmented	CTD_diseases	4
MESH:C537840	MESH:C537840	Mal de debarquement	CTD_diseases	4
MESH:C537841	MESH:C537841	NADH cytochrome B5 reductase deficiency	CTD_diseases	4
MESH:C537844	MESH:C537844	Nonseminomatous germ cell tumor	CTD_diseases	4
MESH:C537858	MESH:C537858	O'Donnell Pappas syndrome	CTD_diseases	4
MESH:C537862	MESH:C537862	Ochronosis, hereditary	CTD_diseases	4
MESH:C537865	MESH:C537865	Oculoauriculofrontonasal syndrome	CTD_diseases	4
MESH:C537866	MESH:C537866	Oculocerebral hypopigmentation syndrome type Preus	CTD_diseases	4
MESH:C537878	MESH:C537878	Lateral meningocele syndrome	CTD_diseases	4
MESH:C537879	MESH:C537879	Lateral semicircular canal malformation, familial, with external and middle ear abnormalities	CTD_diseases	4
MESH:C537884	MESH:C537884	Peters anomaly	CTD_diseases	4
MESH:C537885	MESH:C537885	Peters anomaly with cataract	CTD_diseases	4
MESH:C537886	MESH:C537886	Petty Laxova Wiedemann syndrome	CTD_diseases	4
MESH:C537887	MESH:C537887	Pfeiffer Kapferer syndrome	CTD_diseases	4
MESH:C537888	MESH:C537888	Pfeiffer Mayer syndrome	CTD_diseases	4
MESH:C537891	MESH:C537891	Pfeiffer Tietze Welte syndrome	CTD_diseases	4
MESH:C537892	MESH:C537892	PHACE association	CTD_diseases	4
MESH:C537893	MESH:C537893	Phacomatosis pigmentokeratotica	CTD_diseases	4
MESH:C537895	MESH:C537895	Phenol sulfotransferase deficiency	CTD_diseases	4
MESH:C537901	MESH:C537901	Bamforth syndrome	CTD_diseases	4
MESH:C537902	MESH:C537902	Bangstad syndrome	CTD_diseases	4
MESH:C537903	MESH:C537903	Banti's syndrome	CTD_diseases	4
MESH:C537905	MESH:C537905	Baraitser Brett Piesowicz syndrome	CTD_diseases	4
MESH:C537907	MESH:C537907	Barakat syndrome	CTD_diseases	4
MESH:C537915	MESH:C537915	Chondrodysplasia, Grebe type	CTD_diseases	4
MESH:C537917	MESH:C537917	Femur bifid with monodactylous ectrodactyly	CTD_diseases	4
MESH:C537918	MESH:C537918	Femur fibula ulna syndrome	CTD_diseases	4
MESH:C537921	MESH:C537921	Fetal akinesia syndrome, X-linked	CTD_diseases	4
MESH:C537922	MESH:C537922	Fetal hydantoin syndrome	CTD_diseases	4
MESH:C537927	MESH:C537927	Fibrocartilaginous embolism	CTD_diseases	4
MESH:C537933	MESH:C537933	Fine-Lubinsky syndrome	CTD_diseases	4
MESH:C537934	MESH:C537934	Finnish lethal neonatal metabolic syndrome	CTD_diseases	4
MESH:C537936	MESH:C537936	Fitz-Hugh-Curtis syndrome	CTD_diseases	4
MESH:C537955	MESH:C537955	Cerulean cataract	CTD_diseases	4
MESH:C537959	MESH:C537959	CAHMR syndrome	CTD_diseases	4
MESH:C537960	MESH:C537960	Calabro syndrome	CTD_diseases	4
MESH:C537961	MESH:C537961	Calcifying Epithelial Odontogenic Tumor	CTD_diseases	4
MESH:C537963	MESH:C537963	Calvarial hyperostosis	CTD_diseases	4
MESH:C537974	MESH:C537974	Camptodactyly, fibrous tissue hyperplasia, and skeletal dysplasia	CTD_diseases	4
MESH:C537975	MESH:C537975	CATSHL syndrome	CTD_diseases	4
MESH:C537981	MESH:C537981	Cantalamessa Baldini Ambrosi syndrome	CTD_diseases	4
MESH:C537997	MESH:C537997	Dysplasia epiphysealis hemimelica	CTD_diseases	4
MESH:C538010	MESH:C538010	Eagle syndrome	CTD_diseases	4
MESH:C538012	MESH:C538012	Meier-Gorlin syndrome	CTD_diseases	4
MESH:C538036	MESH:C538036	Partial Duplication 15q Syndrome	CTD_diseases	4
MESH:C538051	MESH:C538051	Adrenomyodystrophy	CTD_diseases	4
MESH:C538052	MESH:C538052	Propping Zerres syndrome	CTD_diseases	4
MESH:C538055	MESH:C538055	Agammaglobulinemia, microcephaly, and severe dermatitis	CTD_diseases	4
MESH:C538057	MESH:C538057	Agammaglobulinemia, X-linked, type 2	CTD_diseases	4
MESH:C538061	MESH:C538061	Friedreich ataxia congenital glaucoma	CTD_diseases	4
MESH:C538063	MESH:C538063	Fronto-facio-nasal dysplasia	CTD_diseases	4
MESH:C538069	MESH:C538069	Fryns Hofkens Fabry syndrome	CTD_diseases	4
MESH:C538072	MESH:C538072	Cervical ribs sprengel anomaly anal atresia urethral obstruction	CTD_diseases	4
MESH:C538075	MESH:C538075	Chang Davidson Carlson syndrome	CTD_diseases	4
MESH:C538079	MESH:C538079	Charcot-Marie-Tooth disease with ptosis and parkinsonism	CTD_diseases	4
MESH:C538087	MESH:C538087	Distal Trisomy 10q Syndrome	CTD_diseases	4
MESH:C538088	MESH:C538088	Oculocerebrocutaneous syndrome	CTD_diseases	4
MESH:C538090	MESH:C538090	Ovarian epithelial cancer	CTD_diseases	4
MESH:C538098	MESH:C538098	Familial Paget's disease of bone	CTD_diseases	4
MESH:C538102	MESH:C538102	Palant cleft palate syndrome	CTD_diseases	4
MESH:C538104	MESH:C538104	Pallidopyramidal syndrome	CTD_diseases	4
MESH:C538105	MESH:C538105	Pallister Killian syndrome	CTD_diseases	4
MESH:C538106	MESH:C538106	Pallister W syndrome	CTD_diseases	4
MESH:C538114	MESH:C538114	Hersh Podruch Weisskopk syndrome	CTD_diseases	4
MESH:C538115	MESH:C538115	Heterochromia iridis	CTD_diseases	4
MESH:C538116	MESH:C538116	Heterotaxy, visceral, X-linked	CTD_diseases	4
MESH:C538125	MESH:C538125	Kuster Majewski Hammerstein syndrome	CTD_diseases	4
MESH:C538128	MESH:C538128	Kyphomelic dysplasia	CTD_diseases	4
MESH:C538130	MESH:C538130	Kyrle disease	CTD_diseases	4
MESH:C538135	MESH:C538135	Ladda Zonana Ramer syndrome	CTD_diseases	4
MESH:C538137	MESH:C538137	Hyperferritinemia, hereditary, with congenital cataracts	CTD_diseases	4
MESH:C538147	MESH:C538147	Symmastia	CTD_diseases	4
MESH:C538152	MESH:C538152	Filippi syndrome	CTD_diseases	4
MESH:C538158	MESH:C538158	McDonough syndrome	CTD_diseases	4
MESH:C538159	MESH:C538159	McKusick Kaufman syndrome	CTD_diseases	4
MESH:C538160	MESH:C538160	McPherson Clemens syndrome	CTD_diseases	4
MESH:C538161	MESH:C538161	McPherson Robertson Cammarano syndrome	CTD_diseases	4
MESH:C538164	MESH:C538164	Bowen syndrome	CTD_diseases	4
MESH:C538165	MESH:C538165	Achromatopsia incomplete, X-linked	CTD_diseases	4
MESH:C538169	MESH:C538169	Acitretin embryopathy	CTD_diseases	4
MESH:C538170	MESH:C538170	Ackerman syndrome	CTD_diseases	4
MESH:C538172	MESH:C538172	Acquired amegakaryocytic thrombocytopenia	CTD_diseases	4
MESH:C538176	MESH:C538176	Acquired pure megakaryocytic aplasia	CTD_diseases	4
MESH:C538191	MESH:C538191	Fumaric aciduria	CTD_diseases	4
MESH:C538209	MESH:C538209	Dementia, familial Danish	CTD_diseases	4
MESH:C538212	MESH:C538212	Dent disease 1	CTD_diseases	4
MESH:C538217	MESH:C538217	Der Kaloustian Mcintosh Silver syndrome	CTD_diseases	4
MESH:C538224	MESH:C538224	Adams Nance syndrome	CTD_diseases	4
MESH:C538225	MESH:C538225	Adams Oliver syndrome	CTD_diseases	4
MESH:C538228	MESH:C538228	Adenine phosphoribosyltransferase deficiency	CTD_diseases	4
MESH:C538245	MESH:C538245	Ameloonychohypohidrotic syndrome	CTD_diseases	4
MESH:C538269	MESH:C538269	Aughton syndrome	CTD_diseases	4
MESH:C538271	MESH:C538271	Auriculoosteodysplasia	CTD_diseases	4
MESH:C538273	MESH:C538273	Autoimmune enteropathy	CTD_diseases	4
MESH:C538274	MESH:C538274	Autoimmune oophoritis	CTD_diseases	4
MESH:C538275	MESH:C538275	Autoimmune polyendocrinopathy syndrome, type 1	CTD_diseases	4
MESH:C538278	MESH:C538278	Preaxial deficiency, postaxial polydactyly and hypospadias	CTD_diseases	4
MESH:C538279	MESH:C538279	Catamenial pneumothorax	CTD_diseases	4
MESH:C538280	MESH:C538280	Cataract and cardiomyopathy	CTD_diseases	4
MESH:C538281	MESH:C538281	Cataract and congenital ichthyosis	CTD_diseases	4
MESH:C538282	MESH:C538282	Cataract anterior polar dominant	CTD_diseases	4
MESH:C538283	MESH:C538283	Cataract ataxia deafness	CTD_diseases	4
MESH:C538284	MESH:C538284	Cataract congenital dominant non nuclear	CTD_diseases	4
MESH:C538285	MESH:C538285	Cataract congenital Volkmann type	CTD_diseases	4
MESH:C538286	MESH:C538286	Cataract Hutterite type	CTD_diseases	4
MESH:C538288	MESH:C538288	10p Deletion Syndrome (Partial)	CTD_diseases	4
MESH:C538309	MESH:C538309	Chromosome 18p deletion syndrome	CTD_diseases	4
MESH:C538322	MESH:C538322	Histiocytosis with joint contractures and sensorineural deafness	CTD_diseases	4
MESH:C538323	MESH:C538323	Hittner Hirsch Kreh syndrome	CTD_diseases	4
MESH:C538326	MESH:C538326	Hodgkin disease, X-linked pseudoautosomal	CTD_diseases	4
MESH:C538333	MESH:C538333	Nail dysplasia, isolated congenital	CTD_diseases	4
MESH:C538336	MESH:C538336	Nance-Horan syndrome	CTD_diseases	4
MESH:C538337	MESH:C538337	Nasodigitoacoustic syndrome	CTD_diseases	4
MESH:C538338	MESH:C538338	Nasopalpebral lipoma coloboma syndrome	CTD_diseases	4
MESH:C538340	MESH:C538340	Nasopharyngeal teratoma with Dandy Walker diaphragmatic hernia	CTD_diseases	4
MESH:C538342	MESH:C538342	Nathalie syndrome	CTD_diseases	4
MESH:C538346	MESH:C538346	Naxos disease	CTD_diseases	4
MESH:C538347	MESH:C538347	Negative rheumatoid factor polyarthritis	CTD_diseases	4
MESH:C538356	MESH:C538356	Potocki-Shaffer syndrome	CTD_diseases	4
MESH:C538357	MESH:C538357	Powell Chandra Saal syndrome	CTD_diseases	4
MESH:C538362	MESH:C538362	Reticuloendotheliosis, X-linked	CTD_diseases	4
MESH:C538364	MESH:C538364	MacKay Shek Carr syndrome	CTD_diseases	4
MESH:C538371	MESH:C538371	Revesz Debuse syndrome	CTD_diseases	4
MESH:C538377	MESH:C538377	Hyperkeratosis lenticularis perstans	CTD_diseases	4
MESH:C538380	MESH:C538380	HHH syndrome	CTD_diseases	4
MESH:C538381	MESH:C538381	Hyperostosis-hyperphosphatemia syndrome	CTD_diseases	4
MESH:C538388	MESH:C538388	Hypertrichosis congenital generalized X-linked	CTD_diseases	4
MESH:C538406	MESH:C538406	Canaliculitis	CTD_diseases	4
MESH:C538407	MESH:C538407	Acute rheumatism	CTD_diseases	4
MESH:C538416	MESH:C538416	Chondrodysplasia punctata 2, X-linked dominant	CTD_diseases	4
MESH:C538421	MESH:C538421	Neurodegeneration with brain iron accumulation (NBIA)	CTD_diseases	4
MESH:C538429	MESH:C538429	Hypoadrenocorticism, familial	CTD_diseases	4
MESH:C538472	MESH:C538472	Mesoectodermal dysplasia	CTD_diseases	4
MESH:C538539	MESH:C538539	Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells	CTD_diseases	4
MESH:C538542	MESH:C538542	Sexual precocity	CTD_diseases	4
MESH:C538613	MESH:C538613	Panhypopituitarism X-linked	CTD_diseases	4
MESH:C538641	MESH:C538641	Congenital facial linear porokeratosis	CTD_diseases	4
MESH:C540694	MESH:C540694	Thrombophilia, hereditary	CTD_diseases	4
MESH:C541083	MESH:C541083	Non-alcoholic Fatty Liver Disease	CTD_diseases	4
MESH:C543092	MESH:C543092	Lubinsky syndrome	CTD_diseases	4
MESH:C543241	MESH:C543241	Cardiomyopathy, fatal fetal, due to myocardial calcification	CTD_diseases	4
MESH:C543758	MESH:C543758	Juvenile linear scleroderma	CTD_diseases	4
MESH:C543759	MESH:C543759	Juvenile-onset scleroderma	CTD_diseases	4
MESH:C548028	MESH:C548028	Inherited Peripheral Neuropathy	CTD_diseases	4
MESH:C548030	MESH:C548030	Knobloch Syndrome Type II	CTD_diseases	4
MESH:C548031	MESH:C548031	Knobloch Syndrome Type III	CTD_diseases	4
MESH:C548071	MESH:C548071	Megarbane Jalkh Syndrome	CTD_diseases	4
MESH:C548080	MESH:C548080	Neuroferritinopathy	CTD_diseases	4
MESH:C548086	MESH:C548086	Stargardt Macular Degeneration Absent or Hypoplastic Corpus Callosum Mental Retardation and Dysmorph	CTD_diseases	4
MESH:C553654	MESH:C553654	Congenital Deficiency of Pulmonary Surfactant Protein B	CTD_diseases	4
MESH:C557818	MESH:C557818	Orofaciodigital syndrome 9	CTD_diseases	4
MESH:C557830	MESH:C557830	Duplication 15q11-q13 Syndrome	CTD_diseases	4
MESH:C562379	MESH:C562379	Dermatosis Papulosa Nigra	CTD_diseases	4
MESH:C562386	MESH:C562386	Hypertension, Essential	CTD_diseases	4
MESH:C562388	MESH:C562388	Bicuspid Aortic Valve	CTD_diseases	4
MESH:C562397	MESH:C562397	Hymen, Imperforate	CTD_diseases	4
MESH:C562398	MESH:C562398	Madelung Deformity	CTD_diseases	4
MESH:C562401	MESH:C562401	Pseudopapilledema	CTD_diseases	4
MESH:C562406	MESH:C562406	Bladder Diverticulum	CTD_diseases	4
MESH:C562419	MESH:C562419	Blepharophimosis, Ptosis, and Epicanthus Inversus	CTD_diseases	4
MESH:C562438	MESH:C562438	Hemangiomatosis, Cutaneous, with Associated Features	CTD_diseases	4
MESH:C562443	MESH:C562443	Weaver-Like Syndrome	CTD_diseases	4
MESH:C562446	MESH:C562446	Russell-Silver Syndrome, X-Linked	CTD_diseases	4
MESH:C562447	MESH:C562447	Spondyloepiphyseal Dysplasia Tarda, X-Linked	CTD_diseases	4
MESH:C562456	MESH:C562456	Volvulus Of Midgut	CTD_diseases	4
MESH:C562461	MESH:C562461	Annular Erythema	CTD_diseases	4
MESH:C562465	MESH:C562465	Phobia, Specific	CTD_diseases	4
MESH:D012888	MESH:D012888	Skull Neoplasms	CTD_diseases	4
MESH:D012899	MESH:D012899	Smallpox	CTD_diseases	4
MESH:D012909	MESH:D012909	Snake Bites	CTD_diseases	4
MESH:D012912	MESH:D012912	Sneezing	CTD_diseases	4
MESH:D013117	MESH:D013117	Spinal Cord Compression	CTD_diseases	4
MESH:D013120	MESH:D013120	Spinal Cord Neoplasms	CTD_diseases	4
MESH:D013121	MESH:D013121	Spinal Curvatures	CTD_diseases	4
MESH:D013125	MESH:D013125	Spinal Neoplasms	CTD_diseases	4
MESH:D013128	MESH:D013128	Spinal Osteophytosis	CTD_diseases	4
MESH:D013130	MESH:D013130	Spinal Stenosis	CTD_diseases	4
MESH:D013132	MESH:D013132	Spinocerebellar Degenerations	CTD_diseases	4
MESH:D013163	MESH:D013163	Splenomegaly	CTD_diseases	4
MESH:D013166	MESH:D013166	Spondylitis	CTD_diseases	4
MESH:D013167	MESH:D013167	Spondylitis, Ankylosing	CTD_diseases	4
MESH:D013202	MESH:D013202	Staphylococcal Food Poisoning	CTD_diseases	4
MESH:D013203	MESH:D013203	Staphylococcal Infections	CTD_diseases	4
MESH:D013217	MESH:D013217	Starvation	CTD_diseases	4
MESH:D013262	MESH:D013262	Stevens-Johnson Syndrome	CTD_diseases	4
MESH:D013271	MESH:D013271	Gastric Dilatation	CTD_diseases	4
MESH:D013273	MESH:D013273	Diverticulum, Stomach	CTD_diseases	4
MESH:D013274	MESH:D013274	Stomach Neoplasms	CTD_diseases	4
MESH:D013277	MESH:D013277	Stomach Volvulus	CTD_diseases	4
MESH:D013281	MESH:D013281	Stomatitis, Aphthous	CTD_diseases	4
MESH:D013282	MESH:D013282	Stomatitis, Denture	CTD_diseases	4
MESH:D013283	MESH:D013283	Stomatitis, Herpetic	CTD_diseases	4
MESH:D013285	MESH:D013285	Strabismus	CTD_diseases	4
MESH:D013290	MESH:D013290	Streptococcal Infections	CTD_diseases	4
MESH:D013313	MESH:D013313	Stress Disorders, Post-Traumatic	CTD_diseases	4
MESH:D013341	MESH:D013341	Sturge-Weber Syndrome	CTD_diseases	4
MESH:D013352	MESH:D013352	Subcutaneous Emphysema	CTD_diseases	4
MESH:D013353	MESH:D013353	Subdural Effusion	CTD_diseases	4
MESH:D013354	MESH:D013354	Empyema, Subdural	CTD_diseases	4
MESH:D013364	MESH:D013364	Submandibular Gland Diseases	CTD_diseases	4
MESH:D013474	MESH:D013474	Sunstroke	CTD_diseases	4
MESH:D013494	MESH:D013494	Supranuclear Palsy, Progressive	CTD_diseases	4
MESH:D013529	MESH:D013529	Surgical Wound Dehiscence	CTD_diseases	4
MESH:D013530	MESH:D013530	Surgical Wound Infection	CTD_diseases	4
MESH:D013544	MESH:D013544	Sweat Gland Neoplasms	CTD_diseases	4
MESH:D013577	MESH:D013577	Syndrome	CTD_diseases	4
MESH:D013580	MESH:D013580	Synostosis	CTD_diseases	4
MESH:D013581	MESH:D013581	Synovial Cyst	CTD_diseases	4
MESH:D013586	MESH:D013586	Synovitis, Pigmented Villonodular	CTD_diseases	4
MESH:D013589	MESH:D013589	Syphilis, Cardiovascular	CTD_diseases	4
MESH:D013595	MESH:D013595	Syringomyelia	CTD_diseases	4
MESH:D013606	MESH:D013606	Tabes Dorsalis	CTD_diseases	4
MESH:D013610	MESH:D013610	Tachycardia	CTD_diseases	4
MESH:D013622	MESH:D013622	Taeniasis	CTD_diseases	4
MESH:D013625	MESH:D013625	Takayasu Arteritis	CTD_diseases	4
MESH:D013683	MESH:D013683	Telangiectasia, Hereditary Hemorrhagic	CTD_diseases	4
MESH:D013700	MESH:D013700	Giant Cell Arteritis	CTD_diseases	4
MESH:D013724	MESH:D013724	Teratoma	CTD_diseases	4
MESH:D013734	MESH:D013734	Androgen-Insensitivity Syndrome	CTD_diseases	4
MESH:D013736	MESH:D013736	Testicular Neoplasms	CTD_diseases	4
MESH:D013786	MESH:D013786	Thalamic Diseases	CTD_diseases	4
MESH:D013789	MESH:D013789	Thalassemia	CTD_diseases	4
MESH:D013851	MESH:D013851	Thinness	CTD_diseases	4
MESH:D013915	MESH:D013915	Thrombasthenia	CTD_diseases	4
MESH:D013919	MESH:D013919	Thromboangiitis Obliterans	CTD_diseases	4
MESH:D013920	MESH:D013920	Thrombocythemia, Essential	CTD_diseases	4
MESH:D013921	MESH:D013921	Thrombocytopenia	CTD_diseases	4
MESH:D013922	MESH:D013922	Thrombocytosis	CTD_diseases	4
MESH:D013923	MESH:D013923	Thromboembolism	CTD_diseases	4
MESH:D013927	MESH:D013927	Thrombosis	CTD_diseases	4
MESH:D013945	MESH:D013945	Thymoma	CTD_diseases	4
MESH:D013955	MESH:D013955	Thyroglossal Cyst	CTD_diseases	4
MESH:D013968	MESH:D013968	Thyroiditis, Subacute	CTD_diseases	4
MESH:D013969	MESH:D013969	Thyroiditis, Suppurative	CTD_diseases	4
MESH:D013991	MESH:D013991	Tietze's Syndrome	CTD_diseases	4
MESH:D014006	MESH:D014006	Tinea Capitis	CTD_diseases	4
MESH:D014009	MESH:D014009	Onychomycosis	CTD_diseases	4
MESH:D014062	MESH:D014062	Tongue Neoplasms	CTD_diseases	4
MESH:D014063	MESH:D014063	Tongue, Fissured	CTD_diseases	4
MESH:D014064	MESH:D014064	Tongue, Hairy	CTD_diseases	4
MESH:D014072	MESH:D014072	Tooth Abrasion	CTD_diseases	4
MESH:D014077	MESH:D014077	Tooth Erosion	CTD_diseases	4
MESH:D014082	MESH:D014082	Tooth Fractures	CTD_diseases	4
MESH:D014084	MESH:D014084	Tooth Avulsion	CTD_diseases	4
MESH:D014085	MESH:D014085	Tooth Migration	CTD_diseases	4
MESH:D014086	MESH:D014086	Tooth Mobility	CTD_diseases	4
MESH:D014120	MESH:D014120	Toxocariasis	CTD_diseases	4
MESH:D014123	MESH:D014123	Toxoplasmosis	CTD_diseases	4
MESH:D014124	MESH:D014124	Toxoplasmosis, Animal	CTD_diseases	4
MESH:D014178	MESH:D014178	Translocation, Genetic	CTD_diseases	4
MESH:D014189	MESH:D014189	Transsexualism	CTD_diseases	4
MESH:D014211	MESH:D014211	Treponemal Infections	CTD_diseases	4
MESH:D014247	MESH:D014247	Trichomonas Vaginitis	CTD_diseases	4
MESH:D014262	MESH:D014262	Tricuspid Valve Insufficiency	CTD_diseases	4
MESH:D014264	MESH:D014264	Tricuspid Valve Stenosis	CTD_diseases	4
MESH:D014277	MESH:D014277	Trigeminal Neuralgia	CTD_diseases	4
MESH:D014328	MESH:D014328	Trophoblastic Neoplasms	CTD_diseases	4
MESH:D014352	MESH:D014352	Trypanosomiasis	CTD_diseases	4
MESH:D014381	MESH:D014381	Tuberculosis, Cardiovascular	CTD_diseases	4
MESH:D014384	MESH:D014384	Tuberculosis, Female Genital	CTD_diseases	4
MESH:D014394	MESH:D014394	Tuberculosis, Osteoarticular	CTD_diseases	4
MESH:D014400	MESH:D014400	Tuberculosis, Splenic	CTD_diseases	4
MESH:D014406	MESH:D014406	Tularemia	CTD_diseases	4
MESH:D014428	MESH:D014428	Twins, Conjoined	CTD_diseases	4
MESH:D014496	MESH:D014496	Urachal Cyst	CTD_diseases	4
MESH:D014515	MESH:D014515	Ureteral Diseases	CTD_diseases	4
MESH:D014522	MESH:D014522	Urethral Diseases	CTD_diseases	4
MESH:D014545	MESH:D014545	Urinary Calculi	CTD_diseases	4
MESH:D014548	MESH:D014548	Urinary Fistula	CTD_diseases	4
MESH:D014555	MESH:D014555	Urination Disorders	CTD_diseases	4
MESH:D014571	MESH:D014571	Urologic Neoplasms	CTD_diseases	4
MESH:D014581	MESH:D014581	Urticaria	CTD_diseases	4
MESH:D014582	MESH:D014582	Urticaria Pigmentosa	CTD_diseases	4
MESH:D014591	MESH:D014591	Uterine Diseases	CTD_diseases	4
MESH:D014592	MESH:D014592	Uterine Hemorrhage	CTD_diseases	4
MESH:D014607	MESH:D014607	Uveomeningoencephalitic Syndrome	CTD_diseases	4
MESH:D014615	MESH:D014615	Vaccinia	CTD_diseases	4
MESH:D014623	MESH:D014623	Vaginal Diseases	CTD_diseases	4
MESH:D014624	MESH:D014624	Vaginal Fistula	CTD_diseases	4
MESH:D014647	MESH:D014647	Varicose Ulcer	CTD_diseases	4
MESH:D014693	MESH:D014693	Ventricular Fibrillation	CTD_diseases	4
MESH:D014717	MESH:D014717	Vertigo	CTD_diseases	4
MESH:D014735	MESH:D014735	Vibrio Infections	CTD_diseases	4
MESH:D014813	MESH:D014813	Vitamin K Deficiency	CTD_diseases	4
MESH:D014839	MESH:D014839	Vomiting	CTD_diseases	4
MESH:D014842	MESH:D014842	von Willebrand Diseases	CTD_diseases	4
MESH:D014845	MESH:D014845	Vulvar Diseases	CTD_diseases	4
MESH:D014849	MESH:D014849	Waardenburg Syndrome	CTD_diseases	4
MESH:D014855	MESH:D014855	Wallerian Degeneration	CTD_diseases	4
MESH:D014860	MESH:D014860	Warts	CTD_diseases	4
MESH:D014884	MESH:D014884	Waterhouse-Friderichsen Syndrome	CTD_diseases	4
MESH:D014890	MESH:D014890	Wegener Granulomatosis	CTD_diseases	4
MESH:D014897	MESH:D014897	Spinal Muscular Atrophies of Childhood	CTD_diseases	4
MESH:D014899	MESH:D014899	Wernicke Encephalopathy	CTD_diseases	4
MESH:D014917	MESH:D014917	Whooping Cough	CTD_diseases	4
MESH:D014929	MESH:D014929	Wolfram Syndrome	CTD_diseases	4
MESH:D014973	MESH:D014973	Xanthomatosis	CTD_diseases	4
MESH:D014987	MESH:D014987	Xerostomia	CTD_diseases	4
MESH:D015043	MESH:D015043	Zollinger-Ellison Syndrome	CTD_diseases	4
MESH:D015160	MESH:D015160	Hydrops Fetalis	CTD_diseases	4
MESH:D015163	MESH:D015163	Superinfection	CTD_diseases	4
MESH:D015208	MESH:D015208	Smoke Inhalation Injury	CTD_diseases	4
MESH:D015212	MESH:D015212	Inflammatory Bowel Diseases	CTD_diseases	4
MESH:D015218	MESH:D015218	Hyperostosis, Sternocostoclavicular	CTD_diseases	4
MESH:D015266	MESH:D015266	Carcinoma, Merkel Cell	CTD_diseases	4
MESH:D015275	MESH:D015275	Tumor Lysis Syndrome	CTD_diseases	4
MESH:D015324	MESH:D015324	Pyruvate Carboxylase Deficiency Disease	CTD_diseases	4
MESH:D015325	MESH:D015325	Pyruvate Dehydrogenase Complex Deficiency Disease	CTD_diseases	4
MESH:D015355	MESH:D015355	Glaucoma, Neovascular	CTD_diseases	4
MESH:D015417	MESH:D015417	Hereditary Sensory and Motor Neuropathy	CTD_diseases	4
MESH:D015418	MESH:D015418	Optic Atrophies, Hereditary	CTD_diseases	4
MESH:D015428	MESH:D015428	Myocardial Reperfusion Injury	CTD_diseases	4
MESH:D015435	MESH:D015435	Panniculitis, Lupus Erythematosus	CTD_diseases	4
MESH:D015499	MESH:D015499	Renal Tubular Transport, Inborn Errors	CTD_diseases	4
MESH:D015518	MESH:D015518	Rett Syndrome	CTD_diseases	4
MESH:D015529	MESH:D015529	Choledochal Cyst	CTD_diseases	4
MESH:D015535	MESH:D015535	Arthritis, Psoriatic	CTD_diseases	4
MESH:D015593	MESH:D015593	Retinal Drusen	CTD_diseases	4
MESH:D015594	MESH:D015594	Optic Disk Drusen	CTD_diseases	4
MESH:D015605	MESH:D015605	Cowpox	CTD_diseases	4
MESH:D015616	MESH:D015616	Histiocytosis, Non-Langerhans-Cell	CTD_diseases	4
MESH:D015746	MESH:D015746	Abdominal Pain	CTD_diseases	4
MESH:D015783	MESH:D015783	Aniridia	CTD_diseases	4
MESH:D015787	MESH:D015787	Erythema Chronicum Migrans	CTD_diseases	4
MESH:D015794	MESH:D015794	Choroideremia	CTD_diseases	4
MESH:D015799	MESH:D015799	Gyrate Atrophy	CTD_diseases	4
MESH:D015811	MESH:D015811	Iris Neoplasms	CTD_diseases	4
MESH:D015812	MESH:D015812	Glaucoma, Angle-Closure	CTD_diseases	4
MESH:D015823	MESH:D015823	Acanthamoeba Keratitis	CTD_diseases	4
MESH:D015829	MESH:D015829	Uveitis, Suppurative	CTD_diseases	4
MESH:D015834	MESH:D015834	Cochlear Diseases	CTD_diseases	4
MESH:D015837	MESH:D015837	Vestibular Diseases	CTD_diseases	4
MESH:D015863	MESH:D015863	Iridocyclitis	CTD_diseases	4
MESH:D015864	MESH:D015864	Panuveitis	CTD_diseases	4
MESH:D015867	MESH:D015867	Uveitis, Intermediate	CTD_diseases	4
MESH:D015882	MESH:D015882	Retinal Necrosis Syndrome, Acute	CTD_diseases	4
MESH:D016063	MESH:D016063	Blood Loss, Surgical	CTD_diseases	4
MESH:D016066	MESH:D016066	Pleural Effusion, Malignant	CTD_diseases	4
MESH:D016080	MESH:D016080	Arachnoid Cysts	CTD_diseases	4
MESH:D016098	MESH:D016098	Gerstmann-Straussler-Scheinker Disease	CTD_diseases	4
MESH:D016108	MESH:D016108	Epidermolysis Bullosa Dystrophica	CTD_diseases	4
MESH:D016111	MESH:D016111	Sjogren-Larsson Syndrome	CTD_diseases	4
MESH:D016112	MESH:D016112	Ichthyosis Vulgaris	CTD_diseases	4
MESH:D016113	MESH:D016113	Ichthyosiform Erythroderma, Congenital	CTD_diseases	4
MESH:D016114	MESH:D016114	Ichthyosis, X-Linked	CTD_diseases	4
MESH:D016127	MESH:D016127	Heart Valve Prolapse	CTD_diseases	4
MESH:D016142	MESH:D016142	Holoprosencephaly	CTD_diseases	4
MESH:D016180	MESH:D016180	Lentivirus Infections	CTD_diseases	4
MESH:D016301	MESH:D016301	Alveolar Bone Loss	CTD_diseases	4
MESH:D016369	MESH:D016369	Smear Layer	CTD_diseases	4
MESH:D016463	MESH:D016463	Sweet Syndrome	CTD_diseases	4
MESH:D016464	MESH:D016464	Lysosomal Storage Diseases	CTD_diseases	4
MESH:D016481	MESH:D016481	Helicobacter Infections	CTD_diseases	4
MESH:D016506	MESH:D016506	Pemphigus, Benign Familial	CTD_diseases	4
MESH:D016523	MESH:D016523	Foot Ulcer	CTD_diseases	4
MESH:D016543	MESH:D016543	Central Nervous System Neoplasms	CTD_diseases	4
MESH:D016574	MESH:D016574	Seasonal Affective Disorder	CTD_diseases	4
MESH:D016575	MESH:D016575	Hidradenitis	CTD_diseases	4
MESH:D016602	MESH:D016602	Needlestick Injuries	CTD_diseases	4
MESH:D016603	MESH:D016603	Eosinophilia-Myalgia Syndrome	CTD_diseases	4
MESH:D016638	MESH:D016638	Critical Illness	CTD_diseases	4
MESH:D016715	MESH:D016715	Proteus Syndrome	CTD_diseases	4
MESH:D016731	MESH:D016731	Erythema Infectiosum	CTD_diseases	4
MESH:D016757	MESH:D016757	Death, Sudden, Cardiac	CTD_diseases	4
MESH:D016776	MESH:D016776	Blastocystis Infections	CTD_diseases	4
MESH:D016778	MESH:D016778	Malaria, Falciparum	CTD_diseases	4
MESH:D016779	MESH:D016779	Malaria, Cerebral	CTD_diseases	4
MESH:D016780	MESH:D016780	Malaria, Vivax	CTD_diseases	4
MESH:D016849	MESH:D016849	Keratitis, Herpetic	CTD_diseases	4
MESH:D016857	MESH:D016857	Hypocapnia	CTD_diseases	4
MESH:D016863	MESH:D016863	Bacillaceae Infections	CTD_diseases	4
MESH:D016864	MESH:D016864	Li-Fraumeni Syndrome	CTD_diseases	4
MESH:D016866	MESH:D016866	Bacteroidaceae Infections	CTD_diseases	4
MESH:D016870	MESH:D016870	Neisseriaceae Infections	CTD_diseases	4
MESH:D016871	MESH:D016871	Pasteurellaceae Infections	CTD_diseases	4
MESH:D016878	MESH:D016878	POEMS Syndrome	CTD_diseases	4
MESH:D016890	MESH:D016890	Encephalitozoonosis	CTD_diseases	4
MESH:D016893	MESH:D016893	Carotid Stenosis	CTD_diseases	4
MESH:D016917	MESH:D016917	Angiomatosis, Bacillary	CTD_diseases	4
MESH:D016919	MESH:D016919	Meningitis, Cryptococcal	CTD_diseases	4
MESH:D017088	MESH:D017088	AIDS-Related Opportunistic Infections	CTD_diseases	4
MESH:D017092	MESH:D017092	Porphyria, Erythropoietic	CTD_diseases	4
MESH:D017093	MESH:D017093	Liver Failure	CTD_diseases	4
MESH:D017188	MESH:D017188	Adenophorea Infections	CTD_diseases	4
MESH:D017190	MESH:D017190	Secernentea Infections	CTD_diseases	4
MESH:D017204	MESH:D017204	Angelman Syndrome	CTD_diseases	4
MESH:D017219	MESH:D017219	Gastric Outlet Obstruction	CTD_diseases	4
MESH:D017240	MESH:D017240	Mitochondrial Myopathies	CTD_diseases	4
MESH:D017246	MESH:D017246	Ophthalmoplegia, Chronic Progressive External	CTD_diseases	4
MESH:D017253	MESH:D017253	Neurofibromatoses	CTD_diseases	4
MESH:D017271	MESH:D017271	Craniomandibular Disorders	CTD_diseases	4
MESH:D017449	MESH:D017449	Dermatitis, Allergic Contact	CTD_diseases	4
MESH:D017454	MESH:D017454	Dermatitis, Photoallergic	CTD_diseases	4
MESH:D017484	MESH:D017484	Dermatitis, Phototoxic	CTD_diseases	4
MESH:D017492	MESH:D017492	Keratosis, Seborrheic	CTD_diseases	4
MESH:D017495	MESH:D017495	Hyperpigmentation	CTD_diseases	4
MESH:D017496	MESH:D017496	Hypopigmentation	CTD_diseases	4
MESH:D017499	MESH:D017499	Porokeratosis	CTD_diseases	4
MESH:D017511	MESH:D017511	Pyoderma Gangrenosum	CTD_diseases	4
MESH:D017512	MESH:D017512	Lichenoid Eruptions	CTD_diseases	4
MESH:D017541	MESH:D017541	Aneurysm, False	CTD_diseases	4
MESH:D017542	MESH:D017542	Aneurysm, Ruptured	CTD_diseases	4
MESH:D017543	MESH:D017543	Iliac Aneurysm	CTD_diseases	4
MESH:D017565	MESH:D017565	Sarcoidosis, Pulmonary	CTD_diseases	4
MESH:D017574	MESH:D017574	Parasystole	CTD_diseases	4
MESH:D017599	MESH:D017599	Neuroectodermal Tumors	CTD_diseases	4
MESH:D017624	MESH:D017624	WAGR Syndrome	CTD_diseases	4
MESH:D017674	MESH:D017674	Hypophosphatemia	CTD_diseases	4
MESH:D017675	MESH:D017675	CREST Syndrome	CTD_diseases	4
MESH:D017682	MESH:D017682	Myocardial Stunning	CTD_diseases	4
MESH:D017688	MESH:D017688	Cholera Morbus	CTD_diseases	4
MESH:D017726	MESH:D017726	Cytomegalovirus Retinitis	CTD_diseases	4
MESH:D017769	MESH:D017769	Ulnar Nerve Compression Syndromes	CTD_diseases	4
MESH:D017772	MESH:D017772	Amyloid Neuropathies	CTD_diseases	4
MESH:D017823	MESH:D017823	Furcation Defects	CTD_diseases	4
MESH:D017825	MESH:D017825	Canavan Disease	CTD_diseases	4
MESH:D017880	MESH:D017880	Limb Deformities, Congenital	CTD_diseases	4
MESH:D017887	MESH:D017887	Ossification of Posterior Longitudinal Ligament	CTD_diseases	4
MESH:D017889	MESH:D017889	Exfoliation Syndrome	CTD_diseases	4
MESH:D018159	MESH:D018159	Endolymphatic Hydrops	CTD_diseases	4
MESH:D018174	MESH:D018174	Arterivirus Infections	CTD_diseases	4
MESH:D018177	MESH:D018177	Flavivirus Infections	CTD_diseases	4
MESH:D018182	MESH:D018182	Pestivirus Infections	CTD_diseases	4
MESH:D018184	MESH:D018184	Paramyxoviridae Infections	CTD_diseases	4
MESH:D018188	MESH:D018188	Cardiovirus Infections	CTD_diseases	4
MESH:D018194	MESH:D018194	Adenomyoma	CTD_diseases	4
MESH:D018195	MESH:D018195	Adenosarcoma	CTD_diseases	4
MESH:D018196	MESH:D018196	Carcinoma, Adenosquamous	CTD_diseases	4
MESH:D018197	MESH:D018197	Hepatoblastoma	CTD_diseases	4
MESH:D018198	MESH:D018198	Mixed Tumor, Malignant	CTD_diseases	4
MESH:D018199	MESH:D018199	Mixed Tumor, Mesodermal	CTD_diseases	4
MESH:D018200	MESH:D018200	Mixed Tumor, Mullerian	CTD_diseases	4
MESH:D018201	MESH:D018201	Nephroma, Mesoblastic	CTD_diseases	4
MESH:D018202	MESH:D018202	Pulmonary Blastoma	CTD_diseases	4
MESH:D018203	MESH:D018203	Sarcoma, Endometrial Stromal	CTD_diseases	4
MESH:D018205	MESH:D018205	Neoplasms, Adipose Tissue	CTD_diseases	4
MESH:D018225	MESH:D018225	Neoplasms, Fibroepithelial	CTD_diseases	4
MESH:D018236	MESH:D018236	Carcinoma, Embryonal	CTD_diseases	4
MESH:D018237	MESH:D018237	Germinoma	CTD_diseases	4
MESH:D018238	MESH:D018238	Gonadoblastoma	CTD_diseases	4
MESH:D018243	MESH:D018243	Teratocarcinoma	CTD_diseases	4
MESH:D018294	MESH:D018294	Neoplasms, Adnexal and Skin Appendage	CTD_diseases	4
MESH:D018295	MESH:D018295	Neoplasms, Basal Cell	CTD_diseases	4
MESH:D018297	MESH:D018297	Neoplasms, Cystic, Mucinous, and Serous	CTD_diseases	4
MESH:D018299	MESH:D018299	Neoplasms, Ductal, Lobular, and Medullary	CTD_diseases	4
MESH:D018301	MESH:D018301	Neoplasms, Mesothelial	CTD_diseases	4
MESH:D018302	MESH:D018302	Neoplasms, Neuroepithelial	CTD_diseases	4
MESH:D018304	MESH:D018304	Esthesioneuroblastoma, Olfactory	CTD_diseases	4
MESH:D018307	MESH:D018307	Neoplasms, Squamous Cell	CTD_diseases	4
MESH:D018312	MESH:D018312	Sex Cord-Gonadal Stromal Tumors	CTD_diseases	4
MESH:D018317	MESH:D018317	Nerve Sheath Neoplasms	CTD_diseases	4
MESH:D018322	MESH:D018322	Angiofibroma	CTD_diseases	4
MESH:D018333	MESH:D018333	Odontogenic Cyst, Calcifying	CTD_diseases	4
MESH:D018335	MESH:D018335	Rhabdoid Tumor	CTD_diseases	4
MESH:D018353	MESH:D018353	Rhabdoviridae Infections	CTD_diseases	4
MESH:D018354	MESH:D018354	Alphavirus Infections	CTD_diseases	4
MESH:D018355	MESH:D018355	Rubivirus Infections	CTD_diseases	4
MESH:D018365	MESH:D018365	Neoplasm, Residual	CTD_diseases	4
MESH:D018366	MESH:D018366	Vasculitis, Leukocytoclastic, Cutaneous	CTD_diseases	4
MESH:D018382	MESH:D018382	Thyroid Hormone Resistance Syndrome	CTD_diseases	4
MESH:D018404	MESH:D018404	Isochromosomes	CTD_diseases	4
MESH:D018438	MESH:D018438	Blue Toe Syndrome	CTD_diseases	4
MESH:D018450	MESH:D018450	Disease Progression	CTD_diseases	4
MESH:D018455	MESH:D018455	Protein S Deficiency	CTD_diseases	4
MESH:D018457	MESH:D018457	Placenta, Retained	CTD_diseases	4
MESH:D018467	MESH:D018467	Positive-Pressure Respiration, Intrinsic	CTD_diseases	4
MESH:D018487	MESH:D018487	Ventricular Dysfunction, Left	CTD_diseases	4
MESH:D018488	MESH:D018488	Bone Demineralization, Pathologic	CTD_diseases	4
MESH:D018489	MESH:D018489	Space Motion Sickness	CTD_diseases	4
MESH:D018496	MESH:D018496	Hyperoxia	CTD_diseases	4
MESH:D018497	MESH:D018497	Ventricular Dysfunction, Right	CTD_diseases	4
MESH:D018589	MESH:D018589	Gastroparesis	CTD_diseases	4
MESH:D018602	MESH:D018602	Milk Sickness	CTD_diseases	4
MESH:D018633	MESH:D018633	Pulmonary Atresia	CTD_diseases	4
MESH:D018702	MESH:D018702	Filoviridae Infections	CTD_diseases	4
MESH:D018746	MESH:D018746	Systemic Inflammatory Response Syndrome	CTD_diseases	4
MESH:D018777	MESH:D018777	Multiple Chemical Sensitivity	CTD_diseases	4
MESH:D018778	MESH:D018778	Hantavirus Infections	CTD_diseases	4
MESH:D018785	MESH:D018785	Tricuspid Atresia	CTD_diseases	4
MESH:D018798	MESH:D018798	Anemia, Iron-Deficiency	CTD_diseases	4
MESH:D018804	MESH:D018804	Hantavirus Pulmonary Syndrome	CTD_diseases	4
MESH:D018860	MESH:D018860	Sneddon Syndrome	CTD_diseases	4
MESH:D018877	MESH:D018877	Sick Building Syndrome	CTD_diseases	4
MESH:D018901	MESH:D018901	Peroxisomal Disorders	CTD_diseases	4
MESH:D018921	MESH:D018921	Leukostasis	CTD_diseases	4
MESH:D018980	MESH:D018980	Williams Syndrome	CTD_diseases	4
MESH:D019042	MESH:D019042	Muscle Neoplasms	CTD_diseases	4
MESH:D019046	MESH:D019046	Bone Marrow Neoplasms	CTD_diseases	4
MESH:D019052	MESH:D019052	Depression, Postpartum	CTD_diseases	4
MESH:D019053	MESH:D019053	HIV Enteropathy	CTD_diseases	4
MESH:D019066	MESH:D019066	Facies	CTD_diseases	4
MESH:D019080	MESH:D019080	Cafe-au-Lait Spots	CTD_diseases	4
MESH:D019082	MESH:D019082	Smith-Lemli-Opitz Syndrome	CTD_diseases	4
MESH:D019106	MESH:D019106	Postoperative Hemorrhage	CTD_diseases	4
MESH:D019121	MESH:D019121	Burkholderia Infections	CTD_diseases	4
MESH:D019142	MESH:D019142	Hemorrhagic Fever, Ebola	CTD_diseases	4
MESH:D019150	MESH:D019150	Neuroaxonal Dystrophies	CTD_diseases	4
MESH:D019190	MESH:D019190	Iron Overload	CTD_diseases	4
MESH:D019217	MESH:D019217	Tooth Attrition	CTD_diseases	4
MESH:D019247	MESH:D019247	HIV Wasting Syndrome	CTD_diseases	4
MESH:D019263	MESH:D019263	Dysthymic Disorder	CTD_diseases	4
MESH:D019280	MESH:D019280	Branchio-Oto-Renal Syndrome	CTD_diseases	4
MESH:D019283	MESH:D019283	Pancreatitis, Acute Necrotizing	CTD_diseases	4
MESH:D019339	MESH:D019339	Port-Wine Stain	CTD_diseases	4
MESH:D019349	MESH:D019349	Roseolovirus Infections	CTD_diseases	4
MESH:D019446	MESH:D019446	Endotoxemia	CTD_diseases	4
MESH:D019457	MESH:D019457	Chromosome Breakage	CTD_diseases	4
MESH:D019465	MESH:D019465	Craniofacial Abnormalities	CTD_diseases	4
MESH:D019512	MESH:D019512	Pancreatitis, Alcoholic	CTD_diseases	4
MESH:D019553	MESH:D019553	Tooth, Nonvital	CTD_diseases	4
MESH:D019557	MESH:D019557	Dermatitis, Perioral	CTD_diseases	4
MESH:D019571	MESH:D019571	Arrhythmogenic Right Ventricular Dysplasia	CTD_diseases	4
MESH:D019574	MESH:D019574	Optic Nerve Neoplasms	CTD_diseases	4
MESH:D019585	MESH:D019585	Intracranial Hypotension	CTD_diseases	4
MESH:D019586	MESH:D019586	Intracranial Hypertension	CTD_diseases	4
MESH:D019687	MESH:D019687	Uterine Inversion	CTD_diseases	4
MESH:D019767	MESH:D019767	Maxillofacial Abnormalities	CTD_diseases	4
MESH:D019846	MESH:D019846	Miller Fisher Syndrome	CTD_diseases	4
MESH:D019871	MESH:D019871	Dyskeratosis Congenita	CTD_diseases	4
MESH:D019954	MESH:D019954	Neurobehavioral Manifestations	CTD_diseases	4
MESH:D019955	MESH:D019955	Conduct Disorder	CTD_diseases	4
MESH:D020016	MESH:D020016	Activated Protein C Resistance	CTD_diseases	4
MESH:D020031	MESH:D020031	Epstein-Barr Virus Infections	CTD_diseases	4
MESH:D020042	MESH:D020042	Histiocytic Necrotizing Lymphadenitis	CTD_diseases	4
MESH:D020078	MESH:D020078	Neurogenic Inflammation	CTD_diseases	4
MESH:D020139	MESH:D020139	Gastroschisis	CTD_diseases	4
MESH:D020147	MESH:D020147	Coagulation Protein Disorders	CTD_diseases	4
MESH:D020151	MESH:D020151	Protein C Deficiency	CTD_diseases	4
MESH:D020152	MESH:D020152	Antithrombin III Deficiency	CTD_diseases	4
MESH:D020157	MESH:D020157	Amino Acid Transport Disorders, Inborn	CTD_diseases	4
MESH:D020163	MESH:D020163	Ornithine Carbamoyltransferase Deficiency Disease	CTD_diseases	4
MESH:D020165	MESH:D020165	Carbamoyl-Phosphate Synthase I Deficiency Disease	CTD_diseases	4
MESH:D020186	MESH:D020186	Sleep Bruxism	CTD_diseases	4
MESH:D020192	MESH:D020192	Lafora Disease	CTD_diseases	4
MESH:D020194	MESH:D020194	Unverricht-Lundborg Syndrome	CTD_diseases	4
MESH:D020198	MESH:D020198	Intracranial Hemorrhage, Traumatic	CTD_diseases	4
MESH:D020207	MESH:D020207	Coma, Post-Head Injury	CTD_diseases	4
MESH:D020220	MESH:D020220	Facial Nerve Injuries	CTD_diseases	4
MESH:D020221	MESH:D020221	Optic Nerve Injuries	CTD_diseases	4
MESH:D020222	MESH:D020222	Abducens Nerve Injury	CTD_diseases	4
MESH:D020232	MESH:D020232	Kluver-Bucy Syndrome	CTD_diseases	4
MESH:D020233	MESH:D020233	Gait Disorders, Neurologic	CTD_diseases	4
MESH:D020236	MESH:D020236	Amnesia, Transient Global	CTD_diseases	4
MESH:D020250	MESH:D020250	Postoperative Nausea and Vomiting	CTD_diseases	4
MESH:D020252	MESH:D020252	Gastric Antral Vascular Ectasia	CTD_diseases	4
MESH:D020256	MESH:D020256	Choroidal Neovascularization	CTD_diseases	4
MESH:D020260	MESH:D020260	Heavy Metal Poisoning, Nervous System	CTD_diseases	4
MESH:D020262	MESH:D020262	Mercury Poisoning, Nervous System	CTD_diseases	4
MESH:D020263	MESH:D020263	Lead Poisoning, Nervous System	CTD_diseases	4
MESH:D020267	MESH:D020267	MPTP Poisoning	CTD_diseases	4
MESH:D020268	MESH:D020268	Alcohol-Induced Disorders, Nervous System	CTD_diseases	4
MESH:D020270	MESH:D020270	Alcohol Withdrawal Seizures	CTD_diseases	4
MESH:D020275	MESH:D020275	Guillain-Barre Syndrome	CTD_diseases	4
MESH:D020293	MESH:D020293	Vasculitis, Central Nervous System	CTD_diseases	4
MESH:D020300	MESH:D020300	Intracranial Hemorrhages	CTD_diseases	4
MESH:D020329	MESH:D020329	Essential Tremor	CTD_diseases	4
MESH:D020333	MESH:D020333	Tolosa-Hunt Syndrome	CTD_diseases	4
MESH:D020371	MESH:D020371	Pelizaeus-Merzbacher Disease	CTD_diseases	4
MESH:D020388	MESH:D020388	Muscular Dystrophy, Duchenne	CTD_diseases	4
MESH:D020389	MESH:D020389	Muscular Dystrophy, Emery-Dreifuss	CTD_diseases	4
MESH:D020422	MESH:D020422	Mononeuropathies	CTD_diseases	4
MESH:D020516	MESH:D020516	Brachial Plexus Neuropathies	CTD_diseases	4
MESH:D020567	MESH:D020567	Fetal Weight	CTD_diseases	4
MESH:D020721	MESH:D020721	Nervous System Autoimmune Disease, Experimental	CTD_diseases	4
MESH:D020734	MESH:D020734	Parkinsonian Disorders	CTD_diseases	4
MESH:D020739	MESH:D020739	Brain Diseases, Metabolic, Inborn	CTD_diseases	4
MESH:D020751	MESH:D020751	Alcohol-Induced Disorders	CTD_diseases	4
MESH:D020773	MESH:D020773	Headache Disorders	CTD_diseases	4
MESH:D020785	MESH:D020785	Central Nervous System Vascular Malformations	CTD_diseases	4
MESH:D020788	MESH:D020788	Bardet-Biedl Syndrome	CTD_diseases	4
MESH:D020792	MESH:D020792	Salivary Calculi	CTD_diseases	4
MESH:D020802	MESH:D020802	Epidural Abscess	CTD_diseases	4
MESH:D020803	MESH:D020803	Encephalitis, Herpes Simplex	CTD_diseases	4
MESH:D020804	MESH:D020804	Encephalitis, Varicella Zoster	CTD_diseases	4
MESH:D020817	MESH:D020817	Asperger Syndrome	CTD_diseases	4
MESH:D020819	MESH:D020819	Perimeningeal Infections	CTD_diseases	4
MESH:D020820	MESH:D020820	Dyskinesias	CTD_diseases	4
MESH:D020821	MESH:D020821	Dystonic Disorders	CTD_diseases	4
MESH:D020863	MESH:D020863	Central Nervous System Cysts	CTD_diseases	4
MESH:D020879	MESH:D020879	Neuromuscular Manifestations	CTD_diseases	4
MESH:D020914	MESH:D020914	Myopathies, Structural, Congenital	CTD_diseases	4
MESH:D020945	MESH:D020945	Lupus Vasculitis, Central Nervous System	CTD_diseases	4
MESH:D020964	MESH:D020964	Embryo Loss	CTD_diseases	4
MESH:D020967	MESH:D020967	Myotonic Disorders	CTD_diseases	4
MESH:D021782	MESH:D021782	Multicystic Dysplastic Kidney	CTD_diseases	4
MESH:D021821	MESH:D021821	Communicable Diseases, Emerging	CTD_diseases	4
MESH:D021865	MESH:D021865	Isosporiasis	CTD_diseases	4
MESH:D021866	MESH:D021866	Cyclosporiasis	CTD_diseases	4
MESH:D024343	MESH:D024343	Open Bite	CTD_diseases	4
MESH:D025064	MESH:D025064	Sex Chromosome Disorders	CTD_diseases	4
MESH:D025241	MESH:D025241	Spondylarthritis	CTD_diseases	4
MESH:D025962	MESH:D025962	Septo-Optic Dysplasia	CTD_diseases	4
MESH:D028226	MESH:D028226	Amyloidosis, Familial	CTD_diseases	4
MESH:D028227	MESH:D028227	Amyloid Neuropathies, Familial	CTD_diseases	4
MESH:D029241	MESH:D029241	Optic Atrophy, Autosomal Dominant	CTD_diseases	4
MESH:D029242	MESH:D029242	Optic Atrophy, Hereditary, Leber	CTD_diseases	4
MESH:D029424	MESH:D029424	Pulmonary Disease, Chronic Obstructive	CTD_diseases	4
MESH:D030401	MESH:D030401	Cytochrome-c Oxidase Deficiency	CTD_diseases	4
MESH:D030981	MESH:D030981	Acro-Osteolysis	CTD_diseases	4
MESH:D031261	MESH:D031261	Poult Enteritis Mortality Syndrome	CTD_diseases	4
MESH:D035583	MESH:D035583	Rare Diseases	CTD_diseases	4
MESH:D036841	MESH:D036841	Ciguatera Poisoning	CTD_diseases	4
MESH:D036982	MESH:D036982	Heel Spur	CTD_diseases	4
MESH:D037081	MESH:D037081	Posterior Tibial Tendon Dysfunction	CTD_diseases	4
MESH:D038261	MESH:D038261	Alexander Disease	CTD_diseases	4
MESH:D038901	MESH:D038901	Mental Retardation, X-Linked	CTD_diseases	4
MESH:D039941	MESH:D039941	Bifidobacteriales Infections	CTD_diseases	4
MESH:D040701	MESH:D040701	Stress Disorders, Traumatic, Acute	CTD_diseases	4
MESH:D041441	MESH:D041441	Retinoschisis	CTD_diseases	4
MESH:D041761	MESH:D041761	Cholecystolithiasis	CTD_diseases	4
MESH:D042882	MESH:D042882	Gallstones	CTD_diseases	4
MESH:D042883	MESH:D042883	Choledocholithiasis	CTD_diseases	4
MESH:D043171	MESH:D043171	Chromosomal Instability	CTD_diseases	4
MESH:D043202	MESH:D043202	Steroid Metabolism, Inborn Errors	CTD_diseases	4
MESH:D044225	MESH:D044225	Piscirickettsiaceae Infections	CTD_diseases	4
MESH:D044483	MESH:D044483	Intestinal Polyposis	CTD_diseases	4
MESH:D044542	MESH:D044542	LEOPARD Syndrome	CTD_diseases	4
MESH:D045169	MESH:D045169	Severe Acute Respiratory Syndrome	CTD_diseases	4
MESH:D045723	MESH:D045723	Diverticulosis, Esophageal	CTD_diseases	4
MESH:D045724	MESH:D045724	Diverticulosis, Stomach	CTD_diseases	4
MESH:D045743	MESH:D045743	Scleroderma, Diffuse	CTD_diseases	4
MESH:D045745	MESH:D045745	Scleroderma, Limited	CTD_diseases	4
MESH:D045822	MESH:D045822	Intestinal Volvulus	CTD_diseases	4
MESH:D045824	MESH:D045824	Desulfovibrionaceae Infections	CTD_diseases	4
MESH:D045825	MESH:D045825	Fusobacteriaceae Infections	CTD_diseases	4
MESH:D045826	MESH:D045826	Flavobacteriaceae Infections	CTD_diseases	4
MESH:D045827	MESH:D045827	Cytophagaceae Infections	CTD_diseases	4
MESH:D045828	MESH:D045828	Moraxellaceae Infections	CTD_diseases	4
MESH:D045888	MESH:D045888	Ganglion Cysts	CTD_diseases	4
MESH:D046151	MESH:D046151	Lingual Thyroid	CTD_diseases	4
MESH:D046449	MESH:D046449	Hernia, Abdominal	CTD_diseases	4
MESH:D046789	MESH:D046789	Chondromalacia Patellae	CTD_diseases	4
MESH:D047268	MESH:D047268	Lingual Goiter	CTD_diseases	4
MESH:D047688	MESH:D047688	Breast Cyst	CTD_diseases	4
MESH:D047728	MESH:D047728	Myopia, Degenerative	CTD_diseases	4
MESH:D048070	MESH:D048070	Fetal Nutrition Disorders	CTD_diseases	4
MESH:D048629	MESH:D048629	Micronuclei, Chromosome-Defective	CTD_diseases	4
MESH:D049291	MESH:D049291	Seroma	CTD_diseases	4
MESH:D049309	MESH:D049309	Acanthoma	CTD_diseases	4
MESH:D049932	MESH:D049932	Nijmegen Breakage Syndrome	CTD_diseases	4
MESH:D049950	MESH:D049950	Hyperparathyroidism, Primary	CTD_diseases	4
MESH:D049970	MESH:D049970	Graves Ophthalmopathy	CTD_diseases	4
MESH:D050032	MESH:D050032	Postpartum Thyroiditis	CTD_diseases	4
MESH:D050035	MESH:D050035	Sexual Infantilism	CTD_diseases	4
MESH:D050171	MESH:D050171	Dyslipidemias	CTD_diseases	4
MESH:D050177	MESH:D050177	Overweight	CTD_diseases	4
MESH:D050398	MESH:D050398	Adamantinoma	CTD_diseases	4
MESH:D050489	MESH:D050489	Bunion, Tailor's	CTD_diseases	4
MESH:D050500	MESH:D050500	Pancreatitis, Chronic	CTD_diseases	4
MESH:D050805	MESH:D050805	Wandering Spleen	CTD_diseases	4
MESH:D051527	MESH:D051527	Odontogenic Tumor, Squamous	CTD_diseases	4
MESH:D052065	MESH:D052065	Vaginismus	CTD_diseases	4
MESH:D052120	MESH:D052120	Glycogen Storage Disease Type IIb	CTD_diseases	4
MESH:D052178	MESH:D052178	Cephalopelvic Disproportion	CTD_diseases	4
MESH:D052878	MESH:D052878	Urolithiasis	CTD_diseases	4
MESH:D052958	MESH:D052958	Tarlov Cysts	CTD_diseases	4
MESH:D053307	MESH:D053307	Hyper-IgM Immunodeficiency Syndrome, Type 1	CTD_diseases	4
MESH:D053358	MESH:D053358	Ectodermal Dysplasia 1, Anhidrotic	CTD_diseases	4
MESH:D053529	MESH:D053529	Leukokeratosis, Hereditary Mucosal	CTD_diseases	4
MESH:D053549	MESH:D053549	Pachyonychia Congenita	CTD_diseases	4
MESH:D053560	MESH:D053560	Ichthyosis Bullosa of Siemens	CTD_diseases	4
MESH:D053565	MESH:D053565	Hypercalciuria	CTD_diseases	4
MESH:D053578	MESH:D053578	Opsoclonus-Myoclonus Syndrome	CTD_diseases	4
MESH:D053584	MESH:D053584	Urinoma	CTD_diseases	4
MESH:D053632	MESH:D053632	X-Linked Combined Immunodeficiency Diseases	CTD_diseases	4
MESH:D053706	MESH:D053706	Typhlitis	CTD_diseases	4
MESH:D053717	MESH:D053717	Pneumonia, Ventilator-Associated	CTD_diseases	4
MESH:D053718	MESH:D053718	Scleromyxedema	CTD_diseases	4
MESH:D053836	MESH:D053836	DNA Degradation, Necrotic	CTD_diseases	4
MESH:D053842	MESH:D053842	Microsatellite Instability	CTD_diseases	4
MESH:D054000	MESH:D054000	Nevus, Sebaceous of Jadassohn	CTD_diseases	4
MESH:D054039	MESH:D054039	Onycholysis	CTD_diseases	4
MESH:D054058	MESH:D054058	Acute Coronary Syndrome	CTD_diseases	4
MESH:D054062	MESH:D054062	Deaf-Blind Disorders	CTD_diseases	4
MESH:D054068	MESH:D054068	Livedo Reticularis	CTD_diseases	4
MESH:D054069	MESH:D054069	Multiple Acyl Coenzyme A Dehydrogenase Deficiency	CTD_diseases	4
MESH:D054070	MESH:D054070	Postthrombotic Syndrome	CTD_diseases	4
MESH:D054079	MESH:D054079	Vascular Malformations	CTD_diseases	4
MESH:D054141	MESH:D054141	Ventricular Flutter	CTD_diseases	4
MESH:D054143	MESH:D054143	Heart Failure, Systolic	CTD_diseases	4
MESH:D054144	MESH:D054144	Heart Failure, Diastolic	CTD_diseases	4
MESH:D054160	MESH:D054160	Systolic Murmurs	CTD_diseases	4
MESH:D054220	MESH:D054220	Malformations of Cortical Development	CTD_diseases	4
MESH:D054312	MESH:D054312	Buruli Ulcer	CTD_diseases	4
MESH:D054318	MESH:D054318	No-Reflow Phenomenon	CTD_diseases	4
MESH:D054437	MESH:D054437	Myelodysplastic-Myeloproliferative Diseases	CTD_diseases	4
MESH:D054463	MESH:D054463	Trichothiodystrophy Syndromes	CTD_diseases	4
MESH:D054514	MESH:D054514	Persistent Hyperplastic Primary Vitreous	CTD_diseases	4
MESH:D054546	MESH:D054546	Neuroacanthocytosis	CTD_diseases	4
MESH:D054559	MESH:D054559	Hyperphosphatemia	CTD_diseases	4
MESH:D054853	MESH:D054853	Malignant Atrophic Papulosis	CTD_diseases	4
MESH:D054868	MESH:D054868	Jacobsen Distal 11q Deletion Syndrome	CTD_diseases	4
MESH:D054877	MESH:D054877	Wolf-Hirschhorn Syndrome	CTD_diseases	4
MESH:D054970	MESH:D054970	Pure Autonomic Failure	CTD_diseases	4
MESH:D054971	MESH:D054971	Orthostatic Intolerance	CTD_diseases	4
MESH:D054973	MESH:D054973	Perivascular Epithelioid Cell Neoplasms	CTD_diseases	4
MESH:D054988	MESH:D054988	Idiopathic Interstitial Pneumonias	CTD_diseases	4
MESH:D054990	MESH:D054990	Idiopathic Pulmonary Fibrosis	CTD_diseases	4
MESH:D055009	MESH:D055009	Spondylosis	CTD_diseases	4
MESH:D055010	MESH:D055010	Posterior Cervical Sympathetic Syndrome	CTD_diseases	4
MESH:D055035	MESH:D055035	Spinal Osteochondrosis	CTD_diseases	4
MESH:D055036	MESH:D055036	Campomelic Dysplasia	CTD_diseases	4
MESH:D055093	MESH:D055093	Periodontal Atrophy	CTD_diseases	4
MESH:D055111	MESH:D055111	Failed Back Surgery Syndrome	CTD_diseases	4
MESH:D055191	MESH:D055191	Delayed Emergence from Anesthesia	CTD_diseases	4
MESH:D055331	MESH:D055331	Adenomyoepithelioma	CTD_diseases	4
MESH:D055371	MESH:D055371	Acute Lung Injury	CTD_diseases	4
MESH:D055397	MESH:D055397	Ventilator-Induced Lung Injury	CTD_diseases	4
MESH:D055501	MESH:D055501	Macrophage Activation Syndrome	CTD_diseases	4
MESH:D055534	MESH:D055534	Bulbo-Spinal Atrophy, X-Linked	CTD_diseases	4
MESH:D055589	MESH:D055589	Pancreatitis, Graft	CTD_diseases	4
MESH:D055652	MESH:D055652	Gray Platelet Syndrome	CTD_diseases	4
MESH:D055653	MESH:D055653	Muir-Torre Syndrome	CTD_diseases	4
MESH:D055677	MESH:D055677	Refeeding Syndrome	CTD_diseases	4
MESH:D055949	MESH:D055949	Vasa Previa	CTD_diseases	4
MESH:D055956	MESH:D055956	Diffuse Neurofibrillary Tangles with Calcification	CTD_diseases	4
MESH:D055959	MESH:D055959	Intervertebral Disc Degeneration	CTD_diseases	4
MESH:D055963	MESH:D055963	Asthma, Aspirin-Induced	CTD_diseases	4
MESH:D056104	MESH:D056104	Commotio Cordis	CTD_diseases	4
MESH:D056124	MESH:D056124	Slit Ventricle Syndrome	CTD_diseases	4
MESH:D056266	MESH:D056266	Erythrokeratodermia Variabilis	CTD_diseases	4
MESH:D056364	MESH:D056364	Colloid Cysts	CTD_diseases	4
MESH:D056487	MESH:D056487	Drug-Induced Liver Injury, Chronic	CTD_diseases	4
MESH:D056647	MESH:D056647	Systemic Vasculitis	CTD_diseases	4
MESH:D056730	MESH:D056730	Silver-Russell Syndrome	CTD_diseases	4
MESH:D056732	MESH:D056732	Prolidase Deficiency	CTD_diseases	4
MESH:D056733	MESH:D056733	Carney Complex	CTD_diseases	4
MESH:D056734	MESH:D056734	Monilethrix	CTD_diseases	4
MESH:D056768	MESH:D056768	Giant Axonal Neuropathy	CTD_diseases	4
MESH:D056769	MESH:D056769	Alstrom Syndrome	CTD_diseases	4
MESH:D056770	MESH:D056770	Netherton Syndrome	CTD_diseases	4
MESH:D056784	MESH:D056784	Leukoencephalopathies	CTD_diseases	4
MESH:D056830	MESH:D056830	Isolated Noncompaction of the Ventricular Myocardium	CTD_diseases	4
MESH:D056887	MESH:D056887	Pelvic Organ Prolapse	CTD_diseases	4
MESH:D056889	MESH:D056889	Barth Syndrome	CTD_diseases	4
MESH:D057066	MESH:D057066	Low Tension Glaucoma	CTD_diseases	4
MESH:D057096	MESH:D057096	Shellfish Poisoning	CTD_diseases	4
MESH:D057765	MESH:D057765	Eosinophilic Esophagitis	CTD_diseases	4
MESH:D057768	MESH:D057768	Infantile Apparent Life-Threatening Event	CTD_diseases	4
MESH:D057770	MESH:D057770	Hyalinosis, Systemic	CTD_diseases	4
MESH:D057774	MESH:D057774	Post-Exercise Hypotension	CTD_diseases	4
MESH:D057826	MESH:D057826	Vitelliform Macular Dystrophy	CTD_diseases	4
MESH:D057867	MESH:D057867	Endoleak	CTD_diseases	4
MESH:D057868	MESH:D057868	Anastomotic Leak	CTD_diseases	4
MESH:D057896	MESH:D057896	Striae Distensae	CTD_diseases	4
MESH:D057973	MESH:D057973	Dent Disease	CTD_diseases	4
MESH:D058065	MESH:D058065	Diabetic Cardiomyopathies	CTD_diseases	4
MESH:D058069	MESH:D058069	Neglected Diseases	CTD_diseases	4
MESH:D058070	MESH:D058070	Asymptomatic Diseases	CTD_diseases	4
MESH:D058165	MESH:D058165	22q11 Deletion Syndrome	CTD_diseases	4
MESH:D058249	MESH:D058249	Birt-Hogg-Dube Syndrome	CTD_diseases	4
MESH:D058288	MESH:D058288	Sister Mary Joseph's Nodule	CTD_diseases	4
MESH:D058365	MESH:D058365	Candidiasis, Invasive	CTD_diseases	4
MESH:D058442	MESH:D058442	Capsule Opacification	CTD_diseases	4
MESH:D058447	MESH:D058447	Eye Pain	CTD_diseases	4
MESH:D058494	MESH:D058494	Walker-Warburg Syndrome	CTD_diseases	4
MESH:D058495	MESH:D058495	Sotos Syndrome	CTD_diseases	4
MESH:D058497	MESH:D058497	Fraser Syndrome	CTD_diseases	4
MESH:D058499	MESH:D058499	Retinal Dystrophies	CTD_diseases	4
MESH:D058502	MESH:D058502	Pentalogy of Cantrell	CTD_diseases	4
MESH:D058535	MESH:D058535	Echogenic Bowel	CTD_diseases	4
MESH:D058536	MESH:D058536	Pyelectasis	CTD_diseases	4
MESH:D058566	MESH:D058566	Sacroiliitis	CTD_diseases	4
MESH:D058617	MESH:D058617	Composite Lymphoma	CTD_diseases	4
MESH:D058674	MESH:D058674	Chromosome Duplication	CTD_diseases	4
MESH:D058686	MESH:D058686	Coronary-Subclavian Steal Syndrome	CTD_diseases	4
MESH:D058687	MESH:D058687	Out-of-Hospital Cardiac Arrest	CTD_diseases	4
MESH:D058729	MESH:D058729	Peripheral Arterial Disease	CTD_diseases	4
MESH:D058734	MESH:D058734	Exsanguination	CTD_diseases	4
MESH:D058736	MESH:D058736	Intrauterine Device Migration	CTD_diseases	4
MESH:D058745	MESH:D058745	Iliotibial Band Syndrome	CTD_diseases	4
MESH:D058926	MESH:D058926	Intraoperative Awareness	CTD_diseases	4
MESH:D059347	MESH:D059347	Cardio-Renal Syndrome	CTD_diseases	4
MESH:D059352	MESH:D059352	Musculoskeletal Pain	CTD_diseases	4
MESH:D059411	MESH:D059411	Lower Urinary Tract Symptoms	CTD_diseases	4
MESH:D059446	MESH:D059446	Heterotaxy Syndrome	CTD_diseases	4
MESH:D059466	MESH:D059466	White Coat Hypertension	CTD_diseases	4
MESH:D059468	MESH:D059468	Masked Hypertension	CTD_diseases	4
MESH:D059607	MESH:D059607	Polydipsia, Psychogenic	CTD_diseases	4
MESH:D059707	MESH:D059707	Aliivibrio Infections	CTD_diseases	4
MESH:D059786	MESH:D059786	Abnormal Karyotype	CTD_diseases	4
MESH:D059905	MESH:D059905	Endocarditis, Non-Infective	CTD_diseases	4
MESH:D060048	MESH:D060048	Slipped Capital Femoral Epiphyses	CTD_diseases	4
MESH:D060426	MESH:D060426	Anti-N-Methyl-D-Aspartate Receptor Encephalitis	CTD_diseases	4
MESH:D060467	MESH:D060467	Disease Resistance	CTD_diseases	4
MESH:D060725	MESH:D060725	Uterine Retroversion	CTD_diseases	4
MESH:D060750	MESH:D060750	Bone Anteversion	CTD_diseases	4
MESH:D060751	MESH:D060751	Bone Retroversion	CTD_diseases	4
MESH:D060825	MESH:D060825	Mild Cognitive Impairment	CTD_diseases	4
MESH:D060845	MESH:D060845	Obsessive Hoarding	CTD_diseases	4
MESH:D061218	MESH:D061218	Depressive Disorder, Treatment-Resistant	CTD_diseases	4
MESH:D061219	MESH:D061219	Olfactory Nerve Injuries	CTD_diseases	4
MESH:D061221	MESH:D061221	Trigeminal Nerve Injuries	CTD_diseases	4
MESH:D061223	MESH:D061223	Vagus Nerve Injuries	CTD_diseases	4
MESH:D061227	MESH:D061227	Accessory Nerve Injuries	CTD_diseases	4
MESH:D061228	MESH:D061228	Hypoglossal Nerve Injuries	CTD_diseases	4
MESH:D061287	MESH:D061287	Glossopharyngeal Nerve Injuries	CTD_diseases	4
MESH:D061325	MESH:D061325	Hereditary Breast and Ovarian Cancer Syndrome	CTD_diseases	4
MESH:D061686	MESH:D061686	Premature Ejaculation	CTD_diseases	4
MESH:D062108	MESH:D062108	May-Thurner Syndrome	CTD_diseases	4
MESH:D062846	MESH:D062846	Non-Filarial Lymphedema	CTD_diseases	4
MESH:D063129	MESH:D063129	Parental Death	CTD_diseases	4
MESH:D063173	MESH:D063173	Retrognathia	CTD_diseases	4
MESH:D063205	MESH:D063205	Pneumorrhachis	CTD_diseases	4
MESH:D063425	MESH:D063425	Binge Drinking	CTD_diseases	4
MESH:D063466	MESH:D063466	Respiratory Aspiration of Gastric Contents	CTD_diseases	4
MESH:D063646	MESH:D063646	Carcinogenesis	CTD_diseases	4
MESH:D063647	MESH:D063647	Fetal Alcohol Spectrum Disorders	CTD_diseases	4
MESH:D063806	MESH:D063806	Myalgia	CTD_diseases	4
MESH:D063807	MESH:D063807	Dandruff	CTD_diseases	4
MESH:D064090	MESH:D064090	Intraocular Lymphoma	CTD_diseases	4
MESH:D064749	MESH:D064749	Retrocaval Ureter	CTD_diseases	4
MESH:D064927	MESH:D064927	Tick Bites	CTD_diseases	4
MESH:D065008	MESH:D065008	Scorpion Stings	CTD_diseases	4
OMIM:102510	OMIM:102510	ACROPECTOROVERTEBRAL DYSPLASIA	CTD_diseases	4
OMIM:115650	OMIM:115650	CATARACT 32, MULTIPLE TYPES	CTD_diseases	4
OMIM:115700	OMIM:115700	CATARACT 4, MULTIPLE TYPES	CTD_diseases	4
OMIM:116600	OMIM:116600	CATARACT 6, MULTIPLE TYPES	CTD_diseases	4
OMIM:123320	OMIM:123320	CREATINE PHOSPHOKINASE, ELEVATED SERUM	CTD_diseases	4
OMIM:132100	OMIM:132100	PHOTOPAROXYSMAL RESPONSE 1	CTD_diseases	4
OMIM:138900	OMIM:138900	URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 1	CTD_diseases	4
OMIM:143860	OMIM:143860	HYPERCHLORHIDROSIS, ISOLATED	CTD_diseases	4
OMIM:155600	OMIM:155600	MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 1	CTD_diseases	4
OMIM:155601	OMIM:155601	MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2	CTD_diseases	4
OMIM:162000	OMIM:162000	HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 1	CTD_diseases	4
OMIM:165800	OMIM:165800	OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS	CTD_diseases	4
OMIM:176430	OMIM:176430	PREMATURE CHROMATID SEPARATION TRAIT	CTD_diseases	4
OMIM:180500	OMIM:180500	AXENFELD-RIEGER SYNDROME, TYPE 1	CTD_diseases	4
OMIM:181750	OMIM:181750	SCLERODERMA, FAMILIAL PROGRESSIVE	CTD_diseases	4
OMIM:188890	OMIM:188890	TOBACCO ADDICTION, SUSCEPTIBILITY TO	CTD_diseases	4
OMIM:190320	OMIM:190320	TRICHODENTOOSSEOUS SYNDROME	CTD_diseases	4
OMIM:193235	OMIM:193235	VITREORETINOPATHY, NEOVASCULAR INFLAMMATORY	CTD_diseases	4
OMIM:194300	OMIM:194300	WOOLLY HAIR, AUTOSOMAL DOMINANT	CTD_diseases	4
OMIM:201750	OMIM:201750	ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS	CTD_diseases	4
OMIM:203700	OMIM:203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)	CTD_diseases	4
OMIM:212500	OMIM:212500	CATARACT, CONGENITAL OR JUVENILE	CTD_diseases	4
OMIM:222800	OMIM:222800	BISPHOSPHOGLYCERATE MUTASE DEFICIENCY	CTD_diseases	4
OMIM:231050	OMIM:231050	GELEOPHYSIC DYSPLASIA 1	CTD_diseases	4
OMIM:235700	OMIM:235700	HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY	CTD_diseases	4
OMIM:239000	OMIM:239000	PAGET DISEASE, JUVENILE	CTD_diseases	4
OMIM:242860	OMIM:242860	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 1	CTD_diseases	4
OMIM:245400	OMIM:245400	MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITH METHYLMALONIC ACIDURIA)	CTD_diseases	4
OMIM:248310	OMIM:248310	PLASMODIUM FALCIPARUM BLOOD INFECTION LEVEL	CTD_diseases	4
OMIM:251290	OMIM:251290	BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA	CTD_diseases	4
OMIM:251880	OMIM:251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)	CTD_diseases	4
OMIM:253290	OMIM:253290	MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE	CTD_diseases	4
OMIM:256810	OMIM:256810	MITOCHONDRIAL DNA DEPLETION SYNDROME 6 (HEPATOCEREBRAL TYPE)	CTD_diseases	4
OMIM:259100	OMIM:259100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1	CTD_diseases	4
OMIM:260660	OMIM:260660	COUSIN SYNDROME	CTD_diseases	4
OMIM:261515	OMIM:261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY	CTD_diseases	4
OMIM:270100	OMIM:270100	HETEROTAXY, VISCERAL, 5, AUTOSOMAL	CTD_diseases	4
OMIM:275120	OMIM:275120	THYROTROPIN-RELEASING HORMONE DEFICIENCY	CTD_diseases	4
OMIM:277580	OMIM:277580	WAARDENBURG SYNDROME, TYPE 4A	CTD_diseases	4
OMIM:300147	OMIM:300147	PROSTATE CANCER, HEREDITARY, X-LINKED 1	CTD_diseases	4
OMIM:300244	OMIM:300244	TERMINAL OSSEOUS DYSPLASIA	CTD_diseases	4
OMIM:300354	OMIM:300354	MENTAL RETARDATION, X-LINKED, WITH SHORT STATURE, HYPOGONADISM, AND ABNORMAL GAIT	CTD_diseases	4
OMIM:300845	OMIM:300845	MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM, AND FACIAL DYSMORPHISM	CTD_diseases	4
OMIM:305390	OMIM:305390	EXUDATIVE VITREORETINOPATHY 2, X-LINKED	CTD_diseases	4
OMIM:311250	OMIM:311250	ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO	CTD_diseases	4
OMIM:600803	OMIM:600803	GALLBLADDER DISEASE 1	CTD_diseases	4
OMIM:601419	OMIM:601419	MYOPATHY, MYOFIBRILLAR, 1	CTD_diseases	4
OMIM:601499	OMIM:601499	AXENFELD-RIEGER SYNDROME, TYPE 2	CTD_diseases	4
OMIM:601547	OMIM:601547	CATARACT 3, MULTIPLE TYPES	CTD_diseases	4
OMIM:601675	OMIM:601675	TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL	CTD_diseases	4
OMIM:602032	OMIM:602032	ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE	CTD_diseases	4
OMIM:603855	OMIM:603855	CYSTIC FIBROSIS, MODIFIER OF, 1	CTD_diseases	4
OMIM:604201	OMIM:604201	HEPATIC FIBROSIS, SEVERE, SUSCEPTIBILITY TO, DUE TO SCHISTOSOMA MANSONI INFECTION	CTD_diseases	4
OMIM:604273	OMIM:604273	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (AT	CTD_diseases	4
OMIM:605376	OMIM:605376	HETEROTAXY, VISCERAL, 2, AUTOSOMAL	CTD_diseases	4
OMIM:605711	OMIM:605711	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1	CTD_diseases	4
OMIM:606657	OMIM:606657	GLAUCOMA, NORMAL TENSION, SUSCEPTIBILITY TO	CTD_diseases	4
OMIM:607279	OMIM:607279	SYSTEMIC LUPUS ERYTHEMATOSUS WITH HEMOLYTIC ANEMIA, SUSCEPTIBILITY TO, 1	CTD_diseases	4
OMIM:607965	OMIM:607965	SYSTEMIC LUPUS ERYTHEMATOSUS WITH NEPHRITIS, SUSCEPTIBILITY TO, 1	CTD_diseases	4
OMIM:607966	OMIM:607966	SYSTEMIC LUPUS ERYTHEMATOSUS WITH NEPHRITIS, SUSCEPTIBILITY TO, 2	CTD_diseases	4
OMIM:607967	OMIM:607967	SYSTEMIC LUPUS ERYTHEMATOSUS WITH NEPHRITIS, SUSCEPTIBILITY TO, 3	CTD_diseases	4
OMIM:608035	OMIM:608035	MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 4	CTD_diseases	4
OMIM:608688	OMIM:608688	AICAR TRANSFORMYLASE/IMP CYCLOHYDROLASE DEFICIENCY	CTD_diseases	4
OMIM:609016	OMIM:609016	LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY	CTD_diseases	4
OMIM:609048	OMIM:609048	MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 3	CTD_diseases	4
OMIM:609452	OMIM:609452	MYOPATHY, MYOFIBRILLAR, 4	CTD_diseases	4
OMIM:609572	OMIM:609572	PHOTOPAROXYSMAL RESPONSE 2	CTD_diseases	4
OMIM:609821	OMIM:609821	BLEEDING DISORDER, PLATELET-TYPE, 8	CTD_diseases	4
OMIM:610141	OMIM:610141	QT INTERVAL, VARIATION IN	CTD_diseases	4
OMIM:610251	OMIM:610251	ALCOHOL SENSITIVITY, ACUTE	CTD_diseases	4
OMIM:610425	OMIM:610425	CATARACT 23	CTD_diseases	4
OMIM:610460	OMIM:610460	THIOPURINE S-METHYLTRANSFERASE DEFICIENCY	CTD_diseases	4
OMIM:610644	OMIM:610644	PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL	CTD_diseases	4
OMIM:612263	OMIM:612263	MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 7	CTD_diseases	4
OMIM:612348	OMIM:612348	THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINO	CTD_diseases	4
OMIM:612671	OMIM:612671	URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 4	CTD_diseases	4
OMIM:612862	OMIM:612862	PULMONARY HYPERTENSION, CHRONIC THROMBOEMBOLIC, WITHOUT DEEP VEIN THROMBOSIS, SUSCEPTIBILITY TO	CTD_diseases	4
OMIM:612954	OMIM:612954	MYOPATHY, MYOFIBRILLAR, 6	CTD_diseases	4
OMIM:613085	OMIM:613085	GLAUCOMA 3, PRIMARY CONGENITAL, C	CTD_diseases	4
OMIM:613092	OMIM:613092	HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 2	CTD_diseases	4
OMIM:613099	OMIM:613099	MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 5	CTD_diseases	4
OMIM:613376	OMIM:613376	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC	CTD_diseases	4
OMIM:613382	OMIM:613382	BRACHYDACTYLY, TYPE E2	CTD_diseases	4
OMIM:613402	OMIM:613402	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 10	CTD_diseases	4
OMIM:613418	OMIM:613418	BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 15	CTD_diseases	4
OMIM:613443	OMIM:613443	MENTAL RETARDATION, AUTOSOMAL DOMINANT 20	CTD_diseases	4
OMIM:613470	OMIM:613470	HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY	CTD_diseases	4
OMIM:613471	OMIM:613471	REYNOLDS SYNDROME	CTD_diseases	4
OMIM:613480	OMIM:613480	LYMPHEDEMA, HEREDITARY, IC	CTD_diseases	4
OMIM:613606	OMIM:613606	FORSYTHE-WAKELING SYNDROME	CTD_diseases	4
OMIM:613611	OMIM:613611	CHOANAL ATRESIA AND LYMPHEDEMA	CTD_diseases	4
OMIM:613630	OMIM:613630	COCOON SYNDROME	CTD_diseases	4
OMIM:613658	OMIM:613658	RAJAB SYNDROME	CTD_diseases	4
OMIM:613668	OMIM:613668	MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY	CTD_diseases	4
OMIM:613680	OMIM:613680	BEAULIEU-BOYCOTT-INNES SYNDROME	CTD_diseases	4
OMIM:613689	OMIM:613689	MAMMARY-DIGITAL-NAIL SYNDROME	CTD_diseases	4
OMIM:613730	OMIM:613730	HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION, AND CATARACTS	CTD_diseases	4
OMIM:613789	OMIM:613789	COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II	CTD_diseases	4
OMIM:613790	OMIM:613790	COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE I	CTD_diseases	4
OMIM:613792	OMIM:613792	CHROMOSOME 3pter-p25 DELETION SYNDROME	CTD_diseases	4
OMIM:613884	OMIM:613884	CHROMOSOME 13q14 DELETION SYNDROME	CTD_diseases	4
OMIM:613969	OMIM:613969	MYOPIA 19, AUTOSOMAL DOMINANT	CTD_diseases	4
OMIM:614149	OMIM:614149	NAIL DISORDER, NONSYNDROMIC CONGENITAL, 9	CTD_diseases	4
OMIM:614166	OMIM:614166	MYOPIA 20, AUTOSOMAL DOMINANT	CTD_diseases	4
OMIM:614227	OMIM:614227	HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 3	CTD_diseases	4
MESH:C567276	MESH:C567276	Coumarin Sensitivity	CTD_diseases	4
MESH:C567289	MESH:C567289	Chromosome 2p16.1-P15 Deletion Syndrome	CTD_diseases	4
MESH:C567291	MESH:C567291	Chromosome 1q21.1 Deletion Syndrome, 1.35-Mb	CTD_diseases	4
MESH:C567298	MESH:C567298	Craniofaciofrontodigital Syndrome	CTD_diseases	4
MESH:C567300	MESH:C567300	Skin/Hair/Eye Pigmentation, Variation In, 4	CTD_diseases	4
MESH:C567306	MESH:C567306	Skeletal Defects, Genital Hypoplasia, And Mental Retardation	CTD_diseases	4
MESH:C567313	MESH:C567313	Leukodystrophy, Hypomyelinating, with Hypodontia and Hypogonadotropic Hypogonadism	CTD_diseases	4
MESH:C567337	MESH:C567337	Cowden-Like Syndrome	CTD_diseases	4
MESH:C567341	MESH:C567341	Thrombophilia, Familial, Due To Decreased Release Of Tissue Plasminogen Activator	CTD_diseases	4
MESH:C567344	MESH:C567344	Chromosome 2q31.2 Deletion Syndrome	CTD_diseases	4
MESH:C567346	MESH:C567346	Chromosome 1q43-Q44 Deletion Syndrome	CTD_diseases	4
MESH:C567350	MESH:C567350	Chromosome 2q32-Q33 Deletion Syndrome	CTD_diseases	4
MESH:C567358	MESH:C567358	Joubert Syndrome 8	CTD_diseases	4
MESH:C567360	MESH:C567360	Progeroid Syndrome, Congenital, Petty Type	CTD_diseases	4
MESH:C567364	MESH:C567364	Joubert Syndrome 9	CTD_diseases	4
MESH:C567365	MESH:C567365	Meckel Syndrome, Type 6	CTD_diseases	4
MESH:C567374	MESH:C567374	Skin/Hair/Eye Pigmentation, Variation In, 11	CTD_diseases	4
MESH:C567376	MESH:C567376	Skin/Hair/Eye Pigmentation, Variation In, 10	CTD_diseases	4
MESH:C567390	MESH:C567390	Leukodystrophy, Hypomyelinating, 4	CTD_diseases	4
MESH:C567398	MESH:C567398	Lymphedema, Cardiac Septal Defects, And Characteristic Facies	CTD_diseases	4
MESH:C567416	MESH:C567416	Oculoauricular Syndrome	CTD_diseases	4
MESH:C567418	MESH:C567418	Trichoepithelioma, Multiple Familial, 2	CTD_diseases	4
MESH:C567421	MESH:C567421	Otosclerosis 8	CTD_diseases	4
MESH:C567434	MESH:C567434	Cataract, Juvenile, With Microcornea And Glucosuria	CTD_diseases	4
MESH:C567439	MESH:C567439	Chromosome 15q13.3 Microdeletion Syndrome	CTD_diseases	4
MESH:C567443	MESH:C567443	Ichthyosis, X-Linked, Complicated	CTD_diseases	4
MESH:C567444	MESH:C567444	Congenital Heart Defects, X-Linked	CTD_diseases	4
MESH:C567445	MESH:C567445	Hunter-Macdonald Syndrome	CTD_diseases	4
MESH:C567446	MESH:C567446	Stevenson-Carey Syndrome	CTD_diseases	4
MESH:C567452	MESH:C567452	Lymphedema, Hereditary, IB	CTD_diseases	4
MESH:C567461	MESH:C567461	Surfactant Metabolism Dysfunction, Pulmonary, 4	CTD_diseases	4
MESH:C567462	MESH:C567462	Hypospadias 2, X-Linked	CTD_diseases	4
MESH:C567463	MESH:C567463	Alzheimer Disease 16	CTD_diseases	4
MESH:C567464	MESH:C567464	Protoporphyria, Erythropoietic, X-Linked Dominant	CTD_diseases	4
MESH:C567465	MESH:C567465	Spastic Paraplegia 34, X-Linked	CTD_diseases	4
MESH:C567467	MESH:C567467	Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities	CTD_diseases	4
MESH:C567468	MESH:C567468	Myopathy, Reducing Body, X-Linked, Childhood-Onset	CTD_diseases	4
MESH:C567469	MESH:C567469	Myopathy, Reducing Body, X-Linked, Early-Onset, Severe	CTD_diseases	4
MESH:C567471	MESH:C567471	Craniofacioskeletal Syndrome	CTD_diseases	4
MESH:C567475	MESH:C567475	Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations	CTD_diseases	4
MESH:C567476	MESH:C567476	Mental Retardation, X-Linked, Syndromic, Turner Type	CTD_diseases	4
MESH:C567477	MESH:C567477	Prostate Cancer, Hereditary, X-Linked 2	CTD_diseases	4
MESH:C567478	MESH:C567478	Spinocerebellar Ataxia, X-Linked 5	CTD_diseases	4
MESH:C567482	MESH:C567482	Hypospadias 1, X-Linked	CTD_diseases	4
MESH:C567484	MESH:C567484	Mental Retardation, X-Linked, Syndromic, Christianson Type	CTD_diseases	4
MESH:C567485	MESH:C567485	Mental Retardation, X-Linked, With Panhypopituitarism	CTD_diseases	4
MESH:C567490	MESH:C567490	Diarrhea 3, Secretory Sodium, Congenital, Syndromic	CTD_diseases	4
MESH:C567491	MESH:C567491	Renal Tubular Dysgenesis With Choanal Atresia And Athelia	CTD_diseases	4
MESH:C567492	MESH:C567492	Pituitary Hormone Deficiency, Combined, 4	CTD_diseases	4
MESH:C567502	MESH:C567502	Lethal Arthrogryposis With Anterior Horn Cell Disease	CTD_diseases	4
MESH:C567503	MESH:C567503	Mesomelic Dysplasia, Camera Type	CTD_diseases	4
MESH:C567510	MESH:C567510	Prostate Cancer, Hereditary, 12	CTD_diseases	4
MESH:C567511	MESH:C567511	Chromosome 22q11.2 Deletion Syndrome, Distal	CTD_diseases	4
MESH:C567516	MESH:C567516	Temple-Baraitser Syndrome	CTD_diseases	4
MESH:C567533	MESH:C567533	Anemia, Nonspherocytic Hemolytic, Due To G6pd Deficiency	CTD_diseases	4
MESH:C567551	MESH:C567551	Spondyloepimetaphyseal Dysplasia, Pakistani Type	CTD_diseases	4
MESH:C567552	MESH:C567552	Spondylodysplasia And Premature Pubarche	CTD_diseases	4
MESH:C567555	MESH:C567555	Leukocyte Adhesion Deficiency, Type III	CTD_diseases	4
MESH:C567558	MESH:C567558	Spondyloepimetaphyseal Dysplasia, Aggrecan Type	CTD_diseases	4
MESH:C567566	MESH:C567566	Hypotonia, Seizures, And Precocious Puberty	CTD_diseases	4
MESH:C567570	MESH:C567570	Mitchell-Riley Syndrome	CTD_diseases	4
MESH:C567572	MESH:C567572	Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement	CTD_diseases	4
MESH:C567579	MESH:C567579	Glycogen Storage Disease, Type IXA2	CTD_diseases	4
MESH:C567580	MESH:C567580	Chromosome Xq28 Duplication Syndrome	CTD_diseases	4
MESH:C567581	MESH:C567581	Thrombophilia, X-Linked, Due To Factor Ix Defect	CTD_diseases	4
MESH:C567582	MESH:C567582	Joubert Syndrome 10	CTD_diseases	4
MESH:C567583	MESH:C567583	Mental Retardation, X-Linked, Znf711-Related	CTD_diseases	4
MESH:C567585	MESH:C567585	Chromosome Xp11.23-P11.22 Duplication Syndrome	CTD_diseases	4
MESH:C567586	MESH:C567586	Mental Retardation, X-Linked, Syndromic, Zdhhc9-Related	CTD_diseases	4
MESH:C567595	MESH:C567595	Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness	CTD_diseases	4
MESH:C567596	MESH:C567596	Mineralocorticoid Deficiency, Isolated	CTD_diseases	4
MESH:C567605	MESH:C567605	Oculodentodigital Dysplasia, Autosomal Recessive	CTD_diseases	4
MESH:C567606	MESH:C567606	Myopia 18, Autosomal Recessive	CTD_diseases	4
MESH:C567618	MESH:C567618	Bronchiectasis With Or Without Elevated Sweat Chloride 1	CTD_diseases	4
MESH:C567624	MESH:C567624	Mitochondrial Dna Depletion Syndrome, Encephalomyopathic Form, With Methylmalonic Aciduria, Autosoma	CTD_diseases	4
MESH:C567626	MESH:C567626	Chromosome 3q29 Duplication Syndrome	CTD_diseases	4
MESH:C567640	MESH:C567640	Plasminogen Activator Inhibitor-1 Deficiency	CTD_diseases	4
MESH:C567644	MESH:C567644	Chondrodysplasia, Megarbane-Dagher-Melki Type	CTD_diseases	4
MESH:C567666	MESH:C567666	Fibrosis of Extraocular Muscles, Congenital, 3C	CTD_diseases	4
MESH:C567704	MESH:C567704	CSNB1C	CTD_diseases	4
MESH:C567705	MESH:C567705	Chromosome 17p13.3 Duplication Syndrome	CTD_diseases	4
MESH:C567710	MESH:C567710	Weill-Marchesani-Like Syndrome	CTD_diseases	4
MESH:C567717	MESH:C567717	Chromosome 5p13 Duplication Syndrome	CTD_diseases	4
MESH:C567719	MESH:C567719	Dystransthyretinemic Euthyroidal Hyperthyroxinemia	CTD_diseases	4
MESH:C567731	MESH:C567731	Hydrops Fetalis, Nonimmune, With Gracile Bones And Dysmorphic Features	CTD_diseases	4
MESH:C567737	MESH:C567737	Thrombophilia Due To Elevated Histidine-Rich Glycoprotein	CTD_diseases	4
MESH:C567739	MESH:C567739	Fibrosis of Extraocular Muscles, Congenital, 3B	CTD_diseases	4
MESH:C567753	MESH:C567753	Glaucoma 1, Open Angle, O	CTD_diseases	4
MESH:C567759	MESH:C567759	Achromatopsia 5	CTD_diseases	4
MESH:C567760	MESH:C567760	Hyperuricemic Nephropathy, Familial Juvenile 2	CTD_diseases	4
MESH:C567761	MESH:C567761	Asphyxiating Thoracic Dystrophy 3	CTD_diseases	4
MESH:C567765	MESH:C567765	Glaucoma 3, Primary Congenital, D	CTD_diseases	4
MESH:C567767	MESH:C567767	Nijmegen Breakage Syndrome-Like Disorder	CTD_diseases	4
MESH:C567768	MESH:C567768	Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5	CTD_diseases	4
MESH:C567769	MESH:C567769	Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay	CTD_diseases	4
MESH:C567772	MESH:C567772	Bronchiectasis With Or Without Elevated Sweat Chloride 3	CTD_diseases	4
MESH:C567784	MESH:C567784	3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency	CTD_diseases	4
MESH:C567786	MESH:C567786	Prostaglandin-Endoperoxide Synthase 1 Deficiency, Platelet	CTD_diseases	4
MESH:C567803	MESH:C567803	Pituitary Hormone Deficiency, Combined, 1	CTD_diseases	4
MESH:C567804	MESH:C567804	Dursun Syndrome	CTD_diseases	4
MESH:C567810	MESH:C567810	Chromosome 19q13.11 Deletion Syndrome	CTD_diseases	4
MESH:C567813	MESH:C567813	Bronchiectasis With Or Without Elevated Sweat Chloride 2	CTD_diseases	4
MESH:C567814	MESH:C567814	Cataract, Age-Related Cortical, 2	CTD_diseases	4
MESH:C567815	MESH:C567815	Lymphoproliferative Syndrome, Ebv-Associated, Autosomal, 1	CTD_diseases	4
MESH:C567819	MESH:C567819	Santos Syndrome	CTD_diseases	4
MESH:C567835	MESH:C567835	Cataract, Autosomal Recessive Congenital 3	CTD_diseases	4
MESH:C567845	MESH:C567845	Leukoencephalopathy, Cystic, Without Megalencephaly	CTD_diseases	4
MESH:C567847	MESH:C567847	Hypomyelination, Global Cerebral	CTD_diseases	4
MESH:C567849	MESH:C567849	Microcephaly, Growth Retardation, Cataract, Hearing Loss, And Unusual Appearance	CTD_diseases	4
MESH:C567850	MESH:C567850	Hadziselimovic Syndrome	CTD_diseases	4
MESH:C567856	MESH:C567856	Growth Retardation, Developmental Delay, Coarse Facies, And Early Death	CTD_diseases	4
MESH:C567863	MESH:C567863	Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi	CTD_diseases	4
MESH:C567865	MESH:C567865	Zechi-Ceide Syndrome	CTD_diseases	4
MESH:C567878	MESH:C567878	Erythrocyte Amp Deaminase Deficiency	CTD_diseases	4
MESH:C567932	MESH:C567932	Opitz GBBB Syndrome, X-Linked	CTD_diseases	4
MESH:C571912	MESH:C571912	Inhalation anthrax	CTD_diseases	4
MESH:C573722	MESH:C573722	Acrocephalopolydactylous Dysplasia	CTD_diseases	4
MESH:C576084	MESH:C576084	Bleeding Disorder Due To P2rx1 Defect	CTD_diseases	4
MESH:C579395	MESH:C579395	Ruvalcaba Syndrome	CTD_diseases	4
MESH:C579849	MESH:C579849	15q24 Microdeletion	CTD_diseases	4
MESH:C579850	MESH:C579850	16p11.2 Deletion Syndrome	CTD_diseases	4
MESH:C579867	MESH:C579867	3-Methylglutaconic Aciduria	CTD_diseases	4
MESH:C579873	MESH:C579873	9q22.3 Microdeletion	CTD_diseases	4
MESH:C579922	MESH:C579922	Ataxia Neuropathy Spectrum	CTD_diseases	4
MESH:C579990	MESH:C579990	Childhood Myocerebrohepatopathy Spectrum	CTD_diseases	4
MESH:C580002	MESH:C580002	Combined Malonic and Methylmalonic Aciduria	CTD_diseases	4
MESH:C580012	MESH:C580012	Congenital Fibrosis of the Extraocular Muscles	CTD_diseases	4
MESH:C580039	MESH:C580039	Deoxyguanosine Kinase Deficiency	CTD_diseases	4
MESH:C580055	MESH:C580055	Early-Onset Glaucoma	CTD_diseases	4
MESH:C580102	MESH:C580102	Fatty Acid Hydroxylase-Associated Neurodegeneration	CTD_diseases	4
MESH:C580174	MESH:C580174	Huntington Disease-Like Syndrome	CTD_diseases	4
MESH:C580192	MESH:C580192	Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome	CTD_diseases	4
MESH:C580205	MESH:C580205	Isodicentric Chromosome 15 Syndrome	CTD_diseases	4
MESH:C580212	MESH:C580212	Agenesis of Cerebellar Vermis	CTD_diseases	4
MESH:C580224	MESH:C580224	Keratitis-Ichthyosis-Deafness Syndrome	CTD_diseases	4
MESH:C580280	MESH:C580280	Congenital Methemoglobinemia	CTD_diseases	4
MESH:C580305	MESH:C580305	Multiple Cutaneous and Mucosal Venous Malformations	CTD_diseases	4
MESH:C580430	MESH:C580430	Salih Myopathy	CTD_diseases	4
MESH:C580439	MESH:C580439	Short Qt Syndrome	CTD_diseases	4
MESH:C580472	MESH:C580472	Stickler Syndrome	CTD_diseases	4
MESH:C580473	MESH:C580473	Succinate-Coa Ligase Deficiency	CTD_diseases	4
MESH:C580477	MESH:C580477	Surfactant Dysfunction	CTD_diseases	4
MESH:C580533	MESH:C580533	X-Linked Chondrodysplasia Punctata 1	CTD_diseases	4
MESH:C580539	MESH:C580539	X-Linked Infantile Nystagmus	CTD_diseases	4
MESH:C581942	MESH:C581942	Hemoglobin M Disease	CTD_diseases	4
MESH:D000026	MESH:D000026	Abortion, Habitual	CTD_diseases	4
MESH:D000027	MESH:D000027	Abortion, Incomplete	CTD_diseases	4
MESH:D000030	MESH:D000030	Abortion, Missed	CTD_diseases	4
MESH:D000031	MESH:D000031	Abortion, Septic	CTD_diseases	4
MESH:D000033	MESH:D000033	Abortion, Threatened	CTD_diseases	4
MESH:D000037	MESH:D000037	Abruptio Placentae	CTD_diseases	4
MESH:D000126	MESH:D000126	Achlorhydria	CTD_diseases	4
MESH:D000138	MESH:D000138	Acidosis	CTD_diseases	4
MESH:D000142	MESH:D000142	Acidosis, Respiratory	CTD_diseases	4
MESH:D000152	MESH:D000152	Acne Vulgaris	CTD_diseases	4
MESH:D000169	MESH:D000169	Acrodermatitis	CTD_diseases	4
MESH:D000170	MESH:D000170	Acrodynia	CTD_diseases	4
MESH:D000172	MESH:D000172	Acromegaly	CTD_diseases	4
MESH:D000193	MESH:D000193	Actinomycetales Infections	CTD_diseases	4
MESH:D000208	MESH:D000208	Acute Disease	CTD_diseases	4
MESH:D000210	MESH:D000210	Acute-Phase Reaction	CTD_diseases	4
MESH:D000235	MESH:D000235	Adenolymphoma	CTD_diseases	4
MESH:D000236	MESH:D000236	Adenoma	CTD_diseases	4
MESH:D000258	MESH:D000258	Adenovirus Infections, Human	CTD_diseases	4
MESH:D000291	MESH:D000291	Adnexal Diseases	CTD_diseases	4
MESH:D000292	MESH:D000292	Pelvic Inflammatory Disease	CTD_diseases	4
MESH:D000306	MESH:D000306	Adrenal Cortex Neoplasms	CTD_diseases	4
MESH:D000326	MESH:D000326	Adrenoleukodystrophy	CTD_diseases	4
MESH:D000334	MESH:D000334	Aerophagy	CTD_diseases	4
MESH:D000343	MESH:D000343	Afferent Loop Syndrome	CTD_diseases	4
MESH:D000347	MESH:D000347	Afibrinogenemia	CTD_diseases	4
MESH:D000387	MESH:D000387	Ainhum	CTD_diseases	4
MESH:D000402	MESH:D000402	Airway Obstruction	CTD_diseases	4
MESH:D000405	MESH:D000405	Akinetic Mutism	CTD_diseases	4
MESH:D000417	MESH:D000417	Albinism	CTD_diseases	4
MESH:D000425	MESH:D000425	Alcohol Amnestic Disorder	CTD_diseases	4
MESH:D000430	MESH:D000430	Alcohol Withdrawal Delirium	CTD_diseases	4
MESH:D000435	MESH:D000435	Alcoholic Intoxication	CTD_diseases	4
MESH:D000437	MESH:D000437	Alcoholism	CTD_diseases	4
MESH:D000471	MESH:D000471	Alkalosis	CTD_diseases	4
MESH:D000507	MESH:D000507	Mucinosis, Follicular	CTD_diseases	4
MESH:D000542	MESH:D000542	Alveolitis, Extrinsic Allergic	CTD_diseases	4
MESH:D000544	MESH:D000544	Alzheimer Disease	CTD_diseases	4
MESH:D000550	MESH:D000550	Amblyopia	CTD_diseases	4
MESH:D000564	MESH:D000564	Ameloblastoma	CTD_diseases	4
MESH:D000568	MESH:D000568	Amenorrhea	CTD_diseases	4
MESH:D000592	MESH:D000592	Amino Acid Metabolism, Inborn Errors	CTD_diseases	4
MESH:D000686	MESH:D000686	Amyloidosis	CTD_diseases	4
MESH:D000690	MESH:D000690	Amyotrophic Lateral Sclerosis	CTD_diseases	4
MESH:D000707	MESH:D000707	Anaphylaxis	CTD_diseases	4
MESH:D000708	MESH:D000708	Anaplasia	CTD_diseases	4
MESH:D000711	MESH:D000711	Anaplasmataceae Infections	CTD_diseases	4
MESH:D000741	MESH:D000741	Anemia, Aplastic	CTD_diseases	4
MESH:D000743	MESH:D000743	Anemia, Hemolytic	CTD_diseases	4
MESH:D000747	MESH:D000747	Anemia, Hypochromic	CTD_diseases	4
MESH:D000748	MESH:D000748	Anemia, Macrocytic	CTD_diseases	4
MESH:D000750	MESH:D000750	Anemia, Myelophthisic	CTD_diseases	4
MESH:D000753	MESH:D000753	Anemia, Refractory	CTD_diseases	4
MESH:D000755	MESH:D000755	Anemia, Sickle Cell	CTD_diseases	4
MESH:D000756	MESH:D000756	Anemia, Sideroblastic	CTD_diseases	4
MESH:D000757	MESH:D000757	Anencephaly	CTD_diseases	4
MESH:D000782	MESH:D000782	Aneuploidy	CTD_diseases	4
MESH:D000784	MESH:D000784	Aneurysm, Dissecting	CTD_diseases	4
MESH:D000787	MESH:D000787	Angina Pectoris	CTD_diseases	4
MESH:D000794	MESH:D000794	Angiokeratoma	CTD_diseases	4
MESH:D000795	MESH:D000795	Fabry Disease	CTD_diseases	4
MESH:D000853	MESH:D000853	Anophthalmos	CTD_diseases	4
MESH:D000855	MESH:D000855	Anorexia	CTD_diseases	4
MESH:D000860	MESH:D000860	Anoxia	CTD_diseases	4
MESH:D001006	MESH:D001006	Anus, Imperforate	CTD_diseases	4
MESH:D001014	MESH:D001014	Aortic Aneurysm	CTD_diseases	4
MESH:D001015	MESH:D001015	Aortic Arch Syndromes	CTD_diseases	4
MESH:D001022	MESH:D001022	Aortic Valve Insufficiency	CTD_diseases	4
MESH:D001024	MESH:D001024	Aortic Valve Stenosis	CTD_diseases	4
MESH:D001025	MESH:D001025	Aortitis	CTD_diseases	4
MESH:D001036	MESH:D001036	Aphakia, Postcataract	CTD_diseases	4
MESH:D001064	MESH:D001064	Appendicitis	CTD_diseases	4
MESH:D001098	MESH:D001098	Spider Bites	CTD_diseases	4
MESH:D001112	MESH:D001112	Arcus Senilis	CTD_diseases	4
MESH:D001146	MESH:D001146	Arrhythmia, Sinus	CTD_diseases	4
MESH:D001161	MESH:D001161	Arteriosclerosis	CTD_diseases	4
MESH:D001169	MESH:D001169	Arthritis, Experimental	CTD_diseases	4
MESH:D001183	MESH:D001183	Arthus Reaction	CTD_diseases	4
MESH:D001281	MESH:D001281	Atrial Fibrillation	CTD_diseases	4
MESH:D001282	MESH:D001282	Atrial Flutter	CTD_diseases	4
MESH:D001289	MESH:D001289	Attention Deficit Disorder with Hyperactivity	CTD_diseases	4
MESH:D001304	MESH:D001304	Auditory Diseases, Central	CTD_diseases	4
MESH:D001308	MESH:D001308	Auditory Perceptual Disorders	CTD_diseases	4
MESH:D001321	MESH:D001321	Autistic Disorder	CTD_diseases	4
MESH:D001446	MESH:D001446	Balanitis	CTD_diseases	4
MESH:D001447	MESH:D001447	Balantidiasis	CTD_diseases	4
MESH:D001471	MESH:D001471	Barrett Esophagus	CTD_diseases	4
MESH:D001476	MESH:D001476	Bartonellaceae Infections	CTD_diseases	4
MESH:D001478	MESH:D001478	Basal Cell Nevus Syndrome	CTD_diseases	4
MESH:D001480	MESH:D001480	Basal Ganglia Diseases	CTD_diseases	4
MESH:D001506	MESH:D001506	Beckwith-Wiedemann Syndrome	CTD_diseases	4
MESH:D001606	MESH:D001606	Bernard-Soulier Syndrome	CTD_diseases	4
MESH:D001650	MESH:D001650	Bile Duct Neoplasms	CTD_diseases	4
MESH:D001656	MESH:D001656	Biliary Atresia	CTD_diseases	4
MESH:D001714	MESH:D001714	Bipolar Disorder	CTD_diseases	4
MESH:D001724	MESH:D001724	Birth Weight	CTD_diseases	4
MESH:D001734	MESH:D001734	Bites, Human	CTD_diseases	4
MESH:D001745	MESH:D001745	Urinary Bladder Diseases	CTD_diseases	4
MESH:D001746	MESH:D001746	Bladder Exstrophy	CTD_diseases	4
MESH:D001750	MESH:D001750	Urinary Bladder, Neurogenic	CTD_diseases	4
MESH:D001816	MESH:D001816	Bloom Syndrome	CTD_diseases	4
MESH:D001836	MESH:D001836	Body Weight Changes	CTD_diseases	4
MESH:D001885	MESH:D001885	Bordetella Infections	CTD_diseases	4
MESH:D001899	MESH:D001899	Borrelia Infections	CTD_diseases	4
MESH:D001906	MESH:D001906	Botulism	CTD_diseases	4
MESH:D001919	MESH:D001919	Bradycardia	CTD_diseases	4
MESH:D001925	MESH:D001925	Brain Damage, Chronic	CTD_diseases	4
MESH:D001926	MESH:D001926	Brain Death	CTD_diseases	4
MESH:D001929	MESH:D001929	Brain Edema	CTD_diseases	4
MESH:D001930	MESH:D001930	Brain Injuries	CTD_diseases	4
MESH:D001932	MESH:D001932	Brain Neoplasms	CTD_diseases	4
MESH:D001935	MESH:D001935	Branchioma	CTD_diseases	4
MESH:D001946	MESH:D001946	Breech Presentation	CTD_diseases	4
MESH:D001997	MESH:D001997	Bronchopulmonary Dysplasia	CTD_diseases	4
MESH:D001998	MESH:D001998	Bronchopulmonary Sequestration	CTD_diseases	4
MESH:D002006	MESH:D002006	Brucellosis	CTD_diseases	4
MESH:D002102	MESH:D002102	Cadaver	CTD_diseases	4
MESH:D002114	MESH:D002114	Calcinosis	CTD_diseases	4
MESH:D002145	MESH:D002145	Callosities	CTD_diseases	4
MESH:D002169	MESH:D002169	Campylobacter Infections	CTD_diseases	4
MESH:D002178	MESH:D002178	Candidiasis, Chronic Mucocutaneous	CTD_diseases	4
MESH:D002179	MESH:D002179	Candidiasis, Cutaneous	CTD_diseases	4
MESH:D002181	MESH:D002181	Candidiasis, Vulvovaginal	CTD_diseases	4
MESH:D002239	MESH:D002239	Carbohydrate Metabolism, Inborn Errors	CTD_diseases	4
MESH:D002249	MESH:D002249	Carbon Monoxide Poisoning	CTD_diseases	4
MESH:D002277	MESH:D002277	Carcinoma	CTD_diseases	4
MESH:D002296	MESH:D002296	Carcinosarcoma	CTD_diseases	4
MESH:D002310	MESH:D002310	Cardiomyopathy, Alcoholic	CTD_diseases	4
MESH:D002311	MESH:D002311	Cardiomyopathy, Dilated	CTD_diseases	4
MESH:D002312	MESH:D002312	Cardiomyopathy, Hypertrophic	CTD_diseases	4
MESH:D002313	MESH:D002313	Cardiomyopathy, Restrictive	CTD_diseases	4
MESH:D002349	MESH:D002349	Carpal Tunnel Syndrome	CTD_diseases	4
MESH:D002372	MESH:D002372	Cat-Scratch Disease	CTD_diseases	4
MESH:D002388	MESH:D002388	Catastrophic Illness	CTD_diseases	4
MESH:D002429	MESH:D002429	Cecal Diseases	CTD_diseases	4
MESH:D002485	MESH:D002485	Cementoma	CTD_diseases	4
MESH:D002526	MESH:D002526	Cerebellar Diseases	CTD_diseases	4
MESH:D002532	MESH:D002532	Intracranial Aneurysm	CTD_diseases	4
MESH:D002534	MESH:D002534	Hypoxia, Brain	CTD_diseases	4
MESH:D002549	MESH:D002549	Diffuse Cerebral Sclerosis of Schilder	CTD_diseases	4
MESH:D002558	MESH:D002558	Cerebrospinal Fluid Otorrhea	CTD_diseases	4
MESH:D002559	MESH:D002559	Cerebrospinal Fluid Rhinorrhea	CTD_diseases	4
MESH:D002573	MESH:D002573	Cervical Rib Syndrome	CTD_diseases	4
MESH:D002598	MESH:D002598	Chagas Cardiomyopathy	CTD_diseases	4
MESH:D002613	MESH:D002613	Cheilitis	CTD_diseases	4
MESH:D002644	MESH:D002644	Chickenpox	CTD_diseases	4
MESH:D002694	MESH:D002694	Chlamydiaceae Infections	CTD_diseases	4
MESH:D002761	MESH:D002761	Cholangitis	CTD_diseases	4
MESH:D002764	MESH:D002764	Cholecystitis	CTD_diseases	4
MESH:D002779	MESH:D002779	Cholestasis	CTD_diseases	4
MESH:D002781	MESH:D002781	Cholesteatoma	CTD_diseases	4
MESH:D002805	MESH:D002805	Chondrocalcinosis	CTD_diseases	4
MESH:D002817	MESH:D002817	Chordoma	CTD_diseases	4
MESH:D002821	MESH:D002821	Chorioamnionitis	CTD_diseases	4
MESH:D002825	MESH:D002825	Chorioretinitis	CTD_diseases	4
MESH:D002830	MESH:D002830	Choroid Neoplasms	CTD_diseases	4
MESH:D002832	MESH:D002832	Choroid Hemorrhage	CTD_diseases	4
MESH:D002833	MESH:D002833	Choroiditis	CTD_diseases	4
MESH:D002836	MESH:D002836	Hemophilia B	CTD_diseases	4
MESH:D002908	MESH:D002908	Chronic Disease	CTD_diseases	4
MESH:D002921	MESH:D002921	Cicatrix	CTD_diseases	4
MESH:D002971	MESH:D002971	Cleft Lip	CTD_diseases	4
MESH:D003003	MESH:D003003	Clonorchiasis	CTD_diseases	4
MESH:D003015	MESH:D003015	Clostridium Infections	CTD_diseases	4
MESH:D003057	MESH:D003057	Cockayne Syndrome	CTD_diseases	4
MESH:D003092	MESH:D003092	Colitis	CTD_diseases	4
MESH:D003103	MESH:D003103	Coloboma	CTD_diseases	4
MESH:D003108	MESH:D003108	Colonic Diseases	CTD_diseases	4
MESH:D003121	MESH:D003121	Colorado Tick Fever	CTD_diseases	4
MESH:D003123	MESH:D003123	Colorectal Neoplasms, Hereditary Nonpolyposis	CTD_diseases	4
MESH:D003130	MESH:D003130	Combat Disorders	CTD_diseases	4
MESH:D003137	MESH:D003137	Common Bile Duct Diseases	CTD_diseases	4
MESH:D003139	MESH:D003139	Common Cold	CTD_diseases	4
MESH:D003233	MESH:D003233	Conjunctivitis, Allergic	CTD_diseases	4
MESH:D003234	MESH:D003234	Conjunctivitis, Bacterial	CTD_diseases	4
MESH:D003236	MESH:D003236	Conjunctivitis, Viral	CTD_diseases	4
MESH:D003248	MESH:D003248	Constipation	CTD_diseases	4
MESH:D003289	MESH:D003289	Convalescence	CTD_diseases	4
MESH:D003320	MESH:D003320	Corneal Ulcer	CTD_diseases	4
MESH:D003323	MESH:D003323	Coronary Aneurysm	CTD_diseases	4
MESH:D003327	MESH:D003327	Coronary Disease	CTD_diseases	4
MESH:D003333	MESH:D003333	Coronaviridae Infections	CTD_diseases	4
MESH:D003409	MESH:D003409	Congenital Hypothyroidism	CTD_diseases	4
MESH:D003410	MESH:D003410	Cri-du-Chat Syndrome	CTD_diseases	4
MESH:D003456	MESH:D003456	Cryptorchidism	CTD_diseases	4
MESH:D003457	MESH:D003457	Cryptosporidiosis	CTD_diseases	4
MESH:D003480	MESH:D003480	Cushing Syndrome	CTD_diseases	4
MESH:D003586	MESH:D003586	Cytomegalovirus Infections	CTD_diseases	4
MESH:D003616	MESH:D003616	Dandy-Walker Syndrome	CTD_diseases	4
MESH:D003635	MESH:D003635	De Lange Syndrome	CTD_diseases	4
MESH:D003645	MESH:D003645	Death, Sudden	CTD_diseases	4
MESH:D003649	MESH:D003649	Decalcification, Pathologic	CTD_diseases	4
MESH:D003655	MESH:D003655	Decerebrate State	CTD_diseases	4
MESH:D003668	MESH:D003668	Pressure Ulcer	CTD_diseases	4
MESH:D003677	MESH:D003677	Deficiency Diseases	CTD_diseases	4
MESH:D003728	MESH:D003728	Dental Calculus	CTD_diseases	4
MESH:D003731	MESH:D003731	Dental Caries	CTD_diseases	4
MESH:D003769	MESH:D003769	Dental Occlusion, Traumatic	CTD_diseases	4
MESH:D003773	MESH:D003773	Dental Plaque	CTD_diseases	4
MESH:D003784	MESH:D003784	Dental Pulp Calcification	CTD_diseases	4
MESH:D003789	MESH:D003789	Dental Pulp Exposure	CTD_diseases	4
MESH:D003790	MESH:D003790	Dental Pulp Necrosis	CTD_diseases	4
MESH:D003809	MESH:D003809	Dentin, Secondary	CTD_diseases	4
MESH:D003865	MESH:D003865	Depressive Disorder, Major	CTD_diseases	4
MESH:D003873	MESH:D003873	Dermatitis, Exfoliative	CTD_diseases	4
MESH:D003875	MESH:D003875	Drug Eruptions	CTD_diseases	4
MESH:D003876	MESH:D003876	Dermatitis, Atopic	CTD_diseases	4
MESH:D003877	MESH:D003877	Dermatitis, Contact	CTD_diseases	4
MESH:D003884	MESH:D003884	Dermoid Cyst	CTD_diseases	4
MESH:D003914	MESH:D003914	Dextrocardia	CTD_diseases	4
MESH:D003929	MESH:D003929	Diabetic Neuropathies	CTD_diseases	4
MESH:D003965	MESH:D003965	Diaphragmatic Eventration	CTD_diseases	4
MESH:D003967	MESH:D003967	Diarrhea	CTD_diseases	4
MESH:D003970	MESH:D003970	Diastema	CTD_diseases	4
MESH:D004011	MESH:D004011	Dicrocoeliasis	CTD_diseases	4
MESH:D004022	MESH:D004022	Dictyocaulus Infections	CTD_diseases	4
MESH:D004057	MESH:D004057	Hyperostosis, Diffuse Idiopathic Skeletal	CTD_diseases	4
MESH:D004169	MESH:D004169	Diphyllobothriasis	CTD_diseases	4
MESH:D004184	MESH:D004184	Dirofilariasis	CTD_diseases	4
MESH:D004198	MESH:D004198	Disease Susceptibility	CTD_diseases	4
MESH:D004200	MESH:D004200	Diseases in Twins	CTD_diseases	4
MESH:D004211	MESH:D004211	Disseminated Intravascular Coagulation	CTD_diseases	4
MESH:D004238	MESH:D004238	Diverticulitis	CTD_diseases	4
MESH:D004241	MESH:D004241	Diverticulum, Colon	CTD_diseases	4
MESH:D004313	MESH:D004313	Dourine	CTD_diseases	4
MESH:D004314	MESH:D004314	Down Syndrome	CTD_diseases	4
MESH:D004370	MESH:D004370	Duane Retraction Syndrome	CTD_diseases	4
MESH:D004378	MESH:D004378	Duodenal Diseases	CTD_diseases	4
MESH:D004383	MESH:D004383	Duodenogastric Reflux	CTD_diseases	4
MESH:D004393	MESH:D004393	Dwarfism, Pituitary	CTD_diseases	4
MESH:D004402	MESH:D004402	Dysautonomia, Familial	CTD_diseases	4
MESH:D004403	MESH:D004403	Dysentery	CTD_diseases	4
MESH:D004404	MESH:D004404	Dysentery, Amebic	CTD_diseases	4
MESH:D004412	MESH:D004412	Dysmenorrhea	CTD_diseases	4
MESH:D004413	MESH:D004413	Dysostoses	CTD_diseases	4
MESH:D004414	MESH:D004414	Dyspareunia	CTD_diseases	4
MESH:D004415	MESH:D004415	Dyspepsia	CTD_diseases	4
MESH:D004416	MESH:D004416	Dysplastic Nevus Syndrome	CTD_diseases	4
MESH:D004418	MESH:D004418	Dyspnea, Paroxysmal	CTD_diseases	4
MESH:D004420	MESH:D004420	Dystocia	CTD_diseases	4
MESH:D004422	MESH:D004422	Dystonia Musculorum Deformans	CTD_diseases	4
MESH:D004438	MESH:D004438	Ecchymosis	CTD_diseases	4
MESH:D004443	MESH:D004443	Echinococcosis	CTD_diseases	4
MESH:D004444	MESH:D004444	Echinococcosis, Hepatic	CTD_diseases	4
MESH:D004451	MESH:D004451	Echinostomiasis	CTD_diseases	4
MESH:D004473	MESH:D004473	Ecthyma	CTD_diseases	4
MESH:D004476	MESH:D004476	Ectodermal Dysplasia	CTD_diseases	4
MESH:D004479	MESH:D004479	Ectopia Lentis	CTD_diseases	4
MESH:D004485	MESH:D004485	Eczema	CTD_diseases	4
MESH:D004489	MESH:D004489	Edema, Cardiac	CTD_diseases	4
MESH:D004535	MESH:D004535	Ehlers-Danlos Syndrome	CTD_diseases	4
MESH:D004604	MESH:D004604	Elephantiasis	CTD_diseases	4
MESH:D004605	MESH:D004605	Elephantiasis, Filarial	CTD_diseases	4
MESH:D004617	MESH:D004617	Embolism	CTD_diseases	4
MESH:D004619	MESH:D004619	Embolism, Amniotic Fluid	CTD_diseases	4
MESH:D004630	MESH:D004630	Emergencies	CTD_diseases	4
MESH:D004660	MESH:D004660	Encephalitis	CTD_diseases	4
MESH:D004670	MESH:D004670	Encephalitis, California	CTD_diseases	4
MESH:D004677	MESH:D004677	Encephalocele	CTD_diseases	4
MESH:D004678	MESH:D004678	Encephalomalacia	CTD_diseases	4
MESH:D004684	MESH:D004684	Leukoencephalitis, Acute Hemorrhagic	CTD_diseases	4
MESH:D004688	MESH:D004688	Encopresis	CTD_diseases	4
MESH:D004695	MESH:D004695	Endocardial Fibroelastosis	CTD_diseases	4
MESH:D004715	MESH:D004715	Endometriosis	CTD_diseases	4
MESH:D004719	MESH:D004719	Endomyocardial Fibrosis	CTD_diseases	4
MESH:D004749	MESH:D004749	Entamoebiasis	CTD_diseases	4
MESH:D004751	MESH:D004751	Enteritis	CTD_diseases	4
MESH:D004753	MESH:D004753	Enteritis, Transmissible, of Turkeys	CTD_diseases	4
MESH:D004756	MESH:D004756	Enterobacteriaceae Infections	CTD_diseases	4
MESH:D004760	MESH:D004760	Enterocolitis	CTD_diseases	4
MESH:D004769	MESH:D004769	Enterovirus Infections	CTD_diseases	4
MESH:D004775	MESH:D004775	Enuresis	CTD_diseases	4
MESH:D004802	MESH:D004802	Eosinophilia	CTD_diseases	4
MESH:D004814	MESH:D004814	Epidermal Cyst	CTD_diseases	4
MESH:D004820	MESH:D004820	Epidermolysis Bullosa	CTD_diseases	4
MESH:D004827	MESH:D004827	Epilepsy	CTD_diseases	4
MESH:D004842	MESH:D004842	Epispadias	CTD_diseases	4
MESH:D004863	MESH:D004863	Equinus Deformity	CTD_diseases	4
MESH:D004884	MESH:D004884	Eructation	CTD_diseases	4
MESH:D004891	MESH:D004891	Erythema Induratum	CTD_diseases	4
MESH:D004892	MESH:D004892	Erythema Multiforme	CTD_diseases	4
MESH:D004893	MESH:D004893	Erythema Nodosum	CTD_diseases	4
MESH:D004916	MESH:D004916	Erythromelalgia	CTD_diseases	4
MESH:D004932	MESH:D004932	Esophageal and Gastric Varices	CTD_diseases	4
MESH:D004933	MESH:D004933	Esophageal Atresia	CTD_diseases	4
MESH:D004934	MESH:D004934	Esophageal Cyst	CTD_diseases	4
MESH:D004936	MESH:D004936	Diverticulum, Esophageal	CTD_diseases	4
MESH:D004937	MESH:D004937	Esophageal Fistula	CTD_diseases	4
MESH:D004938	MESH:D004938	Esophageal Neoplasms	CTD_diseases	4
MESH:D004940	MESH:D004940	Esophageal Stenosis	CTD_diseases	4
MESH:D004941	MESH:D004941	Esophagitis	CTD_diseases	4
MESH:D005058	MESH:D005058	Eunuchism	CTD_diseases	4
MESH:D005077	MESH:D005077	Exanthema Subitum	CTD_diseases	4
MESH:D005096	MESH:D005096	Exostoses	CTD_diseases	4
MESH:D005097	MESH:D005097	Exostoses, Multiple Hereditary	CTD_diseases	4
MESH:D005117	MESH:D005117	Cardiac Complexes, Premature	CTD_diseases	4
MESH:D005151	MESH:D005151	Facial Injuries	CTD_diseases	4
MESH:D005153	MESH:D005153	Facial Neoplasms	CTD_diseases	4
MESH:D005166	MESH:D005166	Factor V Deficiency	CTD_diseases	4
MESH:D005168	MESH:D005168	Factor VII Deficiency	CTD_diseases	4
MESH:D005171	MESH:D005171	Factor X Deficiency	CTD_diseases	4
MESH:D005173	MESH:D005173	Factor XI Deficiency	CTD_diseases	4
MESH:D005175	MESH:D005175	Factor XII Deficiency	CTD_diseases	4
MESH:D005177	MESH:D005177	Factor XIII Deficiency	CTD_diseases	4
MESH:D005199	MESH:D005199	Fanconi Anemia	CTD_diseases	4
MESH:D005211	MESH:D005211	Fascioliasis	CTD_diseases	4
MESH:D005213	MESH:D005213	Fascioloidiasis	CTD_diseases	4
MESH:D005218	MESH:D005218	Fat Necrosis	CTD_diseases	4
MESH:D005222	MESH:D005222	Mental Fatigue	CTD_diseases	4
MESH:D005235	MESH:D005235	Fatty Liver, Alcoholic	CTD_diseases	4
MESH:D005236	MESH:D005236	Favism	CTD_diseases	4
MESH:D005266	MESH:D005266	Femoral Neoplasms	CTD_diseases	4
MESH:D005311	MESH:D005311	Fetal Hypoxia	CTD_diseases	4
MESH:D005317	MESH:D005317	Fetal Growth Retardation	CTD_diseases	4
MESH:D005320	MESH:D005320	Fetal Macrosomia	CTD_diseases	4
MESH:D005322	MESH:D005322	Fetal Membranes, Premature Rupture	CTD_diseases	4
MESH:D005334	MESH:D005334	Fever	CTD_diseases	4
MESH:D005348	MESH:D005348	Fibrocystic Breast Disease	CTD_diseases	4
MESH:D005352	MESH:D005352	Fibromuscular Dysplasia	CTD_diseases	4
MESH:D005356	MESH:D005356	Fibromyalgia	CTD_diseases	4
MESH:D005414	MESH:D005414	Flatulence	CTD_diseases	4
MESH:D005489	MESH:D005489	Focal Dermal Hypoplasia	CTD_diseases	4
MESH:D005497	MESH:D005497	Follicular Cyst	CTD_diseases	4
MESH:D005499	MESH:D005499	Folliculitis	CTD_diseases	4
MESH:D005512	MESH:D005512	Food Hypersensitivity	CTD_diseases	4
MESH:D005533	MESH:D005533	Foot Dermatoses	CTD_diseases	4
MESH:D005621	MESH:D005621	Friedreich Ataxia	CTD_diseases	4
MESH:D005660	MESH:D005660	Funnel Chest	CTD_diseases	4
MESH:D005683	MESH:D005683	Gagging	CTD_diseases	4
MESH:D005706	MESH:D005706	Gallbladder Neoplasms	CTD_diseases	4
MESH:D005734	MESH:D005734	Gangrene	CTD_diseases	4
MESH:D005736	MESH:D005736	Gardner Syndrome	CTD_diseases	4
MESH:D005756	MESH:D005756	Gastritis	CTD_diseases	4
MESH:D005833	MESH:D005833	Genital Neoplasms, Female	CTD_diseases	4
MESH:D005871	MESH:D005871	Giant Lymph Node Hyperplasia	CTD_diseases	4
MESH:D005877	MESH:D005877	Gigantism	CTD_diseases	4
MESH:D005879	MESH:D005879	Tourette Syndrome	CTD_diseases	4
MESH:D005882	MESH:D005882	Gingival Diseases	CTD_diseases	4
MESH:D005902	MESH:D005902	Glaucoma, Open-Angle	CTD_diseases	4
MESH:D005918	MESH:D005918	Glomus Tumor	CTD_diseases	4
MESH:D005926	MESH:D005926	Glossalgia	CTD_diseases	4
MESH:D005928	MESH:D005928	Glossitis	CTD_diseases	4
MESH:D006015	MESH:D006015	Glycogen Storage Disease Type VIII	CTD_diseases	4
MESH:D006029	MESH:D006029	Glycosuria	CTD_diseases	4
MESH:D006043	MESH:D006043	Goiter, Endemic	CTD_diseases	4
MESH:D006044	MESH:D006044	Goiter, Nodular	CTD_diseases	4
MESH:D006045	MESH:D006045	Goiter, Substernal	CTD_diseases	4
MESH:D006073	MESH:D006073	Gout	CTD_diseases	4
MESH:D006083	MESH:D006083	Graft Occlusion, Vascular	CTD_diseases	4
MESH:D006105	MESH:D006105	Granulomatous Disease, Chronic	CTD_diseases	4
MESH:D006175	MESH:D006175	Gynatresia	CTD_diseases	4
MESH:D006177	MESH:D006177	Gynecomastia	CTD_diseases	4
MESH:D006209	MESH:D006209	Halitosis	CTD_diseases	4
MESH:D006211	MESH:D006211	Pantothenate Kinase-Associated Neurodegeneration	CTD_diseases	4
MESH:D006327	MESH:D006327	Heart Block	CTD_diseases	4
MESH:D006342	MESH:D006342	Heart Rupture, Post-Infarction	CTD_diseases	4
MESH:D006356	MESH:D006356	Heartburn	CTD_diseases	4
MESH:D006362	MESH:D006362	Heavy Chain Disease	CTD_diseases	4
MESH:D006391	MESH:D006391	Hemangioma	CTD_diseases	4
MESH:D006393	MESH:D006393	Hemangiopericytoma	CTD_diseases	4
MESH:D006394	MESH:D006394	Hemangiosarcoma	CTD_diseases	4
MESH:D006406	MESH:D006406	Hematoma	CTD_diseases	4
MESH:D006417	MESH:D006417	Hematuria	CTD_diseases	4
MESH:D006431	MESH:D006431	Hemobilia	CTD_diseases	4
MESH:D006445	MESH:D006445	Hemoglobin C Disease	CTD_diseases	4
MESH:D006467	MESH:D006467	Hemophilia A	CTD_diseases	4
MESH:D006473	MESH:D006473	Postpartum Hemorrhage	CTD_diseases	4
MESH:D006478	MESH:D006478	Hemorrhagic Fever, American	CTD_diseases	4
MESH:D006479	MESH:D006479	Hemorrhagic Fever, Crimean	CTD_diseases	4
MESH:D006480	MESH:D006480	Hemorrhagic Fever with Renal Syndrome	CTD_diseases	4
MESH:D006481	MESH:D006481	Hemorrhagic Fever, Omsk	CTD_diseases	4
MESH:D006509	MESH:D006509	Hepatitis B	CTD_diseases	4
MESH:D006519	MESH:D006519	Hepatitis, Alcoholic	CTD_diseases	4
MESH:D006521	MESH:D006521	Hepatitis, Chronic	CTD_diseases	4
MESH:D006526	MESH:D006526	Hepatitis C	CTD_diseases	4
MESH:D006548	MESH:D006548	Hernia, Diaphragmatic	CTD_diseases	4
MESH:D006553	MESH:D006553	Hernia, Obturator	CTD_diseases	4
MESH:D006556	MESH:D006556	Heroin Dependence	CTD_diseases	4
MESH:D006560	MESH:D006560	Herpes Labialis	CTD_diseases	4
MESH:D006561	MESH:D006561	Herpes Simplex	CTD_diseases	4
MESH:D006562	MESH:D006562	Herpes Zoster	CTD_diseases	4
MESH:D006606	MESH:D006606	Hiccup	CTD_diseases	4
MESH:D006618	MESH:D006618	Hip Dislocation, Congenital	CTD_diseases	4
MESH:D006623	MESH:D006623	von Hippel-Lindau Disease	CTD_diseases	4
MESH:D006627	MESH:D006627	Hirschsprung Disease	CTD_diseases	4
MESH:D006628	MESH:D006628	Hirsutism	CTD_diseases	4
MESH:D006646	MESH:D006646	Histiocytosis, Langerhans-Cell	CTD_diseases	4
MESH:D006816	MESH:D006816	Huntington Disease	CTD_diseases	4
MESH:D006832	MESH:D006832	Hydranencephaly	CTD_diseases	4
MESH:D006837	MESH:D006837	Hydroa Vacciniforme	CTD_diseases	4
MESH:D006849	MESH:D006849	Hydrocephalus	CTD_diseases	4
MESH:D006925	MESH:D006925	Hymenolepiasis	CTD_diseases	4
MESH:D006929	MESH:D006929	Hyperaldosteronism	CTD_diseases	4
MESH:D006933	MESH:D006933	Hyperbilirubinemia, Hereditary	CTD_diseases	4
MESH:D006934	MESH:D006934	Hypercalcemia	CTD_diseases	4
MESH:D006935	MESH:D006935	Hypercapnia	CTD_diseases	4
MESH:D006943	MESH:D006943	Hyperglycemia	CTD_diseases	4
MESH:D006945	MESH:D006945	Hyperhidrosis	CTD_diseases	4
MESH:D006946	MESH:D006946	Hyperinsulinism	CTD_diseases	4
MESH:D006947	MESH:D006947	Hyperkalemia	CTD_diseases	4
MESH:D006955	MESH:D006955	Hypernatremia	CTD_diseases	4
MESH:D006957	MESH:D006957	Hyperostosis Frontalis Interna	CTD_diseases	4
MESH:D006962	MESH:D006962	Hyperparathyroidism, Secondary	CTD_diseases	4
MESH:D006963	MESH:D006963	Hyperphagia	CTD_diseases	4
MESH:D006971	MESH:D006971	Hypersplenism	CTD_diseases	4
MESH:D006974	MESH:D006974	Hypertension, Malignant	CTD_diseases	4
MESH:D006977	MESH:D006977	Hypertension, Renal	CTD_diseases	4
MESH:D006983	MESH:D006983	Hypertrichosis	CTD_diseases	4
MESH:D006994	MESH:D006994	Hypoaldosteronism	CTD_diseases	4
MESH:D006996	MESH:D006996	Hypocalcemia	CTD_diseases	4
MESH:D007003	MESH:D007003	Hypoglycemia	CTD_diseases	4
MESH:D007007	MESH:D007007	Hypohidrosis	CTD_diseases	4
MESH:D007008	MESH:D007008	Hypokalemia	CTD_diseases	4
MESH:D007010	MESH:D007010	Hyponatremia	CTD_diseases	4
MESH:D007019	MESH:D007019	Hypoproteinemia	CTD_diseases	4
MESH:D007020	MESH:D007020	Hypoprothrombinemias	CTD_diseases	4
MESH:D007021	MESH:D007021	Hypospadias	CTD_diseases	4
MESH:D007024	MESH:D007024	Hypotension, Orthostatic	CTD_diseases	4
MESH:D007027	MESH:D007027	Hypothalamic Diseases	CTD_diseases	4
MESH:D007035	MESH:D007035	Hypothermia	CTD_diseases	4
MESH:D007039	MESH:D007039	Hypotrichosis	CTD_diseases	4
MESH:D007040	MESH:D007040	Hypoventilation	CTD_diseases	4
MESH:D007046	MESH:D007046	Hysteria	CTD_diseases	4
MESH:D007049	MESH:D007049	Iatrogenic Disease	CTD_diseases	4
MESH:D007077	MESH:D007077	Ileal Diseases	CTD_diseases	4
MESH:D007102	MESH:D007102	Immersion Foot	CTD_diseases	4
MESH:D007119	MESH:D007119	Immunoblastic Lymphadenopathy	CTD_diseases	4
MESH:D007161	MESH:D007161	Immunoproliferative Small Intestinal Disease	CTD_diseases	4
MESH:D007172	MESH:D007172	Erectile Dysfunction	CTD_diseases	4
MESH:D007177	MESH:D007177	Inappropriate ADH Syndrome	CTD_diseases	4
MESH:D007184	MESH:D007184	Incontinentia Pigmenti	CTD_diseases	4
MESH:D007238	MESH:D007238	Infarction	CTD_diseases	4
MESH:D007244	MESH:D007244	Infectious Mononucleosis	CTD_diseases	4
MESH:D007251	MESH:D007251	Influenza, Human	CTD_diseases	4
MESH:D007299	MESH:D007299	Insect Bites and Stings	CTD_diseases	4
MESH:D007402	MESH:D007402	Intertrigo	CTD_diseases	4
MESH:D007405	MESH:D007405	Intervertebral Disc Displacement	CTD_diseases	4
MESH:D007409	MESH:D007409	Intestinal Atresia	CTD_diseases	4
MESH:D007412	MESH:D007412	Intestinal Fistula	CTD_diseases	4
MESH:D007414	MESH:D007414	Intestinal Neoplasms	CTD_diseases	4
MESH:D007415	MESH:D007415	Intestinal Obstruction	CTD_diseases	4
MESH:D007416	MESH:D007416	Intestinal Perforation	CTD_diseases	4
MESH:D007417	MESH:D007417	Intestinal Polyps	CTD_diseases	4
MESH:D007446	MESH:D007446	Chromosome Inversion	CTD_diseases	4
MESH:D007500	MESH:D007500	Iritis	CTD_diseases	4
MESH:D007565	MESH:D007565	Jaundice	CTD_diseases	4
MESH:D007579	MESH:D007579	Jejunal Diseases	CTD_diseases	4
MESH:D007625	MESH:D007625	Kearns-Sayre Syndrome	CTD_diseases	4
MESH:D007627	MESH:D007627	Keloid	CTD_diseases	4
MESH:D007637	MESH:D007637	Keratoconjunctivitis	CTD_diseases	4
MESH:D007638	MESH:D007638	Keratoconjunctivitis Sicca	CTD_diseases	4
MESH:D007644	MESH:D007644	Darier Disease	CTD_diseases	4
MESH:D007645	MESH:D007645	Keratoderma, Palmoplantar	CTD_diseases	4
MESH:D007647	MESH:D007647	Kernicterus	CTD_diseases	4
MESH:D007674	MESH:D007674	Kidney Diseases	CTD_diseases	4
MESH:D007706	MESH:D007706	Menkes Kinky Hair Syndrome	CTD_diseases	4
MESH:D007713	MESH:D007713	Klinefelter Syndrome	CTD_diseases	4
MESH:D007714	MESH:D007714	Klippel-Feil Syndrome	CTD_diseases	4
MESH:D007715	MESH:D007715	Klippel-Trenaunay-Weber Syndrome	CTD_diseases	4
MESH:D007733	MESH:D007733	Kyasanur Forest Disease	CTD_diseases	4
MESH:D007752	MESH:D007752	Obstetric Labor, Premature	CTD_diseases	4
MESH:D007762	MESH:D007762	Labyrinthitis	CTD_diseases	4
MESH:D007775	MESH:D007775	Lactation Disorders	CTD_diseases	4
MESH:D007815	MESH:D007815	Larva Migrans	CTD_diseases	4
MESH:D007826	MESH:D007826	Laryngismus	CTD_diseases	4
MESH:D007835	MESH:D007835	Lassa Fever	CTD_diseases	4
MESH:D007842	MESH:D007842	Lathyrism	CTD_diseases	4
MESH:D007849	MESH:D007849	Laurence-Moon Syndrome	CTD_diseases	4
MESH:D007871	MESH:D007871	Leg Ulcer	CTD_diseases	4
MESH:D007876	MESH:D007876	Legionellosis	CTD_diseases	4
MESH:D007888	MESH:D007888	Leigh Disease	CTD_diseases	4
MESH:D007896	MESH:D007896	Leishmaniasis	CTD_diseases	4
MESH:D007922	MESH:D007922	Leptospirosis	CTD_diseases	4
MESH:D007925	MESH:D007925	Leriche Syndrome	CTD_diseases	4
MESH:D007926	MESH:D007926	Lesch-Nyhan Syndrome	CTD_diseases	4
MESH:D007943	MESH:D007943	Leukemia, Hairy Cell	CTD_diseases	4
MESH:D007945	MESH:D007945	Leukemia, Lymphoid	CTD_diseases	4
MESH:D007946	MESH:D007946	Leukemia, Mast-Cell	CTD_diseases	4
MESH:D007951	MESH:D007951	Leukemia, Myeloid	CTD_diseases	4
MESH:D007952	MESH:D007952	Leukemia, Plasma Cell	CTD_diseases	4
MESH:D007969	MESH:D007969	Leukomalacia, Periventricular	CTD_diseases	4
MESH:D007970	MESH:D007970	Leukopenia	CTD_diseases	4
MESH:D007972	MESH:D007972	Leukoplakia, Oral	CTD_diseases	4
MESH:D007979	MESH:D007979	Levocardia	CTD_diseases	4
MESH:D008048	MESH:D008048	Lip Neoplasms	CTD_diseases	4
MESH:D008052	MESH:D008052	Lipid Metabolism, Inborn Errors	CTD_diseases	4
MESH:D008060	MESH:D008060	Lipodystrophy	CTD_diseases	4
MESH:D008064	MESH:D008064	Lipidoses	CTD_diseases	4
MESH:D008065	MESH:D008065	Lipoid Proteinosis of Urbach and Wiethe	CTD_diseases	4
MESH:D008088	MESH:D008088	Listeriosis	CTD_diseases	4
MESH:D008101	MESH:D008101	Liver Abscess, Amebic	CTD_diseases	4
MESH:D008104	MESH:D008104	Liver Cirrhosis, Alcoholic	CTD_diseases	4
MESH:D008105	MESH:D008105	Liver Cirrhosis, Biliary	CTD_diseases	4
MESH:D008106	MESH:D008106	Liver Cirrhosis, Experimental	CTD_diseases	4
MESH:D008133	MESH:D008133	Long QT Syndrome	CTD_diseases	4
MESH:D008179	MESH:D008179	Lupus Erythematosus, Discoid	CTD_diseases	4
MESH:D008181	MESH:D008181	Lupus Nephritis	CTD_diseases	4
MESH:D008201	MESH:D008201	Lymphangiectasis, Intestinal	CTD_diseases	4
MESH:D008202	MESH:D008202	Lymphangioma	CTD_diseases	4
MESH:D008203	MESH:D008203	Lymphangiomyoma	CTD_diseases	4
MESH:D008204	MESH:D008204	Lymphangiosarcoma	CTD_diseases	4
MESH:D008216	MESH:D008216	Lymphocytic Choriomeningitis	CTD_diseases	4
MESH:D008258	MESH:D008258	Waldenstrom Macroglobulinemia	CTD_diseases	4
MESH:D008260	MESH:D008260	Macroglossia	CTD_diseases	4
MESH:D008268	MESH:D008268	Macular Degeneration	CTD_diseases	4
MESH:D008305	MESH:D008305	Malignant Hyperthermia	CTD_diseases	4
MESH:D008311	MESH:D008311	Malocclusion, Angle Class I	CTD_diseases	4
MESH:D008312	MESH:D008312	Malocclusion, Angle Class II	CTD_diseases	4
MESH:D008313	MESH:D008313	Malocclusion, Angle Class III	CTD_diseases	4
MESH:D008339	MESH:D008339	Mandibular Neoplasms	CTD_diseases	4
MESH:D008379	MESH:D008379	Marburg Virus Disease	CTD_diseases	4
MESH:D008413	MESH:D008413	Mastitis	CTD_diseases	4
MESH:D008441	MESH:D008441	Maxillary Neoplasms	CTD_diseases	4
MESH:D008467	MESH:D008467	Meckel Diverticulum	CTD_diseases	4
MESH:D008476	MESH:D008476	Mediastinal Cyst	CTD_diseases	4
MESH:D008478	MESH:D008478	Mediastinal Emphysema	CTD_diseases	4
MESH:D008479	MESH:D008479	Mediastinal Neoplasms	CTD_diseases	4
MESH:D008480	MESH:D008480	Mediastinitis	CTD_diseases	4
MESH:D008545	MESH:D008545	Melanoma	CTD_diseases	4
MESH:D008579	MESH:D008579	Meningioma	CTD_diseases	4
MESH:D008580	MESH:D008580	Meningism	CTD_diseases	4
MESH:D008588	MESH:D008588	Meningocele	CTD_diseases	4
MESH:D008590	MESH:D008590	Meningoencephalitis	CTD_diseases	4
MESH:D008595	MESH:D008595	Menorrhagia	CTD_diseases	4
MESH:D008637	MESH:D008637	Mesenchymoma	CTD_diseases	4
MESH:D008639	MESH:D008639	Mesenteric Cyst	CTD_diseases	4
MESH:D008649	MESH:D008649	Mesonephroma	CTD_diseases	4
MESH:D008664	MESH:D008664	Metal Metabolism, Inborn Errors	CTD_diseases	4
MESH:D008850	MESH:D008850	Microphthalmos	CTD_diseases	4
MESH:D008878	MESH:D008878	Middle Lobe Syndrome	CTD_diseases	4
MESH:D008882	MESH:D008882	Mikulicz' Disease	CTD_diseases	4
MESH:D008883	MESH:D008883	Miliaria	CTD_diseases	4
MESH:D008944	MESH:D008944	Mitral Valve Insufficiency	CTD_diseases	4
MESH:D008946	MESH:D008946	Mitral Valve Stenosis	CTD_diseases	4
MESH:D008949	MESH:D008949	Adenoma, Pleomorphic	CTD_diseases	4
MESH:D008976	MESH:D008976	Molluscum Contagiosum	CTD_diseases	4
MESH:D008989	MESH:D008989	Monieziasis	CTD_diseases	4
MESH:D009021	MESH:D009021	Morphine Dependence	CTD_diseases	4
MESH:D009072	MESH:D009072	Moyamoya Disease	CTD_diseases	4
MESH:D009078	MESH:D009078	Mucocele	CTD_diseases	4
MESH:D009081	MESH:D009081	Mucolipidoses	CTD_diseases	4
MESH:D009083	MESH:D009083	Mucopolysaccharidoses	CTD_diseases	4
MESH:D009091	MESH:D009091	Mucormycosis	CTD_diseases	4
MESH:D009101	MESH:D009101	Multiple Myeloma	CTD_diseases	4
MESH:D009102	MESH:D009102	Multiple Organ Failure	CTD_diseases	4
MESH:D009120	MESH:D009120	Muscle Cramp	CTD_diseases	4
MESH:D009127	MESH:D009127	Muscle Rigidity	CTD_diseases	4
MESH:D009128	MESH:D009128	Muscle Spasticity	CTD_diseases	4
MESH:D009133	MESH:D009133	Muscular Atrophy	CTD_diseases	4
MESH:D009145	MESH:D009145	Mushroom Poisoning	CTD_diseases	4
MESH:D009157	MESH:D009157	Myasthenia Gravis	CTD_diseases	4
MESH:D009180	MESH:D009180	Mycoplasmatales Infections	CTD_diseases	4
MESH:D009187	MESH:D009187	Myelitis	CTD_diseases	4
MESH:D009190	MESH:D009190	Myelodysplastic Syndromes	CTD_diseases	4
MESH:D009196	MESH:D009196	Myeloproliferative Disorders	CTD_diseases	4
MESH:D009203	MESH:D009203	Myocardial Infarction	CTD_diseases	4
MESH:D009205	MESH:D009205	Myocarditis	CTD_diseases	4
MESH:D009208	MESH:D009208	Myoepithelioma	CTD_diseases	4
MESH:D009209	MESH:D009209	Myofascial Pain Syndromes	CTD_diseases	4
MESH:D009220	MESH:D009220	Myositis	CTD_diseases	4
MESH:D009223	MESH:D009223	Myotonic Dystrophy	CTD_diseases	4
MESH:D009224	MESH:D009224	Myotonia Congenita	CTD_diseases	4
MESH:D009230	MESH:D009230	Myxedema	CTD_diseases	4
MESH:D009263	MESH:D009263	Nails, Ingrown	CTD_diseases	4
MESH:D009303	MESH:D009303	Nasopharyngeal Neoplasms	CTD_diseases	4
MESH:D009304	MESH:D009304	Nasopharyngitis	CTD_diseases	4
MESH:D009325	MESH:D009325	Nausea	CTD_diseases	4
MESH:D009335	MESH:D009335	Necrobiosis Lipoidica	CTD_diseases	4
MESH:D009361	MESH:D009361	Neoplasm Invasiveness	CTD_diseases	4
MESH:D009362	MESH:D009362	Neoplasm Metastasis	CTD_diseases	4
MESH:D009364	MESH:D009364	Neoplasm Recurrence, Local	CTD_diseases	4
MESH:D009365	MESH:D009365	Neoplasm Regression, Spontaneous	CTD_diseases	4
MESH:D009379	MESH:D009379	Neoplasms, Muscle Tissue	CTD_diseases	4
MESH:D009389	MESH:D009389	Neovascularization, Pathologic	CTD_diseases	4
MESH:D009394	MESH:D009394	Nephritis, Hereditary	CTD_diseases	4
MESH:D009396	MESH:D009396	Wilms Tumor	CTD_diseases	4
MESH:D009408	MESH:D009408	Nerve Compression Syndromes	CTD_diseases	4
MESH:D009436	MESH:D009436	Neural Tube Defects	CTD_diseases	4
MESH:D009437	MESH:D009437	Neuralgia	CTD_diseases	4
MESH:D009443	MESH:D009443	Neuritis	CTD_diseases	4
MESH:D009450	MESH:D009450	Neurodermatitis	CTD_diseases	4
MESH:D009456	MESH:D009456	Neurofibromatosis 1	CTD_diseases	4
MESH:D009459	MESH:D009459	Neuroleptic Malignant Syndrome	CTD_diseases	4
MESH:D009472	MESH:D009472	Neuronal Ceroid-Lipofuscinoses	CTD_diseases	4
MESH:D009477	MESH:D009477	Hereditary Sensory and Autonomic Neuropathies	CTD_diseases	4
MESH:D009506	MESH:D009506	Nevus	CTD_diseases	4
MESH:D009630	MESH:D009630	Nondisjunction, Genetic	CTD_diseases	4
MESH:D009759	MESH:D009759	Nystagmus, Pathologic	CTD_diseases	4
MESH:D009765	MESH:D009765	Obesity	CTD_diseases	4
MESH:D009800	MESH:D009800	Oculocerebrorenal Syndrome	CTD_diseases	4
MESH:D009810	MESH:D009810	Odontoma	CTD_diseases	4
MESH:D009839	MESH:D009839	Oligomenorrhea	CTD_diseases	4
MESH:D009846	MESH:D009846	Oliguria	CTD_diseases	4
MESH:D009877	MESH:D009877	Endophthalmitis	CTD_diseases	4
MESH:D009886	MESH:D009886	Ophthalmoplegia	CTD_diseases	4
MESH:D009889	MESH:D009889	Opisthorchiasis	CTD_diseases	4
MESH:D009896	MESH:D009896	Optic Atrophy	CTD_diseases	4
MESH:D009902	MESH:D009902	Optic Neuritis	CTD_diseases	4
MESH:D009920	MESH:D009920	Orchitis	CTD_diseases	4
MESH:D009958	MESH:D009958	Orofaciodigital Syndromes	CTD_diseases	4
MESH:D010002	MESH:D010002	Osteitis Fibrosa Cystica	CTD_diseases	4
MESH:D010003	MESH:D010003	Osteoarthritis	CTD_diseases	4
MESH:D010009	MESH:D010009	Osteochondrodysplasias	CTD_diseases	4
MESH:D010014	MESH:D010014	Osteolysis	CTD_diseases	4
MESH:D010015	MESH:D010015	Osteolysis, Essential	CTD_diseases	4
MESH:D010019	MESH:D010019	Osteomyelitis	CTD_diseases	4
MESH:D010024	MESH:D010024	Osteoporosis	CTD_diseases	4
MESH:D010032	MESH:D010032	Otitis Externa	CTD_diseases	4
MESH:D010033	MESH:D010033	Otitis Media	CTD_diseases	4
MESH:D010048	MESH:D010048	Ovarian Cysts	CTD_diseases	4
MESH:D010051	MESH:D010051	Ovarian Neoplasms	CTD_diseases	4
MESH:D010149	MESH:D010149	Pain, Postoperative	CTD_diseases	4
MESH:D010167	MESH:D010167	Pallor	CTD_diseases	4
MESH:D010201	MESH:D010201	Panniculitis, Nodular Nonsuppurative	CTD_diseases	4
MESH:D010211	MESH:D010211	Papilledema	CTD_diseases	4
MESH:D010237	MESH:D010237	Paragonimiasis	CTD_diseases	4
MESH:D010241	MESH:D010241	Parakeratosis	CTD_diseases	4
MESH:D010243	MESH:D010243	Paralysis	CTD_diseases	4
MESH:D010244	MESH:D010244	Bulbar Palsy, Progressive	CTD_diseases	4
MESH:D010245	MESH:D010245	Paralyses, Familial Periodic	CTD_diseases	4
MESH:D010246	MESH:D010246	Paralysis, Obstetric	CTD_diseases	4
MESH:D010255	MESH:D010255	Paranasal Sinus Neoplasms	CTD_diseases	4
MESH:D010262	MESH:D010262	Paraphilias	CTD_diseases	4
MESH:D010267	MESH:D010267	Parapsoriasis	CTD_diseases	4
MESH:D010291	MESH:D010291	Paresis	CTD_diseases	4
MESH:D010304	MESH:D010304	Paronychia	CTD_diseases	4
MESH:D010305	MESH:D010305	Parotid Diseases	CTD_diseases	4
MESH:D010310	MESH:D010310	Parovarian Cyst	CTD_diseases	4
MESH:D010412	MESH:D010412	Penile Neoplasms	CTD_diseases	4
MESH:D010488	MESH:D010488	Polyarteritis Nodosa	CTD_diseases	4
MESH:D010489	MESH:D010489	Periarthritis	CTD_diseases	4
MESH:D010494	MESH:D010494	Pericarditis, Constrictive	CTD_diseases	4
MESH:D010495	MESH:D010495	Pericarditis, Tuberculous	CTD_diseases	4
MESH:D010509	MESH:D010509	Periodontal Cyst	CTD_diseases	4
MESH:D010518	MESH:D010518	Periodontitis	CTD_diseases	4
MESH:D010522	MESH:D010522	Periostitis	CTD_diseases	4
MESH:D010524	MESH:D010524	Peripheral Nervous System Neoplasms	CTD_diseases	4
MESH:D010580	MESH:D010580	Peutz-Jeghers Syndrome	CTD_diseases	4
MESH:D010688	MESH:D010688	Phimosis	CTD_diseases	4
MESH:D010689	MESH:D010689	Phlebitis	CTD_diseases	4
MESH:D010864	MESH:D010864	Pilonidal Sinus	CTD_diseases	4
MESH:D010911	MESH:D010911	Pituitary Neoplasms	CTD_diseases	4
MESH:D010915	MESH:D010915	Pityriasis	CTD_diseases	4
MESH:D010921	MESH:D010921	Placenta Accreta	CTD_diseases	4
MESH:D010923	MESH:D010923	Placenta Previa	CTD_diseases	4
MESH:D010927	MESH:D010927	Placental Insufficiency	CTD_diseases	4
MESH:D010954	MESH:D010954	Plasmacytoma	CTD_diseases	4
MESH:D010981	MESH:D010981	Platelet Storage Pool Deficiency	CTD_diseases	4
MESH:D010985	MESH:D010985	Platybasia	CTD_diseases	4
MESH:D011006	MESH:D011006	Pneumatosis Cystoides Intestinalis	CTD_diseases	4
MESH:D011020	MESH:D011020	Pneumonia, Pneumocystis	CTD_diseases	4
MESH:D011081	MESH:D011081	Polychondritis, Relapsing	CTD_diseases	4
MESH:D011111	MESH:D011111	Polymyalgia Rheumatica	CTD_diseases	4
MESH:D011115	MESH:D011115	Polyneuropathies	CTD_diseases	4
MESH:D011123	MESH:D011123	Polyploidy	CTD_diseases	4
MESH:D011125	MESH:D011125	Adenomatous Polyposis Coli	CTD_diseases	4
MESH:D011141	MESH:D011141	Polyuria	CTD_diseases	4
MESH:D011146	MESH:D011146	Eczema, Dyshidrotic	CTD_diseases	4
MESH:D011178	MESH:D011178	Postgastrectomy Syndromes	CTD_diseases	4
MESH:D011186	MESH:D011186	Postphlebitic Syndrome	CTD_diseases	4
MESH:D011218	MESH:D011218	Prader-Willi Syndrome	CTD_diseases	4
MESH:D011226	MESH:D011226	Pre-Excitation Syndromes	CTD_diseases	4
MESH:D011269	MESH:D011269	Pregnancy, Abdominal	CTD_diseases	4
MESH:D011274	MESH:D011274	Pregnancy, Tubal	CTD_diseases	4
MESH:D011293	MESH:D011293	Premenstrual Syndrome	CTD_diseases	4
MESH:D011297	MESH:D011297	Prenatal Exposure Delayed Effects	CTD_diseases	4
MESH:D011317	MESH:D011317	Priapism	CTD_diseases	4
MESH:D011349	MESH:D011349	Proctitis	CTD_diseases	4
MESH:D011371	MESH:D011371	Progeria	CTD_diseases	4
MESH:D011378	MESH:D011378	Prognathism	CTD_diseases	4
MESH:D011470	MESH:D011470	Prostatic Hyperplasia	CTD_diseases	4
MESH:D011471	MESH:D011471	Prostatic Neoplasms	CTD_diseases	4
MESH:D011472	MESH:D011472	Prostatitis	CTD_diseases	4
MESH:D011475	MESH:D011475	Prosthesis Failure	CTD_diseases	4
MESH:D011504	MESH:D011504	Protein-Losing Enteropathies	CTD_diseases	4
MESH:D011507	MESH:D011507	Proteinuria	CTD_diseases	4
MESH:D011535	MESH:D011535	Prune Belly Syndrome	CTD_diseases	4
MESH:D011542	MESH:D011542	Pseudarthrosis	CTD_diseases	4
MESH:D011547	MESH:D011547	Pseudohypoparathyroidism	CTD_diseases	4
MESH:D011552	MESH:D011552	Pseudomonas Infections	CTD_diseases	4
MESH:D011565	MESH:D011565	Psoriasis	CTD_diseases	4
MESH:D011602	MESH:D011602	Psychophysiologic Disorders	CTD_diseases	4
MESH:D011604	MESH:D011604	Psychoses, Alcoholic	CTD_diseases	4
MESH:D011645	MESH:D011645	Puerperal Infection	CTD_diseases	4
MESH:D011665	MESH:D011665	Pulmonary Valve Insufficiency	CTD_diseases	4
MESH:D011666	MESH:D011666	Pulmonary Valve Stenosis	CTD_diseases	4
MESH:D011671	MESH:D011671	Pulpitis	CTD_diseases	4
MESH:D011686	MESH:D011686	Purine-Pyrimidine Metabolism, Inborn Errors	CTD_diseases	4
MESH:D011693	MESH:D011693	Purpura	CTD_diseases	4
MESH:D011695	MESH:D011695	Purpura, Schoenlein-Henoch	CTD_diseases	4
MESH:D011697	MESH:D011697	Purpura, Thrombotic Thrombocytopenic	CTD_diseases	4
MESH:D011778	MESH:D011778	Q Fever	CTD_diseases	4
MESH:D011843	MESH:D011843	Radiculopathy	CTD_diseases	4
MESH:D011906	MESH:D011906	Rat-Bite Fever	CTD_diseases	4
MESH:D011928	MESH:D011928	Raynaud Disease	CTD_diseases	4
MESH:D012002	MESH:D012002	Rectal Diseases	CTD_diseases	4
MESH:D012008	MESH:D012008	Recurrence	CTD_diseases	4
MESH:D012010	MESH:D012010	Red-Cell Aplasia, Pure	CTD_diseases	4
MESH:D012021	MESH:D012021	Reflex, Abnormal	CTD_diseases	4
MESH:D012078	MESH:D012078	Renal Artery Obstruction	CTD_diseases	4
MESH:D012080	MESH:D012080	Renal Osteodystrophy	CTD_diseases	4
MESH:D012133	MESH:D012133	Respiratory Paralysis	CTD_diseases	4
MESH:D012135	MESH:D012135	Respiratory Sounds	CTD_diseases	4
MESH:D012174	MESH:D012174	Retinitis Pigmentosa	CTD_diseases	4
MESH:D012183	MESH:D012183	Retrograde Degeneration	CTD_diseases	4
MESH:D012185	MESH:D012185	Retroperitoneal Fibrosis	CTD_diseases	4
MESH:D012186	MESH:D012186	Retroperitoneal Neoplasms	CTD_diseases	4
MESH:D012202	MESH:D012202	Reye Syndrome	CTD_diseases	4
MESH:D012203	MESH:D012203	Rh Isoimmunization	CTD_diseases	4
MESH:D012206	MESH:D012206	Rhabdomyolysis	CTD_diseases	4
MESH:D012213	MESH:D012213	Rheumatic Fever	CTD_diseases	4
MESH:D012224	MESH:D012224	Rhinophyma	CTD_diseases	4
MESH:D012279	MESH:D012279	Rickets	CTD_diseases	4
MESH:D012288	MESH:D012288	Rickettsiaceae Infections	CTD_diseases	4
MESH:D012303	MESH:D012303	Ring Chromosomes	CTD_diseases	4
MESH:D012391	MESH:D012391	Root Resorption	CTD_diseases	4
MESH:D012400	MESH:D012400	Rotavirus Infections	CTD_diseases	4
MESH:D012410	MESH:D012410	Rubella Syndrome, Congenital	CTD_diseases	4
MESH:D012415	MESH:D012415	Rubinstein-Taybi Syndrome	CTD_diseases	4
MESH:D012467	MESH:D012467	Salivary Gland Fistula	CTD_diseases	4
MESH:D012468	MESH:D012468	Salivary Gland Neoplasms	CTD_diseases	4
MESH:D012478	MESH:D012478	Salmonella Food Poisoning	CTD_diseases	4
MESH:D012507	MESH:D012507	Sarcoidosis	CTD_diseases	4
MESH:D012509	MESH:D012509	Sarcoma	CTD_diseases	4
MESH:D012514	MESH:D012514	Sarcoma, Kaposi	CTD_diseases	4
MESH:D012523	MESH:D012523	Sarcocystosis	CTD_diseases	4
MESH:D012552	MESH:D012552	Schistosomiasis	CTD_diseases	4
MESH:D012560	MESH:D012560	Schizophrenia, Catatonic	CTD_diseases	4
MESH:D012562	MESH:D012562	Schizophrenia, Disorganized	CTD_diseases	4
MESH:D012563	MESH:D012563	Schizophrenia, Paranoid	CTD_diseases	4
MESH:D012626	MESH:D012626	Sebaceous Gland Neoplasms	CTD_diseases	4
MESH:D012628	MESH:D012628	Dermatitis, Seborrheic	CTD_diseases	4
MESH:D012640	MESH:D012640	Seizures	CTD_diseases	4
MESH:D012678	MESH:D012678	Sensation Disorders	CTD_diseases	4
MESH:D012700	MESH:D012700	Serositis	CTD_diseases	4
MESH:D012713	MESH:D012713	Serum Sickness	CTD_diseases	4
MESH:D012719	MESH:D012719	Setariasis	CTD_diseases	4
MESH:D012729	MESH:D012729	Sex Chromosome Aberrations	CTD_diseases	4
MESH:D012751	MESH:D012751	Sezary Syndrome	CTD_diseases	4
MESH:D012753	MESH:D012753	Shared Paranoid Disorder	CTD_diseases	4
MESH:D012770	MESH:D012770	Shock, Cardiogenic	CTD_diseases	4
MESH:D012771	MESH:D012771	Shock, Hemorrhagic	CTD_diseases	4
MESH:D012773	MESH:D012773	Shock, Surgical	CTD_diseases	4
MESH:D012778	MESH:D012778	Short Bowel Syndrome	CTD_diseases	4
MESH:D012779	MESH:D012779	Short Rib-Polydactyly Syndrome	CTD_diseases	4
MESH:D012790	MESH:D012790	Shwartzman Phenomenon	CTD_diseases	4
MESH:D012793	MESH:D012793	Sialadenitis	CTD_diseases	4
MESH:D012797	MESH:D012797	Sialometaplasia, Necrotizing	CTD_diseases	4
MESH:D012798	MESH:D012798	Sialorrhea	CTD_diseases	4
MESH:D012852	MESH:D012852	Sinusitis	CTD_diseases	4
MESH:D012859	MESH:D012859	Sjogren's Syndrome	CTD_diseases	4
MESH:C567275	MESH:C567275	Craniodiaphyseal Dysplasia, Autosomal Dominant	CTD_diseases	5
MESH:C567278	MESH:C567278	Holoprosencephaly 10	CTD_diseases	5
MESH:C567290	MESH:C567290	Chromosome 1q21.1 Duplication Syndrome	CTD_diseases	5
MESH:C567308	MESH:C567308	C6 Deficiency, Subtotal	CTD_diseases	5
MESH:C567316	MESH:C567316	Cardiomyopathy, Familial Restrictive, 3	CTD_diseases	5
MESH:C567319	MESH:C567319	Dystonia 17, Torsion, Autosomal Recessive	CTD_diseases	5
MESH:C567324	MESH:C567324	Pontocerebellar Hypoplasia Type 2C	CTD_diseases	5
MESH:C567325	MESH:C567325	Pontocerebellar Hypoplasia Type 2B	CTD_diseases	5
MESH:C567326	MESH:C567326	Inflammatory Bowel Disease 23	CTD_diseases	5
MESH:C567327	MESH:C567327	Inflammatory Bowel Disease 22	CTD_diseases	5
MESH:C567338	MESH:C567338	Inflammatory Bowel Disease 21	CTD_diseases	5
MESH:C567339	MESH:C567339	Porokeratosis, Disseminated Superficial Actinic, 4	CTD_diseases	5
MESH:C567340	MESH:C567340	Spondylocheirodysplasia, Ehlers-Danlos Syndrome-Like	CTD_diseases	5
MESH:C567347	MESH:C567347	Thrombophilia, Hereditary, Due To Protein S Deficiency, Autosomal Dominant	CTD_diseases	5
MESH:C567348	MESH:C567348	Thrombophilia, Hereditary, Due To Protein S Deficiency, Autosomal Recessive	CTD_diseases	5
MESH:C567354	MESH:C567354	Osteopetrosis, Autosomal Recessive 7	CTD_diseases	5
MESH:C567355	MESH:C567355	CD59 Deficiency	CTD_diseases	5
MESH:C567356	MESH:C567356	Porokeratosis, Disseminated Superficial Actinic, 3	CTD_diseases	5
MESH:C567357	MESH:C567357	Birk-Barel Mental Retardation Dysmorphism Syndrome	CTD_diseases	5
MESH:C567361	MESH:C567361	Inflammatory Bowel Disease 20	CTD_diseases	5
MESH:C567362	MESH:C567362	Nephrolithiasis-Osteoporosis, Hypophosphatemic, 2	CTD_diseases	5
MESH:C567363	MESH:C567363	Nephrolithiasis-Osteoporosis, Hypophosphatemic, 1	CTD_diseases	5
MESH:C567370	MESH:C567370	Ichthyosis, Congenital, Autosomal Recessive, Ichthyin-Related	CTD_diseases	5
MESH:C567372	MESH:C567372	Inflammatory Bowel Disease 19	CTD_diseases	5
MESH:C567377	MESH:C567377	Inflammatory Bowel Disease 18	CTD_diseases	5
MESH:C567378	MESH:C567378	Inflammatory Bowel Disease 17	CTD_diseases	5
MESH:C567380	MESH:C567380	Inflammatory Bowel Disease 16	CTD_diseases	5
MESH:C567381	MESH:C567381	Inflammatory Bowel Disease 15	CTD_diseases	5
MESH:C567383	MESH:C567383	Inflammatory Bowel Disease 14	CTD_diseases	5
MESH:C567384	MESH:C567384	Inflammatory Bowel Disease 13	CTD_diseases	5
MESH:C567388	MESH:C567388	Inflammatory Bowel Disease 12	CTD_diseases	5
MESH:C567389	MESH:C567389	Atrial Fibrillation, Familial, 7	CTD_diseases	5
MESH:C567400	MESH:C567400	Atrial Fibrillation, Familial, 6	CTD_diseases	5
MESH:C567402	MESH:C567402	Diastasis Recti And Weakness Of The Linea Alba	CTD_diseases	5
MESH:C567412	MESH:C567412	Paroxysmal Exertion-Induced Dyskinesia And Hemolytic Anemia	CTD_diseases	5
MESH:C567423	MESH:C567423	Hypophosphatemic Rickets And Hyperparathyroidism	CTD_diseases	5
MESH:C567430	MESH:C567430	Dystonia 16	CTD_diseases	5
MESH:C567438	MESH:C567438	Thrombocytopenia 4	CTD_diseases	5
MESH:C567450	MESH:C567450	Macular Degeneration, Age-Related, 11	CTD_diseases	5
MESH:C567487	MESH:C567487	Thrombocytopenia 3	CTD_diseases	5
MESH:C567498	MESH:C567498	Nanophthalmos 3	CTD_diseases	5
MESH:C567508	MESH:C567508	Brugada Syndrome 4	CTD_diseases	5
MESH:C567509	MESH:C567509	Brugada Syndrome 3	CTD_diseases	5
MESH:C567512	MESH:C567512	Microtia With Nasolacrimal Duct Imperforation And Eye Coloboma	CTD_diseases	5
MESH:C567519	MESH:C567519	Tremor, Hereditary Essential, And Idiopathic Normal Pressure Hydrocephalus	CTD_diseases	5
MESH:C567524	MESH:C567524	Nevus Flammeus of Nape of Neck	CTD_diseases	5
MESH:C567529	MESH:C567529	Major Affective Disorder 7	CTD_diseases	5
MESH:C567530	MESH:C567530	Major Affective Disorder 8	CTD_diseases	5
MESH:C567531	MESH:C567531	Major Affective Disorder 9	CTD_diseases	5
MESH:C567545	MESH:C567545	Metaphyseal Anadysplasia 1	CTD_diseases	5
MESH:C567546	MESH:C567546	Corneal Dystrophy, Posterior Amorphous	CTD_diseases	5
MESH:C567547	MESH:C567547	Corneal Dystrophy, Subepithelial Mucinous	CTD_diseases	5
MESH:C567553	MESH:C567553	Keratosis Follicularis Spinulosa Decalvans, Autosomal Dominant	CTD_diseases	5
MESH:C567554	MESH:C567554	Hypotrichosis 5	CTD_diseases	5
MESH:C567556	MESH:C567556	Brugada Syndrome 5	CTD_diseases	5
MESH:C567557	MESH:C567557	Cardiac Conduction Defect, Nonspecific	CTD_diseases	5
MESH:C567559	MESH:C567559	Inflammatory Bowel Disease 27	CTD_diseases	5
MESH:C567564	MESH:C567564	Isolated Growth Hormone Deficiency, Type IB	CTD_diseases	5
MESH:C567577	MESH:C567577	Otopalatodigital Spectrum Disorder	CTD_diseases	5
MESH:C567578	MESH:C567578	Frontootopalatodigital Osteodysplasia	CTD_diseases	5
MESH:C567587	MESH:C567587	Corneal Dystrophy, Endothelial, X-Linked	CTD_diseases	5
MESH:C567588	MESH:C567588	Corneal Dystrophy, Lisch Epithelial	CTD_diseases	5
MESH:C567594	MESH:C567594	Myopathy, Congenital, With Fiber-Type Disproportion, X-Linked	CTD_diseases	5
MESH:C567608	MESH:C567608	Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form, Autosomal Recessive	CTD_diseases	5
MESH:C567616	MESH:C567616	Split-Hand/Foot Malformation 6	CTD_diseases	5
MESH:C567627	MESH:C567627	Musician's Dystonia	CTD_diseases	5
MESH:C567628	MESH:C567628	Spastic Paraplegia 18, Autosomal Recessive	CTD_diseases	5
MESH:C567632	MESH:C567632	Growth Hormone Deficiency With Pituitary Anomalies	CTD_diseases	5
MESH:C567636	MESH:C567636	Leber Congenital Amaurosis 14	CTD_diseases	5
MESH:C567639	MESH:C567639	Spondylo-Megaepiphyseal-Metaphyseal Dysplasia	CTD_diseases	5
MESH:C567643	MESH:C567643	Rhabdoid Tumor Predisposition Syndrome 2	CTD_diseases	5
MESH:C567652	MESH:C567652	Bile Acid Malabsorption, Primary	CTD_diseases	5
MESH:C567657	MESH:C567657	Pitt-Hopkins-Like Syndrome 1	CTD_diseases	5
MESH:C567658	MESH:C567658	Polymicrogyria, Asymmetric	CTD_diseases	5
MESH:C567661	MESH:C567661	Progeria Syndrome, Childhood-Onset	CTD_diseases	5
MESH:C567664	MESH:C567664	Omodysplasia 2	CTD_diseases	5
MESH:C567672	MESH:C567672	Bifid Nose With Or Without Anorectal And Renal Anomalies	CTD_diseases	5
MESH:C567679	MESH:C567679	Waardenburg Syndrome, Type 4c	CTD_diseases	5
MESH:C567680	MESH:C567680	Waardenburg Syndrome, Type 4b	CTD_diseases	5
MESH:C567703	MESH:C567703	Diarrhea 5, With Tufting Enteropathy, Congenital	CTD_diseases	5
MESH:C567715	MESH:C567715	Polymicrogyria With Optic Nerve Hypoplasia	CTD_diseases	5
MESH:C567718	MESH:C567718	Marie Unna Hereditary Hypotrichosis 1	CTD_diseases	5
MESH:C567728	MESH:C567728	Inflammatory Bowel Disease 28, Autosomal Recessive	CTD_diseases	5
MESH:C567729	MESH:C567729	Choroidal Dystrophy, Central Areolar 3	CTD_diseases	5
MESH:C567730	MESH:C567730	Parkinsonism-Dystonia, Infantile	CTD_diseases	5
MESH:C567732	MESH:C567732	Brugada Syndrome 8	CTD_diseases	5
MESH:C567734	MESH:C567734	Brugada Syndrome 7	CTD_diseases	5
MESH:C567735	MESH:C567735	Brugada Syndrome 6	CTD_diseases	5
MESH:C567743	MESH:C567743	Epilepsy, Benign Neonatal, 1, And/Or Myokymia	CTD_diseases	5
MESH:C567747	MESH:C567747	Macrothrombocytopenia, Autosomal Dominant, Tubb1-Related	CTD_diseases	5
MESH:C567750	MESH:C567750	Choroidal Dystrophy, Central Areolar 2	CTD_diseases	5
MESH:C567751	MESH:C567751	Hypotrichosis And Recurrent Skin Vesicles	CTD_diseases	5
MESH:C567755	MESH:C567755	Tooth Agenesis, Selective, 6	CTD_diseases	5
MESH:C567757	MESH:C567757	Microphthalmia, Isolated 4	CTD_diseases	5
MESH:C567770	MESH:C567770	Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis	CTD_diseases	5
MESH:C567771	MESH:C567771	Metaphyseal Anadysplasia 2	CTD_diseases	5
MESH:C567773	MESH:C567773	46,Xy Gonadal Dysgenesis, Partial, With Minifascicular Neuropathy	CTD_diseases	5
MESH:C567791	MESH:C567791	Neurodegeneration Due To Cerebral Folate Transport Deficiency	CTD_diseases	5
MESH:C567796	MESH:C567796	Dermatitis, Atopic, 7	CTD_diseases	5
MESH:C567802	MESH:C567802	Atrial Fibrillation, Familial, 8	CTD_diseases	5
MESH:C567841	MESH:C567841	Ventricular Fibrillation, Paroxysmal Familial, 2	CTD_diseases	5
MESH:C567843	MESH:C567843	Myopathy, Myofibrillar, Bag3-Related	CTD_diseases	5
MESH:C567844	MESH:C567844	Dystonia-Parkinsonism, Adult-Onset	CTD_diseases	5
MESH:C567851	MESH:C567851	Ventricular Fibrillation, Paroxysmal Familial, 1	CTD_diseases	5
MESH:C567855	MESH:C567855	Cutis Laxa, Autosomal Recessive, Type IIB	CTD_diseases	5
MESH:C567862	MESH:C567862	Three M Syndrome 2	CTD_diseases	5
MESH:C567864	MESH:C567864	Giacheti Syndrome	CTD_diseases	5
MESH:C567886	MESH:C567886	Xeroderma Pigmentosum, Complementation Group C	CTD_diseases	5
MESH:C567893	MESH:C567893	Split hand foot deformity 1	CTD_diseases	5
MESH:C567934	MESH:C567934	Thyroid Hormone Resistance, Generalized, Autosomal Dominant	CTD_diseases	5
MESH:C567936	MESH:C567936	Thyroid Hormone Resistance, Generalized, Autosomal Recessive	CTD_diseases	5
MESH:C567938	MESH:C567938	Anorectal Anomalies	CTD_diseases	5
MESH:C574275	MESH:C574275	Ectrodactyly	CTD_diseases	5
MESH:C579872	MESH:C579872	6q24-Related Transient Neonatal Diabetes Mellitus	CTD_diseases	5
MESH:C579878	MESH:C579878	Achondrogenesis	CTD_diseases	5
MESH:C579880	MESH:C579880	Actin-Accumulation Myopathy	CTD_diseases	5
MESH:C579928	MESH:C579928	Atelosteogenesis Type 3	CTD_diseases	5
MESH:C579969	MESH:C579969	Cap Myopathy	CTD_diseases	5
MESH:C580011	MESH:C580011	Congenital Fiber-Type Disproportion	CTD_diseases	5
MESH:C580017	MESH:C580017	Congenital Plasminogen Deficiency	CTD_diseases	5
MESH:C580044	MESH:C580044	Distal Hereditary Motor Neuropathy, Type Ii	CTD_diseases	5
MESH:C580054	MESH:C580054	Dyserythropoietic Anemia and Thrombocytopenia	CTD_diseases	5
MESH:C580062	MESH:C580062	Epidermal Nevus	CTD_diseases	5
MESH:C580087	MESH:C580087	Familial Hyperaldosteronism	CTD_diseases	5
MESH:C580109	MESH:C580109	Fragile X-Associated Tremor/Ataxia Syndrome	CTD_diseases	5
MESH:C580150	MESH:C580150	Hereditary Diffuse Leukoencephalopathy with Spheroids	CTD_diseases	5
MESH:C580151	MESH:C580151	Hereditary Folate Malabsorption	CTD_diseases	5
MESH:C580182	MESH:C580182	Hyperparathyroidism-Jaw Tumor Syndrome	CTD_diseases	5
MESH:C580183	MESH:C580183	Hyperphosphatemic Familial Tumoral Calcinosis	CTD_diseases	5
MESH:C580202	MESH:C580202	Intranuclear Rod Myopathy	CTD_diseases	5
MESH:C580233	MESH:C580233	Lactate Dehydrogenase Deficiency	CTD_diseases	5
MESH:C580241	MESH:C580241	Larsen Syndrome	CTD_diseases	5
MESH:C580273	MESH:C580273	Mecp2-Related Severe Neonatal Encephalopathy	CTD_diseases	5
MESH:C580316	MESH:C580316	Myofibrillar Myopathy	CTD_diseases	5
MESH:C580359	MESH:C580359	Palmoplantar Keratoderma with Deafness	CTD_diseases	5
MESH:C580369	MESH:C580369	Permanent Neonatal Diabetes Mellitus	CTD_diseases	5
MESH:C580383	MESH:C580383	Pontocerebellar Hypoplasia	CTD_diseases	5
MESH:C580420	MESH:C580420	Ren-Related Kidney Disease	CTD_diseases	5
MESH:C580424	MESH:C580424	Ring Chromosome 20 Syndrome	CTD_diseases	5
MESH:C580470	MESH:C580470	Stargardt Macular Degeneration	CTD_diseases	5
MESH:C580482	MESH:C580482	Task-Specific Focal Dystonia	CTD_diseases	5
MESH:C581628	MESH:C581628	Metatropic Dwarfism, Type II	CTD_diseases	5
MESH:D000038	MESH:D000038	Abscess	CTD_diseases	5
MESH:D000130	MESH:D000130	Achondroplasia	CTD_diseases	5
MESH:D000140	MESH:D000140	Acidosis, Lactic	CTD_diseases	5
MESH:D000141	MESH:D000141	Acidosis, Renal Tubular	CTD_diseases	5
MESH:D000151	MESH:D000151	Acinetobacter Infections	CTD_diseases	5
MESH:D000153	MESH:D000153	Acne Keloid	CTD_diseases	5
MESH:D000182	MESH:D000182	ACTH Syndrome, Ectopic	CTD_diseases	5
MESH:D000189	MESH:D000189	Actinobacillus Infections	CTD_diseases	5
MESH:D000196	MESH:D000196	Actinomycosis	CTD_diseases	5
MESH:D000197	MESH:D000197	Actinomycosis, Cervicofacial	CTD_diseases	5
MESH:D000219	MESH:D000219	Adams-Stokes Syndrome	CTD_diseases	5
MESH:D000230	MESH:D000230	Adenocarcinoma	CTD_diseases	5
MESH:D000237	MESH:D000237	Adenoma, Basophil	CTD_diseases	5
MESH:D000238	MESH:D000238	Adenoma, Chromophobe	CTD_diseases	5
MESH:D000239	MESH:D000239	Adenoma, Acidophil	CTD_diseases	5
MESH:D000267	MESH:D000267	Tissue Adhesions	CTD_diseases	5
MESH:D000274	MESH:D000274	Adiposis Dolorosa	CTD_diseases	5
MESH:D000314	MESH:D000314	Adrenal Rest Tumor	CTD_diseases	5
MESH:D000380	MESH:D000380	Agranulocytosis	CTD_diseases	5
MESH:D000472	MESH:D000472	Alkalosis, Respiratory	CTD_diseases	5
MESH:D000474	MESH:D000474	Alkaptonuria	CTD_diseases	5
MESH:D000749	MESH:D000749	Anemia, Megaloblastic	CTD_diseases	5
MESH:D000848	MESH:D000848	Anodontia	CTD_diseases	5
MESH:D000857	MESH:D000857	Olfaction Disorders	CTD_diseases	5
MESH:D000868	MESH:D000868	Anterior Compartment Syndrome	CTD_diseases	5
MESH:D000881	MESH:D000881	Anthrax	CTD_diseases	5
MESH:D001002	MESH:D001002	Anuria	CTD_diseases	5
MESH:D001004	MESH:D001004	Anus Diseases	CTD_diseases	5
MESH:D001017	MESH:D001017	Aortic Coarctation	CTD_diseases	5
MESH:D001020	MESH:D001020	Aortic Stenosis, Subvalvular	CTD_diseases	5
MESH:D001023	MESH:D001023	Aortic Valve Prolapse	CTD_diseases	5
MESH:D001044	MESH:D001044	Aphonia	CTD_diseases	5
MESH:D001072	MESH:D001072	Apraxias	CTD_diseases	5
MESH:D001079	MESH:D001079	Apudoma	CTD_diseases	5
MESH:D001100	MESH:D001100	Arachnoiditis	CTD_diseases	5
MESH:D001139	MESH:D001139	Arnold-Chiari Malformation	CTD_diseases	5
MESH:D001159	MESH:D001159	Arterio-Arterial Fistula	CTD_diseases	5
MESH:D001162	MESH:D001162	Arteriosclerosis Obliterans	CTD_diseases	5
MESH:D001195	MESH:D001195	Asbestosis	CTD_diseases	5
MESH:D001229	MESH:D001229	Aspergillosis, Allergic Bronchopulmonary	CTD_diseases	5
MESH:D001259	MESH:D001259	Ataxia	CTD_diseases	5
MESH:D001264	MESH:D001264	Athetosis	CTD_diseases	5
MESH:D001361	MESH:D001361	Avitaminosis	CTD_diseases	5
MESH:D001405	MESH:D001405	Reflex, Babinski	CTD_diseases	5
MESH:D001416	MESH:D001416	Back Pain	CTD_diseases	5
MESH:D001437	MESH:D001437	Bacteriuria	CTD_diseases	5
MESH:D001442	MESH:D001442	Bacteroides Infections	CTD_diseases	5
MESH:D001474	MESH:D001474	Bartonella Infections	CTD_diseases	5
MESH:D001477	MESH:D001477	Bartter Syndrome	CTD_diseases	5
MESH:D001607	MESH:D001607	Berylliosis	CTD_diseases	5
MESH:D001651	MESH:D001651	Cholestasis, Extrahepatic	CTD_diseases	5
MESH:D001657	MESH:D001657	Biliary Dyskinesia	CTD_diseases	5
MESH:D001658	MESH:D001658	Biliary Fistula	CTD_diseases	5
MESH:D001742	MESH:D001742	Blackwater Fever	CTD_diseases	5
MESH:D001744	MESH:D001744	Urinary Bladder Calculi	CTD_diseases	5
MESH:D001747	MESH:D001747	Urinary Bladder Fistula	CTD_diseases	5
MESH:D001748	MESH:D001748	Urinary Bladder Neck Obstruction	CTD_diseases	5
MESH:D001749	MESH:D001749	Urinary Bladder Neoplasms	CTD_diseases	5
MESH:D001765	MESH:D001765	Blind Loop Syndrome	CTD_diseases	5
MESH:D001907	MESH:D001907	Boutonneuse Fever	CTD_diseases	5
MESH:D001988	MESH:D001988	Bronchiolitis	CTD_diseases	5
MESH:D002032	MESH:D002032	Bulimia	CTD_diseases	5
MESH:D002037	MESH:D002037	Bundle-Branch Block	CTD_diseases	5
MESH:D002051	MESH:D002051	Burkitt Lymphoma	CTD_diseases	5
MESH:D002095	MESH:D002095	Byssinosis	CTD_diseases	5
MESH:D002115	MESH:D002115	Calciphylaxis	CTD_diseases	5
MESH:D002205	MESH:D002205	Caplan Syndrome	CTD_diseases	5
MESH:D002278	MESH:D002278	Carcinoma in Situ	CTD_diseases	5
MESH:D002280	MESH:D002280	Carcinoma, Basal Cell	CTD_diseases	5
MESH:D002281	MESH:D002281	Carcinoma, Basosquamous	CTD_diseases	5
MESH:D002285	MESH:D002285	Carcinoma, Intraductal, Noninfiltrating	CTD_diseases	5
MESH:D002288	MESH:D002288	Adenocarcinoma, Mucinous	CTD_diseases	5
MESH:D002291	MESH:D002291	Carcinoma, Papillary	CTD_diseases	5
MESH:D002294	MESH:D002294	Carcinoma, Squamous Cell	CTD_diseases	5
MESH:D002295	MESH:D002295	Carcinoma, Transitional Cell	CTD_diseases	5
MESH:D002340	MESH:D002340	Carotid Artery Diseases	CTD_diseases	5
MESH:D002375	MESH:D002375	Catalepsy	CTD_diseases	5
MESH:D002389	MESH:D002389	Catatonia	CTD_diseases	5
MESH:D002422	MESH:D002422	Causalgia	CTD_diseases	5
MESH:D002430	MESH:D002430	Cecal Neoplasms	CTD_diseases	5
MESH:D002446	MESH:D002446	Celiac Disease	CTD_diseases	5
MESH:D002471	MESH:D002471	Cell Transformation, Neoplastic	CTD_diseases	5
MESH:D002524	MESH:D002524	Cerebellar Ataxia	CTD_diseases	5
MESH:D002528	MESH:D002528	Cerebellar Neoplasms	CTD_diseases	5
MESH:D002537	MESH:D002537	Intracranial Arteriosclerosis	CTD_diseases	5
MESH:D002538	MESH:D002538	Intracranial Arteriovenous Malformations	CTD_diseases	5
MESH:D002542	MESH:D002542	Intracranial Embolism and Thrombosis	CTD_diseases	5
MESH:D002545	MESH:D002545	Brain Ischemia	CTD_diseases	5
MESH:D002547	MESH:D002547	Cerebral Palsy	CTD_diseases	5
MESH:D002577	MESH:D002577	Uterine Cervical Diseases	CTD_diseases	5
MESH:D002581	MESH:D002581	Uterine Cervical Incompetence	CTD_diseases	5
MESH:D002609	MESH:D002609	Chediak-Higashi Syndrome	CTD_diseases	5
MESH:D002637	MESH:D002637	Chest Pain	CTD_diseases	5
MESH:D002690	MESH:D002690	Chlamydia Infections	CTD_diseases	5
MESH:D002759	MESH:D002759	Adenoma, Bile Duct	CTD_diseases	5
MESH:D002771	MESH:D002771	Cholera	CTD_diseases	5
MESH:D002804	MESH:D002804	Chondroblastoma	CTD_diseases	5
MESH:D002806	MESH:D002806	Chondrodysplasia Punctata	CTD_diseases	5
MESH:D002812	MESH:D002812	Chondroma	CTD_diseases	5
MESH:D002813	MESH:D002813	Chondrosarcoma	CTD_diseases	5
MESH:D002819	MESH:D002819	Chorea	CTD_diseases	5
MESH:D002822	MESH:D002822	Choriocarcinoma	CTD_diseases	5
MESH:D002862	MESH:D002862	Chromoblastomycosis	CTD_diseases	5
MESH:D002873	MESH:D002873	Chromosome Fragility	CTD_diseases	5
MESH:D002972	MESH:D002972	Cleft Palate	CTD_diseases	5
MESH:D002973	MESH:D002973	Cleidocranial Dysplasia	CTD_diseases	5
MESH:D003043	MESH:D003043	Cocarcinogenesis	CTD_diseases	5
MESH:D003093	MESH:D003093	Colitis, Ulcerative	CTD_diseases	5
MESH:D003100	MESH:D003100	Colles' Fracture	CTD_diseases	5
MESH:D003109	MESH:D003109	Colonic Diseases, Functional	CTD_diseases	5
MESH:D003111	MESH:D003111	Colonic Polyps	CTD_diseases	5
MESH:D003138	MESH:D003138	Common Bile Duct Neoplasms	CTD_diseases	5
MESH:D003221	MESH:D003221	Confusion	CTD_diseases	5
MESH:D003232	MESH:D003232	Conjunctivitis, Acute Hemorrhagic	CTD_diseases	5
MESH:D003294	MESH:D003294	Seizures, Febrile	CTD_diseases	5
MESH:D003310	MESH:D003310	Cor Triatriatum	CTD_diseases	5
MESH:D003324	MESH:D003324	Coronary Artery Disease	CTD_diseases	5
MESH:D003328	MESH:D003328	Coronary Thrombosis	CTD_diseases	5
MESH:D003329	MESH:D003329	Coronary Vasospasm	CTD_diseases	5
MESH:D003330	MESH:D003330	Coronary Vessel Anomalies	CTD_diseases	5
MESH:D003354	MESH:D003354	Corynebacterium Infections	CTD_diseases	5
MESH:D003384	MESH:D003384	Coxsackievirus Infections	CTD_diseases	5
MESH:D003387	MESH:D003387	Cracked Tooth Syndrome	CTD_diseases	5
MESH:D003394	MESH:D003394	Craniofacial Dysostosis	CTD_diseases	5
MESH:D003397	MESH:D003397	Craniopharyngioma	CTD_diseases	5
MESH:D003398	MESH:D003398	Craniosynostoses	CTD_diseases	5
MESH:D003414	MESH:D003414	Crigler-Najjar Syndrome	CTD_diseases	5
MESH:D003420	MESH:D003420	Crisscross Heart	CTD_diseases	5
MESH:D003424	MESH:D003424	Crohn Disease	CTD_diseases	5
MESH:D003440	MESH:D003440	Croup	CTD_diseases	5
MESH:D003444	MESH:D003444	Crush Syndrome	CTD_diseases	5
MESH:D003449	MESH:D003449	Cryoglobulinemia	CTD_diseases	5
MESH:D003527	MESH:D003527	Cyclothymic Disorder	CTD_diseases	5
MESH:D003536	MESH:D003536	Cystadenocarcinoma	CTD_diseases	5
MESH:D003537	MESH:D003537	Cystadenoma	CTD_diseases	5
MESH:D003551	MESH:D003551	Cysticercosis	CTD_diseases	5
MESH:D003554	MESH:D003554	Cystinosis	CTD_diseases	5
MESH:D003556	MESH:D003556	Cystitis	CTD_diseases	5
MESH:D003557	MESH:D003557	Phyllodes Tumor	CTD_diseases	5
MESH:D003719	MESH:D003719	Dens in Dente	CTD_diseases	5
MESH:D003744	MESH:D003744	Dental Enamel Hypoplasia	CTD_diseases	5
MESH:D003750	MESH:D003750	Dental Fissures	CTD_diseases	5
MESH:D003751	MESH:D003751	Dental Fistula	CTD_diseases	5
MESH:D003805	MESH:D003805	Dentin Dysplasia	CTD_diseases	5
MESH:D003811	MESH:D003811	Dentinogenesis Imperfecta	CTD_diseases	5
MESH:D003919	MESH:D003919	Diabetes Insipidus	CTD_diseases	5
MESH:D003921	MESH:D003921	Diabetes Mellitus, Experimental	CTD_diseases	5
MESH:D003924	MESH:D003924	Diabetes Mellitus, Type 2	CTD_diseases	5
MESH:D003928	MESH:D003928	Diabetic Nephropathies	CTD_diseases	5
MESH:D003968	MESH:D003968	Diarrhea, Infantile	CTD_diseases	5
MESH:D004244	MESH:D004244	Dizziness	CTD_diseases	5
MESH:D004374	MESH:D004374	Ductus Arteriosus, Patent	CTD_diseases	5
MESH:D004377	MESH:D004377	Dumping Syndrome	CTD_diseases	5
MESH:D004379	MESH:D004379	Duodenal Neoplasms	CTD_diseases	5
MESH:D004380	MESH:D004380	Duodenal Obstruction	CTD_diseases	5
MESH:D004382	MESH:D004382	Duodenitis	CTD_diseases	5
MESH:D004405	MESH:D004405	Dysentery, Bacillary	CTD_diseases	5
MESH:D004407	MESH:D004407	Dysgerminoma	CTD_diseases	5
MESH:D004421	MESH:D004421	Dystonia	CTD_diseases	5
MESH:D004437	MESH:D004437	Ebstein Anomaly	CTD_diseases	5
MESH:D004445	MESH:D004445	Echinococcosis, Pulmonary	CTD_diseases	5
MESH:D004457	MESH:D004457	Echovirus Infections	CTD_diseases	5
MESH:D004461	MESH:D004461	Eclampsia	CTD_diseases	5
MESH:D004478	MESH:D004478	Ectoparasitic Infestations	CTD_diseases	5
MESH:D004480	MESH:D004480	Ectromelia	CTD_diseases	5
MESH:D004541	MESH:D004541	Eisenmenger Complex	CTD_diseases	5
MESH:D004613	MESH:D004613	Ellis-Van Creveld Syndrome	CTD_diseases	5
MESH:D004618	MESH:D004618	Embolism, Air	CTD_diseases	5
MESH:D004620	MESH:D004620	Embolism, Fat	CTD_diseases	5
MESH:D004653	MESH:D004653	Empyema	CTD_diseases	5
MESH:D004672	MESH:D004672	Encephalitis, Japanese	CTD_diseases	5
MESH:D004674	MESH:D004674	Encephalitis, St. Louis	CTD_diseases	5
MESH:D004675	MESH:D004675	Encephalitis, Tick-Borne	CTD_diseases	5
MESH:D004681	MESH:D004681	Encephalomyelitis, Autoimmune, Experimental	CTD_diseases	5
MESH:D004687	MESH:D004687	Enchondromatosis	CTD_diseases	5
MESH:D004692	MESH:D004692	Endarteritis	CTD_diseases	5
MESH:D004698	MESH:D004698	Endocarditis, Subacute Bacterial	CTD_diseases	5
MESH:D004714	MESH:D004714	Endometrial Hyperplasia	CTD_diseases	5
MESH:D004716	MESH:D004716	Endometritis	CTD_diseases	5
MESH:D004761	MESH:D004761	Enterocolitis, Pseudomembranous	CTD_diseases	5
MESH:D004826	MESH:D004826	Epiglottitis	CTD_diseases	5
MESH:D004828	MESH:D004828	Epilepsies, Partial	CTD_diseases	5
MESH:D004829	MESH:D004829	Epilepsy, Generalized	CTD_diseases	5
MESH:D004831	MESH:D004831	Epilepsies, Myoclonic	CTD_diseases	5
MESH:D004834	MESH:D004834	Epilepsy, Post-Traumatic	CTD_diseases	5
MESH:D004886	MESH:D004886	Erysipelas	CTD_diseases	5
MESH:D004887	MESH:D004887	Erysipeloid	CTD_diseases	5
MESH:D004894	MESH:D004894	Erythrasma	CTD_diseases	5
MESH:D004915	MESH:D004915	Leukemia, Erythroblastic, Acute	CTD_diseases	5
MESH:D004927	MESH:D004927	Escherichia coli Infections	CTD_diseases	5
MESH:D004942	MESH:D004942	Esophagitis, Peptic	CTD_diseases	5
MESH:D004948	MESH:D004948	Esotropia	CTD_diseases	5
MESH:D005084	MESH:D005084	Exhibitionism	CTD_diseases	5
MESH:D005099	MESH:D005099	Exotropia	CTD_diseases	5
MESH:D005157	MESH:D005157	Facial Pain	CTD_diseases	5
MESH:D005184	MESH:D005184	Fallopian Tube Diseases	CTD_diseases	5
MESH:D005185	MESH:D005185	Fallopian Tube Neoplasms	CTD_diseases	5
MESH:D005198	MESH:D005198	Fanconi Syndrome	CTD_diseases	5
MESH:D005207	MESH:D005207	Fasciculation	CTD_diseases	5
MESH:D005242	MESH:D005242	Fecal Incontinence	CTD_diseases	5
MESH:D005244	MESH:D005244	Fecal Impaction	CTD_diseases	5
MESH:D005258	MESH:D005258	Felty Syndrome	CTD_diseases	5
MESH:D005265	MESH:D005265	Femoral Neck Fractures	CTD_diseases	5
MESH:D005271	MESH:D005271	Femur Head Necrosis	CTD_diseases	5
MESH:D005327	MESH:D005327	Fetal Resorption	CTD_diseases	5
MESH:D005329	MESH:D005329	Fetishism (Psychiatric)	CTD_diseases	5
MESH:D005330	MESH:D005330	Fetofetal Transfusion	CTD_diseases	5
MESH:D005331	MESH:D005331	Fetomaternal Transfusion	CTD_diseases	5
MESH:D005335	MESH:D005335	Fever of Unknown Origin	CTD_diseases	5
MESH:D005351	MESH:D005351	Fibromatosis, Gingival	CTD_diseases	5
MESH:D005354	MESH:D005354	Fibrosarcoma	CTD_diseases	5
MESH:D005357	MESH:D005357	Fibrous Dysplasia of Bone	CTD_diseases	5
MESH:D005588	MESH:D005588	Fox-Fordyce Disease	CTD_diseases	5
MESH:D005600	MESH:D005600	Fragile X Syndrome	CTD_diseases	5
MESH:D005642	MESH:D005642	Fuchs' Endothelial Dystrophy	CTD_diseases	5
MESH:D005645	MESH:D005645	Fucosidosis	CTD_diseases	5
MESH:D005671	MESH:D005671	Fused Teeth	CTD_diseases	5
MESH:D005674	MESH:D005674	Fusobacterium Infections	CTD_diseases	5
MESH:D005687	MESH:D005687	Galactorrhea	CTD_diseases	5
MESH:D005693	MESH:D005693	Galactosemias	CTD_diseases	5
MESH:D005738	MESH:D005738	Gas Gangrene	CTD_diseases	5
MESH:D005747	MESH:D005747	Gastric Fistula	CTD_diseases	5
MESH:D005757	MESH:D005757	Gastritis, Atrophic	CTD_diseases	5
MESH:D005758	MESH:D005758	Gastritis, Hypertrophic	CTD_diseases	5
MESH:D005870	MESH:D005870	Giant Cell Tumors	CTD_diseases	5
MESH:D005878	MESH:D005878	Gilbert Disease	CTD_diseases	5
MESH:D005884	MESH:D005884	Gingival Hemorrhage	CTD_diseases	5
MESH:D005887	MESH:D005887	Gingival Neoplasms	CTD_diseases	5
MESH:D005889	MESH:D005889	Gingival Recession	CTD_diseases	5
MESH:D005891	MESH:D005891	Gingivitis	CTD_diseases	5
MESH:D005929	MESH:D005929	Glossitis, Benign Migratory	CTD_diseases	5
MESH:D005955	MESH:D005955	Glucosephosphate Dehydrogenase Deficiency	CTD_diseases	5
MESH:D006008	MESH:D006008	Glycogen Storage Disease	CTD_diseases	5
MESH:D006059	MESH:D006059	Gonadal Dysgenesis	CTD_diseases	5
MESH:D006069	MESH:D006069	Gonorrhea	CTD_diseases	5
MESH:D006100	MESH:D006100	Granuloma Inguinale	CTD_diseases	5
MESH:D006104	MESH:D006104	Granuloma, Plasma Cell	CTD_diseases	5
MESH:D006106	MESH:D006106	Granulosa Cell Tumor	CTD_diseases	5
MESH:D006192	MESH:D006192	Haemophilus Infections	CTD_diseases	5
MESH:D006250	MESH:D006250	Hartnup Disease	CTD_diseases	5
MESH:D006255	MESH:D006255	Rhinitis, Allergic, Seasonal	CTD_diseases	5
MESH:D006261	MESH:D006261	Headache	CTD_diseases	5
MESH:D006313	MESH:D006313	Hearing Loss, Central	CTD_diseases	5
MESH:D006343	MESH:D006343	Heart Septal Defects	CTD_diseases	5
MESH:D006390	MESH:D006390	Hemangioendothelioma	CTD_diseases	5
MESH:D006392	MESH:D006392	Hemangioma, Cavernous	CTD_diseases	5
MESH:D006396	MESH:D006396	Hematemesis	CTD_diseases	5
MESH:D006399	MESH:D006399	Hematocolpos	CTD_diseases	5
MESH:D006407	MESH:D006407	Hematoma, Epidural, Cranial	CTD_diseases	5
MESH:D006408	MESH:D006408	Hematoma, Subdural	CTD_diseases	5
MESH:D006409	MESH:D006409	Hematometra	CTD_diseases	5
MESH:D006429	MESH:D006429	Hemiplegia	CTD_diseases	5
MESH:D006432	MESH:D006432	Hemochromatosis	CTD_diseases	5
MESH:D006457	MESH:D006457	Hemoglobinuria, Paroxysmal	CTD_diseases	5
MESH:D006463	MESH:D006463	Hemolytic-Uremic Syndrome	CTD_diseases	5
MESH:D006486	MESH:D006486	Hemosiderosis	CTD_diseases	5
MESH:D006501	MESH:D006501	Hepatic Encephalopathy	CTD_diseases	5
MESH:D006506	MESH:D006506	Hepatitis A	CTD_diseases	5
MESH:D006528	MESH:D006528	Carcinoma, Hepatocellular	CTD_diseases	5
MESH:D006550	MESH:D006550	Hernia, Femoral	CTD_diseases	5
MESH:D006551	MESH:D006551	Hernia, Hiatal	CTD_diseases	5
MESH:D006552	MESH:D006552	Hernia, Inguinal	CTD_diseases	5
MESH:D006555	MESH:D006555	Hernia, Ventral	CTD_diseases	5
MESH:D006563	MESH:D006563	Herpes Zoster Ophthalmicus	CTD_diseases	5
MESH:D006607	MESH:D006607	Adenoma, Sweat Gland	CTD_diseases	5
MESH:D006616	MESH:D006616	Hip Contracture	CTD_diseases	5
MESH:D006689	MESH:D006689	Hodgkin Disease	CTD_diseases	5
MESH:D006819	MESH:D006819	Hyaline Membrane Disease	CTD_diseases	5
MESH:D006869	MESH:D006869	Hydronephrosis	CTD_diseases	5
MESH:D006938	MESH:D006938	Hyperlipoproteinemia Type II	CTD_diseases	5
MESH:D006948	MESH:D006948	Hyperkinesis	CTD_diseases	5
MESH:D006949	MESH:D006949	Hyperlipidemias	CTD_diseases	5
MESH:D006950	MESH:D006950	Hyperlipidemia, Familial Combined	CTD_diseases	5
MESH:D006952	MESH:D006952	Hyperlipoproteinemia Type III	CTD_diseases	5
MESH:D006953	MESH:D006953	Hyperlipoproteinemia Type IV	CTD_diseases	5
MESH:D006954	MESH:D006954	Hyperlipoproteinemia Type V	CTD_diseases	5
MESH:D006959	MESH:D006959	Hyperoxaluria	CTD_diseases	5
MESH:D006960	MESH:D006960	Hyperoxaluria, Primary	CTD_diseases	5
MESH:D006988	MESH:D006988	Hyphema	CTD_diseases	5
MESH:D007009	MESH:D007009	Hypolipoproteinemias	CTD_diseases	5
MESH:D007014	MESH:D007014	Hypophosphatasia	CTD_diseases	5
MESH:D007015	MESH:D007015	Hypophosphatemia, Familial	CTD_diseases	5
MESH:D007029	MESH:D007029	Hypothalamic Neoplasms	CTD_diseases	5
MESH:D007078	MESH:D007078	Ileal Neoplasms	CTD_diseases	5
MESH:D007079	MESH:D007079	Ileitis	CTD_diseases	5
MESH:D007169	MESH:D007169	Impetigo	CTD_diseases	5
MESH:D007247	MESH:D007247	Infertility, Female	CTD_diseases	5
MESH:D007248	MESH:D007248	Infertility, Male	CTD_diseases	5
MESH:D007331	MESH:D007331	Insulin Coma	CTD_diseases	5
MESH:D007333	MESH:D007333	Insulin Resistance	CTD_diseases	5
MESH:D007443	MESH:D007443	Intussusception	CTD_diseases	5
MESH:D007516	MESH:D007516	Adenoma, Islet Cell	CTD_diseases	5
MESH:D007562	MESH:D007562	Creutzfeldt-Jakob Syndrome	CTD_diseases	5
MESH:D007566	MESH:D007566	Jaundice, Chronic Idiopathic	CTD_diseases	5
MESH:D007567	MESH:D007567	Jaundice, Neonatal	CTD_diseases	5
MESH:D007572	MESH:D007572	Jaw Fractures	CTD_diseases	5
MESH:D007576	MESH:D007576	Jaw, Edentulous, Partially	CTD_diseases	5
MESH:D007580	MESH:D007580	Jejunal Neoplasms	CTD_diseases	5
MESH:D007589	MESH:D007589	Job Syndrome	CTD_diseases	5
MESH:D007662	MESH:D007662	Ketosis	CTD_diseases	5
MESH:D007673	MESH:D007673	Kidney Cortex Necrosis	CTD_diseases	5
MESH:D007680	MESH:D007680	Kidney Neoplasms	CTD_diseases	5
MESH:D007681	MESH:D007681	Kidney Papillary Necrosis	CTD_diseases	5
MESH:D007710	MESH:D007710	Klebsiella Infections	CTD_diseases	5
MESH:D007724	MESH:D007724	Vulvar Lichen Sclerosus	CTD_diseases	5
MESH:D007729	MESH:D007729	Kuru	CTD_diseases	5
MESH:D007738	MESH:D007738	Kyphosis	CTD_diseases	5
MESH:D007787	MESH:D007787	Lactose Intolerance	CTD_diseases	5
MESH:D007877	MESH:D007877	Legionnaires' Disease	CTD_diseases	5
MESH:D007889	MESH:D007889	Leiomyoma	CTD_diseases	5
MESH:D007890	MESH:D007890	Leiomyosarcoma	CTD_diseases	5
MESH:D007939	MESH:D007939	Leukemia L1210	CTD_diseases	5
MESH:D007940	MESH:D007940	Leukemia L5178	CTD_diseases	5
MESH:D007941	MESH:D007941	Leukemia P388	CTD_diseases	5
MESH:D007955	MESH:D007955	Leukemoid Reaction	CTD_diseases	5
MESH:D008010	MESH:D008010	Lichen Planus	CTD_diseases	5
MESH:D008061	MESH:D008061	Whipple Disease	CTD_diseases	5
MESH:D008067	MESH:D008067	Lipoma	CTD_diseases	5
MESH:D008069	MESH:D008069	Lipomatosis, Multiple Symmetrical	CTD_diseases	5
MESH:D008072	MESH:D008072	Hyperlipoproteinemia Type I	CTD_diseases	5
MESH:D008080	MESH:D008080	Liposarcoma	CTD_diseases	5
MESH:D008141	MESH:D008141	Lordosis	CTD_diseases	5
MESH:D008151	MESH:D008151	Lown-Ganong-Levine Syndrome	CTD_diseases	5
MESH:D008193	MESH:D008193	Lyme Disease	CTD_diseases	5
MESH:D008207	MESH:D008207	Lymphatic Metastasis	CTD_diseases	5
MESH:D008218	MESH:D008218	Lymphocytosis	CTD_diseases	5
MESH:D008228	MESH:D008228	Lymphoma, Non-Hodgkin	CTD_diseases	5
MESH:D008265	MESH:D008265	Macrostomia	CTD_diseases	5
MESH:D008269	MESH:D008269	Macular Edema	CTD_diseases	5
MESH:D008271	MESH:D008271	Mycetoma	CTD_diseases	5
MESH:D008275	MESH:D008275	Magnesium Deficiency	CTD_diseases	5
MESH:D008309	MESH:D008309	Mallory-Weiss Syndrome	CTD_diseases	5
MESH:D008375	MESH:D008375	Maple Syrup Urine Disease	CTD_diseases	5
MESH:D008398	MESH:D008398	Masochism	CTD_diseases	5
MESH:D008417	MESH:D008417	Mastoiditis	CTD_diseases	5
MESH:D008446	MESH:D008446	Maxillofacial Injuries	CTD_diseases	5
MESH:D008531	MESH:D008531	Megacolon	CTD_diseases	5
MESH:D008538	MESH:D008538	Meige Syndrome	CTD_diseases	5
MESH:D008548	MESH:D008548	Melanosis	CTD_diseases	5
MESH:D008551	MESH:D008551	Melena	CTD_diseases	5
MESH:D008554	MESH:D008554	Melioidosis	CTD_diseases	5
MESH:D008569	MESH:D008569	Memory Disorders	CTD_diseases	5
MESH:D008575	MESH:D008575	Meniere Disease	CTD_diseases	5
MESH:D008577	MESH:D008577	Meningeal Neoplasms	CTD_diseases	5
MESH:D008582	MESH:D008582	Meningitis, Aseptic	CTD_diseases	5
MESH:D008584	MESH:D008584	Meningitis, Listeria	CTD_diseases	5
MESH:D008589	MESH:D008589	Meningococcal Infections	CTD_diseases	5
MESH:D008591	MESH:D008591	Meningomyelocele	CTD_diseases	5
MESH:D008644	MESH:D008644	Mesial Movement of Teeth	CTD_diseases	5
MESH:D008654	MESH:D008654	Mesothelioma	CTD_diseases	5
MESH:D008831	MESH:D008831	Microcephaly	CTD_diseases	5
MESH:D008865	MESH:D008865	Microstomia	CTD_diseases	5
MESH:D008945	MESH:D008945	Mitral Valve Prolapse	CTD_diseases	5
MESH:D008998	MESH:D008998	Monoclonal Gammopathy of Undetermined Significance	CTD_diseases	5
MESH:D009006	MESH:D009006	Monosomy	CTD_diseases	5
MESH:D009011	MESH:D009011	Monteggia's Fracture	CTD_diseases	5
MESH:D009100	MESH:D009100	Multiple Carboxylase Deficiency	CTD_diseases	5
MESH:D009122	MESH:D009122	Muscle Hypertonia	CTD_diseases	5
MESH:D009123	MESH:D009123	Muscle Hypotonia	CTD_diseases	5
MESH:D009164	MESH:D009164	Mycobacterium Infections	CTD_diseases	5
MESH:D009175	MESH:D009175	Mycoplasma Infections	CTD_diseases	5
MESH:D009188	MESH:D009188	Myelitis, Transverse	CTD_diseases	5
MESH:D009207	MESH:D009207	Myoclonus	CTD_diseases	5
MESH:D009212	MESH:D009212	Myoglobinuria	CTD_diseases	5
MESH:D009214	MESH:D009214	Myoma	CTD_diseases	5
MESH:D009217	MESH:D009217	Myosarcoma	CTD_diseases	5
MESH:D009221	MESH:D009221	Myositis Ossificans	CTD_diseases	5
MESH:D009222	MESH:D009222	Myotonia	CTD_diseases	5
MESH:D009232	MESH:D009232	Myxoma	CTD_diseases	5
MESH:D009236	MESH:D009236	Myxosarcoma	CTD_diseases	5
MESH:D009360	MESH:D009360	Neoplastic Cells, Circulating	CTD_diseases	5
MESH:D009366	MESH:D009366	Neoplasm Seeding	CTD_diseases	5
MESH:D009382	MESH:D009382	Neoplasms, Unknown Primary	CTD_diseases	5
MESH:D009393	MESH:D009393	Nephritis	CTD_diseases	5
MESH:D009397	MESH:D009397	Nephrocalcinosis	CTD_diseases	5
MESH:D009400	MESH:D009400	Nephrosclerosis	CTD_diseases	5
MESH:D009401	MESH:D009401	Nephrosis	CTD_diseases	5
MESH:D009444	MESH:D009444	Neuritis, Autoimmune, Experimental	CTD_diseases	5
MESH:D009464	MESH:D009464	Neuroma, Acoustic	CTD_diseases	5
MESH:D009471	MESH:D009471	Neuromyelitis Optica	CTD_diseases	5
MESH:D009494	MESH:D009494	Neurosyphilis	CTD_diseases	5
MESH:D009508	MESH:D009508	Nevus, Pigmented	CTD_diseases	5
MESH:D009542	MESH:D009542	Niemann-Pick Diseases	CTD_diseases	5
MESH:D009617	MESH:D009617	Nocardia Infections	CTD_diseases	5
MESH:D009855	MESH:D009855	Onchocerciasis	CTD_diseases	5
MESH:D009917	MESH:D009917	Orbital Fractures	CTD_diseases	5
MESH:D009957	MESH:D009957	Oroantral Fistula	CTD_diseases	5
MESH:D010008	MESH:D010008	Osteochondritis Dissecans	CTD_diseases	5
MESH:D010026	MESH:D010026	Osteosclerosis	CTD_diseases	5
MESH:D010034	MESH:D010034	Otitis Media with Effusion	CTD_diseases	5
MESH:D010035	MESH:D010035	Otitis Media, Suppurative	CTD_diseases	5
MESH:D010145	MESH:D010145	Paget Disease, Extramammary	CTD_diseases	5
MESH:D010148	MESH:D010148	Pain, Intractable	CTD_diseases	5
MESH:D010157	MESH:D010157	Palatal Neoplasms	CTD_diseases	5
MESH:D010192	MESH:D010192	Pancreatic Pseudocyst	CTD_diseases	5
MESH:D010212	MESH:D010212	Papilloma	CTD_diseases	5
MESH:D010214	MESH:D010214	Papillon-Lefevre Disease	CTD_diseases	5
MESH:D010253	MESH:D010253	Respirovirus Infections	CTD_diseases	5
MESH:D010263	MESH:D010263	Paraphimosis	CTD_diseases	5
MESH:D010264	MESH:D010264	Paraplegia	CTD_diseases	5
MESH:D010307	MESH:D010307	Parotid Neoplasms	CTD_diseases	5
MESH:D010309	MESH:D010309	Parotitis	CTD_diseases	5
MESH:D010326	MESH:D010326	Pasteurella Infections	CTD_diseases	5
MESH:D010373	MESH:D010373	Lice Infestations	CTD_diseases	5
MESH:D010378	MESH:D010378	Pedophilia	CTD_diseases	5
MESH:D010438	MESH:D010438	Peptic Ulcer Hemorrhage	CTD_diseases	5
MESH:D010468	MESH:D010468	Perceptual Disorders	CTD_diseases	5
MESH:D010485	MESH:D010485	Periapical Periodontitis	CTD_diseases	5
MESH:D010497	MESH:D010497	Pericoronitis	CTD_diseases	5
MESH:D010501	MESH:D010501	Perinephritis	CTD_diseases	5
MESH:D010505	MESH:D010505	Familial Mediterranean Fever	CTD_diseases	5
MESH:D010508	MESH:D010508	Periodontal Abscess	CTD_diseases	5
MESH:D010514	MESH:D010514	Periodontal Pocket	CTD_diseases	5
MESH:D010520	MESH:D010520	Aggressive Periodontitis	CTD_diseases	5
MESH:D010661	MESH:D010661	Phenylketonurias	CTD_diseases	5
MESH:D010677	MESH:D010677	Philadelphia Chromosome	CTD_diseases	5
MESH:D010845	MESH:D010845	Obesity Hypoventilation Syndrome	CTD_diseases	5
MESH:D010874	MESH:D010874	Pinta	CTD_diseases	5
MESH:D010916	MESH:D010916	Pityriasis Rubra Pilaris	CTD_diseases	5
MESH:D011001	MESH:D011001	Pleuropneumonia	CTD_diseases	5
MESH:D011008	MESH:D011008	Pneumococcal Infections	CTD_diseases	5
MESH:D011015	MESH:D011015	Pneumonia, Aspiration	CTD_diseases	5
MESH:D011016	MESH:D011016	Pneumonia, Atypical Interstitial, of Cattle	CTD_diseases	5
MESH:D011022	MESH:D011022	Pneumonia, Rickettsial	CTD_diseases	5
MESH:D011023	MESH:D011023	Pneumonia, Staphylococcal	CTD_diseases	5
MESH:D011087	MESH:D011087	Polycythemia Vera	CTD_diseases	5
MESH:D011151	MESH:D011151	Popliteal Cyst	CTD_diseases	5
MESH:D011180	MESH:D011180	Postmortem Changes	CTD_diseases	5
MESH:D011191	MESH:D011191	Potassium Deficiency	CTD_diseases	5
MESH:D011225	MESH:D011225	Pre-Eclampsia	CTD_diseases	5
MESH:D011227	MESH:D011227	Pre-Excitation, Mahaim-Type	CTD_diseases	5
MESH:D011236	MESH:D011236	Prediabetic State	CTD_diseases	5
MESH:D011488	MESH:D011488	Protein Deficiency	CTD_diseases	5
MESH:D011512	MESH:D011512	Proteus Infections	CTD_diseases	5
MESH:D011538	MESH:D011538	Pruritus Ani	CTD_diseases	5
MESH:D011539	MESH:D011539	Pruritus Vulvae	CTD_diseases	5
MESH:D011553	MESH:D011553	Pseudomyxoma Peritonei	CTD_diseases	5
MESH:D011559	MESH:D011559	Pseudotumor Cerebri	CTD_diseases	5
MESH:D011595	MESH:D011595	Psychomotor Agitation	CTD_diseases	5
MESH:D011596	MESH:D011596	Psychomotor Disorders	CTD_diseases	5
MESH:D011656	MESH:D011656	Pulmonary Emphysema	CTD_diseases	5
MESH:D011662	MESH:D011662	Pulmonary Subvalvular Stenosis	CTD_diseases	5
MESH:D011694	MESH:D011694	Purpura, Hyperglobulinemic	CTD_diseases	5
MESH:D011707	MESH:D011707	Pyloric Stenosis	CTD_diseases	5
MESH:D011776	MESH:D011776	Pyuria	CTD_diseases	5
MESH:D011782	MESH:D011782	Quadriplegia	CTD_diseases	5
MESH:D011818	MESH:D011818	Rabies	CTD_diseases	5
MESH:D011842	MESH:D011842	Radicular Cyst	CTD_diseases	5
MESH:D012003	MESH:D012003	Rectal Fistula	CTD_diseases	5
MESH:D012005	MESH:D012005	Rectal Prolapse	CTD_diseases	5
MESH:D012019	MESH:D012019	Reflex Sympathetic Dystrophy	CTD_diseases	5
MESH:D012061	MESH:D012061	Relapsing Fever	CTD_diseases	5
MESH:D012075	MESH:D012075	Remission, Spontaneous	CTD_diseases	5
MESH:D012175	MESH:D012175	Retinoblastoma	CTD_diseases	5
MESH:D012218	MESH:D012218	Rheumatoid Nodule	CTD_diseases	5
MESH:D012221	MESH:D012221	Rhinitis, Allergic, Perennial	CTD_diseases	5
MESH:D012222	MESH:D012222	Rhinitis, Atrophic	CTD_diseases	5
MESH:D012223	MESH:D012223	Rhinitis, Vasomotor	CTD_diseases	5
MESH:D012282	MESH:D012282	Rickettsia Infections	CTD_diseases	5
MESH:D012373	MESH:D012373	Rocky Mountain Spotted Fever	CTD_diseases	5
MESH:D012409	MESH:D012409	Rubella	CTD_diseases	5
MESH:D012448	MESH:D012448	Sadism	CTD_diseases	5
MESH:D012465	MESH:D012465	Salivary Duct Calculi	CTD_diseases	5
MESH:D012480	MESH:D012480	Salmonella Infections	CTD_diseases	5
MESH:D012516	MESH:D012516	Osteosarcoma	CTD_diseases	5
MESH:D012532	MESH:D012532	Scabies	CTD_diseases	5
MESH:D012541	MESH:D012541	Scarlet Fever	CTD_diseases	5
MESH:D012544	MESH:D012544	Scheuermann Disease	CTD_diseases	5
MESH:D012553	MESH:D012553	Schistosomiasis haematobia	CTD_diseases	5
MESH:D012554	MESH:D012554	Schistosomiasis japonica	CTD_diseases	5
MESH:D012555	MESH:D012555	Schistosomiasis mansoni	CTD_diseases	5
MESH:D012600	MESH:D012600	Scoliosis	CTD_diseases	5
MESH:D012612	MESH:D012612	Scrub Typhus	CTD_diseases	5
MESH:D012614	MESH:D012614	Scurvy	CTD_diseases	5
MESH:D012618	MESH:D012618	Sea-Blue Histiocyte Syndrome	CTD_diseases	5
MESH:D012766	MESH:D012766	Pasteurellosis, Pneumonic	CTD_diseases	5
MESH:D012772	MESH:D012772	Shock, Septic	CTD_diseases	5
MESH:D012804	MESH:D012804	Sick Sinus Syndrome	CTD_diseases	5
MESH:D012806	MESH:D012806	Siderosis	CTD_diseases	5
MESH:D012810	MESH:D012810	Sigmoid Diseases	CTD_diseases	5
MESH:D012829	MESH:D012829	Silicosis	CTD_diseases	5
MESH:D012848	MESH:D012848	Sinoatrial Block	CTD_diseases	5
MESH:C531616	MESH:C531616	Primary amyloidosis	CTD_diseases	5
MESH:C531619	MESH:C531619	Happy puppet syndrome (formerly)	CTD_diseases	5
MESH:C531621	MESH:C531621	Cutaneous anthrax	CTD_diseases	5
MESH:C531638	MESH:C531638	Sudden unexpected nocturnal death syndrome	CTD_diseases	5
MESH:C531660	MESH:C531660	Generalized elastolysis	CTD_diseases	5
MESH:C531700	MESH:C531700	Diarrhea prodrome + Hemolytic-Uremic Syndrome	CTD_diseases	5
MESH:C531716	MESH:C531716	Incontinentia pigmenti, familial male-lethal type	CTD_diseases	5
MESH:C531731	MESH:C531731	Lissencephaly and agenesis of corpus callosum	CTD_diseases	5
MESH:C531735	MESH:C531735	Congenital macroglossia	CTD_diseases	5
MESH:C531737	MESH:C531737	Malignant fever	CTD_diseases	5
MESH:C531747	MESH:C531747	Congenital facial diplegia	CTD_diseases	5
MESH:C531763	MESH:C531763	Irritable heart	CTD_diseases	5
MESH:C531766	MESH:C531766	Inflammation of the whole uveal tract	CTD_diseases	5
MESH:C531767	MESH:C531767	Edema of the optic disc	CTD_diseases	5
MESH:C531777	MESH:C531777	Islet cell tumor syndrome	CTD_diseases	5
MESH:C531791	MESH:C531791	Priapism, familial idiopathic	CTD_diseases	5
MESH:C531815	MESH:C531815	Hypopituitarism and septooptic 'dysplasia'	CTD_diseases	5
MESH:C531816	MESH:C531816	Severe combined immunodeficiency due to adenosine deaminase deficiency	CTD_diseases	5
MESH:C531833	MESH:C531833	Ophthalmoplegia, painful	CTD_diseases	5
MESH:C531841	MESH:C531841	Benign non-infected urachal cyst	CTD_diseases	5
MESH:C531847	MESH:C531847	Wallerian degeneration of the pyramidal tract	CTD_diseases	5
MESH:C535273	MESH:C535273	Presenile dementia, Kraepelin type	CTD_diseases	5
MESH:C535274	MESH:C535274	Prieto X-linked mental retardation syndrome	CTD_diseases	5
MESH:C535288	MESH:C535288	Rapadilino syndrome	CTD_diseases	5
MESH:C535289	MESH:C535289	Rapp-Hodgkin syndrome	CTD_diseases	5
MESH:C535292	MESH:C535292	Ray Peterson Scott syndrome	CTD_diseases	5
MESH:C535294	MESH:C535294	Reardon Hall Slaney syndrome	CTD_diseases	5
MESH:C535300	MESH:C535300	Autosomal dominant compelling helio ophthalmic outburst syndrome	CTD_diseases	5
MESH:C535307	MESH:C535307	2-Methylacetoacetyl CoA thiolase deficiency	CTD_diseases	5
MESH:C535312	MESH:C535312	3-Hydroxyisobutyric aciduria	CTD_diseases	5
MESH:C535314	MESH:C535314	Miller-McKusick-Malvaux-Syndrome (3M Syndrome)	CTD_diseases	5
MESH:C535317	MESH:C535317	47, XYY syndrome	CTD_diseases	5
MESH:C535318	MESH:C535318	Triple X syndrome	CTD_diseases	5
MESH:C535319	MESH:C535319	49,XXXXX syndrome	CTD_diseases	5
MESH:C535322	MESH:C535322	5-oxoprolinase deficiency	CTD_diseases	5
MESH:C535323	MESH:C535323	5q- syndrome	CTD_diseases	5
MESH:C535328	MESH:C535328	Homocarnosinosis	CTD_diseases	5
MESH:C535334	MESH:C535334	ABCD syndrome	CTD_diseases	5
MESH:C535350	MESH:C535350	Cerebellar ataxia ectodermal dysplasia	CTD_diseases	5
MESH:C535351	MESH:C535351	CAPOS syndrome	CTD_diseases	5
MESH:C535356	MESH:C535356	Chorioretinal atrophy, progressive bifocal	CTD_diseases	5
MESH:C535357	MESH:C535357	Choroid plexus calcification with mental retardation	CTD_diseases	5
MESH:C535361	MESH:C535361	Chromosome 1 ring	CTD_diseases	5
MESH:C535369	MESH:C535369	Chromosome 20 ring	CTD_diseases	5
MESH:C535375	MESH:C535375	Dermochondrocorneal dystrophy of François	CTD_diseases	5
MESH:C535377	MESH:C535377	Epidermolysis bullosa with pyloric atresia	CTD_diseases	5
MESH:C535378	MESH:C535378	Arthrogryposis multiplex congenita, distal type 1	CTD_diseases	5
MESH:C535379	MESH:C535379	Arthrogryposis multiplex congenita, distal type 2	CTD_diseases	5
MESH:C535381	MESH:C535381	Arthrogryposis multiplex with deafness, inguinal hernias, and early death	CTD_diseases	5
MESH:C535382	MESH:C535382	Arthrogryposis renal dysfunction cholestasis syndrome	CTD_diseases	5
MESH:C535384	MESH:C535384	Arthrogryposis, distal, type 2E	CTD_diseases	5
MESH:C535385	MESH:C535385	Arthrogryposis, distal, with hypopituitarism, mental retardation, and facial anomalies	CTD_diseases	5
MESH:C535386	MESH:C535386	Arthrogryposis-like hand anomaly and sensorineural deafness	CTD_diseases	5
MESH:C535390	MESH:C535390	Aspergillus niger infection	CTD_diseases	5
MESH:C535392	MESH:C535392	Astley-Kendall syndrome	CTD_diseases	5
MESH:C535395	MESH:C535395	Atelosteogenesis type 2	CTD_diseases	5
MESH:C535396	MESH:C535396	Atelosteogenesis, type 1	CTD_diseases	5
MESH:C535407	MESH:C535407	Gamma aminobutyric acid transaminase deficiency	CTD_diseases	5
MESH:C535434	MESH:C535434	Beta ketothiolase deficiency	CTD_diseases	5
MESH:C535436	MESH:C535436	Bethlem myopathy	CTD_diseases	5
MESH:C535438	MESH:C535438	Bidirectional tachycardia	CTD_diseases	5
MESH:C535442	MESH:C535442	Bile acid synthesis defect, congenital, 1	CTD_diseases	5
MESH:C535443	MESH:C535443	Bile acid synthesis defect, congenital, 2	CTD_diseases	5
MESH:C535455	MESH:C535455	Chromosomes 1 and 2, monosomy 2q duplication 1p	CTD_diseases	5
MESH:C535456	MESH:C535456	Chronic recurrent multifocal osteomyelitis	CTD_diseases	5
MESH:C535459	MESH:C535459	Chudley-Mccullough syndrome	CTD_diseases	5
MESH:C535460	MESH:C535460	Chylomicron retention disease	CTD_diseases	5
MESH:C535464	MESH:C535464	Conotruncal cardiac defects	CTD_diseases	5
MESH:C535472	MESH:C535472	Corneal cerebellar syndrome	CTD_diseases	5
MESH:C535473	MESH:C535473	Corneal dystrophy and perceptive deafness	CTD_diseases	5
MESH:C535474	MESH:C535474	Corneal dystrophy Avellino type	CTD_diseases	5
MESH:C535475	MESH:C535475	Corneal Dystrophy, Crystalline, of Schnyder	CTD_diseases	5
MESH:C535476	MESH:C535476	Corneal dystrophy of Bowman layer, type 1	CTD_diseases	5
MESH:C535480	MESH:C535480	Corneal dystrophy, gelatinous drop-like	CTD_diseases	5
MESH:C535487	MESH:C535487	Ring Chromosome 14 Syndrome	CTD_diseases	5
MESH:C535493	MESH:C535493	Epidermolysis bullosa, lethal acantholytic	CTD_diseases	5
MESH:C535496	MESH:C535496	Epilepsy occipital calcifications	CTD_diseases	5
MESH:C535499	MESH:C535499	Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp	CTD_diseases	5
MESH:C535501	MESH:C535501	Epiphyseal dysplasia, multiple, 1	CTD_diseases	5
MESH:C535502	MESH:C535502	Epiphyseal dysplasia, multiple, 2	CTD_diseases	5
MESH:C535503	MESH:C535503	Epiphyseal dysplasia, multiple, 3	CTD_diseases	5
MESH:C535504	MESH:C535504	Epiphyseal dysplasia, multiple, 4	CTD_diseases	5
MESH:C535505	MESH:C535505	Epiphyseal dysplasia, multiple, 5	CTD_diseases	5
MESH:C535506	MESH:C535506	Episodic ataxia with nystagmus	CTD_diseases	5
MESH:C535507	MESH:C535507	MYH9-Related Disorders	CTD_diseases	5
MESH:C535509	MESH:C535509	Erythema elevatum diutinum	CTD_diseases	5
MESH:C535512	MESH:C535512	Erythroderma desquamativa of Leiner	CTD_diseases	5
MESH:C535513	MESH:C535513	Lethal congenital erythroderma	CTD_diseases	5
MESH:C535521	MESH:C535521	Stargardt disease 4	CTD_diseases	5
MESH:C535522	MESH:C535522	Infantile convulsions and paroxysmal choreoathetosis, familial	CTD_diseases	5
MESH:C535531	MESH:C535531	Intervertebral disc disease	CTD_diseases	5
MESH:C535533	MESH:C535533	Intrahepatic cholangiocarcinoma	CTD_diseases	5
MESH:C535541	MESH:C535541	Isobutyryl-CoA dehydrogenase deficiency	CTD_diseases	5
MESH:C535548	MESH:C535548	Pelvic dysplasia arthrogryposis of lower limbs	CTD_diseases	5
MESH:C535549	MESH:C535549	Pelvic lipomatosis	CTD_diseases	5
MESH:C535550	MESH:C535550	Pelviscapular dysplasia	CTD_diseases	5
MESH:C535551	MESH:C535551	Pemphigus and fogo selvagem	CTD_diseases	5
MESH:C535553	MESH:C535553	Abdominal cystic lymphangioma	CTD_diseases	5
MESH:C535556	MESH:C535556	Abidi X-linked mental retardation syndrome	CTD_diseases	5
MESH:C535562	MESH:C535562	Absence of septum pellucidum	CTD_diseases	5
MESH:C535570	MESH:C535570	Acalvaria	CTD_diseases	5
MESH:C535577	MESH:C535577	Cardioauditory syndrome of Sanchez Cascos	CTD_diseases	5
MESH:C535578	MESH:C535578	Cardiocranial syndrome	CTD_diseases	5
MESH:C535588	MESH:C535588	Carnitine palmitoyl transferase 1A deficiency	CTD_diseases	5
MESH:C535602	MESH:C535602	Doyne honeycomb retinal dystrophy	CTD_diseases	5
MESH:C535609	MESH:C535609	Akaba Hayasaka syndrome	CTD_diseases	5
MESH:C535612	MESH:C535612	Al Awadi syndrome	CTD_diseases	5
MESH:C535619	MESH:C535619	Hairy nose tip	CTD_diseases	5
MESH:C535621	MESH:C535621	Halal Setton Wang syndrome	CTD_diseases	5
MESH:C535626	MESH:C535626	Hand and foot deformity with flat facies	CTD_diseases	5
MESH:C535632	MESH:C535632	Hardikar syndrome	CTD_diseases	5
MESH:C535636	MESH:C535636	Freiberg's disease	CTD_diseases	5
MESH:C535637	MESH:C535637	Freire-Maia odontotrichomelic syndrome	CTD_diseases	5
MESH:C535646	MESH:C535646	Garret Tripp syndrome	CTD_diseases	5
MESH:C535650	MESH:C535650	Gastro-enteropancreatic neuroendocrine tumor	CTD_diseases	5
MESH:C535653	MESH:C535653	Acrokeratoelastoidosis of Costa	CTD_diseases	5
MESH:C535655	MESH:C535655	Acromegaloid facial appearance syndrome	CTD_diseases	5
MESH:C535658	MESH:C535658	Acromesomelic dysplasia	CTD_diseases	5
MESH:C535659	MESH:C535659	Acromesomelic dysplasia Campailla-Martinelli type	CTD_diseases	5
MESH:C535664	MESH:C535664	Acropectoral syndrome	CTD_diseases	5
MESH:C535669	MESH:C535669	Actinic cheilitis	CTD_diseases	5
MESH:C535681	MESH:C535681	Familial anomalous origin of right pulmonary artery	CTD_diseases	5
MESH:C535682	MESH:C535682	Right ventricle hypoplasia	CTD_diseases	5
MESH:C535687	MESH:C535687	Roberts Syndrome	CTD_diseases	5
MESH:C535690	MESH:C535690	Long-chain acyl-CoA dehydrogenase deficiency	CTD_diseases	5
MESH:C535694	MESH:C535694	Malignant hyperthermia susceptibility type 1	CTD_diseases	5
MESH:C535695	MESH:C535695	Malignant hyperthermia susceptibility type 2	CTD_diseases	5
MESH:C535696	MESH:C535696	Malignant hyperthermia susceptibility type 3	CTD_diseases	5
MESH:C535697	MESH:C535697	Malignant hyperthermia susceptibility type 4	CTD_diseases	5
MESH:C535698	MESH:C535698	Malignant hyperthermia susceptibility type 5	CTD_diseases	5
MESH:C535699	MESH:C535699	Malignant hyperthermia susceptibility type 6	CTD_diseases	5
MESH:C535700	MESH:C535700	Malignant mesenchymal tumor	CTD_diseases	5
MESH:C535701	MESH:C535701	Malignant Teratocarcinosarcoma	CTD_diseases	5
MESH:C535705	MESH:C535705	Mandibuloacral dysplasia with type A lipodystrophy	CTD_diseases	5
MESH:C535706	MESH:C535706	Mandibuloacral dysplasia with type B lipodystrophy	CTD_diseases	5
MESH:C535714	MESH:C535714	Neuropathy, congenital, with arthrogryposis multiplex	CTD_diseases	5
MESH:C535715	MESH:C535715	Spinal muscular atrophy, Jerash type	CTD_diseases	5
MESH:C535722	MESH:C535722	Duodenojejunal atresia with volvulus, absent dorsal mesentery and absent superior mesenteric artery	CTD_diseases	5
MESH:C535725	MESH:C535725	Dwarfism tall vertebrae	CTD_diseases	5
MESH:C535727	MESH:C535727	Dykes Markes Harper syndrome	CTD_diseases	5
MESH:C535734	MESH:C535734	Muscular dystrophy, tardive Emery-Dreifuss type, with contractures	CTD_diseases	5
MESH:C535737	MESH:C535737	Ethylmalonic encephalopathy	CTD_diseases	5
MESH:C535751	MESH:C535751	Congenital disorder of glycosylation type 1X	CTD_diseases	5
MESH:C535757	MESH:C535757	Congenital ectodermal dysplasia with hearing loss	CTD_diseases	5
MESH:C535758	MESH:C535758	Congenital heart block	CTD_diseases	5
MESH:C535759	MESH:C535759	Congenital myasthenic syndrome with episodic apnea	CTD_diseases	5
MESH:C535762	MESH:C535762	Congenital pseudoarthrosis	CTD_diseases	5
MESH:C535764	MESH:C535764	Eunuchoidism, familial hypogonadotropic	CTD_diseases	5
MESH:C535766	MESH:C535766	Czech dysplasia, metatarsal type	CTD_diseases	5
MESH:C535767	MESH:C535767	D-glycericacidemia	CTD_diseases	5
MESH:C535773	MESH:C535773	Mental retardation, X-linked, syndromic 5	CTD_diseases	5
MESH:C535775	MESH:C535775	Pierre Robin sequence with pectus excavatum and rib and scapular anomalies	CTD_diseases	5
MESH:C535776	MESH:C535776	Pierre Robin syndrome with fetal chondrodysplasia	CTD_diseases	5
MESH:C535777	MESH:C535777	Split hand foot deformity	CTD_diseases	5
MESH:C535781	MESH:C535781	Spondylocostal dysostosis, autosomal recessive	CTD_diseases	5
MESH:C535783	MESH:C535783	Spondyloepimetaphyseal dysplasia with hypotrichosis	CTD_diseases	5
MESH:C535785	MESH:C535785	Spondyloepimetaphyseal dysplasia, Genevieve type	CTD_diseases	5
MESH:C535786	MESH:C535786	Spondyloepimetaphyseal dysplasia, sponastrime type	CTD_diseases	5
MESH:C535788	MESH:C535788	Spondyloepiphyseal dysplasia, congenita	CTD_diseases	5
MESH:C535789	MESH:C535789	Spondyloepiphyseal dysplasia, Omani type	CTD_diseases	5
MESH:C535791	MESH:C535791	Spondylometaphyseal dysplasia with bowed forearms and facial dysmorphism	CTD_diseases	5
MESH:C535792	MESH:C535792	Spondylometaphyseal dysplasia with dentinogenesis imperfecta	CTD_diseases	5
MESH:C535794	MESH:C535794	Spondylometaphyseal dysplasia, Algerian type	CTD_diseases	5
MESH:C535795	MESH:C535795	Spondylometaphyseal dysplasia, axial	CTD_diseases	5
MESH:C535796	MESH:C535796	Spondylometaphyseal dysplasia, east-African type	CTD_diseases	5
MESH:C535797	MESH:C535797	Spondylometaphyseal dysplasia, Kozlowski type	CTD_diseases	5
MESH:C535798	MESH:C535798	Spondylometaphyseal dysplasia, Sedaghatian type	CTD_diseases	5
MESH:C535799	MESH:C535799	Spondyloperipheral dysplasia short ulna	CTD_diseases	5
MESH:C535800	MESH:C535800	Amyloidosis, Cerebral, with Spongiform Encephalopathy	CTD_diseases	5
MESH:C535803	MESH:C535803	succinic semialdehyde dehydrogenase deficiency	CTD_diseases	5
MESH:C535804	MESH:C535804	Stargardt disease 1	CTD_diseases	5
MESH:C535805	MESH:C535805	Stargardt disease 3	CTD_diseases	5
MESH:C535807	MESH:C535807	Moebius syndrome 1	CTD_diseases	5
MESH:C535808	MESH:C535808	Mohr-Tranebjaerg syndrome	CTD_diseases	5
MESH:C535810	MESH:C535810	Moloney syndrome	CTD_diseases	5
MESH:C535811	MESH:C535811	Molybdenum cofactor deficiency	CTD_diseases	5
MESH:C535816	MESH:C535816	Nevi flammei, familial multiple	CTD_diseases	5
MESH:C535826	MESH:C535826	Pseudodiastrophic dysplasia	CTD_diseases	5
MESH:C535827	MESH:C535827	Pseudohyperkalemia Cardiff	CTD_diseases	5
MESH:C535828	MESH:C535828	Pseudoinflammatory fundus dystrophy, Finnish type	CTD_diseases	5
MESH:C535830	MESH:C535830	Pseudovaginal Perineoscrotal Hypospadias	CTD_diseases	5
MESH:C535836	MESH:C535836	Pancreatic cancer, adult	CTD_diseases	5
MESH:C535837	MESH:C535837	Pancreatic carcinoma, familial	CTD_diseases	5
MESH:C535840	MESH:C535840	Selig Benacerraf Greene syndrome	CTD_diseases	5
MESH:C535843	MESH:C535843	Hashimoto-Pritzker syndrome	CTD_diseases	5
MESH:C535846	MESH:C535846	Hay Wells syndrome recessive type	CTD_diseases	5
MESH:C535849	MESH:C535849	Heart defect, tongue hamartoma and polysyndactyly	CTD_diseases	5
MESH:C535852	MESH:C535852	Heart-hand syndrome, Slovenian type	CTD_diseases	5
MESH:C535853	MESH:C535853	Heart-hand syndrome, Spanish type	CTD_diseases	5
MESH:C535858	MESH:C535858	HEM dysplasia	CTD_diseases	5
MESH:C535863	MESH:C535863	Robinow syndrome, autosomal recessive	CTD_diseases	5
MESH:C535864	MESH:C535864	Robinson Miller Bensimon syndrome	CTD_diseases	5
MESH:C535885	MESH:C535885	Jones Hersh Yusk syndrome	CTD_diseases	5
MESH:C535890	MESH:C535890	Levator syndrome	CTD_diseases	5
MESH:C535903	MESH:C535903	Limb-mammary syndrome	CTD_diseases	5
MESH:C535904	MESH:C535904	Lipase deficiency combined	CTD_diseases	5
MESH:C535912	MESH:C535912	Marie Unna congenital hypotrichosis	CTD_diseases	5
MESH:C535921	MESH:C535921	Cheilitis glandularis	CTD_diseases	5
MESH:C535923	MESH:C535923	Chikungunya virus infection	CTD_diseases	5
MESH:C535937	MESH:C535937	Cholesterol pneumonia	CTD_diseases	5
MESH:C535938	MESH:C535938	Chondrocalcinosis 1	CTD_diseases	5
MESH:C535939	MESH:C535939	Chondrocalcinosis due to Apatite crystal deposition	CTD_diseases	5
MESH:C535942	MESH:C535942	Corneal dystrophy, Thiel-Behnke type	CTD_diseases	5
MESH:C535949	MESH:C535949	Schofer Beetz Bohl syndrome	CTD_diseases	5
MESH:C535950	MESH:C535950	Dianzani autoimmune lymphoproliferative syndrome	CTD_diseases	5
MESH:C535952	MESH:C535952	Eosinophilic enteropathy	CTD_diseases	5
MESH:C535964	MESH:C535964	Collagenopathy, type 2 alpha 1	CTD_diseases	5
MESH:C535967	MESH:C535967	Coloboma of Alar-nasal cartilages with telecanthus	CTD_diseases	5
MESH:C535968	MESH:C535968	Hereditary macular coloboma	CTD_diseases	5
MESH:C535969	MESH:C535969	Coloboma of macula type B brachydactyly	CTD_diseases	5
MESH:C535970	MESH:C535970	Coloboma of optic nerve	CTD_diseases	5
MESH:C535971	MESH:C535971	Coloboma, cleft lip/palate and mental retardation syndrome	CTD_diseases	5
MESH:C535974	MESH:C535974	Complete atrioventricular septal defect	CTD_diseases	5
MESH:C535982	MESH:C535982	Congenital amegakaryocytic thrombocytopenia	CTD_diseases	5
MESH:C535986	MESH:C535986	Daneman Davy Mancer syndrome	CTD_diseases	5
MESH:C535989	MESH:C535989	Davis Lafer syndrome	CTD_diseases	5
MESH:C535998	MESH:C535998	Galactocele	CTD_diseases	5
MESH:C536000	MESH:C536000	Acanthosis nigricans muscle cramps acral enlargement	CTD_diseases	5
MESH:C536005	MESH:C536005	Cytosolic acetoacetyl-CoA thiolase deficiency	CTD_diseases	5
MESH:C536020	MESH:C536020	Achondroplasia and Swiss type agammaglobulinemia	CTD_diseases	5
MESH:C536031	MESH:C536031	Massa Casaer Ceulemans syndrome	CTD_diseases	5
MESH:C536038	MESH:C536038	Medium chain acyl CoA dehydrogenase deficiency	CTD_diseases	5
MESH:C536050	MESH:C536050	Osteoglophonic dwarfism	CTD_diseases	5
MESH:C536051	MESH:C536051	Osteolysis hereditary multicentric	CTD_diseases	5
MESH:C536055	MESH:C536055	Osteopetrosis and infantile neuroaxonal dystrophy	CTD_diseases	5
MESH:C536060	MESH:C536060	Whyte Murphy Fallon Sly syndrome	CTD_diseases	5
MESH:C536065	MESH:C536065	Oto-Palato-digital syndrome type 1	CTD_diseases	5
MESH:C536068	MESH:C536068	Hoyeraal Hreidarsson syndrome	CTD_diseases	5
MESH:C536071	MESH:C536071	Hunter Carpenter Macdonald syndrome	CTD_diseases	5
MESH:C536077	MESH:C536077	Hydroa vacciniforme, familial	CTD_diseases	5
MESH:C536079	MESH:C536079	Hydrolethalus syndrome	CTD_diseases	5
MESH:C536080	MESH:C536080	Hydroxyacyl-CoA Dehydrogenase, Type 2, Deficiency	CTD_diseases	5
MESH:C536081	MESH:C536081	Hydroxykynureninuria	CTD_diseases	5
MESH:C536082	MESH:C536082	Hypercalciuria, childhood idiopathic	CTD_diseases	5
MESH:C536084	MESH:C536084	Ichthyosis cheek eyebrow syndrome	CTD_diseases	5
MESH:C536085	MESH:C536085	Ichthyosis follicularis atrichia photophobia syndrome	CTD_diseases	5
MESH:C536087	MESH:C536087	Ichthyosis hystrix gravior	CTD_diseases	5
MESH:C536088	MESH:C536088	Ichthyosis hystrix, Curth Macklin type	CTD_diseases	5
MESH:C536089	MESH:C536089	Congenital myasthenic syndrome ib	CTD_diseases	5
MESH:C536090	MESH:C536090	Myasthenic syndrome, congenital, type Id	CTD_diseases	5
MESH:C536091	MESH:C536091	Myasthenic syndrome, congenital, postsynaptic slow-channel	CTD_diseases	5
MESH:C536092	MESH:C536092	Mycobacterium tuberculosis, susceptibility to infection by	CTD_diseases	5
MESH:C536094	MESH:C536094	Myeloid splenomegaly	CTD_diseases	5
MESH:C536096	MESH:C536096	Myoclonic dystonia	CTD_diseases	5
MESH:C536111	MESH:C536111	Partial agenesis of corpus callosum	CTD_diseases	5
MESH:C536113	MESH:C536113	Nevo syndrome	CTD_diseases	5
MESH:C536116	MESH:C536116	Nicolaides Baraitser syndrome	CTD_diseases	5
MESH:C536120	MESH:C536120	Nievergelt syndrome	CTD_diseases	5
MESH:C536123	MESH:C536123	Nivelon Nivelon Mabille syndrome	CTD_diseases	5
MESH:C536126	MESH:C536126	Non functioning pancreatic endocrine tumor	CTD_diseases	5
MESH:C536140	MESH:C536140	Megaepiphyseal dwarfism	CTD_diseases	5
MESH:C536152	MESH:C536152	Keratoderma palmoplantar deafness	CTD_diseases	5
MESH:C536157	MESH:C536157	Keratosis focal palmoplantar gingival	CTD_diseases	5
MESH:C536161	MESH:C536161	Keratosis palmoplantaris papulosa	CTD_diseases	5
MESH:C536162	MESH:C536162	Keratosis palmoplantaris striata 1	CTD_diseases	5
MESH:C536163	MESH:C536163	Keratosis palmoplantaris striata 3	CTD_diseases	5
MESH:C536164	MESH:C536164	Keratosis palmoplantaris with esophageal cancer	CTD_diseases	5
MESH:C536170	MESH:C536170	Diastrophic dysplasia	CTD_diseases	5
MESH:C536172	MESH:C536172	Dieterich's disease	CTD_diseases	5
MESH:C536180	MESH:C536180	Ectodermal dysplasia, hidrotic, Christianson-Fourie type	CTD_diseases	5
MESH:C536182	MESH:C536182	Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features	CTD_diseases	5
MESH:C536184	MESH:C536184	Familial ectopia lentis	CTD_diseases	5
MESH:C536185	MESH:C536185	Ectopia pupillae	CTD_diseases	5
MESH:C536189	MESH:C536189	Ectrodactyly-cleft lip/palate syndrome	CTD_diseases	5
MESH:C536190	MESH:C536190	Ectodermal dysplasia, ectrodactyly, and macular dystrophy	CTD_diseases	5
MESH:C536209	MESH:C536209	Congenital central hypoventilation syndrome	CTD_diseases	5
MESH:C536211	MESH:C536211	Congenital contractural arachnodactyly	CTD_diseases	5
MESH:C536214	MESH:C536214	Crisponi syndrome	CTD_diseases	5
MESH:C536225	MESH:C536225	Cutis laxa, recessive	CTD_diseases	5
MESH:C536228	MESH:C536228	Familial cyclic vomiting syndrome	CTD_diseases	5
MESH:C536241	MESH:C536241	Bobble-head doll syndrome	CTD_diseases	5
MESH:C536249	MESH:C536249	Purpura simplex	CTD_diseases	5
MESH:C536252	MESH:C536252	Pyle disease	CTD_diseases	5
MESH:C536253	MESH:C536253	Pyogenic arthritis, pyoderma gangrenosum, and acne	CTD_diseases	5
MESH:C536254	MESH:C536254	Pyridoxine-dependent epilepsy	CTD_diseases	5
MESH:C536267	MESH:C536267	Radio renal syndrome	CTD_diseases	5
MESH:C536272	MESH:C536272	Ichthyosis tapered fingers midline groove up	CTD_diseases	5
MESH:C536273	MESH:C536273	Ichthyosis with hypotrichosis, autosomal recessive	CTD_diseases	5
MESH:C536274	MESH:C536274	Ichthyosis, mental retardation, dwarfism, and renal impairment	CTD_diseases	5
MESH:C536276	MESH:C536276	Idiopathic basal ganglia calcification, childhood onset	CTD_diseases	5
MESH:C536284	MESH:C536284	Iida Kannari syndrome	CTD_diseases	5
MESH:C536297	MESH:C536297	Male sterility due to Y-chromosome deletions	CTD_diseases	5
MESH:C536302	MESH:C536302	Pascual Castroviejo syndrome	CTD_diseases	5
MESH:C536303	MESH:C536303	Pashayan syndrome	CTD_diseases	5
MESH:C536308	MESH:C536308	Patella hypoplasia mental retardation	CTD_diseases	5
MESH:C536309	MESH:C536309	Patterned dystrophy of retinal pigment epithelium	CTD_diseases	5
MESH:C536312	MESH:C536312	Juvenile pauciarticular chronic arthritis	CTD_diseases	5
MESH:C536320	MESH:C536320	Sabinas brittle hair syndrome	CTD_diseases	5
MESH:C536324	MESH:C536324	Polycystic bone disease	CTD_diseases	5
MESH:C536329	MESH:C536329	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy	CTD_diseases	5
MESH:C536335	MESH:C536335	Polyostotic osteolytic dysplasia, hereditary expansile	CTD_diseases	5
MESH:C536336	MESH:C536336	Porencephaly cerebellar hypoplasia malformations	CTD_diseases	5
MESH:C536338	MESH:C536338	Porokeratosis punctata palmaris et plantaris	CTD_diseases	5
MESH:C536339	MESH:C536339	Porokeratosis, disseminated superficial actinic 1	CTD_diseases	5
MESH:C536341	MESH:C536341	Porphyria, Chester type	CTD_diseases	5
MESH:C536342	MESH:C536342	Posterior column ataxia	CTD_diseases	5
MESH:C536346	MESH:C536346	Vestibulocochlear Dysfunction, Progressive	CTD_diseases	5
MESH:C536348	MESH:C536348	Vibrio vulnificus infection	CTD_diseases	5
MESH:C536357	MESH:C536357	Anemia, hypochromic microcytic	CTD_diseases	5
MESH:C536362	MESH:C536362	Angiofollicular ganglionic hyperplasia	CTD_diseases	5
MESH:C536364	MESH:C536364	Angioma hereditary neurocutaneous	CTD_diseases	5
MESH:C536368	MESH:C536368	Angiosarcoma of the breast	CTD_diseases	5
MESH:C536370	MESH:C536370	Aniridia cerebellar ataxia mental deficiency	CTD_diseases	5
MESH:C536372	MESH:C536372	Aniridia, type 2	CTD_diseases	5
MESH:C536380	MESH:C536380	Evan's syndrome	CTD_diseases	5
MESH:C536388	MESH:C536388	Faciocardiorenal syndrome	CTD_diseases	5
MESH:C536393	MESH:C536393	Fairbank disease	CTD_diseases	5
MESH:C536406	MESH:C536406	Neuhauser Daly Magnelli syndrome	CTD_diseases	5
MESH:C536407	MESH:C536407	Neuhauser Eichner Opitz syndrome	CTD_diseases	5
MESH:C536408	MESH:C536408	Neural crest tumor	CTD_diseases	5
MESH:C536411	MESH:C536411	Neuraminidase deficiency with beta-galactosidase deficiency	CTD_diseases	5
MESH:C536423	MESH:C536423	Progeroid syndrome, neonatal	CTD_diseases	5
MESH:C536425	MESH:C536425	Split-hand/foot malformation with long bone deficiency	CTD_diseases	5
MESH:C536428	MESH:C536428	Cleidorhizomelic syndrome	CTD_diseases	5
MESH:C536444	MESH:C536444	Corneodermatoosseous syndrome	CTD_diseases	5
MESH:C536445	MESH:C536445	Coronal synostosis, syndactyly and jejunal atresia	CTD_diseases	5
MESH:C536447	MESH:C536447	Cortisone reductase deficiency	CTD_diseases	5
MESH:C536455	MESH:C536455	Craniofacial dyssynostosis	CTD_diseases	5
MESH:C536456	MESH:C536456	Craniofrontonasal dysplasia	CTD_diseases	5
MESH:C536463	MESH:C536463	Waardenburg syndrome type 2	CTD_diseases	5
MESH:C536464	MESH:C536464	Waardenburg syndrome type 2A	CTD_diseases	5
MESH:C536465	MESH:C536465	Waardenburg syndrome type 2B	CTD_diseases	5
MESH:C536467	MESH:C536467	Waardenburg syndrome, type 4	CTD_diseases	5
MESH:C536472	MESH:C536472	Upington disease	CTD_diseases	5
MESH:C536479	MESH:C536479	Urocanase deficiency	CTD_diseases	5
MESH:C536494	MESH:C536494	Uveal melanoma	CTD_diseases	5
MESH:C536495	MESH:C536495	VACTERL association	CTD_diseases	5
MESH:C536502	MESH:C536502	Tetrasomy X	CTD_diseases	5
MESH:C536504	MESH:C536504	Thalamic degeneration symmetrical infantile	CTD_diseases	5
MESH:C536510	MESH:C536510	Thiamine responsive megaloblastic anemia syndrome	CTD_diseases	5
MESH:C536516	MESH:C536516	Thoraco limb dysplasia Rivera type	CTD_diseases	5
MESH:C536521	MESH:C536521	VACTERL hydrocephaly	CTD_diseases	5
MESH:C536524	MESH:C536524	Valinemia	CTD_diseases	5
MESH:C536527	MESH:C536527	Van Buchem disease type 2	CTD_diseases	5
MESH:C536534	MESH:C536534	VATER association	CTD_diseases	5
MESH:C536537	MESH:C536537	Ventricular extrasystoles perodactyly Robin sequence	CTD_diseases	5
MESH:C536538	MESH:C536538	Verloes Bourguignon syndrome	CTD_diseases	5
MESH:C536539	MESH:C536539	Verloes Gillerot Fryns syndrome	CTD_diseases	5
MESH:C536540	MESH:C536540	Verloes Van Maldergem Marneffe syndrome	CTD_diseases	5
MESH:C536545	MESH:C536545	Tremor hereditary essential, 1	CTD_diseases	5
MESH:C536551	MESH:C536551	Trichodental syndrome	CTD_diseases	5
MESH:C536556	MESH:C536556	Trichorrhexis nodosa syndrome	CTD_diseases	5
MESH:C536557	MESH:C536557	Trichoscyphodysplasia	CTD_diseases	5
MESH:C536565	MESH:C536565	Trueb Burg Bottani syndrome	CTD_diseases	5
MESH:C536568	MESH:C536568	Walker Dyson syndrome	CTD_diseases	5
MESH:C536573	MESH:C536573	Boomerang dysplasia	CTD_diseases	5
MESH:C536574	MESH:C536574	Bor-Duane hydrocephalus contiguous gene syndrome	CTD_diseases	5
MESH:C536582	MESH:C536582	Alpha-ketoglutarate dehydrogenase deficiency	CTD_diseases	5
MESH:C536588	MESH:C536588	Alsing syndrome	CTD_diseases	5
MESH:C536590	MESH:C536590	Alveolar capillary dysplasia	CTD_diseases	5
MESH:C536593	MESH:C536593	Alves Castelo dos Santos syndrome	CTD_diseases	5
MESH:C536600	MESH:C536600	Amaurosis congenita of Leber, type 1	CTD_diseases	5
MESH:C536601	MESH:C536601	Amaurosis congenita of Leber, type 2	CTD_diseases	5
MESH:C536602	MESH:C536602	Amaurosis congenita of Leber, type 5	CTD_diseases	5
MESH:C536603	MESH:C536603	Amaurosis congenita of Leber, type 9	CTD_diseases	5
MESH:C536604	MESH:C536604	Amaurosis hypertrichosis	CTD_diseases	5
MESH:C536605	MESH:C536605	Ambras syndrome	CTD_diseases	5
MESH:C536612	MESH:C536612	Familial dermographism	CTD_diseases	5
MESH:C536614	MESH:C536614	Arthrogryposis multiplex congenita neurogenic type	CTD_diseases	5
MESH:C536616	MESH:C536616	Satoyoshi syndrome	CTD_diseases	5
MESH:C536618	MESH:C536618	Say Barber Miller syndrome	CTD_diseases	5
MESH:C536631	MESH:C536631	Schindler Disease, Type I	CTD_diseases	5
MESH:C536637	MESH:C536637	Schneckenbecken dysplasia	CTD_diseases	5
MESH:C536645	MESH:C536645	Pemphigus vulgaris, familial	CTD_diseases	5
MESH:C536647	MESH:C536647	Pena Shokeir syndrome, type 1	CTD_diseases	5
MESH:C536648	MESH:C536648	Pendred syndrome	CTD_diseases	5
MESH:C536652	MESH:C536652	Pentosuria	CTD_diseases	5
MESH:C536653	MESH:C536653	Penttinen-Aula syndrome	CTD_diseases	5
MESH:C536656	MESH:C536656	Peptide growth factors deficiency	CTD_diseases	5
MESH:C536657	MESH:C536657	Periodic fever, familial, autosomal dominant	CTD_diseases	5
MESH:C536662	MESH:C536662	Peroxisomal ACYL-COA oxidase deficiency	CTD_diseases	5
MESH:C536669	MESH:C536669	Sjögren-Mikulicz syndrome	CTD_diseases	5
MESH:C536693	MESH:C536693	Wells syndrome	CTD_diseases	5
MESH:C536698	MESH:C536698	Whispering dysphonia, hereditary	CTD_diseases	5
MESH:C536708	MESH:C536708	Wilson-Turner X-linked mental retardation syndrome	CTD_diseases	5
MESH:C536719	MESH:C536719	Yunis Varon syndrome	CTD_diseases	5
MESH:C536720	MESH:C536720	Yusho Disease	CTD_diseases	5
MESH:C536722	MESH:C536722	ZAP70 deficiency	CTD_diseases	5
MESH:C536723	MESH:C536723	Zazam Sheriff Phillips syndrome	CTD_diseases	5
MESH:C536726	MESH:C536726	Zlotogora-Ogur syndrome	CTD_diseases	5
MESH:C536729	MESH:C536729	Zunich neuroectodermal syndrome	CTD_diseases	5
MESH:C536731	MESH:C536731	X chromosome, trisomy Xpter Xq13	CTD_diseases	5
MESH:C536732	MESH:C536732	Chromosome Xq duplication syndrome	CTD_diseases	5
MESH:C536733	MESH:C536733	X chromosome, trisomy Xq25	CTD_diseases	5
MESH:C536739	MESH:C536739	Wolcott-Rallison syndrome	CTD_diseases	5
MESH:C536741	MESH:C536741	Wolffian tumor	CTD_diseases	5
MESH:C536744	MESH:C536744	Woods Leversha Rogers syndrome	CTD_diseases	5
MESH:C536747	MESH:C536747	Worster Drought syndrome	CTD_diseases	5
MESH:C536749	MESH:C536749	Wright Dyck syndrome	CTD_diseases	5
MESH:C536750	MESH:C536750	Wrinkly skin syndrome	CTD_diseases	5
MESH:C536753	MESH:C536753	X chromosome, duplication Xq13 1 q21 1	CTD_diseases	5
MESH:C536754	MESH:C536754	X chromosome, monosomy Xp22 pter	CTD_diseases	5
MESH:C536755	MESH:C536755	X chromosome, monosomy Xq28	CTD_diseases	5
MESH:C536756	MESH:C536756	X chromosome, trisomy Xp3	CTD_diseases	5
MESH:C536759	MESH:C536759	X-linked mental retardation Gustavson type	CTD_diseases	5
MESH:C536762	MESH:C536762	Xanthogranulomatous cholecystitis	CTD_diseases	5
MESH:C536763	MESH:C536763	Xanthogranulomatous sialadenitis	CTD_diseases	5
MESH:C536765	MESH:C536765	Xeroderma pigmentosum, type 9	CTD_diseases	5
MESH:C536766	MESH:C536766	Xeroderma pigmentosum, variant type	CTD_diseases	5
MESH:C536784	MESH:C536784	Tabatznik syndrome	CTD_diseases	5
MESH:C536786	MESH:C536786	Athabaskan severe combined immunodeficiency	CTD_diseases	5
MESH:C536793	MESH:C536793	Chromosome 21, tetrasomy 21q	CTD_diseases	5
MESH:C536795	MESH:C536795	Chromosome 22 ring	CTD_diseases	5
MESH:C536814	MESH:C536814	Distal arthrogryposis Moore Weaver type	CTD_diseases	5
MESH:C536827	MESH:C536827	Glomus vagale tumors	CTD_diseases	5
MESH:C536830	MESH:C536830	De Vivo disease	CTD_diseases	5
MESH:C536832	MESH:C536832	Glutamine deficiency, congenital	CTD_diseases	5
MESH:C536833	MESH:C536833	Glutaric aciduria 1	CTD_diseases	5
MESH:C536835	MESH:C536835	Glutathione synthetase deficiency	CTD_diseases	5
MESH:C536836	MESH:C536836	Glutathionuria	CTD_diseases	5
MESH:C536840	MESH:C536840	Aplasia cutis congenita of limbs recessive	CTD_diseases	5
MESH:C536861	MESH:C536861	Spastic paraplegia 25, autosomal recessive	CTD_diseases	5
MESH:C536870	MESH:C536870	Spastic paraplegia neuropathy poikiloderma	CTD_diseases	5
MESH:C536880	MESH:C536880	Spinal muscular atrophy with respiratory distress 1	CTD_diseases	5
MESH:C536881	MESH:C536881	Spinal muscular atrophy, Ryukyuan type	CTD_diseases	5
MESH:C536883	MESH:C536883	King Denborough syndrome	CTD_diseases	5
MESH:C536889	MESH:C536889	Weber Klippel Trenaunay	CTD_diseases	5
MESH:C536892	MESH:C536892	Kaplan Plauchu Fitch syndrome	CTD_diseases	5
MESH:C536893	MESH:C536893	Kaplowitz Bodurtha syndrome	CTD_diseases	5
MESH:C536899	MESH:C536899	Thrombocytopenia, cyclic	CTD_diseases	5
MESH:C536907	MESH:C536907	Thymic-Renal-Anal-Lung dysplasia	CTD_diseases	5
MESH:C536909	MESH:C536909	Thyroglossal tract cyst	CTD_diseases	5
MESH:C536910	MESH:C536910	Thyroid cancer, anaplastic	CTD_diseases	5
MESH:C536911	MESH:C536911	Familial medullary thyroid carcinoma	CTD_diseases	5
MESH:C536913	MESH:C536913	Thyroid cancer, Hurthle cell	CTD_diseases	5
MESH:C536914	MESH:C536914	Thyroid cancer, medullary	CTD_diseases	5
MESH:C536915	MESH:C536915	Thyroid cancer, papillary	CTD_diseases	5
MESH:C536921	MESH:C536921	Tiglic acidemia	CTD_diseases	5
MESH:C536932	MESH:C536932	Uhl anomaly	CTD_diseases	5
MESH:C536935	MESH:C536935	Ulna metaphyseal dysplasia syndrome	CTD_diseases	5
MESH:C536940	MESH:C536940	Absent radii and thrombocytopenia	CTD_diseases	5
MESH:C536942	MESH:C536942	TARP syndrome	CTD_diseases	5
MESH:C536944	MESH:C536944	Thrombocytopenia absent ulnar syndrome	CTD_diseases	5
MESH:C536945	MESH:C536945	Taurodontia absent teeth sparse hair	CTD_diseases	5
MESH:C536946	MESH:C536946	Taurodontism	CTD_diseases	5
MESH:C536947	MESH:C536947	Taurodontism, microdontia, and dens invaginatus	CTD_diseases	5
MESH:C536949	MESH:C536949	Teebi Naguib Al Awadi syndrome	CTD_diseases	5
MESH:C536954	MESH:C536954	Telencephalic leukoencephalopathy	CTD_diseases	5
MESH:C536958	MESH:C536958	Temtamy preaxial brachydactyly syndrome	CTD_diseases	5
MESH:C536959	MESH:C536959	Temtamy syndrome	CTD_diseases	5
MESH:C536965	MESH:C536965	Tomaculous neuropathy	CTD_diseases	5
MESH:C536978	MESH:C536978	Tranebjaerg Svejgaard syndrome	CTD_diseases	5
MESH:C536990	MESH:C536990	Mowat-Wilson syndrome	CTD_diseases	5
MESH:C536998	MESH:C536998	Leber congenital amaurosis type 3	CTD_diseases	5
MESH:C536999	MESH:C536999	Leber congenital amaurosis, type 4	CTD_diseases	5
MESH:C537003	MESH:C537003	Leichtman Wood Rohn syndrome	CTD_diseases	5
MESH:C537004	MESH:C537004	Leigh syndrome , French Canadian type	CTD_diseases	5
MESH:C537014	MESH:C537014	Infantile polyarteritis	CTD_diseases	5
MESH:C537018	MESH:C537018	Kennerknecht Sorgo Oberhoffer syndrome	CTD_diseases	5
MESH:C537020	MESH:C537020	Kenny Caffey syndrome	CTD_diseases	5
MESH:C537023	MESH:C537023	Koone Rizzo Elias syndrome	CTD_diseases	5
MESH:C537029	MESH:C537029	Lipomatous hemangiopericytoma	CTD_diseases	5
MESH:C537031	MESH:C537031	Littoral cell angioma of the spleen	CTD_diseases	5
MESH:C537050	MESH:C537050	Alopecia congenita keratosis palmoplantaris	CTD_diseases	5
MESH:C537051	MESH:C537051	Alopecia contractures dwarfism mental retardation	CTD_diseases	5
MESH:C537052	MESH:C537052	Alopecia epilepsy oligophrenia syndrome of Moynahan	CTD_diseases	5
MESH:C537057	MESH:C537057	Alopecia, epilepsy, pyorrhea, mental subnormality	CTD_diseases	5
MESH:C537058	MESH:C537058	Fitzsimmons-McLachlan-Gilbert syndrome	CTD_diseases	5
MESH:C537061	MESH:C537061	Flavimonas oryzihabitans Bacteremia	CTD_diseases	5
MESH:C537063	MESH:C537063	Florid cemento-osseous dysplasia	CTD_diseases	5
MESH:C537068	MESH:C537068	Focal facial dermal dysplasia	CTD_diseases	5
MESH:C537069	MESH:C537069	Foix Chavany Marie syndrome	CTD_diseases	5
MESH:C537072	MESH:C537072	Nonpuerperal galactorrhea	CTD_diseases	5
MESH:C537079	MESH:C537079	Bare lymphocyte syndrome 2	CTD_diseases	5
MESH:C537080	MESH:C537080	Baritosis	CTD_diseases	5
MESH:C537081	MESH:C537081	Bowen-Conradi syndrome	CTD_diseases	5
MESH:C537098	MESH:C537098	Brachyolmia	CTD_diseases	5
MESH:C537099	MESH:C537099	Brachyolmia, recessive Hobaek type	CTD_diseases	5
MESH:C537100	MESH:C537100	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia	CTD_diseases	5
MESH:C537101	MESH:C537101	Brachytelephalangy characteristic facies Kallmann	CTD_diseases	5
MESH:C537104	MESH:C537104	Branchiootic syndrome	CTD_diseases	5
MESH:C537109	MESH:C537109	Chromosome 21 ring	CTD_diseases	5
MESH:C537111	MESH:C537111	Brown-Vialetto-Van Laere syndrome	CTD_diseases	5
MESH:C537122	MESH:C537122	Opsismodysplasia	CTD_diseases	5
MESH:C537129	MESH:C537129	Optic atrophy polyneuropathy deafness	CTD_diseases	5
MESH:C537130	MESH:C537130	Optic nerve hypoplasia, familial bilateral	CTD_diseases	5
MESH:C537131	MESH:C537131	Orbital lymphoma	CTD_diseases	5
MESH:C537136	MESH:C537136	Oroticaciduria 1	CTD_diseases	5
MESH:C537143	MESH:C537143	Ossification of the posterior longitudinal ligament of the spine	CTD_diseases	5
MESH:C537145	MESH:C537145	Hypocalciuric hypercalcemia, familial, type 1	CTD_diseases	5
MESH:C537146	MESH:C537146	Hypocalciuric hypercalcemia, familial, type 2	CTD_diseases	5
MESH:C537147	MESH:C537147	Familial benign hypercalcemia, type 3	CTD_diseases	5
MESH:C537150	MESH:C537150	Hypoglycemia, leucine-induced	CTD_diseases	5
MESH:C537153	MESH:C537153	Hypomagnesemia primary	CTD_diseases	5
MESH:C537160	MESH:C537160	Hypotrichosis simplex	CTD_diseases	5
MESH:C537162	MESH:C537162	Pancreatoblastoma	CTD_diseases	5
MESH:C537167	MESH:C537167	Papillomatosis, florid, of nipple	CTD_diseases	5
MESH:C537168	MESH:C537168	Papillorenal syndrome	CTD_diseases	5
MESH:C537172	MESH:C537172	Parastremmatic dwarfism	CTD_diseases	5
MESH:C537173	MESH:C537173	Parathyroid cancer, adult	CTD_diseases	5
MESH:C537174	MESH:C537174	PARC syndrome	CTD_diseases	5
MESH:C537182	MESH:C537182	Paroxysmal ventricular fibrillation	CTD_diseases	5
MESH:C537190	MESH:C537190	Ruvalcaba Churesigaew Myhre syndrome	CTD_diseases	5
MESH:C537192	MESH:C537192	Ruzicka Goerz Anton syndrome	CTD_diseases	5
MESH:C537194	MESH:C537194	Lethal congenital contracture syndrome 1	CTD_diseases	5
MESH:C537213	MESH:C537213	Kohlschutter Tonz syndrome	CTD_diseases	5
MESH:C537222	MESH:C537222	Sacral hemangiomas multiple congenital abnormalities	CTD_diseases	5
MESH:C537228	MESH:C537228	Salcedo syndrome	CTD_diseases	5
MESH:C537229	MESH:C537229	Sammartino De Crecchio Syndrome	CTD_diseases	5
MESH:C537245	MESH:C537245	Prostatic stromal proliferation of uncertain malignant potential	CTD_diseases	5
MESH:C537262	MESH:C537262	Hereditary pancreatitis	CTD_diseases	5
MESH:C537268	MESH:C537268	Formaldehyde poisoning	CTD_diseases	5
MESH:C537271	MESH:C537271	Fowler Christmas Chapple syndrome	CTD_diseases	5
MESH:C537272	MESH:C537272	Franceschini Vardeu Guala syndrome	CTD_diseases	5
MESH:C537279	MESH:C537279	Goldberg-Shprintzen megacolon syndrome	CTD_diseases	5
MESH:C537280	MESH:C537280	Goldblatt Viljoen syndrome	CTD_diseases	5
MESH:C537288	MESH:C537288	Gordon syndrome	CTD_diseases	5
MESH:C537292	MESH:C537292	Graham Boyle Troxell syndrome	CTD_diseases	5
MESH:C537297	MESH:C537297	Autosomal Dominant Lateral Temporal Lobe Epilepsy	CTD_diseases	5
MESH:C537304	MESH:C537304	Groenouw type I corneal dystrophy	CTD_diseases	5
MESH:C537306	MESH:C537306	Grover's disease	CTD_diseases	5
MESH:C537318	MESH:C537318	Splenogonadal fusion limb defects micrognatia	CTD_diseases	5
MESH:C537319	MESH:C537319	Split hand split foot nystagmus	CTD_diseases	5
MESH:C537320	MESH:C537320	Microcephalic osteodysplastic primordial dwarfism, type 3	CTD_diseases	5
MESH:C537326	MESH:C537326	Microcephaly deafness syndrome	CTD_diseases	5
MESH:C537339	MESH:C537339	Simosa cranio facial syndrome	CTD_diseases	5
MESH:C537344	MESH:C537344	Sinonasal undifferentiated carcinoma	CTD_diseases	5
MESH:C537349	MESH:C537349	Mesomelic dwarfism Reinhardt Pfeiffer type	CTD_diseases	5
MESH:C537351	MESH:C537351	Metaphyseal anadysplasia	CTD_diseases	5
MESH:C537352	MESH:C537352	Metaphyseal chondrodysplasia Schmid type	CTD_diseases	5
MESH:C537353	MESH:C537353	Metaphyseal chondrodysplasia Spahr type	CTD_diseases	5
MESH:C537354	MESH:C537354	Metaphyseal chondrodysplasia with cone-shaped epiphyses, normal hair, and normal hands	CTD_diseases	5
MESH:C537355	MESH:C537355	Metaphyseal undermodeling, spondylar dysplasia, and overgrowth	CTD_diseases	5
MESH:C537356	MESH:C537356	Metatropic dwarfism	CTD_diseases	5
MESH:C537358	MESH:C537358	Methylmalonic acidemia	CTD_diseases	5
MESH:C537359	MESH:C537359	Methylmalonic acidemia with homocystinuria	CTD_diseases	5
MESH:C537360	MESH:C537360	Methylmalonic aciduria cblA type	CTD_diseases	5
MESH:C537361	MESH:C537361	Methylmalonic aciduria cblB type	CTD_diseases	5
MESH:C537363	MESH:C537363	Ichthyosiform erythroderma, corneal involvement, deafness	CTD_diseases	5
MESH:C537372	MESH:C537372	Multi-centric Castleman's Disease	CTD_diseases	5
MESH:C537375	MESH:C537375	Multifocal fibrosclerosis	CTD_diseases	5
MESH:C537386	MESH:C537386	Neuroaxonal dystrophy renal tubular acidosis	CTD_diseases	5
MESH:C537396	MESH:C537396	Neuropathy ataxia and retinis pigmentosa	CTD_diseases	5
MESH:C537401	MESH:C537401	Pineal Teratoma	CTD_diseases	5
MESH:C537403	MESH:C537403	Pitt-Hopkins syndrome	CTD_diseases	5
MESH:C537406	MESH:C537406	Bruck syndrome 1	CTD_diseases	5
MESH:C537407	MESH:C537407	Bruck syndrome 2	CTD_diseases	5
MESH:C537408	MESH:C537408	Brunoni syndrome	CTD_diseases	5
MESH:C537411	MESH:C537411	Burn-Mckeown syndrome	CTD_diseases	5
MESH:C537421	MESH:C537421	Cafe au lait spots, multiple	CTD_diseases	5
MESH:C537426	MESH:C537426	Arakawa syndrome 2	CTD_diseases	5
MESH:C537427	MESH:C537427	AREDYLD Syndrome	CTD_diseases	5
MESH:C537429	MESH:C537429	Arhinia, choanal atresia, and microphthalmia	CTD_diseases	5
MESH:C537430	MESH:C537430	Arima syndrome	CTD_diseases	5
MESH:C537437	MESH:C537437	Aromatic amino acid decarboxylase deficiency	CTD_diseases	5
MESH:C537439	MESH:C537439	Arroyo Garcia Cimadevilla syndrome	CTD_diseases	5
MESH:C537441	MESH:C537441	Arthrogryposis and ectodermal dysplasia	CTD_diseases	5
MESH:C537446	MESH:C537446	Mental retardation spasticity ectrodactyly	CTD_diseases	5
MESH:C537453	MESH:C537453	Mental retardation, macrocephaly, short stature and craniofacial dysmorphism	CTD_diseases	5
MESH:C537458	MESH:C537458	Meralgia paresthetica	CTD_diseases	5
MESH:C537459	MESH:C537459	Meretoja syndrome	CTD_diseases	5
MESH:C537464	MESH:C537464	Microphthalmia, syndromic 1	CTD_diseases	5
MESH:C537470	MESH:C537470	Microvillus inclusion disease	CTD_diseases	5
MESH:C537471	MESH:C537471	Midphalangeal hair	CTD_diseases	5
MESH:C537474	MESH:C537474	Minicore myopathy, antenatal onset, with arthrogryposis	CTD_diseases	5
MESH:C537490	MESH:C537490	Lyngstadaas syndrome	CTD_diseases	5
MESH:C537501	MESH:C537501	Strudwick syndrome	CTD_diseases	5
MESH:C537502	MESH:C537502	Stuve-Wiedemann syndrome	CTD_diseases	5
MESH:C537508	MESH:C537508	Kozlowski Ouvrier syndrome	CTD_diseases	5
MESH:C537510	MESH:C537510	Kozlowski Tsuruta Taki syndrome	CTD_diseases	5
MESH:C537514	MESH:C537514	Plasmacytoma anaplastic	CTD_diseases	5
MESH:C537527	MESH:C537527	Succinyl-CoA:3-oxoacid CoA transferase deficiency	CTD_diseases	5
MESH:C537533	MESH:C537533	Seckel syndrome 1	CTD_diseases	5
MESH:C537534	MESH:C537534	Seckel syndrome 2	CTD_diseases	5
MESH:C537535	MESH:C537535	Secretory breast carcinoma	CTD_diseases	5
MESH:C537537	MESH:C537537	Segawa syndrome, autosomal recessive	CTD_diseases	5
MESH:C537541	MESH:C537541	Microcephaly microphthalmos blindness	CTD_diseases	5
MESH:C537543	MESH:C537543	Microcephaly pontocerebellar hypoplasia dyskinesia	CTD_diseases	5
MESH:C537549	MESH:C537549	Lambotte syndrome	CTD_diseases	5
MESH:C537550	MESH:C537550	Microcoria, congenital	CTD_diseases	5
MESH:C537551	MESH:C537551	Microcornea corectopia macular hypoplasia	CTD_diseases	5
MESH:C537555	MESH:C537555	Microhydranencephaly	CTD_diseases	5
MESH:C537556	MESH:C537556	Micromelic dwarfism Fryns type	CTD_diseases	5
MESH:C537557	MESH:C537557	Micromelic dysplasia, congenital, with dislocation of radius	CTD_diseases	5
MESH:C537564	MESH:C537564	Jansen type metaphyseal chondrodysplasia	CTD_diseases	5
MESH:C537567	MESH:C537567	Jejunal atresia with renal adysplasia	CTD_diseases	5
MESH:C537568	MESH:C537568	Jensen syndrome	CTD_diseases	5
MESH:C537577	MESH:C537577	Microcephalic osteodysplastic primordial dwarfism, type 1	CTD_diseases	5
MESH:C537580	MESH:C537580	Senior Loken Syndrome	CTD_diseases	5
MESH:C537585	MESH:C537585	Seres-Santamaria Arimany Muniz syndrome	CTD_diseases	5
MESH:C537589	MESH:C537589	Severe combined immunodeficiency with sensitivity to ionizing radiation	CTD_diseases	5
MESH:C537590	MESH:C537590	Severe combined immunodeficiency, atypical	CTD_diseases	5
MESH:C537593	MESH:C537593	Severe infantile axonal neuropathy	CTD_diseases	5
MESH:C537594	MESH:C537594	Shapiro syndrome	CTD_diseases	5
MESH:C537596	MESH:C537596	Short chain Acyl CoA dehydrogenase deficiency	CTD_diseases	5
MESH:C537598	MESH:C537598	Short limb dwarfism Al Gazali type	CTD_diseases	5
MESH:C537656	MESH:C537656	Basal cell carcinoma, multiple	CTD_diseases	5
MESH:C537657	MESH:C537657	Basal ganglia calcification, idiopathic 2	CTD_diseases	5
MESH:C537658	MESH:C537658	Basal ganglia disease, biotin-responsive	CTD_diseases	5
MESH:C537668	MESH:C537668	Beemer Ertbruggen syndrome	CTD_diseases	5
MESH:C537669	MESH:C537669	Behr syndrome	CTD_diseases	5
MESH:C537670	MESH:C537670	Behrens Baumann Dust syndrome	CTD_diseases	5
MESH:C537683	MESH:C537683	Genito palato cardiac syndrome	CTD_diseases	5
MESH:C537686	MESH:C537686	Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism	CTD_diseases	5
MESH:C537698	MESH:C537698	Juvenile macular degeneration and hypotrichosis	CTD_diseases	5
MESH:C537700	MESH:C537700	Juvenile osteoporosis	CTD_diseases	5
MESH:C537704	MESH:C537704	Juvenile-onset dystonia	CTD_diseases	5
MESH:C537708	MESH:C537708	Kifafa seizure disorder	CTD_diseases	5
MESH:C537713	MESH:C537713	Lynch Lee Murday syndrome	CTD_diseases	5
MESH:C537715	MESH:C537715	Macleod Fraser syndrome	CTD_diseases	5
MESH:C537724	MESH:C537724	Lujan Fryns syndrome	CTD_diseases	5
MESH:C537732	MESH:C537732	Oculodental syndrome Rutherfurd syndrome	CTD_diseases	5
MESH:C537734	MESH:C537734	Oculodigitoesophagoduodenal syndrome	CTD_diseases	5
MESH:C537740	MESH:C537740	Odontoma dysphagia syndrome	CTD_diseases	5
MESH:C537742	MESH:C537742	Odontoonychodermal dysplasia	CTD_diseases	5
MESH:C537751	MESH:C537751	Oncogenic osteomalacia	CTD_diseases	5
MESH:C537766	MESH:C537766	Anonychia-onychodystrophy with hypoplasia or absence of distal phalanges	CTD_diseases	5
MESH:C537767	MESH:C537767	Anophthalmia plus syndrome	CTD_diseases	5
MESH:C537769	MESH:C537769	Anophthalmos with limb anomalies	CTD_diseases	5
MESH:C537771	MESH:C537771	Anorectal atresia	CTD_diseases	5
MESH:C537778	MESH:C537778	Antisynthetase syndrome	CTD_diseases	5
MESH:C537785	MESH:C537785	Aortic arch anomaly with peculiar facies and mental retardation	CTD_diseases	5
MESH:C537788	MESH:C537788	Aplasia cutis congenita intestinal lymphangiectasia	CTD_diseases	5
MESH:C537793	MESH:C537793	Ayazi syndrome	CTD_diseases	5
MESH:C537795	MESH:C537795	Baetz-Greenwalt syndrome	CTD_diseases	5
MESH:C537805	MESH:C537805	17-Hydroxysteroid Dehydrogenase Deficiency	CTD_diseases	5
MESH:C537806	MESH:C537806	18-Hydroxylase deficiency	CTD_diseases	5
MESH:C537824	MESH:C537824	Chromosome 8 ring	CTD_diseases	5
MESH:C537831	MESH:C537831	Macrothrombocytopenia progressive deafness	CTD_diseases	5
MESH:C537833	MESH:C537833	Macular dystrophy, concentric annular	CTD_diseases	5
MESH:C537834	MESH:C537834	Macular dystrophy, corneal type 1	CTD_diseases	5
MESH:C537835	MESH:C537835	Macular dystrophy, retinal, 1, North Carolina type	CTD_diseases	5
MESH:C537838	MESH:C537838	Madokoro Ohdo Sonoda syndrome	CTD_diseases	5
MESH:C537839	MESH:C537839	Majeed syndrome	CTD_diseases	5
MESH:C537842	MESH:C537842	Nonmedullary thyroid carcinoma, with or without cell oxyphilia	CTD_diseases	5
MESH:C537857	MESH:C537857	Hereditary vertical nystagmus	CTD_diseases	5
MESH:C537860	MESH:C537860	Occipital horn syndrome	CTD_diseases	5
MESH:C537880	MESH:C537880	Lathosterolosis	CTD_diseases	5
MESH:C537881	MESH:C537881	Lattice corneal dystrophy type 1	CTD_diseases	5
MESH:C537890	MESH:C537890	Pfeiffer Rockelein syndrome	CTD_diseases	5
MESH:C537897	MESH:C537897	Phosphoribosylpyrophosphate synthetase deficiency	CTD_diseases	5
MESH:C537899	MESH:C537899	Baker Vinters syndrome	CTD_diseases	5
MESH:C537906	MESH:C537906	Baraitser Rodeck Garner syndrome	CTD_diseases	5
MESH:C537913	MESH:C537913	Chondrodysplasia, acromesomelic, with genital anomalies	CTD_diseases	5
MESH:C537914	MESH:C537914	Chondrodysplasia, blomstrand type	CTD_diseases	5
MESH:C537919	MESH:C537919	Fertile eunuch syndrome	CTD_diseases	5
MESH:C537923	MESH:C537923	Opitz-Kaveggia syndrome	CTD_diseases	5
MESH:C537929	MESH:C537929	Fibromuscular dysplasia of arteries	CTD_diseases	5
MESH:C537943	MESH:C537943	Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome	CTD_diseases	5
MESH:C537946	MESH:C537946	Cerebral sarcoma	CTD_diseases	5
MESH:C537947	MESH:C537947	Cerebrospinal fluid leak	CTD_diseases	5
MESH:C537956	MESH:C537956	Cervical hypertrichosis neuropathy	CTD_diseases	5
MESH:C537962	MESH:C537962	Calloso-genital dysplasia	CTD_diseases	5
MESH:C537966	MESH:C537966	Campomelia Cumming type	CTD_diseases	5
MESH:C537967	MESH:C537967	Camptobrachydactyly	CTD_diseases	5
MESH:C537968	MESH:C537968	Camptocormia	CTD_diseases	5
MESH:C537969	MESH:C537969	Camptodactyly joint contractures and facial skeletal dysplasia	CTD_diseases	5
MESH:C537971	MESH:C537971	Camptodactyly syndrome Guadalajara type 2	CTD_diseases	5
MESH:C537972	MESH:C537972	Camptodactyly taurinuria	CTD_diseases	5
MESH:C537976	MESH:C537976	Camptodactyly-ichthyosis syndrome	CTD_diseases	5
MESH:C537977	MESH:C537977	Camptomelic syndrome long limb type	CTD_diseases	5
MESH:C537998	MESH:C537998	Dyssegmental dysplasia	CTD_diseases	5
MESH:C537999	MESH:C537999	Dyssegmental dysplasia, Rolland-Desbuquois type	CTD_diseases	5
MESH:C538001	MESH:C538001	Dystonia 12	CTD_diseases	5
MESH:C538007	MESH:C538007	Dystonia, Dopa-responsive	CTD_diseases	5
MESH:C538009	MESH:C538009	Dystrophia myotonica 2	CTD_diseases	5
MESH:C538011	MESH:C538011	Eales disease	CTD_diseases	5
MESH:C538016	MESH:C538016	Ectodermal dysplasia alopecia preaxial polydactyly	CTD_diseases	5
MESH:C538018	MESH:C538018	Ectodermal dysplasia mental retardation syndactyly	CTD_diseases	5
MESH:C538021	MESH:C538021	Chromosome 9 inversion or duplication	CTD_diseases	5
MESH:C538022	MESH:C538022	Chromosome 9 Ring	CTD_diseases	5
MESH:C538023	MESH:C538023	Chromosome 9, duplication 9q21	CTD_diseases	5
MESH:C538027	MESH:C538027	Chromosome 9, tetrasomy 9p	CTD_diseases	5
MESH:C538035	MESH:C538035	Chromosome 15 ring	CTD_diseases	5
MESH:C538039	MESH:C538039	Chromosome 15q, tetrasomy	CTD_diseases	5
MESH:C538046	MESH:C538046	Chromosome 17 ring	CTD_diseases	5
MESH:C538056	MESH:C538056	Agammaglobulinemia, non-Bruton type	CTD_diseases	5
MESH:C538064	MESH:C538064	Frontometaphyseal dysplasia	CTD_diseases	5
MESH:C538065	MESH:C538065	Frontonasal dysplasia	CTD_diseases	5
MESH:C538070	MESH:C538070	Fryns syndrome	CTD_diseases	5
MESH:C538080	MESH:C538080	Congenital diaphragmatic hernia	CTD_diseases	5
MESH:C538081	MESH:C538081	Congenital dislocation of the patella	CTD_diseases	5
MESH:C538086	MESH:C538086	Chromosome 10 ring	CTD_diseases	5
MESH:C538089	MESH:C538089	Oto-palato-digital syndrome, type 2	CTD_diseases	5
MESH:C538091	MESH:C538091	Kuzniecky syndrome	CTD_diseases	5
MESH:C538100	MESH:C538100	Pagon Stephan syndrome	CTD_diseases	5
MESH:C538103	MESH:C538103	Palindromic rheumatism	CTD_diseases	5
MESH:C538110	MESH:C538110	Pancreatic adenoma	CTD_diseases	5
MESH:C538111	MESH:C538111	Pancreatic beta cell agenesis with neonatal diabetes mellitus	CTD_diseases	5
MESH:C538113	MESH:C538113	Herrmann syndrome	CTD_diseases	5
MESH:C538117	MESH:C538117	Human Herpesvirus 6 encephalitis	CTD_diseases	5
MESH:C538124	MESH:C538124	Kuskokwim disease	CTD_diseases	5
MESH:C538126	MESH:C538126	Kuster syndrome	CTD_diseases	5
MESH:C538138	MESH:C538138	Hyperglycerolemia	CTD_diseases	5
MESH:C538139	MESH:C538139	Sucrase-isomaltase deficiency, congenital	CTD_diseases	5
MESH:C538141	MESH:C538141	Sulfite oxidase deficiency	CTD_diseases	5
MESH:C538144	MESH:C538144	Supraumbilical midabdominal raphe and facial cavernous hemangiomas	CTD_diseases	5
MESH:C538145	MESH:C538145	Sutton disease 2	CTD_diseases	5
MESH:C538148	MESH:C538148	Symphalangism, distal, with microdontia, dental pulp stones, and narrowed zygomatic arch	CTD_diseases	5
MESH:C538167	MESH:C538167	Acidemia, isovaleric	CTD_diseases	5
MESH:C538175	MESH:C538175	Acquired ichthyosis	CTD_diseases	5
MESH:C538178	MESH:C538178	Acrodermatitis enteropathica	CTD_diseases	5
MESH:C538179	MESH:C538179	Acrodysostosis	CTD_diseases	5
MESH:C538180	MESH:C538180	Acrodysplasia scoliosis	CTD_diseases	5
MESH:C538181	MESH:C538181	Acrodysplasia with ossification abnormalities, short stature, and fibular hypoplasia	CTD_diseases	5
MESH:C538187	MESH:C538187	Acrogeria, gottron type	CTD_diseases	5
MESH:C538193	MESH:C538193	Furukawa Takagi Nakao syndrome	CTD_diseases	5
MESH:C538218	MESH:C538218	Dermatitis herpetiformis, familial	CTD_diseases	5
MESH:C538229	MESH:C538229	Adenoameloblastoma	CTD_diseases	5
MESH:C538234	MESH:C538234	Adenosine monophosphate deaminase deficiency	CTD_diseases	5
MESH:C538235	MESH:C538235	Adenylosuccinate lyase deficiency	CTD_diseases	5
MESH:C538238	MESH:C538238	Adrenal incidentaloma	CTD_diseases	5
MESH:C538246	MESH:C538246	Aminoacylase 1 deficiency	CTD_diseases	5
MESH:C538254	MESH:C538254	Anal sphincter dysplasia	CTD_diseases	5
MESH:C538256	MESH:C538256	Anauxetic dysplasia	CTD_diseases	5
MESH:C538259	MESH:C538259	Congenital atransferrinemia	CTD_diseases	5
MESH:C538260	MESH:C538260	Atresia of small intestine	CTD_diseases	5
MESH:C538261	MESH:C538261	Atrial fibrillation, familial 1	CTD_diseases	5
MESH:C538262	MESH:C538262	Atrial myxoma, familial	CTD_diseases	5
MESH:C538276	MESH:C538276	Prader-Willi habitus, osteopenia, and camptodactyly	CTD_diseases	5
MESH:C538298	MESH:C538298	Chromosome 12 ring	CTD_diseases	5
MESH:C538303	MESH:C538303	Chromosome 13 ring	CTD_diseases	5
MESH:C538304	MESH:C538304	Chromosome 18 ring	CTD_diseases	5
MESH:C538306	MESH:C538306	Chromosome 18, tetrasomy 18p	CTD_diseases	5
MESH:C538310	MESH:C538310	Chromosome 19 ring	CTD_diseases	5
MESH:C538320	MESH:C538320	Histidinemia	CTD_diseases	5
MESH:C538324	MESH:C538324	3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency	CTD_diseases	5
MESH:C538328	MESH:C538328	Holoprosencephaly, recurrent infections, and monocytosis	CTD_diseases	5
MESH:C538330	MESH:C538330	Inclusion body myopathy, autosomal dominant	CTD_diseases	5
MESH:C538331	MESH:C538331	Naegeli syndrome	CTD_diseases	5
MESH:C538332	MESH:C538332	Naguib-Richieri-Costa syndrome	CTD_diseases	5
MESH:C538335	MESH:C538335	Nakamura Osame syndrome	CTD_diseases	5
MESH:C538343	MESH:C538343	Native American myopathy	CTD_diseases	5
MESH:C538345	MESH:C538345	Navajo poikiloderma	CTD_diseases	5
MESH:C538354	MESH:C538354	Potato nose	CTD_diseases	5
MESH:C538355	MESH:C538355	Potocki-Lupski syndrome	CTD_diseases	5
MESH:C538358	MESH:C538358	Powell Venencie Gordon syndrome	CTD_diseases	5
MESH:C538359	MESH:C538359	RDS - infants	CTD_diseases	5
MESH:C538361	MESH:C538361	Reticular dysgenesis	CTD_diseases	5
MESH:C538369	MESH:C538369	Retinoschisis of Fovea	CTD_diseases	5
MESH:C538370	MESH:C538370	Retroperitoneal liposarcoma	CTD_diseases	5
MESH:C538374	MESH:C538374	Hyperinsulinemic hypoglycemia, familial, 3	CTD_diseases	5
MESH:C538375	MESH:C538375	Hyperinsulinemic hypoglycemia, familial, 6	CTD_diseases	5
MESH:C538376	MESH:C538376	Hyperinsulinemic hypoglycemia, familial, 7	CTD_diseases	5
MESH:C538384	MESH:C538384	Hyperprolinemia	CTD_diseases	5
MESH:C538385	MESH:C538385	Hyperprolinemia type 2	CTD_diseases	5
MESH:C538387	MESH:C538387	Hypertelorism with esophageal abnormality and hypospadias	CTD_diseases	5
MESH:C538389	MESH:C538389	Congenital hypertrichosis lanuginosa	CTD_diseases	5
MESH:C538390	MESH:C538390	Hypertrichosis, anterior cervical	CTD_diseases	5
MESH:C538391	MESH:C538391	Hypertrichosis, hyperkeratosis, mental retardation, and distinctive facial features	CTD_diseases	5
MESH:C538393	MESH:C538393	Hypertryptophanemia	CTD_diseases	5
MESH:C538396	MESH:C538396	Lambert syndrome	CTD_diseases	5
MESH:C538400	MESH:C538400	Distal arthrogryposis type 2B	CTD_diseases	5
MESH:C538401	MESH:C538401	Arthrogryposis multiplex congenita whistling face	CTD_diseases	5
MESH:C538405	MESH:C538405	Dichuchwa	CTD_diseases	5
MESH:C538417	MESH:C538417	Spinal muscular atrophy 4	CTD_diseases	5
MESH:C538420	MESH:C538420	Black hairy tongue	CTD_diseases	5
MESH:C538459	MESH:C538459	Ovarian gynandroblastoma	CTD_diseases	5
MESH:C538465	MESH:C538465	HLA class 1 deficiency	CTD_diseases	5
MESH:C538478	MESH:C538478	Muscular dystrophy, tardive, Dreifuss-Emery type, with contractures	CTD_diseases	5
MESH:C538494	MESH:C538494	Aplastic anemia, idiopathic	CTD_diseases	5
MESH:C538505	MESH:C538505	Cytomegalic inclusion body disease	CTD_diseases	5
MESH:C538514	MESH:C538514	Familial schizencephaly	CTD_diseases	5
MESH:C538556	MESH:C538556	Imerslund-Grasbeck syndrome	CTD_diseases	5
MESH:C538558	MESH:C538558	Bilateral Kienbock's disease	CTD_diseases	5
MESH:C538564	MESH:C538564	Reticuloendotheliosis, familial, with eosinophilia	CTD_diseases	5
MESH:C538596	MESH:C538596	Peritoneal retractile mesenteritis	CTD_diseases	5
MESH:C538616	MESH:C538616	Paramyotonia congenita of Von Eulenburg	CTD_diseases	5
MESH:C538636	MESH:C538636	Familial Letterer-Siwe disease	CTD_diseases	5
MESH:C538639	MESH:C538639	Sarcoma family syndrome of Li and Fraumeni	CTD_diseases	5
MESH:C538647	MESH:C538647	Myotubular myopathy, X-linked	CTD_diseases	5
MESH:C538648	MESH:C538648	Lysosomal Alpha-N-Acetylgalactosaminidase Deficiency	CTD_diseases	5
MESH:C538657	MESH:C538657	Van der Hoeve Halbertsma Waardenburg Gualdi Syndrome	CTD_diseases	5
MESH:C538665	MESH:C538665	Watermelon stomach disease	CTD_diseases	5
MESH:C538678	MESH:C538678	Lymphedema of the lower extremities, recurrent pneumonia, bronchiectasis, and yellowed nails	CTD_diseases	5
MESH:C540770	MESH:C540770	Mitochondrial cytopathy	CTD_diseases	5
MESH:C548011	MESH:C548011	Deafness with Labyrinthine Aplasia Microtia and Microdontia (LAMM)	CTD_diseases	5
MESH:C548012	MESH:C548012	Diploid-Triploid Mosaicism	CTD_diseases	5
MESH:C548027	MESH:C548027	Idiopathic Juxtafoveal Retinal Telangiectasia	CTD_diseases	5
MESH:C548029	MESH:C548029	Karak Syndrome	CTD_diseases	5
MESH:C548032	MESH:C548032	Legius syndrome	CTD_diseases	5
MESH:C548078	MESH:C548078	Mungan Syndrome	CTD_diseases	5
MESH:C548085	MESH:C548085	Progressive Transformation of Germinal Centers	CTD_diseases	5
MESH:C557815	MESH:C557815	Deficiency of interleukin-1 receptor antagonist	CTD_diseases	5
MESH:C557826	MESH:C557826	Immune dysfunction with T-cell inactivation due to calcium entry defect 1	CTD_diseases	5
MESH:C557827	MESH:C557827	Immune dysfunction with T-cell inactivation due to calcium entry defect 2	CTD_diseases	5
MESH:C559045	MESH:C559045	Recurrent spontaneous hypothermia with hypoplasia of the corpus callosum	CTD_diseases	5
MESH:C562377	MESH:C562377	Glutamate Monosodium Sensitivity	CTD_diseases	5
MESH:C562396	MESH:C562396	Ankyloglossia	CTD_diseases	5
MESH:C562399	MESH:C562399	Corneal Dystrophy, Band-Shaped	CTD_diseases	5
MESH:C562435	MESH:C562435	Choanal Atresia, Posterior	CTD_diseases	5
MESH:C562441	MESH:C562441	Intestinal Atresia, Multiple	CTD_diseases	5
MESH:C562448	MESH:C562448	Lipodystrophy, Partial, Acquired	CTD_diseases	5
MESH:C562451	MESH:C562451	Hyperbilirubinemia, Shunt	CTD_diseases	5
MESH:C562463	MESH:C562463	Pancreatic Carcinoma	CTD_diseases	5
MESH:C562472	MESH:C562472	Teratoma, Testicular	CTD_diseases	5
MESH:C562479	MESH:C562479	Macular Degeneration, Age-Related, 2	CTD_diseases	5
MESH:C562481	MESH:C562481	Urticaria, Aquagenic	CTD_diseases	5
MESH:C562484	MESH:C562484	Hairy Ears	CTD_diseases	5
MESH:C562503	MESH:C562503	Otocephaly	CTD_diseases	5
MESH:C562546	MESH:C562546	Megalodactyly	CTD_diseases	5
MESH:C562548	MESH:C562548	Clavicle, Pseudarthrosis Of, Congenital	CTD_diseases	5
MESH:C562561	MESH:C562561	Pyloric Atresia	CTD_diseases	5
MESH:C562562	MESH:C562562	Colonic Atresia	CTD_diseases	5
MESH:C562563	MESH:C562563	Microcolon	CTD_diseases	5
MESH:C562587	MESH:C562587	Purine Nucleoside Phosphorylase Deficiency	CTD_diseases	5
MESH:C562589	MESH:C562589	Orotic Aciduria II	CTD_diseases	5
MESH:C562590	MESH:C562590	Xeroderma Pigmentosum, Complementation Group B	CTD_diseases	5
MESH:C562591	MESH:C562591	Xeroderma Pigmentosum, Complementation Group D	CTD_diseases	5
MESH:C562592	MESH:C562592	Xeroderma Pigmentosum, Complementation Group F	CTD_diseases	5
MESH:C562593	MESH:C562593	Xeroderma Pigmentosum, Complementation Group G	CTD_diseases	5
MESH:C562600	MESH:C562600	Lactase Deficiency, Congenital	CTD_diseases	5
MESH:C562602	MESH:C562602	Glucose-Galactose Malabsorption	CTD_diseases	5
MESH:C562603	MESH:C562603	Trehalase Deficiency	CTD_diseases	5
MESH:C562627	MESH:C562627	Cutis Laxa, Autosomal Dominant	CTD_diseases	5
MESH:C562628	MESH:C562628	Cutis Laxa, Autosomal Recessive, Type I	CTD_diseases	5
MESH:C562632	MESH:C562632	Cutis Laxa, Autosomal Recessive, Type IIA	CTD_diseases	5
MESH:C562658	MESH:C562658	Tryptophanuria With Dwarfism	CTD_diseases	5
MESH:C562659	MESH:C562659	Tyrosinosis	CTD_diseases	5
MESH:C562669	MESH:C562669	Hydroxyprolinemia	CTD_diseases	5
MESH:C562670	MESH:C562670	Glucoglycinuria	CTD_diseases	5
MESH:C562674	MESH:C562674	Hyperleucine-Isoleucinemia	CTD_diseases	5
MESH:C562678	MESH:C562678	Acetyl-Coa Carboxylase Deficiency	CTD_diseases	5
MESH:C562680	MESH:C562680	Cystathionase Deficiency	CTD_diseases	5
MESH:C562681	MESH:C562681	Methionine Adenosyltransferase Deficiency	CTD_diseases	5
MESH:C562687	MESH:C562687	Lysinuric Protein Intolerance	CTD_diseases	5
MESH:C562692	MESH:C562692	Hyperbilirubinemia, Transient Familial Neonatal	CTD_diseases	5
MESH:C562710	MESH:C562710	Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans	CTD_diseases	5
MESH:C562722	MESH:C562722	Eosinophilia, Familial	CTD_diseases	5
MESH:C562724	MESH:C562724	Dysprothrombinemia	CTD_diseases	5
MESH:C562731	MESH:C562731	Teratoma, Ovarian	CTD_diseases	5
MESH:C562732	MESH:C562732	Euthyroid Goiter	CTD_diseases	5
MESH:C562737	MESH:C562737	Connective Tissue Nevus	CTD_diseases	5
MESH:C562740	MESH:C562740	Hemangiopericytoma, Malignant	CTD_diseases	5
MESH:C562741	MESH:C562741	Adamantinoma Of Long Bones	CTD_diseases	5
MESH:C562742	MESH:C562742	Blepharochalasis And Double Lip	CTD_diseases	5
MESH:C562745	MESH:C562745	Corneal Dystrophy, Posterior Polymorphous, 1	CTD_diseases	5
MESH:C562746	MESH:C562746	Macular Dystrophy, Retinal, 2	CTD_diseases	5
MESH:C562750	MESH:C562750	Glaucoma, Primary Open Angle	CTD_diseases	5
MESH:C562760	MESH:C562760	Capillary Malformations, Congenital, 1	CTD_diseases	5
MESH:C562761	MESH:C562761	Splenoportal Vascular Anomalies	CTD_diseases	5
MESH:C562765	MESH:C562765	Esophageal Ring, Lower	CTD_diseases	5
MESH:C562774	MESH:C562774	Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus	CTD_diseases	5
MESH:C562776	MESH:C562776	Hyperproinsulinemia	CTD_diseases	5
MESH:C562790	MESH:C562790	Hypercalciuria, Absorptive, 2	CTD_diseases	5
MESH:C562793	MESH:C562793	Hypophosphatemic Rickets with Hypercalciuria, Hereditary	CTD_diseases	5
MESH:C562799	MESH:C562799	Folate Malabsorption, Hereditary	CTD_diseases	5
MESH:C562812	MESH:C562812	Carnitine-Acylcarnitine Translocase Deficiency	CTD_diseases	5
MESH:C562818	MESH:C562818	Glutaric Aciduria III	CTD_diseases	5
MESH:C562823	MESH:C562823	Milia, Multiple Eruptive	CTD_diseases	5
MESH:C562830	MESH:C562830	Patent Ductus Venosus	CTD_diseases	5
MESH:C562832	MESH:C562832	Pulmonary Atresia with Intact Ventricular Septum	CTD_diseases	5
MESH:C562840	MESH:C562840	Breast Cancer, Familial	CTD_diseases	5
MESH:C562858	MESH:C562858	Cholesteatoma, Congenital	CTD_diseases	5
MESH:C562865	MESH:C562865	Heparin Cofactor II Deficiency	CTD_diseases	5
MESH:C562875	MESH:C562875	Complement Factor H Deficiency	CTD_diseases	5
MESH:C562876	MESH:C562876	Carboxypeptidase N Deficiency	CTD_diseases	5
MESH:C562885	MESH:C562885	Hyperbilirubinemia, Conjugated, Type III	CTD_diseases	5
MESH:C562886	MESH:C562886	Ichthyosis Congenita With Biliary Atresia	CTD_diseases	5
MESH:C562894	MESH:C562894	Prune Belly Syndrome with Pulmonic Stenosis, Mental Retardation, and Deafness	CTD_diseases	5
MESH:C562895	MESH:C562895	Pulmonic Stenosis and Congenital Nephrosis	CTD_diseases	5
MESH:C562934	MESH:C562934	Myopathy, Centronuclear, Autosomal Recessive	CTD_diseases	5
MESH:C562935	MESH:C562935	Myopathy with Abnormal Lipid Metabolism	CTD_diseases	5
MESH:C562937	MESH:C562937	Hypochondroplasia	CTD_diseases	5
MESH:C562940	MESH:C562940	Craniodiaphyseal Dysplasia	CTD_diseases	5
MESH:C562941	MESH:C562941	Telecanthus	CTD_diseases	5
MESH:C562942	MESH:C562942	Aortic Valve, Calcification of	CTD_diseases	5
MESH:C562943	MESH:C562943	Choroid Plexus Carcinoma	CTD_diseases	5
MESH:C562952	MESH:C562952	Cervical Vertebrae, Agenesis Of	CTD_diseases	5
MESH:C562958	MESH:C562958	Spondyloepimetaphyseal Dysplasia, Irapa Type	CTD_diseases	5
MESH:C562963	MESH:C562963	Brachyolmia Type 3	CTD_diseases	5
MESH:C562966	MESH:C562966	Cranioectodermal Dysplasia	CTD_diseases	5
MESH:C562995	MESH:C562995	Hexokinase Deficiency Hemolytic Anemia	CTD_diseases	5
MESH:C562999	MESH:C562999	Hypercalcemia, Infantile	CTD_diseases	5
MESH:C563007	MESH:C563007	Hypochondrogenesis	CTD_diseases	5
MESH:C563009	MESH:C563009	Glycinuria with or without Oxalate Urolithiasis	CTD_diseases	5
MESH:C563015	MESH:C563015	Preauricular Fistulae, Congenital	CTD_diseases	5
MESH:C563017	MESH:C563017	Gigantiform Cementoma, Familial	CTD_diseases	5
MESH:C563032	MESH:C563032	Preterm Premature Rupture of the Membranes	CTD_diseases	5
MESH:C563043	MESH:C563043	Kleefstra Syndrome	CTD_diseases	5
MESH:C563047	MESH:C563047	Cleft Palate-Lateral Synechia Syndrome	CTD_diseases	5
MESH:C563080	MESH:C563080	Lysine Malabsorption Syndrome	CTD_diseases	5
MESH:C563085	MESH:C563085	Mercaptolactate-Cysteine Disulfiduria	CTD_diseases	5
MESH:C563087	MESH:C563087	Mexican Cardiomelic Dysplasia	CTD_diseases	5
MESH:C563129	MESH:C563129	Van Den Bosch Syndrome	CTD_diseases	5
MESH:C563162	MESH:C563162	Chondrocalcinosis 2	CTD_diseases	5
MESH:C563177	MESH:C563177	Glucocorticoid-Remediable Aldosteronism	CTD_diseases	5
MESH:C563184	MESH:C563184	Glaucoma-Related Pigment Dispersion Syndrome	CTD_diseases	5
MESH:C563185	MESH:C563185	Hyperhidrosis Palmaris Et Plantaris	CTD_diseases	5
MESH:C563192	MESH:C563192	Epidermolysis Bullosa Pruriginosa	CTD_diseases	5
MESH:C563207	MESH:C563207	Transaldolase Deficiency	CTD_diseases	5
MESH:C563212	MESH:C563212	Ribose 5-Phosphate Isomerase Deficiency	CTD_diseases	5
MESH:C563213	MESH:C563213	Myositis, Eosinophilic	CTD_diseases	5
MESH:C563218	MESH:C563218	Brachyolmia Type 2	CTD_diseases	5
MESH:C563256	MESH:C563256	Corneal Dystrophy, Fleck	CTD_diseases	5
MESH:C563262	MESH:C563262	Corneal Dystrophy, Central Type	CTD_diseases	5
MESH:C563268	MESH:C563268	Ectopia Lentis with Ectopia of Pupil	CTD_diseases	5
MESH:C563270	MESH:C563270	Macular Corneal Dystrophy, Type II	CTD_diseases	5
MESH:C563277	MESH:C563277	Papillary Thyroid Microcarcinoma	CTD_diseases	5
MESH:C563291	MESH:C563291	Multiple Epiphyseal Dysplasia with Robin Phenotype	CTD_diseases	5
MESH:C563293	MESH:C563293	Ectopia Lentis, Spontaneous Filtering Blebs, and Craniofacial Dysmorphism	CTD_diseases	5
MESH:C563305	MESH:C563305	Agammaglobulinemia, Non-Bruton Type, Autosomal Dominant	CTD_diseases	5
MESH:C563310	MESH:C563310	Inflammatory Bowel Disease 2	CTD_diseases	5
MESH:C563330	MESH:C563330	Chondrodysplasia, Lethal, with Long Bone Angulation and Mixed Bone Density	CTD_diseases	5
MESH:C563339	MESH:C563339	Sebaceous Nevus Syndrome and Hemimegalencephaly	CTD_diseases	5
MESH:C563341	MESH:C563341	Microcephaly, Congenital Heart Disease, Unilateral Renal Agenesis, and Hyposegmented Lungs	CTD_diseases	5
MESH:C563344	MESH:C563344	Ectrodactyly of Lower Limbs, Congenital Heart Defect, and Micrognathia	CTD_diseases	5
MESH:C563347	MESH:C563347	Ectodermal Dysplasia with Natal Teeth, Turnpenny Type	CTD_diseases	5
MESH:C563348	MESH:C563348	Spinal Dysplasia, Anhalt Type	CTD_diseases	5
MESH:C563373	MESH:C563373	Hypercalciuric Hypercalcemia	CTD_diseases	5
MESH:C563374	MESH:C563374	Hypocalcemia, Autosomal Dominant, with Bartter Syndrome	CTD_diseases	5
MESH:C563387	MESH:C563387	Rhabdomyolysis, Cerivastatin-Induced	CTD_diseases	5
MESH:C563401	MESH:C563401	Choreoathetosis/Spasticity, Episodic	CTD_diseases	5
MESH:C563412	MESH:C563412	Juvenile Polyposis with Hereditary Hemorrhagic Telangiectasia	CTD_diseases	5
MESH:C563414	MESH:C563414	Cardiac Malformation, Cleft Lip-Palate, Microcephaly and Digital Anomalies	CTD_diseases	5
MESH:C563425	MESH:C563425	Diabetes Mellitus, Permanent Neonatal	CTD_diseases	5
MESH:C563440	MESH:C563440	Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, NK Cell-Neg	CTD_diseases	5
MESH:C563443	MESH:C563443	Neuronopathy, Distal Hereditary Motor, Type V	CTD_diseases	5
MESH:C563447	MESH:C563447	Dwarfism, Familial, With Muscle Spasms	CTD_diseases	5
MESH:C563458	MESH:C563458	Varicella, Severe Recurrent	CTD_diseases	5
MESH:C563464	MESH:C563464	Orofacial Cleft 7	CTD_diseases	5
MESH:C563467	MESH:C563467	Hypertryptophanemia, Familial	CTD_diseases	5
MESH:C563475	MESH:C563475	Paroxysmal Extreme Pain Disorder	CTD_diseases	5
MESH:C563481	MESH:C563481	Otofaciocervical Syndrome	CTD_diseases	5
MESH:C563488	MESH:C563488	Ossified Ear Cartilages	CTD_diseases	5
MESH:C563490	MESH:C563490	Orbital Margin, Hypoplasia of	CTD_diseases	5
MESH:C563498	MESH:C563498	Ophthalmoplegia, Progressive, with Scrotal Tongue and Mental Deficiency	CTD_diseases	5
MESH:C563509	MESH:C563509	Schilbach-Rott Syndrome Ocular Hypotelorism, Submucosal Cleft Palate, and Hypospadias	CTD_diseases	5
MESH:C563522	MESH:C563522	Neurofibromatosis-Pheochromocytoma-Duodenal Carcinoid Syndrome	CTD_diseases	5
MESH:C563524	MESH:C563524	NF1 Microdeletion Syndrome	CTD_diseases	5
MESH:C563535	MESH:C563535	Myotonic Myopathy with Cylindrical Spirals	CTD_diseases	5
MESH:C563542	MESH:C563542	Myopathy with Storage of Glycoproteins and Glycosaminoglycans	CTD_diseases	5
MESH:C563544	MESH:C563544	Myopathy, Centronuclear, Autosomal Dominant	CTD_diseases	5
MESH:C563552	MESH:C563552	Myasthenia, Limb-Girdle, Autoimmune	CTD_diseases	5
MESH:C563561	MESH:C563561	Neuropathy, Distal Hereditary Motor, Type IIA	CTD_diseases	5
MESH:C563562	MESH:C563562	Neuropathy, Distal Hereditary Motor, Type VIIA	CTD_diseases	5
MESH:C563564	MESH:C563564	Cerebelloparenchymal Disorder VI	CTD_diseases	5
MESH:C563565	MESH:C563565	Cerebellar Granule Cell Hypertrophy and Megalencephaly	CTD_diseases	5
MESH:C563572	MESH:C563572	Mitral Regurgitation, Conductive Deafness, and Fusion of Cervical Vertebrae and of Carpal and Tarsal	CTD_diseases	5
MESH:C563574	MESH:C563574	Metaphyseal Dysplasia without Hypotrichosis	CTD_diseases	5
MESH:C563586	MESH:C563586	Metaphyseal Dysplasia with Maxillary Hypoplasia and Brachydactyly	CTD_diseases	5
MESH:C563589	MESH:C563589	Mesomelic Dwarfism of Hypoplastic Tibia and Radius Type	CTD_diseases	5
MESH:C563590	MESH:C563590	Meralgia Paraesthetica, Familial	CTD_diseases	5
MESH:C563594	MESH:C563594	Melanosis, Universal	CTD_diseases	5
MESH:C563607	MESH:C563607	Macular Dystrophy, Fenestrated Sheen Type	CTD_diseases	5
MESH:C563610	MESH:C563610	Sebaceous Tumors, Somatic	CTD_diseases	5
MESH:C563618	MESH:C563618	Lp(A) Deficiency, Congenital	CTD_diseases	5
MESH:C563620	MESH:C563620	Lipoma of the Conjunctiva	CTD_diseases	5
MESH:C563632	MESH:C563632	Leg Ulcers, Familial, of Juvenile Onset	CTD_diseases	5
MESH:C563634	MESH:C563634	Tooth Agenesis, Selective, 4	CTD_diseases	5
MESH:C563646	MESH:C563646	Keratosis Palmaris et Plantaris with Clinodactyly	CTD_diseases	5
MESH:C563654	MESH:C563654	Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency	CTD_diseases	5
MESH:C563661	MESH:C563661	Renal Hypodysplasia, Nonsyndromic, 1	CTD_diseases	5
MESH:C563664	MESH:C563664	Epiphyseal Dysplasia, Baumann Type	CTD_diseases	5
MESH:C563673	MESH:C563673	Diarrhea 4, Malabsorptive, Congenital	CTD_diseases	5
MESH:C563674	MESH:C563674	Macular Degeneration, Age-Related, 6	CTD_diseases	5
MESH:C563682	MESH:C563682	Oculootofacial Dysplasia	CTD_diseases	5
MESH:C563692	MESH:C563692	Glaucoma 1, Open Angle, G	CTD_diseases	5
MESH:C563700	MESH:C563700	Nanophthalmos 2	CTD_diseases	5
MESH:C563702	MESH:C563702	Spastic Paraplegia, Optic Atrophy, and Neuropathy	CTD_diseases	5
MESH:C563714	MESH:C563714	Sarcoidosis, Early-Onset	CTD_diseases	5
MESH:C563731	MESH:C563731	Cerebrorenodigital Syndrome with Limb Malformations and Triradiate Acetabula	CTD_diseases	5
MESH:C563735	MESH:C563735	Epiphyseal Dysplasia, Multiple, with Miniepiphyses	CTD_diseases	5
MESH:C563736	MESH:C563736	Epiphyseal Dysplasia, Multiple, with Severe Proximal Femoral Dysplasia	CTD_diseases	5
MESH:C563737	MESH:C563737	Teratoid Tumor, Atypical	CTD_diseases	5
MESH:C563738	MESH:C563738	Rhabdoid Tumor Predisposition Syndrome 1	CTD_diseases	5
MESH:C563739	MESH:C563739	Erythrokeratodermia Variabilis 3	CTD_diseases	5
MESH:C563754	MESH:C563754	Li-Fraumeni Syndrome 3	CTD_diseases	5
MESH:C563755	MESH:C563755	Li-Fraumeni Syndrome 2	CTD_diseases	5
MESH:C563763	MESH:C563763	Senior-Loken Syndrome 5	CTD_diseases	5
MESH:C563765	MESH:C563765	Hypotrichosis, Progressive Patterned Scalp, with Wiry Hair, Onycholysis, and Cleft Lip/Palate	CTD_diseases	5
MESH:C563772	MESH:C563772	Spondyloepiphyseal Dysplasia Tarda, Autosomal Recessive, Leroy-Spranger Type	CTD_diseases	5
MESH:C563775	MESH:C563775	Myotilinopathy	CTD_diseases	5
MESH:C563781	MESH:C563781	Erythrokeratoderma, Reticular	CTD_diseases	5
MESH:C563785	MESH:C563785	Pseudohyperkalemia, Familial, 2, due to Red Cell Leak	CTD_diseases	5
MESH:C563787	MESH:C563787	Tibia, Bowing of, with Pseudarthrosis and Pectus Excavatum	CTD_diseases	5
MESH:C563788	MESH:C563788	Corneal Dystrophy, Posterior Polymorphous, 3	CTD_diseases	5
MESH:C563791	MESH:C563791	Arthrogryposis, Distal, Type 4	CTD_diseases	5
MESH:C563796	MESH:C563796	Diabetes Mellitus, Permanent Neonatal, with Cerebellar Agenesis	CTD_diseases	5
MESH:C563798	MESH:C563798	Nephropathy with Pretibial Epidermolysis Bullosa and Deafness	CTD_diseases	5
MESH:C563799	MESH:C563799	Amish Infantile Epilepsy Syndrome	CTD_diseases	5
MESH:C563803	MESH:C563803	Spondylometaphyseal Dysplasia, Type A4	CTD_diseases	5
MESH:C563817	MESH:C563817	Atrial Fibrillation, Familial, 3	CTD_diseases	5
MESH:C563821	MESH:C563821	Meacham Syndrome	CTD_diseases	5
MESH:C563822	MESH:C563822	Severe Combined Immunodeficiency, Autosomal Recessive, T Cell Negative, B Cell Positive, NK Cell Pos	CTD_diseases	5
MESH:C563825	MESH:C563825	Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy	CTD_diseases	5
MESH:C563829	MESH:C563829	Myasthenic Syndrome, Congenital, with Facial Dysmorphism, associated with Acetylcholine Receptor Def	CTD_diseases	5
MESH:C563831	MESH:C563831	Myasthenic Syndrome, Congenital, Ie	CTD_diseases	5
MESH:C563832	MESH:C563832	Myasthenic Syndrome, Congenital, Fast-Channel	CTD_diseases	5
MESH:C563838	MESH:C563838	Macular Degeneration, Age-Related, 3	CTD_diseases	5
MESH:C563839	MESH:C563839	Waardenburg Syndrome, Type 2D	CTD_diseases	5
MESH:C563869	MESH:C563869	Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related	CTD_diseases	5
MESH:C563873	MESH:C563873	Glaucoma 1, Open Angle, K	CTD_diseases	5
MESH:C563874	MESH:C563874	Glaucoma 1, Open Angle, J	CTD_diseases	5
MESH:C563875	MESH:C563875	Major Depressive Disorder 2	CTD_diseases	5
MESH:C563880	MESH:C563880	Robin Sequence with Distinctive Facial Appearance and Brachydactyly	CTD_diseases	5
MESH:C563881	MESH:C563881	Seckel Syndrome 3	CTD_diseases	5
MESH:C563901	MESH:C563901	Brachial Palsy, Familial Congenital	CTD_diseases	5
MESH:C563903	MESH:C563903	Atrial Fibrillation, Familial, 2	CTD_diseases	5
MESH:C563919	MESH:C563919	Major Depressive Disorder 1	CTD_diseases	5
MESH:C563920	MESH:C563920	Alopecia Universalis Congenita, XY Gonadal Dysgenesis, and Laryngomalacia	CTD_diseases	5
MESH:C563921	MESH:C563921	Congenital Corneal Opacities, Cornea Guttata, and Corectopia	CTD_diseases	5
MESH:C563923	MESH:C563923	Corneal Dystrophy, Lattice Type IIIA	CTD_diseases	5
MESH:C563926	MESH:C563926	Inflammatory Bowel Disease 9	CTD_diseases	5
MESH:C563948	MESH:C563948	Spinal Muscular Atrophy, Type IV	CTD_diseases	5
MESH:C563963	MESH:C563963	Fryns Macrocephaly	CTD_diseases	5
MESH:C563969	MESH:C563969	Aplasia Cutis Congenita with Epibulbar Dermoids	CTD_diseases	5
MESH:C563974	MESH:C563974	Cleidocranial Dysplasia, Forme Fruste, Dental Anomalies Only	CTD_diseases	5
MESH:C563978	MESH:C563978	Ichthyosis Exfoliativa	CTD_diseases	5
MESH:C563981	MESH:C563981	Spinal Muscular Atrophy, Distal, Congenital Nonprogressive	CTD_diseases	5
MESH:C563982	MESH:C563982	Hyperparathyroidism, Primary, Caused By Water Clear Cell Hyperplasia	CTD_diseases	5
MESH:C564003	MESH:C564003	Spondyloepiphyseal Dysplasia Tarda with Characteristic Facies	CTD_diseases	5
MESH:C564010	MESH:C564010	Eiken Skeletal Dysplasia	CTD_diseases	5
MESH:C564011	MESH:C564011	Pancreatic Hypoplasia, Congenital, with Diabetes Mellitus and Congenital Heart Disease	CTD_diseases	5
MESH:C564012	MESH:C564012	Wolfram Syndrome, Mitochondrial Form	CTD_diseases	5
MESH:C564014	MESH:C564014	Renal Tubulopathy, Diabetes Mellitus, and Cerebellar Ataxia due to Duplication of Mitochondrial DNA	CTD_diseases	5
MESH:C564017	MESH:C564017	Myopathy, Mitochondrial, Lethal Infantile	CTD_diseases	5
MESH:C564019	MESH:C564019	Diarrhea, Chronic, with Villous Atrophy	CTD_diseases	5
MESH:C564023	MESH:C564023	Cyclic Vomiting Syndrome-Plus	CTD_diseases	5
MESH:C564026	MESH:C564026	Mitochondrial Myopathy with Diabetes	CTD_diseases	5
MESH:C564051	MESH:C564051	Thrombocytopenia with Elevated Serum Iga and Renal Disease	CTD_diseases	5
MESH:C564078	MESH:C564078	Pierre Robin Sequence with Facial and Digital Anomalies	CTD_diseases	5
MESH:C564088	MESH:C564088	Nystagmus, Myoclonic	CTD_diseases	5
MESH:C564107	MESH:C564107	Mental Retardation associated with Psoriasis	CTD_diseases	5
MESH:C564128	MESH:C564128	Indifference to Pain, Congenital, Autosomal Dominant	CTD_diseases	5
MESH:C564133	MESH:C564133	Ige Responsiveness, Atopic	CTD_diseases	5
MESH:C564140	MESH:C564140	Leber Congenital Amaurosis 11	CTD_diseases	5
MESH:C564143	MESH:C564143	Hypotrichosis Simplex of Scalp	CTD_diseases	5
MESH:C564151	MESH:C564151	Hypocalciuric Hypercalcemia, Acquired	CTD_diseases	5
MESH:C564156	MESH:C564156	Hyperthermia, Cutaneous, With Headaches And Nausea	CTD_diseases	5
MESH:C564159	MESH:C564159	Hyperproglucagonemia	CTD_diseases	5
MESH:C564163	MESH:C564163	Hyperpigmentation, Familial Progressive	CTD_diseases	5
MESH:C564164	MESH:C564164	Hyperpigmentation of Fuldauer and Kuijpers	CTD_diseases	5
MESH:C564165	MESH:C564165	Parathyroid Adenomatosis, Familial Cystic	CTD_diseases	5
MESH:C564166	MESH:C564166	Hyperparathyroidism 1	CTD_diseases	5
MESH:C564171	MESH:C564171	Palmoplantar Keratoderma, Epidermolytic, with Knuckle Pads	CTD_diseases	5
MESH:C564172	MESH:C564172	Hyperkeratosis-Hyperpigmentation Syndrome	CTD_diseases	5
MESH:C564173	MESH:C564173	Hyperimmunoglobulin G1(A1) Syndrome	CTD_diseases	5
MESH:C564188	MESH:C564188	Diaphragmatic Hernia 1	CTD_diseases	5
MESH:C564189	MESH:C564189	Diaphragm, Complete Agenesis Of	CTD_diseases	5
MESH:C564190	MESH:C564190	Hepatic Adenomas, Familial	CTD_diseases	5
MESH:C564197	MESH:C564197	Hemolytic Poikilocytic Anemia due to Reduced Ankyrin Binding Sites	CTD_diseases	5
MESH:C564201	MESH:C564201	Hemangiomas of Small Intestine	CTD_diseases	5
MESH:C564202	MESH:C564202	Progressive Familial Heart Block, Type II	CTD_diseases	5
MESH:C564207	MESH:C564207	Prolonged Bleeding Time, Brachydactyly, and Mental Retardation	CTD_diseases	5
MESH:C564211	MESH:C564211	Granddad Syndrome	CTD_diseases	5
MESH:C564217	MESH:C564217	Glutathione Peroxidase Deficiency, Hemolytic Anemia possibly due to	CTD_diseases	5
MESH:C564218	MESH:C564218	Glutathione Reductase, Hemolytic Anemia due to Deficiency of, in Red Cells	CTD_diseases	5
MESH:C564233	MESH:C564233	Glaucoma 1, Open Angle, E	CTD_diseases	5
MESH:C564234	MESH:C564234	Glaucoma 1, Open Angle, A	CTD_diseases	5
MESH:C564235	MESH:C564235	Glaucoma with Elevated Episcleral Venous Pressure	CTD_diseases	5
MESH:C564237	MESH:C564237	Giant Platelet Syndrome with Thrombocytopenia	CTD_diseases	5
MESH:C564239	MESH:C564239	Geographic Tongue and Fissured Tongue	CTD_diseases	5
MESH:C564241	MESH:C564241	Craniosynostosis, Calcification of Basal Ganglia, and Facial Dysmorphism	CTD_diseases	5
MESH:C564248	MESH:C564248	Branchiootic Syndrome 3	CTD_diseases	5
MESH:C564252	MESH:C564252	Spondyloepiphyseal Dysplasia, Kimberley Type	CTD_diseases	5
MESH:C564254	MESH:C564254	Capillary Malformation-Arteriovenous Malformation	CTD_diseases	5
MESH:C564258	MESH:C564258	Coronary Artery Disease, Autosomal Dominant, 1	CTD_diseases	5
MESH:C564261	MESH:C564261	Lelis Syndrome	CTD_diseases	5
MESH:C564262	MESH:C564262	Scimitar Anomaly, Multiple Cardiac Malformations, and Craniofacial and Central Nervous System Abnorm	CTD_diseases	5
MESH:C564276	MESH:C564276	Tropical Calcific Pancreatitis	CTD_diseases	5
MESH:C564282	MESH:C564282	Campomelic Dysplasia with Autosomal Sex Reversal	CTD_diseases	5
MESH:C564286	MESH:C564286	Zinc Deficiency, Neonatal, due to Low Breast Milk Zinc	CTD_diseases	5
MESH:C564288	MESH:C564288	Dystonia 18	CTD_diseases	5
MESH:C564296	MESH:C564296	Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux	CTD_diseases	5
MESH:C564305	MESH:C564305	Diaphanospondylodysostosis	CTD_diseases	5
MESH:C564312	MESH:C564312	Hypotrichosis, Localized, Autosomal Recessive 1	CTD_diseases	5
MESH:C564336	MESH:C564336	Hypercholanemia, Familial	CTD_diseases	5
MESH:C564357	MESH:C564357	Hypotrichosis-Osteolysis-Periodontitis-Palmoplantar Keratoderma Syndrome	CTD_diseases	5
MESH:C564362	MESH:C564362	Neuronopathy, Distal Hereditary Motor, Type Viib	CTD_diseases	5
MESH:C564369	MESH:C564369	Lethal Congenital Contracture Syndrome 2	CTD_diseases	5
MESH:C564370	MESH:C564370	Microphthalmia with Cyst, Bilateral Facial Clefts, and Limb Anomalies	CTD_diseases	5
MESH:C564372	MESH:C564372	Brain Small Vessel Disease with Hemorrhage	CTD_diseases	5
MESH:C564393	MESH:C564393	Vitamin K-Dependent Clotting Factors, Combined Deficiency Of, Type 2	CTD_diseases	5
MESH:C564409	MESH:C564409	Holoprosencephaly with Fetal Akinesia/Hypokinesia Sequence	CTD_diseases	5
MESH:C564411	MESH:C564411	Hhhh Syndrome	CTD_diseases	5
MESH:C564413	MESH:C564413	Hernia, Anterior Diaphragmatic	CTD_diseases	5
MESH:C564415	MESH:C564415	Hemophilia A with Vascular Abnormality	CTD_diseases	5
MESH:C564416	MESH:C564416	Gynecomastia, Familial	CTD_diseases	5
MESH:C564457	MESH:C564457	Microphthalmia, Syndromic 4	CTD_diseases	5
MESH:C564509	MESH:C564509	Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia	CTD_diseases	5
MESH:C564510	MESH:C564510	Cubitus Valgus with Mental Retardation and Unusual Facies	CTD_diseases	5
MESH:C564516	MESH:C564516	Mental Retardation, X-Linked, with Epilepsy	CTD_diseases	5
MESH:C564542	MESH:C564542	Hyper-IgM Immunodeficiency, X-Linked, with Ectodermal Dysplasia, Hypohidrotic	CTD_diseases	5
MESH:C564546	MESH:C564546	Goiter, Multinodular 2	CTD_diseases	5
MESH:C564560	MESH:C564560	Mental Retardation, X-Linked, Syndromic 10	CTD_diseases	5
MESH:C564583	MESH:C564583	Cortical Dysplasia of Taylor without Balloon Cells	CTD_diseases	5
MESH:C564589	MESH:C564589	Smith-McCort Dysplasia	CTD_diseases	5
MESH:C564591	MESH:C564591	Cholesteryl Ester Transfer Protein Deficiency	CTD_diseases	5
MESH:C564595	MESH:C564595	Mammographic Density	CTD_diseases	5
MESH:C564600	MESH:C564600	Hypercalciuria, Absorptive, 1	CTD_diseases	5
MESH:C564621	MESH:C564621	Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies	CTD_diseases	5
MESH:C564626	MESH:C564626	Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3	CTD_diseases	5
MESH:C564628	MESH:C564628	Myasthenia Gravis with Thymus Hyperplasia	CTD_diseases	5
MESH:C564637	MESH:C564637	Senior-Loken Syndrome 3	CTD_diseases	5
MESH:C564638	MESH:C564638	Hyperreninemic Hypoaldosteronism, Familial, 2	CTD_diseases	5
MESH:C564641	MESH:C564641	Pulmonary Disease, Chronic Obstructive, Severe Early-Onset	CTD_diseases	5
MESH:C564648	MESH:C564648	Vascular Malformation, Primary Intraosseous	CTD_diseases	5
MESH:C564652	MESH:C564652	Polymicrogyria, Bilateral Frontoparietal	CTD_diseases	5
MESH:C564656	MESH:C564656	Digital Arthropathy-Brachydactyly, Familial	CTD_diseases	5
MESH:C564674	MESH:C564674	Split-Hand/Foot Malformation 5	CTD_diseases	5
MESH:C564676	MESH:C564676	Dyskinesia, Familial, with Facial Myokymia	CTD_diseases	5
MESH:C564680	MESH:C564680	Inflammatory Bowel Disease 4	CTD_diseases	5
MESH:C564681	MESH:C564681	Inflammatory Bowel Disease 6	CTD_diseases	5
MESH:C564682	MESH:C564682	Inflammatory Bowel Disease 8	CTD_diseases	5
MESH:C564683	MESH:C564683	Glycine N-Methyltransferase Deficiency	CTD_diseases	5
MESH:C564684	MESH:C564684	Waardenburg Syndrome, Type 2C	CTD_diseases	5
MESH:C564690	MESH:C564690	Noncompaction of Left Ventricular Myocardium with Congenital Heart Defects	CTD_diseases	5
MESH:C564730	MESH:C564730	Xylosidase Deficiency	CTD_diseases	5
MESH:C564731	MESH:C564731	Xeroderma Pigmentosum IX	CTD_diseases	5
MESH:C564732	MESH:C564732	Xeroderma Pigmentosum, Complementation Group E	CTD_diseases	5
MESH:C564733	MESH:C564733	Trichothiodystrophy with Sun Sensitivity	CTD_diseases	5
MESH:C564734	MESH:C564734	Trichothiodystrophy, Type 1	CTD_diseases	5
MESH:C564741	MESH:C564741	Vitamin K-Dependent Clotting Factors, Combined Deficiency Of, 1	CTD_diseases	5
MESH:C564742	MESH:C564742	Chondrodysplasia Punctata with Coagulation Factor Deficiency	CTD_diseases	5
MESH:C564743	MESH:C564743	Methylmalonic Aciduria and Homocystinuria, CblD Type	CTD_diseases	5
MESH:C564747	MESH:C564747	Methylmalonic Aciduria and Homocystinuria, CblF Type	CTD_diseases	5
MESH:C564752	MESH:C564752	Vater Association With Hydrocephalus	CTD_diseases	5
MESH:C564756	MESH:C564756	Ulnar Agenesis and Endocardial Fibroelastosis	CTD_diseases	5
MESH:C564771	MESH:C564771	Tetraphocomelia-Thrombocytopenia Syndrome	CTD_diseases	5
MESH:C564773	MESH:C564773	Thoracomelic Dysplasia	CTD_diseases	5
MESH:C564774	MESH:C564774	Thoracic Dysplasia-Hydrocephalus Syndrome	CTD_diseases	5
MESH:C564787	MESH:C564787	Tatsumi Factor Deficiency	CTD_diseases	5
MESH:C564793	MESH:C564793	Subaortic Stenosis, Membranous	CTD_diseases	5
MESH:C564794	MESH:C564794	Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type	CTD_diseases	5
MESH:C564796	MESH:C564796	Spondyloepiphyseal Dysplasia Tarda with Mental Retardation	CTD_diseases	5
MESH:C564797	MESH:C564797	Spondyloepiphyseal Dysplasia Tarda, Autosomal Recessive	CTD_diseases	5
MESH:C564802	MESH:C564802	Spinocerebellar Ataxia with Dysmorphism	CTD_diseases	5
MESH:C564807	MESH:C564807	Spinal Muscular Atrophy with Mental Retardation	CTD_diseases	5
MESH:C564815	MESH:C564815	Spastic Ataxia	CTD_diseases	5
MESH:C564819	MESH:C564819	Skeletal Dysplasia with Telangiectases and Mesodermal Dysgenesis of the Iris	CTD_diseases	5
MESH:C564821	MESH:C564821	Short Stature-Obesity Syndrome	CTD_diseases	5
MESH:C564844	MESH:C564844	Retinal Dystrophy, Reticular Pigmentary, of Posterior Pole	CTD_diseases	5
MESH:C564854	MESH:C564854	Reese Retinal Dysplasia	CTD_diseases	5
MESH:C564864	MESH:C564864	Pseudouridinuria and Mental Defect	CTD_diseases	5
MESH:C564871	MESH:C564871	Progesterone Resistance	CTD_diseases	5
MESH:C564875	MESH:C564875	Bonneau Syndrome	CTD_diseases	5
MESH:C564877	MESH:C564877	Polysaccharide, Storage of Unusual	CTD_diseases	5
MESH:C564880	MESH:C564880	Polydactyly, Postaxial, with Dental and Vertebral Anomalies	CTD_diseases	5
MESH:C564883	MESH:C564883	Pleoconial Myopathy with Salt Craving	CTD_diseases	5
MESH:C564906	MESH:C564906	Pancreatitis, Sclerosing Cholangitis, and Sicca Complex	CTD_diseases	5
MESH:C564910	MESH:C564910	Pallidal Degeneration, Progressive, with Retinitis Pigmentosa	CTD_diseases	5
MESH:C564916	MESH:C564916	Osteomalacia, Sclerosing, with Cerebral Calcification	CTD_diseases	5
MESH:C564922	MESH:C564922	Osteodysplasty, Precocious, Of Danks, Mayne, And Kozlowski	CTD_diseases	5
MESH:C564923	MESH:C564923	Osteodysplasia, Familial, Anderson Type	CTD_diseases	5
MESH:C564943	MESH:C564943	Neutropenia, Lethal Congenital, with Eosinophilia	CTD_diseases	5
MESH:C564968	MESH:C564968	Myosclerosis, Autosomal Recessive	CTD_diseases	5
MESH:C564969	MESH:C564969	Minicore Myopathy with External Ophthalmoplegia	CTD_diseases	5
MESH:C564977	MESH:C564977	Myeloproliferative Disease, Autosomal Recessive	CTD_diseases	5
MESH:C564979	MESH:C564979	Myasthenia, Congenital, Refractory to Acetylcholinesterase Inhibitors	CTD_diseases	5
MESH:C564985	MESH:C564985	Muscular Dystrophy, Congenital, Producing Arthrogryposis	CTD_diseases	5
MESH:C564989	MESH:C564989	Gastric Volvulus, Intrathoracic	CTD_diseases	5
MESH:C564990	MESH:C564990	Gastric Sneezing	CTD_diseases	5
MESH:C564992	MESH:C564992	Fundus Dystrophy, Pseudoinflammatory, Of Sorsby	CTD_diseases	5
MESH:C565009	MESH:C565009	Flood Factor Deficiency	CTD_diseases	5
MESH:C565016	MESH:C565016	Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia	CTD_diseases	5
MESH:C565018	MESH:C565018	Dysfibrinogenemia Causing Recurrent Thrombosis	CTD_diseases	5
MESH:C565020	MESH:C565020	Iron Overload, Autosomal Dominant	CTD_diseases	5
MESH:C565022	MESH:C565022	Familial Multiple Coagulation Factor Deficiency VI	CTD_diseases	5
MESH:C565023	MESH:C565023	Factors VIII, IX And XI, Combined Deficiency of	CTD_diseases	5
MESH:C565024	MESH:C565024	Familial Multiple Coagulation Factor Deficiency II	CTD_diseases	5
MESH:C565025	MESH:C565025	Familial Multiple Coagulation Factor Deficiency IV	CTD_diseases	5
MESH:C565029	MESH:C565029	Facial Hypertrichosis	CTD_diseases	5
MESH:C565034	MESH:C565034	Exostoses with Anetodermia and Brachydactyly, Type E	CTD_diseases	5
MESH:C565036	MESH:C565036	Exchondrosis Of Pinna, Posterior	CTD_diseases	5
MESH:C565049	MESH:C565049	Epidermolysis Bullosa with Deficiency of Galactosylhydroxylysyl Glucosyltransferase	CTD_diseases	5
MESH:C565054	MESH:C565054	Myeloproliferative Disorder, Chronic, with Eosinophilia	CTD_diseases	5
MESH:C565062	MESH:C565062	Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1	CTD_diseases	5
MESH:C565065	MESH:C565065	Ectrodactyly and Ectodermal Dysplasia without Cleft Lip/Palate	CTD_diseases	5
MESH:C565067	MESH:C565067	Ectodermal Dysplasia Syndrome with Distinctive Facial Appearance and Preaxial Polydactyly of Feet	CTD_diseases	5
MESH:C565068	MESH:C565068	Ectodermal Dysplasia, Trichoodontoonychial Type	CTD_diseases	5
MESH:C565070	MESH:C565070	Cleft Lip with or without Cleft Palate, Nonsyndromic, 8	CTD_diseases	5
MESH:C565071	MESH:C565071	Echo Virus 11 Sensitivity	CTD_diseases	5
MESH:C565079	MESH:C565079	Dyskeratosis Congenita, Autosomal Dominant	CTD_diseases	5
MESH:C565081	MESH:C565081	Dwarfism, Levi Type	CTD_diseases	5
MESH:C565092	MESH:C565092	Distichiasis with Congenital Anomalies of the Heart and Peripheral Vasculature	CTD_diseases	5
MESH:C565098	MESH:C565098	Diastema, Dental Medial	CTD_diseases	5
MESH:C565102	MESH:C565102	Keratosis Palmoplantaris Striata II	CTD_diseases	5
MESH:C565111	MESH:C565111	Major Affective Disorder 1	CTD_diseases	5
MESH:C565118	MESH:C565118	Deafness-Craniofacial Syndrome	CTD_diseases	5
MESH:C565119	MESH:C565119	Deafness with Anhidrotic Ectodermal Dysplasia	CTD_diseases	5
MESH:C565120	MESH:C565120	Deafness, Sensorineural, with Peripheral Neuropathy and Arterial Disease	CTD_diseases	5
MESH:C565125	MESH:C565125	Darier Disease, Acral Hemorrhagic Type	CTD_diseases	5
MESH:C565126	MESH:C565126	Darier Disease, Segmental	CTD_diseases	5
MESH:C565144	MESH:C565144	Craniorhiny	CTD_diseases	5
MESH:C565145	MESH:C565145	Craniometaphyseal Dysplasia, Autosomal Dominant	CTD_diseases	5
MESH:C565147	MESH:C565147	Cranioacrofacial Syndrome	CTD_diseases	5
MESH:C565149	MESH:C565149	Spondylocostal Dysostosis 4, Autosomal Dominant	CTD_diseases	5
MESH:C565155	MESH:C565155	Epithelial Recurrent Erosion Dystrophy	CTD_diseases	5
MESH:C565156	MESH:C565156	Corneal Endothelial Dystrophy 1	CTD_diseases	5
MESH:C565157	MESH:C565157	Corneal Degeneration, Ribbonlike, with Deafness	CTD_diseases	5
MESH:C565171	MESH:C565171	Branchiootic Syndrome 2	CTD_diseases	5
MESH:C565173	MESH:C565173	Coloboma, Uveal, with Cleft Lip and Palate and Mental Retardation	CTD_diseases	5
MESH:C565176	MESH:C565176	Corneal Dystrophy, Posterior Polymorphous, 2	CTD_diseases	5
MESH:C565195	MESH:C565195	Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia	CTD_diseases	5
MESH:C565196	MESH:C565196	Macular Degeneration, Age-Related, 4	CTD_diseases	5
MESH:C565199	MESH:C565199	Split-Hand/Foot Malformation With Long Bone Deficiency 2	CTD_diseases	5
MESH:C565220	MESH:C565220	Bleeding Disorder Due To P2RY12 Defect	CTD_diseases	5
MESH:C565234	MESH:C565234	Inflammatory Bowel Disease 5	CTD_diseases	5
MESH:C565247	MESH:C565247	Thyroid Carcinoma, Nonmedullary 1	CTD_diseases	5
MESH:C565252	MESH:C565252	Laryngeal Abductor Paralysis with Cerebellar Ataxia and Motor Neuropathy	CTD_diseases	5
MESH:C565258	MESH:C565258	Fryns-Aftimos Syndrome	CTD_diseases	5
MESH:C565260	MESH:C565260	Goiter, Multinodular 3	CTD_diseases	5
MESH:C565271	MESH:C565271	Metaphyseal Dysplasia, Braun-Tinschert Type	CTD_diseases	5
MESH:C565278	MESH:C565278	Dimethylglycine Dehydrogenase Deficiency	CTD_diseases	5
MESH:C565279	MESH:C565279	Dermatitis, Atopic, 6	CTD_diseases	5
MESH:C565280	MESH:C565280	Dermatitis, Atopic, 5	CTD_diseases	5
MESH:C565289	MESH:C565289	Myasthenia, Familial Infantile, 1	CTD_diseases	5
MESH:C565291	MESH:C565291	Dermatitis, Atopic, 4	CTD_diseases	5
MESH:C565292	MESH:C565292	Dermatitis, Atopic, 3	CTD_diseases	5
MESH:C565293	MESH:C565293	Dermatitis, Atopic, 2	CTD_diseases	5
MESH:C565300	MESH:C565300	Microphthalmia, Isolated, with Coloboma 2	CTD_diseases	5
MESH:C565310	MESH:C565310	Thyroid Carcinoma, Papillary, With Papillary Renal Neoplasia	CTD_diseases	5
MESH:C565311	MESH:C565311	Inclusion Body Myopathy 3, Autosomal Dominant	CTD_diseases	5
MESH:C565312	MESH:C565312	Hyperaldosteronism, Familial, Type II	CTD_diseases	5
MESH:C565313	MESH:C565313	Cerebrooculonasal Syndrome	CTD_diseases	5
MESH:C565327	MESH:C565327	Leber Congenital Amaurosis 6	CTD_diseases	5
MESH:C565328	MESH:C565328	Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia	CTD_diseases	5
MESH:C565336	MESH:C565336	Breast Cancer 3	CTD_diseases	5
MESH:C565342	MESH:C565342	Macrocephaly Autism Syndrome	CTD_diseases	5
MESH:C565344	MESH:C565344	Split-Hand/Foot Malformation 4	CTD_diseases	5
MESH:C565349	MESH:C565349	Mesomelic Dysplasia, Savarirayan Type	CTD_diseases	5
MESH:C565353	MESH:C565353	Inflammatory Bowel Disease 7	CTD_diseases	5
MESH:C565361	MESH:C565361	Muscular Dystrophy, Adult-Onset, with Leukoencephalopathy	CTD_diseases	5
MESH:C565366	MESH:C565366	Mucus Inspissation of Respiratory Tract	CTD_diseases	5
MESH:C565372	MESH:C565372	Molybdenum Cofactor Deficiency, Complementation Group A	CTD_diseases	5
MESH:C565373	MESH:C565373	Molybdenum Cofactor Deficiency, Complementation Group B	CTD_diseases	5
MESH:C565374	MESH:C565374	Molybdenum Cofactor Deficiency, Complementation Group C	CTD_diseases	5
MESH:C565376	MESH:C565376	Mitochondrial Myopathy with a Defect in Mitochondrial Protein Transport	CTD_diseases	5
MESH:C565377	MESH:C565377	Microphthalmia, Isolated 1	CTD_diseases	5
MESH:C565378	MESH:C565378	Microphthalmia, Isolated, with Coloboma 4	CTD_diseases	5
MESH:C565381	MESH:C565381	Microcephaly with Chemotactic Defect and Transient Hypogammaglobulinemia	CTD_diseases	5
MESH:C565382	MESH:C565382	Microcephaly-Micromelia Syndrome	CTD_diseases	5
MESH:C565386	MESH:C565386	Methylmalonyl-CoA Epimerase Deficiency	CTD_diseases	5
MESH:C565387	MESH:C565387	Methylmalonyl-CoA Epimerase Deficiency with Sepiapterin Reductase Deficiency	CTD_diseases	5
MESH:C565390	MESH:C565390	Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency	CTD_diseases	5
MESH:C565395	MESH:C565395	Metaphyseal Dysplasia, Anetoderma, and Optic Atrophy	CTD_diseases	5
MESH:C565396	MESH:C565396	Metaphyseal Dysostosis, Mental Retardation, and Conductive Deafness	CTD_diseases	5
MESH:C565398	MESH:C565398	Metaphyseal Chondrodysplasia with Retinitis Pigmentosa	CTD_diseases	5
MESH:C565399	MESH:C565399	Metaphyseal Chondrodysplasia, Pena Type	CTD_diseases	5
MESH:C565400	MESH:C565400	Metaphyseal Chondrodysplasia, Kaitila Type	CTD_diseases	5
MESH:C565409	MESH:C565409	MAST Syndrome	CTD_diseases	5
MESH:C565410	MESH:C565410	Marfanoid Mental Retardation Syndrome, Autosomal	CTD_diseases	5
MESH:C565436	MESH:C565436	Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome	CTD_diseases	5
MESH:C565437	MESH:C565437	Limb Deficiencies, Distal, with Micrognathia	CTD_diseases	5
MESH:C565438	MESH:C565438	Limb Defects, Distal Transverse, with Mental Retardation and Spasticity	CTD_diseases	5
MESH:C565452	MESH:C565452	Kniest-Like Dysplasia with Pursed Lips and Ectopia Lentis	CTD_diseases	5
MESH:C565454	MESH:C565454	Keratoderma, Palmoplantar, Norrbotten Recessive Type	CTD_diseases	5
MESH:C565466	MESH:C565466	Indolylacroyl Glycinuria with Mental Retardation	CTD_diseases	5
MESH:C565471	MESH:C565471	Ichthyosis, Split Hairs, and Amino Aciduria	CTD_diseases	5
MESH:C565492	MESH:C565492	Hypertrichosis, Congenital Anterior Cervical, with Peripheral Sensory and Motor Neuropathy	CTD_diseases	5
MESH:C565494	MESH:C565494	Hyperphosphatemia, Polyuria, and Seizures	CTD_diseases	5
MESH:C565496	MESH:C565496	Hyperparathyroidism, Neonatal Self-Limited Primary, With Hypercalciuria	CTD_diseases	5
MESH:C565507	MESH:C565507	Hydranencephaly with Renal Aplasia-Dysplasia	CTD_diseases	5
MESH:C565522	MESH:C565522	Hemolytic Anemia with Thermal Sensitivity of Red Cells	CTD_diseases	5
MESH:C565535	MESH:C565535	Granulocytopenia with Immunoglobulin Abnormality	CTD_diseases	5
MESH:C565545	MESH:C565545	Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to	CTD_diseases	5
MESH:C565551	MESH:C565551	Ghosal Hematodiaphyseal Dysplasia	CTD_diseases	5
MESH:C565557	MESH:C565557	Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to	CTD_diseases	5
MESH:C565558	MESH:C565558	Fructose and Galactose Intolerance	CTD_diseases	5
MESH:C565567	MESH:C565567	Fibromatosis, Gingival, with Distinctive Facies	CTD_diseases	5
MESH:C565578	MESH:C565578	Faciocardiomelic Dysplasia, Lethal	CTD_diseases	5
MESH:C565587	MESH:C565587	Epilepsy, Photogenic, with Spastic Diplegia and Mental Retardation	CTD_diseases	5
MESH:C565588	MESH:C565588	Epidermolysis Bullosa With Diaphragmatic Hernia	CTD_diseases	5
MESH:C565592	MESH:C565592	Endocardial Fibroelastosis and Coarctation of Abdominal Aorta	CTD_diseases	5
MESH:C565593	MESH:C565593	Encephaloclastic Proliferative Vasculopathy	CTD_diseases	5
MESH:C565597	MESH:C565597	Encephalomalacia, Multilocular	CTD_diseases	5
MESH:C565601	MESH:C565601	Ectrodactyly-Polydactyly	CTD_diseases	5
MESH:C565605	MESH:C565605	Ectodermal Dysplasia, Hypohidrotic, with Hypothyroidism and Agenesis of the Corpus Callosum	CTD_diseases	5
MESH:C565606	MESH:C565606	Ectodermal Dysplasia and Neurosensory Deafness	CTD_diseases	5
MESH:C565607	MESH:C565607	Schopf-Schulz-Passarge Syndrome	CTD_diseases	5
MESH:C565608	MESH:C565608	Dystonia with Ringbinden	CTD_diseases	5
MESH:C565610	MESH:C565610	Dysmyelination With Jaundice	CTD_diseases	5
MESH:C565611	MESH:C565611	Dyskeratosis Congenita, Autosomal Recessive	CTD_diseases	5
MESH:C565614	MESH:C565614	Dwarfism, Proportionate, with Hip Dislocation	CTD_diseases	5
MESH:C565615	MESH:C565615	Dwarfism, Low-Birth-Weight Type, with Unresponsiveness to Growth Hormone	CTD_diseases	5
MESH:C565624	MESH:C565624	2,4-Dienoyl-CoA Reductase Deficiency	CTD_diseases	5
MESH:C565626	MESH:C565626	Diastrophic Dysplasia, Broad Bone-Platyspondylic Variant	CTD_diseases	5
MESH:C565629	MESH:C565629	Diaphragmatic Hernia 2	CTD_diseases	5
MESH:C565630	MESH:C565630	Diaminopentanuria	CTD_diseases	5
MESH:C565632	MESH:C565632	Diabetes Insipidus, Nephrogenic, with Mental Retardation and Intracerebral Calcification	CTD_diseases	5
MESH:C565639	MESH:C565639	Deafness, Neural, with Atypical Atopic Dermatitis	CTD_diseases	5
MESH:C565659	MESH:C565659	Cysteine Peptiduria	CTD_diseases	5
MESH:C565662	MESH:C565662	Acth-Independent Macronodular Adrenal Hyperplasia	CTD_diseases	5
MESH:C565667	MESH:C565667	Craniosynostosis Microcephaly with Chromosomal Breakage and Other Abnormalities	CTD_diseases	5
MESH:C565674	MESH:C565674	Cortical Blindness, Retardation, and Postaxial Polydactyly	CTD_diseases	5
MESH:C565679	MESH:C565679	Contractures, Congenital, Torticollis, and Malignant Hyperthermia	CTD_diseases	5
MESH:C565686	MESH:C565686	Coloboma of Macula and Skeletal Anomalies	CTD_diseases	5
MESH:C565697	MESH:C565697	Leber Congenital Amaurosis 12	CTD_diseases	5
MESH:C565705	MESH:C565705	Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism	CTD_diseases	5
MESH:C565708	MESH:C565708	Senior-Loken Syndrome 6	CTD_diseases	5
MESH:C565710	MESH:C565710	Diaphragmatic Hernia 3	CTD_diseases	5
MESH:C565718	MESH:C565718	Macular Degeneration, Age-Related, 7	CTD_diseases	5
MESH:C565720	MESH:C565720	Leber Congenital Amaurosis 10	CTD_diseases	5
MESH:C565724	MESH:C565724	Glaucoma 1, Open Angle, I	CTD_diseases	5
MESH:C565731	MESH:C565731	Craniofacial Anomalies, Empty Sella Turcica, Corneal Endothelial Changes, and Abnormal Retinal and A	CTD_diseases	5
MESH:C565736	MESH:C565736	Hydronephrosis, Congenital, with Cleft Palate, Characteristic Facies, Hypotonia, and Mental Retardat	CTD_diseases	5
MESH:C565739	MESH:C565739	Asthma and Nasal Polyps	CTD_diseases	5
MESH:C565740	MESH:C565740	Osteoarthritis with Mild Chondrodysplasia	CTD_diseases	5
MESH:C565744	MESH:C565744	Mandibulofacial Dysostosis Syndrome, Bauru Type	CTD_diseases	5
MESH:C565749	MESH:C565749	Ichthyosis, Nonlamellar and Nonerythrodermic, Congenital, Autosomal Recessive	CTD_diseases	5
MESH:C565757	MESH:C565757	Tooth Agenesis, Selective, 5	CTD_diseases	5
MESH:C565758	MESH:C565758	Aortic Aneurysm, Giant Congenital	CTD_diseases	5
MESH:C565759	MESH:C565759	Bare Lymphocyte Syndrome, Type I	CTD_diseases	5
MESH:C565764	MESH:C565764	Inflammatory Bowel Disease 3	CTD_diseases	5
MESH:C565771	MESH:C565771	Human Herpesvirus Type 6, Integrated	CTD_diseases	5
MESH:C565778	MESH:C565778	Leber Congenital Amaurosis 4	CTD_diseases	5
MESH:C565784	MESH:C565784	Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency	CTD_diseases	5
MESH:C565797	MESH:C565797	Blepharophimosis with Facial and Genital Anomalies and Mental Retardation	CTD_diseases	5
MESH:C565798	MESH:C565798	Rheumatoid Arthritis, Systemic Juvenile	CTD_diseases	5
MESH:C565799	MESH:C565799	Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3	CTD_diseases	5
MESH:C565814	MESH:C565814	Leber Congenital Amaurosis 3	CTD_diseases	5
MESH:C565830	MESH:C565830	Myasthenic Syndrome due to Mutation in SCN4A	CTD_diseases	5
MESH:C565833	MESH:C565833	Autoimmune Lymphoproliferative Syndrome, Type IIA	CTD_diseases	5
MESH:C565836	MESH:C565836	Vanishing White Matter Leukodystrophy with Ovarian Failure	CTD_diseases	5
MESH:C565855	MESH:C565855	Chondrodysplasia Calcificans Metaphysealis	CTD_diseases	5
MESH:C565867	MESH:C565867	Cerebellar Vermis Aplasia with Associated Features suggesting Smith-Lemli-Opitz Syndrome and Meckel 	CTD_diseases	5
MESH:C565898	MESH:C565898	Microcephalic Osteodysplastic Primordial Dwarfism, Type II	CTD_diseases	5
MESH:C565902	MESH:C565902	Biemond Syndrome II	CTD_diseases	5
MESH:C565904	MESH:C565904	Beta-Aminoisobutyric Acid, Urinary Excretion of	CTD_diseases	5
MESH:C565905	MESH:C565905	Berry Aneurysm, Cirrhosis, Pulmonary Emphysema, and Cerebral Calcification	CTD_diseases	5
MESH:C565910	MESH:C565910	Bare Lymphocyte Syndrome, Type II, Complementation Group A	CTD_diseases	5
MESH:C565927	MESH:C565927	Athrombia, Essential	CTD_diseases	5
MESH:C565930	MESH:C565930	Ataxia-Telangiectasia with Generalized Skin Pigmentation and Early Death	CTD_diseases	5
MESH:C565933	MESH:C565933	Ataxia with Myoclonic Epilepsy and Presenile Dementia	CTD_diseases	5
MESH:C565935	MESH:C565935	Asthma, Nasal Polyps, And Aspirin Intolerance	CTD_diseases	5
MESH:C565940	MESH:C565940	Arthrogryposis, Distal, with Mental Retardation and Characteristic Facies	CTD_diseases	5
MESH:C565941	MESH:C565941	Arteriosclerosis, Severe Juvenile	CTD_diseases	5
MESH:C565944	MESH:C565944	Coronary Sclerosis, Medial, of Infancy	CTD_diseases	5
MESH:C565956	MESH:C565956	Amyotrophic Lateral Sclerosis, Juvenile, with Dementia	CTD_diseases	5
MESH:C565960	MESH:C565960	Amino Aciduria with Mental Deficiency, Dwarfism, Muscular Dystrophy, Osteoporosis, and Acidosis	CTD_diseases	5
MESH:C565968	MESH:C565968	Alaninuria with Microcephaly, Dwarfism, Enamel Hypoplasia, and Diabetes Mellitus	CTD_diseases	5
MESH:C565984	MESH:C565984	Short-Limb Skeletal Dysplasia with Severe Combined Immunodeficiency	CTD_diseases	5
MESH:C565988	MESH:C565988	Hyperzincemia and Hypercalprotectinemia	CTD_diseases	5
MESH:C565989	MESH:C565989	Xeroderma Pigmentosum, Autosomal Dominant, Mild	CTD_diseases	5
MESH:C566000	MESH:C566000	Glycoprotein IA Deficiency	CTD_diseases	5
MESH:C566011	MESH:C566011	Urticaria, Familial Localized Heat	CTD_diseases	5
MESH:C566024	MESH:C566024	Transient Myeloproliferative Disorder of Down Syndrome	CTD_diseases	5
MESH:C566029	MESH:C566029	Triosephosphate Isomerase Deficiency	CTD_diseases	5
MESH:C566030	MESH:C566030	Triglyceride Storage Disease, Type II	CTD_diseases	5
MESH:C566031	MESH:C566031	Triglyceride Storage Disease, Type I	CTD_diseases	5
MESH:C566043	MESH:C566043	Torus Palatinus and Torus Mandibularis	CTD_diseases	5
MESH:C566060	MESH:C566060	Thrombasthenia-Thrombocytopenia, Hereditary	CTD_diseases	5
MESH:C566062	MESH:C566062	Thoracopelvic Dysostosis	CTD_diseases	5
MESH:C566063	MESH:C566063	Thoracic Dysostosis, Isolated	CTD_diseases	5
MESH:C566066	MESH:C566066	Tetramelic Monodactyly	CTD_diseases	5
MESH:C566069	MESH:C566069	Arthrogryposis, Distal, Type 10	CTD_diseases	5
MESH:C566076	MESH:C566076	Teeth, Odd Shapes Of	CTD_diseases	5
MESH:C566084	MESH:C566084	Syringomyelia, Isolated	CTD_diseases	5
MESH:C566104	MESH:C566104	Striae Distensae, Familial	CTD_diseases	5
MESH:C566105	MESH:C566105	Stratton-Parker Syndrome	CTD_diseases	5
MESH:C566133	MESH:C566133	Chiari Malformation Type I with Syringomyelia	CTD_diseases	5
MESH:C566137	MESH:C566137	Charcot-Marie-Tooth Disease, Guadalajara Neuronal Type	CTD_diseases	5
MESH:C566142	MESH:C566142	Cervical Hypertrichosis with Underlying Kyphoscoliosis	CTD_diseases	5
MESH:C566168	MESH:C566168	Cardiomyopathy, Familial Restrictive, 1	CTD_diseases	5
MESH:C566172	MESH:C566172	Familial Sudden Death	CTD_diseases	5
MESH:C566175	MESH:C566175	Carabelli Anomaly of Maxillary Molar Teeth	CTD_diseases	5
MESH:C566180	MESH:C566180	Callosities, Hereditary Painful	CTD_diseases	5
MESH:C566185	MESH:C566185	Heart Block, Nonprogressive	CTD_diseases	5
MESH:C566222	MESH:C566222	Bpes With Duane Retraction Syndrome	CTD_diseases	5
MESH:C566237	MESH:C566237	Atrial Tachyarrhythmia with Short PR Interval	CTD_diseases	5
MESH:C566238	MESH:C566238	Atrial Septal Defect with Atrioventricular Conduction Defects	CTD_diseases	5
MESH:C566244	MESH:C566244	Atrial Fibrillation, Familial, 4	CTD_diseases	5
MESH:C566253	MESH:C566253	Arteritis, Familial Granulomatous, with Juvenile Polyarthritis	CTD_diseases	5
MESH:C566256	MESH:C566256	Arrhenoblastoma--Thyroid Adenoma	CTD_diseases	5
MESH:C566258	MESH:C566258	Arms, Malformation of	CTD_diseases	5
MESH:C566260	MESH:C566260	Apolipoprotein E, Deficiency or Defect of	CTD_diseases	5
MESH:C566261	MESH:C566261	Dysbetalipoproteinemia due to Defect in Apolipoprotein E-d	CTD_diseases	5
MESH:C566263	MESH:C566263	Hyperlipemia with Familial Hypercholesterolemic Xanthomatosis	CTD_diseases	5
MESH:C566264	MESH:C566264	Broad-Betalipoproteinemia	CTD_diseases	5
MESH:C566265	MESH:C566265	Floating-Betalipoproteinemia	CTD_diseases	5
MESH:C566271	MESH:C566271	Aortic Arch Interruption, Facial Palsy, and Retinal Coloboma	CTD_diseases	5
MESH:C566281	MESH:C566281	Aniridia and Absent Patella	CTD_diseases	5
MESH:C566282	MESH:C566282	Spinal Arterial Venous Malformations with Cutaneous Hemangiomas	CTD_diseases	5
MESH:C566283	MESH:C566283	Hemangiomatosis, Disseminated	CTD_diseases	5
MESH:C566305	MESH:C566305	Dysalbuminemic Hyperthyroxinemia	CTD_diseases	5
MESH:C566308	MESH:C566308	Hypoglossia-Hypodactylia	CTD_diseases	5
MESH:C566314	MESH:C566314	Adenosine Deaminase, Elevated, Hemolytic Anemia Due To	CTD_diseases	5
MESH:C566319	MESH:C566319	Acropectorovertebral Dysplasia, F-Form	CTD_diseases	5
MESH:C566340	MESH:C566340	Bile Acid Synthesis Defect, Congenital, 3	CTD_diseases	5
MESH:C566356	MESH:C566356	Osteoma of Cranial Vault, Familial	CTD_diseases	5
MESH:C566357	MESH:C566357	Craniosynostosis with Ectopia Lentis	CTD_diseases	5
MESH:C566358	MESH:C566358	Xanthinuria, Type II	CTD_diseases	5
MESH:C566361	MESH:C566361	Microcephaly, Facial Abnormalities, Micromelia, and Mental Retardation	CTD_diseases	5
MESH:C566369	MESH:C566369	Dehydrated Hereditary Stomatocytosis, Pseudohyperkalemia, and Perinatal Edema	CTD_diseases	5
MESH:C566373	MESH:C566373	Hypospadias, Hypertelorism, Upper Lid Coloboma, and Mixed-Type Hearing Loss	CTD_diseases	5
MESH:C566374	MESH:C566374	Oroacral Syndrome, Verloes-Koulischer Type	CTD_diseases	5
MESH:C566377	MESH:C566377	Microcephaly, Severe, with Skeletal Anomalies including Posterior Rib-Gap Defects	CTD_diseases	5
MESH:C566380	MESH:C566380	Osebold Skeletal Dysplasia Osteolysis Syndrome	CTD_diseases	5
MESH:C566381	MESH:C566381	Megalanecephaly Polymicrogyria-Polydactyly Hydrocephalus Syndrome	CTD_diseases	5
MESH:C566383	MESH:C566383	Glaucoma 1, Open Angle, F	CTD_diseases	5
MESH:C566386	MESH:C566386	Thyroid Adenoma, Hyperfunctioning	CTD_diseases	5
MESH:C566391	MESH:C566391	Erythrokeratodermia Variabilis, Autosomal Recessive	CTD_diseases	5
MESH:C566402	MESH:C566402	Methylmalonate Semialdehyde Dehydrogenase Deficiency	CTD_diseases	5
MESH:C566404	MESH:C566404	Dermatitis, Atopic, 1	CTD_diseases	5
MESH:C566411	MESH:C566411	Macular Degeneration, Age-Related, 1	CTD_diseases	5
MESH:C566415	MESH:C566415	Endplate Acetylcholinesterase Deficiency	CTD_diseases	5
MESH:C566432	MESH:C566432	Diabetes Mellitus, Transient Neonatal, 3	CTD_diseases	5
MESH:C566434	MESH:C566434	Myasthenia, Limb-Girdle, with Tubular Aggregates	CTD_diseases	5
MESH:C566436	MESH:C566436	Glaucoma 1, Open Angle, M	CTD_diseases	5
MESH:C566441	MESH:C566441	Microphthalmia, Syndromic 5	CTD_diseases	5
MESH:C566446	MESH:C566446	Microphthalmia, Isolated 2	CTD_diseases	5
MESH:C566447	MESH:C566447	Microphthalmia, Isolated, with Coloboma 3	CTD_diseases	5
MESH:C566449	MESH:C566449	Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency	CTD_diseases	5
MESH:C566450	MESH:C566450	Hyperparathyroidism 3	CTD_diseases	5
MESH:C566452	MESH:C566452	Corneal Dystrophy, Congenital Stromal	CTD_diseases	5
MESH:C566457	MESH:C566457	Short Stature And Facioauriculothoracic Malformations	CTD_diseases	5
MESH:C566466	MESH:C566466	Maturity-Onset Diabetes of the Young, Type 7	CTD_diseases	5
MESH:C566467	MESH:C566467	Combined Oxidative Phosphorylation Deficiency 3	CTD_diseases	5
MESH:C566468	MESH:C566468	Combined Oxidative Phosphorylation Deficiency 2	CTD_diseases	5
MESH:C566473	MESH:C566473	Tumoral Calcinosis, Normophosphatemic, Familial	CTD_diseases	5
MESH:C566482	MESH:C566482	Cortical Dysplasia-Focal Epilepsy Syndrome	CTD_diseases	5
MESH:C566484	MESH:C566484	Brachydactyly, Coloboma, And Anterior Segment Dysgenesis	CTD_diseases	5
MESH:C566487	MESH:C566487	2-Methylbutyryl-CoA Dehydrogenase Deficiency	CTD_diseases	5
MESH:C566493	MESH:C566493	Hyperinsulinemic Hypoglycemia, Familial, 4	CTD_diseases	5
MESH:C566494	MESH:C566494	Hyperinsulinemic Hypoglycemia, Familial, 5	CTD_diseases	5
MESH:C566501	MESH:C566501	Major Affective Disorder 3	CTD_diseases	5
MESH:C566507	MESH:C566507	Spondylomegaepiphyseal Dysplasia With Upper Limb Mesomelia, Punctate Calcifications, And Deafness	CTD_diseases	5
MESH:C566509	MESH:C566509	External Ophthalmoplegia, Synergistic Divergence, Jaw Winking, and Oculocutaneous Hypopigmentation	CTD_diseases	5
MESH:C566512	MESH:C566512	Cardiomyopathy, Familial Restrictive, 2	CTD_diseases	5
MESH:C566513	MESH:C566513	Tooth Agenesis, Selective, 2	CTD_diseases	5
MESH:C566516	MESH:C566516	Pancreatic Lymphoma, Familial	CTD_diseases	5
MESH:C566520	MESH:C566520	Mandibulofacial Dysostosis with Macroblepharon and Macrostomia	CTD_diseases	5
MESH:C566523	MESH:C566523	Spondyloepimetaphyseal Dysplasia, Shohat Type	CTD_diseases	5
MESH:C566524	MESH:C566524	Facial Dysmorphism, Cleft Palate, Hearing Loss, and Camptodactyly	CTD_diseases	5
MESH:C566526	MESH:C566526	Anal Atresia, Hypospadias, and Penoscrotal Inversion	CTD_diseases	5
MESH:C566528	MESH:C566528	HID Syndrome	CTD_diseases	5
MESH:C566551	MESH:C566551	Glaucoma 1, Open Angle, D	CTD_diseases	5
MESH:C566553	MESH:C566553	Ectodermal Dysplasia, Hidrotic, Autosomal Recessive	CTD_diseases	5
MESH:C566554	MESH:C566554	Ichthyosis, Follicular Atrophoderma, Hypotrichosis, and Hypohidrosis	CTD_diseases	5
MESH:C566563	MESH:C566563	Progeroid Facial Appearance with Hand Anomalies	CTD_diseases	5
MESH:C566574	MESH:C566574	Spondyloepimetaphyseal Dysplasia, Missouri Type	CTD_diseases	5
MESH:C566591	MESH:C566591	Erythrokeratodermia, Progressive Symmetric	CTD_diseases	5
MESH:C566592	MESH:C566592	Ectodermal Dysplasia, Pure Hair-Nail Type	CTD_diseases	5
MESH:C566593	MESH:C566593	Hypomagnesemia 1, Intestinal	CTD_diseases	5
MESH:C566595	MESH:C566595	Hyperzincemia with Functional Zinc Depletion	CTD_diseases	5
MESH:C566597	MESH:C566597	Otofacioosseous-Gonadal Syndrome	CTD_diseases	5
MESH:C566598	MESH:C566598	Odontotrichoungual-Digital-Palmar Syndrome	CTD_diseases	5
MESH:C566604	MESH:C566604	Deafness, Congenital Heart Defects, and Posterior Embryotoxon	CTD_diseases	5
MESH:C566613	MESH:C566613	Autoimmune Lymphoproliferative Syndrome, Type IA	CTD_diseases	5
MESH:C566614	MESH:C566614	Autoimmune Lymphoproliferative Syndrome, Type IB	CTD_diseases	5
MESH:C566615	MESH:C566615	Autoimmune Lymphoproliferative Syndrome, Type I, Autosomal Recessive	CTD_diseases	5
MESH:C566618	MESH:C566618	Phosphoglycerate Dehydrogenase Deficiency	CTD_diseases	5
MESH:C566621	MESH:C566621	Premature Aging Syndrome, Okamoto Type	CTD_diseases	5
MESH:C566622	MESH:C566622	Spondylospinal Thoracic Dysostosis	CTD_diseases	5
MESH:C566623	MESH:C566623	Coloboma-Obesity-Hypogenitalism-Mental Retardation Syndrome	CTD_diseases	5
MESH:C566636	MESH:C566636	Pten Hamartoma Tumor Syndrome With Granular Cell Tumor	CTD_diseases	5
MESH:C566641	MESH:C566641	Glaucoma 1, Open Angle, C	CTD_diseases	5
MESH:C566643	MESH:C566643	Ichthyosis, Congenital, with Trichothiodystrophy	CTD_diseases	5
MESH:C566644	MESH:C566644	Spondyloepimetaphyseal Dysplasia With Abnormal Dentition	CTD_diseases	5
MESH:C566652	MESH:C566652	Spastic Paraplegia And Evans Syndrome	CTD_diseases	5
MESH:C566654	MESH:C566654	Leukoencephalopathy with Dystonia and Motor Neuropathy, SCPx-Deficient	CTD_diseases	5
MESH:C566655	MESH:C566655	Steinfeld Syndrome	CTD_diseases	5
MESH:C566658	MESH:C566658	Spondyloepiphyseal Dysplasia Tarda, Autosomal Dominant	CTD_diseases	5
MESH:C566660	MESH:C566660	Spondyloepiphyseal Dysplasia With Punctate Corneal Dystrophy	CTD_diseases	5
MESH:C566665	MESH:C566665	Split-Hand And Split-Foot With Hypodontia	CTD_diseases	5
MESH:C566666	MESH:C566666	Splenomegaly Syndrome With Splenic Germinal Center Hypoplasia And Reduced Circulating T-Helper Cells	CTD_diseases	5
MESH:C566670	MESH:C566670	Spinal Muscular Atrophy, Segmental	CTD_diseases	5
MESH:C566672	MESH:C566672	Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant	CTD_diseases	5
MESH:C566673	MESH:C566673	Spinal Muscular Atrophy, Late-Onset, Finkel Type	CTD_diseases	5
MESH:C566674	MESH:C566674	Spinal Muscular Atrophy, Facioscapulohumeral Type	CTD_diseases	5
MESH:C566675	MESH:C566675	Neuronopathy, Distal Hereditary Motor, Type I	CTD_diseases	5
MESH:C566677	MESH:C566677	Speech Development, Delayed, With Facial Asymmetry, Strabismus, And Transverse Earlobe Crease	CTD_diseases	5
MESH:C566679	MESH:C566679	Spastic Paraplegia, Optic Atrophy, And Dementia	CTD_diseases	5
MESH:C566681	MESH:C566681	Spastic Paraplegia With Associated Extrapyramidal Signs	CTD_diseases	5
MESH:C566682	MESH:C566682	Spastic Paraplegia, Sensorineural Deafness, Mental Retardation, And Progressive Nephropathy	CTD_diseases	5
MESH:C566700	MESH:C566700	Hypermethioninemia with Deficiency of S-Adenosylhomocysteine Hydrolase	CTD_diseases	5
MESH:C566702	MESH:C566702	Parotid Aplasia or Hypoplasia	CTD_diseases	5
MESH:C566713	MESH:C566713	Retinopathy, Pericentral Pigmentary, Dominant	CTD_diseases	5
MESH:C566721	MESH:C566721	Reticular Dystrophy Of Retinal Pigment Epithelium	CTD_diseases	5
MESH:C566724	MESH:C566724	Raindrop Hypopigmentation	CTD_diseases	5
MESH:C566733	MESH:C566733	Ciuffo Syndrome	CTD_diseases	5
MESH:C566735	MESH:C566735	Pubic Bone Dysplasia	CTD_diseases	5
MESH:C566739	MESH:C566739	Multiple Pterygium Syndrome, Autosomal Dominant	CTD_diseases	5
MESH:C566754	MESH:C566754	Pruritus, Hereditary Localized	CTD_diseases	5
MESH:C566762	MESH:C566762	Sacral Agenesis Syndrome	CTD_diseases	5
MESH:C566767	MESH:C566767	Postaxial Oligodactyly, Tetramelic	CTD_diseases	5
MESH:C566774	MESH:C566774	Polyps, Multiple And Recurrent Inflammatory Fibroid, Gastrointestinal	CTD_diseases	5
MESH:C566794	MESH:C566794	Platelet Alpha/Delta Storage Pool Deficiency	CTD_diseases	5
MESH:C566807	MESH:C566807	Pheochromocytoma Islet Cell Tumor Syndrome	CTD_diseases	5
MESH:C566812	MESH:C566812	Pelvic Lipomatosis with Crossed Renal Ectopia	CTD_diseases	5
MESH:C566814	MESH:C566814	Pechet Factor Deficiency	CTD_diseases	5
MESH:C566820	MESH:C566820	Passovoy Factor	CTD_diseases	5
MESH:C566822	MESH:C566822	Perry Syndrome	CTD_diseases	5
MESH:C566837	MESH:C566837	Pancreatitis, Calcific	CTD_diseases	5
MESH:C566870	MESH:C566870	Tumoral Calcinosis, Hyperphosphatemic, Familial	CTD_diseases	5
MESH:C566873	MESH:C566873	Hereditary bundle branch system defect	CTD_diseases	5
MESH:C566879	MESH:C566879	Xeroderma Pigmentosum, Type G/Cockayne Syndrome	CTD_diseases	5
MESH:C566881	MESH:C566881	Respiratory Distress Syndrome In Premature Infants	CTD_diseases	5
MESH:C566888	MESH:C566888	Humeroradial Synostosis with Craniofacial Anomalies	CTD_diseases	5
MESH:C566899	MESH:C566899	Microphthalmia, Isolated, with Coloboma 5	CTD_diseases	5
MESH:C566910	MESH:C566910	Renal Tubular Acidosis, Distal, With Hemolytic Anemia	CTD_diseases	5
MESH:C566932	MESH:C566932	Atrial Fibrillation, Familial, 5	CTD_diseases	5
MESH:C566935	MESH:C566935	Macular Degeneration, Age-Related, 10	CTD_diseases	5
MESH:C566946	MESH:C566946	Periodontitis, Aggressive, 2	CTD_diseases	5
MESH:C566948	MESH:C566948	Kallmann Syndrome 2 with Selective Tooth Agenesis	CTD_diseases	5
MESH:C566949	MESH:C566949	Tremor, Hereditary Essential, 3	CTD_diseases	5
MESH:C566950	MESH:C566950	Hypotrichosis, Localized, Autosomal Recessive, 3	CTD_diseases	5
MESH:C566956	MESH:C566956	Ataxia, Spastic, 3, Autosomal Recessive	CTD_diseases	5
MESH:C566958	MESH:C566958	Macular Degeneration, Age-Related, 9	CTD_diseases	5
MESH:C566961	MESH:C566961	Lethal Congenital Contractural Syndrome 3	CTD_diseases	5
MESH:C566973	MESH:C566973	Dystonia, Focal, Task-Specific	CTD_diseases	5
MESH:C566976	MESH:C566976	Glaucoma 1, Open Angle, H	CTD_diseases	5
MESH:C566977	MESH:C566977	Glaucoma 1, Open Angle, N	CTD_diseases	5
MESH:C566978	MESH:C566978	COPD, Severe Early-Onset	CTD_diseases	5
MESH:C567021	MESH:C567021	Inflammatory Bowel Disease 10	CTD_diseases	5
MESH:C567024	MESH:C567024	Microphthalmia, Posterior, With Retinitis Pigmentosa, Foveoschisis, And Optic Disc Drusen	CTD_diseases	5
MESH:C567025	MESH:C567025	Microphthalmia, Isolated 3	CTD_diseases	5
MESH:C567026	MESH:C567026	Episodic Kinesigenic Dyskinesia 2	CTD_diseases	5
MESH:C567034	MESH:C567034	Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress	CTD_diseases	5
MESH:C567036	MESH:C567036	Tooth Agenesis, Selective, 3	CTD_diseases	5
MESH:C567037	MESH:C567037	Progressive Familial Heart Block, Type Ib	CTD_diseases	5
MESH:C567039	MESH:C567039	Facial Dysmorphism, Selective Tooth Agenesis, and Choroid Calcification	CTD_diseases	5
MESH:C567043	MESH:C567043	XFE Progeroid Syndrome	CTD_diseases	5
MESH:C567045	MESH:C567045	Coronary Artery Disease, Autosomal Dominant 2	CTD_diseases	5
MESH:C567055	MESH:C567055	Sakoda Complex	CTD_diseases	5
MESH:C567059	MESH:C567059	Multiple Endocrine Neoplasia, Type IV	CTD_diseases	5
MESH:C567061	MESH:C567061	Xeroderma Pigmentosum B/Cockayne Syndrome	CTD_diseases	5
MESH:C567064	MESH:C567064	Phosphoribosylpyrophosphate Synthetase Superactivity	CTD_diseases	5
MESH:C567073	MESH:C567073	Major Affective Disorder 4	CTD_diseases	5
MESH:C567074	MESH:C567074	Major Affective Disorder 5	CTD_diseases	5
MESH:C567075	MESH:C567075	Major Affective Disorder 6	CTD_diseases	5
MESH:C567077	MESH:C567077	Acquired Protein S Deficiency	CTD_diseases	5
MESH:C567084	MESH:C567084	Neuronopathy, Distal Hereditary Motor, Type IIB	CTD_diseases	5
MESH:C567085	MESH:C567085	Aortic Aneurysm, Familial Thoracic 6	CTD_diseases	5
MESH:C567087	MESH:C567087	Brugada Syndrome 2	CTD_diseases	5
MESH:C567088	MESH:C567088	Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps	CTD_diseases	5
MESH:C567089	MESH:C567089	Lipoprotein Glomerulopathy	CTD_diseases	5
MESH:C567115	MESH:C567115	Combined Cellular And Humoral Immune Defects With Granulomas	CTD_diseases	5
MESH:C567124	MESH:C567124	Ectopia Lentis, Isolated, Autosomal Recessive	CTD_diseases	5
MESH:C567128	MESH:C567128	Spondyloepiphyseal Dysplasia-Brachydactyly and Distinctive Speech	CTD_diseases	5
MESH:C567131	MESH:C567131	Dystonia with Cerebellar Atrophy	CTD_diseases	5
MESH:C567132	MESH:C567132	Dibasic Amino Aciduria I	CTD_diseases	5
MESH:C567154	MESH:C567154	Inflammatory Bowel Disease 11	CTD_diseases	5
MESH:C567165	MESH:C567165	Palmoplantar Hyperkeratosis And True Hermaphroditism	CTD_diseases	5
MESH:C567171	MESH:C567171	Osteolysis, Hereditary, Of Carpal Bones With Or Without Nephropathy	CTD_diseases	5
MESH:C567176	MESH:C567176	Faciocardiomelic Syndrome	CTD_diseases	5
MESH:C567182	MESH:C567182	Chromosome 10q26 Deletion Syndrome	CTD_diseases	5
MESH:C567189	MESH:C567189	Li-Fraumeni-Like Syndrome	CTD_diseases	5
MESH:C567190	MESH:C567190	Keratosis, Familial Actinic	CTD_diseases	5
MESH:C567191	MESH:C567191	Hypospadias 3, Autosomal	CTD_diseases	5
MESH:C567197	MESH:C567197	Leber Congenital Amaurosis 13	CTD_diseases	5
MESH:C567201	MESH:C567201	Polymicrogyria, Bilateral Occipital	CTD_diseases	5
MESH:C567217	MESH:C567217	Inflammatory Bowel Disease 26	CTD_diseases	5
MESH:C567228	MESH:C567228	Adenylate Kinase Deficiency, Hemolytic Anemia Due To	CTD_diseases	5
MESH:C567245	MESH:C567245	Split-Hand/Foot Malformation With Long Bone Deficiency 3	CTD_diseases	5
MESH:C567251	MESH:C567251	Inflammatory Bowel Disease 25, Autosomal Recessive	CTD_diseases	5
MESH:C567252	MESH:C567252	Inflammatory Bowel Disease 24	CTD_diseases	5
MESH:C567261	MESH:C567261	Myopathy, Congenital, Compton-North	CTD_diseases	5
MESH:D012891	MESH:D012891	Sleep Apnea Syndromes	CTD_diseases	5
MESH:D012892	MESH:D012892	Sleep Deprivation	CTD_diseases	5
MESH:D012913	MESH:D012913	Snoring	CTD_diseases	5
MESH:D013031	MESH:D013031	Sparganosis	CTD_diseases	5
MESH:D013035	MESH:D013035	Spasm	CTD_diseases	5
MESH:D013169	MESH:D013169	Spondylolysis	CTD_diseases	5
MESH:D013174	MESH:D013174	Sporotrichosis	CTD_diseases	5
MESH:D013182	MESH:D013182	Sprue, Tropical	CTD_diseases	5
MESH:D013207	MESH:D013207	Staphylococcal Skin Infections	CTD_diseases	5
MESH:D013226	MESH:D013226	Status Epilepticus	CTD_diseases	5
MESH:D013330	MESH:D013330	Struma Ovarii	CTD_diseases	5
MESH:D013365	MESH:D013365	Submandibular Gland Neoplasms	CTD_diseases	5
MESH:D013369	MESH:D013369	Subphrenic Abscess	CTD_diseases	5
MESH:D013398	MESH:D013398	Sudden Infant Death	CTD_diseases	5
MESH:D013576	MESH:D013576	Syndactyly	CTD_diseases	5
MESH:D013584	MESH:D013584	Sarcoma, Synovial	CTD_diseases	5
MESH:D013587	MESH:D013587	Syphilis	CTD_diseases	5
MESH:D013591	MESH:D013591	Syphilis, Cutaneous	CTD_diseases	5
MESH:D013614	MESH:D013614	Tachycardia, Paroxysmal	CTD_diseases	5
MESH:D013617	MESH:D013617	Tachycardia, Supraventricular	CTD_diseases	5
MESH:D013631	MESH:D013631	Tangier Disease	CTD_diseases	5
MESH:D013641	MESH:D013641	Tarsal Tunnel Syndrome	CTD_diseases	5
MESH:D013651	MESH:D013651	Taste Disorders	CTD_diseases	5
MESH:D013706	MESH:D013706	Temporomandibular Joint Dysfunction Syndrome	CTD_diseases	5
MESH:D013717	MESH:D013717	Tenosynovitis	CTD_diseases	5
MESH:D013742	MESH:D013742	Tetanus	CTD_diseases	5
MESH:D013746	MESH:D013746	Tetany	CTD_diseases	5
MESH:D013771	MESH:D013771	Tetralogy of Fallot	CTD_diseases	5
MESH:D013798	MESH:D013798	Thecoma	CTD_diseases	5
MESH:D013924	MESH:D013924	Thrombophlebitis	CTD_diseases	5
MESH:D013958	MESH:D013958	Thyroid Crisis	CTD_diseases	5
MESH:D013986	MESH:D013986	Tick Toxicoses	CTD_diseases	5
MESH:D014005	MESH:D014005	Tinea	CTD_diseases	5
MESH:D014008	MESH:D014008	Tinea Pedis	CTD_diseases	5
MESH:D014010	MESH:D014010	Tinea Versicolor	CTD_diseases	5
MESH:D014069	MESH:D014069	Tonsillitis	CTD_diseases	5
MESH:D014096	MESH:D014096	Tooth, Supernumerary	CTD_diseases	5
MESH:D014103	MESH:D014103	Torticollis	CTD_diseases	5
MESH:D014126	MESH:D014126	Toxoplasmosis, Ocular	CTD_diseases	5
MESH:D014188	MESH:D014188	Transposition of Great Vessels	CTD_diseases	5
MESH:D014190	MESH:D014190	Transvestism	CTD_diseases	5
MESH:D014202	MESH:D014202	Tremor	CTD_diseases	5
MESH:D014263	MESH:D014263	Tricuspid Valve Prolapse	CTD_diseases	5
MESH:D014286	MESH:D014286	Trilogy of Fallot	CTD_diseases	5
MESH:D014314	MESH:D014314	Trisomy	CTD_diseases	5
MESH:D014353	MESH:D014353	Trypanosomiasis, African	CTD_diseases	5
MESH:D014355	MESH:D014355	Chagas Disease	CTD_diseases	5
MESH:D014382	MESH:D014382	Tuberculosis, Cutaneous	CTD_diseases	5
MESH:D014392	MESH:D014392	Tuberculosis, Ocular	CTD_diseases	5
MESH:D014395	MESH:D014395	Peritonitis, Tuberculous	CTD_diseases	5
MESH:D014398	MESH:D014398	Tuberculosis, Renal	CTD_diseases	5
MESH:D014399	MESH:D014399	Tuberculosis, Spinal	CTD_diseases	5
MESH:D014424	MESH:D014424	Turner Syndrome	CTD_diseases	5
MESH:D014511	MESH:D014511	Uremia	CTD_diseases	5
MESH:D014516	MESH:D014516	Ureteral Neoplasms	CTD_diseases	5
MESH:D014517	MESH:D014517	Ureteral Obstruction	CTD_diseases	5
MESH:D014518	MESH:D014518	Ureterocele	CTD_diseases	5
MESH:D014523	MESH:D014523	Urethral Neoplasms	CTD_diseases	5
MESH:D014524	MESH:D014524	Urethral Obstruction	CTD_diseases	5
MESH:D014526	MESH:D014526	Urethritis	CTD_diseases	5
MESH:D014549	MESH:D014549	Urinary Incontinence	CTD_diseases	5
MESH:D014593	MESH:D014593	Uterine Inertia	CTD_diseases	5
MESH:D014594	MESH:D014594	Uterine Neoplasms	CTD_diseases	5
MESH:D014596	MESH:D014596	Uterine Prolapse	CTD_diseases	5
MESH:D014606	MESH:D014606	Uveitis, Anterior	CTD_diseases	5
MESH:D014608	MESH:D014608	Uveoparotid Fever	CTD_diseases	5
MESH:D014625	MESH:D014625	Vaginal Neoplasms	CTD_diseases	5
MESH:D014627	MESH:D014627	Vaginitis	CTD_diseases	5
MESH:D014653	MESH:D014653	Vascular Headaches	CTD_diseases	5
MESH:D014715	MESH:D014715	Vertebrobasilar Insufficiency	CTD_diseases	5
MESH:D014718	MESH:D014718	Vesico-Ureteral Reflux	CTD_diseases	5
MESH:D014820	MESH:D014820	Vitiligo	CTD_diseases	5
MESH:D014823	MESH:D014823	Vitreous Hemorrhage	CTD_diseases	5
MESH:D014840	MESH:D014840	Vomiting, Anticipatory	CTD_diseases	5
MESH:D014843	MESH:D014843	Voyeurism	CTD_diseases	5
MESH:D014846	MESH:D014846	Vulvar Neoplasms	CTD_diseases	5
MESH:D014847	MESH:D014847	Vulvitis	CTD_diseases	5
MESH:D014895	MESH:D014895	Weil Disease	CTD_diseases	5
MESH:D014901	MESH:D014901	West Nile Fever	CTD_diseases	5
MESH:D014927	MESH:D014927	Wolff-Parkinson-White Syndrome	CTD_diseases	5
MESH:D014997	MESH:D014997	XYY Karyotype	CTD_diseases	5
MESH:D015001	MESH:D015001	Yaws	CTD_diseases	5
MESH:D015009	MESH:D015009	Yersinia Infections	CTD_diseases	5
MESH:D015051	MESH:D015051	Zygomatic Fractures	CTD_diseases	5
MESH:D015140	MESH:D015140	Dementia, Vascular	CTD_diseases	5
MESH:D015154	MESH:D015154	Esophageal Motility Disorders	CTD_diseases	5
MESH:D015175	MESH:D015175	Prolactinoma	CTD_diseases	5
MESH:D015179	MESH:D015179	Colorectal Neoplasms	CTD_diseases	5
MESH:D015207	MESH:D015207	Osteoarthritis, Hip	CTD_diseases	5
MESH:D015209	MESH:D015209	Cholangitis, Sclerosing	CTD_diseases	5
MESH:D015217	MESH:D015217	Cholesterol Ester Storage Disease	CTD_diseases	5
MESH:D015229	MESH:D015229	Sexually Transmitted Diseases, Viral	CTD_diseases	5
MESH:D015267	MESH:D015267	Churg-Strauss Syndrome	CTD_diseases	5
MESH:D015299	MESH:D015299	Discitis	CTD_diseases	5
MESH:D015318	MESH:D015318	Fructose Metabolism, Inborn Errors	CTD_diseases	5
MESH:D015323	MESH:D015323	Pyruvate Metabolism, Inborn Errors	CTD_diseases	5
MESH:D015430	MESH:D015430	Weight Gain	CTD_diseases	5
MESH:D015431	MESH:D015431	Weight Loss	CTD_diseases	5
MESH:D015448	MESH:D015448	Leukemia, B-Cell	CTD_diseases	5
MESH:D015456	MESH:D015456	Leukemia, Biphenotypic, Acute	CTD_diseases	5
MESH:D015458	MESH:D015458	Leukemia, T-Cell	CTD_diseases	5
MESH:D015463	MESH:D015463	Leukemia, Prolymphocytic	CTD_diseases	5
MESH:D015464	MESH:D015464	Leukemia, Myelogenous, Chronic, BCR-ABL Positive	CTD_diseases	5
MESH:D015467	MESH:D015467	Leukemia, Neutrophilic, Chronic	CTD_diseases	5
MESH:D015470	MESH:D015470	Leukemia, Myeloid, Acute	CTD_diseases	5
MESH:D015477	MESH:D015477	Leukemia, Myelomonocytic, Chronic	CTD_diseases	5
MESH:D015479	MESH:D015479	Leukemia, Myelomonocytic, Acute	CTD_diseases	5
MESH:D015490	MESH:D015490	HTLV-I Infections	CTD_diseases	5
MESH:D015491	MESH:D015491	HTLV-II Infections	CTD_diseases	5
MESH:D015494	MESH:D015494	Salivary Gland Calculi	CTD_diseases	5
MESH:D015521	MESH:D015521	Ethmoid Sinusitis	CTD_diseases	5
MESH:D015522	MESH:D015522	Frontal Sinusitis	CTD_diseases	5
MESH:D015523	MESH:D015523	Maxillary Sinusitis	CTD_diseases	5
MESH:D015524	MESH:D015524	Sphenoid Sinusitis	CTD_diseases	5
MESH:D015526	MESH:D015526	AIDS Dementia Complex	CTD_diseases	5
MESH:D015618	MESH:D015618	Histiocytosis, Sinus	CTD_diseases	5
MESH:D015663	MESH:D015663	Osteoporosis, Postmenopausal	CTD_diseases	5
MESH:D015701	MESH:D015701	Near Drowning	CTD_diseases	5
MESH:D015745	MESH:D015745	Granuloma, Foreign-Body	CTD_diseases	5
MESH:D015776	MESH:D015776	Keratoderma, Palmoplantar, Diffuse	CTD_diseases	5
MESH:D015826	MESH:D015826	Langer-Giedion Syndrome	CTD_diseases	5
MESH:D015827	MESH:D015827	Onchocerciasis, Ocular	CTD_diseases	5
MESH:D015831	MESH:D015831	Osteochondroma	CTD_diseases	5
MESH:D015845	MESH:D015845	Tonic Pupil	CTD_diseases	5
MESH:D015866	MESH:D015866	Uveitis, Posterior	CTD_diseases	5
MESH:D015868	MESH:D015868	Pars Planitis	CTD_diseases	5
MESH:D015875	MESH:D015875	Anisocoria	CTD_diseases	5
MESH:D015877	MESH:D015877	Miosis	CTD_diseases	5
MESH:D015878	MESH:D015878	Mydriasis	CTD_diseases	5
MESH:D016055	MESH:D016055	Urinary Retention	CTD_diseases	5
MESH:D016107	MESH:D016107	Epidermolysis Bullosa Acquisita	CTD_diseases	5
MESH:D016109	MESH:D016109	Epidermolysis Bullosa, Junctional	CTD_diseases	5
MESH:D016110	MESH:D016110	Epidermolysis Bullosa Simplex	CTD_diseases	5
MESH:D016135	MESH:D016135	Spinal Dysraphism	CTD_diseases	5
MESH:D016263	MESH:D016263	AIDS-Associated Nephropathy	CTD_diseases	5
MESH:D016269	MESH:D016269	Milk Hypersensitivity	CTD_diseases	5
MESH:D016460	MESH:D016460	Granuloma Annulare	CTD_diseases	5
MESH:D016586	MESH:D016586	Granular Cell Tumor	CTD_diseases	5
MESH:D016606	MESH:D016606	Thyroid Nodule	CTD_diseases	5
MESH:D016657	MESH:D016657	Cerebral Amyloid Angiopathy	CTD_diseases	5
MESH:D016672	MESH:D016672	Zenker Diverticulum	CTD_diseases	5
MESH:D016706	MESH:D016706	Still's Disease, Adult-Onset	CTD_diseases	5
MESH:D016767	MESH:D016767	Caroli Disease	CTD_diseases	5
MESH:D016781	MESH:D016781	Toxoplasmosis, Cerebral	CTD_diseases	5
MESH:D016868	MESH:D016868	Serratia Infections	CTD_diseases	5
MESH:D016869	MESH:D016869	Ureaplasma Infections	CTD_diseases	5
MESH:D016873	MESH:D016873	Ehrlichiosis	CTD_diseases	5
MESH:D016883	MESH:D016883	Diabetic Ketoacidosis	CTD_diseases	5
MESH:D016918	MESH:D016918	Arthritis, Reactive	CTD_diseases	5
MESH:D016920	MESH:D016920	Meningitis, Bacterial	CTD_diseases	5
MESH:D016921	MESH:D016921	Meningitis, Fungal	CTD_diseases	5
MESH:D017098	MESH:D017098	IgA Deficiency	CTD_diseases	5
MESH:D017099	MESH:D017099	IgG Deficiency	CTD_diseases	5
MESH:D017114	MESH:D017114	Liver Failure, Acute	CTD_diseases	5
MESH:D017129	MESH:D017129	Anisakiasis	CTD_diseases	5
MESH:D017180	MESH:D017180	Tachycardia, Ventricular	CTD_diseases	5
MESH:D017189	MESH:D017189	Enoplida Infections	CTD_diseases	5
MESH:D017191	MESH:D017191	Ascaridida Infections	CTD_diseases	5
MESH:D017194	MESH:D017194	Oxyurida Infections	CTD_diseases	5
MESH:D017196	MESH:D017196	Rhabditida Infections	CTD_diseases	5
MESH:D017205	MESH:D017205	Spirurida Infections	CTD_diseases	5
MESH:D017206	MESH:D017206	Strongylida Infections	CTD_diseases	5
MESH:D017213	MESH:D017213	Root Caries	CTD_diseases	5
MESH:D017237	MESH:D017237	Mitochondrial Encephalomyopathies	CTD_diseases	5
MESH:D017254	MESH:D017254	Leukemic Infiltration	CTD_diseases	5
MESH:D017285	MESH:D017285	Polymyositis	CTD_diseases	5
MESH:D017359	MESH:D017359	HELLP Syndrome	CTD_diseases	5
MESH:D017379	MESH:D017379	Hypertrophy, Left Ventricular	CTD_diseases	5
MESH:D017380	MESH:D017380	Hypertrophy, Right Ventricular	CTD_diseases	5
MESH:D017439	MESH:D017439	Cicatrix, Hypertrophic	CTD_diseases	5
MESH:D017453	MESH:D017453	Dermatitis, Irritant	CTD_diseases	5
MESH:D017497	MESH:D017497	Hidradenitis Suppurativa	CTD_diseases	5
MESH:D017513	MESH:D017513	Lichen Nitidus	CTD_diseases	5
MESH:D017514	MESH:D017514	Pityriasis Lichenoides	CTD_diseases	5
MESH:D017515	MESH:D017515	Pityriasis Rosea	CTD_diseases	5
MESH:D017544	MESH:D017544	Aortic Aneurysm, Abdominal	CTD_diseases	5
MESH:D017545	MESH:D017545	Aortic Aneurysm, Thoracic	CTD_diseases	5
MESH:D017600	MESH:D017600	Neuroectodermal Tumor, Melanotic	CTD_diseases	5
MESH:D017622	MESH:D017622	Periodontal Attachment Loss	CTD_diseases	5
MESH:D017681	MESH:D017681	Hypereosinophilic Syndrome	CTD_diseases	5
MESH:D017689	MESH:D017689	Polydactyly	CTD_diseases	5
MESH:D017696	MESH:D017696	Myopathies, Nemaline	CTD_diseases	5
MESH:D017699	MESH:D017699	Pelvic Pain	CTD_diseases	5
MESH:D017703	MESH:D017703	Retropharyngeal Abscess	CTD_diseases	5
MESH:D017733	MESH:D017733	Leukoplakia, Hairy	CTD_diseases	5
MESH:D017789	MESH:D017789	Granuloma, Pyogenic	CTD_diseases	5
MESH:D017824	MESH:D017824	Bone Cysts, Aneurysmal	CTD_diseases	5
MESH:D017890	MESH:D017890	Splenosis	CTD_diseases	5
MESH:D018126	MESH:D018126	Odontodysplasia	CTD_diseases	5
MESH:D018149	MESH:D018149	Glucose Intolerance	CTD_diseases	5
MESH:D018176	MESH:D018176	Torovirus Infections	CTD_diseases	5
MESH:D018185	MESH:D018185	Morbillivirus Infections	CTD_diseases	5
MESH:D018186	MESH:D018186	Pneumovirus Infections	CTD_diseases	5
MESH:D018191	MESH:D018191	Lymphangioma, Cystic	CTD_diseases	5
MESH:D018192	MESH:D018192	Lymphangioleiomyomatosis	CTD_diseases	5
MESH:D018206	MESH:D018206	Angiolipoma	CTD_diseases	5
MESH:D018207	MESH:D018207	Angiomyolipoma	CTD_diseases	5
MESH:D018209	MESH:D018209	Myelolipoma	CTD_diseases	5
MESH:D018213	MESH:D018213	Neoplasms, Bone Tissue	CTD_diseases	5
MESH:D018218	MESH:D018218	Neoplasms, Fibrous Tissue	CTD_diseases	5
MESH:D018227	MESH:D018227	Sarcoma, Clear Cell	CTD_diseases	5
MESH:D018228	MESH:D018228	Sarcoma, Small Cell	CTD_diseases	5
MESH:D018234	MESH:D018234	Sarcoma, Alveolar Soft Part	CTD_diseases	5
MESH:D018235	MESH:D018235	Smooth Muscle Tumor	CTD_diseases	5
MESH:D018239	MESH:D018239	Seminoma	CTD_diseases	5
MESH:D018240	MESH:D018240	Endodermal Sinus Tumor	CTD_diseases	5
MESH:D018248	MESH:D018248	Adenoma, Liver Cell	CTD_diseases	5
MESH:D018249	MESH:D018249	Adenoma, Oxyphilic	CTD_diseases	5
MESH:D018253	MESH:D018253	Adenoma, Villous	CTD_diseases	5
MESH:D018254	MESH:D018254	Adenomatoid Tumor	CTD_diseases	5
MESH:D018255	MESH:D018255	Adenomatosis, Pulmonary	CTD_diseases	5
MESH:D018256	MESH:D018256	Adenomatous Polyps	CTD_diseases	5
MESH:D018266	MESH:D018266	Adenocarcinoma, Sebaceous	CTD_diseases	5
MESH:D018270	MESH:D018270	Carcinoma, Ductal, Breast	CTD_diseases	5
MESH:D018273	MESH:D018273	Carcinoma, Islet Cell	CTD_diseases	5
MESH:D018275	MESH:D018275	Carcinoma, Lobular	CTD_diseases	5
MESH:D018276	MESH:D018276	Carcinoma, Medullary	CTD_diseases	5
MESH:D018277	MESH:D018277	Carcinoma, Mucoepidermoid	CTD_diseases	5
MESH:D018279	MESH:D018279	Carcinoma, Signet Ring Cell	CTD_diseases	5
MESH:D018280	MESH:D018280	Carcinoma, Skin Appendage	CTD_diseases	5
MESH:D018286	MESH:D018286	Carcinoma, Giant Cell	CTD_diseases	5
MESH:D018287	MESH:D018287	Carcinoma, Large Cell	CTD_diseases	5
MESH:D018288	MESH:D018288	Carcinoma, Small Cell	CTD_diseases	5
MESH:D018289	MESH:D018289	Carcinoma, Verrucous	CTD_diseases	5
MESH:D018296	MESH:D018296	Pilomatrixoma	CTD_diseases	5
MESH:D018298	MESH:D018298	Mucoepidermoid Tumor	CTD_diseases	5
MESH:D018300	MESH:D018300	Papilloma, Intraductal	CTD_diseases	5
MESH:D018310	MESH:D018310	Sertoli-Leydig Cell Tumor	CTD_diseases	5
MESH:D018311	MESH:D018311	Luteoma	CTD_diseases	5
MESH:D018324	MESH:D018324	Hemangioma, Capillary	CTD_diseases	5
MESH:D018330	MESH:D018330	Nevus, Intradermal	CTD_diseases	5
MESH:D018352	MESH:D018352	Coronavirus Infections	CTD_diseases	5
MESH:D018358	MESH:D018358	Neuroendocrine Tumors	CTD_diseases	5
MESH:D018458	MESH:D018458	Persistent Vegetative State	CTD_diseases	5
MESH:D018459	MESH:D018459	Lichen Sclerosus et Atrophicus	CTD_diseases	5
MESH:D018476	MESH:D018476	Hypokinesia	CTD_diseases	5
MESH:D018549	MESH:D018549	Cryptogenic Organizing Pneumonia	CTD_diseases	5
MESH:D018567	MESH:D018567	Breast Neoplasms, Male	CTD_diseases	5
MESH:D018614	MESH:D018614	Sweating Sickness	CTD_diseases	5
MESH:D018636	MESH:D018636	Hypoplastic Left Heart Syndrome	CTD_diseases	5
MESH:D018658	MESH:D018658	Ventricular Septal Rupture	CTD_diseases	5
MESH:D018761	MESH:D018761	Multiple Endocrine Neoplasia Type 1	CTD_diseases	5
MESH:D018813	MESH:D018813	Multiple Endocrine Neoplasia Type 2a	CTD_diseases	5
MESH:D018814	MESH:D018814	Multiple Endocrine Neoplasia Type 2b	CTD_diseases	5
MESH:D018879	MESH:D018879	Ventricular Premature Complexes	CTD_diseases	5
MESH:D018880	MESH:D018880	Atrial Premature Complexes	CTD_diseases	5
MESH:D018887	MESH:D018887	Landau-Kleffner Syndrome	CTD_diseases	5
MESH:D018888	MESH:D018888	Aphasia, Primary Progressive	CTD_diseases	5
MESH:D018979	MESH:D018979	Myositis, Inclusion Body	CTD_diseases	5
MESH:D018981	MESH:D018981	Congenital Disorders of Glycosylation	CTD_diseases	5
MESH:D019214	MESH:D019214	Gingival Overgrowth	CTD_diseases	5
MESH:D019292	MESH:D019292	Skull Base Neoplasms	CTD_diseases	5
MESH:D019294	MESH:D019294	Xanthomatosis, Cerebrotendinous	CTD_diseases	5
MESH:D019351	MESH:D019351	Rubulavirus Infections	CTD_diseases	5
MESH:D019462	MESH:D019462	Syncope, Vasovagal	CTD_diseases	5
MESH:D019522	MESH:D019522	Vaginal Discharge	CTD_diseases	5
MESH:D019547	MESH:D019547	Neck Pain	CTD_diseases	5
MESH:D019694	MESH:D019694	Hepatitis B, Chronic	CTD_diseases	5
MESH:D019698	MESH:D019698	Hepatitis C, Chronic	CTD_diseases	5
MESH:D019701	MESH:D019701	Hepatitis D, Chronic	CTD_diseases	5
MESH:D020022	MESH:D020022	Genetic Predisposition to Disease	CTD_diseases	5
MESH:D020047	MESH:D020047	Rectocele	CTD_diseases	5
MESH:D020069	MESH:D020069	Shoulder Pain	CTD_diseases	5
MESH:D020083	MESH:D020083	Acquired Hyperostosis Syndrome	CTD_diseases	5
MESH:D020138	MESH:D020138	Hyperhomocysteinemia	CTD_diseases	5
MESH:D020140	MESH:D020140	Lysosomal Storage Diseases, Nervous System	CTD_diseases	5
MESH:D020144	MESH:D020144	Basal Ganglia Cerebrovascular Disease	CTD_diseases	5
MESH:D020158	MESH:D020158	Hyperglycinemia, Nonketotic	CTD_diseases	5
MESH:D020167	MESH:D020167	Hyperlysinemias	CTD_diseases	5
MESH:D020176	MESH:D020176	Tyrosinemias	CTD_diseases	5
MESH:D020195	MESH:D020195	Epilepsy, Reflex	CTD_diseases	5
MESH:D020201	MESH:D020201	Brain Hemorrhage, Traumatic	CTD_diseases	5
MESH:D020204	MESH:D020204	Skull Fracture, Depressed	CTD_diseases	5
MESH:D020205	MESH:D020205	Skull Fracture, Basilar	CTD_diseases	5
MESH:D020208	MESH:D020208	Brain Injury, Chronic	CTD_diseases	5
MESH:D020210	MESH:D020210	Central Cord Syndrome	CTD_diseases	5
MESH:D020215	MESH:D020215	Carotid Artery, Internal, Dissection	CTD_diseases	5
MESH:D020217	MESH:D020217	Vertebral Artery Dissection	CTD_diseases	5
MESH:D020234	MESH:D020234	Gait Ataxia	CTD_diseases	5
MESH:D020235	MESH:D020235	Gait Apraxia	CTD_diseases	5
MESH:D020246	MESH:D020246	Venous Thrombosis	CTD_diseases	5
MESH:D020269	MESH:D020269	Alcoholic Neuropathy	CTD_diseases	5
MESH:D020301	MESH:D020301	Vasospasm, Intracranial	CTD_diseases	5
MESH:D020306	MESH:D020306	Tuberculosis, Central Nervous System	CTD_diseases	5
MESH:D020323	MESH:D020323	Tics	CTD_diseases	5
MESH:D020335	MESH:D020335	Paraparesis	CTD_diseases	5
MESH:D020338	MESH:D020338	Vestibular Neuronitis	CTD_diseases	5
MESH:D020343	MESH:D020343	Hypertensive Encephalopathy	CTD_diseases	5
MESH:D020345	MESH:D020345	Enterocolitis, Necrotizing	CTD_diseases	5
MESH:D020362	MESH:D020362	Paraneoplastic Cerebellar Degeneration	CTD_diseases	5
MESH:D020363	MESH:D020363	Limbic Encephalitis	CTD_diseases	5
MESH:D020364	MESH:D020364	Paraneoplastic Polyneuropathy	CTD_diseases	5
MESH:D020370	MESH:D020370	Osteoarthritis, Knee	CTD_diseases	5
MESH:D020385	MESH:D020385	Myokymia	CTD_diseases	5
MESH:D020423	MESH:D020423	Median Neuropathy	CTD_diseases	5
MESH:D020424	MESH:D020424	Ulnar Neuropathies	CTD_diseases	5
MESH:D020425	MESH:D020425	Radial Neuropathy	CTD_diseases	5
MESH:D020426	MESH:D020426	Sciatic Neuropathy	CTD_diseases	5
MESH:D020427	MESH:D020427	Peroneal Neuropathies	CTD_diseases	5
MESH:D020428	MESH:D020428	Femoral Neuropathy	CTD_diseases	5
MESH:D020429	MESH:D020429	Tibial Neuropathy	CTD_diseases	5
MESH:D020447	MESH:D020447	Parasomnias	CTD_diseases	5
MESH:D020512	MESH:D020512	Myopathy, Central Core	CTD_diseases	5
MESH:D020521	MESH:D020521	Stroke	CTD_diseases	5
MESH:D020720	MESH:D020720	Myasthenia Gravis, Autoimmune, Experimental	CTD_diseases	5
MESH:D020759	MESH:D020759	Anterior Spinal Artery Syndrome	CTD_diseases	5
MESH:D020760	MESH:D020760	Spinal Cord Ischemia	CTD_diseases	5
MESH:D020765	MESH:D020765	Intracranial Arterial Diseases	CTD_diseases	5
MESH:D020787	MESH:D020787	Central Nervous System Venous Angioma	CTD_diseases	5
MESH:D020809	MESH:D020809	Central Nervous System Helminthiasis	CTD_diseases	5
MESH:D020818	MESH:D020818	Neuroschistosomiasis	CTD_diseases	5
MESH:D020828	MESH:D020828	Pseudobulbar Palsy	CTD_diseases	5
MESH:D020833	MESH:D020833	Diffuse Axonal Injury	CTD_diseases	5
MESH:D020852	MESH:D020852	Lyme Neuroborreliosis	CTD_diseases	5
MESH:D020886	MESH:D020886	Somatosensory Disorders	CTD_diseases	5
MESH:D020920	MESH:D020920	Dyssomnias	CTD_diseases	5
MESH:D020925	MESH:D020925	Hypoxia-Ischemia, Brain	CTD_diseases	5
MESH:D020941	MESH:D020941	Myasthenia Gravis, Neonatal	CTD_diseases	5
MESH:D020943	MESH:D020943	AIDS Arteritis, Central Nervous System	CTD_diseases	5
MESH:D020953	MESH:D020953	Neuroaspergillosis	CTD_diseases	5
MESH:D020968	MESH:D020968	Brachial Plexus Neuritis	CTD_diseases	5
MESH:D021181	MESH:D021181	Egg Hypersensitivity	CTD_diseases	5
MESH:D021182	MESH:D021182	Wheat Hypersensitivity	CTD_diseases	5
MESH:D021183	MESH:D021183	Peanut Hypersensitivity	CTD_diseases	5
MESH:D021184	MESH:D021184	Nut Hypersensitivity	CTD_diseases	5
MESH:D021441	MESH:D021441	Carcinoma, Pancreatic Ductal	CTD_diseases	5
MESH:D021501	MESH:D021501	Flank Pain	CTD_diseases	5
MESH:D021921	MESH:D021921	Aortic Stenosis, Supravalvular	CTD_diseases	5
MESH:D022861	MESH:D022861	Hermanski-Pudlak Syndrome	CTD_diseases	5
MESH:D023521	MESH:D023521	Chlamydophila Infections	CTD_diseases	5
MESH:D023921	MESH:D023921	Coronary Stenosis	CTD_diseases	5
MESH:D023981	MESH:D023981	Sarcoma, Myeloid	CTD_diseases	5
MESH:D024182	MESH:D024182	Uniparental Disomy	CTD_diseases	5
MESH:D029481	MESH:D029481	Bronchitis, Chronic	CTD_diseases	5
MESH:D029503	MESH:D029503	Anemia, Diamond-Blackfan	CTD_diseases	5
MESH:D031249	MESH:D031249	Erdheim-Chester Disease	CTD_diseases	5
MESH:D031368	MESH:D031368	Zoster Sine Herpete	CTD_diseases	5
MESH:D031901	MESH:D031901	Gestational Trophoblastic Disease	CTD_diseases	5
MESH:D034062	MESH:D034062	Insomnia, Fatal Familial	CTD_diseases	5
MESH:D034141	MESH:D034141	Hypoalbuminemia	CTD_diseases	5
MESH:D036821	MESH:D036821	Endometrial Stromal Tumors	CTD_diseases	5
MESH:D038061	MESH:D038061	Lower Extremity Deformities, Congenital	CTD_diseases	5
MESH:D038062	MESH:D038062	Upper Extremity Deformities, Congenital	CTD_diseases	5
MESH:D038642	MESH:D038642	Shaken Baby Syndrome	CTD_diseases	5
MESH:D039682	MESH:D039682	HIV-Associated Lipodystrophy Syndrome	CTD_diseases	5
MESH:D041781	MESH:D041781	Jaundice, Obstructive	CTD_diseases	5
MESH:D041881	MESH:D041881	Cholecystitis, Acute	CTD_diseases	5
MESH:D042101	MESH:D042101	Acalculous Cholecystitis	CTD_diseases	5
MESH:D043204	MESH:D043204	Mineralocorticoid Excess Syndrome, Apparent	CTD_diseases	5
MESH:D043963	MESH:D043963	Diverticulosis, Colonic	CTD_diseases	5
MESH:D044504	MESH:D044504	Enterocolitis, Neutropenic	CTD_diseases	5
MESH:D044584	MESH:D044584	Carcinoma, Ductal	CTD_diseases	5
MESH:D044904	MESH:D044904	Mannosidase Deficiency Diseases	CTD_diseases	5
MESH:D045463	MESH:D045463	Avulavirus Infections	CTD_diseases	5
MESH:D045464	MESH:D045464	Henipavirus Infections	CTD_diseases	5
MESH:D045602	MESH:D045602	Steatorrhea	CTD_diseases	5
MESH:D045823	MESH:D045823	Ileus	CTD_diseases	5
MESH:D046150	MESH:D046150	Laron Syndrome	CTD_diseases	5
MESH:D046152	MESH:D046152	Gastrointestinal Stromal Tumors	CTD_diseases	5
MESH:D046608	MESH:D046608	Synkinesis	CTD_diseases	5
MESH:D046748	MESH:D046748	Hematoma, Epidural, Spinal	CTD_diseases	5
MESH:D047708	MESH:D047708	Myofibroma	CTD_diseases	5
MESH:D047808	MESH:D047808	Adrenogenital Syndrome	CTD_diseases	5
MESH:D047928	MESH:D047928	Premature Birth	CTD_diseases	5
MESH:D048089	MESH:D048089	Pneumonia of Calves, Enzootic	CTD_diseases	5
MESH:D048909	MESH:D048909	Diabetes Complications	CTD_diseases	5
MESH:D048949	MESH:D048949	Labor Pain	CTD_diseases	5
MESH:D049912	MESH:D049912	Growth Hormone-Secreting Pituitary Adenoma	CTD_diseases	5
MESH:D049913	MESH:D049913	ACTH-Secreting Pituitary Adenoma	CTD_diseases	5
MESH:D050031	MESH:D050031	Hashimoto Disease	CTD_diseases	5
MESH:D050090	MESH:D050090	Ovotesticular Disorders of Sex Development	CTD_diseases	5
MESH:D050197	MESH:D050197	Atherosclerosis	CTD_diseases	5
MESH:D050336	MESH:D050336	Mulibrey Nanism	CTD_diseases	5
MESH:D050379	MESH:D050379	Arteriolosclerosis	CTD_diseases	5
MESH:D051270	MESH:D051270	Headache Disorders, Primary	CTD_diseases	5
MESH:D051271	MESH:D051271	Headache Disorders, Secondary	CTD_diseases	5
MESH:D051359	MESH:D051359	Lymphohistiocytosis, Hemophagocytic	CTD_diseases	5
MESH:D051437	MESH:D051437	Renal Insufficiency	CTD_diseases	5
MESH:D051677	MESH:D051677	Histiocytoma, Malignant Fibrous	CTD_diseases	5
MESH:D052177	MESH:D052177	Kidney Diseases, Cystic	CTD_diseases	5
MESH:D052202	MESH:D052202	Hydrocolpos	CTD_diseases	5
MESH:D052496	MESH:D052496	Lipodystrophy, Familial Partial	CTD_diseases	5
MESH:D052497	MESH:D052497	Lipodystrophy, Congenital Generalized	CTD_diseases	5
MESH:D052798	MESH:D052798	Balanitis Xerotica Obliterans	CTD_diseases	5
MESH:D052858	MESH:D052858	Cystocele	CTD_diseases	5
MESH:D052880	MESH:D052880	Pyomyositis	CTD_diseases	5
MESH:D053039	MESH:D053039	Ureterolithiasis	CTD_diseases	5
MESH:D053040	MESH:D053040	Nephrolithiasis	CTD_diseases	5
MESH:D053158	MESH:D053158	Nocturia	CTD_diseases	5
MESH:D053159	MESH:D053159	Dysuria	CTD_diseases	5
MESH:D053201	MESH:D053201	Urinary Bladder, Overactive	CTD_diseases	5
MESH:D053359	MESH:D053359	Ectodermal Dysplasia 3, Anhidrotic	CTD_diseases	5
MESH:D053360	MESH:D053360	Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive	CTD_diseases	5
MESH:D053448	MESH:D053448	Prostatism	CTD_diseases	5
MESH:D053559	MESH:D053559	Corneal Dystrophy, Juvenile Epithelial of Meesmann	CTD_diseases	5
MESH:D053591	MESH:D053591	Pain, Referred	CTD_diseases	5
MESH:D053609	MESH:D053609	Lethargy	CTD_diseases	5
MESH:D054038	MESH:D054038	Posterior Leukoencephalopathy Syndrome	CTD_diseases	5
MESH:D054059	MESH:D054059	Coronary Occlusion	CTD_diseases	5
MESH:D054061	MESH:D054061	Ischemic Contracture	CTD_diseases	5
MESH:D054067	MESH:D054067	Dihydropyrimidine Dehydrogenase Deficiency	CTD_diseases	5
MESH:D054078	MESH:D054078	Mevalonate Kinase Deficiency	CTD_diseases	5
MESH:D054081	MESH:D054081	Neuronal Migration Disorders	CTD_diseases	5
MESH:D054082	MESH:D054082	Lissencephaly	CTD_diseases	5
MESH:D054083	MESH:D054083	Ectopia Cordis	CTD_diseases	5
MESH:D054119	MESH:D054119	Arachnodactyly	CTD_diseases	5
MESH:D054138	MESH:D054138	Sinus Arrest, Cardiac	CTD_diseases	5
MESH:D054139	MESH:D054139	Tachycardia, Reciprocating	CTD_diseases	5
MESH:D054198	MESH:D054198	Precursor Cell Lymphoblastic Leukemia-Lymphoma	CTD_diseases	5
MESH:D054429	MESH:D054429	Leukemia, Myelomonocytic, Juvenile	CTD_diseases	5
MESH:D054438	MESH:D054438	Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative	CTD_diseases	5
MESH:D054506	MESH:D054506	Chloracne	CTD_diseases	5
MESH:D054537	MESH:D054537	Atrioventricular Block	CTD_diseases	5
MESH:D054549	MESH:D054549	Takotsubo Cardiomyopathy	CTD_diseases	5
MESH:D054739	MESH:D054739	Dendritic Cell Sarcoma, Interdigitating	CTD_diseases	5
MESH:D054740	MESH:D054740	Dendritic Cell Sarcoma, Follicular	CTD_diseases	5
MESH:D054747	MESH:D054747	Histiocytic Sarcoma	CTD_diseases	5
MESH:D054752	MESH:D054752	Langerhans Cell Sarcoma	CTD_diseases	5
MESH:D054850	MESH:D054850	Osteophyte	CTD_diseases	5
MESH:D054880	MESH:D054880	Aspartylglucosaminuria	CTD_diseases	5
MESH:D054882	MESH:D054882	Antley-Bixler Syndrome Phenotype	CTD_diseases	5
MESH:D054972	MESH:D054972	Postural Orthostatic Tachycardia Syndrome	CTD_diseases	5
MESH:D055008	MESH:D055008	Anthracosis	CTD_diseases	5
MESH:D055013	MESH:D055013	Osteoarthritis, Spine	CTD_diseases	5
MESH:D055031	MESH:D055031	Primary Graft Dysfunction	CTD_diseases	5
MESH:D055090	MESH:D055090	Tracheomalacia	CTD_diseases	5
MESH:D055091	MESH:D055091	Bronchomalacia	CTD_diseases	5
MESH:D055112	MESH:D055112	Pyometra	CTD_diseases	5
MESH:D055113	MESH:D055113	Chronic Periodontitis	CTD_diseases	5
MESH:D055154	MESH:D055154	Dysphonia	CTD_diseases	5
MESH:D055665	MESH:D055665	Purpura Fulminans	CTD_diseases	5
MESH:D055673	MESH:D055673	Acrocallosal Syndrome	CTD_diseases	5
MESH:D055728	MESH:D055728	Primary Myelofibrosis	CTD_diseases	5
MESH:D055732	MESH:D055732	Pulmonary Aspergillosis	CTD_diseases	5
MESH:D055882	MESH:D055882	Nevus, Halo	CTD_diseases	5
MESH:D055958	MESH:D055958	Piriformis Muscle Syndrome	CTD_diseases	5
MESH:D056150	MESH:D056150	Acute Generalized Exanthematous Pustulosis	CTD_diseases	5
MESH:D056587	MESH:D056587	Cryopyrin-Associated Periodic Syndromes	CTD_diseases	5
MESH:D056650	MESH:D056650	Vulvodynia	CTD_diseases	5
MESH:D056653	MESH:D056653	Rheumatoid Vasculitis	CTD_diseases	5
MESH:D056693	MESH:D056693	Propionic Acidemia	CTD_diseases	5
MESH:D056806	MESH:D056806	Urea Cycle Disorders, Inborn	CTD_diseases	5
MESH:D056988	MESH:D056988	Anterior Wall Myocardial Infarction	CTD_diseases	5
MESH:D056989	MESH:D056989	Inferior Wall Myocardial Infarction	CTD_diseases	5
MESH:D057049	MESH:D057049	Thrombotic Microangiopathies	CTD_diseases	5
MESH:D057092	MESH:D057092	Geographic Atrophy	CTD_diseases	5
MESH:D057135	MESH:D057135	Wet Macular Degeneration	CTD_diseases	5
MESH:D057174	MESH:D057174	Frontotemporal Lobar Degeneration	CTD_diseases	5
MESH:D057767	MESH:D057767	Kashin-Beck Disease	CTD_diseases	5
MESH:D057792	MESH:D057792	Mirizzi Syndrome	CTD_diseases	5
MESH:D057885	MESH:D057885	Triploidy	CTD_diseases	5
MESH:D057887	MESH:D057887	Overbite	CTD_diseases	5
MESH:D057891	MESH:D057891	Tetraploidy	CTD_diseases	5
MESH:D057910	MESH:D057910	Implant Capsular Contracture	CTD_diseases	5
MESH:D058252	MESH:D058252	Necrobiotic Xanthogranuloma	CTD_diseases	5
MESH:D058345	MESH:D058345	Asymptomatic Infections	CTD_diseases	5
MESH:D058387	MESH:D058387	Candidemia	CTD_diseases	5
MESH:D058405	MESH:D058405	Desmoplastic Small Round Cell Tumor	CTD_diseases	5
MESH:D058489	MESH:D058489	46, XX Disorders of Sex Development	CTD_diseases	5
MESH:D058490	MESH:D058490	46, XY Disorders of Sex Development	CTD_diseases	5
MESH:D058529	MESH:D058529	Single Umbilical Artery	CTD_diseases	5
MESH:D058533	MESH:D058533	Sex Chromosome Disorders of Sex Development	CTD_diseases	5
MESH:D058625	MESH:D058625	End Stage Liver Disease	CTD_diseases	5
MESH:D058627	MESH:D058627	Macrocephaly	CTD_diseases	5
MESH:D058670	MESH:D058670	Tetrasomy	CTD_diseases	5
MESH:D058890	MESH:D058890	Granulomatous Mastitis	CTD_diseases	5
MESH:D058922	MESH:D058922	Inflammatory Breast Neoplasms	CTD_diseases	5
MESH:D059041	MESH:D059041	Plagiocephaly	CTD_diseases	5
MESH:D059226	MESH:D059226	Nociceptive Pain	CTD_diseases	5
MESH:D059228	MESH:D059228	Renal Nutcracker Syndrome	CTD_diseases	5
MESH:D059245	MESH:D059245	Transient Tachypnea of the Newborn	CTD_diseases	5
MESH:D059269	MESH:D059269	Chilaiditi Syndrome	CTD_diseases	5
MESH:D059270	MESH:D059270	Petrositis	CTD_diseases	5
MESH:D059325	MESH:D059325	Intra-Abdominal Hypertension	CTD_diseases	5
MESH:D059327	MESH:D059327	Brachydactyly	CTD_diseases	5
MESH:D059345	MESH:D059345	Cerebral Small Vessel Diseases	CTD_diseases	5
MESH:D059350	MESH:D059350	Chronic Pain	CTD_diseases	5
MESH:D059373	MESH:D059373	Mastodynia	CTD_diseases	5
MESH:D059390	MESH:D059390	Breakthrough Pain	CTD_diseases	5
MESH:D059445	MESH:D059445	Anhedonia	CTD_diseases	5
MESH:D059787	MESH:D059787	Acute Pain	CTD_diseases	5
MESH:D059885	MESH:D059885	Kasabach-Merritt Syndrome	CTD_diseases	5
MESH:D060368	MESH:D060368	Lobomycosis	CTD_diseases	5
MESH:D060545	MESH:D060545	Pudendal Neuralgia	CTD_diseases	5
MESH:D060831	MESH:D060831	Hand-Foot Syndrome	CTD_diseases	5
MESH:D060905	MESH:D060905	Coxa Vara	CTD_diseases	5
MESH:D061205	MESH:D061205	Vascular Calcification	CTD_diseases	5
MESH:D061206	MESH:D061206	Neoplasm Micrometastasis	CTD_diseases	5
MESH:D061220	MESH:D061220	Oculomotor Nerve Injuries	CTD_diseases	5
MESH:D061247	MESH:D061247	Trochlear Nerve Injuries	CTD_diseases	5
MESH:D061285	MESH:D061285	Vestibulocochlear Nerve Injuries	CTD_diseases	5
MESH:D062625	MESH:D062625	Cystadenofibroma	CTD_diseases	5
MESH:D062788	MESH:D062788	Adenomyosis	CTD_diseases	5
MESH:D063730	MESH:D063730	Rickets, Hypophosphatemic	CTD_diseases	5
MESH:D063926	MESH:D063926	Drug Hypersensitivity Syndrome	CTD_diseases	5
MESH:D064068	MESH:D064068	Collagenous Sprue	CTD_diseases	5
MESH:D064726	MESH:D064726	Triple Negative Breast Neoplasms	CTD_diseases	5
OMIM:105500	OMIM:105500	AMYOTROPHIC LATERAL SCLEROSIS-PARKINSONISM/DEMENTIA COMPLEX 1	CTD_diseases	5
OMIM:108120	OMIM:108120	ARTHROGRYPOSIS, DISTAL, TYPE 1A	CTD_diseases	5
OMIM:108721	OMIM:108721	ATELOSTEOGENESIS, TYPE III	CTD_diseases	5
OMIM:109660	OMIM:109660	BETA-AMINO ACIDS, RENAL TRANSPORT OF	CTD_diseases	5
OMIM:120100	OMIM:120100	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 1	CTD_diseases	5
OMIM:121700	OMIM:121700	CORNEAL ENDOTHELIAL DYSTROPHY 1, AUTOSOMAL DOMINANT	CTD_diseases	5
OMIM:122600	OMIM:122600	SPONDYLOCOSTAL DYSOSTOSIS 5, AUTOSOMAL DOMINANT	CTD_diseases	5
OMIM:123700	OMIM:123700	CUTIS LAXA, AUTOSOMAL DOMINANT 1	CTD_diseases	5
OMIM:125420	OMIM:125420	DENTIN DYSPLASIA, TYPE II	CTD_diseases	5
OMIM:125630	OMIM:125630	DERMODISTORTIVE URTICARIA	CTD_diseases	5
OMIM:132850	OMIM:132850	EPSTEIN-BARR VIRUS INSERTION SITE 1;EBVS1 EPSTEIN-BARR VIRUS INTEGRATION SITE	CTD_diseases	5
OMIM:136760	OMIM:136760	FRONTONASAL DYSPLASIA 1	CTD_diseases	5
OMIM:138500	OMIM:138500	HYPERGLYCINURIA	CTD_diseases	5
OMIM:142700	OMIM:142700	DEVELOPMENTAL DYSPLASIA OF THE HIP 1	CTD_diseases	5
OMIM:145250	OMIM:145250	HYPERPIGMENTATION, FAMILIAL PROGRESSIVE, 2	CTD_diseases	5
OMIM:151900	OMIM:151900	LIPOMATOSIS, MULTIPLE	CTD_diseases	5
OMIM:157600	OMIM:157600	MIRROR MOVEMENTS 1	CTD_diseases	5
OMIM:160150	OMIM:160150	MYOPATHY, CENTRONUCLEAR, 1	CTD_diseases	5
OMIM:163000	OMIM:163000	CAPILLARY MALFORMATIONS, CONGENITAL	CTD_diseases	5
OMIM:181405	OMIM:181405	SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY	CTD_diseases	5
OMIM:184095	OMIM:184095	SPONDYLOEPIPHYSEAL DYSPLASIA, MAROTEAUX TYPE	CTD_diseases	5
OMIM:188000	OMIM:188000	THROMBOCYTOPENIA 2	CTD_diseases	5
OMIM:188580	OMIM:188580	THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 1	CTD_diseases	5
OMIM:191900	OMIM:191900	MUCKLE-WELLS SYNDROME	CTD_diseases	5
OMIM:193520	OMIM:193520	WATSON SYNDROME	CTD_diseases	5
OMIM:194470	OMIM:194470	ZINC, ELEVATED PLASMA	CTD_diseases	5
OMIM:215140	OMIM:215140	GREENBERG DYSPLASIA	CTD_diseases	5
OMIM:215150	OMIM:215150	OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA	CTD_diseases	5
OMIM:255200	OMIM:255200	MYOPATHY, CENTRONUCLEAR, 2	CTD_diseases	5
OMIM:255310	OMIM:255310	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION	CTD_diseases	5
OMIM:258660	OMIM:258660	NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY, SUSCEPTIBILITY TO	CTD_diseases	5
OMIM:267430	OMIM:267430	RENAL TUBULAR DYSGENESIS	CTD_diseases	5
OMIM:271700	OMIM:271700	SPONDYLOPERIPHERAL DYSPLASIA	CTD_diseases	5
OMIM:300049	OMIM:300049	HETEROTOPIA, PERIVENTRICULAR, X-LINKED DOMINANT	CTD_diseases	5
OMIM:300158	OMIM:300158	ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED	CTD_diseases	5
OMIM:300337	OMIM:300337	HYPOMELANOSIS OF ITO	CTD_diseases	5
OMIM:300351	OMIM:300351	GRAVES DISEASE, SUSCEPTIBILITY TO, X-LINKED 1	CTD_diseases	5
OMIM:300367	OMIM:300367	THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA	CTD_diseases	5
OMIM:300425	OMIM:300425	AUTISM, SUSCEPTIBILITY TO, X-LINKED 1	CTD_diseases	5
OMIM:300494	OMIM:300494	ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1	CTD_diseases	5
OMIM:300495	OMIM:300495	AUTISM, SUSCEPTIBILITY TO, X-LINKED 2	CTD_diseases	5
OMIM:300496	OMIM:300496	AUTISM, SUSCEPTIBILITY TO, X-LINKED 3	CTD_diseases	5
OMIM:300497	OMIM:300497	ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 2	CTD_diseases	5
OMIM:300831	OMIM:300831	CK SYNDROME	CTD_diseases	5
OMIM:300856	OMIM:300856	HYPOSPADIAS 4, X-LINKED, SUSCEPTIBILITY TO	CTD_diseases	5
OMIM:304020	OMIM:304020	CONE-ROD DYSTROPHY, X-LINKED, 1	CTD_diseases	5
OMIM:310400	OMIM:310400	MYOPATHY, CENTRONUCLEAR, X-LINKED	CTD_diseases	5
OMIM:311050	OMIM:311050	OPTIC ATROPHY 2	CTD_diseases	5
OMIM:551000	OMIM:551000	MITOCHONDRIAL MYOPATHY, LETHAL, INFANTILE	CTD_diseases	5
OMIM:600048	OMIM:600048	BREAST CANCER, 11-22 TRANSLOCATION-ASSOCIATED	CTD_diseases	5
OMIM:600630	OMIM:600630	UV-SENSITIVE SYNDROME 1	CTD_diseases	5
OMIM:601308	OMIM:601308	MYELOID TUMOR SUPPRESSOR	CTD_diseases	5
OMIM:601495	OMIM:601495	AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE	CTD_diseases	5
OMIM:601682	OMIM:601682	GLAUCOMA 1, PRIMARY OPEN ANGLE, C	CTD_diseases	5
OMIM:601776	OMIM:601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1	CTD_diseases	5
OMIM:602197	OMIM:602197	CEREBELLAR DEGENERATION-RELATED AUTOANTIGEN 3	CTD_diseases	5
OMIM:602482	OMIM:602482	AXENFELD-RIEGER SYNDROME, TYPE 3	CTD_diseases	5
OMIM:603663	OMIM:603663	MENTAL HEALTH WELLNESS 1	CTD_diseases	5
OMIM:603664	OMIM:603664	MENTAL HEALTH WELLNESS 2	CTD_diseases	5
OMIM:604370	OMIM:604370	BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1	CTD_diseases	5
OMIM:606240	OMIM:606240	THYROID CARCINOMA, NONMEDULLARY, SUSCEPTIBILITY TO, 1	CTD_diseases	5
OMIM:606613	OMIM:606613	HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 1	CTD_diseases	5
OMIM:606689	OMIM:606689	GLAUCOMA 1, OPEN ANGLE, B	CTD_diseases	5
OMIM:607053	OMIM:607053	HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 2	CTD_diseases	5
OMIM:607473	OMIM:607473	VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 2	CTD_diseases	5
OMIM:607687	OMIM:607687	HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 3	CTD_diseases	5
OMIM:608850	OMIM:608850	MACULAR DYSTROPHY, RETINAL, 3	CTD_diseases	5
OMIM:608931	OMIM:608931	MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY	CTD_diseases	5
OMIM:608971	OMIM:608971	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-POS	CTD_diseases	5
OMIM:609560	OMIM:609560	MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)	CTD_diseases	5
OMIM:610031	OMIM:610031	POLYMICROGYRIA, SYMMETRIC OR ASYMMETRIC	CTD_diseases	5
OMIM:610239	OMIM:610239	HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 4	CTD_diseases	5
OMIM:610761	OMIM:610761	HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 5	CTD_diseases	5
OMIM:610762	OMIM:610762	HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 6	CTD_diseases	5
OMIM:612073	OMIM:612073	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)	CTD_diseases	5
OMIM:612075	OMIM:612075	MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY)	CTD_diseases	5
OMIM:612281	OMIM:612281	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6	CTD_diseases	5
OMIM:612286	OMIM:612286	NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 1	CTD_diseases	5
OMIM:612287	OMIM:612287	NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 2	CTD_diseases	5
OMIM:612336	OMIM:612336	THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT	CTD_diseases	5
OMIM:612353	OMIM:612353	POROKERATOSIS 6, DISSEMINATED SUPERFICIAL ACTINIC TYPE	CTD_diseases	5
OMIM:612555	OMIM:612555	BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2	CTD_diseases	5
OMIM:612692	OMIM:612692	AGAMMAGLOBULINEMIA 6, AUTOSOMAL RECESSIVE	CTD_diseases	5
OMIM:612775	OMIM:612775	CONE-ROD DYSTROPHY 9	CTD_diseases	5
OMIM:612797	OMIM:612797	HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 12	CTD_diseases	5
OMIM:613159	OMIM:613159	NEPHRONOPHTHISIS-LIKE NEPHROPATHY 1	CTD_diseases	5
OMIM:613339	OMIM:613339	EPILEPSY, HOT WATER, 1	CTD_diseases	5
OMIM:613340	OMIM:613340	EPILEPSY, HOT WATER, 2	CTD_diseases	5
OMIM:613353	OMIM:613353	MONONEUROPATHY OF THE MEDIAN NERVE, MILD	CTD_diseases	5
OMIM:613370	OMIM:613370	MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 10	CTD_diseases	5
OMIM:613375	OMIM:613375	MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 11	CTD_diseases	5
OMIM:613398	OMIM:613398	WARSAW BREAKAGE SYNDROME	CTD_diseases	5
OMIM:613399	OMIM:613399	BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 3	CTD_diseases	5
OMIM:613451	OMIM:613451	FRONTONASAL DYSPLASIA 2	CTD_diseases	5
OMIM:613456	OMIM:613456	FRONTONASAL DYSPLASIA 3	CTD_diseases	5
OMIM:613502	OMIM:613502	AGAMMAGLOBULINEMIA 4, AUTOSOMAL RECESSIVE	CTD_diseases	5
OMIM:613508	OMIM:613508	SODIUM SERUM LEVEL QUANTITATIVE TRAIT LOCUS 1	CTD_diseases	5
OMIM:613517	OMIM:613517	MICROPHTHALMIA, ISOLATED 6	CTD_diseases	5
OMIM:613573	OMIM:613573	ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1	CTD_diseases	5
OMIM:613576	OMIM:613576	ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 2	CTD_diseases	5
OMIM:613587	OMIM:613587	OCCULT MACULAR DYSTROPHY	CTD_diseases	5
OMIM:613660	OMIM:613660	CONE-ROD DYSTROPHY 15	CTD_diseases	5
OMIM:613670	OMIM:613670	MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES	CTD_diseases	5
OMIM:613671	OMIM:613671	MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS	CTD_diseases	5
OMIM:613676	OMIM:613676	SECKEL SYNDROME 4	CTD_diseases	5
OMIM:613703	OMIM:613703	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 6	CTD_diseases	5
OMIM:613704	OMIM:613704	MICROPHTHALMIA, ISOLATED 7	CTD_diseases	5
OMIM:613724	OMIM:613724	LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY	CTD_diseases	5
OMIM:613729	OMIM:613729	CHROMOSOME 7q11.23 DELETION SYNDROME, DISTAL, 1.2-MB	CTD_diseases	5
OMIM:613843	OMIM:613843	LEBER CONGENITAL AMAUROSIS 15	CTD_diseases	5
OMIM:614230	OMIM:614230	CHROMOSOME 8q21.11 DELETION SYNDROME	CTD_diseases	5
MESH:D013036	MESH:D013036	Spasms, Infantile	CTD_diseases	6
MESH:D013103	MESH:D013103	Spherocytosis, Hereditary	CTD_diseases	6
MESH:D013106	MESH:D013106	Sphingolipidoses	CTD_diseases	6
MESH:D013168	MESH:D013168	Spondylolisthesis	CTD_diseases	6
MESH:D013206	MESH:D013206	Staphylococcal Scalded Skin Syndrome	CTD_diseases	6
MESH:D013224	MESH:D013224	Status Asthmaticus	CTD_diseases	6
MESH:D013276	MESH:D013276	Stomach Ulcer	CTD_diseases	6
MESH:D013322	MESH:D013322	Strongyloidiasis	CTD_diseases	6
MESH:D013345	MESH:D013345	Subarachnoid Hemorrhage	CTD_diseases	6
MESH:D013362	MESH:D013362	Sublingual Gland Neoplasms	CTD_diseases	6
MESH:D013478	MESH:D013478	Superior Mesenteric Artery Syndrome	CTD_diseases	6
MESH:D013611	MESH:D013611	Tachycardia, Atrioventricular Nodal Reentry	CTD_diseases	6
MESH:D013612	MESH:D013612	Tachycardia, Ectopic Atrial	CTD_diseases	6
MESH:D013613	MESH:D013613	Tachycardia, Ectopic Junctional	CTD_diseases	6
MESH:D013615	MESH:D013615	Tachycardia, Sinoatrial Nodal Reentry	CTD_diseases	6
MESH:D013616	MESH:D013616	Tachycardia, Sinus	CTD_diseases	6
MESH:D013984	MESH:D013984	Tick Infestations	CTD_diseases	6
MESH:D013985	MESH:D013985	Tick Paralysis	CTD_diseases	6
MESH:D014012	MESH:D014012	Tinnitus	CTD_diseases	6
MESH:D014205	MESH:D014205	Trench Fever	CTD_diseases	6
MESH:D014235	MESH:D014235	Trichinellosis	CTD_diseases	6
MESH:D014252	MESH:D014252	Trichostrongyloidiasis	CTD_diseases	6
MESH:D014257	MESH:D014257	Trichuriasis	CTD_diseases	6
MESH:D014313	MESH:D014313	Trismus	CTD_diseases	6
MESH:D014376	MESH:D014376	Tuberculosis	CTD_diseases	6
MESH:D014390	MESH:D014390	Tuberculosis, Meningeal	CTD_diseases	6
MESH:D014435	MESH:D014435	Typhoid Fever	CTD_diseases	6
MESH:D014437	MESH:D014437	Typhus, Endemic Flea-Borne	CTD_diseases	6
MESH:D014438	MESH:D014438	Typhus, Epidemic Louse-Borne	CTD_diseases	6
MESH:D014474	MESH:D014474	Unconsciousness	CTD_diseases	6
MESH:D014514	MESH:D014514	Ureteral Calculi	CTD_diseases	6
MESH:D014525	MESH:D014525	Urethral Stricture	CTD_diseases	6
MESH:D014550	MESH:D014550	Urinary Incontinence, Stress	CTD_diseases	6
MESH:D014595	MESH:D014595	Uterine Perforation	CTD_diseases	6
MESH:D014719	MESH:D014719	Vesicovaginal Fistula	CTD_diseases	6
MESH:D014802	MESH:D014802	Vitamin A Deficiency	CTD_diseases	6
MESH:D014804	MESH:D014804	Vitamin B Deficiency	CTD_diseases	6
MESH:D014808	MESH:D014808	Vitamin D Deficiency	CTD_diseases	6
MESH:D014811	MESH:D014811	Vitamin E Deficiency	CTD_diseases	6
MESH:D014848	MESH:D014848	Vulvovaginitis	CTD_diseases	6
MESH:D015012	MESH:D015012	Yersinia pseudotuberculosis Infections	CTD_diseases	6
MESH:D015155	MESH:D015155	Esophageal Spasm, Diffuse	CTD_diseases	6
MESH:D015173	MESH:D015173	Supratentorial Neoplasms	CTD_diseases	6
MESH:D015174	MESH:D015174	Epidural Neoplasms	CTD_diseases	6
MESH:D015192	MESH:D015192	Infratentorial Neoplasms	CTD_diseases	6
MESH:D015210	MESH:D015210	Arthritis, Gouty	CTD_diseases	6
MESH:D015228	MESH:D015228	Hypertriglyceridemia	CTD_diseases	6
MESH:D015319	MESH:D015319	Fructose-1,6-Diphosphatase Deficiency	CTD_diseases	6
MESH:D015354	MESH:D015354	Vision, Low	CTD_diseases	6
MESH:D015419	MESH:D015419	Spastic Paraplegia, Hereditary	CTD_diseases	6
MESH:D015451	MESH:D015451	Leukemia, Lymphocytic, Chronic, B-Cell	CTD_diseases	6
MESH:D015452	MESH:D015452	Precursor B-Cell Lymphoblastic Leukemia-Lymphoma	CTD_diseases	6
MESH:D015459	MESH:D015459	Leukemia-Lymphoma, Adult T-Cell	CTD_diseases	6
MESH:D015461	MESH:D015461	Leukemia, Prolymphocytic, T-Cell	CTD_diseases	6
MESH:D015465	MESH:D015465	Leukemia, Myeloid, Accelerated Phase	CTD_diseases	6
MESH:D015466	MESH:D015466	Leukemia, Myeloid, Chronic-Phase	CTD_diseases	6
MESH:D015471	MESH:D015471	Leukemia, Basophilic, Acute	CTD_diseases	6
MESH:D015472	MESH:D015472	Leukemia, Eosinophilic, Acute	CTD_diseases	6
MESH:D015473	MESH:D015473	Leukemia, Promyelocytic, Acute	CTD_diseases	6
MESH:D015493	MESH:D015493	Paraparesis, Tropical Spastic	CTD_diseases	6
MESH:D016115	MESH:D016115	Albinism, Oculocutaneous	CTD_diseases	6
MESH:D016116	MESH:D016116	Piebaldism	CTD_diseases	6
MESH:D016117	MESH:D016117	Albinism, Ocular	CTD_diseases	6
MESH:D016136	MESH:D016136	Spina Bifida Occulta	CTD_diseases	6
MESH:D016137	MESH:D016137	Spina Bifida Cystica	CTD_diseases	6
MESH:D016170	MESH:D016170	Accelerated Idioventricular Rhythm	CTD_diseases	6
MESH:D016171	MESH:D016171	Torsades de Pointes	CTD_diseases	6
MESH:D016393	MESH:D016393	Lymphoma, B-Cell	CTD_diseases	6
MESH:D016399	MESH:D016399	Lymphoma, T-Cell	CTD_diseases	6
MESH:D016400	MESH:D016400	Lymphoma, Large-Cell, Immunoblastic	CTD_diseases	6
MESH:D016471	MESH:D016471	Ovarian Hyperstimulation Syndrome	CTD_diseases	6
MESH:D016532	MESH:D016532	Mucopolysaccharidosis II	CTD_diseases	6
MESH:D016538	MESH:D016538	Mucopolysaccharidosis VII	CTD_diseases	6
MESH:D016649	MESH:D016649	Primary Ovarian Insufficiency	CTD_diseases	6
MESH:D016659	MESH:D016659	Psoas Abscess	CTD_diseases	6
MESH:D016773	MESH:D016773	Leishmaniasis, Cutaneous	CTD_diseases	6
MESH:D016889	MESH:D016889	Endometrial Neoplasms	CTD_diseases	6
MESH:D017029	MESH:D017029	Epilepsy, Complex Partial	CTD_diseases	6
MESH:D017034	MESH:D017034	Epilepsy, Frontal Lobe	CTD_diseases	6
MESH:D017036	MESH:D017036	Epilepsia Partialis Continua	CTD_diseases	6
MESH:D017116	MESH:D017116	Low Back Pain	CTD_diseases	6
MESH:D017118	MESH:D017118	Porphyria, Acute Intermittent	CTD_diseases	6
MESH:D017119	MESH:D017119	Porphyria Cutanea Tarda	CTD_diseases	6
MESH:D017121	MESH:D017121	Porphyria, Hepatoerythropoietic	CTD_diseases	6
MESH:D017227	MESH:D017227	Toxascariasis	CTD_diseases	6
MESH:D017241	MESH:D017241	MELAS Syndrome	CTD_diseases	6
MESH:D017243	MESH:D017243	MERRF Syndrome	CTD_diseases	6
MESH:D017488	MESH:D017488	Hyperkeratosis, Epidermolytic	CTD_diseases	6
MESH:D017490	MESH:D017490	Ichthyosis, Lamellar	CTD_diseases	6
MESH:D017588	MESH:D017588	Hyperandrogenism	CTD_diseases	6
MESH:D017700	MESH:D017700	Embolism, Cholesterol	CTD_diseases	6
MESH:D017719	MESH:D017719	Diabetic Foot	CTD_diseases	6
MESH:D017728	MESH:D017728	Lymphoma, Large-Cell, Anaplastic	CTD_diseases	6
MESH:D018208	MESH:D018208	Liposarcoma, Myxoid	CTD_diseases	6
MESH:D018210	MESH:D018210	Chondromatosis	CTD_diseases	6
MESH:D018211	MESH:D018211	Chondrosarcoma, Mesenchymal	CTD_diseases	6
MESH:D018212	MESH:D018212	Giant Cell Tumor of Bone	CTD_diseases	6
MESH:D018214	MESH:D018214	Fibroma, Ossifying	CTD_diseases	6
MESH:D018215	MESH:D018215	Osteoblastoma	CTD_diseases	6
MESH:D018224	MESH:D018224	Myofibromatosis	CTD_diseases	6
MESH:D018229	MESH:D018229	Angiomyoma	CTD_diseases	6
MESH:D018230	MESH:D018230	Leiomyoma, Epithelioid	CTD_diseases	6
MESH:D018231	MESH:D018231	Leiomyomatosis	CTD_diseases	6
MESH:D018242	MESH:D018242	Neuroectodermal Tumors, Primitive	CTD_diseases	6
MESH:D018246	MESH:D018246	Adrenocortical Adenoma	CTD_diseases	6
MESH:D018250	MESH:D018250	Acrospiroma	CTD_diseases	6
MESH:D018251	MESH:D018251	Hidrocystoma	CTD_diseases	6
MESH:D018252	MESH:D018252	Syringoma	CTD_diseases	6
MESH:D018261	MESH:D018261	Mesothelioma, Cystic	CTD_diseases	6
MESH:D018262	MESH:D018262	Adenocarcinoma, Clear Cell	CTD_diseases	6
MESH:D018263	MESH:D018263	Adenocarcinoma, Follicular	CTD_diseases	6
MESH:D018267	MESH:D018267	Carcinoma, Acinar Cell	CTD_diseases	6
MESH:D018268	MESH:D018268	Adrenocortical Carcinoma	CTD_diseases	6
MESH:D018269	MESH:D018269	Carcinoma, Endometrioid	CTD_diseases	6
MESH:D018278	MESH:D018278	Carcinoma, Neuroendocrine	CTD_diseases	6
MESH:D018281	MESH:D018281	Cholangiocarcinoma	CTD_diseases	6
MESH:D018285	MESH:D018285	Klatskin's Tumor	CTD_diseases	6
MESH:D018290	MESH:D018290	Cervical Intraepithelial Neoplasia	CTD_diseases	6
MESH:D018291	MESH:D018291	Cystadenoma, Mucinous	CTD_diseases	6
MESH:D018292	MESH:D018292	Cystadenoma, Papillary	CTD_diseases	6
MESH:D018293	MESH:D018293	Cystadenoma, Serous	CTD_diseases	6
MESH:D018306	MESH:D018306	Neurocytoma	CTD_diseases	6
MESH:D018308	MESH:D018308	Papilloma, Inverted	CTD_diseases	6
MESH:D018319	MESH:D018319	Neurofibrosarcoma	CTD_diseases	6
MESH:D018321	MESH:D018321	Neurothekeoma	CTD_diseases	6
MESH:D018323	MESH:D018323	Hemangioendothelioma, Epithelioid	CTD_diseases	6
MESH:D018325	MESH:D018325	Hemangioblastoma	CTD_diseases	6
MESH:D018329	MESH:D018329	Nevus, Blue	CTD_diseases	6
MESH:D018331	MESH:D018331	Nevus, Spindle Cell	CTD_diseases	6
MESH:D018344	MESH:D018344	T-Lymphocytopenia, Idiopathic CD4-Positive	CTD_diseases	6
MESH:D018357	MESH:D018357	Respiratory Syncytial Virus Infections	CTD_diseases	6
MESH:D018437	MESH:D018437	Brown-Sequard Syndrome	CTD_diseases	6
MESH:D018781	MESH:D018781	Tension-Type Headache	CTD_diseases	6
MESH:D018783	MESH:D018783	Impotence, Vasculogenic	CTD_diseases	6
MESH:D018784	MESH:D018784	Abdominal Abscess	CTD_diseases	6
MESH:D018856	MESH:D018856	Cystitis, Interstitial	CTD_diseases	6
MESH:D018902	MESH:D018902	Chondrodysplasia Punctata, Rhizomelic	CTD_diseases	6
MESH:D019048	MESH:D019048	Prostatic Intraepithelial Neoplasia	CTD_diseases	6
MESH:D019305	MESH:D019305	Epilepsy, Rolandic	CTD_diseases	6
MESH:D019320	MESH:D019320	Embolism, Paradoxical	CTD_diseases	6
MESH:D019449	MESH:D019449	Pouchitis	CTD_diseases	6
MESH:D019595	MESH:D019595	Severe Dengue	CTD_diseases	6
MESH:D019873	MESH:D019873	Schnitzler Syndrome	CTD_diseases	6
MESH:D020019	MESH:D020019	Neurocysticercosis	CTD_diseases	6
MESH:D020132	MESH:D020132	Anticipation, Genetic	CTD_diseases	6
MESH:D020145	MESH:D020145	Basal Ganglia Hemorrhage	CTD_diseases	6
MESH:D020183	MESH:D020183	Nocturnal Paroxysmal Dystonia	CTD_diseases	6
MESH:D020189	MESH:D020189	Nocturnal Myoclonus Syndrome	CTD_diseases	6
MESH:D020190	MESH:D020190	Myoclonic Epilepsy, Juvenile	CTD_diseases	6
MESH:D020191	MESH:D020191	Myoclonic Epilepsies, Progressive	CTD_diseases	6
MESH:D020206	MESH:D020206	Subarachnoid Hemorrhage, Traumatic	CTD_diseases	6
MESH:D020212	MESH:D020212	Carotid Artery Injuries	CTD_diseases	6
MESH:D020216	MESH:D020216	Carotid-Cavernous Sinus Fistula	CTD_diseases	6
MESH:D020264	MESH:D020264	Lead Poisoning, Nervous System, Childhood	CTD_diseases	6
MESH:D020265	MESH:D020265	Lead Poisoning, Nervous System, Adult	CTD_diseases	6
MESH:D020277	MESH:D020277	Polyradiculoneuropathy, Chronic Inflammatory Demyelinating	CTD_diseases	6
MESH:D020299	MESH:D020299	Intracranial Hemorrhage, Hypertensive	CTD_diseases	6
MESH:D020336	MESH:D020336	Paraparesis, Spastic	CTD_diseases	6
MESH:D020391	MESH:D020391	Muscular Dystrophy, Facioscapulohumeral	CTD_diseases	6
MESH:D020430	MESH:D020430	Cubital Tunnel Syndrome	CTD_diseases	6
MESH:D020513	MESH:D020513	Paralysis, Hyperkalemic Periodic	CTD_diseases	6
MESH:D020514	MESH:D020514	Hypokalemic Periodic Paralysis	CTD_diseases	6
MESH:D020520	MESH:D020520	Brain Infarction	CTD_diseases	6
MESH:D020522	MESH:D020522	Lymphoma, Mantle-Cell	CTD_diseases	6
MESH:D020754	MESH:D020754	Spinocerebellar Ataxias	CTD_diseases	6
MESH:D020779	MESH:D020779	Sinus Pericranii	CTD_diseases	6
MESH:D020786	MESH:D020786	Hemangioma, Cavernous, Central Nervous System	CTD_diseases	6
MESH:D020795	MESH:D020795	Photophobia	CTD_diseases	6
MESH:D020814	MESH:D020814	Meningitis, Escherichia coli	CTD_diseases	6
MESH:D020915	MESH:D020915	Korsakoff Syndrome	CTD_diseases	6
MESH:D020919	MESH:D020919	Sleep Disorders, Intrinsic	CTD_diseases	6
MESH:D020921	MESH:D020921	Sleep Arousal Disorders	CTD_diseases	6
MESH:D020922	MESH:D020922	Sleep-Wake Transition Disorders	CTD_diseases	6
MESH:D020923	MESH:D020923	REM Sleep Parasomnias	CTD_diseases	6
MESH:D020937	MESH:D020937	Epilepsy, Partial, Sensory	CTD_diseases	6
MESH:D020938	MESH:D020938	Epilepsy, Partial, Motor	CTD_diseases	6
MESH:D020955	MESH:D020955	Striatonigral Degeneration	CTD_diseases	6
MESH:D021922	MESH:D021922	Discrete Subaortic Stenosis	CTD_diseases	6
MESH:D023903	MESH:D023903	Coronary Restenosis	CTD_diseases	6
MESH:D023961	MESH:D023961	Gonadal Dysgenesis, 46,XX	CTD_diseases	6
MESH:D025242	MESH:D025242	Spondylarthropathies	CTD_diseases	6
MESH:D028243	MESH:D028243	Cerebral Amyloid Angiopathy, Familial	CTD_diseases	6
MESH:D028921	MESH:D028921	Biotinidase Deficiency	CTD_diseases	6
MESH:D028922	MESH:D028922	Holocarboxylase Synthetase Deficiency	CTD_diseases	6
MESH:D029593	MESH:D029593	Jervell-Lange Nielsen Syndrome	CTD_diseases	6
MESH:D029597	MESH:D029597	Romano-Ward Syndrome	CTD_diseases	6
MESH:D030321	MESH:D030321	Denys-Drash Syndrome	CTD_diseases	6
MESH:D034381	MESH:D034381	Hearing Loss	CTD_diseases	6
MESH:D034701	MESH:D034701	Mastocytosis, Cutaneous	CTD_diseases	6
MESH:D034721	MESH:D034721	Mastocytosis, Systemic	CTD_diseases	6
MESH:D034801	MESH:D034801	Mastocytoma	CTD_diseases	6
MESH:D038223	MESH:D038223	Post-Concussion Syndrome	CTD_diseases	6
MESH:D039141	MESH:D039141	Muscular Dystrophy, Oculopharyngeal	CTD_diseases	6
MESH:D041882	MESH:D041882	Emphysematous Cholecystitis	CTD_diseases	6
MESH:D043183	MESH:D043183	Irritable Bowel Syndrome	CTD_diseases	6
MESH:D044905	MESH:D044905	beta-Mannosidosis	CTD_diseases	6
MESH:D046248	MESH:D046248	Pyloric Stenosis, Hypertrophic	CTD_diseases	6
MESH:D046349	MESH:D046349	Coproporphyria, Hereditary	CTD_diseases	6
MESH:D046350	MESH:D046350	Porphyria, Variegate	CTD_diseases	6
MESH:D046351	MESH:D046351	Protoporphyria, Erythropoietic	CTD_diseases	6
MESH:D046628	MESH:D046628	Sphincter of Oddi Dysfunction	CTD_diseases	6
MESH:D046728	MESH:D046728	Colitis, Microscopic	CTD_diseases	6
MESH:D046768	MESH:D046768	Nesidioblastosis	CTD_diseases	6
MESH:D047508	MESH:D047508	Massive Hepatic Necrosis	CTD_diseases	6
MESH:D047868	MESH:D047868	Pulmonary Sclerosing Hemangioma	CTD_diseases	6
MESH:D049068	MESH:D049068	Plagiocephaly, Nonsynostotic	CTD_diseases	6
MESH:D049288	MESH:D049288	Muscular Dystrophies, Limb-Girdle	CTD_diseases	6
MESH:D049310	MESH:D049310	Distal Myopathies	CTD_diseases	6
MESH:D049328	MESH:D049328	Mongolian Spot	CTD_diseases	6
MESH:D050030	MESH:D050030	Andersen Syndrome	CTD_diseases	6
MESH:D050380	MESH:D050380	Monckeberg Medial Calcific Sclerosis	CTD_diseases	6
MESH:D051298	MESH:D051298	Post-Traumatic Headache	CTD_diseases	6
MESH:D051299	MESH:D051299	Post-Dural Puncture Headache	CTD_diseases	6
MESH:D051303	MESH:D051303	Trigeminal Autonomic Cephalalgias	CTD_diseases	6
MESH:D051436	MESH:D051436	Renal Insufficiency, Chronic	CTD_diseases	6
MESH:D051474	MESH:D051474	Neuralgia, Postherpetic	CTD_diseases	6
MESH:D051642	MESH:D051642	Histiocytoma	CTD_diseases	6
MESH:D052245	MESH:D052245	Usher Syndromes	CTD_diseases	6
MESH:D052456	MESH:D052456	Hypoalphalipoproteinemias	CTD_diseases	6
MESH:D053018	MESH:D053018	Pyonephrosis	CTD_diseases	6
MESH:D053202	MESH:D053202	Urinary Incontinence, Urge	CTD_diseases	6
MESH:D053206	MESH:D053206	Nocturnal Enuresis	CTD_diseases	6
MESH:D053207	MESH:D053207	Diurnal Enuresis	CTD_diseases	6
MESH:D053546	MESH:D053546	Keratoderma, Palmoplantar, Epidermolytic	CTD_diseases	6
MESH:D053579	MESH:D053579	Gitelman Syndrome	CTD_diseases	6
MESH:D053627	MESH:D053627	Asthenozoospermia	CTD_diseases	6
MESH:D053653	MESH:D053653	Pyelocystitis	CTD_diseases	6
MESH:D053682	MESH:D053682	Tendon Entrapment	CTD_diseases	6
MESH:D053713	MESH:D053713	Azoospermia	CTD_diseases	6
MESH:D053714	MESH:D053714	Aspermia	CTD_diseases	6
MESH:D054060	MESH:D054060	Pulmonary Infarction	CTD_diseases	6
MESH:D054066	MESH:D054066	Leukemia, Large Granular Lymphocytic	CTD_diseases	6
MESH:D054084	MESH:D054084	Myocardial Bridging	CTD_diseases	6
MESH:D054091	MESH:D054091	Periventricular Nodular Heterotopia	CTD_diseases	6
MESH:D054218	MESH:D054218	Precursor T-Cell Lymphoblastic Leukemia-Lymphoma	CTD_diseases	6
MESH:D054221	MESH:D054221	Classical Lissencephalies and Subcortical Band Heterotopias	CTD_diseases	6
MESH:D054222	MESH:D054222	Cobblestone Lissencephaly	CTD_diseases	6
MESH:D054331	MESH:D054331	Sertoli Cell-Only Syndrome	CTD_diseases	6
MESH:D054363	MESH:D054363	Solitary Fibrous Tumor, Pleural	CTD_diseases	6
MESH:D054364	MESH:D054364	Solitary Fibrous Tumors	CTD_diseases	6
MESH:D054403	MESH:D054403	Leukemia, Prolymphocytic, B-Cell	CTD_diseases	6
MESH:D054515	MESH:D054515	Vulvar Vestibulitis	CTD_diseases	6
MESH:D054556	MESH:D054556	Venous Thromboembolism	CTD_diseases	6
MESH:D055496	MESH:D055496	Neurogenic Bowel	CTD_diseases	6
MESH:D055613	MESH:D055613	Multiple Pulmonary Nodules	CTD_diseases	6
MESH:D055744	MESH:D055744	Invasive Pulmonary Aspergillosis	CTD_diseases	6
MESH:D055756	MESH:D055756	Meningeal Carcinomatosis	CTD_diseases	6
MESH:D055948	MESH:D055948	Sarcopenia	CTD_diseases	6
MESH:D055953	MESH:D055953	Microscopic Polyangiitis	CTD_diseases	6
MESH:D056128	MESH:D056128	Obesity, Abdominal	CTD_diseases	6
MESH:D056725	MESH:D056725	von Willebrand Disease, Type 1	CTD_diseases	6
MESH:D056728	MESH:D056728	von Willebrand Disease, Type 2	CTD_diseases	6
MESH:D056729	MESH:D056729	von Willebrand Disease, Type 3	CTD_diseases	6
MESH:D056824	MESH:D056824	Upper Extremity Deep Vein Thrombosis	CTD_diseases	6
MESH:D056844	MESH:D056844	Renal Colic	CTD_diseases	6
MESH:D056929	MESH:D056929	Liddle Syndrome	CTD_diseases	6
MESH:D057090	MESH:D057090	Eccrine Porocarcinoma	CTD_diseases	6
MESH:D057178	MESH:D057178	Primary Progressive Nonfluent Aphasia	CTD_diseases	6
MESH:D057180	MESH:D057180	Frontotemporal Dementia	CTD_diseases	6
MESH:D057851	MESH:D057851	Posterior Capsular Rupture, Ocular	CTD_diseases	6
MESH:D057971	MESH:D057971	Anterior Capsular Rupture, Ocular	CTD_diseases	6
MESH:D058186	MESH:D058186	Acute Kidney Injury	CTD_diseases	6
MESH:D058247	MESH:D058247	Loose Anagen Hair Syndrome	CTD_diseases	6
MESH:D058267	MESH:D058267	Flea Infestations	CTD_diseases	6
MESH:D058429	MESH:D058429	Gnathostomiasis	CTD_diseases	6
MESH:D058531	MESH:D058531	46, XX Testicular Disorders of Sex Development	CTD_diseases	6
MESH:D058565	MESH:D058565	Cerebral Ventriculitis	CTD_diseases	6
MESH:D059265	MESH:D059265	Visceral Pain	CTD_diseases	6
MESH:D059268	MESH:D059268	Atrophic Vaginitis	CTD_diseases	6
MESH:D059388	MESH:D059388	Pelvic Girdle Pain	CTD_diseases	6
MESH:D059409	MESH:D059409	Stroke, Lacunar	CTD_diseases	6
MESH:D060425	MESH:D060425	Cerebral Phaeohyphomycosis	CTD_diseases	6
MESH:D060487	MESH:D060487	Alternariosis	CTD_diseases	6
MESH:D060585	MESH:D060585	Fusariosis	CTD_diseases	6
MESH:D061222	MESH:D061222	Lingual Nerve Injuries	CTD_diseases	6
MESH:D061387	MESH:D061387	Chlamydial Pneumonia	CTD_diseases	6
MESH:D062026	MESH:D062026	Alice in Wonderland Syndrome	CTD_diseases	6
MESH:D062685	MESH:D062685	Steatocystoma Multiplex	CTD_diseases	6
MESH:D062688	MESH:D062688	Buschke-Lowenstein Tumor	CTD_diseases	6
MESH:D062689	MESH:D062689	Lipoblastoma	CTD_diseases	6
MESH:D063169	MESH:D063169	Dentofacial Deformities	CTD_diseases	6
MESH:D063748	MESH:D063748	Bland White Garland Syndrome	CTD_diseases	6
MESH:D063766	MESH:D063766	Pediatric Obesity	CTD_diseases	6
MESH:D064128	MESH:D064128	Nodding Syndrome	CTD_diseases	6
MESH:D064129	MESH:D064129	Prostatic Neoplasms, Castration-Resistant	CTD_diseases	6
OMIM:100070	OMIM:100070	AORTIC ANEURYSM, FAMILIAL ABDOMINAL, 1	CTD_diseases	6
OMIM:102530	OMIM:102530	SPERMATOGENIC FAILURE 6	CTD_diseases	6
OMIM:103580	OMIM:103580	PSEUDOHYPOPARATHYROIDISM, TYPE IA	CTD_diseases	6
OMIM:105550	OMIM:105550	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS	CTD_diseases	6
OMIM:108420	OMIM:108420	SPERMATOGENIC FAILURE 2	CTD_diseases	6
OMIM:108600	OMIM:108600	SPASTIC ATAXIA 1, AUTOSOMAL DOMINANT	CTD_diseases	6
OMIM:108900	OMIM:108900	ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS	CTD_diseases	6
OMIM:109730	OMIM:109730	AORTIC VALVE DISEASE 1	CTD_diseases	6
OMIM:113900	OMIM:113900	PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA	CTD_diseases	6
OMIM:120050	OMIM:120050	COXSACKIEVIRUS B3 SUSCEPTIBILITY	CTD_diseases	6
OMIM:120970	OMIM:120970	CONE-ROD DYSTROPHY 2	CTD_diseases	6
OMIM:121200	OMIM:121200	SEIZURES, BENIGN FAMILIAL NEONATAL, 1	CTD_diseases	6
OMIM:121201	OMIM:121201	SEIZURES, BENIGN FAMILIAL NEONATAL, 2	CTD_diseases	6
OMIM:129600	OMIM:129600	ECTOPIA LENTIS 1, ISOLATED, AUTOSOMAL DOMINANT	CTD_diseases	6
OMIM:138800	OMIM:138800	GOITER, MULTINODULAR 1, WITH OR WITHOUT SERTOLI-LEYDIG CELL TUMORS	CTD_diseases	6
OMIM:143095	OMIM:143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS	CTD_diseases	6
OMIM:146520	OMIM:146520	HYPOTRICHOSIS 2	CTD_diseases	6
OMIM:153670	OMIM:153670	BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT	CTD_diseases	6
OMIM:157700	OMIM:157700	MITRAL VALVE PROLAPSE, FAMILIAL	CTD_diseases	6
OMIM:160800	OMIM:160800	MYOTONIA CONGENITA, AUTOSOMAL DOMINANT	CTD_diseases	6
OMIM:166260	OMIM:166260	GNATHODIAPHYSEAL DYSPLASIA	CTD_diseases	6
OMIM:171200	OMIM:171200	THIOUREA TASTING	CTD_diseases	6
OMIM:174500	OMIM:174500	POLYDACTYLY, PREAXIAL II	CTD_diseases	6
OMIM:181800	OMIM:181800	SCOLIOSIS, IDIOPATHIC, SUSCEPTIBILITY TO, 1	CTD_diseases	6
OMIM:182920	OMIM:182920	MYOPATHY, SPHEROID BODY	CTD_diseases	6
OMIM:186500	OMIM:186500	MULTIPLE SYNOSTOSES SYNDROME 1	CTD_diseases	6
OMIM:190350	OMIM:190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I	CTD_diseases	6
OMIM:192605	OMIM:192605	VENTRICULAR TACHYCARDIA, FAMILIAL	CTD_diseases	6
OMIM:201250	OMIM:201250	ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE	CTD_diseases	6
OMIM:212050	OMIM:212050	CANDIDIASIS, FAMILIAL, 2	CTD_diseases	6
OMIM:217095	OMIM:217095	CONOTRUNCAL HEART MALFORMATIONS	CTD_diseases	6
OMIM:219100	OMIM:219100	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA	CTD_diseases	6
OMIM:225100	OMIM:225100	ECTOPIA LENTIS 2, ISOLATED, AUTOSOMAL RECESSIVE	CTD_diseases	6
OMIM:225753	OMIM:225753	PONTOCEREBELLAR HYPOPLASIA, TYPE 4	CTD_diseases	6
OMIM:227300	OMIM:227300	FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 1	CTD_diseases	6
OMIM:233300	OMIM:233300	OVARIAN DYSGENESIS 1	CTD_diseases	6
OMIM:246560	OMIM:246560	SPLIT-HAND/FOOT MALFORMATION 3	CTD_diseases	6
OMIM:251200	OMIM:251200	MICROCEPHALY 1, PRIMARY, AUTOSOMAL RECESSIVE	CTD_diseases	6
OMIM:254900	OMIM:254900	EPILEPSY, PROGRESSIVE MYOCLONIC 4, WITH OR WITHOUT RENAL FAILURE	CTD_diseases	6
OMIM:261100	OMIM:261100	MEGALOBLASTIC ANEMIA 1	CTD_diseases	6
OMIM:277300	OMIM:277300	SPONDYLOCOSTAL DYSOSTOSIS 1, AUTOSOMAL RECESSIVE	CTD_diseases	6
OMIM:300136	OMIM:300136	DIABETES MELLITUS, INSULIN-DEPENDENT, X-LINKED, SUSCEPTIBILITY TO	CTD_diseases	6
OMIM:300306	OMIM:300306	BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 11	CTD_diseases	6
OMIM:300331	OMIM:300331	THROMBOCYTHEMIA, X-LINKED	CTD_diseases	6
OMIM:300589	OMIM:300589	NYSTAGMUS 5, CONGENITAL, X-LINKED	CTD_diseases	6
OMIM:300814	OMIM:300814	NYSTAGMUS 6, CONGENITAL, X-LINKED	CTD_diseases	6
OMIM:300816	OMIM:300816	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6	CTD_diseases	6
OMIM:302045	OMIM:302045	CARDIOMYOPATHY, DILATED, 3B	CTD_diseases	6
OMIM:306000	OMIM:306000	GLYCOGEN STORAGE DISEASE IXa1	CTD_diseases	6
OMIM:313000	OMIM:313000	SPATIAL VISUALIZATION, APTITUDE FOR	CTD_diseases	6
OMIM:313350	OMIM:313350	SPLIT-HAND/FOOT MALFORMATION 2	CTD_diseases	6
OMIM:400044	OMIM:400044	46,XY SEX REVERSAL 1	CTD_diseases	6
OMIM:600176	OMIM:600176	PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS	CTD_diseases	6
OMIM:600309	OMIM:600309	ATRIOVENTRICULAR SEPTAL DEFECT 3	CTD_diseases	6
OMIM:600430	OMIM:600430	BRACHYDACTYLY-MENTAL RETARDATION SYNDROME	CTD_diseases	6
OMIM:601518	OMIM:601518	PROSTATE CANCER, HEREDITARY, 1	CTD_diseases	6
OMIM:602025	OMIM:602025	BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 9	CTD_diseases	6
OMIM:603188	OMIM:603188	BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 8	CTD_diseases	6
OMIM:603688	OMIM:603688	PROSTATE CANCER/BRAIN CANCER SUSCEPTIBILITY	CTD_diseases	6
OMIM:604169	OMIM:604169	LEFT VENTRICULAR NONCOMPACTION 1	CTD_diseases	6
OMIM:604317	OMIM:604317	MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICAL MALFORMATIONS	CTD_diseases	6
OMIM:604321	OMIM:604321	MICROCEPHALY 4, PRIMARY, AUTOSOMAL RECESSIVE	CTD_diseases	6
OMIM:604804	OMIM:604804	MICROCEPHALY 3, PRIMARY, AUTOSOMAL RECESSIVE	CTD_diseases	6
OMIM:605021	OMIM:605021	MYOCLONIC EPILEPSY, FAMILIAL INFANTILE	CTD_diseases	6
OMIM:605479	OMIM:605479	CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC, 2	CTD_diseases	6
OMIM:605751	OMIM:605751	SEIZURES, BENIGN FAMILIAL INFANTILE, 2	CTD_diseases	6
OMIM:606035	OMIM:606035	FASTING INSULIN LEVEL QUANTITATIVE TRAIT LOCUS 1	CTD_diseases	6
OMIM:606612	OMIM:606612	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5	CTD_diseases	6
OMIM:607277	OMIM:607277	ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 1	CTD_diseases	6
OMIM:607354	OMIM:607354	SCOLIOSIS, IDIOPATHIC, SUSCEPTIBILITY TO, 2	CTD_diseases	6
OMIM:607447	OMIM:607447	BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 4	CTD_diseases	6
OMIM:607485	OMIM:607485	FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED	CTD_diseases	6
OMIM:607514	OMIM:607514	BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 10	CTD_diseases	6
OMIM:607706	OMIM:607706	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE	CTD_diseases	6
OMIM:607876	OMIM:607876	EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2	CTD_diseases	6
OMIM:608393	OMIM:608393	MICROCEPHALY 6, PRIMARY, AUTOSOMAL RECESSIVE	CTD_diseases	6
OMIM:608410	OMIM:608410	BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 7	CTD_diseases	6
OMIM:608584	OMIM:608584	ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 2	CTD_diseases	6
OMIM:608681	OMIM:608681	SPONDYLOCOSTAL DYSOSTOSIS 2, AUTOSOMAL RECESSIVE	CTD_diseases	6
OMIM:608716	OMIM:608716	MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE	CTD_diseases	6
OMIM:608765	OMIM:608765	SCOLIOSIS, IDIOPATHIC, SUSCEPTIBILITY TO, 3	CTD_diseases	6
OMIM:608840	OMIM:608840	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6	CTD_diseases	6
OMIM:608864	OMIM:608864	OROFACIAL CLEFT 6, SUSCEPTIBILITY TO	CTD_diseases	6
OMIM:608984	OMIM:608984	ATAXIA, SENSORY, 1, AUTOSOMAL DOMINANT	CTD_diseases	6
OMIM:609165	OMIM:609165	ERYTHRODERMA, ICHTHYOSIFORM, CONGENITAL RETICULAR	CTD_diseases	6
OMIM:609470	OMIM:609470	LEFT VENTRICULAR NONCOMPACTION 2	CTD_diseases	6
OMIM:609782	OMIM:609782	AORTIC ANEURYSM, FAMILIAL ABDOMINAL, 2	CTD_diseases	6
OMIM:609813	OMIM:609813	SPONDYLOCOSTAL DYSOSTOSIS 3, AUTOSOMAL RECESSIVE	CTD_diseases	6
OMIM:609958	OMIM:609958	ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 3	CTD_diseases	6
OMIM:610906	OMIM:610906	ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 4	CTD_diseases	6
OMIM:611064	OMIM:611064	ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 5	CTD_diseases	6
OMIM:611302	OMIM:611302	SPASTIC ATAXIA 2, AUTOSOMAL RECESSIVE	CTD_diseases	6
OMIM:611377	OMIM:611377	BRACHYDACTYLY, TYPE B2	CTD_diseases	6
OMIM:611390	OMIM:611390	SPASTIC ATAXIA 3, AUTOSOMAL RECESSIVE	CTD_diseases	6
OMIM:611403	OMIM:611403	ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 6	CTD_diseases	6
OMIM:611891	OMIM:611891	AORTIC ANEURYSM, FAMILIAL ABDOMINAL, 3	CTD_diseases	6
OMIM:611960	OMIM:611960	ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 7	CTD_diseases	6
OMIM:612126	OMIM:612126	GLUT1 DEFICIENCY SYNDROME 2	CTD_diseases	6
OMIM:612238	OMIM:612238	SCOLIOSIS, IDIOPATHIC, SUSCEPTIBILITY TO, 4	CTD_diseases	6
OMIM:612239	OMIM:612239	SCOLIOSIS, IDIOPATHIC, SUSCEPTIBILITY TO, 5	CTD_diseases	6
OMIM:612362	OMIM:612362	BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 12	CTD_diseases	6
OMIM:612379	OMIM:612379	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iq	CTD_diseases	6
OMIM:612459	OMIM:612459	BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 13	CTD_diseases	6
OMIM:612460	OMIM:612460	BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 14	CTD_diseases	6
OMIM:612703	OMIM:612703	MICROCEPHALY 7, PRIMARY, AUTOSOMAL RECESSIVE	CTD_diseases	6
OMIM:613070	OMIM:613070	LIVER FAILURE, INFANTILE, TRANSIENT	CTD_diseases	6
OMIM:613151	OMIM:613151	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3	CTD_diseases	6
OMIM:613152	OMIM:613152	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4	CTD_diseases	6
OMIM:613155	OMIM:613155	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1	CTD_diseases	6
OMIM:613156	OMIM:613156	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2	CTD_diseases	6
OMIM:613194	OMIM:613194	RETINITIS PIGMENTOSA 50	CTD_diseases	6
OMIM:613207	OMIM:613207	ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 8	CTD_diseases	6
OMIM:613428	OMIM:613428	RETINITIS PIGMENTOSA 54	CTD_diseases	6
OMIM:613435	OMIM:613435	AMYOTROPHIC LATERAL SCLEROSIS 12	CTD_diseases	6
OMIM:613464	OMIM:613464	RETINITIS PIGMENTOSA 51	CTD_diseases	6
OMIM:613477	OMIM:613477	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5	CTD_diseases	6
OMIM:613485	OMIM:613485	LONG QT SYNDROME 13	CTD_diseases	6
OMIM:613489	OMIM:613489	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj	CTD_diseases	6
OMIM:613507	OMIM:613507	GLYCOGEN STORAGE DISEASE XV	CTD_diseases	6
OMIM:613550	OMIM:613550	NEPHRONOPHTHISIS 11	CTD_diseases	6
OMIM:613559	OMIM:613559	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7	CTD_diseases	6
OMIM:613563	OMIM:613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA	CTD_diseases	6
OMIM:613575	OMIM:613575	RETINITIS PIGMENTOSA 55	CTD_diseases	6
OMIM:613581	OMIM:613581	RETINITIS PIGMENTOSA 56	CTD_diseases	6
OMIM:613582	OMIM:613582	RETINITIS PIGMENTOSA 57	CTD_diseases	6
OMIM:613612	OMIM:613612	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi	CTD_diseases	6
OMIM:613617	OMIM:613617	RETINITIS PIGMENTOSA 58	CTD_diseases	6
OMIM:613625	OMIM:613625	FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 2	CTD_diseases	6
OMIM:613646	OMIM:613646	METHYLMALONIC ACIDURIA DUE TO TRANSCOBALAMIN RECEPTOR DEFECT	CTD_diseases	6
OMIM:613661	OMIM:613661	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip	CTD_diseases	6
OMIM:613672	OMIM:613672	SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE	CTD_diseases	6
OMIM:613674	OMIM:613674	VESICOURETERAL REFLUX 3	CTD_diseases	6
OMIM:613679	OMIM:613679	PROTHROMBIN DEFICIENCY, CONGENITAL	CTD_diseases	6
OMIM:613686	OMIM:613686	SPONDYLOCOSTAL DYSOSTOSIS 4, AUTOSOMAL RECESSIVE	CTD_diseases	6
OMIM:613706	OMIM:613706	NOONAN SYNDROME 7	CTD_diseases	6
OMIM:613720	OMIM:613720	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7	CTD_diseases	6
OMIM:613721	OMIM:613721	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11	CTD_diseases	6
OMIM:613722	OMIM:613722	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 12	CTD_diseases	6
OMIM:613776	OMIM:613776	CHROMOSOME 17p13.1 DELETION SYNDROME	CTD_diseases	6
OMIM:613828	OMIM:613828	GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 8	CTD_diseases	6
OMIM:613857	OMIM:613857	OROFACIAL CLEFT 13	CTD_diseases	6
OMIM:613930	OMIM:613930	ALOPECIA-MENTAL RETARDATION SYNDROME 3	CTD_diseases	6
OMIM:614208	OMIM:614208	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 16	CTD_diseases	6
MESH:C032598	MESH:C032598	heavy chain disease proteins, human	CTD_diseases	6
MESH:C041229	MESH:C041229	BOT heavy chain disease protein, human	CTD_diseases	6
MESH:C483996	MESH:C483996	FOR heavy chain disease protein, human	CTD_diseases	6
MESH:C483997	MESH:C483997	Wis heavy-chain disease protein, human	CTD_diseases	6
MESH:C483999	MESH:C483999	CHA heavy chain disease protein, human	CTD_diseases	6
MESH:C484001	MESH:C484001	RIV immunoglobulin variant protein, human	CTD_diseases	6
MESH:C531599	MESH:C531599	Achondroplastic dwarfism	CTD_diseases	6
MESH:C531602	MESH:C531602	Anders' syndrome	CTD_diseases	6
MESH:C531603	MESH:C531603	Afibrinogenemia congenital	CTD_diseases	6
MESH:C531615	MESH:C531615	Amyloid Neuropathies, Primary (nonfamilial)	CTD_diseases	6
MESH:C531617	MESH:C531617	Amyotrophic lateral sclerosis 1	CTD_diseases	6
MESH:C531624	MESH:C531624	Familial spinal arachnoiditis	CTD_diseases	6
MESH:C531625	MESH:C531625	Chiari malformation type 2	CTD_diseases	6
MESH:C531629	MESH:C531629	Human balantidiasis	CTD_diseases	6
MESH:C531641	MESH:C531641	Monday morning fever	CTD_diseases	6
MESH:C531647	MESH:C531647	Caroli disease isolated	CTD_diseases	6
MESH:C531649	MESH:C531649	Neutropenia and hyperlymphocytosis with large granular lymphocytes	CTD_diseases	6
MESH:C531662	MESH:C531662	Submacular Cysticercosis	CTD_diseases	6
MESH:C531665	MESH:C531665	Opalescent dentin	CTD_diseases	6
MESH:C531667	MESH:C531667	5 alpha Fluorouracil toxicity	CTD_diseases	6
MESH:C531684	MESH:C531684	Hereditary spinal ataxia	CTD_diseases	6
MESH:C531691	MESH:C531691	Platelet granule deficiency disorder	CTD_diseases	6
MESH:C531719	MESH:C531719	Keratitis sicca	CTD_diseases	6
MESH:C531728	MESH:C531728	Canicola fever	CTD_diseases	6
MESH:C531732	MESH:C531732	Ascending aortic aneurysm, hypertelorism, bifid uvula, cleft palate, and arterial tortuosity	CTD_diseases	6
MESH:C531742	MESH:C531742	Marfanoid hypermobility syndrome	CTD_diseases	6
MESH:C531755	MESH:C531755	Kidney disorder involving deposition of calcium and oxalate or phosphate in the renal tubules	CTD_diseases	6
MESH:C531768	MESH:C531768	Colangite esclerosante porracoccidiodomicose	CTD_diseases	6
MESH:C531782	MESH:C531782	Endemic treponematosis caused by Treponema carateum	CTD_diseases	6
MESH:C531784	MESH:C531784	Familial pityriasis rubra pilaris	CTD_diseases	6
MESH:C531795	MESH:C531795	Idiopathic intracranial hypertension with papilledema	CTD_diseases	6
MESH:C531836	MESH:C531836	Congenital agenesis of the tricuspid valve	CTD_diseases	6
MESH:C531844	MESH:C531844	Von willebrand factor, deficiency	CTD_diseases	6
MESH:C535276	MESH:C535276	Primary angiitis of the central nervous system	CTD_diseases	6
MESH:C535284	MESH:C535284	Ramer Ladda syndrome	CTD_diseases	6
MESH:C535290	MESH:C535290	Rasmussen Johnsen Thomsen syndrome	CTD_diseases	6
MESH:C535305	MESH:C535305	2-hydroxyethyl methacrylate sensitization	CTD_diseases	6
MESH:C535306	MESH:C535306	2-Hydroxyglutaricaciduria	CTD_diseases	6
MESH:C535316	MESH:C535316	46,XX Gonadal dysgenesis epibulbar dermoid	CTD_diseases	6
MESH:C535335	MESH:C535335	Abderhalden-Kaufmann-Lignac syndrome	CTD_diseases	6
MESH:C535349	MESH:C535349	Cayler cardiofacial syndrome	CTD_diseases	6
MESH:C535353	MESH:C535353	Cerebellar hypoplasia with endosteal sclerosis	CTD_diseases	6
MESH:C535354	MESH:C535354	Cerebral astrocytoma, adult	CTD_diseases	6
MESH:C535355	MESH:C535355	Chorea, remitting with nystagmus and cataracts	CTD_diseases	6
MESH:C535364	MESH:C535364	Chromosome 1, duplication 1p21 p32	CTD_diseases	6
MESH:C535365	MESH:C535365	Chromosome 2, trisomy 2p13 p21	CTD_diseases	6
MESH:C535366	MESH:C535366	Chromosome 2, trisomy 2pter p24	CTD_diseases	6
MESH:C535367	MESH:C535367	Chromosome 2, trisomy 2q	CTD_diseases	6
MESH:C535368	MESH:C535368	Chromosome 2, trisomy 2q37	CTD_diseases	6
MESH:C535371	MESH:C535371	Trisomy 20p	CTD_diseases	6
MESH:C535372	MESH:C535372	Chromosome 20, trisomy	CTD_diseases	6
MESH:C535393	MESH:C535393	Ataxia with vitamin E deficiency	CTD_diseases	6
MESH:C535402	MESH:C535402	Galactorrhea-Hyperprolactinemia	CTD_diseases	6
MESH:C535424	MESH:C535424	Congenital thrombotic disease, due to Protein C deficiency	CTD_diseases	6
MESH:C535426	MESH:C535426	Congenitally corrected transposition of the great arteries	CTD_diseases	6
MESH:C535431	MESH:C535431	Benign paroxysmal positional vertigo	CTD_diseases	6
MESH:C535444	MESH:C535444	Bile acid synthesis defect, congenital, 4	CTD_diseases	6
MESH:C535450	MESH:C535450	Chromosome 13p duplication	CTD_diseases	6
MESH:C535453	MESH:C535453	Chromosome 9, trisomy 9q32	CTD_diseases	6
MESH:C535454	MESH:C535454	Chromosome 9, trisomy mosaic	CTD_diseases	6
MESH:C535463	MESH:C535463	Mainzer-Saldino Disease	CTD_diseases	6
MESH:C535466	MESH:C535466	Convulsions benign familial neonatal dominant form	CTD_diseases	6
MESH:C535470	MESH:C535470	CoQ-responsive OXPHOS deficiency	CTD_diseases	6
MESH:C535477	MESH:C535477	Corneal dystrophy, epithelial basement membrane	CTD_diseases	6
MESH:C535478	MESH:C535478	Corneal dystrophy, Fuchs' endothelial, 1	CTD_diseases	6
MESH:C535479	MESH:C535479	Corneal dystrophy, Fuchs' endothelial, 2	CTD_diseases	6
MESH:C535483	MESH:C535483	Freeman-Sheldon syndrome	CTD_diseases	6
MESH:C535485	MESH:C535485	Chromosome 13q trisomy	CTD_diseases	6
MESH:C535488	MESH:C535488	Chromosome 14 trisomy	CTD_diseases	6
MESH:C535489	MESH:C535489	Chromosome 14, trisomy mosaic	CTD_diseases	6
MESH:C535494	MESH:C535494	Epidermolysis bullosa, pretibial	CTD_diseases	6
MESH:C535500	MESH:C535500	Epileptic encephalopathy, Lennox-Gastaut type	CTD_diseases	6
MESH:C535510	MESH:C535510	Erythema nodosum, familial	CTD_diseases	6
MESH:C535511	MESH:C535511	Erythema nodosum, idiopathic	CTD_diseases	6
MESH:C535523	MESH:C535523	Infantile onset spinocerebellar ataxia	CTD_diseases	6
MESH:C535563	MESH:C535563	Absence of Tibia	CTD_diseases	6
MESH:C535564	MESH:C535564	Absence of tibia with polydactyly	CTD_diseases	6
MESH:C535598	MESH:C535598	Creatine deficiency, X-linked	CTD_diseases	6
MESH:C535601	MESH:C535601	Dosage-sensitive sex reversal	CTD_diseases	6
MESH:C535630	MESH:C535630	Hantavirosis	CTD_diseases	6
MESH:C535648	MESH:C535648	Familial primary gastric lymphoma	CTD_diseases	6
MESH:C535663	MESH:C535663	Acroosteolysis dominant type	CTD_diseases	6
MESH:C535675	MESH:C535675	Richieri Costa Da Silva syndrome	CTD_diseases	6
MESH:C535683	MESH:C535683	Rigid spine syndrome	CTD_diseases	6
MESH:C535692	MESH:C535692	Male pseudohermaphroditism due to defective LH molecule	CTD_diseases	6
MESH:C535709	MESH:C535709	Manz syndrome	CTD_diseases	6
MESH:C535717	MESH:C535717	Neuropathy, hereditary motor and sensory, Okinawa type	CTD_diseases	6
MESH:C535720	MESH:C535720	Familial duodenal atresia	CTD_diseases	6
MESH:C535731	MESH:C535731	Dysequilibrium syndrome	CTD_diseases	6
MESH:C535735	MESH:C535735	Congenital lobar emphysema	CTD_diseases	6
MESH:C535739	MESH:C535739	Congenital disorder of glycosylation type 1A	CTD_diseases	6
MESH:C535740	MESH:C535740	Congenital disorder of glycosylation type 1B	CTD_diseases	6
MESH:C535741	MESH:C535741	Congenital disorder of glycosylation type 1C	CTD_diseases	6
MESH:C535742	MESH:C535742	Congenital disorder of glycosylation type 1D	CTD_diseases	6
MESH:C535743	MESH:C535743	Congenital disorder of glycosylation type 1E	CTD_diseases	6
MESH:C535744	MESH:C535744	Congenital disorder of glycosylation type 1F	CTD_diseases	6
MESH:C535745	MESH:C535745	Congenital disorder of glycosylation type 1G	CTD_diseases	6
MESH:C535746	MESH:C535746	Congenital disorder of glycosylation type 1H	CTD_diseases	6
MESH:C535747	MESH:C535747	Congenital disorder of glycosylation type II	CTD_diseases	6
MESH:C535748	MESH:C535748	Congenital disorder of glycosylation type 1J	CTD_diseases	6
MESH:C535749	MESH:C535749	Congenital disorder of glycosylation type 1K	CTD_diseases	6
MESH:C535750	MESH:C535750	Congenital disorder of glycosylation type 1L	CTD_diseases	6
MESH:C535753	MESH:C535753	Congenital disorder of glycosylation type 2D	CTD_diseases	6
MESH:C535754	MESH:C535754	Congenital disorder of glycosylation type 2E	CTD_diseases	6
MESH:C535755	MESH:C535755	Congenital disorder of glycosylation, type 2C	CTD_diseases	6
MESH:C535756	MESH:C535756	Congenital disorder of glycosylation, type 2G	CTD_diseases	6
MESH:C535765	MESH:C535765	Cystinosis, ocular nonnephropathic	CTD_diseases	6
MESH:C535771	MESH:C535771	Dandy Walker malformation postaxial polydactyly	CTD_diseases	6
MESH:C535813	MESH:C535813	Neuropathy, hereditary motor and sensory, Russe type	CTD_diseases	6
MESH:C535819	MESH:C535819	Pseudoachondroplasia	CTD_diseases	6
MESH:C535820	MESH:C535820	Pseudoachondroplastic dysplasia 2	CTD_diseases	6
MESH:C535829	MESH:C535829	Pseudotrisomy 13 syndrome	CTD_diseases	6
MESH:C535835	MESH:C535835	Schwartz Cohen-Addad Lambert syndrome	CTD_diseases	6
MESH:C535838	MESH:C535838	Pancreatic islet cell tumors	CTD_diseases	6
MESH:C535869	MESH:C535869	Rokitansky-Aschoff sinuses of the gallbladder	CTD_diseases	6
MESH:C535879	MESH:C535879	Rudd Klimek syndrome	CTD_diseases	6
MESH:C535881	MESH:C535881	Johnson Munson syndrome	CTD_diseases	6
MESH:C535884	MESH:C535884	Joint laxity, familial	CTD_diseases	6
MESH:C535892	MESH:C535892	Lichen planus follicularis	CTD_diseases	6
MESH:C535911	MESH:C535911	Marfan Syndrome type 2	CTD_diseases	6
MESH:C535933	MESH:C535933	Cholestasis, progressive familial intrahepatic 1	CTD_diseases	6
MESH:C535934	MESH:C535934	Cholestasis, progressive familial intrahepatic 2	CTD_diseases	6
MESH:C535935	MESH:C535935	Cholestasis, progressive familial intrahepatic 3	CTD_diseases	6
MESH:C535945	MESH:C535945	Desmoplastic cerebral astrocytoma of infancy	CTD_diseases	6
MESH:C535955	MESH:C535955	Epidermolysa bullosa simplex and limb girdle muscular dystrophy	CTD_diseases	6
MESH:C535956	MESH:C535956	Epidermolysis bullosa dystrophica, Pasini type	CTD_diseases	6
MESH:C535958	MESH:C535958	Epidermolysis bullosa inversa dystrophica	CTD_diseases	6
MESH:C535959	MESH:C535959	Epidermolysis bullosa simplex with mottled pigmentation	CTD_diseases	6
MESH:C535962	MESH:C535962	Epidermolysis bullosa simplex, Ogna type	CTD_diseases	6
MESH:C535976	MESH:C535976	Cone rod dystrophy amelogenesis imperfecta	CTD_diseases	6
MESH:C535983	MESH:C535983	Congenital anosmia	CTD_diseases	6
MESH:C536010	MESH:C536010	Achalasia microcephaly	CTD_diseases	6
MESH:C536015	MESH:C536015	Achondrogenesis type 1A	CTD_diseases	6
MESH:C536016	MESH:C536016	Achondrogenesis type 1B	CTD_diseases	6
MESH:C536017	MESH:C536017	Achondrogenesis type 2	CTD_diseases	6
MESH:C536018	MESH:C536018	Achondrogenesis, type 3	CTD_diseases	6
MESH:C536019	MESH:C536019	Achondrogenesis, type 4	CTD_diseases	6
MESH:C536023	MESH:C536023	Maroteaux Fonfria syndrome	CTD_diseases	6
MESH:C536024	MESH:C536024	Marsden syndrome	CTD_diseases	6
MESH:C536032	MESH:C536032	Mastocytic enterocolitis	CTD_diseases	6
MESH:C536036	MESH:C536036	Maxillonasal dysplasia, Binder type	CTD_diseases	6
MESH:C536039	MESH:C536039	Osteogenesis imperfecta, Levin type	CTD_diseases	6
MESH:C536041	MESH:C536041	Osteogenesis imperfecta, type 1A	CTD_diseases	6
MESH:C536042	MESH:C536042	Osteogenesis imperfecta, type 2A	CTD_diseases	6
MESH:C536043	MESH:C536043	Osteogenesis imperfecta, type 2B	CTD_diseases	6
MESH:C536044	MESH:C536044	Osteogenesis imperfecta, type 3	CTD_diseases	6
MESH:C536045	MESH:C536045	Osteogenesis imperfecta, type 4	CTD_diseases	6
MESH:C536046	MESH:C536046	Osteogenesis imperfecta, type 5	CTD_diseases	6
MESH:C536047	MESH:C536047	Osteogenesis imperfecta, type 6	CTD_diseases	6
MESH:C536048	MESH:C536048	Osteogenesis imperfecta, type 7	CTD_diseases	6
MESH:C536049	MESH:C536049	Osteogenesis imperfecta, type VIII	CTD_diseases	6
MESH:C536053	MESH:C536053	Osteopathia striata cranial sclerosis	CTD_diseases	6
MESH:C536063	MESH:C536063	Osteoporosis-pseudoglioma syndrome	CTD_diseases	6
MESH:C536099	MESH:C536099	Myokymia with neonatal epilepsy	CTD_diseases	6
MESH:C536103	MESH:C536103	Myopathy, desmin storage	CTD_diseases	6
MESH:C536154	MESH:C536154	Keratoderma palmoplantaris transgrediens	CTD_diseases	6
MESH:C536171	MESH:C536171	Dicarboxylicaminoaciduria	CTD_diseases	6
MESH:C536173	MESH:C536173	Diffuse palmoplantar keratoderma, Bothnian type	CTD_diseases	6
MESH:C536174	MESH:C536174	Diffuse panbronchiolitis	CTD_diseases	6
MESH:C536192	MESH:C536192	Ehlers-Danlos syndrome 6B	CTD_diseases	6
MESH:C536193	MESH:C536193	Ehlers-Danlos syndrome caused by tenascin-X deficiency	CTD_diseases	6
MESH:C536194	MESH:C536194	Ehlers-Danlos syndrome type 1	CTD_diseases	6
MESH:C536195	MESH:C536195	Ehlers-Danlos syndrome type 2	CTD_diseases	6
MESH:C536196	MESH:C536196	Ehlers-Danlos syndrome type 3	CTD_diseases	6
MESH:C536198	MESH:C536198	Ehlers-Danlos syndrome type 6	CTD_diseases	6
MESH:C536199	MESH:C536199	Ehlers-Danlos syndrome, Beasley Cohen type	CTD_diseases	6
MESH:C536200	MESH:C536200	Ehlers-Danlos syndrome, cardiac valvular form	CTD_diseases	6
MESH:C536201	MESH:C536201	Ehlers-Danlos syndrome, progeroid form	CTD_diseases	6
MESH:C536213	MESH:C536213	Crigler Najjar syndrome, type 2	CTD_diseases	6
MESH:C536215	MESH:C536215	Pediatric Crohn's disease	CTD_diseases	6
MESH:C536218	MESH:C536218	Cryofibrinogenemia	CTD_diseases	6
MESH:C536231	MESH:C536231	Familial dilated cardiomyopathy	CTD_diseases	6
MESH:C536245	MESH:C536245	Nondystrophic myotonia	CTD_diseases	6
MESH:C536246	MESH:C536246	Noninsulin-dependent diabetes mellitus with deafness	CTD_diseases	6
MESH:C536251	MESH:C536251	Pyknoachondrogenesis	CTD_diseases	6
MESH:C536258	MESH:C536258	Pyruvate dehydrogenase phosphatase deficiency	CTD_diseases	6
MESH:C536260	MESH:C536260	Quebec platelet disorder	CTD_diseases	6
MESH:C536277	MESH:C536277	Idiopathic dilation cardiomyopathy	CTD_diseases	6
MESH:C536285	MESH:C536285	Iminoglycinuria	CTD_diseases	6
MESH:C536290	MESH:C536290	Immunoglobulin a deficiency 1	CTD_diseases	6
MESH:C536291	MESH:C536291	Immunoglobulin a deficiency 2	CTD_diseases	6
MESH:C536298	MESH:C536298	Partial lissencephaly	CTD_diseases	6
MESH:C536300	MESH:C536300	Partington X-linked mental retardation syndrome	CTD_diseases	6
MESH:C536301	MESH:C536301	Parvovirus antenatal infection	CTD_diseases	6
MESH:C536307	MESH:C536307	Patella aplasia, coxa vara, tarsal synostosis	CTD_diseases	6
MESH:C536332	MESH:C536332	Polydactyly preaxial type 1	CTD_diseases	6
MESH:C536333	MESH:C536333	Polydactyly, preaxial 4	CTD_diseases	6
MESH:C536334	MESH:C536334	Polymorphic catecholergic ventricular tachycardia	CTD_diseases	6
MESH:C536343	MESH:C536343	Posterior column ataxia with retinitis pigmentosa	CTD_diseases	6
MESH:C536354	MESH:C536354	Vocal cord dysfunction familial	CTD_diseases	6
MESH:C536356	MESH:C536356	Anemia, hereditary spherocytic hemolytic	CTD_diseases	6
MESH:C536369	MESH:C536369	Angiostrongyliasis	CTD_diseases	6
MESH:C536386	MESH:C536386	Facial paresis, hereditary, congenital	CTD_diseases	6
MESH:C536392	MESH:C536392	Factor 8 deficiency, acquired	CTD_diseases	6
MESH:C536394	MESH:C536394	Neonatal hemochromatosis	CTD_diseases	6
MESH:C536409	MESH:C536409	Neural tube defect, folate-sensitive	CTD_diseases	6
MESH:C536413	MESH:C536413	Primary granulocytic sarcoma	CTD_diseases	6
MESH:C536418	MESH:C536418	Primary orthostatic tremor	CTD_diseases	6
MESH:C536439	MESH:C536439	Corneal endothelial dystrophy type 2	CTD_diseases	6
MESH:C536458	MESH:C536458	Von Willebrand disease, platelet type	CTD_diseases	6
MESH:C536461	MESH:C536461	Waaler Aarskog syndrome	CTD_diseases	6
MESH:C536468	MESH:C536468	Uniparental disomy of 11	CTD_diseases	6
MESH:C536469	MESH:C536469	Uniparental disomy of 13	CTD_diseases	6
MESH:C536470	MESH:C536470	Uniparental disomy of chromosome 2	CTD_diseases	6
MESH:C536471	MESH:C536471	Uniparental disomy, paternal, chromosome 14	CTD_diseases	6
MESH:C536474	MESH:C536474	Urachal adenocarcinoma	CTD_diseases	6
MESH:C536475	MESH:C536475	Urachal cancer	CTD_diseases	6
MESH:C536498	MESH:C536498	Tetra-amelia autosomal recessive	CTD_diseases	6
MESH:C536531	MESH:C536531	Orofaciodigital syndrome 6	CTD_diseases	6
MESH:C536546	MESH:C536546	Tremor hereditary essential, 2	CTD_diseases	6
MESH:C536570	MESH:C536570	Craniometaphyseal dysplasia, autosomal recessive type	CTD_diseases	6
MESH:C536572	MESH:C536572	Bone Marrow failure syndromes	CTD_diseases	6
MESH:C536578	MESH:C536578	Chromosome 17, trisomy 17p11 2	CTD_diseases	6
MESH:C536579	MESH:C536579	Chromosome 17, trisomy 17q22	CTD_diseases	6
MESH:C536581	MESH:C536581	Chromosome 18 mosaic monosomy	CTD_diseases	6
MESH:C536589	MESH:C536589	Alternating hemiplegia of childhood	CTD_diseases	6
MESH:C536591	MESH:C536591	Alveolar echinococcosis	CTD_diseases	6
MESH:C536594	MESH:C536594	Alzheimer disease type 1	CTD_diseases	6
MESH:C536595	MESH:C536595	Alzheimer disease type 2	CTD_diseases	6
MESH:C536596	MESH:C536596	Alzheimer disease type 4	CTD_diseases	6
MESH:C536598	MESH:C536598	Alzheimer disease, familial, type 3	CTD_diseases	6
MESH:C536599	MESH:C536599	Alzheimer's disease without Neurofibrillary tangles	CTD_diseases	6
MESH:C536607	MESH:C536607	Brody myopathy	CTD_diseases	6
MESH:C536622	MESH:C536622	Scalp defects postaxial polydactyly	CTD_diseases	6
MESH:C536660	MESH:C536660	Perniola Krajewska Carnevale syndrome	CTD_diseases	6
MESH:C536665	MESH:C536665	Persistent Mullerian duct syndrome	CTD_diseases	6
MESH:C536684	MESH:C536684	Warman Mulliken Hayward syndrome	CTD_diseases	6
MESH:C536699	MESH:C536699	Whistling face syndrome, recessive form	CTD_diseases	6
MESH:C536711	MESH:C536711	Winship Viljoen Leary syndrome	CTD_diseases	6
MESH:C536743	MESH:C536743	Woods Black Norbury syndrome	CTD_diseases	6
MESH:C536748	MESH:C536748	Worth syndrome	CTD_diseases	6
MESH:C536752	MESH:C536752	Wyburn Mason's syndrome	CTD_diseases	6
MESH:C536764	MESH:C536764	Xerocytosis, hereditary	CTD_diseases	6
MESH:C536779	MESH:C536779	Systemic necrotizing angiitis	CTD_diseases	6
MESH:C536783	MESH:C536783	T-Lymphocytopenia	CTD_diseases	6
MESH:C536794	MESH:C536794	Chromosome 21, uniparental disomy of	CTD_diseases	6
MESH:C536799	MESH:C536799	Chromosome 22, trisomy	CTD_diseases	6
MESH:C536800	MESH:C536800	Chromosome 22, trisomy q11 q13	CTD_diseases	6
MESH:C536811	MESH:C536811	Chromosome 3, trisomy 3p	CTD_diseases	6
MESH:C536812	MESH:C536812	Chromosome 3, trisomy 3p25	CTD_diseases	6
MESH:C536813	MESH:C536813	Chromosome 3, trisomy 3q	CTD_diseases	6
MESH:C536834	MESH:C536834	Glutaric aciduria 2	CTD_diseases	6
MESH:C536846	MESH:C536846	Familial hypersensitivity pneumonitis	CTD_diseases	6
MESH:C536848	MESH:C536848	Familial myelofibrosis	CTD_diseases	6
MESH:C536852	MESH:C536852	Familial streblodactyly	CTD_diseases	6
MESH:C536869	MESH:C536869	Spastic paraplegia epilepsy mental retardation	CTD_diseases	6
MESH:C536879	MESH:C536879	Muscular atrophy, spinal, infantile chronic form	CTD_diseases	6
MESH:C536887	MESH:C536887	Klippel Feil syndrome dominant type	CTD_diseases	6
MESH:C536888	MESH:C536888	Klippel Feil syndrome recessive type	CTD_diseases	6
MESH:C536917	MESH:C536917	Hypothyroidism, Congenital, Nongoitrous, 4	CTD_diseases	6
MESH:C536918	MESH:C536918	Tibia absent polydactyly arachnoid cyst	CTD_diseases	6
MESH:C536936	MESH:C536936	Ulnar hypoplasia lobster claw deformity of feet	CTD_diseases	6
MESH:C536943	MESH:C536943	NOG-Related-Symphalangism Spectrum Disorder	CTD_diseases	6
MESH:C536962	MESH:C536962	Timothy syndrome	CTD_diseases	6
MESH:C536968	MESH:C536968	Torsion dystonia 7	CTD_diseases	6
MESH:C536973	MESH:C536973	Total Hypotrichosis, Mari type	CTD_diseases	6
MESH:C536976	MESH:C536976	Tracheal agenesis without tracheoesophageal fistula	CTD_diseases	6
MESH:C536979	MESH:C536979	Transient bullous dermolysis of the newborn	CTD_diseases	6
MESH:C536980	MESH:C536980	Transient erythroblastopenia of childhood	CTD_diseases	6
MESH:C537006	MESH:C537006	Leiomyoma of vulva and esophagus	CTD_diseases	6
MESH:C537007	MESH:C537007	Kaposiform Hemangioendothelioma	CTD_diseases	6
MESH:C537017	MESH:C537017	Bulbospinal neuronopathy, X-linked recessive	CTD_diseases	6
MESH:C537021	MESH:C537021	Kenny-Caffey syndrome, Type 1	CTD_diseases	6
MESH:C537027	MESH:C537027	Lipoid congenital adrenal hyperplasia	CTD_diseases	6
MESH:C537030	MESH:C537030	Lipomyelomeningocele	CTD_diseases	6
MESH:C537034	MESH:C537034	Long QT syndrome type 3	CTD_diseases	6
MESH:C537042	MESH:C537042	Albinism deafness syndrome	CTD_diseases	6
MESH:C537045	MESH:C537045	Albright's hereditary osteodystrophy	CTD_diseases	6
MESH:C537046	MESH:C537046	Aldred syndrome	CTD_diseases	6
MESH:C537047	MESH:C537047	Allan-Herndon-Dudley syndrome	CTD_diseases	6
MESH:C537055	MESH:C537055	Alopecia universalis	CTD_diseases	6
MESH:C537077	MESH:C537077	Febrile Ulceronecrotic Mucha-Habermann disease	CTD_diseases	6
MESH:C537088	MESH:C537088	Brachydactyly type A1	CTD_diseases	6
MESH:C537089	MESH:C537089	Brachydactyly type A2	CTD_diseases	6
MESH:C537090	MESH:C537090	Brachydactyly type A3	CTD_diseases	6
MESH:C537092	MESH:C537092	Brachydactyly type A6	CTD_diseases	6
MESH:C537093	MESH:C537093	Brachydactyly type C	CTD_diseases	6
MESH:C537094	MESH:C537094	Brachydactyly types B and E combined	CTD_diseases	6
MESH:C537097	MESH:C537097	Brachymesophalangy 2 and 5	CTD_diseases	6
MESH:C537108	MESH:C537108	Chromosome 21 monosomy	CTD_diseases	6
MESH:C537124	MESH:C537124	Optic atrophy 1 and deafness	CTD_diseases	6
MESH:C537126	MESH:C537126	Optic atrophy 5	CTD_diseases	6
MESH:C537127	MESH:C537127	Optic atrophy 6	CTD_diseases	6
MESH:C537133	MESH:C537133	Orofaciodigital syndrome 4	CTD_diseases	6
MESH:C537134	MESH:C537134	Orofaciodigital syndrome type1	CTD_diseases	6
MESH:C537139	MESH:C537139	Osler-rendu-weber syndrome 2	CTD_diseases	6
MESH:C537140	MESH:C537140	Osler-rendu-weber syndrome 3	CTD_diseases	6
MESH:C537142	MESH:C537142	Ossicular Malformations, familial	CTD_diseases	6
MESH:C537148	MESH:C537148	Hypodontia, X-linked	CTD_diseases	6
MESH:C537152	MESH:C537152	Hypomagnesemia 2, renal	CTD_diseases	6
MESH:C537154	MESH:C537154	Hypomandibular faciocranial dysostosis	CTD_diseases	6
MESH:C537170	MESH:C537170	Paraomphalocele	CTD_diseases	6
MESH:C537177	MESH:C537177	Parkinson disease 9	CTD_diseases	6
MESH:C537180	MESH:C537180	Familial paroxysmal dystonia	CTD_diseases	6
MESH:C537181	MESH:C537181	Paroxysmal nonkinesigenic dyskinesia	CTD_diseases	6
MESH:C537195	MESH:C537195	Spinocerebellar ataxia 13	CTD_diseases	6
MESH:C537196	MESH:C537196	Spinocerebellar ataxia 14	CTD_diseases	6
MESH:C537197	MESH:C537197	Sensorimotor neuropathy with ataxia, autosomal dominant	CTD_diseases	6
MESH:C537198	MESH:C537198	Spinocerebellar ataxia 19	CTD_diseases	6
MESH:C537200	MESH:C537200	Spinocerebellar ataxia 21	CTD_diseases	6
MESH:C537201	MESH:C537201	Spinocerebellar ataxia 23	CTD_diseases	6
MESH:C537204	MESH:C537204	Spinocerebellar ataxia 27	CTD_diseases	6
MESH:C537205	MESH:C537205	Spinocerebellar ataxia 28	CTD_diseases	6
MESH:C537206	MESH:C537206	Spinocerebellar Ataxia 29	CTD_diseases	6
MESH:C537214	MESH:C537214	Konigsmark Knox Hussels syndrome	CTD_diseases	6
MESH:C537235	MESH:C537235	Santos Mateus Leal syndrome	CTD_diseases	6
MESH:C537243	MESH:C537243	Prostate cancer, familial	CTD_diseases	6
MESH:C537247	MESH:C537247	Hemochromatosis, type 2	CTD_diseases	6
MESH:C537248	MESH:C537248	Hemochromatosis, type 3	CTD_diseases	6
MESH:C537249	MESH:C537249	Hemochromatosis, type 4	CTD_diseases	6
MESH:C537250	MESH:C537250	Hemophagocytic lymphohistiocytosis, familial, 2	CTD_diseases	6
MESH:C537251	MESH:C537251	Hemophagocytic lymphohistiocytosis, familial, 3	CTD_diseases	6
MESH:C537252	MESH:C537252	Hemophagocytic lymphohistiocytosis, familial, 4	CTD_diseases	6
MESH:C537256	MESH:C537256	Vascular purpura	CTD_diseases	6
MESH:C537277	MESH:C537277	Glycosylphosphatidylinositol deficiency	CTD_diseases	6
MESH:C537295	MESH:C537295	Granulomatous Angiitis of the Central Nervous System	CTD_diseases	6
MESH:C537307	MESH:C537307	Spinocerebellar ataxia 8	CTD_diseases	6
MESH:C537308	MESH:C537308	Spinocerebellar ataxia, autosomal recessive 1	CTD_diseases	6
MESH:C537309	MESH:C537309	Spinocerebellar ataxia, autosomal recessive 3	CTD_diseases	6
MESH:C537310	MESH:C537310	Spinocerebellar ataxia, autosomal recessive 4	CTD_diseases	6
MESH:C537311	MESH:C537311	Spinocerebellar ataxia, autosomal recessive 5	CTD_diseases	6
MESH:C537312	MESH:C537312	Spinocerebellar ataxia, autosomal recessive 6	CTD_diseases	6
MESH:C537313	MESH:C537313	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy	CTD_diseases	6
MESH:C537314	MESH:C537314	Spinocerebellar ataxia, X-linked, 2	CTD_diseases	6
MESH:C537316	MESH:C537316	Spinocerebellar ataxia, X-linked, 4	CTD_diseases	6
MESH:C537323	MESH:C537323	Microcephaly autosomal dominant	CTD_diseases	6
MESH:C537328	MESH:C537328	Shprintzen Golberg craniosynostosis	CTD_diseases	6
MESH:C537334	MESH:C537334	Sideroblastic anemia, autosomal	CTD_diseases	6
MESH:C537337	MESH:C537337	Silicosiderosis	CTD_diseases	6
MESH:C537338	MESH:C537338	Sillence syndrome	CTD_diseases	6
MESH:C537342	MESH:C537342	Single upper central incisor	CTD_diseases	6
MESH:C537373	MESH:C537373	Multicystic renal dysplasia, bilateral	CTD_diseases	6
MESH:C537380	MESH:C537380	Multiple synostoses syndrome 2	CTD_diseases	6
MESH:C537381	MESH:C537381	Multiple system atrophy (MSA) with orthostatic hypotension	CTD_diseases	6
MESH:C537384	MESH:C537384	Muscular dystrophy congenital, merosin negative	CTD_diseases	6
MESH:C537387	MESH:C537387	Neurocutaneous melanosis	CTD_diseases	6
MESH:C537393	MESH:C537393	Neurofibromatosis-Noonan syndrome	CTD_diseases	6
MESH:C537405	MESH:C537405	Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate	CTD_diseases	6
MESH:C537418	MESH:C537418	Opitz trigonocephaly syndrome	CTD_diseases	6
MESH:C537419	MESH:C537419	Bohring syndrome	CTD_diseases	6
MESH:C537422	MESH:C537422	Apparent mineralocorticoid excess	CTD_diseases	6
MESH:C537423	MESH:C537423	Apraxia, oculomotor, Cogan type	CTD_diseases	6
MESH:C537440	MESH:C537440	Arterial calcification of infancy	CTD_diseases	6
MESH:C537445	MESH:C537445	Mental retardation Smith Fineman Myers type	CTD_diseases	6
MESH:C537447	MESH:C537447	Mental retardation syndrome, Belgian type	CTD_diseases	6
MESH:C537448	MESH:C537448	Mental retardation Wolff type	CTD_diseases	6
MESH:C537461	MESH:C537461	Merlob Grunebaum Reisner syndrome	CTD_diseases	6
MESH:C537477	MESH:C537477	Mitochondrial neurogastrointestinal encephalopathy syndrome	CTD_diseases	6
MESH:C537479	MESH:C537479	Mixed sclerosing bone dystrophy	CTD_diseases	6
MESH:C537480	MESH:C537480	Miyoshi myopathy	CTD_diseases	6
MESH:C537481	MESH:C537481	Spastic diplegia infantile type	CTD_diseases	6
MESH:C537486	MESH:C537486	Spastic paraplegia 14, autosomal recessive	CTD_diseases	6
MESH:C537491	MESH:C537491	Stewart Treves syndrome	CTD_diseases	6
MESH:C537497	MESH:C537497	Stoll Alembik Dott syndrome	CTD_diseases	6
MESH:C537504	MESH:C537504	Kousseff Nichols syndrome	CTD_diseases	6
MESH:C537538	MESH:C537538	Segmentation syndrome 1	CTD_diseases	6
MESH:C537542	MESH:C537542	Microcephaly nonsyndromal	CTD_diseases	6
MESH:C537545	MESH:C537545	Microcephaly sparse hair mental retardation seizures	CTD_diseases	6
MESH:C537546	MESH:C537546	Microcephaly with spastic quadriplegia	CTD_diseases	6
MESH:C537548	MESH:C537548	Galloway Mowat syndrome	CTD_diseases	6
MESH:C537563	MESH:C537563	Jankovic Rivera syndrome	CTD_diseases	6
MESH:C537571	MESH:C537571	Jeune syndrome	CTD_diseases	6
MESH:C537581	MESH:C537581	Senior-Loken syndrome 4	CTD_diseases	6
MESH:C537582	MESH:C537582	Sennetsu Fever	CTD_diseases	6
MESH:C537583	MESH:C537583	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis	CTD_diseases	6
MESH:C537605	MESH:C537605	Rhabdomyosarcoma of the orbit	CTD_diseases	6
MESH:C537612	MESH:C537612	RHYNS syndrome	CTD_diseases	6
MESH:C537613	MESH:C537613	Ribbing disease	CTD_diseases	6
MESH:C537626	MESH:C537626	Hagemoser Weinstein Bresnick syndrome	CTD_diseases	6
MESH:C537627	MESH:C537627	Keratosis palmoplantaris with periodontopathia and onychogryposis	CTD_diseases	6
MESH:C537629	MESH:C537629	HAIR-AN syndrome	CTD_diseases	6
MESH:C537634	MESH:C537634	Chromosome 3, trisomy 3q13 2 q25	CTD_diseases	6
MESH:C537642	MESH:C537642	Chromosome 4, partial trisomy distal 4q	CTD_diseases	6
MESH:C537644	MESH:C537644	Chromosome 4, trisomy 4q	CTD_diseases	6
MESH:C537645	MESH:C537645	Chromosome 4, trisomy 4q21	CTD_diseases	6
MESH:C537646	MESH:C537646	Chromosome 4, trisomy 4q25 qter	CTD_diseases	6
MESH:C537647	MESH:C537647	Chromosome 5, monosomy 5q35	CTD_diseases	6
MESH:C537649	MESH:C537649	Chromosome 5, trisomy 5pter p13 3	CTD_diseases	6
MESH:C537650	MESH:C537650	Chromosome 5, trisomy 5q	CTD_diseases	6
MESH:C537655	MESH:C537655	Basal cell carcinoma, infundibulocystic	CTD_diseases	6
MESH:C537665	MESH:C537665	Beardwell syndrome	CTD_diseases	6
MESH:C537684	MESH:C537684	Genoa syndrome	CTD_diseases	6
MESH:C537690	MESH:C537690	Juberg Hayward syndrome	CTD_diseases	6
MESH:C537699	MESH:C537699	Nephronophthisis, familial juvenile	CTD_diseases	6
MESH:C537714	MESH:C537714	MacDermot Winter syndrome	CTD_diseases	6
MESH:C537716	MESH:C537716	Macrocephaly mesodermal hamartoma spectrum	CTD_diseases	6
MESH:C537717	MESH:C537717	Macrocephaly, benign familial	CTD_diseases	6
MESH:C537750	MESH:C537750	Oncocytoma, renal	CTD_diseases	6
MESH:C537757	MESH:C537757	Renal hypouricemia	CTD_diseases	6
MESH:C537760	MESH:C537760	Renoprival hypertension	CTD_diseases	6
MESH:C537761	MESH:C537761	Renpenning syndrome 1	CTD_diseases	6
MESH:C537762	MESH:C537762	Chromosome 5, uniparental disomy	CTD_diseases	6
MESH:C537776	MESH:C537776	Anterior spinal artery stroke	CTD_diseases	6
MESH:C537783	MESH:C537783	Aortic aneurysm, familial thoracic 3	CTD_diseases	6
MESH:C537784	MESH:C537784	Aortic aneurysm, familial thoracic 4	CTD_diseases	6
MESH:C537792	MESH:C537792	Axial osteosclerosis	CTD_diseases	6
MESH:C537794	MESH:C537794	Baby rattle pelvic dysplasia	CTD_diseases	6
MESH:C537811	MESH:C537811	Chromosome 6, trisomy 6p	CTD_diseases	6
MESH:C537812	MESH:C537812	Chromosome 6, trisomy 6q	CTD_diseases	6
MESH:C537819	MESH:C537819	Chromosome 7, trisomy 7p	CTD_diseases	6
MESH:C537820	MESH:C537820	Chromosome 7, trisomy 7p13 p12 2	CTD_diseases	6
MESH:C537821	MESH:C537821	Chromosome 7, trisomy 7q	CTD_diseases	6
MESH:C537822	MESH:C537822	Chromosome 7, trisomy mosaic	CTD_diseases	6
MESH:C537823	MESH:C537823	Chromosome 8 deletion	CTD_diseases	6
MESH:C537832	MESH:C537832	Macular dystrophy, atypical vitelliform	CTD_diseases	6
MESH:C537837	MESH:C537837	Benign symmetrical lipomatosis	CTD_diseases	6
MESH:C537846	MESH:C537846	Noonan like syndrome	CTD_diseases	6
MESH:C537847	MESH:C537847	Noonan syndrome 3	CTD_diseases	6
MESH:C537848	MESH:C537848	Norman Roberts lissencephaly syndrome	CTD_diseases	6
MESH:C537852	MESH:C537852	Nuchal bleb, familial	CTD_diseases	6
MESH:C537853	MESH:C537853	Nystagmus 1, congenital, X- linked	CTD_diseases	6
MESH:C537854	MESH:C537854	Nystagmus 2, congenital, autosomal dominant	CTD_diseases	6
MESH:C537855	MESH:C537855	Nystagmus 3, congenital, autosomal dominant	CTD_diseases	6
MESH:C537856	MESH:C537856	Nystagmus 4, congenital, autosomal dominant	CTD_diseases	6
MESH:C537871	MESH:C537871	Laron syndrome type 2	CTD_diseases	6
MESH:C537876	MESH:C537876	Laryngeal papillomatosis	CTD_diseases	6
MESH:C537882	MESH:C537882	Laurence Prosser Rocker syndrome	CTD_diseases	6
MESH:C537894	MESH:C537894	Phacomatosis pigmentovascularis	CTD_diseases	6
MESH:C537904	MESH:C537904	Bantu siderosis	CTD_diseases	6
MESH:C537909	MESH:C537909	Bardet-Biedl syndrome 1	CTD_diseases	6
MESH:C537910	MESH:C537910	Bardet-Biedl syndrome 2	CTD_diseases	6
MESH:C537911	MESH:C537911	Bardet-Biedl syndrome 3	CTD_diseases	6
MESH:C537912	MESH:C537912	Bardet-Biedl syndrome 4	CTD_diseases	6
MESH:C537930	MESH:C537930	Fibular aplasia ectrodactyly	CTD_diseases	6
MESH:C537931	MESH:C537931	Fibular hypoplasia and complex brachydactyly	CTD_diseases	6
MESH:C537932	MESH:C537932	Filaminopathy, autosomal dominant	CTD_diseases	6
MESH:C537937	MESH:C537937	Fitzsimmons Walson Mellor syndrome	CTD_diseases	6
MESH:C537938	MESH:C537938	Fitzsimmons-Guilbert syndrome	CTD_diseases	6
MESH:C537940	MESH:C537940	Chromosome 8, mosaic trisomy	CTD_diseases	6
MESH:C537941	MESH:C537941	Chromosome 8, partial trisomy	CTD_diseases	6
MESH:C537942	MESH:C537942	Chromosome 8, trisomy	CTD_diseases	6
MESH:C537944	MESH:C537944	Cerebral hemorrhage with amyloidosis, hereditary, Dutch type	CTD_diseases	6
MESH:C537945	MESH:C537945	Cerebral palsy, spastic, diplegic	CTD_diseases	6
MESH:C537964	MESH:C537964	Camera Marugo Cohen syndrome	CTD_diseases	6
MESH:C537978	MESH:C537978	Camurati Engelmann disease, type 2	CTD_diseases	6
MESH:C537979	MESH:C537979	Candidiasis familial chronic mucocutaneous, autosomal recessive	CTD_diseases	6
MESH:C537980	MESH:C537980	CANOMAD syndrome	CTD_diseases	6
MESH:C537996	MESH:C537996	Dysgnathia complex	CTD_diseases	6
MESH:C538002	MESH:C538002	Dystonia 15, myoclonic	CTD_diseases	6
MESH:C538003	MESH:C538003	Dystonia 6, torsion	CTD_diseases	6
MESH:C538004	MESH:C538004	Dystonia musculorum deformans 4	CTD_diseases	6
MESH:C538005	MESH:C538005	Dystonia musculorum deformans type 1	CTD_diseases	6
MESH:C538006	MESH:C538006	Dystonia musculorum deformans type 2	CTD_diseases	6
MESH:C538013	MESH:C538013	Early-onset ataxia with oculomotor apraxia and hypoalbuminemia	CTD_diseases	6
MESH:C538019	MESH:C538019	Chromosome 8, trisomy 8p	CTD_diseases	6
MESH:C538020	MESH:C538020	Chromosome 8, trisomy 8q	CTD_diseases	6
MESH:C538026	MESH:C538026	Chromosome 9, partial trisomy 9p	CTD_diseases	6
MESH:C538028	MESH:C538028	Chromosome 9, trisomy	CTD_diseases	6
MESH:C538029	MESH:C538029	Chromosome 9, trisomy 9p	CTD_diseases	6
MESH:C538030	MESH:C538030	Chromosome 9, trisomy 9q	CTD_diseases	6
MESH:C538032	MESH:C538032	Chromosome 14q, proximal duplication	CTD_diseases	6
MESH:C538034	MESH:C538034	Chromosome 14q, terminal duplication	CTD_diseases	6
MESH:C538037	MESH:C538037	Chromosome 15, trisomy mosaicism	CTD_diseases	6
MESH:C538040	MESH:C538040	Chromosome 15q, trisomy	CTD_diseases	6
MESH:C538041	MESH:C538041	Chromosome 16, trisomy	CTD_diseases	6
MESH:C538042	MESH:C538042	Chromosome 16, trisomy 16q	CTD_diseases	6
MESH:C538043	MESH:C538043	Chromosome 16, uniparental disomy	CTD_diseases	6
MESH:C538044	MESH:C538044	Chromosome 17 trisomy	CTD_diseases	6
MESH:C538048	MESH:C538048	Chromosome 17, trisomy 17p	CTD_diseases	6
MESH:C538049	MESH:C538049	Deafness oligodontia syndrome	CTD_diseases	6
MESH:C538054	MESH:C538054	Aerobic actinomyces infection	CTD_diseases	6
MESH:C538059	MESH:C538059	Agnathia-microstomia-synotia	CTD_diseases	6
MESH:C538068	MESH:C538068	Fructosuria	CTD_diseases	6
MESH:C538071	MESH:C538071	Fuchs atrophia gyrata chorioideae et retinae	CTD_diseases	6
MESH:C538082	MESH:C538082	Chromosome 1, q42 11 q42 12 duplication	CTD_diseases	6
MESH:C538083	MESH:C538083	Chromosome 1, trisomy 1q32 qter	CTD_diseases	6
MESH:C538084	MESH:C538084	Chromosome 1, trisomy 1q42 qter	CTD_diseases	6
MESH:C538085	MESH:C538085	Chromosome 1, uniparental disomy 1q12 q21	CTD_diseases	6
MESH:C538092	MESH:C538092	Pachygyria, frontotemporal	CTD_diseases	6
MESH:C538094	MESH:C538094	Pachyonychia congenita recessive	CTD_diseases	6
MESH:C538095	MESH:C538095	Pacman dysplasia	CTD_diseases	6
MESH:C538101	MESH:C538101	Paine syndrome	CTD_diseases	6
MESH:C538107	MESH:C538107	Palmer Pagon syndrome	CTD_diseases	6
MESH:C538112	MESH:C538112	Hernandez Aguirre-Negrete syndrome	CTD_diseases	6
MESH:C538118	MESH:C538118	Hidradenitis suppurativa, familial	CTD_diseases	6
MESH:C538120	MESH:C538120	Hirschsprung disease polydactyly heart disease	CTD_diseases	6
MESH:C538133	MESH:C538133	Lactate dehydrogenase deficiency type A	CTD_diseases	6
MESH:C538134	MESH:C538134	Lactic acidosis congenital infantile	CTD_diseases	6
MESH:C538156	MESH:C538156	Synostoses, tarsal, carpal, and digital	CTD_diseases	6
MESH:C538171	MESH:C538171	Acquired agranulocytosis	CTD_diseases	6
MESH:C538173	MESH:C538173	Acquired angioedema	CTD_diseases	6
MESH:C538174	MESH:C538174	Acquired hypoprothrombinemia	CTD_diseases	6
MESH:C538177	MESH:C538177	Acrocallosal syndrome, Schinzel type	CTD_diseases	6
MESH:C538182	MESH:C538182	Acrofacial dysostosis Catania form	CTD_diseases	6
MESH:C538185	MESH:C538185	Acrofacial dysostosis, Palagonia type	CTD_diseases	6
MESH:C538192	MESH:C538192	Furlong syndrome	CTD_diseases	6
MESH:C538204	MESH:C538204	Deafness, congenital onychodystrophy, recessive form	CTD_diseases	6
MESH:C538211	MESH:C538211	Dens in dente and palatal invaginations	CTD_diseases	6
MESH:C538213	MESH:C538213	Dentin dysplasia sclerotic bones	CTD_diseases	6
MESH:C538215	MESH:C538215	Dentin dysplasia, type 1	CTD_diseases	6
MESH:C538216	MESH:C538216	Dentinogenesis imperfecta, shields type 3	CTD_diseases	6
MESH:C538230	MESH:C538230	Adenocarcinoid tumor	CTD_diseases	6
MESH:C538231	MESH:C538231	Adenocarcinoma of lung	CTD_diseases	6
MESH:C538232	MESH:C538232	Adenosarcoma of the uterus	CTD_diseases	6
MESH:C538241	MESH:C538241	Amelogenesis imperfecta nephrocalcinosis	CTD_diseases	6
MESH:C538247	MESH:C538247	Amish lethal microcephaly	CTD_diseases	6
MESH:C538249	MESH:C538249	Amyloidosis, familial visceral	CTD_diseases	6
MESH:C538251	MESH:C538251	Amyotrophic lateral sclerosis, type 6	CTD_diseases	6
MESH:C538253	MESH:C538253	Amyotrophy, monomelic	CTD_diseases	6
MESH:C538255	MESH:C538255	Anaplastic small cell lymphoma	CTD_diseases	6
MESH:C538277	MESH:C538277	Prata Libéral Gonçalves syndrome	CTD_diseases	6
MESH:C538290	MESH:C538290	Chromosome 10, trisomy 10p	CTD_diseases	6
MESH:C538291	MESH:C538291	Chromosome 10, trisomy 10pter p13	CTD_diseases	6
MESH:C538292	MESH:C538292	Chromosome 10, uniparental disomy of	CTD_diseases	6
MESH:C538294	MESH:C538294	Chromosome 11, partial trisomy 11q	CTD_diseases	6
MESH:C538297	MESH:C538297	Chromosome 11q trisomy	CTD_diseases	6
MESH:C538299	MESH:C538299	Chromosome 12, 12p trisomy	CTD_diseases	6
MESH:C538300	MESH:C538300	Chromosome 12, trisomy 12q	CTD_diseases	6
MESH:C538307	MESH:C538307	Chromosome 18, trisomy 18p	CTD_diseases	6
MESH:C538308	MESH:C538308	Chromosome 18, trisomy 18q	CTD_diseases	6
MESH:C538311	MESH:C538311	Chromosome 19, trisomy 19q	CTD_diseases	6
MESH:C538312	MESH:C538312	Chromosome 1q, duplication 1q12 q21	CTD_diseases	6
MESH:C538318	MESH:C538318	Chromosome 2, trisomy 2p	CTD_diseases	6
MESH:C538319	MESH:C538319	Hirschsprung disease type d brachydactyly	CTD_diseases	6
MESH:C538329	MESH:C538329	Inclusion body myopathy autosomal recessive	CTD_diseases	6
MESH:C538334	MESH:C538334	Nakajo syndrome	CTD_diseases	6
MESH:C538341	MESH:C538341	Intestinal Pseudoobstruction with Patent Ductus Arteriosus and Natal Teeth	CTD_diseases	6
MESH:C538348	MESH:C538348	Nemaline myopathy 1	CTD_diseases	6
MESH:C538349	MESH:C538349	Nemaline Myopathy 2	CTD_diseases	6
MESH:C538350	MESH:C538350	Nemaline myopathy 3	CTD_diseases	6
MESH:C538351	MESH:C538351	Nemaline myopathy 4	CTD_diseases	6
MESH:C538353	MESH:C538353	Potassium aggravated myotonia	CTD_diseases	6
MESH:C538363	MESH:C538363	Retinal cone dystrophy 2	CTD_diseases	6
MESH:C538365	MESH:C538365	Retinitis pigmentosa 1	CTD_diseases	6
MESH:C538367	MESH:C538367	Mirhosseini-Holmes-Walton syndrome	CTD_diseases	6
MESH:C538386	MESH:C538386	Hypertelorism and tetralogy of Fallot	CTD_diseases	6
MESH:C538397	MESH:C538397	Nemaline myopathy 5	CTD_diseases	6
MESH:C538398	MESH:C538398	Nemaline myopathy 6	CTD_diseases	6
MESH:C538402	MESH:C538402	Aspartylglucosamidase (AGA) deficiency	CTD_diseases	6
MESH:C538411	MESH:C538411	Diaphyseal dysplasia 1, progressive	CTD_diseases	6
MESH:C538437	MESH:C538437	Immuno-hemolytic anemia	CTD_diseases	6
MESH:C538461	MESH:C538461	Supravalvar aortic stenosis, eisenberg type	CTD_diseases	6
MESH:C538481	MESH:C538481	Acquired CJD	CTD_diseases	6
MESH:C538496	MESH:C538496	Dilated cardiomyopathy, neutropenia, skeletal myopathy, and abnormal mitochondria	CTD_diseases	6
MESH:C538499	MESH:C538499	Erythema migrans	CTD_diseases	6
MESH:C538521	MESH:C538521	Bilateral temporal lobe disorder	CTD_diseases	6
MESH:C538525	MESH:C538525	Mitochondrial encephalopathy	CTD_diseases	6
MESH:C538543	MESH:C538543	Preeclamptic toxemia	CTD_diseases	6
MESH:C538550	MESH:C538550	Subvalvular aortic stenosis, Eisenberg type	CTD_diseases	6
MESH:C538585	MESH:C538585	Oral-facial-digital syndrome, type 2	CTD_diseases	6
MESH:C538586	MESH:C538586	Hyperostosis frontalis interna, obesity, shortness and cognitive impairment	CTD_diseases	6
MESH:C538595	MESH:C538595	Mermaid syndrome	CTD_diseases	6
MESH:C538604	MESH:C538604	Pericardial constriction with growth failure	CTD_diseases	6
MESH:C538617	MESH:C538617	Thrombocytopenia Paris-Trousseau type	CTD_diseases	6
MESH:C538618	MESH:C538618	Donath-Landsteiner hemolytic anemia	CTD_diseases	6
MESH:C538620	MESH:C538620	Acute brachial neuritis	CTD_diseases	6
MESH:C538670	MESH:C538670	X-linked infantile spasm syndrome	CTD_diseases	6
MESH:C538679	MESH:C538679	Transient antero-apical dyskinesia	CTD_diseases	6
MESH:C538682	MESH:C538682	Hyperkeratosis of the palms and soles and esophageal papillomas	CTD_diseases	6
MESH:C539067	MESH:C539067	Amoebic dysentery due to Entamoeba histolytica	CTD_diseases	6
MESH:C540309	MESH:C540309	Abetalipoproteinemia neuropathy	CTD_diseases	6
MESH:C540322	MESH:C540322	Hemorrhagic jaundice	CTD_diseases	6
MESH:C542540	MESH:C542540	Spinocerebellar ataxia 22	CTD_diseases	6
MESH:C544351	MESH:C544351	Idiopathic orthostatic hypotension	CTD_diseases	6
MESH:C548034	MESH:C548034	Orofaciodigital Syndrome 12	CTD_diseases	6
MESH:C548035	MESH:C548035	Orofaciodigital Syndrome 13	CTD_diseases	6
MESH:C548075	MESH:C548075	Pseudohypoparathyroidism Type 1B	CTD_diseases	6
MESH:C548076	MESH:C548076	Pseudohypoparathyroidism Type 1C	CTD_diseases	6
MESH:C548077	MESH:C548077	Pseudohypoparathyroidism Type 2	CTD_diseases	6
MESH:C548081	MESH:C548081	Noonan Syndrome 2	CTD_diseases	6
MESH:C548082	MESH:C548082	Noonan Syndrome 4	CTD_diseases	6
MESH:C548083	MESH:C548083	Noonan Syndrome 5	CTD_diseases	6
MESH:C548084	MESH:C548084	Noonan Syndrome 6	CTD_diseases	6
MESH:C549759	MESH:C549759	Phyllodes Tumor of the Prostate	CTD_diseases	6
MESH:C554497	MESH:C554497	Non-AIDS-related Kaposi sarcoma	CTD_diseases	6
MESH:C554498	MESH:C554498	AIDS-related Kaposi sarcoma	CTD_diseases	6
MESH:C557674	MESH:C557674	SeSAME syndrome	CTD_diseases	6
MESH:C557675	MESH:C557675	Congenital tracheomalacia	CTD_diseases	6
MESH:C557817	MESH:C557817	Orofaciodigital syndrome 3	CTD_diseases	6
MESH:C557819	MESH:C557819	Orofaciodigital syndrome 5	CTD_diseases	6
MESH:C557820	MESH:C557820	Orofaciodigital syndrome 8	CTD_diseases	6
MESH:C557821	MESH:C557821	Orofaciodigital syndrome 11	CTD_diseases	6
MESH:C562385	MESH:C562385	Iron-Refractory Iron Deficiency Anemia	CTD_diseases	6
MESH:C562408	MESH:C562408	Radioulnar Synostosis	CTD_diseases	6
MESH:C562420	MESH:C562420	Brachydactyly, Type D	CTD_diseases	6
MESH:C562424	MESH:C562424	Ehlers-Danlos Syndrome, Autosomal Dominant, Type Unspecified	CTD_diseases	6
MESH:C562429	MESH:C562429	Polydactyly, Postaxial	CTD_diseases	6
MESH:C562434	MESH:C562434	Cerebrooculofacioskeletal Syndrome 1	CTD_diseases	6
MESH:C562440	MESH:C562440	Hypophosphatasia, Childhood	CTD_diseases	6
MESH:C562442	MESH:C562442	Mucopolysaccharidoses, Unclassified Types	CTD_diseases	6
MESH:C562460	MESH:C562460	Synesthesia	CTD_diseases	6
MESH:C562464	MESH:C562464	Polyposis, Gastric	CTD_diseases	6
MESH:C567282	MESH:C567282	Lipodystrophy, Congenital Generalized, Type 3	CTD_diseases	6
MESH:C567284	MESH:C567284	Diabetes Mellitus, Insulin-Dependent, 22	CTD_diseases	6
MESH:C567285	MESH:C567285	Diabetes Mellitus, Insulin-Dependent, 21	CTD_diseases	6
MESH:C567286	MESH:C567286	Diabetes Mellitus, Insulin-Dependent, 20	CTD_diseases	6
MESH:C567292	MESH:C567292	Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome	CTD_diseases	6
MESH:C567309	MESH:C567309	Scoliosis, Arachnodactyly, And Blindness	CTD_diseases	6
MESH:C567317	MESH:C567317	Alopecia, Androgenetic, 3	CTD_diseases	6
MESH:C567328	MESH:C567328	Coloboma, Ocular, And Ichthyosis, Brain Malformations, And Endocrine Abnormalities	CTD_diseases	6
MESH:C567353	MESH:C567353	Thrombophilia, Hereditary, Due To Protein C Deficiency, Autosomal Recessive	CTD_diseases	6
MESH:C567369	MESH:C567369	Retinitis Pigmentosa, Late-Onset Dominant	CTD_diseases	6
MESH:C567371	MESH:C567371	Generalized Epilepsy With Febrile Seizures Plus, Type 6	CTD_diseases	6
MESH:C567382	MESH:C567382	Crouzon Syndrome With Acanthosis Nigricans	CTD_diseases	6
MESH:C567385	MESH:C567385	Chromosome 10q23 Deletion Syndrome	CTD_diseases	6
MESH:C567393	MESH:C567393	Maturity-Onset Diabetes Of The Young, Type 9	CTD_diseases	6
MESH:C567403	MESH:C567403	Retinitis Pigmentosa 29	CTD_diseases	6
MESH:C567407	MESH:C567407	Cardiomyopathy, Dilated, 1AA	CTD_diseases	6
MESH:C567408	MESH:C567408	Epidermolysis Bullosa Simplex With Pyloric Atresia	CTD_diseases	6
MESH:C567410	MESH:C567410	Orofacial Cleft 11	CTD_diseases	6
MESH:C567422	MESH:C567422	Retinitis Pigmentosa 41	CTD_diseases	6
MESH:C567426	MESH:C567426	Hypouricemia, Renal, 2	CTD_diseases	6
MESH:C567429	MESH:C567429	Amyotrophic Lateral Sclerosis 10	CTD_diseases	6
MESH:C567437	MESH:C567437	Congenital Disorder Of Glycosylation, Type In	CTD_diseases	6
MESH:C567447	MESH:C567447	Prostate Cancer, Hereditary, 15	CTD_diseases	6
MESH:C567448	MESH:C567448	Prostate Cancer, Hereditary, 14	CTD_diseases	6
MESH:C567449	MESH:C567449	Prostate Cancer, Hereditary, 11	CTD_diseases	6
MESH:C567455	MESH:C567455	Camptodactyly Syndrome, Guadalajara, Type III	CTD_diseases	6
MESH:C567456	MESH:C567456	Prostate Cancer, Hereditary, 13	CTD_diseases	6
MESH:C567459	MESH:C567459	Episodic Ataxia, Type 7	CTD_diseases	6
MESH:C567466	MESH:C567466	Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia	CTD_diseases	6
MESH:C567473	MESH:C567473	Alopecia, Androgenetic, 2	CTD_diseases	6
MESH:C567474	MESH:C567474	Mental Retardation, X-Linked, Syndromic 9	CTD_diseases	6
MESH:C567499	MESH:C567499	Amyotrophic Lateral Sclerosis 9	CTD_diseases	6
MESH:C567501	MESH:C567501	Aortic Aneurysm, Familial Abdominal 3	CTD_diseases	6
MESH:C567505	MESH:C567505	Cardiomyopathy, Dilated, 2a	CTD_diseases	6
MESH:C567506	MESH:C567506	Cardiomyopathy, Dilated, 1z	CTD_diseases	6
MESH:C567507	MESH:C567507	Cardiomyopathy, Dilated, 1y	CTD_diseases	6
MESH:C567513	MESH:C567513	Long Qt Syndrome 11	CTD_diseases	6
MESH:C567514	MESH:C567514	Long Qt Syndrome 10	CTD_diseases	6
MESH:C567515	MESH:C567515	Long Qt Syndrome 9	CTD_diseases	6
MESH:C567523	MESH:C567523	Retinitis Pigmentosa 2	CTD_diseases	6
MESH:C567527	MESH:C567527	Ehlers-Danlos Syndrome, Type VII, Autosomal Recessive	CTD_diseases	6
MESH:C567528	MESH:C567528	Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency	CTD_diseases	6
MESH:C567535	MESH:C567535	Megalencephaly	CTD_diseases	6
MESH:C567548	MESH:C567548	Orofacial Cleft 12	CTD_diseases	6
MESH:C567575	MESH:C567575	46,Xy True Hermaphroditism, Sry-Related	CTD_diseases	6
MESH:C567614	MESH:C567614	Demyer Sequence	CTD_diseases	6
MESH:C567620	MESH:C567620	Vertigo, Benign Recurrent, 1	CTD_diseases	6
MESH:C567642	MESH:C567642	Lipodystrophy, Congenital Generalized, Type 4	CTD_diseases	6
MESH:C567645	MESH:C567645	Miyoshi Muscular Dystrophy 3	CTD_diseases	6
MESH:C567646	MESH:C567646	Miyoshi Muscular Dystrophy 2	CTD_diseases	6
MESH:C567654	MESH:C567654	Cardiomyopathy, Dilated, 1FF	CTD_diseases	6
MESH:C567656	MESH:C567656	Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2	CTD_diseases	6
MESH:C567674	MESH:C567674	Corneal Dystrophy, Fuchs Endothelial, 7	CTD_diseases	6
MESH:C567675	MESH:C567675	Corneal Dystrophy, Fuchs Endothelial, 6	CTD_diseases	6
MESH:C567676	MESH:C567676	Corneal Dystrophy, Fuchs Endothelial, 5	CTD_diseases	6
MESH:C567677	MESH:C567677	Corneal Dystrophy, Fuchs Endothelial, 4	CTD_diseases	6
MESH:C567678	MESH:C567678	Corneal Dystrophy, Fuchs Endothelial, 3	CTD_diseases	6
MESH:C567682	MESH:C567682	Tsc2 Angiomyolipomas, Renal, Modifier Of	CTD_diseases	6
MESH:C567683	MESH:C567683	Cardiomyopathy, Dilated, 1EE	CTD_diseases	6
MESH:C567688	MESH:C567688	Factor XIII, B Subunit, Deficiency Of	CTD_diseases	6
MESH:C567690	MESH:C567690	Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3	CTD_diseases	6
MESH:C567691	MESH:C567691	Factor Xiii, A Subunit, Deficiency Of	CTD_diseases	6
MESH:C567696	MESH:C567696	Bernard-Soulier Syndrome, Autosomal Dominant	CTD_diseases	6
MESH:C567698	MESH:C567698	Cone-Rod Dystrophy 13	CTD_diseases	6
MESH:C567699	MESH:C567699	Amyotrophic Lateral Sclerosis 6, Autosomal Recessive	CTD_diseases	6
MESH:C567708	MESH:C567708	Muscular Dystrophy, Congenital, Lmna-Related	CTD_diseases	6
MESH:C567709	MESH:C567709	Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency	CTD_diseases	6
MESH:C567712	MESH:C567712	Retinitis Pigmentosa, Concentric	CTD_diseases	6
MESH:C567714	MESH:C567714	Mental Retardation, Autosomal Recessive 13	CTD_diseases	6
MESH:C567725	MESH:C567725	Cardiomyopathy, Dilated, 1DD	CTD_diseases	6
MESH:C567733	MESH:C567733	Cardiomyopathy, Dilated, 1CC	CTD_diseases	6
MESH:C567744	MESH:C567744	Convulsions, Benign Familial Neonatal, 1, And/Or Myokymia	CTD_diseases	6
MESH:C567745	MESH:C567745	Epilepsy, Benign Neonatal, 1, Atypical Severe	CTD_diseases	6
MESH:C567746	MESH:C567746	Convulsions, Benign Familial Neonatal, 1, Atypical Severe	CTD_diseases	6
MESH:C567749	MESH:C567749	Vertigo, Benign Recurrent, 2	CTD_diseases	6
MESH:C567752	MESH:C567752	Hemophagocytic Lymphohistiocytosis, Familial, 5	CTD_diseases	6
MESH:C567758	MESH:C567758	Cone Dystrophy 4	CTD_diseases	6
MESH:C567779	MESH:C567779	Candidiasis, Familial, 1	CTD_diseases	6
MESH:C567781	MESH:C567781	Bifid Nose, Autosomal Dominant	CTD_diseases	6
MESH:C567789	MESH:C567789	Basal Cell Carcinoma, Nonsyndromic	CTD_diseases	6
MESH:C567809	MESH:C567809	Glycogen Storage Disease IXC	CTD_diseases	6
MESH:C567818	MESH:C567818	Diabetes Mellitus, Insulin-Dependent, 24	CTD_diseases	6
MESH:C567820	MESH:C567820	Febrile Convulsions, Familial, 3a	CTD_diseases	6
MESH:C567821	MESH:C567821	Febrile Convulsions, Familial, 3b	CTD_diseases	6
MESH:C567827	MESH:C567827	Generalized Epilepsy With Febrile Seizures Plus, 7	CTD_diseases	6
MESH:C567833	MESH:C567833	Optic Atrophy 7	CTD_diseases	6
MESH:C567839	MESH:C567839	Multiple Synostoses Syndrome 3	CTD_diseases	6
MESH:C567842	MESH:C567842	Long Qt Syndrome 12	CTD_diseases	6
MESH:C567853	MESH:C567853	Cerebral Palsy, Spastic Quadriplegic, 1	CTD_diseases	6
MESH:C567854	MESH:C567854	Retinitis Pigmentosa 42	CTD_diseases	6
MESH:C567857	MESH:C567857	Congenital Disorder of Glycosylation, Type Io	CTD_diseases	6
MESH:C567858	MESH:C567858	Spastic Paraplegia-50, Autosomal Recessive	CTD_diseases	6
MESH:C567859	MESH:C567859	Glycogen Storage Disease XIV	CTD_diseases	6
MESH:C567861	MESH:C567861	Glycogen Storage Disease XIII	CTD_diseases	6
MESH:C567867	MESH:C567867	Cerebral Palsy, Spastic Quadriplegic, 2	CTD_diseases	6
MESH:C567877	MESH:C567877	Cardiomyopathy, Dilated, 1BB	CTD_diseases	6
MESH:C567925	MESH:C567925	Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant	CTD_diseases	6
MESH:C567935	MESH:C567935	Hypothyroidism, Congenital, Nongoitrous, 3	CTD_diseases	6
MESH:C569516	MESH:C569516	Trichophyton infection	CTD_diseases	6
MESH:C569627	MESH:C569627	Cold Hypersensitivity	CTD_diseases	6
MESH:C573012	MESH:C573012	Lactic Acidosis, Congenital Infantile, Due To LAD Deficiency	CTD_diseases	6
MESH:C576203	MESH:C576203	Alcohol fetopathy	CTD_diseases	6
MESH:C576976	MESH:C576976	Hypothyroidism, Congenital, Nongoitrous, 1	CTD_diseases	6
MESH:C579887	MESH:C579887	African Hemochromatosis	CTD_diseases	6
MESH:C579935	MESH:C579935	Autosomal Recessive Primary Microcephaly	CTD_diseases	6
MESH:C579978	MESH:C579978	Catsper1-Related Nonsyndromic Male Infertility	CTD_diseases	6
MESH:C580009	MESH:C580009	Congenital Deafness with Labyrinthine Aplasia, Microtia, and Microdontia	CTD_diseases	6
MESH:C580047	MESH:C580047	Dmd-Associated Dilated Cardiomyopathy	CTD_diseases	6
MESH:C580049	MESH:C580049	Dopa-Responsive Dystonia	CTD_diseases	6
MESH:C580065	MESH:C580065	Episodic Ataxia	CTD_diseases	6
MESH:C580075	MESH:C580075	Familial Acute Myeloid Leukemia with Mutated Cebpa	CTD_diseases	6
MESH:C580095	MESH:C580095	Familial Osteochondritis Dissecans	CTD_diseases	6
MESH:C580130	MESH:C580130	Glycogen Storage Disease Type Ix	CTD_diseases	6
MESH:C580335	MESH:C580335	Nonsyndromic Holoprosencephaly	CTD_diseases	6
MESH:C580364	MESH:C580364	Pdgfra-Associated Chronic Eosinophilic Leukemia	CTD_diseases	6
MESH:C580365	MESH:C580365	Pdgfrb-Associated Chronic Eosinophilic Leukemia	CTD_diseases	6
MESH:C580453	MESH:C580453	Spastic Paraplegia Type 11	CTD_diseases	6
MESH:C580455	MESH:C580455	Spastic Paraplegia Type 3a	CTD_diseases	6
MESH:C580456	MESH:C580456	Spastic Paraplegia Type 4	CTD_diseases	6
MESH:C580457	MESH:C580457	Spastic Paraplegia Type 7	CTD_diseases	6
MESH:C580458	MESH:C580458	Spastic Paraplegia Type 8	CTD_diseases	6
MESH:C580500	MESH:C580500	Trisomy 18	CTD_diseases	6
MESH:D000006	MESH:D000006	Abdomen, Acute	CTD_diseases	6
MESH:D000039	MESH:D000039	Peritonsillar Abscess	CTD_diseases	6
MESH:D000052	MESH:D000052	Acanthosis Nigricans	CTD_diseases	6
MESH:D000231	MESH:D000231	Adenocarcinoma, Papillary	CTD_diseases	6
MESH:D000370	MESH:D000370	Ageusia	CTD_diseases	6
MESH:D000377	MESH:D000377	Agnosia	CTD_diseases	6
MESH:D000419	MESH:D000419	Albuminuria	CTD_diseases	6
MESH:D000506	MESH:D000506	Alopecia Areata	CTD_diseases	6
MESH:D000567	MESH:D000567	Amelogenesis Imperfecta	CTD_diseases	6
MESH:D000608	MESH:D000608	Renal Aminoacidurias	CTD_diseases	6
MESH:D000742	MESH:D000742	Anemia, Dyserythropoietic, Congenital	CTD_diseases	6
MESH:D000746	MESH:D000746	Anemia, Hemolytic, Congenital Nonspherocytic	CTD_diseases	6
MESH:D000752	MESH:D000752	Anemia, Pernicious	CTD_diseases	6
MESH:D000754	MESH:D000754	Anemia, Refractory, with Excess of Blasts	CTD_diseases	6
MESH:D000858	MESH:D000858	Anovulation	CTD_diseases	6
MESH:D000874	MESH:D000874	Anthracosilicosis	CTD_diseases	6
MESH:D001005	MESH:D001005	Anus Neoplasms	CTD_diseases	6
MESH:D001028	MESH:D001028	Aortopulmonary Septal Defect	CTD_diseases	6
MESH:D001164	MESH:D001164	Arteriovenous Fistula	CTD_diseases	6
MESH:D001196	MESH:D001196	Ascariasis	CTD_diseases	6
MESH:D001198	MESH:D001198	Ascaridiasis	CTD_diseases	6
MESH:D001206	MESH:D001206	Ascorbic Acid Deficiency	CTD_diseases	6
MESH:D001228	MESH:D001228	Aspergillosis	CTD_diseases	6
MESH:D001250	MESH:D001250	Asthma, Exercise-Induced	CTD_diseases	6
MESH:D001329	MESH:D001329	Autolysis	CTD_diseases	6
MESH:D001752	MESH:D001752	Blast Crisis	CTD_diseases	6
MESH:D001766	MESH:D001766	Blindness	CTD_diseases	6
MESH:D001913	MESH:D001913	Bowen's Disease	CTD_diseases	6
MESH:D001989	MESH:D001989	Bronchiolitis Obliterans	CTD_diseases	6
MESH:D002276	MESH:D002276	Carcinoid Tumor	CTD_diseases	6
MESH:D002282	MESH:D002282	Adenocarcinoma, Bronchiolo-Alveolar	CTD_diseases	6
MESH:D002283	MESH:D002283	Carcinoma, Bronchogenic	CTD_diseases	6
MESH:D002292	MESH:D002292	Carcinoma, Renal Cell	CTD_diseases	6
MESH:D002293	MESH:D002293	Adenocarcinoma, Scirrhous	CTD_diseases	6
MESH:D002341	MESH:D002341	Carotid Artery Thrombosis	CTD_diseases	6
MESH:D002472	MESH:D002472	Cell Transformation, Viral	CTD_diseases	6
MESH:D002527	MESH:D002527	Myoclonic Cerebellar Dyssynergia	CTD_diseases	6
MESH:D002539	MESH:D002539	Cerebral Arterial Diseases	CTD_diseases	6
MESH:D002543	MESH:D002543	Cerebral Hemorrhage	CTD_diseases	6
MESH:D002546	MESH:D002546	Ischemic Attack, Transient	CTD_diseases	6
MESH:D002551	MESH:D002551	Cerebral Ventricle Neoplasms	CTD_diseases	6
MESH:D002575	MESH:D002575	Uterine Cervicitis	CTD_diseases	6
MESH:D002579	MESH:D002579	Uterine Cervical Erosion	CTD_diseases	6
MESH:D002583	MESH:D002583	Uterine Cervical Neoplasms	CTD_diseases	6
MESH:D002602	MESH:D002602	Chancroid	CTD_diseases	6
MESH:D002607	MESH:D002607	Charcot-Marie-Tooth Disease	CTD_diseases	6
MESH:D002640	MESH:D002640	Chiari-Frommel Syndrome	CTD_diseases	6
MESH:D002872	MESH:D002872	Chromosome Deletion	CTD_diseases	6
MESH:D003085	MESH:D003085	Colic	CTD_diseases	6
MESH:D003112	MESH:D003112	Colonic Pseudo-Obstruction	CTD_diseases	6
MESH:D003117	MESH:D003117	Color Vision Defects	CTD_diseases	6
MESH:D003218	MESH:D003218	Condylomata Acuminata	CTD_diseases	6
MESH:D003235	MESH:D003235	Conjunctivitis, Inclusion	CTD_diseases	6
MESH:D003528	MESH:D003528	Carcinoma, Adenoid Cystic	CTD_diseases	6
MESH:D003923	MESH:D003923	Diabetes Mellitus, Lipoatrophic	CTD_diseases	6
MESH:D003926	MESH:D003926	Diabetic Coma	CTD_diseases	6
MESH:D003963	MESH:D003963	Diaper Rash	CTD_diseases	6
MESH:D004062	MESH:D004062	DiGeorge Syndrome	CTD_diseases	6
MESH:D004165	MESH:D004165	Diphtheria	CTD_diseases	6
MESH:D004172	MESH:D004172	Diplopia	CTD_diseases	6
MESH:D004239	MESH:D004239	Diverticulitis, Colonic	CTD_diseases	6
MESH:D004310	MESH:D004310	Double Outlet Right Ventricle	CTD_diseases	6
MESH:D004320	MESH:D004320	Dracunculiasis	CTD_diseases	6
MESH:D004381	MESH:D004381	Duodenal Ulcer	CTD_diseases	6
MESH:D004408	MESH:D004408	Dysgeusia	CTD_diseases	6
MESH:D004612	MESH:D004612	Elliptocytosis, Hereditary	CTD_diseases	6
MESH:D004614	MESH:D004614	Emaciation	CTD_diseases	6
MESH:D004652	MESH:D004652	Empty Sella Syndrome	CTD_diseases	6
MESH:D004673	MESH:D004673	Encephalomyelitis, Acute Disseminated	CTD_diseases	6
MESH:D004694	MESH:D004694	Endocardial Cushion Defects	CTD_diseases	6
MESH:D004819	MESH:D004819	Epidermodysplasia Verruciformis	CTD_diseases	6
MESH:D004830	MESH:D004830	Epilepsy, Tonic-Clonic	CTD_diseases	6
MESH:D004832	MESH:D004832	Epilepsy, Absence	CTD_diseases	6
MESH:D004833	MESH:D004833	Epilepsy, Temporal Lobe	CTD_diseases	6
MESH:D004931	MESH:D004931	Esophageal Achalasia	CTD_diseases	6
MESH:D005350	MESH:D005350	Fibroma	CTD_diseases	6
MESH:D005358	MESH:D005358	Fibrous Dysplasia, Monostotic	CTD_diseases	6
MESH:D005359	MESH:D005359	Fibrous Dysplasia, Polyostotic	CTD_diseases	6
MESH:D005368	MESH:D005368	Filariasis	CTD_diseases	6
MESH:D005401	MESH:D005401	Fissure in Ano	CTD_diseases	6
MESH:D005633	MESH:D005633	Fructose Intolerance	CTD_diseases	6
MESH:D005729	MESH:D005729	Ganglioneuroma	CTD_diseases	6
MESH:D005764	MESH:D005764	Gastroesophageal Reflux	CTD_diseases	6
MESH:D005885	MESH:D005885	Gingival Hyperplasia	CTD_diseases	6
MESH:D005886	MESH:D005886	Gingival Hypertrophy	CTD_diseases	6
MESH:D005888	MESH:D005888	Gingival Pocket	CTD_diseases	6
MESH:D005910	MESH:D005910	Glioma	CTD_diseases	6
MESH:D005921	MESH:D005921	Glomerulonephritis	CTD_diseases	6
MESH:D005953	MESH:D005953	Glycogen Storage Disease Type I	CTD_diseases	6
MESH:D006009	MESH:D006009	Glycogen Storage Disease Type II	CTD_diseases	6
MESH:D006010	MESH:D006010	Glycogen Storage Disease Type III	CTD_diseases	6
MESH:D006011	MESH:D006011	Glycogen Storage Disease Type IV	CTD_diseases	6
MESH:D006012	MESH:D006012	Glycogen Storage Disease Type V	CTD_diseases	6
MESH:D006013	MESH:D006013	Glycogen Storage Disease Type VI	CTD_diseases	6
MESH:D006014	MESH:D006014	Glycogen Storage Disease Type VII	CTD_diseases	6
MESH:D006030	MESH:D006030	Glycosuria, Renal	CTD_diseases	6
MESH:D006060	MESH:D006060	Gonadal Dysgenesis, Mixed	CTD_diseases	6
MESH:D006061	MESH:D006061	Gonadal Dysgenesis, 46,XY	CTD_diseases	6
MESH:D006210	MESH:D006210	Hallermann's Syndrome	CTD_diseases	6
MESH:D006212	MESH:D006212	Hallucinations	CTD_diseases	6
MESH:D006232	MESH:D006232	Hand, Foot and Mouth Disease	CTD_diseases	6
MESH:D006344	MESH:D006344	Heart Septal Defects, Atrial	CTD_diseases	6
MESH:D006345	MESH:D006345	Heart Septal Defects, Ventricular	CTD_diseases	6
MESH:D006423	MESH:D006423	Hemianopsia	CTD_diseases	6
MESH:D006456	MESH:D006456	Hemoglobinuria	CTD_diseases	6
MESH:D006483	MESH:D006483	Hemorrhagic Septicemia	CTD_diseases	6
MESH:D006557	MESH:D006557	Herpangina	CTD_diseases	6
MESH:D006725	MESH:D006725	Hookworm Infections	CTD_diseases	6
MESH:D006828	MESH:D006828	Hydatidiform Mole	CTD_diseases	6
MESH:D006850	MESH:D006850	Hydrocephalus, Normal Pressure	CTD_diseases	6
MESH:D006930	MESH:D006930	Hyperalgesia	CTD_diseases	6
MESH:D006937	MESH:D006937	Hypercholesterolemia	CTD_diseases	6
MESH:D006939	MESH:D006939	Hyperemesis Gravidarum	CTD_diseases	6
MESH:D006941	MESH:D006941	Hyperesthesia	CTD_diseases	6
MESH:D006951	MESH:D006951	Hyperlipoproteinemias	CTD_diseases	6
MESH:D006964	MESH:D006964	Hyperpituitarism	CTD_diseases	6
MESH:D006972	MESH:D006972	Hypertelorism	CTD_diseases	6
MESH:D006978	MESH:D006978	Hypertension, Renovascular	CTD_diseases	6
MESH:D006987	MESH:D006987	Hypesthesia	CTD_diseases	6
MESH:D006995	MESH:D006995	Hypobetalipoproteinemias	CTD_diseases	6
MESH:D007012	MESH:D007012	Hypopharyngeal Neoplasms	CTD_diseases	6
MESH:D007018	MESH:D007018	Hypopituitarism	CTD_diseases	6
MESH:D007088	MESH:D007088	Illusions	CTD_diseases	6
MESH:D007340	MESH:D007340	Insulinoma	CTD_diseases	6
MESH:D007418	MESH:D007418	Intestinal Pseudo-Obstruction	CTD_diseases	6
MESH:D007617	MESH:D007617	Kaposi Varicelliform Eruption	CTD_diseases	6
MESH:D007669	MESH:D007669	Kidney Calculi	CTD_diseases	6
MESH:D007690	MESH:D007690	Polycystic Kidney Diseases	CTD_diseases	6
MESH:D007691	MESH:D007691	Medullary Sponge Kidney	CTD_diseases	6
MESH:D007806	MESH:D007806	Language Disorders	CTD_diseases	6
MESH:D007816	MESH:D007816	Larva Migrans, Visceral	CTD_diseases	6
MESH:D007873	MESH:D007873	Legg-Calve-Perthes Disease	CTD_diseases	6
MESH:D007898	MESH:D007898	Leishmaniasis, Visceral	CTD_diseases	6
MESH:D007911	MESH:D007911	Lentigo	CTD_diseases	6
MESH:D007918	MESH:D007918	Leprosy	CTD_diseases	6
MESH:D007947	MESH:D007947	Leukemia, Megakaryoblastic, Acute	CTD_diseases	6
MESH:D007948	MESH:D007948	Leukemia, Monocytic, Acute	CTD_diseases	6
MESH:D007973	MESH:D007973	Leukorrhea	CTD_diseases	6
MESH:D008059	MESH:D008059	Mucopolysaccharidosis I	CTD_diseases	6
MESH:D008224	MESH:D008224	Lymphoma, Follicular	CTD_diseases	6
MESH:D008338	MESH:D008338	Mandibular Injuries	CTD_diseases	6
MESH:D008342	MESH:D008342	Mandibulofacial Dysostosis	CTD_diseases	6
MESH:D008363	MESH:D008363	alpha-Mannosidosis	CTD_diseases	6
MESH:D008457	MESH:D008457	Measles	CTD_diseases	6
MESH:D008532	MESH:D008532	Megacolon, Toxic	CTD_diseases	6
MESH:D008557	MESH:D008557	Melorheostosis	CTD_diseases	6
MESH:D008583	MESH:D008583	Meningitis, Haemophilus	CTD_diseases	6
MESH:D008585	MESH:D008585	Meningitis, Meningococcal	CTD_diseases	6
MESH:D008586	MESH:D008586	Meningitis, Pneumococcal	CTD_diseases	6
MESH:D008594	MESH:D008594	Menopause, Premature	CTD_diseases	6
MESH:D008796	MESH:D008796	Metrorrhagia	CTD_diseases	6
MESH:D008881	MESH:D008881	Migraine Disorders	CTD_diseases	6
MESH:D008924	MESH:D008924	Mite Infestations	CTD_diseases	6
MESH:D009084	MESH:D009084	Mucopolysaccharidosis III	CTD_diseases	6
MESH:D009085	MESH:D009085	Mucopolysaccharidosis IV	CTD_diseases	6
MESH:D009087	MESH:D009087	Mucopolysaccharidosis VI	CTD_diseases	6
MESH:D009103	MESH:D009103	Multiple Sclerosis	CTD_diseases	6
MESH:D009107	MESH:D009107	Mumps	CTD_diseases	6
MESH:D009165	MESH:D009165	Mycobacterium Infections, Nontuberculous	CTD_diseases	6
MESH:D009198	MESH:D009198	Myiasis	CTD_diseases	6
MESH:D009395	MESH:D009395	Nephritis, Interstitial	CTD_diseases	6
MESH:D009402	MESH:D009402	Nephrosis, Lipoid	CTD_diseases	6
MESH:D009404	MESH:D009404	Nephrotic Syndrome	CTD_diseases	6
MESH:D009442	MESH:D009442	Neurilemmoma	CTD_diseases	6
MESH:D009455	MESH:D009455	Neurofibroma	CTD_diseases	6
MESH:D009463	MESH:D009463	Neuroma	CTD_diseases	6
MESH:D009503	MESH:D009503	Neutropenia	CTD_diseases	6
MESH:D009507	MESH:D009507	Nevus of Ota	CTD_diseases	6
MESH:D009631	MESH:D009631	Nonodontogenic Cysts	CTD_diseases	6
MESH:D009755	MESH:D009755	Night Blindness	CTD_diseases	6
MESH:D009767	MESH:D009767	Obesity, Morbid	CTD_diseases	6
MESH:D009807	MESH:D009807	Odontogenic Cysts	CTD_diseases	6
MESH:D009814	MESH:D009814	Oesophagostomiasis	CTD_diseases	6
MESH:D009845	MESH:D009845	Oligospermia	CTD_diseases	6
MESH:D009869	MESH:D009869	Oophoritis	CTD_diseases	6
MESH:D009956	MESH:D009956	Psittacosis	CTD_diseases	6
MESH:D009959	MESH:D009959	Oropharyngeal Neoplasms	CTD_diseases	6
MESH:D010016	MESH:D010016	Osteoma	CTD_diseases	6
MESH:D010022	MESH:D010022	Osteopetrosis	CTD_diseases	6
MESH:D010123	MESH:D010123	Oxyuriasis	CTD_diseases	6
MESH:D010178	MESH:D010178	Pancoast Syndrome	CTD_diseases	6
MESH:D010202	MESH:D010202	Panophthalmitis	CTD_diseases	6
MESH:D010235	MESH:D010235	Paraganglioma	CTD_diseases	6
MESH:D010249	MESH:D010249	Parametritis	CTD_diseases	6
MESH:D010284	MESH:D010284	Paratyphoid Fever	CTD_diseases	6
MESH:D010292	MESH:D010292	Paresthesia	CTD_diseases	6
MESH:D010302	MESH:D010302	Parkinson Disease, Secondary	CTD_diseases	6
MESH:D010439	MESH:D010439	Peptic Ulcer Perforation	CTD_diseases	6
MESH:D010482	MESH:D010482	Periapical Abscess	CTD_diseases	6
MESH:D010484	MESH:D010484	Periapical Granuloma	CTD_diseases	6
MESH:D010591	MESH:D010591	Phantom Limb	CTD_diseases	6
MESH:D010871	MESH:D010871	Pinealoma	CTD_diseases	6
MESH:D010899	MESH:D010899	Pituitary Apoplexy	CTD_diseases	6
MESH:D010930	MESH:D010930	Plague	CTD_diseases	6
MESH:D011000	MESH:D011000	Pleurodynia, Epidemic	CTD_diseases	6
MESH:D011004	MESH:D011004	Plummer-Vinson Syndrome	CTD_diseases	6
MESH:D011017	MESH:D011017	Pneumonia, Lipid	CTD_diseases	6
MESH:D011018	MESH:D011018	Pneumonia, Pneumococcal	CTD_diseases	6
MESH:D011019	MESH:D011019	Pneumonia, Mycoplasma	CTD_diseases	6
MESH:D011040	MESH:D011040	Dermatitis, Toxicodendron	CTD_diseases	6
MESH:D011128	MESH:D011128	Polyradiculopathy	CTD_diseases	6
MESH:D011350	MESH:D011350	Proctocolitis	CTD_diseases	6
MESH:D011502	MESH:D011502	Protein-Energy Malnutrition	CTD_diseases	6
MESH:D011546	MESH:D011546	Pseudohypoaldosteronism	CTD_diseases	6
MESH:D011556	MESH:D011556	Pseudopseudohypoparathyroidism	CTD_diseases	6
MESH:D011702	MESH:D011702	Pyelitis	CTD_diseases	6
MESH:D012001	MESH:D012001	Hyperacusis	CTD_diseases	6
MESH:D012006	MESH:D012006	Rectovaginal Fistula	CTD_diseases	6
MESH:D012035	MESH:D012035	Refsum Disease	CTD_diseases	6
MESH:D012207	MESH:D012207	Rhabdomyoma	CTD_diseases	6
MESH:D012208	MESH:D012208	Rhabdomyosarcoma	CTD_diseases	6
MESH:D012215	MESH:D012215	Rheumatic Nodule	CTD_diseases	6
MESH:D012298	MESH:D012298	Rigor Mortis	CTD_diseases	6
MESH:D012488	MESH:D012488	Salpingitis	CTD_diseases	6
MESH:D012510	MESH:D012510	Sarcoma 180	CTD_diseases	6
MESH:D012511	MESH:D012511	Sarcoma 37	CTD_diseases	6
MESH:D012515	MESH:D012515	Mast-Cell Sarcoma	CTD_diseases	6
MESH:D012517	MESH:D012517	Sarcoma, Yoshida	CTD_diseases	6
MESH:D012585	MESH:D012585	Sciatica	CTD_diseases	6
MESH:D012607	MESH:D012607	Scotoma	CTD_diseases	6
MESH:D012811	MESH:D012811	Sigmoid Neoplasms	CTD_diseases	6
MESH:D012830	MESH:D012830	Silicotuberculosis	CTD_diseases	6
MESH:C562476	MESH:C562476	Hematuria, Benign Familial	CTD_diseases	6
MESH:C562538	MESH:C562538	Cerebrocostomandibular Syndrome	CTD_diseases	6
MESH:C562567	MESH:C562567	Leydig Cell Hypoplasia	CTD_diseases	6
MESH:C562573	MESH:C562573	Cyclopia	CTD_diseases	6
MESH:C562583	MESH:C562583	Gout, HPRT-Related	CTD_diseases	6
MESH:C562601	MESH:C562601	Lactose Intolerance, Adult Type	CTD_diseases	6
MESH:C562606	MESH:C562606	Nephrosialidosis	CTD_diseases	6
MESH:C562618	MESH:C562618	Porphyria, Acute Hepatic	CTD_diseases	6
MESH:C562625	MESH:C562625	Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant	CTD_diseases	6
MESH:C562626	MESH:C562626	Ehlers-Danlos Syndrome, Type VIII	CTD_diseases	6
MESH:C562637	MESH:C562637	Epidermolysis Bullosa Dystrophica Neurotrophica	CTD_diseases	6
MESH:C562638	MESH:C562638	Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails	CTD_diseases	6
MESH:C562639	MESH:C562639	Epidermolysis Bullosa, Junctional, Non-Herlitz Type	CTD_diseases	6
MESH:C562646	MESH:C562646	Hypophosphatasia, Infantile	CTD_diseases	6
MESH:C562647	MESH:C562647	Hypophosphatasia, Adult	CTD_diseases	6
MESH:C562683	MESH:C562683	Cystinosis, Late-Onset Juvenile or Adolescent Nephropathic Type	CTD_diseases	6
MESH:C562684	MESH:C562684	Hyper-Beta-Alaninemia	CTD_diseases	6
MESH:C562694	MESH:C562694	Epilepsy, Idiopathic Generalized	CTD_diseases	6
MESH:C562709	MESH:C562709	Insulin Receptor, Defect in	CTD_diseases	6
MESH:C562718	MESH:C562718	Glycogen Storage Disease XII	CTD_diseases	6
MESH:C562727	MESH:C562727	Dysfibrinogenemia, Congenital	CTD_diseases	6
MESH:C562729	MESH:C562729	Esophageal Squamous Cell Carcinoma	CTD_diseases	6
MESH:C562730	MESH:C562730	Adenocarcinoma Of Esophagus	CTD_diseases	6
MESH:C562759	MESH:C562759	Bundle Branch Block, Familial Isolated Complete Right	CTD_diseases	6
MESH:C562768	MESH:C562768	Hypothyroidism, Autoimmune	CTD_diseases	6
MESH:C562770	MESH:C562770	Thyroid Dyshormonogenesis 4	CTD_diseases	6
MESH:C562772	MESH:C562772	Mason-Type Diabetes	CTD_diseases	6
MESH:C562773	MESH:C562773	Diabetes Mellitus, Type Ii, Autosomal Dominant	CTD_diseases	6
MESH:C562805	MESH:C562805	Glycogen Storage Disease IC	CTD_diseases	6
MESH:C562831	MESH:C562831	Atrioventricular Septal Defect	CTD_diseases	6
MESH:C562833	MESH:C562833	Pulmonary Atresia With Ventricular Septal Defect	CTD_diseases	6
MESH:C562834	MESH:C562834	Aortic Aneurysm, Familial Thoracic 1	CTD_diseases	6
MESH:C562835	MESH:C562835	Intestinal Malrotation, Familial	CTD_diseases	6
MESH:C562839	MESH:C562839	Mesothelioma, Malignant	CTD_diseases	6
MESH:C562842	MESH:C562842	Carcinoid Tumors, Intestinal	CTD_diseases	6
MESH:C562844	MESH:C562844	Congenital Disorder Of Glycosylation, Type I/IIX	CTD_diseases	6
MESH:C562851	MESH:C562851	Hereditary Motor And Sensory Neuropathy VI	CTD_diseases	6
MESH:C562859	MESH:C562859	Vertigo, Benign Recurrent	CTD_diseases	6
MESH:C562861	MESH:C562861	Laryngeal Adductor Paralysis	CTD_diseases	6
MESH:C562869	MESH:C562869	Secretory Component Deficiency	CTD_diseases	6
MESH:C562902	MESH:C562902	Oligosynaptic Infertility	CTD_diseases	6
MESH:C562903	MESH:C562903	Male Infertility with Large-Headed, Multiflagellar, Polyploid Spermatozoa	CTD_diseases	6
MESH:C562961	MESH:C562961	Chondrodysplasia Punctata, Tibia-Metacarpal Type	CTD_diseases	6
MESH:C562973	MESH:C562973	Dysosteosclerosis	CTD_diseases	6
MESH:C562974	MESH:C562974	Craniofacial Dysostosis with Diaphyseal Hyperplasia	CTD_diseases	6
MESH:C563008	MESH:C563008	Glycogen Storage Disease IXB	CTD_diseases	6
MESH:C563030	MESH:C563030	Heinz Body Anemias	CTD_diseases	6
MESH:C563050	MESH:C563050	Alpha-Thalassemia Mental Retardation Syndrome, Deletion-Type	CTD_diseases	6
MESH:C563094	MESH:C563094	Mucopolysaccharidosis Type VIII	CTD_diseases	6
MESH:C563104	MESH:C563104	Orofaciodigital Syndrome VII	CTD_diseases	6
MESH:C563161	MESH:C563161	Hypertensive Nephropathy	CTD_diseases	6
MESH:C563164	MESH:C563164	Hernia, Double Inguinal	CTD_diseases	6
MESH:C563203	MESH:C563203	Anodontia of Permanent Dentition	CTD_diseases	6
MESH:C563206	MESH:C563206	Thyroid Dyshormonogenesis 2A	CTD_diseases	6
MESH:C563209	MESH:C563209	Hyaluronidase Deficiency	CTD_diseases	6
MESH:C563241	MESH:C563241	Chronic Motor Tics	CTD_diseases	6
MESH:C563248	MESH:C563248	Chondrodysplasia Punctata, Autosomal Dominant	CTD_diseases	6
MESH:C563250	MESH:C563250	Salivary Gland Adenoma, Pleomorphic	CTD_diseases	6
MESH:C563254	MESH:C563254	Presenile And Senile Dementia	CTD_diseases	6
MESH:C563258	MESH:C563258	Islet Cell Adenomatosis	CTD_diseases	6
MESH:C563278	MESH:C563278	Episodic Ataxia, Type 1	CTD_diseases	6
MESH:C563306	MESH:C563306	Cardiomyopathy, Dilated, 1D	CTD_diseases	6
MESH:C563307	MESH:C563307	Cardiomyopathy, Dilated, 1C	CTD_diseases	6
MESH:C563320	MESH:C563320	Retinitis Pigmentosa 18	CTD_diseases	6
MESH:C563323	MESH:C563323	Diabetes Mellitus, Noninsulin-Dependent, 2	CTD_diseases	6
MESH:C563326	MESH:C563326	Diabetes Mellitus, Insulin-Dependent, 12	CTD_diseases	6
MESH:C563331	MESH:C563331	Aprosencephaly and Cerebellar Dysgenesis	CTD_diseases	6
MESH:C563338	MESH:C563338	Amelia, Autosomal Recessive	CTD_diseases	6
MESH:C563352	MESH:C563352	Diabetes Mellitus, Insulin-Dependent, 13	CTD_diseases	6
MESH:C563359	MESH:C563359	Diabetes Mellitus, Noninsulin-Dependent, 1	CTD_diseases	6
MESH:C563371	MESH:C563371	Diabetes Mellitus, Insulin-Dependent, 11	CTD_diseases	6
MESH:C563384	MESH:C563384	Cardiomyopathy, Dilated, 1E	CTD_diseases	6
MESH:C563391	MESH:C563391	Laterality Defects, Autosomal Dominant	CTD_diseases	6
MESH:C563392	MESH:C563392	Rolandic Epilepsy, Mental Retardation, And Speech Dyspraxia, Autosomal Dominant	CTD_diseases	6
MESH:C563399	MESH:C563399	Epilepsy, Myoclonic, Benign Adult Familial, Type 1	CTD_diseases	6
MESH:C563408	MESH:C563408	Epidermolysis Bullosa Simplex, Autosomal Recessive	CTD_diseases	6
MESH:C563409	MESH:C563409	Arrhythmogenic Right Ventricular Dysplasia, Familial, 2	CTD_diseases	6
MESH:C563415	MESH:C563415	Cone-Rod Dystrophy 5	CTD_diseases	6
MESH:C563422	MESH:C563422	Palmoplantar Keratoderma, Nonepidermolytic	CTD_diseases	6
MESH:C563428	MESH:C563428	Long Qt Syndrome 4	CTD_diseases	6
MESH:C563433	MESH:C563433	Diabetes Mellitus, Insulin-Dependent, 8	CTD_diseases	6
MESH:C563437	MESH:C563437	Retinitis Pigmentosa 17	CTD_diseases	6
MESH:C563448	MESH:C563448	Orofacial Cleft 3	CTD_diseases	6
MESH:C563451	MESH:C563451	Maturity-Onset Diabetes of the Young, Type 4	CTD_diseases	6
MESH:C563455	MESH:C563455	Dermoid Cysts, Familial Frontonasal	CTD_diseases	6
MESH:C563468	MESH:C563468	Cleft Lip, Congenital Healed	CTD_diseases	6
MESH:C563469	MESH:C563469	Cone-Rod Dystrophy 1	CTD_diseases	6
MESH:C563477	MESH:C563477	Nephrolithiasis, Calcium Oxalate	CTD_diseases	6
MESH:C563491	MESH:C563491	Orofaciodigital Syndrome X	CTD_diseases	6
MESH:C563494	MESH:C563494	Optic Atrophy with Negative Electroretinograms	CTD_diseases	6
MESH:C563496	MESH:C563496	Optic Atrophy with Demyelinating Disease of CNS	CTD_diseases	6
MESH:C563499	MESH:C563499	Ophthalmoplegia, Familial Total, with Iris Transillumination	CTD_diseases	6
MESH:C563500	MESH:C563500	Ophthalmoplegia, Familial Static	CTD_diseases	6
MESH:C563508	MESH:C563508	Oculopharyngodistal Myopathy	CTD_diseases	6
MESH:C563513	MESH:C563513	Sick Sinus Syndrome 2, Autosomal Dominant	CTD_diseases	6
MESH:C563526	MESH:C563526	Retinitis Pigmentosa 27	CTD_diseases	6
MESH:C563529	MESH:C563529	Myopathy, Actin, Congenital, with Excess of Thin Myofilaments	CTD_diseases	6
MESH:C563530	MESH:C563530	Necrotizing Encephalomyelopathy, Subacute, of Leigh, Adult	CTD_diseases	6
MESH:C563538	MESH:C563538	Cardiomyopathy, Dilated, 1s	CTD_diseases	6
MESH:C563545	MESH:C563545	Continuous Muscle Fiber Activity, Hereditary	CTD_diseases	6
MESH:C563546	MESH:C563546	Myoglobinuria, Autosomal Dominant	CTD_diseases	6
MESH:C563549	MESH:C563549	Myoclonus, Cerebellar Ataxia, and Deafness	CTD_diseases	6
MESH:C563550	MESH:C563550	Myoclonic Epilepsy, Hartung Type	CTD_diseases	6
MESH:C563551	MESH:C563551	Myeloproliferative Syndrome, Transient	CTD_diseases	6
MESH:C563554	MESH:C563554	Muscular Dystrophy, Pseudohypertrophic, With Internalized Capillaries	CTD_diseases	6
MESH:C563558	MESH:C563558	Muscular Dystrophy, Barnes Type	CTD_diseases	6
MESH:C563559	MESH:C563559	Muscular Atrophy, Malignant Neurogenic	CTD_diseases	6
MESH:C563560	MESH:C563560	Spinal Muscular Atrophy, Childhood, Proximal, Autosomal Dominant	CTD_diseases	6
MESH:C563563	MESH:C563563	Muscle Cramps, Familial	CTD_diseases	6
MESH:C563569	MESH:C563569	Coronary Artery Disease, Development of, in HIV	CTD_diseases	6
MESH:C563573	MESH:C563573	Mitral Valve Prolapse, Myxomatous 1	CTD_diseases	6
MESH:C563579	MESH:C563579	Holoprosencephaly 2	CTD_diseases	6
MESH:C563614	MESH:C563614	Long Qt Syndrome 2	CTD_diseases	6
MESH:C563624	MESH:C563624	Lichen Planus, Familial	CTD_diseases	6
MESH:C563640	MESH:C563640	Lactic Acidosis, Chronic Adult Form	CTD_diseases	6
MESH:C563651	MESH:C563651	Kallmann Syndrome 2 with Cleft Lip or Palate	CTD_diseases	6
MESH:C563652	MESH:C563652	Kallmann Syndrome 2 with Bimanual Synkinesia	CTD_diseases	6
MESH:C563655	MESH:C563655	Mitral Valve Prolapse, Myxomatous 3	CTD_diseases	6
MESH:C563659	MESH:C563659	Holoprosencephaly 9	CTD_diseases	6
MESH:C563660	MESH:C563660	Holoprosencephaly 7	CTD_diseases	6
MESH:C563666	MESH:C563666	Congenital Disorder Of Glycosylation, Type Im	CTD_diseases	6
MESH:C563668	MESH:C563668	Alopecia-Mental Retardation Syndrome 2	CTD_diseases	6
MESH:C563671	MESH:C563671	Cone-Rod Dystrophy 11	CTD_diseases	6
MESH:C563675	MESH:C563675	Orofacial Cleft 9	CTD_diseases	6
MESH:C563676	MESH:C563676	Retinitis Pigmentosa 33	CTD_diseases	6
MESH:C563677	MESH:C563677	Spastic Paraplegia 30, Autosomal Recessive	CTD_diseases	6
MESH:C563678	MESH:C563678	Retinal Cone Dystrophy 3B	CTD_diseases	6
MESH:C563685	MESH:C563685	Retinitis Pigmentosa 31	CTD_diseases	6
MESH:C563688	MESH:C563688	Cardiomyopathy, Dilated, 1q	CTD_diseases	6
MESH:C563689	MESH:C563689	Retinitis Pigmentosa 32	CTD_diseases	6
MESH:C563690	MESH:C563690	Cardiomyopathy, Dilated, 1p	CTD_diseases	6
MESH:C563697	MESH:C563697	Parietal Foramina 3	CTD_diseases	6
MESH:C563699	MESH:C563699	Prostate Cancer, Hereditary, 6	CTD_diseases	6
MESH:C563708	MESH:C563708	Amyotrophic Lateral Sclerosis, Chmp2B-Related	CTD_diseases	6
MESH:C563712	MESH:C563712	Noncompaction of Left Ventricular Myocardium, Familial Isolated, Autosomal Dominant 2	CTD_diseases	6
MESH:C563716	MESH:C563716	Muscular Dystrophy, Congenital, Merosin-Positive	CTD_diseases	6
MESH:C563718	MESH:C563718	Myopathy, Myofibrillar, Zasp-Related	CTD_diseases	6
MESH:C563719	MESH:C563719	Generalized Epilepsy and Paroxysmal Dyskinesia	CTD_diseases	6
MESH:C563723	MESH:C563723	Holoprosencephaly 8	CTD_diseases	6
MESH:C563724	MESH:C563724	Preeclampsia Eclampsia 4	CTD_diseases	6
MESH:C563725	MESH:C563725	Preeclampsia Eclampsia 3	CTD_diseases	6
MESH:C563726	MESH:C563726	Preeclampsia Eclampsia 2	CTD_diseases	6
MESH:C563732	MESH:C563732	Spastic Paraplegia 28, Autosomal Recessive	CTD_diseases	6
MESH:C563733	MESH:C563733	Carotid Intimal Medial Thickness 1	CTD_diseases	6
MESH:C563744	MESH:C563744	Prostate Cancer, Hereditary, 5	CTD_diseases	6
MESH:C563762	MESH:C563762	Febrile Convulsions, Familial, 5	CTD_diseases	6
MESH:C563764	MESH:C563764	Febrile Convulsions, Familial, 6	CTD_diseases	6
MESH:C563784	MESH:C563784	Arrhythmogenic Right Ventricular Dysplasia, Familial, 7	CTD_diseases	6
MESH:C563808	MESH:C563808	Arrhythmogenic Right Ventricular Dysplasia, Familial, 9	CTD_diseases	6
MESH:C563813	MESH:C563813	Peripheral Cone Dystrophy	CTD_diseases	6
MESH:C563818	MESH:C563818	Ataxia, Sensory, Autosomal Dominant	CTD_diseases	6
MESH:C563834	MESH:C563834	Alzheimer Disease 9	CTD_diseases	6
MESH:C563843	MESH:C563843	Orofacial Cleft 5	CTD_diseases	6
MESH:C563844	MESH:C563844	Muscular Dystrophy, Congenital, Type 1D	CTD_diseases	6
MESH:C563853	MESH:C563853	Transposition of the Great Arteries, Dextro-Looped 1	CTD_diseases	6
MESH:C563856	MESH:C563856	Sudden Infant Death with Dysgenesis of the Testes Syndrome	CTD_diseases	6
MESH:C563870	MESH:C563870	Neuropathy, Hereditary Sensory and Autonomic, Adult-Onset, with Anosmia	CTD_diseases	6
MESH:C563871	MESH:C563871	Microcephaly, Primary Autosomal Recessive, 5	CTD_diseases	6
MESH:C563882	MESH:C563882	Prostate Cancer, Hereditary, 4	CTD_diseases	6
MESH:C563883	MESH:C563883	Prostate Cancer, Hereditary, 3	CTD_diseases	6
MESH:C563895	MESH:C563895	Amyotrophic Lateral Sclerosis 8	CTD_diseases	6
MESH:C563898	MESH:C563898	Oligodontia-Colorectal Cancer Syndrome	CTD_diseases	6
MESH:C563905	MESH:C563905	Ulnar/Fibular Ray Defect and Brachydactyly	CTD_diseases	6
MESH:C563906	MESH:C563906	Cardiomyopathy, Dilated, 1o	CTD_diseases	6
MESH:C563907	MESH:C563907	Sick Sinus Syndrome 1, Autosomal Recessive	CTD_diseases	6
MESH:C563909	MESH:C563909	Polydactyly, Postaxial, Type A4	CTD_diseases	6
MESH:C563929	MESH:C563929	Mental Retardation, Autosomal Recessive 3	CTD_diseases	6
MESH:C563933	MESH:C563933	Maturity-Onset Diabetes of the Young, Type 3	CTD_diseases	6
MESH:C563942	MESH:C563942	Aphalangia, Partial, with Syndactyly and Duplication of Metatarsal IV	CTD_diseases	6
MESH:C563957	MESH:C563957	Diabetes Mellitus, Insulin-Dependent, 7	CTD_diseases	6
MESH:C563958	MESH:C563958	Diabetes Mellitus, Insulin-Dependent, 5	CTD_diseases	6
MESH:C563959	MESH:C563959	Diabetes Mellitus, Insulin-Dependent, 4	CTD_diseases	6
MESH:C563960	MESH:C563960	Diabetes Mellitus, Insulin-Dependent, 3	CTD_diseases	6
MESH:C563966	MESH:C563966	Pick Complex	CTD_diseases	6
MESH:C563973	MESH:C563973	Hydrocephalus, Autosomal Dominant	CTD_diseases	6
MESH:C563977	MESH:C563977	Venous Malformations, Multiple Cutaneous and Mucosal	CTD_diseases	6
MESH:C563991	MESH:C563991	Retinitis Pigmentosa 11	CTD_diseases	6
MESH:C563992	MESH:C563992	Retinitis Pigmentosa 14	CTD_diseases	6
MESH:C563999	MESH:C563999	Retinitis Pigmentosa 12	CTD_diseases	6
MESH:C564000	MESH:C564000	Retinitis Pigmentosa with Paraarteriolar Preservation Of Retinal Pigment Epithelium	CTD_diseases	6
MESH:C564008	MESH:C564008	Retinitis Pigmentosa 13	CTD_diseases	6
MESH:C564009	MESH:C564009	Bladder Exstrophy and Epispadias Complex	CTD_diseases	6
MESH:C564018	MESH:C564018	Myoglobinuria, Recurrent	CTD_diseases	6
MESH:C564071	MESH:C564071	Pyruvate Dehydrogenase E1 Alpha Deficiency	CTD_diseases	6
MESH:C564084	MESH:C564084	Optic Atrophy Spastic Paraplegia Syndrome	CTD_diseases	6
MESH:C564096	MESH:C564096	Muscular Dystrophy, Mabry Type	CTD_diseases	6
MESH:C564099	MESH:C564099	Mental Retardation with Spastic Paraplegia	CTD_diseases	6
MESH:C564105	MESH:C564105	Fragile X Tremor Ataxia Syndrome	CTD_diseases	6
MESH:C564118	MESH:C564118	Jaundice, Familial Obstructive, of Infancy	CTD_diseases	6
MESH:C564169	MESH:C564169	Hereditary Renal Cancer Associated 1	CTD_diseases	6
MESH:C564174	MESH:C564174	Orthostatic Hypotensive Disorder, Streeten Type	CTD_diseases	6
MESH:C564180	MESH:C564180	Holoprosencephaly 4	CTD_diseases	6
MESH:C564181	MESH:C564181	Holoprosencephaly 3	CTD_diseases	6
MESH:C564193	MESH:C564193	Erythremia, Beta-Globin Type	CTD_diseases	6
MESH:C564195	MESH:C564195	Erythremia, Alpha-Globin Type	CTD_diseases	6
MESH:C564210	MESH:C564210	Granulomatous Disease, Chronic, Autosomal Dominant Type	CTD_diseases	6
MESH:C564219	MESH:C564219	Maturity-Onset Diabetes of the Young, Type 2	CTD_diseases	6
MESH:C564230	MESH:C564230	Glioma of Brain, Familial	CTD_diseases	6
MESH:C564247	MESH:C564247	Microcephaly, Primary Autosomal Recessive, 6	CTD_diseases	6
MESH:C564249	MESH:C564249	Retinitis Pigmentosa 26	CTD_diseases	6
MESH:C564251	MESH:C564251	Orofacial Cleft 4	CTD_diseases	6
MESH:C564269	MESH:C564269	Slowed Nerve Conduction Velocity, Autosomal Dominant	CTD_diseases	6
MESH:C564274	MESH:C564274	Epilepsy, Benign Neonatal, 3	CTD_diseases	6
MESH:C564277	MESH:C564277	Immunodeficiency With Hyper-Igm, Type 4	CTD_diseases	6
MESH:C564278	MESH:C564278	Synpolydactyly 2	CTD_diseases	6
MESH:C564284	MESH:C564284	Retinitis Pigmentosa 7	CTD_diseases	6
MESH:C564285	MESH:C564285	Pseudoxanthoma Elasticum, Modifier Of Severity Of	CTD_diseases	6
MESH:C564299	MESH:C564299	Diabetes Mellitus, Noninsulin-Dependent, Type 4	CTD_diseases	6
MESH:C564300	MESH:C564300	Amyotrophic Lateral Sclerosis 7	CTD_diseases	6
MESH:C564310	MESH:C564310	Retinitis Pigmentosa 30	CTD_diseases	6
MESH:C564313	MESH:C564313	Epilepsy, Myoclonic, Benign Adult Familial, Type 2	CTD_diseases	6
MESH:C564317	MESH:C564317	Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency	CTD_diseases	6
MESH:C564326	MESH:C564326	Mitral Valve Prolapse, Myxomatous 2	CTD_diseases	6
MESH:C564329	MESH:C564329	Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Unusual Plaques	CTD_diseases	6
MESH:C564330	MESH:C564330	Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia	CTD_diseases	6
MESH:C564342	MESH:C564342	Noonan-Like Syndrome With Loose Anagen Hair	CTD_diseases	6
MESH:C564344	MESH:C564344	Leukodystrophy, Dysmyelinating, with Oligodontia	CTD_diseases	6
MESH:C564368	MESH:C564368	Epidermolysis Bullosa Simplex Superficialis	CTD_diseases	6
MESH:C564375	MESH:C564375	Spastic Paraplegia 24, Autosomal Recessive	CTD_diseases	6
MESH:C564378	MESH:C564378	Spastic Paraplegia, Ataxia, And Mental Retardation	CTD_diseases	6
MESH:C564388	MESH:C564388	Cardiomyopathy, Dilated, 1N	CTD_diseases	6
MESH:C564390	MESH:C564390	Cardiomyopathy, Dilated, 1M	CTD_diseases	6
MESH:C564391	MESH:C564391	Newfoundland Rod-Cone Dystrophy	CTD_diseases	6
MESH:C564400	MESH:C564400	Arrhythmogenic Right Ventricular Dysplasia, Familial, 8	CTD_diseases	6
MESH:C564404	MESH:C564404	Mental Retardation, Autosomal Recessive 2	CTD_diseases	6
MESH:C564405	MESH:C564405	Hypouricemia, Familial Renal, due to Tubular Hypersecretion	CTD_diseases	6
MESH:C564417	MESH:C564417	Granulomatous Disease, Chronic, X-Linked	CTD_diseases	6
MESH:C564481	MESH:C564481	Chromosome Xp11.3 Deletion Syndrome	CTD_diseases	6
MESH:C564484	MESH:C564484	Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate	CTD_diseases	6
MESH:C564557	MESH:C564557	Radioulnar Synostosis, Radial Ray Abnormalities, and Severe Malformations in the Male	CTD_diseases	6
MESH:C564571	MESH:C564571	Noncompaction of Left Ventricular Myocardium, Familial Isolated, X-Linked	CTD_diseases	6
MESH:C564590	MESH:C564590	Polydactyly, Postaxial, Type A3	CTD_diseases	6
MESH:C564593	MESH:C564593	Gaze Palsy, Familial Horizontal, with Progressive Scoliosis	CTD_diseases	6
MESH:C564597	MESH:C564597	Cone-Rod Dystrophy 10	CTD_diseases	6
MESH:C564603	MESH:C564603	Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration	CTD_diseases	6
MESH:C564605	MESH:C564605	Epilepsy, Partial, with Pericentral Spikes	CTD_diseases	6
MESH:C564608	MESH:C564608	Thyroid Dyshormonogenesis 6	CTD_diseases	6
MESH:C564622	MESH:C564622	Alzheimer Disease 8	CTD_diseases	6
MESH:C564625	MESH:C564625	Congenital Disorder Of Glycosylation, Type IIID	CTD_diseases	6
MESH:C564627	MESH:C564627	Aortic Aneurysm, Familial Thoracic 2	CTD_diseases	6
MESH:C564631	MESH:C564631	Parkinson Disease 8	CTD_diseases	6
MESH:C564635	MESH:C564635	Brachydactyly, Type A1, B	CTD_diseases	6
MESH:C564640	MESH:C564640	Nephronophthisis 4	CTD_diseases	6
MESH:C564650	MESH:C564650	Carney-Stratakis Syndrome	CTD_diseases	6
MESH:C564679	MESH:C564679	Cardiomyopathy, Dilated, 1l	CTD_diseases	6
MESH:C564688	MESH:C564688	Amyotrophic Lateral Sclerosis 3	CTD_diseases	6
MESH:C564689	MESH:C564689	Camurati-Engelmann Disease, Type II	CTD_diseases	6
MESH:C564691	MESH:C564691	Muscular Dystrophy, Congenital, 1C	CTD_diseases	6
MESH:C564697	MESH:C564697	Episodic Ataxia, Type 3	CTD_diseases	6
MESH:C564698	MESH:C564698	Episodic Ataxia, Type 4	CTD_diseases	6
MESH:C564707	MESH:C564707	Persistent Polyclonal B-Cell Lymphocytosis	CTD_diseases	6
MESH:C564729	MESH:C564729	Ichthyosis, X-Linked, without Steroid Sulfatase Deficiency	CTD_diseases	6
MESH:C564736	MESH:C564736	Wolman Disease with Hypolipoproteinemia and Acanthocytosis	CTD_diseases	6
MESH:C564759	MESH:C564759	Trigonobrachycephaly, Bulbous Bifid Nose, Micrognathia, and Abnormalities of the Hands and Feet	CTD_diseases	6
MESH:C564762	MESH:C564762	Tricarboxylic Acid Cycle, Defect of	CTD_diseases	6
MESH:C564765	MESH:C564765	Thyrotropin, Biologically Inactive	CTD_diseases	6
MESH:C564766	MESH:C564766	Thyroid Dyshormonogenesis 1	CTD_diseases	6
MESH:C564767	MESH:C564767	Thymoma, Familial	CTD_diseases	6
MESH:C564788	MESH:C564788	Tapetoretinal Degeneration with Ataxia	CTD_diseases	6
MESH:C564792	MESH:C564792	Sucrosuria, Hiatus Hernia and Mental Retardation	CTD_diseases	6
MESH:C564806	MESH:C564806	Spinal Muscular Atrophy with Microcephaly and Mental Subnormality	CTD_diseases	6
MESH:C564808	MESH:C564808	Spastic Quadriplegia, Retinitis Pigmentosa, and Mental Retardation	CTD_diseases	6
MESH:C564810	MESH:C564810	Spastic Paraplegia With Myoclonic Epilepsy	CTD_diseases	6
MESH:C564823	MESH:C564823	Epilepsy, Benign Neonatal, Autosomal Recessive	CTD_diseases	6
MESH:C564829	MESH:C564829	Rod-Cone Dystrophy, Sensorineural Deafness, and Fanconi-Type Renal Dysfunction	CTD_diseases	6
MESH:C564832	MESH:C564832	Myoglobinuria, Acute Recurrent, Autosomal Recessive	CTD_diseases	6
MESH:C564838	MESH:C564838	Retinopathy, Pericentral Pigmentary, Autosomal Recessive	CTD_diseases	6
MESH:C564840	MESH:C564840	Retinitis Pigmentosa, Late-Adult Onset	CTD_diseases	6
MESH:C564842	MESH:C564842	Retinitis Pigmentosa Inversa with Deafness	CTD_diseases	6
MESH:C564857	MESH:C564857	Radiculoneuropathy, Fatal Neonatal	CTD_diseases	6
MESH:C564858	MESH:C564858	Pyruvate Kinase Deficiency of Red Cells	CTD_diseases	6
MESH:C564859	MESH:C564859	Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to	CTD_diseases	6
MESH:C564869	MESH:C564869	Pseudohermaphroditism, Female, with Skeletal Anomalies	CTD_diseases	6
MESH:C564870	MESH:C564870	Prolactin Deficiency with Obesity and Enlarged Testes	CTD_diseases	6
MESH:C564921	MESH:C564921	Osteogenesis Imperfecta, Type IX	CTD_diseases	6
MESH:C564926	MESH:C564926	Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Recessive	CTD_diseases	6
MESH:C564931	MESH:C564931	Oliver Syndrome	CTD_diseases	6
MESH:C564937	MESH:C564937	Ocular Myopathy with Curare Sensitivity	CTD_diseases	6
MESH:C564938	MESH:C564938	Nystagmus, Congenital Motor, Autosomal Recessive	CTD_diseases	6
MESH:C564944	MESH:C564944	Neurovisceral Storage Disease with Curvilinear Bodies	CTD_diseases	6
MESH:C564947	MESH:C564947	Neuropathy, Hereditary Motor and Sensory, with Excessive Myelin Folding Complex, Autosomal Recessive	CTD_diseases	6
MESH:C564948	MESH:C564948	Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive	CTD_diseases	6
MESH:C564967	MESH:C564967	Myotonia with Skeletal Abnormalities and Mental Retardation	CTD_diseases	6
MESH:C564980	MESH:C564980	Musk, Inability to Smell	CTD_diseases	6
MESH:C564982	MESH:C564982	Muscular Hypertonia, Lethal	CTD_diseases	6
MESH:C564983	MESH:C564983	Muscular Dystrophy, Congenital, with Rapid Progression	CTD_diseases	6
MESH:C564991	MESH:C564991	Gamma-A-Globulin, Defect in Assembly of	CTD_diseases	6
MESH:C564999	MESH:C564999	Friedreich Ataxia, So-Called, with Optic Atrophy and Sensorineural Deafness	CTD_diseases	6
MESH:C565021	MESH:C565021	Familial Mediterranean Fever, Autosomal Dominant	CTD_diseases	6
MESH:C565028	MESH:C565028	Facial Palsy, Familial Recurrent Peripheral	CTD_diseases	6
MESH:C565035	MESH:C565035	Cerebrooculofacioskeletal Syndrome 3	CTD_diseases	6
MESH:C565039	MESH:C565039	Erythroleukemia, Familial	CTD_diseases	6
MESH:C565057	MESH:C565057	Emphysema, Hereditary Pulmonary	CTD_diseases	6
MESH:C565061	MESH:C565061	EDS VIIB	CTD_diseases	6
MESH:C565069	MESH:C565069	Orofacial Cleft 8	CTD_diseases	6
MESH:C565078	MESH:C565078	Lewy Body Variant of Alzheimer Disease	CTD_diseases	6
MESH:C565083	MESH:C565083	Dupuytren Contracture 1	CTD_diseases	6
MESH:C565093	MESH:C565093	Distal Osteosclerosis	CTD_diseases	6
MESH:C565095	MESH:C565095	Megaloblastic Anemia due to Dihydrofolate Reductase Deficiency	CTD_diseases	6
MESH:C565100	MESH:C565100	Diabetes Mellitus, Insulin-Dependent, 2	CTD_diseases	6
MESH:C565101	MESH:C565101	Maturity-Onset Diabetes of the Young, Type 1	CTD_diseases	6
MESH:C565142	MESH:C565142	Cryofibrinogenemia, Familial Primary	CTD_diseases	6
MESH:C565143	MESH:C565143	Creutzfeldt-Jakob Disease, Sporadic	CTD_diseases	6
MESH:C565162	MESH:C565162	Febrile Convulsions, Familial, 1	CTD_diseases	6
MESH:C565164	MESH:C565164	Epilepsy, Benign Neonatal, 1	CTD_diseases	6
MESH:C565178	MESH:C565178	OI/EDS Combined Syndrome	CTD_diseases	6
MESH:C565193	MESH:C565193	Brachydactyly-Syndactyly Syndrome	CTD_diseases	6
MESH:C565198	MESH:C565198	Nemaline Myopathy 7	CTD_diseases	6
MESH:C565200	MESH:C565200	Osteogenesis Imperfecta Type VII	CTD_diseases	6
MESH:C565201	MESH:C565201	Prostate Cancer, Hereditary, 7	CTD_diseases	6
MESH:C565206	MESH:C565206	Retinitis Pigmentosa 35	CTD_diseases	6
MESH:C565216	MESH:C565216	Synpolydactyly 3	CTD_diseases	6
MESH:C565225	MESH:C565225	Maturity-Onset Diabetes of the Young, Type 8, with Exocrine Dysfunction	CTD_diseases	6
MESH:C565227	MESH:C565227	Generalized Epilepsy With Febrile Seizures Plus, Type 4	CTD_diseases	6
MESH:C565228	MESH:C565228	Alzheimer Disease 11	CTD_diseases	6
MESH:C565229	MESH:C565229	Aortic Aneurysm, Familial Abdominal 2	CTD_diseases	6
MESH:C565230	MESH:C565230	Aortic Aneurysm, Familial Abdominal 1	CTD_diseases	6
MESH:C565231	MESH:C565231	MODY, Type 6	CTD_diseases	6
MESH:C565237	MESH:C565237	Heterotaxy, Visceral, 3, Autosomal	CTD_diseases	6
MESH:C565249	MESH:C565249	Atrioventricular Septal Defect, Partial, with Heterotaxy Syndrome	CTD_diseases	6
MESH:C565251	MESH:C565251	Alzheimer Disease 7	CTD_diseases	6
MESH:C565264	MESH:C565264	Congenital Disorder Of Glycosylation, Type IIB	CTD_diseases	6
MESH:C565274	MESH:C565274	Holoprosencephaly 6	CTD_diseases	6
MESH:C565277	MESH:C565277	Cardiomyopathy, Dilated, with Left Ventricular Noncompaction	CTD_diseases	6
MESH:C565314	MESH:C565314	Tetralogy Of Fallot Syndrome, Autosomal Recessive	CTD_diseases	6
MESH:C565315	MESH:C565315	Diabetes Mellitus, Insulin-Dependent, 18	CTD_diseases	6
MESH:C565316	MESH:C565316	Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1	CTD_diseases	6
MESH:C565320	MESH:C565320	Cardiomyopathy, Dilated, 1K	CTD_diseases	6
MESH:C565322	MESH:C565322	Cone-Rod Dystrophy 8	CTD_diseases	6
MESH:C565325	MESH:C565325	Alzheimer Disease 6	CTD_diseases	6
MESH:C565337	MESH:C565337	Cardiomyopathy, Dilated, 1J	CTD_diseases	6
MESH:C565343	MESH:C565343	Optic Atrophy 4	CTD_diseases	6
MESH:C565365	MESH:C565365	Multiple Carboxylase Deficiency, Juvenile-Onset	CTD_diseases	6
MESH:C565384	MESH:C565384	Microcephaly, Primary Autosomal Recessive, 1	CTD_diseases	6
MESH:C565406	MESH:C565406	Mental Retardation, Autosomal Recessive 1	CTD_diseases	6
MESH:C565408	MESH:C565408	Megalencephaly with Dysmyelination	CTD_diseases	6
MESH:C565411	MESH:C565411	Marfanoid Habitus with Microcephaly and Glomerulonephritis	CTD_diseases	6
MESH:C565412	MESH:C565412	Maple Syrup Urine Disease, E3 Deficient, with Lactic Acidosis	CTD_diseases	6
MESH:C565420	MESH:C565420	Mandibulofacial Dysostosis with Mental Deficiency	CTD_diseases	6
MESH:C565429	MESH:C565429	Lymphoblastic Leukemia, Acute, with Lymphomatous Features	CTD_diseases	6
MESH:C565441	MESH:C565441	Leukemia, Acute Myelocytic, with Polyposis Coli and Colon Cancer	CTD_diseases	6
MESH:C565447	MESH:C565447	Pyruvate Dehydrogenase E3-Binding Protein Deficiency	CTD_diseases	6
MESH:C565448	MESH:C565448	Pyruvate Dehydrogenase E2 Deficiency	CTD_diseases	6
MESH:C565499	MESH:C565499	Hyperlysinemia Due To Defect In Lysine Transport Into Mitochondria	CTD_diseases	6
MESH:C565501	MESH:C565501	Breastfeeding Jaundice	CTD_diseases	6
MESH:C565502	MESH:C565502	Hydroxylysinuria	CTD_diseases	6
MESH:C565504	MESH:C565504	Hydrolethalus Syndrome 1	CTD_diseases	6
MESH:C565505	MESH:C565505	Muscular Dystrophy, Congenital, plus Mental Retardation	CTD_diseases	6
MESH:C565506	MESH:C565506	Muscular Dystrophy, Congenital, associated with Calf Hypertrophy, Microcephaly, and Severe Mental Re	CTD_diseases	6
MESH:C565509	MESH:C565509	Humeroradial Multiple Synostosis Syndrome	CTD_diseases	6
MESH:C565510	MESH:C565510	Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type	CTD_diseases	6
MESH:C565514	MESH:C565514	Holoprosencephaly 1	CTD_diseases	6
MESH:C565517	MESH:C565517	Hirschsprung Disease with Ulnar Polydactyly, Polysyndactyly of Big Toes, and Ventricular Septal Defe	CTD_diseases	6
MESH:C565518	MESH:C565518	Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness	CTD_diseases	6
MESH:C565531	MESH:C565531	Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II	CTD_diseases	6
MESH:C565532	MESH:C565532	Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I	CTD_diseases	6
MESH:C565533	MESH:C565533	Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative	CTD_diseases	6
MESH:C565534	MESH:C565534	Granulomatous Disease with Defect in Neutrophil Chemotaxis	CTD_diseases	6
MESH:C565548	MESH:C565548	Bernard-Soulier Syndrome, Type A	CTD_diseases	6
MESH:C565549	MESH:C565549	Bernard-Soulier Syndrome, Type B	CTD_diseases	6
MESH:C565550	MESH:C565550	Bernard-Soulier Syndrome, Type C	CTD_diseases	6
MESH:C565563	MESH:C565563	Ehlers-Danlos Syndrome VI Phenotype with Macrocephaly	CTD_diseases	6
MESH:C565569	MESH:C565569	Fever, Familial Lifelong Persistent	CTD_diseases	6
MESH:C565577	MESH:C565577	Familial Multiple Coagulation Factor Deficiency I	CTD_diseases	6
MESH:C565580	MESH:C565580	Facial Abnormalities, Kyphoscoliosis, and Mental Retardation	CTD_diseases	6
MESH:C565603	MESH:C565603	Cleft Lip with or without Cleft Palate, Nonsyndromic, 7	CTD_diseases	6
MESH:C565617	MESH:C565617	Dohle Bodies and Leukemia	CTD_diseases	6
MESH:C565642	MESH:C565642	Deafness, Congenital, with Vitiligo and Achalasia	CTD_diseases	6
MESH:C565649	MESH:C565649	Deafness, Congenital, and Familial Myoclonic Epilepsy	CTD_diseases	6
MESH:C565655	MESH:C565655	Cystinosis, Infantile Nephropathic	CTD_diseases	6
MESH:C565657	MESH:C565657	Cystic Kidney Disease with Ventriculomegaly	CTD_diseases	6
MESH:C565663	MESH:C565663	Craniosynostosis Mental Retardation Clefting Syndrome	CTD_diseases	6
MESH:C565678	MESH:C565678	Convulsive Disorder, Familial, with Prenatal or Early Onset	CTD_diseases	6
MESH:C565691	MESH:C565691	Telangiectasia, Hereditary Hemorrhagic, Type 4	CTD_diseases	6
MESH:C565707	MESH:C565707	Arrhythmogenic Right Ventricular Dysplasia, Familial, 10	CTD_diseases	6
MESH:C565711	MESH:C565711	Kyphoscoliosis 1	CTD_diseases	6
MESH:C565715	MESH:C565715	Diabetes Mellitus, Insulin-Dependent, 19	CTD_diseases	6
MESH:C565728	MESH:C565728	Alzheimer Disease, Familial Early-Onset, With Coexisting Amyloid And Prion Pathology	CTD_diseases	6
MESH:C565738	MESH:C565738	Bardet-Biedl Syndrome 6	CTD_diseases	6
MESH:C565746	MESH:C565746	Microcephaly, Primary Autosomal Recessive, 3	CTD_diseases	6
MESH:C565748	MESH:C565748	Muscular Dystrophy, Congenital, 1B	CTD_diseases	6
MESH:C565752	MESH:C565752	Cardiomyopathy, Dilated, 1i	CTD_diseases	6
MESH:C565773	MESH:C565773	Polyneuropathy, Lethal Neonatal, Axonal Sensorimotor, Autosomal Recessive	CTD_diseases	6
MESH:C565775	MESH:C565775	Arrhythmogenic Right Ventricular Dysplasia, Familial, 6	CTD_diseases	6
MESH:C565776	MESH:C565776	Arrhythmogenic Right Ventricular Dysplasia, Familial, 5	CTD_diseases	6
MESH:C565780	MESH:C565780	Nephronophthisis 3	CTD_diseases	6
MESH:C565781	MESH:C565781	Lissencephaly, Familial, with Cleft Palate and Cerebellar Hypoplasia	CTD_diseases	6
MESH:C565782	MESH:C565782	Patent Ductus Arteriosus and Bicuspid Aortic Valve with Hand Anomalies	CTD_diseases	6
MESH:C565783	MESH:C565783	Ulnar Ray Dysgenesis with Postaxial Polydactyly and Renal Cystic Dysplasia	CTD_diseases	6
MESH:C565785	MESH:C565785	Epilepsy, Partial, with Variable Foci	CTD_diseases	6
MESH:C565788	MESH:C565788	Febrile Convulsions, Familial, 4	CTD_diseases	6
MESH:C565791	MESH:C565791	Acne, Adult	CTD_diseases	6
MESH:C565792	MESH:C565792	Microcephaly, Primary Autosomal Recessive, 4	CTD_diseases	6
MESH:C565794	MESH:C565794	Microcephaly, Primary Autosomal Recessive, 2	CTD_diseases	6
MESH:C565801	MESH:C565801	Hemosiderosis, Systemic, due to Aceruloplasminemia	CTD_diseases	6
MESH:C565803	MESH:C565803	Carney Triad	CTD_diseases	6
MESH:C565808	MESH:C565808	Generalized Epilepsy with Febrile Seizures Plus	CTD_diseases	6
MESH:C565809	MESH:C565809	Generalized Epilepsy With Febrile Seizures Plus, Type 1	CTD_diseases	6
MESH:C565810	MESH:C565810	Generalized Epilepsy With Febrile Seizures Plus, Type 2	CTD_diseases	6
MESH:C565811	MESH:C565811	Generalized Epilepsy With Febrile Seizures Plus, Type 3	CTD_diseases	6
MESH:C565812	MESH:C565812	Generalized Epilepsy With Febrile Seizures Plus, Type 5	CTD_diseases	6
MESH:C565813	MESH:C565813	Febrile Seizures Associated with Afebrile Seizures	CTD_diseases	6
MESH:C565821	MESH:C565821	Noncompaction of Left Ventricular Myocardium, Familial Isolated, Autosomal Dominant 1	CTD_diseases	6
MESH:C565824	MESH:C565824	Cardiomyopathy, Dilated, 1g	CTD_diseases	6
MESH:C565827	MESH:C565827	Cone-Rod Dystrophy 3	CTD_diseases	6
MESH:C565840	MESH:C565840	Long Qt Syndrome 3	CTD_diseases	6
MESH:C565841	MESH:C565841	Long Qt Syndrome 2/3	CTD_diseases	6
MESH:C565843	MESH:C565843	Cleidocranial Dysplasia, Recessive Form	CTD_diseases	6
MESH:C565844	MESH:C565844	Cleft Palate, Deafness, and Oligodontia	CTD_diseases	6
MESH:C565851	MESH:C565851	Chorea, Benign Familial	CTD_diseases	6
MESH:C565853	MESH:C565853	Chondrodysplasia Punctata Syndrome	CTD_diseases	6
MESH:C565864	MESH:C565864	Cerebral Angiopathy, Dysphoric	CTD_diseases	6
MESH:C565865	MESH:C565865	Spinocerebellar Ataxia, Autosomal Recessive 2	CTD_diseases	6
MESH:C565868	MESH:C565868	Cerebellar Ataxia, Benign, with Thermoanalgesia	CTD_diseases	6
MESH:C565872	MESH:C565872	Cephalin Lipidosis	CTD_diseases	6
MESH:C565883	MESH:C565883	Cardiac Septal Defects with Coarctation of the Aorta	CTD_diseases	6
MESH:C565894	MESH:C565894	Brachydactyly, Type A2, With Microcephaly	CTD_diseases	6
MESH:C565916	MESH:C565916	Bardet-Biedl Syndrome 7	CTD_diseases	6
MESH:C565917	MESH:C565917	Bardet-Biedl Syndrome 8	CTD_diseases	6
MESH:C565918	MESH:C565918	Bardet-Biedl Syndrome 9	CTD_diseases	6
MESH:C565919	MESH:C565919	Bardet-Biedl Syndrome 10	CTD_diseases	6
MESH:C565920	MESH:C565920	Bardet-Biedl Syndrome 11	CTD_diseases	6
MESH:C565921	MESH:C565921	Bardet-Biedl Syndrome 12	CTD_diseases	6
MESH:C565926	MESH:C565926	Atonic-Astatic Syndrome of Foerster	CTD_diseases	6
MESH:C565934	MESH:C565934	Asthma, Short Stature, and Elevated IgA	CTD_diseases	6
MESH:C565951	MESH:C565951	Angiolipomatosis, Familial	CTD_diseases	6
MESH:C565954	MESH:C565954	Anemia, Sideroblastic, Pyridoxine-Responsive, Autosomal Recessive	CTD_diseases	6
MESH:C565955	MESH:C565955	Amyotrophic Lateral Sclerosis With Polyglucosan Bodies	CTD_diseases	6
MESH:C565957	MESH:C565957	Amyotrophic Lateral Sclerosis 2, Juvenile	CTD_diseases	6
MESH:C565965	MESH:C565965	Alopecia-Mental Retardation Syndrome 1	CTD_diseases	6
MESH:C565970	MESH:C565970	Hypodysfibrinogenemia, Congenital	CTD_diseases	6
MESH:C566002	MESH:C566002	Vertebral Hypoplasia With Lumbar Kyphosis	CTD_diseases	6
MESH:C566010	MESH:C566010	Uterus Bicornis Bicollis With Partial Vaginal Septum And Unilateral Hematocolpos With Ipsilateral Re	CTD_diseases	6
MESH:C566013	MESH:C566013	Urate-Binding Globulin, Decrease in	CTD_diseases	6
MESH:C566017	MESH:C566017	Parkinson Disease 5	CTD_diseases	6
MESH:C566038	MESH:C566038	Tremor of Intention, Ataxia, and Lipofuscinosis	CTD_diseases	6
MESH:C566046	MESH:C566046	Tibia, Hypoplasia of, with Polydactyly	CTD_diseases	6
MESH:C566052	MESH:C566052	Cardiomyopathy, Dilated, 1t	CTD_diseases	6
MESH:C566054	MESH:C566054	Thumb Deformity And Alopecia	CTD_diseases	6
MESH:C566056	MESH:C566056	Thrombophilia due to Activated Protein C Resistance	CTD_diseases	6
MESH:C566061	MESH:C566061	Glanzmann Thrombasthenia, Autosomal Dominant	CTD_diseases	6
MESH:C566090	MESH:C566090	Synostosis, Carpal, with Dysplastic Elbow Joints and Brachydactyly	CTD_diseases	6
MESH:C566091	MESH:C566091	Syndactyly-Polydactyly-Earlobe Syndrome	CTD_diseases	6
MESH:C566092	MESH:C566092	Syndactyly, Type IV	CTD_diseases	6
MESH:C566095	MESH:C566095	Synpolydactyly With Foot Anomalies	CTD_diseases	6
MESH:C566098	MESH:C566098	Symphalangism with Multiple Anomalies of Hands and Feet	CTD_diseases	6
MESH:C566119	MESH:C566119	Cleidocranial Dysplasia, Forme Fruste, With Brachydactyly	CTD_diseases	6
MESH:C566121	MESH:C566121	Orofacial Cleft 1	CTD_diseases	6
MESH:C566127	MESH:C566127	Choreoathetosis, Familial Inverted	CTD_diseases	6
MESH:C566147	MESH:C566147	Minicore Myopathy, Moderate, with Hand Involvement	CTD_diseases	6
MESH:C566152	MESH:C566152	Cavernous Malformations of CNS and Retina	CTD_diseases	6
MESH:C566178	MESH:C566178	Breast Cancer, Familial Male	CTD_diseases	6
MESH:C566184	MESH:C566184	Prenatal Cortical Hyperostosis, Lethal	CTD_diseases	6
MESH:C566188	MESH:C566188	Branchial Myoclonus with Spastic Paraparesis and Cerebellar Ataxia	CTD_diseases	6
MESH:C566192	MESH:C566192	Brachydactyly-Nystagmus-Cerebellar Ataxia	CTD_diseases	6
MESH:C566193	MESH:C566193	Brachydactyly, Type E, With Atrial Septal Defect, Type Ii	CTD_diseases	6
MESH:C566194	MESH:C566194	Brachydactyly, Type E	CTD_diseases	6
MESH:C566196	MESH:C566196	Brachydactyly, Type B1	CTD_diseases	6
MESH:C566204	MESH:C566204	Brachydactyly, Long-Thumb Type	CTD_diseases	6
MESH:C566210	MESH:C566210	Rh-Null Disease, Amorph Type	CTD_diseases	6
MESH:C566226	MESH:C566226	Basilar Impression, Primary	CTD_diseases	6
MESH:C566228	MESH:C566228	Banki Syndrome	CTD_diseases	6
MESH:C566233	MESH:C566233	Azotemia, Familial	CTD_diseases	6
MESH:C566245	MESH:C566245	External Auditory Canal, Bilateral Atresia Of, With Congenital Vertical Talus	CTD_diseases	6
MESH:C566246	MESH:C566246	Ataxia with Fasciculations	CTD_diseases	6
MESH:C566247	MESH:C566247	Ataxia, Spastic, with Congenital Miosis	CTD_diseases	6
MESH:C566254	MESH:C566254	Arrhythmogenic Right Ventricular Dysplasia, Familial, 1	CTD_diseases	6
MESH:C566255	MESH:C566255	Cardiomyopathy, Right Ventricular Dilated	CTD_diseases	6
MESH:C566273	MESH:C566273	alpha-1-Antitrypsin Deficiency, Autosomal Recessive	CTD_diseases	6
MESH:C566288	MESH:C566288	Frontotemporal Dementia With Motor Neuron Disease	CTD_diseases	6
MESH:C566290	MESH:C566290	Amyotrophic Lateral Sclerosis, Autosomal Recessive	CTD_diseases	6
MESH:C566291	MESH:C566291	Amyotrophic Lateral Sclerosis, Sporadic	CTD_diseases	6
MESH:C566292	MESH:C566292	Amyotrophic Dystonic Paraplegia	CTD_diseases	6
MESH:C566294	MESH:C566294	Amelia and Terminal Transverse Hemimelia	CTD_diseases	6
MESH:C566296	MESH:C566296	Cardiomyopathy, Dilated, 1u	CTD_diseases	6
MESH:C566298	MESH:C566298	Alzheimer Disease, Familial, 1	CTD_diseases	6
MESH:C566299	MESH:C566299	Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy	CTD_diseases	6
MESH:C566301	MESH:C566301	Alopecia, Familial Focal	CTD_diseases	6
MESH:C566309	MESH:C566309	Adenine Nucleotide Translocator Deficiency	CTD_diseases	6
MESH:C566332	MESH:C566332	Microcephaly with Simplified Gyral Pattern	CTD_diseases	6
MESH:C566333	MESH:C566333	Long Qt Syndrome 6	CTD_diseases	6
MESH:C566334	MESH:C566334	Long Qt Syndrome 3/6	CTD_diseases	6
MESH:C566342	MESH:C566342	Diabetes Mellitus, Noninsulin-Dependent, 3	CTD_diseases	6
MESH:C566350	MESH:C566350	Cone-Rod Dystrophy 7	CTD_diseases	6
MESH:C566352	MESH:C566352	Neuroendocrine Carcinoma of Salivary Glands, Sensorineural Hearing Loss, and Enamel Hypoplasia	CTD_diseases	6
MESH:C566359	MESH:C566359	Parotitis, Juvenile Recurrent	CTD_diseases	6
MESH:C566378	MESH:C566378	Osteosclerotic Chondrodysplasia, Lethal, With Intracellular Inclusions	CTD_diseases	6
MESH:C566392	MESH:C566392	Muscular Dystrophy, Congenital, With Cerebellar Atrophy	CTD_diseases	6
MESH:C566393	MESH:C566393	Cerebral Cavernous Malformations 3	CTD_diseases	6
MESH:C566394	MESH:C566394	Cerebral Cavernous Malformations 2	CTD_diseases	6
MESH:C566395	MESH:C566395	Diabetes Mellitus, Insulin-Dependent, 17	CTD_diseases	6
MESH:C566409	MESH:C566409	Spastic Paraplegia, Optic Atrophy, Microcephaly, And Xy Sex Reversal	CTD_diseases	6
MESH:C566419	MESH:C566419	Orofacial Cleft 2	CTD_diseases	6
MESH:C566425	MESH:C566425	Retinitis Pigmentosa 25	CTD_diseases	6
MESH:C566426	MESH:C566426	Prostate Cancer, Hereditary, 8	CTD_diseases	6
MESH:C566429	MESH:C566429	Mental Retardation, Severe, With Spasticity And Pigmentary Tapetoretinal Degeneration	CTD_diseases	6
MESH:C566431	MESH:C566431	Retinitis Pigmentosa 36	CTD_diseases	6
MESH:C566464	MESH:C566464	Holoprosencephaly 5	CTD_diseases	6
MESH:C566465	MESH:C566465	Alzheimer Disease 10	CTD_diseases	6
MESH:C566470	MESH:C566470	Retinal Cone Dystrophy 4	CTD_diseases	6
MESH:C566471	MESH:C566471	Arrhythmogenic Right Ventricular Dysplasia, Familial, 11	CTD_diseases	6
MESH:C566483	MESH:C566483	Retinal Cone Dystrophy 3A	CTD_diseases	6
MESH:C566510	MESH:C566510	Parietal Foramina 2	CTD_diseases	6
MESH:C566511	MESH:C566511	Scaphocephaly, Maxillary Retrusion, And Mental Retardation	CTD_diseases	6
MESH:C566525	MESH:C566525	Microcephaly, Macrotia, And Mental Retardation	CTD_diseases	6
MESH:C566527	MESH:C566527	Muscular Dystrophy, Congenital, Megaconial Type	CTD_diseases	6
MESH:C566531	MESH:C566531	Pseudoacromegaly with Severe Insulin Resistance	CTD_diseases	6
MESH:C566541	MESH:C566541	Febrile Convulsions, Familial, 2	CTD_diseases	6
MESH:C566550	MESH:C566550	Amyotrophic Lateral Sclerosis 4, Juvenile	CTD_diseases	6
MESH:C566556	MESH:C566556	Hemochromatosis, Type 2A	CTD_diseases	6
MESH:C566557	MESH:C566557	Hemochromatosis, Type 2B	CTD_diseases	6
MESH:C566565	MESH:C566565	Ventriculomegaly With Defects Of The Radius And Kidney	CTD_diseases	6
MESH:C566573	MESH:C566573	Nephropathy, Progressive Tubulointerstitial, with Cholestatic Liver Disease	CTD_diseases	6
MESH:C566575	MESH:C566575	Neuropathy, Hereditary Thermosensitive	CTD_diseases	6
MESH:C566576	MESH:C566576	Amyotrophic Lateral Sclerosis 5	CTD_diseases	6
MESH:C566578	MESH:C566578	Alzheimer Disease 5	CTD_diseases	6
MESH:C566579	MESH:C566579	Cone Dystrophy 3	CTD_diseases	6
MESH:C566582	MESH:C566582	Nephronophthisis 2	CTD_diseases	6
MESH:C566583	MESH:C566583	Arrhythmogenic Right Ventricular Dysplasia, Familial, 4	CTD_diseases	6
MESH:C566584	MESH:C566584	Arrhythmogenic Right Ventricular Dysplasia, Familial, 3	CTD_diseases	6
MESH:C566585	MESH:C566585	Polydactyly, Postaxial, Type A2	CTD_diseases	6
MESH:C566596	MESH:C566596	Thrombocytosis, Benign Familial Microcytic	CTD_diseases	6
MESH:C566602	MESH:C566602	Diabetes Mellitus, Insulin-Dependent, 10	CTD_diseases	6
MESH:C566603	MESH:C566603	Diabetes Mellitus, Insulin-Dependent, 6	CTD_diseases	6
MESH:C566605	MESH:C566605	Orofacial Cleft 10	CTD_diseases	6
MESH:C566610	MESH:C566610	Left-Right Axis Malformations	CTD_diseases	6
MESH:C566617	MESH:C566617	Vacuolar Neuromyopathy	CTD_diseases	6
MESH:C566632	MESH:C566632	Preaxial Hallucal Polydactyly	CTD_diseases	6
MESH:C566637	MESH:C566637	Retinitis Pigmentosa 19	CTD_diseases	6
MESH:C566640	MESH:C566640	Platelet-Activating Factor Acetylhydrolase Deficiency	CTD_diseases	6
MESH:C566645	MESH:C566645	Diabetes Mellitus, Insulin-Dependent, 15	CTD_diseases	6
MESH:C566648	MESH:C566648	Spina Bifida, Folate-Sensitive	CTD_diseases	6
MESH:C566706	MESH:C566706	Retinitis Pigmentosa 4	CTD_diseases	6
MESH:C566715	MESH:C566715	Retinitis Pigmentosa 10	CTD_diseases	6
MESH:C566716	MESH:C566716	Retinitis Pigmentosa 9	CTD_diseases	6
MESH:C566718	MESH:C566718	Retinitis Pigmentosa 20	CTD_diseases	6
MESH:C566744	MESH:C566744	Pseudoxanthoma Elasticum, Heterozygous	CTD_diseases	6
MESH:C566765	MESH:C566765	Long Qt Syndrome 2/5	CTD_diseases	6
MESH:C566766	MESH:C566766	Long Qt Syndrome 5	CTD_diseases	6
MESH:C566773	MESH:C566773	Polysyndactyly, Crossed	CTD_diseases	6
MESH:C566783	MESH:C566783	Crossed Polydactyly, Type I	CTD_diseases	6
MESH:C566784	MESH:C566784	Polydactyly, Preaxial III	CTD_diseases	6
MESH:C566809	MESH:C566809	Normokalemic Periodic Paralysis, Potassium-Sensitive	CTD_diseases	6
MESH:C566825	MESH:C566825	Parietal Foramina With Cleidocranial Dysplasia	CTD_diseases	6
MESH:C566826	MESH:C566826	Parietal Foramina	CTD_diseases	6
MESH:C566827	MESH:C566827	Parietal Foramina 1	CTD_diseases	6
MESH:C566847	MESH:C566847	Episodic Kinesigenic Dyskinesia 1	CTD_diseases	6
MESH:C566856	MESH:C566856	Cardiomyopathy, Dilated, 1V	CTD_diseases	6
MESH:C566862	MESH:C566862	Polyasplenia	CTD_diseases	6
MESH:C566864	MESH:C566864	Heterotaxy, Visceroatrial, Autosomal Recessive	CTD_diseases	6
MESH:C566885	MESH:C566885	Lactic Acidosis, Fatal Infantile	CTD_diseases	6
MESH:C566901	MESH:C566901	Febrile Convulsions, Familial, 9	CTD_diseases	6
MESH:C566906	MESH:C566906	Cakut	CTD_diseases	6
MESH:C566907	MESH:C566907	Cardiomyopathy, Dilated, 1x	CTD_diseases	6
MESH:C566908	MESH:C566908	Lissencephaly 3	CTD_diseases	6
MESH:C566917	MESH:C566917	Glycogen Storage Disease 0, Muscle	CTD_diseases	6
MESH:C566925	MESH:C566925	Arrhythmogenic Right Ventricular Dysplasia, Familial, 12	CTD_diseases	6
MESH:C566928	MESH:C566928	Tyrosine Kinase 2 Deficiency	CTD_diseases	6
MESH:C566929	MESH:C566929	Febrile Convulsions, Familial, 7	CTD_diseases	6
MESH:C566930	MESH:C566930	Nephronophthisis 7	CTD_diseases	6
MESH:C566947	MESH:C566947	Mental Retardation, Autosomal Dominant 1	CTD_diseases	6
MESH:C566954	MESH:C566954	Cardiomyopathy, Dilated, 1w	CTD_diseases	6
MESH:C566975	MESH:C566975	Febrile Convulsions, Familial, 8	CTD_diseases	6
MESH:C566981	MESH:C566981	Creutzfeldt-Jakob Disease, Heidenhain Variant	CTD_diseases	6
MESH:C566982	MESH:C566982	Asphyxiating Thoracic Dystrophy 2	CTD_diseases	6
MESH:C566983	MESH:C566983	Spastic Paraplegia 32, Autosomal Recessive	CTD_diseases	6
MESH:C566987	MESH:C566987	Congenital Disorder Of Glycosylation, Type IIH	CTD_diseases	6
MESH:C566991	MESH:C566991	Cleft Palate, Isolated, And Mental Retardation	CTD_diseases	6
MESH:C566994	MESH:C566994	Tooth Agenesis, Selective, With Orofacial Cleft	CTD_diseases	6
MESH:C566995	MESH:C566995	Hypodontia Oligodontia with Orofacial Cleft	CTD_diseases	6
MESH:C566998	MESH:C566998	Alzheimer Disease 15	CTD_diseases	6
MESH:C566999	MESH:C566999	Alzheimer Disease 14	CTD_diseases	6
MESH:C567000	MESH:C567000	Alzheimer Disease 13	CTD_diseases	6
MESH:C567001	MESH:C567001	Paroxysmal Nonkinesigenic Dyskinesia 2	CTD_diseases	6
MESH:C567003	MESH:C567003	Meckel Syndrome, Type 4	CTD_diseases	6
MESH:C567004	MESH:C567004	Meckel-Like Cerebrorenodigital Syndrome	CTD_diseases	6
MESH:C567005	MESH:C567005	Retinitis Pigmentosa 37	CTD_diseases	6
MESH:C567008	MESH:C567008	Mental Retardation, Autosomal Recessive 4	CTD_diseases	6
MESH:C567010	MESH:C567010	Deafness, Sensorineural, And Male Infertility	CTD_diseases	6
MESH:C567011	MESH:C567011	Prostate Cancer, Hereditary, 10	CTD_diseases	6
MESH:C567012	MESH:C567012	Mental Retardation, Autosomal Recessive 11	CTD_diseases	6
MESH:C567013	MESH:C567013	Mental Retardation, Autosomal Recessive 10	CTD_diseases	6
MESH:C567014	MESH:C567014	Mental Retardation, Autosomal Recessive 9	CTD_diseases	6
MESH:C567015	MESH:C567015	Mental Retardation, Autosomal Recessive 8	CTD_diseases	6
MESH:C567016	MESH:C567016	Mental Retardation, Autosomal Recessive 7	CTD_diseases	6
MESH:C567017	MESH:C567017	Mental Retardation, Autosomal Recessive 6	CTD_diseases	6
MESH:C567018	MESH:C567018	Mental Retardation, Autosomal Recessive 5	CTD_diseases	6
MESH:C567019	MESH:C567019	Mental Retardation, Autosomal Recessive 12	CTD_diseases	6
MESH:C567022	MESH:C567022	Alzheimer Disease 12	CTD_diseases	6
MESH:C567023	MESH:C567023	Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4	CTD_diseases	6
MESH:C567031	MESH:C567031	Prostate Cancer, Hereditary, 9	CTD_diseases	6
MESH:C567032	MESH:C567032	Phosphoserine Aminotransferase Deficiency	CTD_diseases	6
MESH:C567040	MESH:C567040	Congenital Disorder Of Glycosylation, Type IIF	CTD_diseases	6
MESH:C567041	MESH:C567041	Osteogenesis Imperfecta, Type VI	CTD_diseases	6
MESH:C567042	MESH:C567042	Osteogenesis Imperfecta, Type V	CTD_diseases	6
MESH:C567053	MESH:C567053	Vesicoureteral Reflux 2	CTD_diseases	6
MESH:C567066	MESH:C567066	Mental Retardation, X-Linked 93	CTD_diseases	6
MESH:C567078	MESH:C567078	Allergic Rhinitis	CTD_diseases	6
MESH:C567090	MESH:C567090	Familial Cold Autoinflammatory Syndrome 2	CTD_diseases	6
MESH:C567098	MESH:C567098	Epilepsy, Familial Adult Myoclonic, 3	CTD_diseases	6
MESH:C567101	MESH:C567101	Microcephaly with Mental Retardation and Digital Anomalies	CTD_diseases	6
MESH:C567107	MESH:C567107	Hypophosphatasia, Perinatal Lethal	CTD_diseases	6
MESH:C567121	MESH:C567121	Epidermolysis Bullosa Dystrophica, Autosomal Recessive, Localisata Variant	CTD_diseases	6
MESH:C567122	MESH:C567122	Epidermolysis Bullosa Dystrophica Inversa, Autosomal Recessive	CTD_diseases	6
MESH:C567123	MESH:C567123	Hypothyroidism, Congenital, Nongoitrous, 5	CTD_diseases	6
MESH:C567127	MESH:C567127	Hypomagnesemia 4, Renal	CTD_diseases	6
MESH:C567138	MESH:C567138	Camptodactyly Syndrome, Guadalajara, Type Ii	CTD_diseases	6
MESH:C567140	MESH:C567140	Bardet-Biedl Syndrome 13	CTD_diseases	6
MESH:C567141	MESH:C567141	Bardet-Biedl Syndrome 14	CTD_diseases	6
MESH:C567144	MESH:C567144	Anemia, Hypochromic Microcytic, With Iron Overload	CTD_diseases	6
MESH:C567145	MESH:C567145	Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive	CTD_diseases	6
MESH:C567156	MESH:C567156	Loeys-Dietz Syndrome, Type 2A	CTD_diseases	6
MESH:C567160	MESH:C567160	Anemia, Sideroblastic, Autosomal Dominant	CTD_diseases	6
MESH:C567162	MESH:C567162	Neuromuscular Disease, Congenital, With Uniform Type 1 Fiber	CTD_diseases	6
MESH:C567163	MESH:C567163	Thrombophilia, Hereditary, Due To Protein C Deficiency, Autosomal Dominant	CTD_diseases	6
MESH:C567164	MESH:C567164	Protein C Deficiency, Acquired	CTD_diseases	6
MESH:C567172	MESH:C567172	Osteopenic Nonfracture Syndrome	CTD_diseases	6
MESH:C567174	MESH:C567174	Myokymia 1	CTD_diseases	6
MESH:C567181	MESH:C567181	Loeys-Dietz Syndrome, Type 1b	CTD_diseases	6
MESH:C567185	MESH:C567185	Dandy-Walker Malformation With Occipital Cephalocele, Autosomal Dominant	CTD_diseases	6
MESH:C567187	MESH:C567187	Best Vitelliform Macular Dystrophy, Multifocal	CTD_diseases	6
MESH:C567198	MESH:C567198	Microcephaly, Primary Autosomal Recessive, 7	CTD_diseases	6
MESH:C567206	MESH:C567206	Cone-Rod Dystrophy 12	CTD_diseases	6
MESH:C567218	MESH:C567218	Febrile Convulsions, Familial, 10	CTD_diseases	6
MESH:C567221	MESH:C567221	Microcephaly, Primary Autosomal Recessive, 5, with Simplified Gyral Pattern	CTD_diseases	6
MESH:C567231	MESH:C567231	Convulsions, Benign Familial Infantile, 4	CTD_diseases	6
MESH:C567233	MESH:C567233	Diabetes Mellitus, Insulin-Dependent, 23	CTD_diseases	6
MESH:C567234	MESH:C567234	Mental Retardation, Autosomal Dominant 5	CTD_diseases	6
MESH:C567240	MESH:C567240	Mental Retardation, Autosomal Dominant 4	CTD_diseases	6
MESH:C567241	MESH:C567241	Mental Retardation, Autosomal Dominant 3	CTD_diseases	6
MESH:C567244	MESH:C567244	Amyotrophic Lateral Sclerosis 11	CTD_diseases	6
MESH:C567249	MESH:C567249	Retinitis Pigmentosa 46	CTD_diseases	6
MESH:C567263	MESH:C567263	Retinitis Pigmentosa 7, Digenic	CTD_diseases	6
MESH:C567264	MESH:C567264	Retinitis Pigmentosa 7 With Bull'S-Eye Maculopathy	CTD_diseases	6
MESH:C567272	MESH:C567272	Epidermolysis Bullosa Dystrophica With Subcorneal Cleavage	CTD_diseases	6
MESH:C562469	MESH:C562469	Paralysis Agitans, Juvenile, Of Hunt	CTD_diseases	7
MESH:C562574	MESH:C562574	Visceral Myopathy, Familial	CTD_diseases	7
MESH:C562594	MESH:C562594	Glycogen Storage Disease IB	CTD_diseases	7
MESH:C562656	MESH:C562656	Hyperphenylalaninemia, BH4-Deficient, B	CTD_diseases	7
MESH:C562662	MESH:C562662	Brown Oculocutaneous Albinism	CTD_diseases	7
MESH:C562695	MESH:C562695	Epileptic Encephalopathy, Early Infantile, 3	CTD_diseases	7
MESH:C562701	MESH:C562701	Fleck Retina of Kandori	CTD_diseases	7
MESH:C562806	MESH:C562806	Glycogen Storage Disease Id	CTD_diseases	7
MESH:C562816	MESH:C562816	Harderoporphyria	CTD_diseases	7
MESH:C562868	MESH:C562868	Posttransfusion Purpura	CTD_diseases	7
MESH:C562879	MESH:C562879	Amelogenesis Imperfecta, Type IB	CTD_diseases	7
MESH:C562880	MESH:C562880	Amelogenesis Imperfecta, Type III	CTD_diseases	7
MESH:C562884	MESH:C562884	Fibromatosis, Gingival, Type 1	CTD_diseases	7
MESH:C562889	MESH:C562889	Renal Failure, Progressive, with Hypertension	CTD_diseases	7
MESH:C562890	MESH:C562890	Alport Syndrome-Like Hereditary Nephritis	CTD_diseases	7
MESH:C562897	MESH:C562897	Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness	CTD_diseases	7
MESH:C562900	MESH:C562900	Glomerulopathy with Giant Fibrillar Deposits	CTD_diseases	7
MESH:C562932	MESH:C562932	Muscular Dystrophy, Scapulohumeral	CTD_diseases	7
MESH:C562951	MESH:C562951	Trigonocephaly, Nonsyndromic	CTD_diseases	7
MESH:C562978	MESH:C562978	Fibromatosis, Congenital Generalized	CTD_diseases	7
MESH:C563003	MESH:C563003	Pallidopontonigral Degeneration	CTD_diseases	7
MESH:C563004	MESH:C563004	Pyropoikilocytosis, Hereditary	CTD_diseases	7
MESH:C563013	MESH:C563013	Membranous Obstruction of Inferior Vena Cava	CTD_diseases	7
MESH:C563135	MESH:C563135	Mental Retardation, X-Linked 2	CTD_diseases	7
MESH:C563136	MESH:C563136	Mental Retardation, X-Linked 3	CTD_diseases	7
MESH:C563137	MESH:C563137	Mental Retardation, X-Linked 9	CTD_diseases	7
MESH:C563139	MESH:C563139	Mental Retardation, X-Linked 16	CTD_diseases	7
MESH:C563140	MESH:C563140	Mental Retardation, X-Linked 17	CTD_diseases	7
MESH:C563141	MESH:C563141	Mental Retardation, X-Linked 19	CTD_diseases	7
MESH:C563142	MESH:C563142	Mental Retardation, X-Linked 20	CTD_diseases	7
MESH:C563144	MESH:C563144	Mental Retardation, X-Linked 23	CTD_diseases	7
MESH:C563146	MESH:C563146	Mental Retardation, X-Linked 30	CTD_diseases	7
MESH:C563147	MESH:C563147	Mental Retardation, X-Linked 31	CTD_diseases	7
MESH:C563148	MESH:C563148	Mental Retardation, X-Linked 34	CTD_diseases	7
MESH:C563150	MESH:C563150	Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related	CTD_diseases	7
MESH:C563151	MESH:C563151	Mental Retardation, X-Linked 47	CTD_diseases	7
MESH:C563159	MESH:C563159	Acrorenal Syndrome	CTD_diseases	7
MESH:C563201	MESH:C563201	Lysine Intolerance	CTD_diseases	7
MESH:C563239	MESH:C563239	Aneurysm Of Interventricular Septum	CTD_diseases	7
MESH:C563240	MESH:C563240	Atrioventricular Canal Defect	CTD_diseases	7
MESH:C563301	MESH:C563301	Peroxisome Biogenesis Disorder, Complementation Group 4	CTD_diseases	7
MESH:C563336	MESH:C563336	Wilms Tumor 4	CTD_diseases	7
MESH:C563337	MESH:C563337	Digeorge Syndrome/Velocardiofacial Syndrome Complex 2	CTD_diseases	7
MESH:C563362	MESH:C563362	Muscular Dystrophy, Limb-Girdle, Type 1C	CTD_diseases	7
MESH:C563363	MESH:C563363	Cerebellar Ataxia, Cayman Type	CTD_diseases	7
MESH:C563368	MESH:C563368	Craniosynostosis, Philadelphia Type	CTD_diseases	7
MESH:C563431	MESH:C563431	Wiskott-Aldrich Syndrome, Autosomal Dominant Form	CTD_diseases	7
MESH:C563439	MESH:C563439	Enuresis, Nocturnal, 2	CTD_diseases	7
MESH:C563442	MESH:C563442	Frontotemporal Dementia, Chromosome 3-Linked	CTD_diseases	7
MESH:C563471	MESH:C563471	Craniosynostosis, Adelaide Type	CTD_diseases	7
MESH:C563479	MESH:C563479	Ovalocytosis, Hereditary Hemolytic, with Defective Erythropoiesis	CTD_diseases	7
MESH:C563480	MESH:C563480	Ovalocytosis, Hereditary Hemolytic	CTD_diseases	7
MESH:C563485	MESH:C563485	Osteomas Of Mandible	CTD_diseases	7
MESH:C563505	MESH:C563505	Olivopontocerebellar Atrophy V	CTD_diseases	7
MESH:C563540	MESH:C563540	Atrial Septal Defect 3	CTD_diseases	7
MESH:C563543	MESH:C563543	Myopathy, Distal, with Onset in Infancy	CTD_diseases	7
MESH:C563557	MESH:C563557	Facioscapulohumeral Muscular Dystrophy 1B	CTD_diseases	7
MESH:C563566	MESH:C563566	Multiple Exostoses with Spastic Tetraparesis	CTD_diseases	7
MESH:C563570	MESH:C563570	Monophalangy of Great Toe	CTD_diseases	7
MESH:C563585	MESH:C563585	Metatarsus Varus, Type I	CTD_diseases	7
MESH:C563593	MESH:C563593	Melorheostosis with Osteopoikilosis	CTD_diseases	7
MESH:C563597	MESH:C563597	Megaduodenum and/or Megacystis	CTD_diseases	7
MESH:C563617	MESH:C563617	Lipoprotein Types--Lp System Lp(A) Hyperlipoproteinemia	CTD_diseases	7
MESH:C563627	MESH:C563627	Platyspondylic Lethal Skeletal Dysplasia, Torrance Type	CTD_diseases	7
MESH:C563630	MESH:C563630	Lentiginosis, Centrofacial Neurodysraphic	CTD_diseases	7
MESH:C563657	MESH:C563657	Fanconi Anemia, Complementation Group N	CTD_diseases	7
MESH:C563679	MESH:C563679	Epilepsy, Nocturnal Frontal Lobe, Type 4	CTD_diseases	7
MESH:C563713	MESH:C563713	Nephropathy, Progressive, with Deafness	CTD_diseases	7
MESH:C563717	MESH:C563717	Supranuclear Palsy, Progressive, 2	CTD_diseases	7
MESH:C563721	MESH:C563721	Syndactyly, Mesoaxial Synostotic, with Phalangeal Reduction	CTD_diseases	7
MESH:C563740	MESH:C563740	Charcot-Marie-Tooth Disease, Type 4H	CTD_diseases	7
MESH:C563747	MESH:C563747	Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3	CTD_diseases	7
MESH:C563750	MESH:C563750	Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2	CTD_diseases	7
MESH:C563757	MESH:C563757	Charcot-Marie-Tooth Disease, Axonal, Type 2A2	CTD_diseases	7
MESH:C563792	MESH:C563792	Aneurysm, Intracranial Berry, 3	CTD_diseases	7
MESH:C563794	MESH:C563794	Limb-Girdle Muscular Dystrophy, Type 1G	CTD_diseases	7
MESH:C563801	MESH:C563801	Fanconi Anemia, Complementation Group J	CTD_diseases	7
MESH:C563802	MESH:C563802	Fanconi Anemia, Complementation Group I	CTD_diseases	7
MESH:C563807	MESH:C563807	Spastic Paraplegia 27, Autosomal Recessive	CTD_diseases	7
MESH:C563816	MESH:C563816	Premature Ovarian Failure 3	CTD_diseases	7
MESH:C563845	MESH:C563845	Carney Complex Variant	CTD_diseases	7
MESH:C563854	MESH:C563854	Muscular Dystrophy, Limb-Girdle, Type 2J	CTD_diseases	7
MESH:C563855	MESH:C563855	Leukodystrophy, Hypomyelinating, 2	CTD_diseases	7
MESH:C563928	MESH:C563928	Speech-Sound Disorder	CTD_diseases	7
MESH:C563930	MESH:C563930	Epilepsy, Nocturnal Frontal Lobe, Type 1	CTD_diseases	7
MESH:C563940	MESH:C563940	Angiokeratoma Corporis Diffusum with Arteriovenous Fistulas	CTD_diseases	7
MESH:C563947	MESH:C563947	Pachydermodactyly, Familial	CTD_diseases	7
MESH:C563964	MESH:C563964	Peroxisome Biogenesis Disorder, Complementation Group 14	CTD_diseases	7
MESH:C563965	MESH:C563965	Peroxisome Biogenesis Disorder, Complementation Group J	CTD_diseases	7
MESH:C563980	MESH:C563980	Fanconi Anemia, Complementation Group D1	CTD_diseases	7
MESH:C563989	MESH:C563989	Ceroid Lipofuscinosis, Neuronal, 7	CTD_diseases	7
MESH:C564016	MESH:C564016	Nephropathy, Chronic Tubulointerstitial	CTD_diseases	7
MESH:C564021	MESH:C564021	Leigh Syndrome Due To Mitochondrial Complex I Deficiency	CTD_diseases	7
MESH:C564025	MESH:C564025	Striatonigral Degeneration, Infantile, Mitochondrial	CTD_diseases	7
MESH:C564032	MESH:C564032	Sertoli Cell-Only Syndrome, Type II	CTD_diseases	7
MESH:C564033	MESH:C564033	Incomplete Sertoli Cell-Only Syndrome	CTD_diseases	7
MESH:C564036	MESH:C564036	Mental Retardation, X-Linked 89	CTD_diseases	7
MESH:C564038	MESH:C564038	Neuroacanthocytosis, Mcleod Type	CTD_diseases	7
MESH:C564058	MESH:C564058	Turner Syndrome-Associated Neurocognitive Phenotype	CTD_diseases	7
MESH:C564064	MESH:C564064	Epileptic Encephalopathy, Early Infantile, 2	CTD_diseases	7
MESH:C564069	MESH:C564069	Mental Retardation, X-Linked, Syndromic, Ube2a-Related	CTD_diseases	7
MESH:C564097	MESH:C564097	Muscular Dystrophy, Hemizygous Lethal Type	CTD_diseases	7
MESH:C564100	MESH:C564100	Metacarpal 4 5 Fusion	CTD_diseases	7
MESH:C564109	MESH:C564109	Male Pseudohermaphroditism due to Deficiency of Testicular 17,20-Desmolase	CTD_diseases	7
MESH:C564160	MESH:C564160	Pseudohypoaldosteronism, Type IIa	CTD_diseases	7
MESH:C564161	MESH:C564161	Pseudohypoaldosteronism, Type IIb	CTD_diseases	7
MESH:C564162	MESH:C564162	Pseudohypoaldosteronism, Type IIc	CTD_diseases	7
MESH:C564170	MESH:C564170	Hyperlipoproteinemia, Type II, and Deafness	CTD_diseases	7
MESH:C564178	MESH:C564178	Horner Syndrome, Congenital	CTD_diseases	7
MESH:C564179	MESH:C564179	Charcot-Marie-Tooth Disease, Foot Deformity of	CTD_diseases	7
MESH:C564198	MESH:C564198	Hemifacial Spasm, Familial	CTD_diseases	7
MESH:C564242	MESH:C564242	Muscular Dystrophy, Limb-Girdle, Type 1F	CTD_diseases	7
MESH:C564256	MESH:C564256	Charcot-Marie-Tooth Disease, Recessive Intermediate A	CTD_diseases	7
MESH:C564257	MESH:C564257	Charcot-Marie-Tooth Disease, Dominant Intermediate C	CTD_diseases	7
MESH:C564291	MESH:C564291	Heterotopia, Periventricular, associated with Chromosome 5p Anomalies	CTD_diseases	7
MESH:C564292	MESH:C564292	Heterotopia, Periventricular, Autosomal Recessive	CTD_diseases	7
MESH:C564325	MESH:C564325	Charcot-Marie-Tooth Disease, Autosomal Dominant, Type 2k	CTD_diseases	7
MESH:C564333	MESH:C564333	Charcot-Marie-Tooth Disease, Dominant Intermediate D	CTD_diseases	7
MESH:C564345	MESH:C564345	Parkinson Disease 11	CTD_diseases	7
MESH:C564356	MESH:C564356	Acute Tubulointerstitial Nephritis	CTD_diseases	7
MESH:C564367	MESH:C564367	Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis	CTD_diseases	7
MESH:C564377	MESH:C564377	Myopathy, Distal, With Early Respiratory Failure, Autosomal Dominant	CTD_diseases	7
MESH:C564383	MESH:C564383	Camptosynpolydactyly, Complex	CTD_diseases	7
MESH:C564385	MESH:C564385	Migraine, Familial Hemiplegic, 4	CTD_diseases	7
MESH:C564440	MESH:C564440	Colorblindness, Partial Tritanomaly	CTD_diseases	7
MESH:C564446	MESH:C564446	Charcot-Marie-Tooth Peroneal Muscular Atrophy and Friedreich Ataxia, Combined	CTD_diseases	7
MESH:C564463	MESH:C564463	Amelogenesis Imperfecta, Hypomaturation Type, with Snow-Capped Teeth	CTD_diseases	7
MESH:C564470	MESH:C564470	Mental Retardation, X-Linked 59	CTD_diseases	7
MESH:C564476	MESH:C564476	Premature Ovarian Failure 2b	CTD_diseases	7
MESH:C564482	MESH:C564482	Mental Retardation, X-Linked 91	CTD_diseases	7
MESH:C564483	MESH:C564483	Mental Retardation, X-Linked 92	CTD_diseases	7
MESH:C564489	MESH:C564489	Mental Retardation, X-Linked 78	CTD_diseases	7
MESH:C564490	MESH:C564490	Mental Retardation, X-Linked Nonsyndromic	CTD_diseases	7
MESH:C564494	MESH:C564494	Mental Retardation, X-Linked, Syndromic, Jarid1c-Related	CTD_diseases	7
MESH:C564496	MESH:C564496	Mental Retardation, X-Linked 82	CTD_diseases	7
MESH:C564497	MESH:C564497	Fanconi Anemia, Complementation Group B	CTD_diseases	7
MESH:C564501	MESH:C564501	Mental Retardation, X-Linked 84	CTD_diseases	7
MESH:C564502	MESH:C564502	Mental Retardation, X-Linked 52	CTD_diseases	7
MESH:C564503	MESH:C564503	Mental Retardation, X-Linked 45	CTD_diseases	7
MESH:C564511	MESH:C564511	Mental Retardation, X-Linked 77	CTD_diseases	7
MESH:C564513	MESH:C564513	Mental Retardation, X-Linked 46	CTD_diseases	7
MESH:C564515	MESH:C564515	Mental Retardation, X-Linked 81	CTD_diseases	7
MESH:C564522	MESH:C564522	Mental Retardation, X-Linked 63	CTD_diseases	7
MESH:C564524	MESH:C564524	Mental Retardation, X-Linked 42	CTD_diseases	7
MESH:C564528	MESH:C564528	Mental Retardation, X-Linked 73	CTD_diseases	7
MESH:C564533	MESH:C564533	Mental Retardation, X-Linked 53	CTD_diseases	7
MESH:C564545	MESH:C564545	Androgen Insensitivity Syndrome due to Coactivator Deficiency	CTD_diseases	7
MESH:C564547	MESH:C564547	Mental Retardation, X-Linked 72	CTD_diseases	7
MESH:C564551	MESH:C564551	Armfield X-Linked Mental Retardation Syndrome	CTD_diseases	7
MESH:C564566	MESH:C564566	Mental Retardation, X-Linked 58	CTD_diseases	7
MESH:C564578	MESH:C564578	Bartter Syndrome, Type 3, with Hypocalciuria	CTD_diseases	7
MESH:C564599	MESH:C564599	Spastic Paraplegia 7, Autosomal Recessive	CTD_diseases	7
MESH:C564607	MESH:C564607	Epilepsy, Intractable Childhood, With Generalized Tonic-Clonic Seizures	CTD_diseases	7
MESH:C564612	MESH:C564612	Muscular Dystrophy, Limb-Girdle, Type 2I	CTD_diseases	7
MESH:C564645	MESH:C564645	Albinism, Oculocutaneous, Type I, Temperature-Sensitive	CTD_diseases	7
MESH:C564653	MESH:C564653	Parkinson Disease 10	CTD_diseases	7
MESH:C564657	MESH:C564657	Friedreich Ataxia with Retained Reflexes	CTD_diseases	7
MESH:C564664	MESH:C564664	Myopathy, Distal, with Anterior Tibial Onset	CTD_diseases	7
MESH:C564665	MESH:C564665	Azoospermia, Nonobstructive	CTD_diseases	7
MESH:C564696	MESH:C564696	Oculocutaneous Albinism, Type IV	CTD_diseases	7
MESH:C564699	MESH:C564699	Ichthyosis, Lamellar, 5	CTD_diseases	7
MESH:C564702	MESH:C564702	Charcot-Marie-Tooth Disease, Dominant Intermediate A	CTD_diseases	7
MESH:C564703	MESH:C564703	Charcot-Marie-Tooth Disease, Dominant Intermediate B	CTD_diseases	7
MESH:C564704	MESH:C564704	Charcot-Marie-Tooth Neuropathy, Dominant Intermediate B, with Neutropenia	CTD_diseases	7
MESH:C564712	MESH:C564712	Mental Retardation, X-Linked, with Isolated Growth Hormone Deficiency	CTD_diseases	7
MESH:C564713	MESH:C564713	Mental Retardation, X-Linked 50	CTD_diseases	7
MESH:C564738	MESH:C564738	Pontocerebellar Hypoplasia Type 2A	CTD_diseases	7
MESH:C564811	MESH:C564811	Spastic Paraplegia 5a, Autosomal Recessive	CTD_diseases	7
MESH:C564824	MESH:C564824	Second Metatarsal-Metacarpal Syndrome	CTD_diseases	7
MESH:C564879	MESH:C564879	Polyneuropathy, Mixed, of Early Onset	CTD_diseases	7
MESH:C564915	MESH:C564915	Osteopetrosis, Autosomal Recessive 1	CTD_diseases	7
MESH:C564917	MESH:C564917	Osteoma of Middle Ear	CTD_diseases	7
MESH:C564930	MESH:C564930	Olivopontocerebellar Atrophy II, Autosomal Recessive	CTD_diseases	7
MESH:C564953	MESH:C564953	Ceroid Lipofuscinosis, Neuronal, 1	CTD_diseases	7
MESH:C564961	MESH:C564961	Leigh Syndrome Due To Mitochondrial Complex II Deficiency	CTD_diseases	7
MESH:C564962	MESH:C564962	Leigh Syndrome due to Mitochondrial Complex III Deficiency	CTD_diseases	7
MESH:C564963	MESH:C564963	Leigh Syndrome due to Mitochondrial Complex IV Deficiency	CTD_diseases	7
MESH:C564964	MESH:C564964	Leigh Syndrome due to Mitochondrial Complex V Deficiency	CTD_diseases	7
MESH:C564976	MESH:C564976	Epilepsy, Progressive Myoclonic 2B	CTD_diseases	7
MESH:C565058	MESH:C565058	Elliptocytosis 2	CTD_diseases	7
MESH:C565064	MESH:C565064	Ectrodactyly-Cleft Palate Syndrome	CTD_diseases	7
MESH:C565086	MESH:C565086	Duodenal Ulcer, Hyperpepsinogenemic I	CTD_diseases	7
MESH:C565097	MESH:C565097	Digitotalar Dysmorphism	CTD_diseases	7
MESH:C565186	MESH:C565186	Alopecia Areata 2	CTD_diseases	7
MESH:C565204	MESH:C565204	Parkinson Disease 13	CTD_diseases	7
MESH:C565208	MESH:C565208	Pyloric Stenosis, Infantile Hypertrophic, 2	CTD_diseases	7
MESH:C565210	MESH:C565210	Spastic Paraplegia 31, Autosomal Dominant	CTD_diseases	7
MESH:C565214	MESH:C565214	Spastic Paraplegia 33, Autosomal Dominant	CTD_diseases	7
MESH:C565223	MESH:C565223	Zygodactyly 1	CTD_diseases	7
MESH:C565236	MESH:C565236	Deafness, Sensorineural, with Hypertrophic Cardiomyopathy	CTD_diseases	7
MESH:C565238	MESH:C565238	Parkinson Disease 7, Autosomal Recessive Early-Onset	CTD_diseases	7
MESH:C565256	MESH:C565256	Diamond-Blackfan Anemia With Microtia And Cleft Palate	CTD_diseases	7
MESH:C565261	MESH:C565261	Hereditary Motor And Sensory Neuropathy, Type IIC	CTD_diseases	7
MESH:C565276	MESH:C565276	Parkinson Disease 6, Autosomal Recessive Early-Onset	CTD_diseases	7
MESH:C565296	MESH:C565296	Convulsions, Benign Familial Infantile, 2	CTD_diseases	7
MESH:C565323	MESH:C565323	Fibromatosis, Gingival, 2	CTD_diseases	7
MESH:C565324	MESH:C565324	Parkinson Disease 4, Autosomal Dominant Lewy Body	CTD_diseases	7
MESH:C565334	MESH:C565334	Epilepsy, Nocturnal Frontal Lobe, Type 3	CTD_diseases	7
MESH:C565346	MESH:C565346	Tuberous Sclerosis 1	CTD_diseases	7
MESH:C565413	MESH:C565413	Maple Syrup Urine Disease, Type IA	CTD_diseases	7
MESH:C565414	MESH:C565414	Maple Syrup Urine Disease, Type IB	CTD_diseases	7
MESH:C565415	MESH:C565415	Maple Syrup Urine Disease, Type II	CTD_diseases	7
MESH:C565418	MESH:C565418	alpha-Mannosidosis, Type II	CTD_diseases	7
MESH:C565473	MESH:C565473	Self-Healing Collodion Baby	CTD_diseases	7
MESH:C565477	MESH:C565477	Hypopituitarism, Congenital, with Central Diabetes Insipidus	CTD_diseases	7
MESH:C565500	MESH:C565500	Hyperlexia	CTD_diseases	7
MESH:C565521	MESH:C565521	Hemolytic Uremic Syndrome, Typical	CTD_diseases	7
MESH:C565537	MESH:C565537	46,XY Gonadal Dysgenesis, Complete or Partial, DHH-Related	CTD_diseases	7
MESH:C565539	MESH:C565539	GSD IV, Classic Hepatic	CTD_diseases	7
MESH:C565561	MESH:C565561	Friedreich Ataxia 1	CTD_diseases	7
MESH:C565568	MESH:C565568	Myofibromatosis, Juvenile	CTD_diseases	7
MESH:C565572	MESH:C565572	Estren-Dameshek Variant of Fanconi Anemia	CTD_diseases	7
MESH:C565573	MESH:C565573	Estren-Dameshek Variant of Fanconi Pancytopenia	CTD_diseases	7
MESH:C565598	MESH:C565598	Elliptocytosis, Atypical	CTD_diseases	7
MESH:C565621	MESH:C565621	Disseminated Sclerosis with Narcolepsy	CTD_diseases	7
MESH:C565646	MESH:C565646	Deafness, Congenital, with Total Albinism	CTD_diseases	7
MESH:C565647	MESH:C565647	Split-Hand/Foot Malformation With Sensorineural Hearing Loss	CTD_diseases	7
MESH:C565665	MESH:C565665	Craniosynostosis with Fibular Aplasia	CTD_diseases	7
MESH:C565666	MESH:C565666	Craniosynostosis with Anomalies of the Cranial Base and Digits	CTD_diseases	7
MESH:C565696	MESH:C565696	Kallmann Syndrome 4	CTD_diseases	7
MESH:C565700	MESH:C565700	Aneurysm, Intracranial Berry, 4	CTD_diseases	7
MESH:C565723	MESH:C565723	Williams-Beuren Region Duplication Syndrome	CTD_diseases	7
MESH:C565732	MESH:C565732	Hypobetalipoproteinemia, Familial, 2	CTD_diseases	7
MESH:C565737	MESH:C565737	North American Indian Childhood Cirrhosis	CTD_diseases	7
MESH:C565747	MESH:C565747	Huntington Disease-Like 3	CTD_diseases	7
MESH:C565753	MESH:C565753	Craniosynostosis, Type 2	CTD_diseases	7
MESH:C565766	MESH:C565766	Hyperlipidemia, Combined, 2	CTD_diseases	7
MESH:C565789	MESH:C565789	Advanced Sleep-Phase Syndrome, Familial	CTD_diseases	7
MESH:C565825	MESH:C565825	Cerebellar Ataxia, Deafness, and Narcolepsy	CTD_diseases	7
MESH:C565866	MESH:C565866	Cerebelloparenchymal Disorder II	CTD_diseases	7
MESH:C565869	MESH:C565869	Cerebellar Ataxia and Neurosensory Deafness	CTD_diseases	7
MESH:C565907	MESH:C565907	BCG Infection, Generalized Familial	CTD_diseases	7
MESH:C565908	MESH:C565908	BCG and Salmonella Infection, Disseminated	CTD_diseases	7
MESH:C565909	MESH:C565909	BCG Infection, Generalized Familial Semibenign, Autosomal Dominant	CTD_diseases	7
MESH:C565952	MESH:C565952	Anemia, Nonspherocytic Hemolytic, possibly due to Defect in Porphyrin Metabolism	CTD_diseases	7
MESH:C565953	MESH:C565953	Anemia, Nonspherocytic Hemolytic, associated with Abnormality of Red Cell Membrane	CTD_diseases	7
MESH:C565969	MESH:C565969	Neutropenia, Severe Congenital, Autosomal Dominant 1	CTD_diseases	7
MESH:C565972	MESH:C565972	Adrenocortical Carcinoma, Hereditary	CTD_diseases	7
MESH:C565973	MESH:C565973	Adrenocortical Carcinoma, Pediatric	CTD_diseases	7
MESH:C565977	MESH:C565977	Hyperandrogenism, Nonclassic Type, due to 21-Hydroxylase Deficiency	CTD_diseases	7
MESH:C565991	MESH:C565991	Wilms Tumor 3	CTD_diseases	7
MESH:C566006	MESH:C566006	Long Qt Syndrome 1/2	CTD_diseases	7
MESH:C566019	MESH:C566019	Tune Deafness	CTD_diseases	7
MESH:C566021	MESH:C566021	Tuberous Sclerosis 2	CTD_diseases	7
MESH:C566023	MESH:C566023	Down Syndrome Critical Region	CTD_diseases	7
MESH:C566025	MESH:C566025	Leukemia, Megakaryoblastic, of Down Syndrome	CTD_diseases	7
MESH:C566028	MESH:C566028	Triphalangeal Thumb with Double Phalanges	CTD_diseases	7
MESH:C566051	MESH:C566051	Takao VCF Syndrome	CTD_diseases	7
MESH:C566068	MESH:C566068	Tendons, Extensor, of Fingers, Anomalous Insertion of	CTD_diseases	7
MESH:C566085	MESH:C566085	Syringomas, Multiple	CTD_diseases	7
MESH:C566094	MESH:C566094	Synpolydactyly 1	CTD_diseases	7
MESH:C566096	MESH:C566096	Syndactyly, Type I	CTD_diseases	7
MESH:C566100	MESH:C566100	Symphalangism, C. S. Lewis Type	CTD_diseases	7
MESH:C566113	MESH:C566113	Progressive Encephalomyelitis with Rigidity	CTD_diseases	7
MESH:C566126	MESH:C566126	Chylomicronemia, Familial, due to Circulating Inhibitor of Lipoprotein Lipase	CTD_diseases	7
MESH:C566136	MESH:C566136	Charcot-Marie-Tooth Disease, Demyelinating, Type 1e	CTD_diseases	7
MESH:C566138	MESH:C566138	Charcot-Marie-Tooth Disease, Axonal, Type 2a1	CTD_diseases	7
MESH:C566187	MESH:C566187	Epidermolytic Hyperkeratosis, Late-Onset	CTD_diseases	7
MESH:C566206	MESH:C566206	Brachmann-De Lange-Like Facial Changes With Microcephaly, Metatarsus Adductus, And Developmental Del	CTD_diseases	7
MESH:C566230	MESH:C566230	Ovalocytosis, Malaysian-Melanesian-Filipino Type	CTD_diseases	7
MESH:C566231	MESH:C566231	Elliptocytosis 4	CTD_diseases	7
MESH:C566235	MESH:C566235	Aurocephalosyndactyly	CTD_diseases	7
MESH:C566239	MESH:C566239	Atrial Septal Defect 1	CTD_diseases	7
MESH:C566240	MESH:C566240	Atrial Septal Defect, Primum Type	CTD_diseases	7
MESH:C566241	MESH:C566241	Atrial Septal Defect, Secundum Type	CTD_diseases	7
MESH:C566270	MESH:C566270	Apolipoprotein C-III Deficiency	CTD_diseases	7
MESH:C566284	MESH:C566284	Aneurysm, Intracranial Berry, 1	CTD_diseases	7
MESH:C566285	MESH:C566285	Erythroreticulosis, Hereditary Benign	CTD_diseases	7
MESH:C566293	MESH:C566293	Amelogenesis Imperfecta, Type IV	CTD_diseases	7
MESH:C566303	MESH:C566303	Alopecia Areata 1	CTD_diseases	7
MESH:C566311	MESH:C566311	Adenosine Triphosphatase Deficiency, Anemia Due To	CTD_diseases	7
MESH:C566331	MESH:C566331	Hypercholesterolemia, Autosomal Recessive	CTD_diseases	7
MESH:C566337	MESH:C566337	Hypercholesterolemia, Autosomal Dominant, 3	CTD_diseases	7
MESH:C566345	MESH:C566345	Acromelic Frontonasal Dysostosis	CTD_diseases	7
MESH:C566346	MESH:C566346	Blue Nevi, Familial Multiple	CTD_diseases	7
MESH:C566370	MESH:C566370	Muscular Dystrophy, Limb-Girdle, Type 1D	CTD_diseases	7
MESH:C566387	MESH:C566387	Peroxisome Biogenesis Disorder, Complementation Group 9	CTD_diseases	7
MESH:C566388	MESH:C566388	Peroxisome Biogenesis Disorder, Complementation Group D	CTD_diseases	7
MESH:C566398	MESH:C566398	Huntington Disease-Like 1	CTD_diseases	7
MESH:C566400	MESH:C566400	Epilepsy, Nocturnal Frontal Lobe, Type 2	CTD_diseases	7
MESH:C566405	MESH:C566405	Peroxisome Biogenesis Disorder, Complementation Group 12	CTD_diseases	7
MESH:C566406	MESH:C566406	Peroxisome Biogenesis Disorder, Complementation Group G	CTD_diseases	7
MESH:C566422	MESH:C566422	Peroxisome Biogenesis Disorder, Complementation Group 7	CTD_diseases	7
MESH:C566428	MESH:C566428	Renal Tubular Acidosis, Distal, Autosomal Recessive, with Late-Onset Sensorineural Hearing Loss	CTD_diseases	7
MESH:C566433	MESH:C566433	Chromosome 16p13.3 Deletion Syndrome	CTD_diseases	7
MESH:C566437	MESH:C566437	Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 4	CTD_diseases	7
MESH:C566438	MESH:C566438	Ceroid Lipofuscinosis, Neuronal, 10	CTD_diseases	7
MESH:C566444	MESH:C566444	Giant Axonal Neuropathy, Autosomal Dominant	CTD_diseases	7
MESH:C566445	MESH:C566445	Myopathy, Distal 3	CTD_diseases	7
MESH:C566500	MESH:C566500	Migraine, Familial Hemiplegic, 3	CTD_diseases	7
MESH:C566502	MESH:C566502	Visceral Neuropathy, Familial, Autosomal Dominant	CTD_diseases	7
MESH:C566530	MESH:C566530	Bartter Syndrome, Type 4A	CTD_diseases	7
MESH:C566535	MESH:C566535	Hyperlipidemia, Combined, 1	CTD_diseases	7
MESH:C566540	MESH:C566540	Migraine, Familial Basilar	CTD_diseases	7
MESH:C566552	MESH:C566552	Parkinson Disease 3, Autosomal Dominant Lewy Body	CTD_diseases	7
MESH:C566568	MESH:C566568	Peroxisome Biogenesis Disorder, Complementation Group 1	CTD_diseases	7
MESH:C566569	MESH:C566569	Peroxisome Biogenesis Disorder, Complementation Group E	CTD_diseases	7
MESH:C566572	MESH:C566572	Cervical Dystonia, Primary	CTD_diseases	7
MESH:C566589	MESH:C566589	Muscular Dystrophy, Limb-Girdle, Type 1E	CTD_diseases	7
MESH:C566594	MESH:C566594	Friedreich Ataxia 2	CTD_diseases	7
MESH:C566599	MESH:C566599	Muscular Dystrophy, Limb-Girdle, Type 2G	CTD_diseases	7
MESH:C566601	MESH:C566601	Episodic Ataxia, Type 5	CTD_diseases	7
MESH:C566624	MESH:C566624	Peroxisome Biogenesis Disorder, Complementation Group K	CTD_diseases	7
MESH:C566625	MESH:C566625	Peroxisome Biogenesis Disorder, Complementation Group 13	CTD_diseases	7
MESH:C566626	MESH:C566626	Peroxisome Biogenesis Disorder, Complementation Group H	CTD_diseases	7
MESH:C566627	MESH:C566627	Ceroid Lipofuscinosis, Neuronal, 6	CTD_diseases	7
MESH:C566633	MESH:C566633	Peroxisome Biogenesis Disorder, Complementation Group 3	CTD_diseases	7
MESH:C566634	MESH:C566634	Peroxisome Biogenesis Disorder, Complementation Group 11	CTD_diseases	7
MESH:C566635	MESH:C566635	Peroxisome Biogenesis Disorder, Complementation Group R	CTD_diseases	7
MESH:C566668	MESH:C566668	Spinocerebellar Atrophy With Pupillary Paralysis	CTD_diseases	7
MESH:C566678	MESH:C566678	Elliptocytosis 3	CTD_diseases	7
MESH:C566709	MESH:C566709	Rhabdomyosarcoma, Embryonal, 2	CTD_diseases	7
MESH:C566714	MESH:C566714	Osteosarcoma, Retinoblastoma-Related	CTD_diseases	7
MESH:C566730	MESH:C566730	Pyloric Stenosis, Infantile Hypertrophic 1	CTD_diseases	7
MESH:C566764	MESH:C566764	Prader-Willi-Like Syndrome Associated With Chromosome 6	CTD_diseases	7
MESH:C566768	MESH:C566768	Porphyria Cutanea Tarda, Type I	CTD_diseases	7
MESH:C566769	MESH:C566769	Porphyria, Acute Intermittent, Nonerythroid Variant	CTD_diseases	7
MESH:C566792	MESH:C566792	Potter Type III Polycystic Kidney Disease	CTD_diseases	7
MESH:C566810	MESH:C566810	Wegener-Like Granulomatosis	CTD_diseases	7
MESH:C566823	MESH:C566823	Parkinson Disease, Familial, Type 1	CTD_diseases	7
MESH:C566831	MESH:C566831	Paragangliomas with Sensorineural Hearing Loss	CTD_diseases	7
MESH:C566844	MESH:C566844	Thanatophoric Dysplasia, Type I	CTD_diseases	7
MESH:C566857	MESH:C566857	Ceroid Lipofuscinosis, Neuronal, 2	CTD_diseases	7
MESH:C566858	MESH:C566858	Copper-Overload Cirrhosis	CTD_diseases	7
MESH:C566872	MESH:C566872	Dilution, Pigmentary	CTD_diseases	7
MESH:C566875	MESH:C566875	Mental Retardation, X-Linked, Syndromic 13	CTD_diseases	7
MESH:C566876	MESH:C566876	Mental Retardation, X-Linked 79	CTD_diseases	7
MESH:C566877	MESH:C566877	Mental Retardation, X-Linked, With Spasticity	CTD_diseases	7
MESH:C566878	MESH:C566878	Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations	CTD_diseases	7
MESH:C566883	MESH:C566883	Osteopetrosis, Autosomal Recessive 5	CTD_diseases	7
MESH:C566889	MESH:C566889	Glycogen Storage Disease IIIA	CTD_diseases	7
MESH:C566890	MESH:C566890	Glycogen Storage Disease IIIB	CTD_diseases	7
MESH:C566891	MESH:C566891	Glycogen Storage Disease IIIC	CTD_diseases	7
MESH:C566892	MESH:C566892	Glycogen Storage Disease IIID	CTD_diseases	7
MESH:C566902	MESH:C566902	Epilepsy, Familial Temporal Lobe, 4	CTD_diseases	7
MESH:C566903	MESH:C566903	Epilepsy, Familial Mesial Temporal Lobe	CTD_diseases	7
MESH:C566911	MESH:C566911	Renal Tubular Acidosis, Distal, With Normal Red Cell Morphology	CTD_diseases	7
MESH:C566912	MESH:C566912	Muscular Dystrophy, Limb-Girdle, Type 2M	CTD_diseases	7
MESH:C566921	MESH:C566921	Premature Ovarian Failure 5	CTD_diseases	7
MESH:C566931	MESH:C566931	Osteopetrosis, Autosomal Recessive 6	CTD_diseases	7
MESH:C566933	MESH:C566933	Osteopetrosis, Autosomal Recessive 4	CTD_diseases	7
MESH:C566963	MESH:C566963	Atrial Septal Defect 4	CTD_diseases	7
MESH:C566968	MESH:C566968	Muscular Dystrophy, Limb-Girdle, Type 2L	CTD_diseases	7
MESH:C566969	MESH:C566969	Ataxia, Spastic, 2, Autosomal Recessive	CTD_diseases	7
MESH:C566984	MESH:C566984	Charcot-Marie-Tooth Disease, Type 4j	CTD_diseases	7
MESH:C566993	MESH:C566993	Ataxia, Spastic, 1, Autosomal Dominant	CTD_diseases	7
MESH:C567002	MESH:C567002	Epilepsy, Childhood Absence, Susceptibility To, 4	CTD_diseases	7
MESH:C567028	MESH:C567028	Fibromatosis, Gingival, 4	CTD_diseases	7
MESH:C567050	MESH:C567050	Supranuclear Palsy, Progressive, 3	CTD_diseases	7
MESH:C567063	MESH:C567063	Mental Retardation, X-Linked, Syndromic 14	CTD_diseases	7
MESH:C567069	MESH:C567069	Mental Retardation, X-Linked, With Brachydactyly And Macroglossia	CTD_diseases	7
MESH:C567076	MESH:C567076	17,20-Lyase Deficiency, Isolated	CTD_diseases	7
MESH:C567095	MESH:C567095	Epilepsy, Progressive Myoclonic 3	CTD_diseases	7
MESH:C567146	MESH:C567146	Amelogenesis Imperfecta, Hypomaturation Type, Iia1	CTD_diseases	7
MESH:C567147	MESH:C567147	Amelogenesis Imperfecta, Type Ic	CTD_diseases	7
MESH:C567159	MESH:C567159	Spherocytosis, Type 1	CTD_diseases	7
MESH:C567186	MESH:C567186	Mullerian Aplasia and Hyperandrogenism	CTD_diseases	7
MESH:C567199	MESH:C567199	Kallmann Syndrome 6	CTD_diseases	7
MESH:C567202	MESH:C567202	Spherocytosis, Type 5	CTD_diseases	7
MESH:C567207	MESH:C567207	Episodic Ataxia, Type 6	CTD_diseases	7
MESH:C567208	MESH:C567208	Spherocytosis, Type 4	CTD_diseases	7
MESH:C567219	MESH:C567219	Deafness, Autosomal Recessive 36, Without Vestibular Involvement	CTD_diseases	7
MESH:C567220	MESH:C567220	Kallmann Syndrome 5	CTD_diseases	7
MESH:C567237	MESH:C567237	Aneurysm, Intracranial Berry, 10	CTD_diseases	7
MESH:C567238	MESH:C567238	Aneurysm, Intracranial Berry, 9	CTD_diseases	7
MESH:C567253	MESH:C567253	Diamond-Blackfan Anemia 8	CTD_diseases	7
MESH:C567254	MESH:C567254	Diamond-Blackfan Anemia 7	CTD_diseases	7
MESH:C567260	MESH:C567260	Neutropenia, Severe Congenital, Autosomal Recessive 4	CTD_diseases	7
MESH:C567262	MESH:C567262	Spastic Paraplegia 42, Autosomal Dominant	CTD_diseases	7
MESH:C567266	MESH:C567266	Deafness, Autosomal Dominant, Due To Mutation In Myo1a	CTD_diseases	7
MESH:C531598	MESH:C531598	Familial acanthosis nigricans	CTD_diseases	7
MESH:C531601	MESH:C531601	Tonic, sluggishly reacting pupil and hypoactive or absent tendon reflexes	CTD_diseases	7
MESH:C531604	MESH:C531604	Primary visual agnosia	CTD_diseases	7
MESH:C531609	MESH:C531609	Diffuse alopecia	CTD_diseases	7
MESH:C531633	MESH:C531633	Biotin deficiency	CTD_diseases	7
MESH:C531690	MESH:C531690	Potassium and magnesium depletion	CTD_diseases	7
MESH:C531699	MESH:C531699	Hb C disease	CTD_diseases	7
MESH:C531743	MESH:C531743	Cystic dilatation of renal collecting tubes	CTD_diseases	7
MESH:C531783	MESH:C531783	Hip socket neuropathy	CTD_diseases	7
MESH:C531834	MESH:C531834	Toxocara canis infection (canine roundworms)	CTD_diseases	7
MESH:C531835	MESH:C531835	Esophageal atresia with or without tracheoesophageal fistula	CTD_diseases	7
MESH:C531849	MESH:C531849	Intestinal lipophagic granulomatosis	CTD_diseases	7
MESH:C535269	MESH:C535269	Preeyasombat Varavithya syndrome	CTD_diseases	7
MESH:C535272	MESH:C535272	Premature ovarian failure, familial	CTD_diseases	7
MESH:C535277	MESH:C535277	Primary ciliary dyskinesia, 2	CTD_diseases	7
MESH:C535278	MESH:C535278	Primary ciliary dyskinesia, 3	CTD_diseases	7
MESH:C535279	MESH:C535279	Primary ciliary dyskinesia, 4	CTD_diseases	7
MESH:C535287	MESH:C535287	Hunt's syndrome	CTD_diseases	7
MESH:C535301	MESH:C535301	Charcot-Marie-Tooth disease, Type 4E	CTD_diseases	7
MESH:C535302	MESH:C535302	Charcot-Marie-Tooth disease, X-linked recessive, 2	CTD_diseases	7
MESH:C535303	MESH:C535303	Charcot-Marie-Tooth disease, X-linked recessive, 3	CTD_diseases	7
MESH:C535308	MESH:C535308	3-methylcrotonyl CoA carboxylase 1 deficiency	CTD_diseases	7
MESH:C535309	MESH:C535309	3-methylcrotonyl CoA carboxylase 2 deficiency	CTD_diseases	7
MESH:C535325	MESH:C535325	6-pyruvoyl-tetrahydropterin synthase deficiency	CTD_diseases	7
MESH:C535347	MESH:C535347	Catel Manzke syndrome	CTD_diseases	7
MESH:C535363	MESH:C535363	Chromosome 1, deletion q21 q25	CTD_diseases	7
MESH:C535370	MESH:C535370	Chromosome 20, deletion 20p	CTD_diseases	7
MESH:C535399	MESH:C535399	Charcot-Marie-Tooth disease, dominant intermediate 1	CTD_diseases	7
MESH:C535400	MESH:C535400	Charcot-Marie-Tooth disease, dominant intermediate 2	CTD_diseases	7
MESH:C535401	MESH:C535401	Charcot-Marie-Tooth disease, dominant intermediate 3	CTD_diseases	7
MESH:C535413	MESH:C535413	Charcot-Marie-Tooth disease, Type 2F	CTD_diseases	7
MESH:C535414	MESH:C535414	Charcot-Marie-Tooth disease, Type 2G	CTD_diseases	7
MESH:C535415	MESH:C535415	Charcot-Marie-Tooth disease, Type 2H	CTD_diseases	7
MESH:C535416	MESH:C535416	Charcot-Marie-Tooth disease, Type 2I	CTD_diseases	7
MESH:C535417	MESH:C535417	Charcot-Marie-Tooth disease, Type 2J	CTD_diseases	7
MESH:C535418	MESH:C535418	Charcot-Marie-Tooth disease, Type 2K	CTD_diseases	7
MESH:C535419	MESH:C535419	Charcot-Marie-Tooth disease, Type 4A	CTD_diseases	7
MESH:C535420	MESH:C535420	Charcot-Marie-Tooth disease, Type 4B1	CTD_diseases	7
MESH:C535421	MESH:C535421	Charcot-Marie-Tooth disease, Type 4B2	CTD_diseases	7
MESH:C535423	MESH:C535423	Charcot-Marie-Tooth disease, Type 4C	CTD_diseases	7
MESH:C535425	MESH:C535425	Congenital torticollis	CTD_diseases	7
MESH:C535435	MESH:C535435	Beta-sarcoglycanopathy	CTD_diseases	7
MESH:C535469	MESH:C535469	Coproporphyria	CTD_diseases	7
MESH:C535508	MESH:C535508	Ermine phenotype	CTD_diseases	7
MESH:C535524	MESH:C535524	Infantile polymyoclonus	CTD_diseases	7
MESH:C535526	MESH:C535526	Infection with Mycobacterium marinum	CTD_diseases	7
MESH:C535554	MESH:C535554	Abdominal obesity metabolic syndrome	CTD_diseases	7
MESH:C535574	MESH:C535574	Carbamoyl phosphate synthase 1 deficiency	CTD_diseases	7
MESH:C535585	MESH:C535585	Carnevale Hernandez Castillo syndrome	CTD_diseases	7
MESH:C535590	MESH:C535590	Carrington syndrome	CTD_diseases	7
MESH:C535591	MESH:C535591	Chromosome 1, monosomy 1p	CTD_diseases	7
MESH:C535592	MESH:C535592	Chromosome 1, monosomy 1p22 p13	CTD_diseases	7
MESH:C535593	MESH:C535593	Chromosome 1, monosomy 1p31 p22	CTD_diseases	7
MESH:C535594	MESH:C535594	Chromosome 1, monosomy 1p32	CTD_diseases	7
MESH:C535595	MESH:C535595	Chromosome 1, monosomy 1p34 p32	CTD_diseases	7
MESH:C535596	MESH:C535596	Chromosome 1, monosomy 1q25 q32	CTD_diseases	7
MESH:C535597	MESH:C535597	Craniotelencephalic dysplasia	CTD_diseases	7
MESH:C535624	MESH:C535624	Hamanishi Ueba Tsuji syndrome	CTD_diseases	7
MESH:C535633	MESH:C535633	Harding ataxia	CTD_diseases	7
MESH:C535673	MESH:C535673	Acute erythroleukemia	CTD_diseases	7
MESH:C535676	MESH:C535676	Richieri Costa Guion-Almeida syndrome	CTD_diseases	7
MESH:C535677	MESH:C535677	Richieri Costa Pereira syndrome	CTD_diseases	7
MESH:C535707	MESH:C535707	Mandibulofacial dysostosis, Treacher Collins type, autosomal recessive	CTD_diseases	7
MESH:C535710	MESH:C535710	Maple syrup urine disease, type 1A	CTD_diseases	7
MESH:C535711	MESH:C535711	Maple syrup urine disease, type 1B	CTD_diseases	7
MESH:C535712	MESH:C535712	Maple syrup urine disease, type 2	CTD_diseases	7
MESH:C535716	MESH:C535716	Neuropathy, hereditary motor and sensory, LOM type	CTD_diseases	7
MESH:C535721	MESH:C535721	Duodenal ulcer due to antral G-cell hyperfunction	CTD_diseases	7
MESH:C535761	MESH:C535761	Nephrosis, congenital	CTD_diseases	7
MESH:C535772	MESH:C535772	Dandy Walker variant	CTD_diseases	7
MESH:C535815	MESH:C535815	Neutropenia, severe chronic	CTD_diseases	7
MESH:C535845	MESH:C535845	Hawkinsinuria	CTD_diseases	7
MESH:C535886	MESH:C535886	Jones syndrome	CTD_diseases	7
MESH:C535895	MESH:C535895	Limb-girdle muscular dystrophy type 2A	CTD_diseases	7
MESH:C535897	MESH:C535897	Limb-girdle muscular dystrophy type 2H	CTD_diseases	7
MESH:C535898	MESH:C535898	Limb-girdle muscular dystrophy, type 1B	CTD_diseases	7
MESH:C535899	MESH:C535899	Limb-girdle muscular dystrophy, type 2B	CTD_diseases	7
MESH:C535906	MESH:C535906	Muscular dystrophy, limb-girdle, type 1A	CTD_diseases	7
MESH:C535919	MESH:C535919	Charcot-Marie-Tooth disease, X-linked, 1	CTD_diseases	7
MESH:C535926	MESH:C535926	Chitayat Meunier Hodgkinson syndrome	CTD_diseases	7
MESH:C535966	MESH:C535966	Colloid cysts of third ventricle	CTD_diseases	7
MESH:C535978	MESH:C535978	Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency	CTD_diseases	7
MESH:C535979	MESH:C535979	Congenital adrenal hyperplasia due to 21 hydroxylase deficiency	CTD_diseases	7
MESH:C536011	MESH:C536011	Achalasia, familial esophageal	CTD_diseases	7
MESH:C536014	MESH:C536014	Acheiropodia	CTD_diseases	7
MESH:C536021	MESH:C536021	Achromatopsia 1	CTD_diseases	7
MESH:C536033	MESH:C536033	Mastocytosis, cutaneous, with short stature, conductive hearing loss and microtia	CTD_diseases	7
MESH:C536035	MESH:C536035	Maternally Inherited Leigh Syndrome	CTD_diseases	7
MESH:C536056	MESH:C536056	Osteopetrosis autosomal dominant type 1	CTD_diseases	7
MESH:C536057	MESH:C536057	Osteopetrosis lethal	CTD_diseases	7
MESH:C536058	MESH:C536058	Osteopetrosis with renal tubular acidosis	CTD_diseases	7
MESH:C536059	MESH:C536059	Osteopetrosis, mild autosomal recessive form	CTD_diseases	7
MESH:C536101	MESH:C536101	Myopathy with lactic acidosis and sideroblastic anemia	CTD_diseases	7
MESH:C536104	MESH:C536104	Myopathy, limb-girdle, with bone fragility	CTD_diseases	7
MESH:C536109	MESH:C536109	N-acetyl glutamate synthetase deficiency	CTD_diseases	7
MESH:C536112	MESH:C536112	Partial atrioventricular canal	CTD_diseases	7
MESH:C536115	MESH:C536115	Nguyen syndrome	CTD_diseases	7
MESH:C536128	MESH:C536128	Achromatopsia 2	CTD_diseases	7
MESH:C536129	MESH:C536129	Achromatopsia 3	CTD_diseases	7
MESH:C536130	MESH:C536130	Anemia, Diamond-Blackfan, 2	CTD_diseases	7
MESH:C536144	MESH:C536144	Megalocytic interstitial nephritis	CTD_diseases	7
MESH:C536156	MESH:C536156	Keratomalacia	CTD_diseases	7
MESH:C536207	MESH:C536207	Citrulline transport defect	CTD_diseases	7
MESH:C536227	MESH:C536227	Cyclic neutropenia	CTD_diseases	7
MESH:C536238	MESH:C536238	Blue cone monochromatism	CTD_diseases	7
MESH:C536247	MESH:C536247	Nonkeratan-sulfate-excreting Morquio syndrome	CTD_diseases	7
MESH:C536255	MESH:C536255	Leigh necrotizing encephalopathy due to pyruvate carboxylase deficiency	CTD_diseases	7
MESH:C536315	MESH:C536315	Pediatric ulcerative colitis	CTD_diseases	7
MESH:C536318	MESH:C536318	Pelizaeus-Merzbacher like brain sclerosis	CTD_diseases	7
MESH:C536319	MESH:C536319	Pelizaeus-Merzbacher-like disease, autosomal recessive, 2	CTD_diseases	7
MESH:C536326	MESH:C536326	Polycystic kidney disease, type 1	CTD_diseases	7
MESH:C536328	MESH:C536328	Polycystic kidneys, severe infantile with tuberous sclerosis	CTD_diseases	7
MESH:C536345	MESH:C536345	Vertical talus, congenital	CTD_diseases	7
MESH:C536350	MESH:C536350	Visceral myopathy familial external ophthalmoplegia	CTD_diseases	7
MESH:C536355	MESH:C536355	Anemia, Diamond-Blackfan, 3	CTD_diseases	7
MESH:C536360	MESH:C536360	Aneurysm, intracranial berry, 2	CTD_diseases	7
MESH:C536389	MESH:C536389	Faciomandibular myoclonus, nocturnal	CTD_diseases	7
MESH:C536391	MESH:C536391	Facioscapulohumeral muscular dystrophy 1a	CTD_diseases	7
MESH:C536396	MESH:C536396	Neonatal ovarian cyst	CTD_diseases	7
MESH:C536399	MESH:C536399	Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor	CTD_diseases	7
MESH:C536404	MESH:C536404	Nephrotic syndrome, idiopathic, steroid-resistant	CTD_diseases	7
MESH:C536414	MESH:C536414	Primary hyperoxaluria type 1	CTD_diseases	7
MESH:C536415	MESH:C536415	Primary hyperoxaluria type 2	CTD_diseases	7
MESH:C536417	MESH:C536417	Primary malignant melanoma of the cervix	CTD_diseases	7
MESH:C536450	MESH:C536450	Cowchock syndrome	CTD_diseases	7
MESH:C536506	MESH:C536506	Thanatophoric dysplasia Glasgow variant	CTD_diseases	7
MESH:C536507	MESH:C536507	Thanatophoric dysplasia, type 1	CTD_diseases	7
MESH:C536508	MESH:C536508	Thanatophoric dysplasia, type 2	CTD_diseases	7
MESH:C536562	MESH:C536562	Triphalangeal thumb non opposable	CTD_diseases	7
MESH:C536584	MESH:C536584	Alpha-mannosidosis type 1	CTD_diseases	7
MESH:C536585	MESH:C536585	Alpha-mannosidosis, type 2	CTD_diseases	7
MESH:C536586	MESH:C536586	Alport syndrome, dominant type	CTD_diseases	7
MESH:C536587	MESH:C536587	Alport syndrome, recessive type	CTD_diseases	7
MESH:C536606	MESH:C536606	Amelogenesis Imperfecta hypomaturation type	CTD_diseases	7
MESH:C536610	MESH:C536610	Familial cerebral cavernous malformation	CTD_diseases	7
MESH:C536624	MESH:C536624	Scapuloperoneal myopathy	CTD_diseases	7
MESH:C536644	MESH:C536644	Spastic paraplegia 17	CTD_diseases	7
MESH:C536664	MESH:C536664	Peroxisome biogenesis disorders	CTD_diseases	7
MESH:C536668	MESH:C536668	Sjogren-Larsson-like syndrome	CTD_diseases	7
MESH:C536670	MESH:C536670	Skeletal dysplasia, San Diego type	CTD_diseases	7
MESH:C536678	MESH:C536678	Snyder Robinson syndrome	CTD_diseases	7
MESH:C536690	MESH:C536690	Welander distal myopathy, Swedish type	CTD_diseases	7
MESH:C536694	MESH:C536694	Westphal disease	CTD_diseases	7
MESH:C536707	MESH:C536707	Wilms tumor and radial bilateral aplasia	CTD_diseases	7
MESH:C536716	MESH:C536716	Young McKeever Squier syndrome	CTD_diseases	7
MESH:C536760	MESH:C536760	X-linked mental retardation type Wittwer	CTD_diseases	7
MESH:C536769	MESH:C536769	46, XY female	CTD_diseases	7
MESH:C536772	MESH:C536772	Syphilis, primary	CTD_diseases	7
MESH:C536773	MESH:C536773	Syphilis, secondary	CTD_diseases	7
MESH:C536774	MESH:C536774	Syphilis, tertiary	CTD_diseases	7
MESH:C536782	MESH:C536782	T-cell lymphoma 1A	CTD_diseases	7
MESH:C536787	MESH:C536787	Spastic ataxia Charlevoix-Saguenay type	CTD_diseases	7
MESH:C536788	MESH:C536788	Craniosynostosis radial aplasia syndrome	CTD_diseases	7
MESH:C536790	MESH:C536790	Craniosynostosis, sagittal, with Dandy-Walker malformation and hydrocephalus	CTD_diseases	7
MESH:C536797	MESH:C536797	Chromosome 22, microdeletion 22 q11	CTD_diseases	7
MESH:C536804	MESH:C536804	Chromosome 3, monosomy 3p	CTD_diseases	7
MESH:C536805	MESH:C536805	Chromosome 3, monosomy 3p14 p11	CTD_diseases	7
MESH:C536806	MESH:C536806	Chromosome 3, monosomy 3p2	CTD_diseases	7
MESH:C536807	MESH:C536807	Chromosome 3, monosomy 3p25	CTD_diseases	7
MESH:C536808	MESH:C536808	Chromosome 3, monosomy 3q13	CTD_diseases	7
MESH:C536809	MESH:C536809	Chromosome 3, monosomy 3q21 23	CTD_diseases	7
MESH:C536810	MESH:C536810	Chromosome 3, monosomy 3q27	CTD_diseases	7
MESH:C536816	MESH:C536816	Distal myopathy, Nonaka type	CTD_diseases	7
MESH:C536823	MESH:C536823	Glassy cell carcinoma of the cervix	CTD_diseases	7
MESH:C536831	MESH:C536831	Glucose-6-phosphate translocase deficiency	CTD_diseases	7
MESH:C536851	MESH:C536851	Familial renal cell carcinoma	CTD_diseases	7
MESH:C536853	MESH:C536853	Familial Wilms tumor 2	CTD_diseases	7
MESH:C536856	MESH:C536856	Spastic paraplegia 19, autosomal dominant	CTD_diseases	7
MESH:C536858	MESH:C536858	Spastic paraplegia 20, autosomal recessive	CTD_diseases	7
MESH:C536860	MESH:C536860	Spastic paraplegia 24	CTD_diseases	7
MESH:C536862	MESH:C536862	Spastic paraplegia 26, autosomal recessive	CTD_diseases	7
MESH:C536863	MESH:C536863	Spastic paraplegia 29, autosomal dominant	CTD_diseases	7
MESH:C536864	MESH:C536864	Spastic paraplegia 3, autosomal dominant	CTD_diseases	7
MESH:C536865	MESH:C536865	Spastic paraplegia 4, autosomal dominant	CTD_diseases	7
MESH:C536866	MESH:C536866	Spastic paraplegia 6, autosomal dominant	CTD_diseases	7
MESH:C536867	MESH:C536867	Spastic paraplegia 8, autosomal dominant	CTD_diseases	7
MESH:C536871	MESH:C536871	Spastic paraplegia type 5A, recessive	CTD_diseases	7
MESH:C536872	MESH:C536872	Spastic paraplegia type 5B, recessive	CTD_diseases	7
MESH:C536873	MESH:C536873	Spastic paraplegia with Kallmann syndrome	CTD_diseases	7
MESH:C536875	MESH:C536875	Arrest of spermatogenesis	CTD_diseases	7
MESH:C536884	MESH:C536884	Kleeblattschaedel syndrome	CTD_diseases	7
MESH:C536890	MESH:C536890	Hemiplegic migraine, familial type 1	CTD_diseases	7
MESH:C536895	MESH:C536895	Talonavicular coalition	CTD_diseases	7
MESH:C536919	MESH:C536919	Tietz syndrome	CTD_diseases	7
MESH:C536956	MESH:C536956	Temporal epilepsy, familial	CTD_diseases	7
MESH:C537043	MESH:C537043	Albinism ocular late onset sensorineural deafness	CTD_diseases	7
MESH:C537044	MESH:C537044	Albinism, minimal pigment type	CTD_diseases	7
MESH:C537064	MESH:C537064	Florid cystic endosalpingiosis of the uterus	CTD_diseases	7
MESH:C537070	MESH:C537070	Follicle-stimulating hormone deficiency, isolated	CTD_diseases	7
MESH:C537074	MESH:C537074	Fara Chlupackova syndrome	CTD_diseases	7
MESH:C537085	MESH:C537085	Brachycephalofrontonasal dysplasia	CTD_diseases	7
MESH:C537110	MESH:C537110	Chromosome 21, monosomy 21q22	CTD_diseases	7
MESH:C537113	MESH:C537113	Leiomyomatosis, esophageal and vulval, with nephropathy	CTD_diseases	7
MESH:C537135	MESH:C537135	Orofaciodigital syndrome, Shashi type	CTD_diseases	7
MESH:C537176	MESH:C537176	Parkinson disease 3	CTD_diseases	7
MESH:C537189	MESH:C537189	Rufous oculocutaneous albinism	CTD_diseases	7
MESH:C537217	MESH:C537217	Hereditary spastic paralysis, infantile onset ascending	CTD_diseases	7
MESH:C537218	MESH:C537218	Saccharopinuria	CTD_diseases	7
MESH:C537234	MESH:C537234	Sandifer syndrome	CTD_diseases	7
MESH:C537240	MESH:C537240	Progressive supranuclear palsy atypical	CTD_diseases	7
MESH:C537258	MESH:C537258	Fibrolamellar hepatocellular carcinoma	CTD_diseases	7
MESH:C537263	MESH:C537263	Lamellar ichthyosis, autosomal dominant form	CTD_diseases	7
MESH:C537264	MESH:C537264	Lamellar ichthyosis, type 2	CTD_diseases	7
MESH:C537265	MESH:C537265	Lamellar ichthyosis, type 3	CTD_diseases	7
MESH:C537275	MESH:C537275	Cirrhosis, familial, with deposition of abnormal glycogen	CTD_diseases	7
MESH:C537283	MESH:C537283	Gollop Coates syndrome	CTD_diseases	7
MESH:C537286	MESH:C537286	Gonadal dysgenesis XX type deafness	CTD_diseases	7
MESH:C537287	MESH:C537287	Goodman camptodactyly	CTD_diseases	7
MESH:C537333	MESH:C537333	Siderius X-linked mental retardation syndrome	CTD_diseases	7
MESH:C537350	MESH:C537350	Metaphyseal acroscyphodysplasia	CTD_diseases	7
MESH:C537369	MESH:C537369	Muenke Syndrome	CTD_diseases	7
MESH:C537374	MESH:C537374	Multifocal choroiditis	CTD_diseases	7
MESH:C537428	MESH:C537428	Arena syndrome	CTD_diseases	7
MESH:C537449	MESH:C537449	Mental retardation X-linked syndromic 7	CTD_diseases	7
MESH:C537450	MESH:C537450	Mental retardation X-linked, South African type	CTD_diseases	7
MESH:C537454	MESH:C537454	Mental retardation, X-linked 14	CTD_diseases	7
MESH:C537456	MESH:C537456	Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance	CTD_diseases	7
MESH:C537472	MESH:C537472	Miles-Carpenter x-linked mental retardation syndrome	CTD_diseases	7
MESH:C537482	MESH:C537482	Spastic paraplegia 10, autosomal dominant	CTD_diseases	7
MESH:C537483	MESH:C537483	Spastic paraplegia 11, autosomal recessive	CTD_diseases	7
MESH:C537484	MESH:C537484	Spastic paraplegia 12, autosomal dominant	CTD_diseases	7
MESH:C537485	MESH:C537485	Spastic paraplegia 13, autosomal dominant	CTD_diseases	7
MESH:C537495	MESH:C537495	Stocco dos Santos syndrome	CTD_diseases	7
MESH:C537500	MESH:C537500	Striatonigral degeneration infantile	CTD_diseases	7
MESH:C537512	MESH:C537512	Plagiocephaly and X-linked mental retardation	CTD_diseases	7
MESH:C537516	MESH:C537516	Pleuropulmonary blastoma	CTD_diseases	7
MESH:C537559	MESH:C537559	Jackson-Weiss syndrome	CTD_diseases	7
MESH:C537586	MESH:C537586	Serpentine fibula polycystic kidney syndrome	CTD_diseases	7
MESH:C537592	MESH:C537592	Neutropenia, Severe Congenital, Autosomal Recessive 3	CTD_diseases	7
MESH:C537597	MESH:C537597	Short limb dwarf lethal Colavita Kozlowski type	CTD_diseases	7
MESH:C537599	MESH:C537599	Short rib-polydactyly syndrome, Beemer type	CTD_diseases	7
MESH:C537602	MESH:C537602	Short rib-polydactyly syndrome, Verma-Naumoff type	CTD_diseases	7
MESH:C537637	MESH:C537637	Chromosome 4 short arm deletion	CTD_diseases	7
MESH:C537638	MESH:C537638	Chromosome 4, monosomy 4p14 p16	CTD_diseases	7
MESH:C537640	MESH:C537640	Chromosome 4, monosomy 4q32	CTD_diseases	7
MESH:C537648	MESH:C537648	Chromosome 5, trisomy 5p	CTD_diseases	7
MESH:C537651	MESH:C537651	Bartter syndrome, antenatal , type 2	CTD_diseases	7
MESH:C537652	MESH:C537652	Bartter syndrome, antenatal type 1	CTD_diseases	7
MESH:C537653	MESH:C537653	Bartter syndrome, type 3	CTD_diseases	7
MESH:C537671	MESH:C537671	Chromosome 1, monosomy 1q32 q42	CTD_diseases	7
MESH:C537672	MESH:C537672	Chromosome 1, monosomy 1q4	CTD_diseases	7
MESH:C537678	MESH:C537678	Gemignani syndrome	CTD_diseases	7
MESH:C537719	MESH:C537719	Macrodactyly of the foot	CTD_diseases	7
MESH:C537720	MESH:C537720	Macrodactyly of the hand	CTD_diseases	7
MESH:C537723	MESH:C537723	Lubs X-linked mental retardation syndrome	CTD_diseases	7
MESH:C537728	MESH:C537728	Oculocutaneous albinism type 1	CTD_diseases	7
MESH:C537729	MESH:C537729	Oculocutaneous albinism type 1B	CTD_diseases	7
MESH:C537730	MESH:C537730	Oculocutaneous albinism type 2	CTD_diseases	7
MESH:C537731	MESH:C537731	Oculocutaneous albinism type 3	CTD_diseases	7
MESH:C537743	MESH:C537743	Oguchi disease	CTD_diseases	7
MESH:C537745	MESH:C537745	Olivopontocerebellar hypoplasia, fetal-onset	CTD_diseases	7
MESH:C537747	MESH:C537747	Omphalocele cleft palate syndrome lethal	CTD_diseases	7
MESH:C537758	MESH:C537758	Renal tubular acidosis, distal, autosomal recessive	CTD_diseases	7
MESH:C537759	MESH:C537759	Renal tubular acidosis, distal, type 3	CTD_diseases	7
MESH:C537764	MESH:C537764	Chromosome 6, deletion 6q13 q15	CTD_diseases	7
MESH:C537765	MESH:C537765	Chromosome 6, monosomy 6p23	CTD_diseases	7
MESH:C537770	MESH:C537770	Anorchia	CTD_diseases	7
MESH:C537782	MESH:C537782	Aorta-pulmonary artery fistula	CTD_diseases	7
MESH:C537807	MESH:C537807	Chromosome 6, monosomy 6q	CTD_diseases	7
MESH:C537808	MESH:C537808	Chromosome 6, monosomy 6q1	CTD_diseases	7
MESH:C537809	MESH:C537809	Chromosome 6, monosomy 6q2	CTD_diseases	7
MESH:C537814	MESH:C537814	Chromosome 7, monosomy	CTD_diseases	7
MESH:C537815	MESH:C537815	Chromosome 7, monosomy 7q2	CTD_diseases	7
MESH:C537816	MESH:C537816	Chromosome 7, monosomy 7q21	CTD_diseases	7
MESH:C537817	MESH:C537817	Chromosome 7, monosomy 7q3	CTD_diseases	7
MESH:C537825	MESH:C537825	Chromosome 8, monosomy 8p	CTD_diseases	7
MESH:C537826	MESH:C537826	Chromosome 8p deletion syndrome (partial)	CTD_diseases	7
MESH:C537827	MESH:C537827	Chromosome 8, monosomy 8p23 1	CTD_diseases	7
MESH:C537828	MESH:C537828	Chromosome 8, monosomy 8q	CTD_diseases	7
MESH:C537863	MESH:C537863	Ocular Albinism type 1	CTD_diseases	7
MESH:C537877	MESH:C537877	Late-onset congenital adrenal hyperplasia	CTD_diseases	7
MESH:C537883	MESH:C537883	Rhabdomyosarcoma 1	CTD_diseases	7
MESH:C537900	MESH:C537900	Baker-Winegrad disease	CTD_diseases	7
MESH:C537928	MESH:C537928	Fibromatosis, gingival, 3	CTD_diseases	7
MESH:C537948	MESH:C537948	Ceroid lipofuscinosis, neuronal 1, infantile	CTD_diseases	7
MESH:C537952	MESH:C537952	Ceroid lipofuscinosis, neuronal 8	CTD_diseases	7
MESH:C537953	MESH:C537953	Ceroid lipofuscinosis, neuronal 9	CTD_diseases	7
MESH:C537970	MESH:C537970	Camptodactyly syndrome Guadalajara type 1	CTD_diseases	7
MESH:C537973	MESH:C537973	Camptodactyly vertebral fusion	CTD_diseases	7
MESH:C537984	MESH:C537984	Charcot-Marie-Tooth disease, Type 1C	CTD_diseases	7
MESH:C537985	MESH:C537985	Charcot-Marie-Tooth disease, Type 1D	CTD_diseases	7
MESH:C537986	MESH:C537986	Charcot-Marie-Tooth disease, Type 1E	CTD_diseases	7
MESH:C537987	MESH:C537987	Charcot-Marie-Tooth disease, Type 1F	CTD_diseases	7
MESH:C537988	MESH:C537988	Charcot-Marie-Tooth disease, Type 2A	CTD_diseases	7
MESH:C537989	MESH:C537989	Charcot-Marie-Tooth disease, Type 2B	CTD_diseases	7
MESH:C537990	MESH:C537990	Charcot-Marie-Tooth disease, Type 2B1	CTD_diseases	7
MESH:C537991	MESH:C537991	Charcot-Marie-Tooth disease, Type 2B2	CTD_diseases	7
MESH:C537992	MESH:C537992	Charcot-Marie-Tooth disease, Type 2C	CTD_diseases	7
MESH:C537993	MESH:C537993	Charcot-Marie-Tooth disease, Type 2D	CTD_diseases	7
MESH:C537994	MESH:C537994	Charcot-Marie-Tooth disease, Type 2E	CTD_diseases	7
MESH:C537995	MESH:C537995	Dysferlinopathy	CTD_diseases	7
MESH:C538000	MESH:C538000	Dystelephalangy	CTD_diseases	7
MESH:C538008	MESH:C538008	Dystrophia myotonica 1	CTD_diseases	7
MESH:C538024	MESH:C538024	Chromosome 9p Deletion Syndrome	CTD_diseases	7
MESH:C538025	MESH:C538025	Chromosome 9, partial monosomy 9p	CTD_diseases	7
MESH:C538031	MESH:C538031	Chromosome 14q, partial deletions	CTD_diseases	7
MESH:C538033	MESH:C538033	Chromosome 14q, terminal deletion	CTD_diseases	7
MESH:C538038	MESH:C538038	Chromosome 15q, partial deletion	CTD_diseases	7
MESH:C538045	MESH:C538045	Chromosome 17 deletion	CTD_diseases	7
MESH:C538047	MESH:C538047	Chromosome 17, deletion 17q23 q24	CTD_diseases	7
MESH:C538058	MESH:C538058	Aganglionosis, total intestinal	CTD_diseases	7
MESH:C538062	MESH:C538062	Frints De Smet Fabry Fryns syndrome	CTD_diseases	7
MESH:C538077	MESH:C538077	Charcot Marie Tooth type 1 aplasia cutis congenita	CTD_diseases	7
MESH:C538078	MESH:C538078	Charcot-Marie-Tooth disease and deafness	CTD_diseases	7
MESH:C538119	MESH:C538119	Hirschsprung disease ganglioneuroblastoma	CTD_diseases	7
MESH:C538121	MESH:C538121	Hirschsprung disease type 3	CTD_diseases	7
MESH:C538136	MESH:C538136	Hyperexplexia hereditary	CTD_diseases	7
MESH:C538150	MESH:C538150	Syndactyly Cenani Lenz type	CTD_diseases	7
MESH:C538153	MESH:C538153	Syndactyly, type 2	CTD_diseases	7
MESH:C538154	MESH:C538154	Syndactyly, type 3	CTD_diseases	7
MESH:C538155	MESH:C538155	Syndactyly, type v	CTD_diseases	7
MESH:C538162	MESH:C538162	Meacham Winn Culler syndrome	CTD_diseases	7
MESH:C538183	MESH:C538183	Acrofacial dysostosis Rodriguez type	CTD_diseases	7
MESH:C538184	MESH:C538184	Acrofacial dysostosis, Nager type	CTD_diseases	7
MESH:C538186	MESH:C538186	Acrofrontofacionasal dysostosis syndrome	CTD_diseases	7
MESH:C538189	MESH:C538189	Fuhrmann syndrome	CTD_diseases	7
MESH:C538194	MESH:C538194	Furunculous myiasis	CTD_diseases	7
MESH:C538195	MESH:C538195	Atkin syndrome	CTD_diseases	7
MESH:C538207	MESH:C538207	Deletion 6q16 q21	CTD_diseases	7
MESH:C538210	MESH:C538210	Dennis Fairhurst Moore syndrome	CTD_diseases	7
MESH:C538221	MESH:C538221	Green Sandford Davison syndrome	CTD_diseases	7
MESH:C538223	MESH:C538223	Acute zonal occult outer retinopathy	CTD_diseases	7
MESH:C538236	MESH:C538236	Adrenal hyperplasia 2	CTD_diseases	7
MESH:C538237	MESH:C538237	Adrenal hyperplasia, congenital, type 5	CTD_diseases	7
MESH:C538240	MESH:C538240	Amelogenesis imperfecta local hypoplastic form	CTD_diseases	7
MESH:C538242	MESH:C538242	Amelogenesis imperfecta pigmented hypomaturation type	CTD_diseases	7
MESH:C538243	MESH:C538243	Amelogenesis imperfecta, hypoplastic/hypomaturation, X-linked 1	CTD_diseases	7
MESH:C538250	MESH:C538250	Amyopathic dermatomyositis	CTD_diseases	7
MESH:C538258	MESH:C538258	ATR-X syndrome	CTD_diseases	7
MESH:C538263	MESH:C538263	Atrial septal defect 2	CTD_diseases	7
MESH:C538266	MESH:C538266	Atypical hemolytic uremic syndrome	CTD_diseases	7
MESH:C538289	MESH:C538289	Chromosome 10, monosomy 10q	CTD_diseases	7
MESH:C538293	MESH:C538293	Chromosome 11, deletion 11p	CTD_diseases	7
MESH:C538295	MESH:C538295	Chromosome 11p, partial deletion	CTD_diseases	7
MESH:C538296	MESH:C538296	Chromosome 11q partial deletion	CTD_diseases	7
MESH:C538301	MESH:C538301	Chromosome 12p deletion	CTD_diseases	7
MESH:C538302	MESH:C538302	Chromosome 12p partial deletion	CTD_diseases	7
MESH:C538305	MESH:C538305	Chromosome 18, deletion 18q23	CTD_diseases	7
MESH:C538313	MESH:C538313	Chromosome 2, monosomy 2p22	CTD_diseases	7
MESH:C538314	MESH:C538314	Chromosome 2, monosomy 2pter p24	CTD_diseases	7
MESH:C538315	MESH:C538315	Chromosome 2, monosomy 2q	CTD_diseases	7
MESH:C538316	MESH:C538316	Chromosome 2, monosomy 2q24	CTD_diseases	7
MESH:C538317	MESH:C538317	Chromosome 2q37 deletion syndrome	CTD_diseases	7
MESH:C538321	MESH:C538321	Histidinuria renal tubular defect	CTD_diseases	7
MESH:C538339	MESH:C538339	Nasopharyngeal carcinoma	CTD_diseases	7
MESH:C538382	MESH:C538382	Hyperphenylalaninemia with primapterinuria	CTD_diseases	7
MESH:C538394	MESH:C538394	Familial HDL deficiency	CTD_diseases	7
MESH:C538424	MESH:C538424	Harlequin type ichthyosis	CTD_diseases	7
MESH:C538427	MESH:C538427	Myoclonic epilepsy with choreoathetosis	CTD_diseases	7
MESH:C538435	MESH:C538435	Lubs syndrome	CTD_diseases	7
MESH:C538442	MESH:C538442	Aase Smith syndrome 2	CTD_diseases	7
MESH:C538445	MESH:C538445	Clear-cell metastatic renal cell carcinoma	CTD_diseases	7
MESH:C538482	MESH:C538482	Monosomy 5p	CTD_diseases	7
MESH:C538507	MESH:C538507	Dandy Walker cyst	CTD_diseases	7
MESH:C538511	MESH:C538511	Cancer of the oviduct	CTD_diseases	7
MESH:C538533	MESH:C538533	Juvenile giant cell arteritis	CTD_diseases	7
MESH:C538534	MESH:C538534	Hypogonadotropic hypogonadism and anosmia, autosomal dominant	CTD_diseases	7
MESH:C538540	MESH:C538540	Hirschsprung disease 1	CTD_diseases	7
MESH:C538544	MESH:C538544	Familial primary biliary cirrhosis	CTD_diseases	7
MESH:C538557	MESH:C538557	Renal cell carcinoma 1	CTD_diseases	7
MESH:C538567	MESH:C538567	Hyperinsulinism, autosomal recessive	CTD_diseases	7
MESH:C538572	MESH:C538572	Familial progressive supranuclear palsy	CTD_diseases	7
MESH:C538590	MESH:C538590	Necrotizing encephalopathy, infantile subacute, of Leigh	CTD_diseases	7
MESH:C538599	MESH:C538599	Lysosomal beta-mannosidase deficiency	CTD_diseases	7
MESH:C538603	MESH:C538603	Ichthyosiform erythroderma, Brocq congenital, nonbullous form	CTD_diseases	7
MESH:C538614	MESH:C538614	Papillary renal cell carcinoma, sporadic	CTD_diseases	7
MESH:C538626	MESH:C538626	Olivopontocerebellar atrophy 1	CTD_diseases	7
MESH:C538631	MESH:C538631	Olivopontocerebellar atrophy 3	CTD_diseases	7
MESH:C538637	MESH:C538637	Autosomal dominant diffuse Lewy body disease	CTD_diseases	7
MESH:C538640	MESH:C538640	Limb-girdle muscular dystrophy autosomal recessive	CTD_diseases	7
MESH:C538655	MESH:C538655	Hepatorenal form of glycogen storage disease	CTD_diseases	7
MESH:C538659	MESH:C538659	Porphyria, South African type	CTD_diseases	7
MESH:C538667	MESH:C538667	Midline granulomatosis	CTD_diseases	7
MESH:C539595	MESH:C539595	Charcot-Marie-Tooth disease, Type 4A, axonal form	CTD_diseases	7
MESH:C541598	MESH:C541598	Chromosome 11p Deletion Syndrome	CTD_diseases	7
MESH:C545036	MESH:C545036	Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis	CTD_diseases	7
MESH:C548006	MESH:C548006	Atrial Septal Defect Ostium Primum	CTD_diseases	7
MESH:C548009	MESH:C548009	Atrial Septal Defect Sinus Venosus	CTD_diseases	7
MESH:C548013	MESH:C548013	Dipsogenic Diabetes Insipidus	CTD_diseases	7
MESH:C548014	MESH:C548014	Gestational Diabetes Insipidus	CTD_diseases	7
MESH:C548069	MESH:C548069	Pontocerebellar Hypoplasia Type 1	CTD_diseases	7
MESH:C548070	MESH:C548070	Pontocerebellar Hypoplasia Type 2	CTD_diseases	7
MESH:C548072	MESH:C548072	Pontocerebellar Hypoplasia Type 3	CTD_diseases	7
MESH:C548074	MESH:C548074	Pontocerebellar Hypoplasia Type 6	CTD_diseases	7
MESH:C548420	MESH:C548420	Vascular Compression of the Duodenum	CTD_diseases	7
MESH:C548479	MESH:C548479	Vulvar dysesthesia localized in the vestibule	CTD_diseases	7
MESH:C548481	MESH:C548481	Periventricular Laminar Heterotopia	CTD_diseases	7
MESH:C548666	MESH:C548666	Mycobacterial disease, Mendelian susceptibility to	CTD_diseases	7
MESH:C548841	MESH:C548841	Parasitic infection caused by Dracunculus medinensis	CTD_diseases	7
MESH:C562391	MESH:C562391	Ovarian Fibromata	CTD_diseases	7
MESH:C562393	MESH:C562393	Melanoma, Cutaneous Malignant	CTD_diseases	7
MESH:C562404	MESH:C562404	Pulmonary Arteriovenous Fistulas	CTD_diseases	7
MESH:C562417	MESH:C562417	Adactylia, Unilateral	CTD_diseases	7
MESH:D013005	MESH:D013005	Somatostatinoma	CTD_diseases	7
MESH:D013009	MESH:D013009	Somnambulism	CTD_diseases	7
MESH:D013064	MESH:D013064	Speech Disorders	CTD_diseases	7
MESH:D013349	MESH:D013349	Subclavian Steal Syndrome	CTD_diseases	7
MESH:D013575	MESH:D013575	Syncope	CTD_diseases	7
MESH:D013592	MESH:D013592	Syphilis, Latent	CTD_diseases	7
MESH:D013832	MESH:D013832	Thiamine Deficiency	CTD_diseases	7
MESH:D014007	MESH:D014007	Tinea Favosa	CTD_diseases	7
MESH:D014067	MESH:D014067	Tonsillar Neoplasms	CTD_diseases	7
MESH:D014253	MESH:D014253	Trichostrongylosis	CTD_diseases	7
MESH:D014323	MESH:D014323	Trombiculiasis	CTD_diseases	7
MESH:D014339	MESH:D014339	Truncus Arteriosus, Persistent	CTD_diseases	7
MESH:D014375	MESH:D014375	Tuberculoma	CTD_diseases	7
MESH:D014391	MESH:D014391	Tuberculosis, Miliary	CTD_diseases	7
MESH:D014806	MESH:D014806	Vitamin B 12 Deficiency	CTD_diseases	7
MESH:D015270	MESH:D015270	Mycobacterium avium-intracellulare Infection	CTD_diseases	7
MESH:D015408	MESH:D015408	Gastrinoma	CTD_diseases	7
MESH:D016403	MESH:D016403	Lymphoma, Large B-Cell, Diffuse	CTD_diseases	7
MESH:D016410	MESH:D016410	Lymphoma, T-Cell, Cutaneous	CTD_diseases	7
MESH:D016411	MESH:D016411	Lymphoma, T-Cell, Peripheral	CTD_diseases	7
MESH:D016483	MESH:D016483	Lymphoma, AIDS-Related	CTD_diseases	7
MESH:D016545	MESH:D016545	Choroid Plexus Neoplasms	CTD_diseases	7
MESH:D016774	MESH:D016774	Leishmaniasis, Diffuse Cutaneous	CTD_diseases	7
MESH:D016891	MESH:D016891	Polycystic Kidney, Autosomal Dominant	CTD_diseases	7
MESH:D017085	MESH:D017085	alpha-Thalassemia	CTD_diseases	7
MESH:D017086	MESH:D017086	beta-Thalassemia	CTD_diseases	7
MESH:D017229	MESH:D017229	Enterobiasis	CTD_diseases	7
MESH:D017566	MESH:D017566	Microvascular Angina	CTD_diseases	7
MESH:D018088	MESH:D018088	Tuberculosis, Multidrug-Resistant	CTD_diseases	7
MESH:D018216	MESH:D018216	Osteochondromatosis	CTD_diseases	7
MESH:D018217	MESH:D018217	Osteosarcoma, Juxtacortical	CTD_diseases	7
MESH:D018219	MESH:D018219	Histiocytoma, Benign Fibrous	CTD_diseases	7
MESH:D018220	MESH:D018220	Fibroma, Desmoplastic	CTD_diseases	7
MESH:D018221	MESH:D018221	Fibromatosis, Abdominal	CTD_diseases	7
MESH:D018222	MESH:D018222	Fibromatosis, Aggressive	CTD_diseases	7
MESH:D018223	MESH:D018223	Dermatofibrosarcoma	CTD_diseases	7
MESH:D018226	MESH:D018226	Fibroadenoma	CTD_diseases	7
MESH:D018232	MESH:D018232	Rhabdomyosarcoma, Alveolar	CTD_diseases	7
MESH:D018233	MESH:D018233	Rhabdomyosarcoma, Embryonal	CTD_diseases	7
MESH:D018241	MESH:D018241	Neuroectodermal Tumors, Primitive, Peripheral	CTD_diseases	7
MESH:D018245	MESH:D018245	Trophoblastic Tumor, Placental Site	CTD_diseases	7
MESH:D018265	MESH:D018265	Carcinoma, Papillary, Follicular	CTD_diseases	7
MESH:D018282	MESH:D018282	Cystadenocarcinoma, Mucinous	CTD_diseases	7
MESH:D018283	MESH:D018283	Cystadenocarcinoma, Papillary	CTD_diseases	7
MESH:D018284	MESH:D018284	Cystadenocarcinoma, Serous	CTD_diseases	7
MESH:D018303	MESH:D018303	Ganglioglioma	CTD_diseases	7
MESH:D018316	MESH:D018316	Gliosarcoma	CTD_diseases	7
MESH:D018318	MESH:D018318	Neurofibroma, Plexiform	CTD_diseases	7
MESH:D018327	MESH:D018327	Hutchinson's Melanotic Freckle	CTD_diseases	7
MESH:D018328	MESH:D018328	Melanoma, Amelanotic	CTD_diseases	7
MESH:D018332	MESH:D018332	Nevus, Epithelioid and Spindle Cell	CTD_diseases	7
MESH:D018442	MESH:D018442	Lymphoma, B-Cell, Marginal Zone	CTD_diseases	7
MESH:D018500	MESH:D018500	Diabetes Insipidus, Nephrogenic	CTD_diseases	7
MESH:D019575	MESH:D019575	Blindness, Cortical	CTD_diseases	7
MESH:D020159	MESH:D020159	Citrullinemia	CTD_diseases	7
MESH:D020162	MESH:D020162	Hyperargininemia	CTD_diseases	7
MESH:D020184	MESH:D020184	Night Terrors	CTD_diseases	7
MESH:D020187	MESH:D020187	REM Sleep Behavior Disorder	CTD_diseases	7
MESH:D020188	MESH:D020188	Sleep Paralysis	CTD_diseases	7
MESH:D020202	MESH:D020202	Cerebral Hemorrhage, Traumatic	CTD_diseases	7
MESH:D020238	MESH:D020238	Prosopagnosia	CTD_diseases	7
MESH:D020240	MESH:D020240	Apraxia, Ideomotor	CTD_diseases	7
MESH:D020243	MESH:D020243	Infarction, Anterior Cerebral Artery	CTD_diseases	7
MESH:D020244	MESH:D020244	Infarction, Middle Cerebral Artery	CTD_diseases	7
MESH:D020295	MESH:D020295	Brain Stem Neoplasms	CTD_diseases	7
MESH:D020324	MESH:D020324	Amnesia, Anterograde	CTD_diseases	7
MESH:D020325	MESH:D020325	Migraine with Aura	CTD_diseases	7
MESH:D020326	MESH:D020326	Migraine without Aura	CTD_diseases	7
MESH:D020339	MESH:D020339	Optic Nerve Glioma	CTD_diseases	7
MESH:D020526	MESH:D020526	Brain Stem Infarctions	CTD_diseases	7
MESH:D020528	MESH:D020528	Multiple Sclerosis, Chronic Progressive	CTD_diseases	7
MESH:D020529	MESH:D020529	Multiple Sclerosis, Relapsing-Remitting	CTD_diseases	7
MESH:D020642	MESH:D020642	Acatalasia	CTD_diseases	7
MESH:D020757	MESH:D020757	Amaurosis Fugax	CTD_diseases	7
MESH:D020762	MESH:D020762	Infarction, Posterior Cerebral Artery	CTD_diseases	7
MESH:D020766	MESH:D020766	Intracranial Embolism	CTD_diseases	7
MESH:D020767	MESH:D020767	Intracranial Thrombosis	CTD_diseases	7
MESH:D020774	MESH:D020774	Pick Disease of the Brain	CTD_diseases	7
MESH:D020790	MESH:D020790	Diabetes Insipidus, Neurogenic	CTD_diseases	7
MESH:D026681	MESH:D026681	Vitamin B 6 Deficiency	CTD_diseases	7
MESH:D029461	MESH:D029461	Sialic Acid Storage Disease	CTD_diseases	7
MESH:D031954	MESH:D031954	Choriocarcinoma, Non-gestational	CTD_diseases	7
MESH:D038921	MESH:D038921	Coffin-Lowry Syndrome	CTD_diseases	7
MESH:D046088	MESH:D046088	Hearing Loss, Unilateral	CTD_diseases	7
MESH:D046089	MESH:D046089	Hearing Loss, Mixed Conductive-Sensorineural	CTD_diseases	7
MESH:D046729	MESH:D046729	Colitis, Collagenous	CTD_diseases	7
MESH:D046730	MESH:D046730	Colitis, Lymphocytic	CTD_diseases	7
MESH:D047748	MESH:D047748	Pituitary ACTH Hypersecretion	CTD_diseases	7
MESH:D050798	MESH:D050798	SUNCT Syndrome	CTD_diseases	7
MESH:D051302	MESH:D051302	Paroxysmal Hemicrania	CTD_diseases	7
MESH:D052476	MESH:D052476	Hypobetalipoproteinemia, Familial, Apolipoprotein B	CTD_diseases	7
MESH:D052582	MESH:D052582	Trigger Finger Disorder	CTD_diseases	7
MESH:D052919	MESH:D052919	Refsum Disease, Infantile	CTD_diseases	7
MESH:D053098	MESH:D053098	Familial Hypophosphatemic Rickets	CTD_diseases	7
MESH:D053608	MESH:D053608	Stupor	CTD_diseases	7
MESH:D053684	MESH:D053684	De Quervain Disease	CTD_diseases	7
MESH:D054080	MESH:D054080	Vein of Galen Malformations	CTD_diseases	7
MESH:D054092	MESH:D054092	Foramen Ovale, Patent	CTD_diseases	7
MESH:D054391	MESH:D054391	Lymphoma, Extranodal NK-T-Cell	CTD_diseases	7
MESH:D054685	MESH:D054685	Lymphoma, Primary Effusion	CTD_diseases	7
MESH:D054705	MESH:D054705	Mastocytoma, Skin	CTD_diseases	7
MESH:D055538	MESH:D055538	delta-Thalassemia	CTD_diseases	7
MESH:D055964	MESH:D055964	Alien Hand Syndrome	CTD_diseases	7
MESH:D055985	MESH:D055985	Latent Tuberculosis	CTD_diseases	7
MESH:D056005	MESH:D056005	Leprosy, Paucibacillary	CTD_diseases	7
MESH:D056006	MESH:D056006	Leprosy, Multibacillary	CTD_diseases	7
MESH:D056807	MESH:D056807	Argininosuccinic Aciduria	CTD_diseases	7
MESH:D056828	MESH:D056828	Hereditary Angioedema Type III	CTD_diseases	7
MESH:D056829	MESH:D056829	Hereditary Angioedema Types I and II	CTD_diseases	7
MESH:D057091	MESH:D057091	Poroma	CTD_diseases	7
MESH:D058285	MESH:D058285	Tungiasis	CTD_diseases	7
MESH:D058527	MESH:D058527	Enteropathy-Associated T-Cell Lymphoma	CTD_diseases	7
MESH:D060050	MESH:D060050	Angina, Stable	CTD_diseases	7
MESH:D060705	MESH:D060705	Dyscalculia	CTD_diseases	7
MESH:D061226	MESH:D061226	Recurrent Laryngeal Nerve Injuries	CTD_diseases	7
MESH:D063485	MESH:D063485	Acanthocheilonemiasis	CTD_diseases	7
MESH:D064147	MESH:D064147	Febrile Neutropenia	CTD_diseases	7
OMIM:113300	OMIM:113300	BRACHYDACTYLY, TYPE E1	CTD_diseases	7
OMIM:115310	OMIM:115310	PARAGANGLIOMAS 4	CTD_diseases	7
OMIM:135300	OMIM:135300	FIBROMATOSIS, GINGIVAL, 1	CTD_diseases	7
OMIM:138110	OMIM:138110	GLUCOSE-6-PHOSPHATE DEHYDROGENASE-LIKE	CTD_diseases	7
OMIM:143460	OMIM:143460	5-HYDROXYTRYPTAMINE OXYGENASE REGULATOR	CTD_diseases	7
OMIM:143470	OMIM:143470	HYPERALPHALIPOPROTEINEMIA 1	CTD_diseases	7
OMIM:143890	OMIM:143890	HYPERCHOLESTEROLEMIA, FAMILIAL	CTD_diseases	7
OMIM:144010	OMIM:144010	HYPERCHOLESTEROLEMIA, AUTOSOMAL DOMINANT, TYPE B	CTD_diseases	7
OMIM:150800	OMIM:150800	HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER	CTD_diseases	7
OMIM:162400	OMIM:162400	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA	CTD_diseases	7
OMIM:167959	OMIM:167959	HUMAN PAPILLOMAVIRUS TYPE 18 INTEGRATION SITE 1	CTD_diseases	7
OMIM:167960	OMIM:167960	HUMAN PAPILLOMAVIRUS TYPE 18 INTEGRATION SITE 2	CTD_diseases	7
OMIM:168600	OMIM:168600	PARKINSON DISEASE, LATE-ONSET	CTD_diseases	7
OMIM:168601	OMIM:168601	PARKINSON DISEASE 1, AUTOSOMAL DOMINANT	CTD_diseases	7
OMIM:170400	OMIM:170400	HYPOKALEMIC PERIODIC PARALYSIS, TYPE 1	CTD_diseases	7
OMIM:179010	OMIM:179010	PYLORIC STENOSIS, INFANTILE HYPERTROPHIC, 1	CTD_diseases	7
OMIM:190440	OMIM:190440	TRIGONOCEPHALY 1	CTD_diseases	7
OMIM:190900	OMIM:190900	TRITANOPIA	CTD_diseases	7
OMIM:191181	OMIM:191181	SUPPRESSOR OF TUMORIGENICITY 3	CTD_diseases	7
OMIM:201300	OMIM:201300	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA	CTD_diseases	7
OMIM:207410	OMIM:207410	ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS	CTD_diseases	7
OMIM:227645	OMIM:227645	FANCONI ANEMIA, COMPLEMENTATION GROUP C	CTD_diseases	7
OMIM:227646	OMIM:227646	FANCONI ANEMIA, COMPLEMENTATION GROUP D2	CTD_diseases	7
OMIM:239300	OMIM:239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1	CTD_diseases	7
OMIM:256370	OMIM:256370	NEPHROTIC SYNDROME, TYPE 4	CTD_diseases	7
OMIM:259710	OMIM:259710	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2	CTD_diseases	7
OMIM:261630	OMIM:261630	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, C	CTD_diseases	7
OMIM:264070	OMIM:264070	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, D	CTD_diseases	7
OMIM:270960	OMIM:270960	SPERMATOGENIC FAILURE 4	CTD_diseases	7
OMIM:271245	OMIM:271245	MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)	CTD_diseases	7
OMIM:277000	OMIM:277000	MAYER-ROKITANSKY-KUSTER-HAUSER SYNDROME	CTD_diseases	7
OMIM:278850	OMIM:278850	46,XX SEX REVERSAL 2	CTD_diseases	7
OMIM:300082	OMIM:300082	COGNITIVE FUNCTION 1, SOCIAL	CTD_diseases	7
OMIM:300114	OMIM:300114	MENTAL RETARDATION, X-LINKED 49	CTD_diseases	7
OMIM:300125	OMIM:300125	MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO, 2	CTD_diseases	7
OMIM:300143	OMIM:300143	MENTAL RETARDATION, X-LINKED 21	CTD_diseases	7
OMIM:300259	OMIM:300259	MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, X-LINKED	CTD_diseases	7
OMIM:300630	OMIM:300630	MENTAL RETARDATION, X-LINKED, SYNDROMIC, FRIED TYPE	CTD_diseases	7
OMIM:300752	OMIM:300752	PROTOPORPHYRIA, ERYTHROPOIETIC, X-LINKED	CTD_diseases	7
OMIM:300799	OMIM:300799	MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE	CTD_diseases	7
OMIM:300802	OMIM:300802	MENTAL RETARDATION, X-LINKED 96	CTD_diseases	7
OMIM:300833	OMIM:300833	46,XX SEX REVERSAL 3	CTD_diseases	7
OMIM:301050	OMIM:301050	ALPORT SYNDROME, X-LINKED	CTD_diseases	7
OMIM:301201	OMIM:301201	AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 2	CTD_diseases	7
OMIM:303800	OMIM:303800	COLORBLINDNESS, PARTIAL, DEUTAN SERIES	CTD_diseases	7
OMIM:303900	OMIM:303900	COLORBLINDNESS, PARTIAL, PROTAN SERIES	CTD_diseases	7
OMIM:309630	OMIM:309630	METACARPAL 4-5 FUSION	CTD_diseases	7
OMIM:400045	OMIM:400045	46,XX SEX REVERSAL 1	CTD_diseases	7
OMIM:600512	OMIM:600512	EPILEPSY, FAMILIAL TEMPORAL LOBE, 1	CTD_diseases	7
OMIM:600901	OMIM:600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E	CTD_diseases	7
OMIM:601583	OMIM:601583	WILMS TUMOR 5	CTD_diseases	7
OMIM:602081	OMIM:602081	SPEECH-LANGUAGE DISORDER 1	CTD_diseases	7
OMIM:603467	OMIM:603467	FANCONI ANEMIA, COMPLEMENTATION GROUP F	CTD_diseases	7
OMIM:603933	OMIM:603933	MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 1	CTD_diseases	7
OMIM:604595	OMIM:604595	CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 1	CTD_diseases	7
OMIM:604772	OMIM:604772	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR	CTD_diseases	7
OMIM:605201	OMIM:605201	HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 14	CTD_diseases	7
OMIM:605990	OMIM:605990	NEPHROLITHIASIS, URIC ACID, SUSCEPTIBILITY TO	CTD_diseases	7
OMIM:607060	OMIM:607060	PARKINSON DISEASE 8, AUTOSOMAL DOMINANT	CTD_diseases	7
OMIM:607155	OMIM:607155	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5	CTD_diseases	7
OMIM:607688	OMIM:607688	PARKINSON DISEASE 11, AUTOSOMAL DOMINANT	CTD_diseases	7
OMIM:607721	OMIM:607721	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR	CTD_diseases	7
OMIM:607948	OMIM:607948	MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO	CTD_diseases	7
OMIM:607949	OMIM:607949	MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, 1	CTD_diseases	7
OMIM:608096	OMIM:608096	EPILEPSY, FAMILIAL TEMPORAL LOBE, 2	CTD_diseases	7
OMIM:608673	OMIM:608673	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L	CTD_diseases	7
OMIM:609308	OMIM:609308	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1	CTD_diseases	7
OMIM:610297	OMIM:610297	PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO	CTD_diseases	7
OMIM:610427	OMIM:610427	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B	CTD_diseases	7
OMIM:610725	OMIM:610725	NEPHROTIC SYNDROME, TYPE 3	CTD_diseases	7
OMIM:611046	OMIM:611046	MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, 2	CTD_diseases	7
OMIM:611490	OMIM:611490	OSTEOPETROSIS,  AUTOSOMAL RECESSIVE 4	CTD_diseases	7
OMIM:611588	OMIM:611588	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4	CTD_diseases	7
OMIM:611630	OMIM:611630	EPILEPSY, FAMILIAL TEMPORAL LOBE, 3	CTD_diseases	7
OMIM:611726	OMIM:611726	EPILEPSY, PROGRESSIVE MYOCLONIC 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS	CTD_diseases	7
OMIM:611938	OMIM:611938	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 2	CTD_diseases	7
OMIM:612304	OMIM:612304	THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE	CTD_diseases	7
OMIM:612319	OMIM:612319	SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE	CTD_diseases	7
OMIM:612561	OMIM:612561	DIAMOND-BLACKFAN ANEMIA 6	CTD_diseases	7
OMIM:612623	OMIM:612623	MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 2	CTD_diseases	7
OMIM:612624	OMIM:612624	MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 3	CTD_diseases	7
OMIM:612628	OMIM:612628	MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 4	CTD_diseases	7
OMIM:612633	OMIM:612633	MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 5	CTD_diseases	7
OMIM:612634	OMIM:612634	MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 6	CTD_diseases	7
OMIM:612635	OMIM:612635	MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7	CTD_diseases	7
OMIM:612929	OMIM:612929	MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, 3	CTD_diseases	7
OMIM:612936	OMIM:612936	SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE	CTD_diseases	7
OMIM:612953	OMIM:612953	PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE	CTD_diseases	7
OMIM:613000	OMIM:613000	PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL	CTD_diseases	7
OMIM:613157	OMIM:613157	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3	CTD_diseases	7
OMIM:613158	OMIM:613158	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2	CTD_diseases	7
OMIM:613162	OMIM:613162	SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE	CTD_diseases	7
OMIM:613239	OMIM:613239	THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 2	CTD_diseases	7
OMIM:613290	OMIM:613290	HEARING LOSS, CISPLATIN-INDUCED, SUSCEPTIBILITY TO	CTD_diseases	7
OMIM:613364	OMIM:613364	SPASTIC PARAPLEGIA 41, AUTOSOMAL DOMINANT	CTD_diseases	7
OMIM:613390	OMIM:613390	FANCONI ANEMIA, COMPLEMENTATION GROUP O	CTD_diseases	7
OMIM:613530	OMIM:613530	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H	CTD_diseases	7
OMIM:613616	OMIM:613616	HYPEROXALURIA, PRIMARY, TYPE III	CTD_diseases	7
OMIM:613640	OMIM:613640	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC	CTD_diseases	7
OMIM:613641	OMIM:613641	CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE B	CTD_diseases	7
OMIM:613643	OMIM:613643	PARKINSON DISEASE 5, AUTOSOMAL DOMINANT	CTD_diseases	7
OMIM:613647	OMIM:613647	SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE	CTD_diseases	7
OMIM:613702	OMIM:613702	KLIPPEL-FEIL SYNDROME 3, AUTOSOMAL DOMINANT	CTD_diseases	7
OMIM:613717	OMIM:613717	TREACHER COLLINS SYNDROME 2	CTD_diseases	7
OMIM:613723	OMIM:613723	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q	CTD_diseases	7
OMIM:614021	OMIM:614021	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 3	CTD_diseases	7
OMIM:614207	OMIM:614207	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 3	CTD_diseases	7
OMIM:615031	OMIM:615031	SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE	CTD_diseases	7
MESH:C567279	MESH:C567279	Amelogenesis Imperfecta, Hypomaturation Type, Iia2	CTD_diseases	7
MESH:C567280	MESH:C567280	Diamond-Blackfan Anemia 5	CTD_diseases	7
MESH:C567281	MESH:C567281	Diamond-Blackfan Anemia 4	CTD_diseases	7
MESH:C567283	MESH:C567283	Pyloric Stenosis, Infantile Hypertrophic, 5	CTD_diseases	7
MESH:C567288	MESH:C567288	Specific Language Impairment 4	CTD_diseases	7
MESH:C567296	MESH:C567296	Hypercarotenemia And Vitamin A Deficiency, Autosomal Dominant	CTD_diseases	7
MESH:C567299	MESH:C567299	Hepatoblastoma Caused By Somatic Mutation	CTD_diseases	7
MESH:C567302	MESH:C567302	Diamond-Blackfan Anemia 1	CTD_diseases	7
MESH:C567310	MESH:C567310	Ciliary Dyskinesia, Primary, 9	CTD_diseases	7
MESH:C567311	MESH:C567311	Leukodystrophy, Dysmyelinating, And Spastic Paraparesis With Or Without Dystonia	CTD_diseases	7
MESH:C567314	MESH:C567314	Leukodystrophy, Hypomyelinating, 6	CTD_diseases	7
MESH:C567315	MESH:C567315	Epilepsy, Progressive Myoclonic, 1b	CTD_diseases	7
MESH:C567343	MESH:C567343	Jervell And Lange-Nielsen Syndrome 2	CTD_diseases	7
MESH:C567349	MESH:C567349	Spastic Paraplegia 38, Autosomal Dominant	CTD_diseases	7
MESH:C567351	MESH:C567351	Premature Ovarian Failure 6	CTD_diseases	7
MESH:C567359	MESH:C567359	Microtia, Hearing Impairment, And Cleft Palate	CTD_diseases	7
MESH:C567373	MESH:C567373	Ciliary Dyskinesia, Primary, 8	CTD_diseases	7
MESH:C567404	MESH:C567404	Epileptic Encephalopathy, Early Infantile, 4	CTD_diseases	7
MESH:C567405	MESH:C567405	Aneurysm, Intracranial Berry, 8	CTD_diseases	7
MESH:C567406	MESH:C567406	Aneurysm, Intracranial Berry, 7	CTD_diseases	7
MESH:C567420	MESH:C567420	Deafness, Unilateral, With Delayed Endolymphatic Hydrops	CTD_diseases	7
MESH:C567433	MESH:C567433	Spastic Paraplegia 39, Autosomal Recessive	CTD_diseases	7
MESH:C567435	MESH:C567435	Pyloric Stenosis, Infantile Hypertrophic, 3	CTD_diseases	7
MESH:C567470	MESH:C567470	Mental Retardation, X-Linked 95	CTD_diseases	7
MESH:C567472	MESH:C567472	Pyloric Stenosis, Infantile Hypertrophic, 4	CTD_diseases	7
MESH:C567479	MESH:C567479	Mental Retardation, X-Linked 94	CTD_diseases	7
MESH:C567480	MESH:C567480	Myopathy, X-Linked, With Postural Muscle Atrophy	CTD_diseases	7
MESH:C567481	MESH:C567481	Scapuloperoneal Myopathy, X-Linked Dominant	CTD_diseases	7
MESH:C567486	MESH:C567486	Hypercarotenemia And Vitamin A Deficiency, Autosomal Recessive	CTD_diseases	7
MESH:C567489	MESH:C567489	Spherocytosis, Type 3	CTD_diseases	7
MESH:C567493	MESH:C567493	Hyperphenylalaninemia, BH4-Deficient, Due To Partial PTS Deficiency	CTD_diseases	7
MESH:C567494	MESH:C567494	Hyperphenylalaninemia, Non-Pku Mild	CTD_diseases	7
MESH:C567500	MESH:C567500	Aneurysm, Intracranial Berry, 6	CTD_diseases	7
MESH:C567504	MESH:C567504	Ciliary Dyskinesia, Primary, 7	CTD_diseases	7
MESH:C567520	MESH:C567520	Elliptocytosis 1	CTD_diseases	7
MESH:C567544	MESH:C567544	Sensorineural Deafness With Mild Renal Dysfunction	CTD_diseases	7
MESH:C567561	MESH:C567561	Atrial Septal Defect 5	CTD_diseases	7
MESH:C567574	MESH:C567574	46,Xy Gonadal Dysgenesis, Complete, Sry-Related	CTD_diseases	7
MESH:C567584	MESH:C567584	Mental Retardation, X-Linked, Syp-Related	CTD_diseases	7
MESH:C567591	MESH:C567591	Emery-Dreifuss Muscular Dystrophy 6, X-Linked	CTD_diseases	7
MESH:C567593	MESH:C567593	Primary Ovarian Insufficiency, Fragile X-Associated	CTD_diseases	7
MESH:C567597	MESH:C567597	46,Xx Gonadal Dysgenesis, Partial Or Complete, Autosomal	CTD_diseases	7
MESH:C567633	MESH:C567633	Emery-Dreifuss Muscular Dystrophy, Atypical, Autosomal Recessive	CTD_diseases	7
MESH:C567635	MESH:C567635	Hypokalemic Periodic Paralysis, Type 2	CTD_diseases	7
MESH:C567649	MESH:C567649	Diamond-Blackfan Anemia 10	CTD_diseases	7
MESH:C567650	MESH:C567650	Diamond-Blackfan Anemia 9	CTD_diseases	7
MESH:C567653	MESH:C567653	Charcot-Marie-Tooth Disease, Axonal, Type 2n	CTD_diseases	7
MESH:C567706	MESH:C567706	Amelogenesis Imperfecta, Hypomaturation Type, Iia3	CTD_diseases	7
MESH:C567707	MESH:C567707	Spastic Paraplegia 44, Autosomal Recessive	CTD_diseases	7
MESH:C567726	MESH:C567726	Parkinson Disease 16	CTD_diseases	7
MESH:C567738	MESH:C567738	Neuropathy, Hereditary Sensory And Autonomic, Type IIB	CTD_diseases	7
MESH:C567748	MESH:C567748	Neutropenia, Severe Congenital, Autosomal Dominant 2	CTD_diseases	7
MESH:C567762	MESH:C567762	Bartter Syndrome, Type 4b	CTD_diseases	7
MESH:C567764	MESH:C567764	Atrial Septal Defect 6	CTD_diseases	7
MESH:C567766	MESH:C567766	46, XY Sex Reversal 5	CTD_diseases	7
MESH:C567780	MESH:C567780	Camptodactyly 1	CTD_diseases	7
MESH:C567782	MESH:C567782	Amyloidosis, Hereditary, Transthyretin-Related	CTD_diseases	7
MESH:C567816	MESH:C567816	Biliary Cirrhosis, Primary, 3	CTD_diseases	7
MESH:C567817	MESH:C567817	Biliary Cirrhosis, Primary, 2	CTD_diseases	7
MESH:C567830	MESH:C567830	Emery-Dreifuss Muscular Dystrophy 5	CTD_diseases	7
MESH:C567831	MESH:C567831	Emery-Dreifuss Muscular Dystrophy 4	CTD_diseases	7
MESH:C567832	MESH:C567832	Spermatogenic Failure 7	CTD_diseases	7
MESH:C567838	MESH:C567838	Premature Ovarian Failure 7	CTD_diseases	7
MESH:C567876	MESH:C567876	Heterotopia, Periventricular, Associated With Chromosome 5q Deletion	CTD_diseases	7
MESH:C567887	MESH:C567887	46,XY Sex Reversal 4	CTD_diseases	7
MESH:C567906	MESH:C567906	Mental Retardation, X-Linked 1	CTD_diseases	7
MESH:C567914	MESH:C567914	Palmoplantar Keratoderma, Vorner Type	CTD_diseases	7
MESH:C567924	MESH:C567924	Epileptic Encephalopathy, Early Infantile, 1	CTD_diseases	7
MESH:C567930	MESH:C567930	Spastic Paraplegia 36, Autosomal Dominant	CTD_diseases	7
MESH:C567931	MESH:C567931	Spastic Paraplegia 37, Autosomal Dominant	CTD_diseases	7
MESH:C570377	MESH:C570377	Benign Pseudohypertrophic Muscular Dystrophy	CTD_diseases	7
MESH:C572845	MESH:C572845	Thyroid cancer, follicular	CTD_diseases	7
MESH:C573023	MESH:C573023	Lentiginosis Profusa	CTD_diseases	7
MESH:C573898	MESH:C573898	Triphalangeal Thumb	CTD_diseases	7
MESH:C575534	MESH:C575534	Ceroid lipofuscinosis, neuronal 5	CTD_diseases	7
MESH:C579862	MESH:C579862	3b-Hydroxysteroid Dehydrogenase Deficiency	CTD_diseases	7
MESH:C579932	MESH:C579932	Autosomal Dominant Nocturnal Frontal Lobe Epilepsy	CTD_diseases	7
MESH:C579934	MESH:C579934	Autosomal Recessive Cerebellar Ataxia Type 1	CTD_diseases	7
MESH:C579991	MESH:C579991	Chmp2b-Related Frontotemporal Dementia	CTD_diseases	7
MESH:C580003	MESH:C580003	Combined Pituitary Hormone Deficiency	CTD_diseases	7
MESH:C580162	MESH:C580162	Hereditary Sensory and Autonomic Neuropathy Type Ie	CTD_diseases	7
MESH:C580329	MESH:C580329	Opticospinal Multiple Sclerosis	CTD_diseases	7
MESH:C580387	MESH:C580387	Ppm-X Syndrome	CTD_diseases	7
MESH:C580388	MESH:C580388	Prickle1-Related Progressive Myoclonus Epilepsy with Ataxia	CTD_diseases	7
MESH:C580471	MESH:C580471	Sebocystomatosis	CTD_diseases	7
MESH:C580551	MESH:C580551	Y Chromosome Infertility	CTD_diseases	7
MESH:D000012	MESH:D000012	Abetalipoproteinemia	CTD_diseases	7
MESH:D000168	MESH:D000168	Acrocephalosyndactylia	CTD_diseases	7
MESH:D000232	MESH:D000232	Adenofibroma	CTD_diseases	7
MESH:D000381	MESH:D000381	Agraphia	CTD_diseases	7
MESH:D000648	MESH:D000648	Amnesia, Retrograde	CTD_diseases	7
MESH:D000724	MESH:D000724	Ancylostomiasis	CTD_diseases	7
MESH:D000789	MESH:D000789	Angina, Unstable	CTD_diseases	7
MESH:D000849	MESH:D000849	Anomia	CTD_diseases	7
MESH:D001063	MESH:D001063	Appendiceal Neoplasms	CTD_diseases	7
MESH:D001254	MESH:D001254	Astrocytoma	CTD_diseases	7
MESH:D001449	MESH:D001449	Balkan Nephropathy	CTD_diseases	7
MESH:D001948	MESH:D001948	Brenner Tumor	CTD_diseases	7
MESH:D002100	MESH:D002100	Cachexia	CTD_diseases	7
MESH:D002270	MESH:D002270	Carbuncle	CTD_diseases	7
MESH:D002544	MESH:D002544	Cerebral Infarction	CTD_diseases	7
MESH:D002601	MESH:D002601	Chancre	CTD_diseases	7
MESH:D002796	MESH:D002796	Choline Deficiency	CTD_diseases	7
MESH:D002820	MESH:D002820	Hydatidiform Mole, Invasive	CTD_diseases	7
MESH:D003025	MESH:D003025	Clubfoot	CTD_diseases	7
MESH:D003027	MESH:D003027	Cluster Headache	CTD_diseases	7
MESH:D003110	MESH:D003110	Colonic Neoplasms	CTD_diseases	7
MESH:D003128	MESH:D003128	Coma	CTD_diseases	7
MESH:D003555	MESH:D003555	Cystinuria	CTD_diseases	7
MESH:D003638	MESH:D003638	Deafness	CTD_diseases	7
MESH:D003639	MESH:D003639	Hearing Loss, Sudden	CTD_diseases	7
MESH:D003803	MESH:D003803	Dentigerous Cyst	CTD_diseases	7
MESH:D003969	MESH:D003969	Vipoma	CTD_diseases	7
MESH:D004154	MESH:D004154	Dipetalonema Infections	CTD_diseases	7
MESH:D004410	MESH:D004410	Dyslexia	CTD_diseases	7
MESH:D004654	MESH:D004654	Empyema, Tuberculous	CTD_diseases	7
MESH:D004806	MESH:D004806	Ependymoma	CTD_diseases	7
MESH:D005494	MESH:D005494	Folic Acid Deficiency	CTD_diseases	7
MESH:D005862	MESH:D005862	Gerstmann Syndrome	CTD_diseases	7
MESH:D005923	MESH:D005923	Glomerulosclerosis, Focal Segmental	CTD_diseases	7
MESH:D005935	MESH:D005935	Glucagonoma	CTD_diseases	7
MESH:D006053	MESH:D006053	Goldenhar Syndrome	CTD_diseases	7
MESH:D006188	MESH:D006188	Haemonchiasis	CTD_diseases	7
MESH:D006312	MESH:D006312	Hearing Loss, Bilateral	CTD_diseases	7
MESH:D006314	MESH:D006314	Hearing Loss, Conductive	CTD_diseases	7
MESH:D006315	MESH:D006315	Hearing Loss, Functional	CTD_diseases	7
MESH:D006316	MESH:D006316	Hearing Loss, High-Frequency	CTD_diseases	7
MESH:D006319	MESH:D006319	Hearing Loss, Sensorineural	CTD_diseases	7
MESH:D006450	MESH:D006450	Hemoglobin SC Disease	CTD_diseases	7
MESH:D006679	MESH:D006679	HIV Seropositivity	CTD_diseases	7
MESH:D006944	MESH:D006944	Hyperglycemic Hyperosmolar Nonketotic Coma	CTD_diseases	7
MESH:D006966	MESH:D006966	Hyperprolactinemia	CTD_diseases	7
MESH:D006970	MESH:D006970	Disorders of Excessive Somnolence	CTD_diseases	7
MESH:D007000	MESH:D007000	Hypodermyiasis	CTD_diseases	7
MESH:D007319	MESH:D007319	Sleep Initiation and Maintenance Disorders	CTD_diseases	7
MESH:D007635	MESH:D007635	Keratitis, Dendritic	CTD_diseases	7
MESH:D007676	MESH:D007676	Kidney Failure, Chronic	CTD_diseases	7
MESH:D007683	MESH:D007683	Kidney Tubular Necrosis, Acute	CTD_diseases	7
MESH:D007725	MESH:D007725	Krukenberg Tumor	CTD_diseases	7
MESH:D007732	MESH:D007732	Kwashiorkor	CTD_diseases	7
MESH:D007805	MESH:D007805	Language Development Disorders	CTD_diseases	7
MESH:D007863	MESH:D007863	Lecithin Acyltransferase Deficiency	CTD_diseases	7
MESH:D007897	MESH:D007897	Leishmaniasis, Mucocutaneous	CTD_diseases	7
MESH:D007965	MESH:D007965	Leukodystrophy, Globoid Cell	CTD_diseases	7
MESH:D007966	MESH:D007966	Leukodystrophy, Metachromatic	CTD_diseases	7
MESH:D008039	MESH:D008039	Linitis Plastica	CTD_diseases	7
MESH:D008118	MESH:D008118	Loiasis	CTD_diseases	7
MESH:D008185	MESH:D008185	Lutembacher Syndrome	CTD_diseases	7
MESH:D008219	MESH:D008219	Lymphogranuloma Venereum	CTD_diseases	7
MESH:D008303	MESH:D008303	Malignant Carcinoid Syndrome	CTD_diseases	7
MESH:D008337	MESH:D008337	Mandibular Fractures	CTD_diseases	7
MESH:D008368	MESH:D008368	Mansonelliasis	CTD_diseases	7
MESH:D008440	MESH:D008440	Maxillary Fractures	CTD_diseases	7
MESH:D008444	MESH:D008444	Maxillary Sinus Neoplasms	CTD_diseases	7
MESH:D008527	MESH:D008527	Medulloblastoma	CTD_diseases	7
MESH:D008539	MESH:D008539	Meigs Syndrome	CTD_diseases	7
MESH:D008844	MESH:D008844	Micrognathism	CTD_diseases	7
MESH:D009332	MESH:D009332	Necatoriasis	CTD_diseases	7
MESH:D009837	MESH:D009837	Oligodendroglioma	CTD_diseases	7
MESH:D010017	MESH:D010017	Osteoma, Osteoid	CTD_diseases	7
MESH:D010029	MESH:D010029	Ostertagiasis	CTD_diseases	7
MESH:D010144	MESH:D010144	Paget's Disease, Mammary	CTD_diseases	7
MESH:D010236	MESH:D010236	Paraganglioma, Extra-Adrenal	CTD_diseases	7
MESH:D010301	MESH:D010301	Parkinson Disease, Postencephalitic	CTD_diseases	7
MESH:D010383	MESH:D010383	Pellagra	CTD_diseases	7
MESH:D010673	MESH:D010673	Pheochromocytoma	CTD_diseases	7
MESH:D010855	MESH:D010855	Pierre Robin Syndrome	CTD_diseases	7
MESH:D011045	MESH:D011045	Poland Syndrome	CTD_diseases	7
MESH:D011052	MESH:D011052	Poliomyelitis, Bulbar	CTD_diseases	7
MESH:D011085	MESH:D011085	Polycystic Ovary Syndrome	CTD_diseases	7
MESH:D011704	MESH:D011704	Pyelonephritis	CTD_diseases	7
MESH:D012004	MESH:D012004	Rectal Neoplasms	CTD_diseases	7
MESH:D012257	MESH:D012257	Riboflavin Deficiency	CTD_diseases	7
MESH:D012512	MESH:D012512	Sarcoma, Ewing	CTD_diseases	7
MESH:D012610	MESH:D012610	Screw Worm Infection	CTD_diseases	7
MESH:D012805	MESH:D012805	Sickle Cell Trait	CTD_diseases	7
MESH:C567277	MESH:C567277	Deafness, Autosomal Dominant 3A	CTD_diseases	8
MESH:C567419	MESH:C567419	Cardiomyopathy, Familial Hypertrophic, 11	CTD_diseases	8
MESH:C567436	MESH:C567436	Spinocerebellar Ataxia, Autosomal Recessive 9	CTD_diseases	8
MESH:C567441	MESH:C567441	Deafness, Autosomal Dominant 2A	CTD_diseases	8
MESH:C567442	MESH:C567442	Rett Syndrome, Zappella Variant	CTD_diseases	8
MESH:C567543	MESH:C567543	Deafness, Autosomal Recessive 77	CTD_diseases	8
MESH:C567562	MESH:C567562	Deafness, Autosomal Recessive 71	CTD_diseases	8
MESH:C567576	MESH:C567576	Rett Syndrome, Atypical	CTD_diseases	8
MESH:C567602	MESH:C567602	Refsum Disease, Adult, 1	CTD_diseases	8
MESH:C567603	MESH:C567603	Refsum Disease, Adult, 2	CTD_diseases	8
MESH:C567651	MESH:C567651	Deafness, Autosomal Recessive 79	CTD_diseases	8
MESH:C567681	MESH:C567681	Cardiomyopathy, Familial Hypertrophic, 15	CTD_diseases	8
MESH:C567684	MESH:C567684	Cardiomyopathy, Familial Hypertrophic, 14	CTD_diseases	8
MESH:C567685	MESH:C567685	Colorectal Cancer, Hereditary Nonpolyposis, Type 8	CTD_diseases	8
MESH:C567686	MESH:C567686	Cardiomyopathy, Familial Hypertrophic, 13	CTD_diseases	8
MESH:C567687	MESH:C567687	Focal Segmental Glomerulosclerosis 5	CTD_diseases	8
MESH:C567727	MESH:C567727	Walker-Warburg Syndrome, Fktn-Related	CTD_diseases	8
MESH:C575214	MESH:C575214	Spinocerebellar ataxia 30	CTD_diseases	8
MESH:C580334	MESH:C580334	Nonsyndromic Deafness	CTD_diseases	8
MESH:D000788	MESH:D000788	Angina Pectoris, Variant	CTD_diseases	8
MESH:D001037	MESH:D001037	Aphasia	CTD_diseases	8
MESH:D001184	MESH:D001184	Articulation Disorders	CTD_diseases	8
MESH:D001602	MESH:D001602	Beriberi	CTD_diseases	8
MESH:D002289	MESH:D002289	Carcinoma, Non-Small-Cell Lung	CTD_diseases	8
MESH:D002345	MESH:D002345	Carotid Body Tumor	CTD_diseases	8
MESH:D004454	MESH:D004454	Echolalia	CTD_diseases	8
MESH:D004685	MESH:D004685	Encephalomyelitis, Venezuelan Equine	CTD_diseases	8
MESH:D005733	MESH:D005733	Gangliosidoses	CTD_diseases	8
MESH:D005776	MESH:D005776	Gaucher Disease	CTD_diseases	8
MESH:D005909	MESH:D005909	Glioblastoma	CTD_diseases	8
MESH:D005925	MESH:D005925	Glomus Jugulare Tumor	CTD_diseases	8
MESH:D006317	MESH:D006317	Hearing Loss, Noise-Induced	CTD_diseases	8
MESH:D007984	MESH:D007984	Leydig Cell Tumor	CTD_diseases	8
MESH:D008177	MESH:D008177	Lupus Vulgaris	CTD_diseases	8
MESH:D009182	MESH:D009182	Mycosis Fungoides	CTD_diseases	8
MESH:D009290	MESH:D009290	Narcolepsy	CTD_diseases	8
MESH:D009447	MESH:D009447	Neuroblastoma	CTD_diseases	8
MESH:D010018	MESH:D010018	Osteomalacia	CTD_diseases	8
MESH:D011304	MESH:D011304	Presbycusis	CTD_diseases	8
MESH:D011705	MESH:D011705	Pyelonephritis, Xanthogranulomatous	CTD_diseases	8
MESH:D012707	MESH:D012707	Sertoli Cell Tumor	CTD_diseases	8
MESH:D012851	MESH:D012851	Sinus Thrombosis, Intracranial	CTD_diseases	8
MESH:C531600	MESH:C531600	Growth hormone excess	CTD_diseases	8
MESH:C531607	MESH:C531607	Alexanders leukodystrophy	CTD_diseases	8
MESH:C531651	MESH:C531651	Rhizomelic chondrodysplasia punctata, type 1	CTD_diseases	8
MESH:C531664	MESH:C531664	Cystinuria type 1	CTD_diseases	8
MESH:C531673	MESH:C531673	Familial ependymoma	CTD_diseases	8
MESH:C531774	MESH:C531774	Familial pars planitis	CTD_diseases	8
MESH:C531854	MESH:C531854	Lysosomal acid lipase deficiency	CTD_diseases	8
MESH:C531857	MESH:C531857	Zellweger leukodystrophy	CTD_diseases	8
MESH:C535280	MESH:C535280	Primary cortisol resistance	CTD_diseases	8
MESH:C535408	MESH:C535408	Gamma-cystathionase deficiency	CTD_diseases	8
MESH:C535525	MESH:C535525	N-Acetylneuraminic acid storage disease	CTD_diseases	8
MESH:C535558	MESH:C535558	Abrikosov's tumor	CTD_diseases	8
MESH:C535631	MESH:C535631	COD (cerebroocular dysgenesis)	CTD_diseases	8
MESH:C535657	MESH:C535657	Acromelic frontonasal dysplasia	CTD_diseases	8
MESH:C535688	MESH:C535688	Robin sequence and oligodactyly	CTD_diseases	8
MESH:C535818	MESH:C535818	Pseudo-Zellweger syndrome	CTD_diseases	8
MESH:C535896	MESH:C535896	Limb-girdle muscular dystrophy type 2F	CTD_diseases	8
MESH:C535900	MESH:C535900	Limb-girdle muscular dystrophy, type 2C	CTD_diseases	8
MESH:C535902	MESH:C535902	Limb-girdle muscular dystrophy, type 2E	CTD_diseases	8
MESH:C535972	MESH:C535972	Colorectal cancer, hereditary nonpolyposis, type 1	CTD_diseases	8
MESH:C536083	MESH:C536083	Hypercholesterolemia due to arg3500 mutation of Apo B-100	CTD_diseases	8
MESH:C536134	MESH:C536134	Medial Medullary Syndrome	CTD_diseases	8
MESH:C536137	MESH:C536137	Medullary cystic kidney disease 1	CTD_diseases	8
MESH:C536398	MESH:C536398	Neonatal-onset citrullinemia type 2	CTD_diseases	8
MESH:C536511	MESH:C536511	Schweitzer Kemink Graham syndrome	CTD_diseases	8
MESH:C536535	MESH:C536535	Vein of Galen aneurysm	CTD_diseases	8
MESH:C536617	MESH:C536617	Saul Wilkes Stevenson syndrome	CTD_diseases	8
MESH:C536655	MESH:C536655	Phosphoenolpyruvate carboxykinase 2 deficiency	CTD_diseases	8
MESH:C536685	MESH:C536685	Fatal pneumococcal Waterhouse-Friderichsen syndrome	CTD_diseases	8
MESH:C536710	MESH:C536710	Winkelman Bethge Pfeiffer syndrome	CTD_diseases	8
MESH:C536775	MESH:C536775	Syphilitic aseptic meningitis	CTD_diseases	8
MESH:C536826	MESH:C536826	Glomerulopathy with fibronectin deposits	CTD_diseases	8
MESH:C536839	MESH:C536839	Cardiac form of generalized glycogenosis	CTD_diseases	8
MESH:C536901	MESH:C536901	Thrombotic thrombocytopenic purpura, acquired	CTD_diseases	8
MESH:C536991	MESH:C536991	Moyamoya disease 1	CTD_diseases	8
MESH:C536992	MESH:C536992	Moyamoya disease 2	CTD_diseases	8
MESH:C536993	MESH:C536993	Moyamoya disease 3	CTD_diseases	8
MESH:C537117	MESH:C537117	LEOPARD syndrome, 2	CTD_diseases	8
MESH:C537183	MESH:C537183	Robinow Sorauf syndrome	CTD_diseases	8
MESH:C537199	MESH:C537199	Spinocerebellar ataxia 20	CTD_diseases	8
MESH:C537202	MESH:C537202	Spinocerebellar ataxia 25	CTD_diseases	8
MESH:C537203	MESH:C537203	Spinocerebellar ataxia 26	CTD_diseases	8
MESH:C537227	MESH:C537227	Sakati syndrome	CTD_diseases	8
MESH:C537239	MESH:C537239	Mengel Konigsmark syndrome	CTD_diseases	8
MESH:C537242	MESH:C537242	Prosopagnosia, hereditary	CTD_diseases	8
MESH:C537246	MESH:C537246	Hemiplegic migraine, familial type 2	CTD_diseases	8
MESH:C537261	MESH:C537261	Lynch syndrome I (site-specific colonic cancer)	CTD_diseases	8
MESH:C537296	MESH:C537296	Granulosa cell tumor of the ovary	CTD_diseases	8
MESH:C537300	MESH:C537300	Greig cephalopolysyndactyly syndrome	CTD_diseases	8
MESH:C537332	MESH:C537332	Sialuria, French type	CTD_diseases	8
MESH:C537366	MESH:C537366	Neuraminidase 1 deficiency	CTD_diseases	8
MESH:C537367	MESH:C537367	Mucolipidosis type 3 A	CTD_diseases	8
MESH:C537389	MESH:C537389	Neurofibromatosis, Type 3, mixed central and peripheral	CTD_diseases	8
MESH:C537390	MESH:C537390	Neurofibromatosis type 5	CTD_diseases	8
MESH:C537391	MESH:C537391	Neurofibromatosis, familial intestinal	CTD_diseases	8
MESH:C537392	MESH:C537392	Neurofibromatosis, type 4, of Riccardi	CTD_diseases	8
MESH:C537404	MESH:C537404	Pituitary dwarfism 1	CTD_diseases	8
MESH:C537469	MESH:C537469	Microtia, meatal atresia and conductive deafness	CTD_diseases	8
MESH:C537505	MESH:C537505	Kowarski syndrome	CTD_diseases	8
MESH:C537588	MESH:C537588	Androblastoma of ovary	CTD_diseases	8
MESH:C537607	MESH:C537607	Rhizomelic chondrodysplasia punctata, type 2	CTD_diseases	8
MESH:C537608	MESH:C537608	Rhizomelic chondrodysplasia punctata, type 3	CTD_diseases	8
MESH:C537630	MESH:C537630	Birdshot chorioretinopathy	CTD_diseases	8
MESH:C537667	MESH:C537667	Bednar's tumor	CTD_diseases	8
MESH:C537709	MESH:C537709	Hermansky Pudlak syndrome 2	CTD_diseases	8
MESH:C537755	MESH:C537755	Renal dysplasia diffuse cystic	CTD_diseases	8
MESH:C537845	MESH:C537845	Nonsyndromic sensorineural hearing loss	CTD_diseases	8
MESH:C537916	MESH:C537916	Femoral facial syndrome	CTD_diseases	8
MESH:C538050	MESH:C538050	Deafness, autosomal dominant nonsyndromic sensorineural 17	CTD_diseases	8
MESH:C538053	MESH:C538053	Adult-onset citrullinemia type 2	CTD_diseases	8
MESH:C538142	MESH:C538142	Summitt syndrome	CTD_diseases	8
MESH:C538190	MESH:C538190	Muscular dystrophy, congenital, with central nervous system involvement	CTD_diseases	8
MESH:C538197	MESH:C538197	Deafness, autosomal dominant nonsyndromic sensorineural 22	CTD_diseases	8
MESH:C538198	MESH:C538198	Deafness, autosomal dominant nonsyndromic sensorineural 23	CTD_diseases	8
MESH:C538199	MESH:C538199	Deafness, autosomal dominant nonsyndromic sensorineural 24	CTD_diseases	8
MESH:C538219	MESH:C538219	Dermatofibrosarcoma protuberans	CTD_diseases	8
MESH:C538248	MESH:C538248	Amyloid angiopathy	CTD_diseases	8
MESH:C538352	MESH:C538352	Pellagra like syndrome	CTD_diseases	8
MESH:C538360	MESH:C538360	Restless legs syndrome 2	CTD_diseases	8
MESH:C538433	MESH:C538433	Ancylostoma duodenale infection	CTD_diseases	8
MESH:C538443	MESH:C538443	Restless legs syndrome 1	CTD_diseases	8
MESH:C538444	MESH:C538444	CTNL1	CTD_diseases	8
MESH:C538446	MESH:C538446	Speech disturbance - use of faulty phrasing and unrelated words	CTD_diseases	8
MESH:C538457	MESH:C538457	Segmental glomerulosclerosis	CTD_diseases	8
MESH:C538475	MESH:C538475	Double cortex	CTD_diseases	8
MESH:C538489	MESH:C538489	Familial hyperchylomicronemia syndrome	CTD_diseases	8
MESH:C538493	MESH:C538493	Familial Burkitt's lymphoma	CTD_diseases	8
MESH:C538523	MESH:C538523	Free sialic acid storage disease	CTD_diseases	8
MESH:C538582	MESH:C538582	Pfeiffer type acrocephalosyndactyly	CTD_diseases	8
MESH:C538602	MESH:C538602	Mucolipidosis 2	CTD_diseases	8
MESH:C538646	MESH:C538646	High serum cholesterol, familial	CTD_diseases	8
MESH:C538662	MESH:C538662	Recurrent trigger thumb	CTD_diseases	8
MESH:C538669	MESH:C538669	Alcohol induced encephalopathy	CTD_diseases	8
MESH:C538676	MESH:C538676	Melanodermic leukodystrophy	CTD_diseases	8
MESH:C548033	MESH:C548033	Medullary Cystic Kidney Disease 2	CTD_diseases	8
MESH:C562423	MESH:C562423	Deafness, Progressive High-Tone Neural	CTD_diseases	8
MESH:C562559	MESH:C562559	Prognathism, Mandibular	CTD_diseases	8
MESH:C562704	MESH:C562704	Isolated Growth Hormone Deficiency, Type II	CTD_diseases	8
MESH:C562705	MESH:C562705	Pituitary Dwarfism with Large Sella Turcica	CTD_diseases	8
MESH:C562716	MESH:C562716	Delta-Beta Thalassemia	CTD_diseases	8
MESH:C562791	MESH:C562791	Hypophosphatemic Rickets, Autosomal Dominant	CTD_diseases	8
MESH:C562950	MESH:C562950	Cleft Soft Palate	CTD_diseases	8
MESH:C563172	MESH:C563172	Pituitary Hormone Deficiency, Combined, 2	CTD_diseases	8
MESH:C563181	MESH:C563181	Histiocytoma, Angiomatoid Fibrous	CTD_diseases	8
MESH:C563187	MESH:C563187	Acrocephalopolysyndactyly Type II	CTD_diseases	8
MESH:C563295	MESH:C563295	Deafness, Autosomal Dominant 12	CTD_diseases	8
MESH:C563316	MESH:C563316	Deafness, Progressive, With Stapes Fixation	CTD_diseases	8
MESH:C563321	MESH:C563321	Deafness, Autosomal Dominant 7	CTD_diseases	8
MESH:C563327	MESH:C563327	Deafness, Autosomal Recessive 12	CTD_diseases	8
MESH:C563335	MESH:C563335	Deafness, Autosomal Dominant 9	CTD_diseases	8
MESH:C563353	MESH:C563353	Deafness, Autosomal Dominant 11	CTD_diseases	8
MESH:C563354	MESH:C563354	Deafness, Autosomal Dominant 10	CTD_diseases	8
MESH:C563395	MESH:C563395	Deafness, Childhood-Onset Neurosensory, Autosomal Recessive 8	CTD_diseases	8
MESH:C563396	MESH:C563396	Deafness, Autosomal Recessive 9	CTD_diseases	8
MESH:C563398	MESH:C563398	Auditory Neuropathy, Nonsyndromic Recessive	CTD_diseases	8
MESH:C563405	MESH:C563405	Migraine, Sporadic Hemiplegic	CTD_diseases	8
MESH:C563410	MESH:C563410	Deafness, Autosomal Dominant 5	CTD_diseases	8
MESH:C563417	MESH:C563417	Deafness, Autosomal Recessive 7	CTD_diseases	8
MESH:C563418	MESH:C563418	Deafness, Autosomal Recessive 6	CTD_diseases	8
MESH:C563421	MESH:C563421	Deafness, Autosomal Dominant 6	CTD_diseases	8
MESH:C563436	MESH:C563436	Cardiomyopathy, Familial Hypertrophic, 6	CTD_diseases	8
MESH:C563444	MESH:C563444	Deafness, Autosomal Recessive 5	CTD_diseases	8
MESH:C563456	MESH:C563456	Colorectal Cancer, Hereditary Nonpolyposis, Type 5	CTD_diseases	8
MESH:C563460	MESH:C563460	Deafness, Autosomal Dominant 4	CTD_diseases	8
MESH:C563523	MESH:C563523	Neurofibromatosis, Familial Spinal	CTD_diseases	8
MESH:C563669	MESH:C563669	Deafness, Autosomal Recessive 68	CTD_diseases	8
MESH:C563705	MESH:C563705	Deafness, Autosomal Recessive 23	CTD_diseases	8
MESH:C563720	MESH:C563720	Deafness, Autosomal Recessive 48	CTD_diseases	8
MESH:C563753	MESH:C563753	Spinocerebellar Ataxia, Autosomal Recessive 7	CTD_diseases	8
MESH:C563815	MESH:C563815	Deafness, Autosomal Recessive 36	CTD_diseases	8
MESH:C563865	MESH:C563865	Cardiomyopathy, Familial Hypertrophic, 10	CTD_diseases	8
MESH:C563866	MESH:C563866	Cardiomyopathy, Familial Hypertrophic, 8	CTD_diseases	8
MESH:C563884	MESH:C563884	Deafness, Autosomal Recessive 32	CTD_diseases	8
MESH:C563885	MESH:C563885	Deafness, Autosomal Dominant 47	CTD_diseases	8
MESH:C563888	MESH:C563888	Deafness, Autosomal Dominant 31	CTD_diseases	8
MESH:C563890	MESH:C563890	Deafness, Autosomal Dominant 28	CTD_diseases	8
MESH:C563908	MESH:C563908	Deafness, Autosomal Recessive 35	CTD_diseases	8
MESH:C563950	MESH:C563950	Band Heterotopia of Brain	CTD_diseases	8
MESH:C563961	MESH:C563961	Deafness, Autosomal Recessive 3	CTD_diseases	8
MESH:C563971	MESH:C563971	Colorectal Cancer, Hereditary Nonpolyposis, Type 4	CTD_diseases	8
MESH:C563972	MESH:C563972	Colorectal Cancer, Hereditary Nonpolyposis, Type 3	CTD_diseases	8
MESH:C564007	MESH:C564007	Deafness, Autosomal Recessive 2	CTD_diseases	8
MESH:C564013	MESH:C564013	Deafness, Aminoglycoside-Induced	CTD_diseases	8
MESH:C564063	MESH:C564063	Rett Syndrome, Preserved Speech Variant	CTD_diseases	8
MESH:C564125	MESH:C564125	Internal Carotid Artery, Spontaneous Dissection of	CTD_diseases	8
MESH:C564246	MESH:C564246	Deafness, Autosomal Dominant 43	CTD_diseases	8
MESH:C564250	MESH:C564250	Deafness, Autosomal Dominant 49	CTD_diseases	8
MESH:C564265	MESH:C564265	Deafness, Autosomal Recessive 39	CTD_diseases	8
MESH:C564266	MESH:C564266	Deafness, Autosomal Recessive 40	CTD_diseases	8
MESH:C564272	MESH:C564272	Deafness, Autosomal Dominant 41	CTD_diseases	8
MESH:C564273	MESH:C564273	Deafness, Autosomal Recessive 38	CTD_diseases	8
MESH:C564322	MESH:C564322	Deafness, Autosomal Dominant 48	CTD_diseases	8
MESH:C564331	MESH:C564331	Deafness, Autosomal Recessive 37	CTD_diseases	8
MESH:C564348	MESH:C564348	Deafness, Autosomal Dominant 52	CTD_diseases	8
MESH:C564399	MESH:C564399	Deafness, Autosomal Dominant 44	CTD_diseases	8
MESH:C564535	MESH:C564535	Lesch-Nyhan Syndrome, Neurologic Variant	CTD_diseases	8
MESH:C564602	MESH:C564602	Deafness, Autosomal Recessive 33	CTD_diseases	8
MESH:C564609	MESH:C564609	Deafness, Autosomal Recessive	CTD_diseases	8
MESH:C564616	MESH:C564616	Spinocerebellar Ataxia 17	CTD_diseases	8
MESH:C564624	MESH:C564624	Deafness, Autosomal Recessive 30	CTD_diseases	8
MESH:C564629	MESH:C564629	Deafness, Autosomal Recessive 31	CTD_diseases	8
MESH:C564633	MESH:C564633	Deafness, Autosomal Recessive 22	CTD_diseases	8
MESH:C564634	MESH:C564634	Deafness, Autosomal Dominant 21	CTD_diseases	8
MESH:C564675	MESH:C564675	Deafness, Autosomal Dominant 36	CTD_diseases	8
MESH:C564685	MESH:C564685	Spinocerebellar Ataxia 15	CTD_diseases	8
MESH:C564706	MESH:C564706	Deafness, Autosomal Dominant 30	CTD_diseases	8
MESH:C564722	MESH:C564722	Subcortical Band Heterotopia, X-Linked	CTD_diseases	8
MESH:C564764	MESH:C564764	Tibia, Absence of, with Congenital Deafness	CTD_diseases	8
MESH:C564868	MESH:C564868	Polycystic Ovarian Disease due to 17-Ketosteroid Reductase Deficiency	CTD_diseases	8
MESH:C564955	MESH:C564955	Sialidosis, Type I	CTD_diseases	8
MESH:C565121	MESH:C565121	Deafness, Autosomal Dominant 1	CTD_diseases	8
MESH:C565122	MESH:C565122	Deafness, Mid-Tone Neural	CTD_diseases	8
MESH:C565188	MESH:C565188	Spinocerebellar Ataxia, Autosomal Recessive 8	CTD_diseases	8
MESH:C565207	MESH:C565207	Deafness, Autosomal Recessive 67	CTD_diseases	8
MESH:C565211	MESH:C565211	Deafness, Autosomal Recessive 65	CTD_diseases	8
MESH:C565218	MESH:C565218	Deafness, Autosomal Recessive 28	CTD_diseases	8
MESH:C565239	MESH:C565239	Deafness, Autosomal Dominant 24	CTD_diseases	8
MESH:C565267	MESH:C565267	Deafness, Autosomal Dominant 18	CTD_diseases	8
MESH:C565287	MESH:C565287	Deafness, Autosomal Recessive 27	CTD_diseases	8
MESH:C565319	MESH:C565319	Deafness, Autosomal Dominant 25	CTD_diseases	8
MESH:C565329	MESH:C565329	Deafness, Autosomal Recessive 26	CTD_diseases	8
MESH:C565341	MESH:C565341	Deafness, Autosomal Recessive 10	CTD_diseases	8
MESH:C565357	MESH:C565357	Deafness, Autosomal Dominant 23	CTD_diseases	8
MESH:C565367	MESH:C565367	Mucolipidosis III Gamma	CTD_diseases	8
MESH:C565637	MESH:C565637	Deafness, Sensorineural, Autosomal-Mitochondrial Type	CTD_diseases	8
MESH:C565644	MESH:C565644	Deafness, Conductive, with Malformed External Ear	CTD_diseases	8
MESH:C565652	MESH:C565652	Cystinuria, Type A	CTD_diseases	8
MESH:C565698	MESH:C565698	Deafness, Autosomal Recessive 59	CTD_diseases	8
MESH:C565701	MESH:C565701	Deafness, Autosomal Recessive 66	CTD_diseases	8
MESH:C565716	MESH:C565716	Deafness, Autosomal Recessive 44	CTD_diseases	8
MESH:C565717	MESH:C565717	Deafness, Autosomal Recessive 49	CTD_diseases	8
MESH:C565719	MESH:C565719	Deafness, Autosomal Recessive 62	CTD_diseases	8
MESH:C565729	MESH:C565729	Clavicular Hypoplasia, Zygomatic Arch Hypoplasia, and Micrognathia	CTD_diseases	8
MESH:C565754	MESH:C565754	Deafness, Autosomal Dominant 20	CTD_diseases	8
MESH:C565772	MESH:C565772	Spinocerebellar Ataxia 11	CTD_diseases	8
MESH:C565777	MESH:C565777	Colorectal Cancer, Hereditary Nonpolyposis, Type 7	CTD_diseases	8
MESH:C565790	MESH:C565790	Spinocerebellar Ataxia 12	CTD_diseases	8
MESH:C565805	MESH:C565805	Short Stature, Idiopathic, Autosomal	CTD_diseases	8
MESH:C565828	MESH:C565828	Deafness, Autosomal Recessive 20	CTD_diseases	8
MESH:C565831	MESH:C565831	Focal Segmental Glomerulosclerosis 2	CTD_diseases	8
MESH:C565832	MESH:C565832	Deafness, Autosomal Dominant 16	CTD_diseases	8
MESH:C565834	MESH:C565834	Beta Thalassemia, Dominant Inclusion Body Type	CTD_diseases	8
MESH:C565861	MESH:C565861	Cerebrohepatorenal Syndrome, Variant Types	CTD_diseases	8
MESH:C566005	MESH:C566005	Cardiomyopathy, Familial Hypertrophic, 1	CTD_diseases	8
MESH:C566039	MESH:C566039	Colorectal Cancer, Hereditary Nonpolyposis, Type 6	CTD_diseases	8
MESH:C566044	MESH:C566044	Cardiomyopathy, Familial Hypertrophic, 9	CTD_diseases	8
MESH:C566065	MESH:C566065	Thalassemia, Beta+, Silent Allele	CTD_diseases	8
MESH:C566117	MESH:C566117	Cluster Headache, Familial	CTD_diseases	8
MESH:C566146	MESH:C566146	Spinocerebellar Ataxia 31	CTD_diseases	8
MESH:C566169	MESH:C566169	Cardiomyopathy, Familial Hypertrophic, 4	CTD_diseases	8
MESH:C566170	MESH:C566170	Cardiomyopathy, Familial Hypertrophic, 3	CTD_diseases	8
MESH:C566171	MESH:C566171	Cardiomyopathy, Familial Hypertrophic, 2	CTD_diseases	8
MESH:C566262	MESH:C566262	Familial Hyperbeta- and Prebetalipoproteinemia	CTD_diseases	8
MESH:C566267	MESH:C566267	Hypobetalipoproteinemia, Familial	CTD_diseases	8
MESH:C566325	MESH:C566325	Saethre-Chotzen Syndrome with Eyelid Anomalies	CTD_diseases	8
MESH:C566327	MESH:C566327	Vogt Cephalodactyly	CTD_diseases	8
MESH:C566339	MESH:C566339	Deafness, Autosomal Recessive 16	CTD_diseases	8
MESH:C566344	MESH:C566344	Deafness, Autosomal Recessive 14	CTD_diseases	8
MESH:C566353	MESH:C566353	Deafness, Autosomal Recessive 21	CTD_diseases	8
MESH:C566366	MESH:C566366	Enlarged Vestibular Aqueduct	CTD_diseases	8
MESH:C566403	MESH:C566403	Homocysteinemia	CTD_diseases	8
MESH:C566410	MESH:C566410	Deafness, Autosomal Recessive 13	CTD_diseases	8
MESH:C566418	MESH:C566418	Deafness, Autosomal Recessive 17	CTD_diseases	8
MESH:C566453	MESH:C566453	Deafness, Autosomal Recessive 53	CTD_diseases	8
MESH:C566459	MESH:C566459	Deafness, Autosomal Recessive 46	CTD_diseases	8
MESH:C566460	MESH:C566460	Deafness, Autosomal Recessive 42	CTD_diseases	8
MESH:C566495	MESH:C566495	Deafness, Autosomal Dominant 53	CTD_diseases	8
MESH:C566498	MESH:C566498	Deafness, Autosomal Recessive 47	CTD_diseases	8
MESH:C566545	MESH:C566545	Deafness, Autosomal Dominant 15	CTD_diseases	8
MESH:C566580	MESH:C566580	Deafness, Autosomal Recessive 18	CTD_diseases	8
MESH:C566611	MESH:C566611	Deafness, Autosomal Recessive 15	CTD_diseases	8
MESH:C566612	MESH:C566612	Deafness, Autosomal Dominant 13	CTD_diseases	8
MESH:C566671	MESH:C566671	Spinocerebellar Ataxia And Plaque-Like Deposits	CTD_diseases	8
MESH:C566729	MESH:C566729	Pyruvate Dehydrogenase E1-Beta Deficiency	CTD_diseases	8
MESH:C566813	MESH:C566813	Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant	CTD_diseases	8
MESH:C566874	MESH:C566874	Spinocerebellar Ataxia 10	CTD_diseases	8
MESH:C566938	MESH:C566938	MPGN II with Complement Factor H Deficiency	CTD_diseases	8
MESH:C566939	MESH:C566939	Glomerulonephritis With Isolated C3 Deposits And Factor H Deficiency	CTD_diseases	8
MESH:C566951	MESH:C566951	Deafness, Autosomal Recessive 63	CTD_diseases	8
MESH:C567027	MESH:C567027	Deafness, Autosomal Recessive, 24	CTD_diseases	8
MESH:C567033	MESH:C567033	Glomerulonephritis With Isolated C3 Deposits And Factor I Deficiency	CTD_diseases	8
MESH:C567079	MESH:C567079	Deafness, Unilateral	CTD_diseases	8
MESH:C567099	MESH:C567099	Mucolipidosis III Alpha Beta, Atypical	CTD_diseases	8
MESH:C567134	MESH:C567134	Deafness, Autosomal Recessive 1A	CTD_diseases	8
MESH:C567213	MESH:C567213	Deafness, Autosomal Recessive 1b	CTD_diseases	8
MESH:C567214	MESH:C567214	Deafness, Autosomal Dominant 2B	CTD_diseases	8
MESH:C567215	MESH:C567215	Deafness, Autosomal Dominant 3B	CTD_diseases	8
MESH:C567216	MESH:C567216	Deafness, Autosomal Dominant 59	CTD_diseases	8
MESH:D013342	MESH:D013342	Stuttering	CTD_diseases	8
MESH:D014854	MESH:D014854	Lateral Medullary Syndrome	CTD_diseases	8
MESH:D015161	MESH:D015161	Dementia, Multi-Infarct	CTD_diseases	8
MESH:D015439	MESH:D015439	Leprosy, Borderline	CTD_diseases	8
MESH:D015440	MESH:D015440	Leprosy, Lepromatous	CTD_diseases	8
MESH:D015441	MESH:D015441	Leprosy, Tuberculoid	CTD_diseases	8
MESH:D016518	MESH:D016518	Neurofibromatosis 2	CTD_diseases	8
MESH:D016862	MESH:D016862	Tuberculoma, Intracranial	CTD_diseases	8
MESH:D017593	MESH:D017593	Kleine-Levin Syndrome	CTD_diseases	8
MESH:D017731	MESH:D017731	Lymphomatoid Papulosis	CTD_diseases	8
MESH:D017827	MESH:D017827	Machado-Joseph Disease	CTD_diseases	8
MESH:D018315	MESH:D018315	Glioma, Subependymal	CTD_diseases	8
MESH:D018601	MESH:D018601	King's Evil	CTD_diseases	8
MESH:D020146	MESH:D020146	Putaminal Hemorrhage	CTD_diseases	8
MESH:D020177	MESH:D020177	Hypersomnolence, Idiopathic	CTD_diseases	8
MESH:D020181	MESH:D020181	Sleep Apnea, Obstructive	CTD_diseases	8
MESH:D020182	MESH:D020182	Sleep Apnea, Central	CTD_diseases	8
MESH:D020199	MESH:D020199	Hematoma, Subdural, Acute	CTD_diseases	8
MESH:D020200	MESH:D020200	Hematoma, Subdural, Chronic	CTD_diseases	8
MESH:D020203	MESH:D020203	Brain Stem Hemorrhage, Traumatic	CTD_diseases	8
MESH:D020241	MESH:D020241	Encephalomyelitis, Western Equine	CTD_diseases	8
MESH:D020242	MESH:D020242	Encephalomyelitis, Eastern Equine	CTD_diseases	8
MESH:D020288	MESH:D020288	Papilloma, Choroid Plexus	CTD_diseases	8
MESH:D043604	MESH:D043604	Glomus Tympanicum Tumor	CTD_diseases	8
MESH:D046290	MESH:D046290	Liver Abscess, Pyogenic	CTD_diseases	8
MESH:D046648	MESH:D046648	Hematoma, Subdural, Intracranial	CTD_diseases	8
MESH:D046649	MESH:D046649	Hematoma, Subdural, Spinal	CTD_diseases	8
MESH:D052516	MESH:D052516	Sulfatidosis	CTD_diseases	8
MESH:D054446	MESH:D054446	Lymphoma, Primary Cutaneous Anaplastic Large Cell	CTD_diseases	8
MESH:D054908	MESH:D054908	Extensively Drug-Resistant Tuberculosis	CTD_diseases	8
MESH:D055577	MESH:D055577	Farber Lipogranulomatosis	CTD_diseases	8
MESH:D055752	MESH:D055752	Small Cell Lung Carcinoma	CTD_diseases	8
MESH:D055847	MESH:D055847	Lynch Syndrome II	CTD_diseases	8
MESH:D064146	MESH:D064146	Chemotherapy-Induced Febrile Neutropenia	CTD_diseases	8
OMIM:100050	OMIM:100050	AARSKOG SYNDROME, AUTOSOMAL DOMINANT	CTD_diseases	8
OMIM:141500	OMIM:141500	MIGRAINE, FAMILIAL HEMIPLEGIC, 1	CTD_diseases	8
OMIM:181430	OMIM:181430	SCAPULOPERONEAL MYOPATHY, MYH7-RELATED	CTD_diseases	8
OMIM:183840	OMIM:183840	SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 2	CTD_diseases	8
OMIM:202370	OMIM:202370	PEROXISOME BIOGENESIS DISORDER 2B	CTD_diseases	8
OMIM:253800	OMIM:253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4	CTD_diseases	8
OMIM:257270	OMIM:257270	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B	CTD_diseases	8
OMIM:275350	OMIM:275350	TRANSCOBALAMIN II DEFICIENCY	CTD_diseases	8
OMIM:277470	OMIM:277470	PONTOCEREBELLAR HYPOPLASIA, TYPE 2A	CTD_diseases	8
OMIM:300071	OMIM:300071	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A	CTD_diseases	8
OMIM:310500	OMIM:310500	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A	CTD_diseases	8
OMIM:400043	OMIM:400043	DEAFNESS, Y-LINKED 1	CTD_diseases	8
OMIM:600652	OMIM:600652	DEAFNESS, AUTOSOMAL DOMINANT 4A	CTD_diseases	8
OMIM:600791	OMIM:600791	DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT	CTD_diseases	8
OMIM:602092	OMIM:602092	DEAFNESS, AUTOSOMAL RECESSIVE 18A	CTD_diseases	8
OMIM:602481	OMIM:602481	MIGRAINE, FAMILIAL HEMIPLEGIC, 2	CTD_diseases	8
OMIM:603041	OMIM:603041	MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE)	CTD_diseases	8
OMIM:603902	OMIM:603902	BETA-THALASSEMIA, DOMINANT INCLUSION BODY TYPE	CTD_diseases	8
OMIM:604588	OMIM:604588	NEVER IN MITOSIS GENE A-RELATED KINASE 1	CTD_diseases	8
OMIM:605429	OMIM:605429	DEAFNESS, NONSYNDROMIC, MODIFIER 1	CTD_diseases	8
OMIM:606346	OMIM:606346	DEAFNESS, AUTOSOMAL DOMINANT 22;DFNA22 DEAFNESS, AUTOSOMAL DOMINANT 22, WITH HYPERTROPHIC CARDIOMYOP	CTD_diseases	8
OMIM:606711	OMIM:606711	SPECIFIC LANGUAGE IMPAIRMENT 1	CTD_diseases	8
OMIM:606712	OMIM:606712	SPECIFIC LANGUAGE IMPAIRMENT 2	CTD_diseases	8
OMIM:607134	OMIM:607134	SPECIFIC LANGUAGE IMPAIRMENT 3	CTD_diseases	8
OMIM:609006	OMIM:609006	DEAFNESS, AUTOSOMAL RECESSIVE 36, WITH OR WITHOUT VESTIBULAR INVOLVEMENT	CTD_diseases	8
OMIM:611022	OMIM:611022	DEAFNESS, AUTOSOMAL RECESSIVE 24	CTD_diseases	8
OMIM:612124	OMIM:612124	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12	CTD_diseases	8
OMIM:612389	OMIM:612389	PONTOCEREBELLAR HYPOPLASIA, TYPE 2B	CTD_diseases	8
OMIM:612390	OMIM:612390	PONTOCEREBELLAR HYPOPLASIA, TYPE 2C	CTD_diseases	8
OMIM:612431	OMIM:612431	DEAFNESS, AUTOSOMAL DOMINANT 27	CTD_diseases	8
OMIM:612433	OMIM:612433	DEAFNESS, AUTOSOMAL RECESSIVE 45	CTD_diseases	8
OMIM:612542	OMIM:612542	VITAMIN B12 PLASMA LEVEL QUANTITATIVE TRAIT LOCUS 1	CTD_diseases	8
OMIM:612551	OMIM:612551	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 4, SUSCEPTIBILITY TO	CTD_diseases	8
OMIM:613074	OMIM:613074	DEAFNESS, AUTOSOMAL DOMINANT 50	CTD_diseases	8
OMIM:613150	OMIM:613150	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2	CTD_diseases	8
OMIM:613153	OMIM:613153	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5	CTD_diseases	8
OMIM:613154	OMIM:613154	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6	CTD_diseases	8
OMIM:613216	OMIM:613216	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C	CTD_diseases	8
OMIM:613238	OMIM:613238	SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 3	CTD_diseases	8
OMIM:613285	OMIM:613285	DEAFNESS, AUTOSOMAL RECESSIVE 25	CTD_diseases	8
OMIM:613391	OMIM:613391	DEAFNESS, AUTOSOMAL RECESSIVE 84A	CTD_diseases	8
OMIM:613392	OMIM:613392	DEAFNESS, AUTOSOMAL RECESSIVE 85	CTD_diseases	8
OMIM:613453	OMIM:613453	DEAFNESS, AUTOSOMAL RECESSIVE 91	CTD_diseases	8
OMIM:613454	OMIM:613454	RETT SYNDROME, CONGENITAL VARIANT	CTD_diseases	8
OMIM:613558	OMIM:613558	DEAFNESS, AUTOSOMAL DOMINANT 51	CTD_diseases	8
OMIM:613610	OMIM:613610	CRANIOECTODERMAL DYSPLASIA 2	CTD_diseases	8
OMIM:613662	OMIM:613662	MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE)	CTD_diseases	8
OMIM:613685	OMIM:613685	DEAFNESS, AUTOSOMAL RECESSIVE 83	CTD_diseases	8
OMIM:613690	OMIM:613690	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7	CTD_diseases	8
OMIM:613707	OMIM:613707	LEOPARD SYNDROME 3	CTD_diseases	8
OMIM:613718	OMIM:613718	DEAFNESS, AUTOSOMAL RECESSIVE 74	CTD_diseases	8
OMIM:613916	OMIM:613916	DEAFNESS, AUTOSOMAL RECESSIVE 89	CTD_diseases	8
OMIM:614129	OMIM:614129	PERRAULT SYNDROME 3	CTD_diseases	8
OMIM:614211	OMIM:614211	DEAFNESS, AUTOSOMAL DOMINANT 33	CTD_diseases	8
MESH:D016537	MESH:D016537	Gangliosidosis, GM1	CTD_diseases	9
MESH:D018305	MESH:D018305	Ganglioneuroblastoma	CTD_diseases	9
MESH:D018886	MESH:D018886	Aphasia, Conduction	CTD_diseases	9
MESH:D020143	MESH:D020143	Gangliosidoses, GM2	CTD_diseases	9
MESH:D020225	MESH:D020225	Sagittal Sinus Thrombosis	CTD_diseases	9
MESH:D020226	MESH:D020226	Cavernous Sinus Thrombosis	CTD_diseases	9
MESH:D020227	MESH:D020227	Lateral Sinus Thrombosis	CTD_diseases	9
MESH:D020237	MESH:D020237	Alexia, Pure	CTD_diseases	9
MESH:D052517	MESH:D052517	Multiple Sulfatase Deficiency Disease	CTD_diseases	9
MESH:D052536	MESH:D052536	Niemann-Pick Disease, Type A	CTD_diseases	9
MESH:D052537	MESH:D052537	Niemann-Pick Disease, Type B	CTD_diseases	9
MESH:D052556	MESH:D052556	Niemann-Pick Disease, Type C	CTD_diseases	9
MESH:D056267	MESH:D056267	Pagetoid Reticulosis	CTD_diseases	9
OMIM:133700	OMIM:133700	EXOSTOSES, MULTIPLE, TYPE I	CTD_diseases	9
OMIM:133701	OMIM:133701	EXOSTOSES, MULTIPLE, TYPE II	CTD_diseases	9
OMIM:184450	OMIM:184450	STUTTERING, FAMILIAL PERSISTENT, 1	CTD_diseases	9
OMIM:252500	OMIM:252500	MUCOLIPIDOSIS II ALPHA/BETA	CTD_diseases	9
OMIM:252600	OMIM:252600	MUCOLIPIDOSIS III ALPHA/BETA	CTD_diseases	9
OMIM:601072	OMIM:601072	DEAFNESS, AUTOSOMAL RECESSIVE 8	CTD_diseases	9
OMIM:603040	OMIM:603040	TUMOR SUPPRESSOR GENE ON CHROMOSOME 11	CTD_diseases	9
OMIM:604391	OMIM:604391	ATAXIA-TELANGIECTASIA-LIKE DISORDER	CTD_diseases	9
OMIM:604547	OMIM:604547	VAN DER WOUDE SYNDROME 1, MODIFIER OF	CTD_diseases	9
OMIM:609261	OMIM:609261	STUTTERING, FAMILIAL PERSISTENT, 2	CTD_diseases	9
MESH:C531642	MESH:C531642	Familial vascular leukoencephalopathy	CTD_diseases	9
MESH:C531689	MESH:C531689	Acute cerebral Gaucher disease	CTD_diseases	9
MESH:C536421	MESH:C536421	Prinzmetal's variant angina	CTD_diseases	9
MESH:C536776	MESH:C536776	Syphilitic myelopathy (tabes dorsalis)	CTD_diseases	9
MESH:C536849	MESH:C536849	Familial neurocardiogenic syncope	CTD_diseases	9
MESH:C537675	MESH:C537675	Gaucher-like disease	CTD_diseases	9
MESH:C537791	MESH:C537791	Axial osteomalacia	CTD_diseases	9
MESH:C538200	MESH:C538200	Deafness, autosomal dominant nonsyndromic sensorineural 3	CTD_diseases	9
MESH:C538201	MESH:C538201	Deafness, autosomal dominant nonsyndromic sensorineural 53	CTD_diseases	9
MESH:C538202	MESH:C538202	Deafness, autosomal recessive 51	CTD_diseases	9
MESH:C538203	MESH:C538203	Deafness, autosomal recessive 55	CTD_diseases	9
MESH:C538205	MESH:C538205	Deafness, neurosensory, autosomal recessive 47	CTD_diseases	9
MESH:C538208	MESH:C538208	Dementia, familial British	CTD_diseases	9
MESH:C538265	MESH:C538265	Attenuated familial adenomatous polyposis	CTD_diseases	9
MESH:C538268	MESH:C538268	Auditory neuropathy	CTD_diseases	9
MESH:C538497	MESH:C538497	Irresistible sleepiness, cataplexy and onset of sleep in desynchronized phase	CTD_diseases	9
MESH:C538553	MESH:C538553	Familial subependymomas	CTD_diseases	9
MESH:C538664	MESH:C538664	PICA syndrome	CTD_diseases	9
MESH:C567305	MESH:C567305	Age-Related Hearing Impairment 1	CTD_diseases	9
MESH:C567787	MESH:C567787	Cerebral Amyloid Angiopathy, App-Related	CTD_diseases	9
MESH:C567834	MESH:C567834	Presbycusis 2	CTD_diseases	9
MESH:D001039	MESH:D001039	Aphasia, Broca	CTD_diseases	9
MESH:D001041	MESH:D001041	Aphasia, Wernicke	CTD_diseases	9
MESH:D002385	MESH:D002385	Cataplexy	CTD_diseases	9
MESH:D004401	MESH:D004401	Dysarthria	CTD_diseases	9
MESH:D012497	MESH:D012497	Sandhoff Disease	CTD_diseases	9
MESH:C562739	MESH:C562739	Cloacogenic Carcinoma	CTD_diseases	9
MESH:C563020	MESH:C563020	Anal Canal Carcinoma	CTD_diseases	9
MESH:C563167	MESH:C563167	Exostoses Of Heel	CTD_diseases	9
MESH:C563242	MESH:C563242	Intrinsic Factor Deficiency	CTD_diseases	9
MESH:C563365	MESH:C563365	Polyposis Syndrome, Hereditary Mixed, 1	CTD_diseases	9
MESH:C563534	MESH:C563534	Narcolepsy 1	CTD_diseases	9
MESH:C563756	MESH:C563756	Stuttering, Familial Persistent 2	CTD_diseases	9
MESH:C563790	MESH:C563790	Auditory Neuropathy, Autosomal Dominant, 1	CTD_diseases	9
MESH:C563924	MESH:C563924	Colorectal Adenomatous Polyposis, Autosomal Recessive	CTD_diseases	9
MESH:C563975	MESH:C563975	Exostoses, Multiple, Type III	CTD_diseases	9
MESH:C563997	MESH:C563997	Dysphasia, Familial Developmental	CTD_diseases	9
MESH:C564306	MESH:C564306	Gaucher Disease, Perinatal Lethal	CTD_diseases	9
MESH:C564366	MESH:C564366	Niemann-Pick Disease, Type F	CTD_diseases	9
MESH:C565380	MESH:C565380	Ataxia-Telangiectasia Variant V2	CTD_diseases	9
MESH:C565512	MESH:C565512	Mthfr Deficiency, Thermolabile Type	CTD_diseases	9
MESH:C565513	MESH:C565513	Homocystinuria, Pyridoxine-Responsive	CTD_diseases	9
MESH:C565553	MESH:C565553	Gaucher Disease, Type Iiic	CTD_diseases	9
MESH:C565554	MESH:C565554	Gaucher Disease, Type IIIa	CTD_diseases	9
MESH:C565555	MESH:C565555	Gaucher Disease, Type IIIb	CTD_diseases	9
MESH:C565556	MESH:C565556	Gaucher Disease, Norrbottnian Type	CTD_diseases	9
MESH:C565640	MESH:C565640	Deafness, Neural, Congenital Moderate	CTD_diseases	9
MESH:C565779	MESH:C565779	Ataxia Telangiectasia Like Disorder	CTD_diseases	9
MESH:C566435	MESH:C566435	Gaucher Disease, Atypical, Due To Saposin C Deficiency	CTD_diseases	9
MESH:C566451	MESH:C566451	Polyposis Syndrome, Hereditary Mixed, 2	CTD_diseases	9
MESH:C566865	MESH:C566865	Ataxia-Telangiectasia Variant	CTD_diseases	9
MESH:C567062	MESH:C567062	Fabry Disease, Cardiac Variant	CTD_diseases	9
MESH:C567097	MESH:C567097	Krabbe Disease, Atypical, due to Saposin A Deficiency	CTD_diseases	9
MESH:C567267	MESH:C567267	Niemann-Pick Disease, Intermediate, With Visceral Involvement And Rapid Progression	CTD_diseases	9
MESH:C567268	MESH:C567268	Niemann-Pick Disease, Intermediate, Protracted Neurovisceral	CTD_diseases	9
MESH:C562609	MESH:C562609	Metachromatic Leukodystrophy due to Saposin B Deficiency	CTD_diseases	10
MESH:C562688	MESH:C562688	Vitamin D Hydroxylation-Deficient Rickets, Type 1A	CTD_diseases	10
MESH:C562689	MESH:C562689	Rickets, Hereditary Vitamin D-Resistant	CTD_diseases	10
MESH:C562792	MESH:C562792	Hypophosphatemic Rickets, Autosomal Recessive, 1	CTD_diseases	10
MESH:C562794	MESH:C562794	Vitamin D-Dependent Rickets, Type 2A	CTD_diseases	10
MESH:C563400	MESH:C563400	Usher Syndrome, Type ID	CTD_diseases	10
MESH:C563587	MESH:C563587	Metachromatic Leukodystrophy, Adult-Onset, with Normal Arylsulfatase A	CTD_diseases	10
MESH:C564005	MESH:C564005	Vitamin D Hydroxylation-Deficient Rickets, Type 1B	CTD_diseases	10
MESH:C564449	MESH:C564449	Cerebral Sclerosis, Diffuse, Scholz Type	CTD_diseases	10
MESH:C564643	MESH:C564643	Usher Syndrome, Type IG	CTD_diseases	10
MESH:C564753	MESH:C564753	Usher Syndrome, Type IC	CTD_diseases	10
MESH:C564755	MESH:C564755	Usher Syndrome, Type Ib	CTD_diseases	10
MESH:C564941	MESH:C564941	Niemann-Pick Disease, Nova Scotian Type	CTD_diseases	10
MESH:C565403	MESH:C565403	Pseudoarylsulfatase A Deficiency	CTD_diseases	10
MESH:C565631	MESH:C565631	Wolfram-Like Syndrome, Autosomal Dominant	CTD_diseases	10
MESH:C566321	MESH:C566321	Pituitary Adenoma, Familial Isolated	CTD_diseases	10
MESH:C566577	MESH:C566577	Usher Syndrome, Type IE	CTD_diseases	10
MESH:C566586	MESH:C566586	Usher Syndrome, Type IF	CTD_diseases	10
MESH:C566778	MESH:C566778	Adenomatous Polyposis Coli, Attenuated	CTD_diseases	10
MESH:C566893	MESH:C566893	Gangliosidosis, Generalized GM1, Late-Infantile Type	CTD_diseases	10
MESH:C567125	MESH:C567125	Combined Saposin Deficiency	CTD_diseases	10
MESH:C567227	MESH:C567227	Usher Syndrome, Type IH	CTD_diseases	10
MESH:C535644	MESH:C535644	Intestinal polyposis, osteomas, sebaceous cysts	CTD_diseases	10
MESH:C536119	MESH:C536119	Niemann-Pick disease, type C2	CTD_diseases	10
MESH:C536485	MESH:C536485	Usher syndrome, type 1B	CTD_diseases	10
MESH:C536486	MESH:C536486	Usher syndrome, type 1C	CTD_diseases	10
MESH:C536487	MESH:C536487	Usher syndrome, type 1D	CTD_diseases	10
MESH:C536488	MESH:C536488	Usher syndrome, type 1E	CTD_diseases	10
MESH:C536489	MESH:C536489	Usher syndrome, type 1F	CTD_diseases	10
MESH:C536490	MESH:C536490	Usher syndrome, type 2A	CTD_diseases	10
MESH:C536491	MESH:C536491	Usher syndrome, type 2B	CTD_diseases	10
MESH:C536492	MESH:C536492	Usher syndrome, type 2C	CTD_diseases	10
MESH:C537230	MESH:C537230	Samson Gardner syndrome	CTD_diseases	10
MESH:C538436	MESH:C538436	Auditory perceptual impairment	CTD_diseases	10
MESH:D013661	MESH:D013661	Tay-Sachs Disease	CTD_diseases	10
MESH:D049290	MESH:D049290	Tay-Sachs Disease, AB Variant	CTD_diseases	10
OMIM:276902	OMIM:276902	USHER SYNDROME, TYPE IIIA	CTD_diseases	10
OMIM:611383	OMIM:611383	USHER SYNDROME, TYPE IID	CTD_diseases	10
OMIM:614869	OMIM:614869	USHER SYNDROME, TYPE IJ	CTD_diseases	10
MESH:C567409	MESH:C567409	Usher Syndrome, Type ID/F	CTD_diseases	10
MESH:C567571	MESH:C567571	Vitamin D-Dependent Rickets, Type 2B, With Normal Vitamin D Receptor	CTD_diseases	10
MESH:C567647	MESH:C567647	Hypophosphatemic Rickets, Autosomal Recessive, 2	CTD_diseases	10
MESH:D009347	MESH:D009347	Nelson Syndrome	CTD_diseases	10
MESH:C567601	MESH:C567601	Gm2-Gangliosidosis, Variant B1	CTD_diseases	11
MESH:C564782	MESH:C564782	Tay-Sachs Disease, Juvenile	CTD_diseases	11
MESH:C564783	MESH:C564783	Hexosaminidase A Deficiency, Adult Type	CTD_diseases	11
MESH:C564784	MESH:C564784	Gm2-Gangliosidosis, Adult Chronic Type	CTD_diseases	11
MESH:C564785	MESH:C564785	Tay-Sachs Disease, Variant B1	CTD_diseases	11
MESH:C564786	MESH:C564786	Tay-Sachs Disease, Pseudo-AB Variant	CTD_diseases	11
MESH:C564825	MESH:C564825	Sandhoff Disease, Adult Type	CTD_diseases	11
MESH:C564826	MESH:C564826	Sandhoff Disease, Juvenile Type	CTD_diseases	11
MESH:C564827	MESH:C564827	Sandhoff Disease, Infantile Type	CTD_diseases	11