ID	Name	Namespace	Distance
HP:0000006	Autosomal dominant inheritance	Mode_of_inheritance	2
HP:0000951	Abnormality of the skin	Phenotypic_abnormality	3
HP:0000952	Jaundice	Phenotypic_abnormality	6
HP:0000961	Cyanosis	Phenotypic_abnormality	4
HP:0001005	Dermatological manifestations of systemic disorders	Phenotypic_abnormality	5
HP:0001392	Abnormality of the liver	Phenotypic_abnormality	4
HP:0001396	Cholestasis	Phenotypic_abnormality	6
HP:0001438	Abnormality of the abdomen	Phenotypic_abnormality	2
HP:0001574	Abnormality of the integument	Phenotypic_abnormality	2
HP:0001743	Abnormality of the spleen	Phenotypic_abnormality	4
HP:0001871	Abnormality of  blood and blood-forming tissues	Phenotypic_abnormality	2
HP:0001877	Abnormality of erythrocytes	Phenotypic_abnormality	3
HP:0001878	Hemolytic anemia	Phenotypic_abnormality	6
HP:0001903	Anemia	Phenotypic_abnormality	4
HP:0001930	Nonspherocytic hemolytic anemia	Phenotypic_abnormality	7
HP:0001935	Microcytic anemia	Phenotypic_abnormality	6
HP:0001939	Abnormality of metabolism/homeostasis	Phenotypic_abnormality	2
HP:0001971	Hypersplenism	Phenotypic_abnormality	5
HP:0002012	Abnormality of the abdominal organs	Phenotypic_abnormality	3
HP:0002086	Abnormality of the respiratory system	Phenotypic_abnormality	2
HP:0002715	Abnormality of the immune system	Phenotypic_abnormality	2
HP:0002795	Functional respiratory abnormality	Phenotypic_abnormality	3
HP:0004297	Abnormality of the biliary system	Phenotypic_abnormality	5
HP:0010472	Abnormality of the heme biosynthetic pathway	Phenotypic_abnormality	3
HP:0010972	Anemia of inadequate production	Phenotypic_abnormality	5
HP:0011354	Generalized abnormality of skin	Phenotypic_abnormality	4
HP:0011895	Anemia due to reduced life span of red cells	Phenotypic_abnormality	5
HP:0011902	Abnormal hemoglobin	Phenotypic_abnormality	4
HP:0100763	Abnormality of the lymphatic system	Phenotypic_abnormality	3
HP:0000707	Abnormality of the nervous system	Phenotypic_abnormality	2
HP:0000478	Abnormality of the eye	Phenotypic_abnormality	2
HP:0000924	Abnormality of the skeletal system	Phenotypic_abnormality	2
HP:0000962	Hyperkeratosis	Phenotypic_abnormality	8
HP:0000972	Palmoplantar hyperkeratosis	Phenotypic_abnormality	6
HP:0000982	Palmoplantar keratoderma	Phenotypic_abnormality	9
HP:0001072	Thickened skin	Phenotypic_abnormality	6
HP:0001155	Abnormality of the hand	Phenotypic_abnormality	7
HP:0002813	Abnormality of limb bone morphology	Phenotypic_abnormality	5
HP:0002817	Abnormality of the upper limb	Phenotypic_abnormality	6
HP:0007556	Plantar hyperkeratosis	Phenotypic_abnormality	9
HP:0008064	Ichthyosis	Phenotypic_abnormality	8
HP:0010765	Palmar hyperkeratosis	Phenotypic_abnormality	9
HP:0011121	Abnormality of skin morphology	Phenotypic_abnormality	5
HP:0011356	Regional abnormality of skin	Phenotypic_abnormality	4
HP:0011368	Epidermal thickening	Phenotypic_abnormality	7
HP:0011842	Abnormality of skeletal morphology	Phenotypic_abnormality	3
HP:0011844	Abnormal appendicular skeleton morphology	Phenotypic_abnormality	4
HP:0100871	Abnormality of the palm	Phenotypic_abnormality	8
HP:0100872	Abnormality of the plantar skin of foot	Phenotypic_abnormality	5
HP:0000587	Abnormality of the optic nerve	Phenotypic_abnormality	7
HP:0000609	Optic nerve hypoplasia	Phenotypic_abnormality	6
HP:0001098	Abnormality of the fundus	Phenotypic_abnormality	6
HP:0002011	Morphological abnormality of the central nervous system	Phenotypic_abnormality	4
HP:0002977	Aplasia/Hypoplasia involving the central nervous system	Phenotypic_abnormality	5
HP:0004329	Abnormality of the posterior segment of the eye	Phenotypic_abnormality	5
HP:0008056	Aplasia/Hypoplasia affecting the eye	Phenotypic_abnormality	5
HP:0008057	Aplasia/Hypoplasia affecting the fundus	Phenotypic_abnormality	6
HP:0008058	Aplasia/Hypoplasia of the optic nerve	Phenotypic_abnormality	8
HP:0012372	Abnormal eye morphology	Phenotypic_abnormality	3
HP:0012374	Abnormality of the globe	Phenotypic_abnormality	4
HP:0012639	Abnormality of nervous system morphology	Phenotypic_abnormality	3
HP:0000152	Abnormality of head and neck	Phenotypic_abnormality	2
HP:0000153	Abnormality of the mouth	Phenotypic_abnormality	5
HP:0000234	Abnormality of the head	Phenotypic_abnormality	3
HP:0000271	Abnormality of the face	Phenotypic_abnormality	4
HP:0000288	Abnormality of the philtrum	Phenotypic_abnormality	6
HP:0001167	Abnormality of finger	Phenotypic_abnormality	7
HP:0002814	Abnormality of the lower limb	Phenotypic_abnormality	6
HP:0005918	Abnormality of phalanx of finger	Phenotypic_abnormality	9
HP:0005927	Aplasia/hypoplasia involving bones of the hand	Phenotypic_abnormality	8
HP:0006265	Aplasia/Hypoplasia of fingers	Phenotypic_abnormality	9
HP:0006493	Aplasia/hypoplasia involving bones of the lower limbs	Phenotypic_abnormality	7
HP:0006496	Aplasia/hypoplasia involving bones of the upper limbs	Phenotypic_abnormality	7
HP:0009115	Aplasia/hypoplasia involving the skeleton	Phenotypic_abnormality	4
HP:0009381	Short finger	Phenotypic_abnormality	8
HP:0009767	Aplasia/Hypoplasia of the phalanges of the hand	Phenotypic_abnormality	10
HP:0009803	Short phalanx of finger	Phenotypic_abnormality	11
HP:0009815	Aplasia/hypoplasia of the extremities	Phenotypic_abnormality	5
HP:0009832	Abnormality of the distal phalanx of finger	Phenotypic_abnormality	10
HP:0009835	Aplasia/Hypoplasia of the distal phalanges of the hand	Phenotypic_abnormality	11
HP:0009882	Short distal phalanx of finger	Phenotypic_abnormality	11
HP:0011297	Abnormality of digit	Phenotypic_abnormality	6
HP:0011927	Short digit	Phenotypic_abnormality	7
HP:0012638	Abnormality of nervous system physiology	Phenotypic_abnormality	3
HP:0001324	Muscle weakness	Phenotypic_abnormality	4
HP:0003011	Abnormality of the musculature	Phenotypic_abnormality	2
HP:0003560	Muscular dystrophy	Phenotypic_abnormality	4
HP:0003701	Proximal muscle weakness	Phenotypic_abnormality	5
HP:0011804	Abnormality of muscle physiology	Phenotypic_abnormality	3
HP:0011805	Abnormality of muscle morphology	Phenotypic_abnormality	3
HP:0000007	Autosomal recessive inheritance	Mode_of_inheritance	2
HP:0001249	Intellectual disability	Phenotypic_abnormality	5
HP:0001251	Ataxia	Phenotypic_abnormality	6
HP:0001252	Muscular hypotonia	Phenotypic_abnormality	5
HP:0001317	Abnormality of the cerebellum	Phenotypic_abnormality	8
HP:0001941	Acidosis	Phenotypic_abnormality	4
HP:0003128	Lactic acidosis	Phenotypic_abnormality	5
HP:0003808	Abnormal muscle tone	Phenotypic_abnormality	4
HP:0004360	Abnormality of acid-base homeostasis	Phenotypic_abnormality	3
HP:0007256	Abnormality of pyramidal motor function	Phenotypic_abnormality	5
HP:0011282	Abnormality of hindbrain morphology	Phenotypic_abnormality	6
HP:0011283	Abnormality of the metencephalon	Phenotypic_abnormality	7
HP:0011442	Abnormality of central motor function	Phenotypic_abnormality	4
HP:0011443	Abnormality of coordination	Phenotypic_abnormality	5
HP:0012443	Abnormality of brain morphology	Phenotypic_abnormality	5
HP:0012759	Neurodevelopmental abnormality	Phenotypic_abnormality	4
HP:0100547	Abnormality of forebrain morphology	Phenotypic_abnormality	6
HP:0000359	Abnormality of the inner ear	Phenotypic_abnormality	3
HP:0000598	Abnormality of the ear	Phenotypic_abnormality	2
HP:0001751	Vestibular dysfunction	Phenotypic_abnormality	5
HP:0002321	Vertigo	Phenotypic_abnormality	6
HP:0011389	Functional abnormality of the inner ear	Phenotypic_abnormality	4
HP:0000944	Abnormality of the metaphyses	Phenotypic_abnormality	5
HP:0005930	Abnormality of the epiphyses	Phenotypic_abnormality	5
HP:0011314	Abnormality of long bone morphology	Phenotypic_abnormality	4
HP:0000079	Abnormality of the urinary system	Phenotypic_abnormality	3
HP:0000119	Abnormality of the genitourinary system	Phenotypic_abnormality	2
HP:0001254	Lethargy	Phenotypic_abnormality	6
HP:0001397	Hepatic steatosis	Phenotypic_abnormality	5
HP:0001943	Hypoglycemia	Phenotypic_abnormality	6
HP:0001992	Organic aciduria	Phenotypic_abnormality	7
HP:0003110	Abnormality of urine homeostasis	Phenotypic_abnormality	3
HP:0003119	Abnormality of lipid metabolism	Phenotypic_abnormality	3
HP:0003215	Dicarboxylic aciduria	Phenotypic_abnormality	5
HP:0003234	Decreased plasma carnitine	Phenotypic_abnormality	6
HP:0003287	Abnormality of mitochondrial metabolism	Phenotypic_abnormality	5
HP:0003674	Onset	Onset_and_clinical_course	2
HP:0004354	Abnormality of carboxylic acid metabolism	Phenotypic_abnormality	3
HP:0004359	Abnormality of fatty-acid metabolism	Phenotypic_abnormality	4
HP:0004372	Reduced consciousness/confusion	Phenotypic_abnormality	5
HP:0010966	Abnormality of fatty-acid anion metabolism	Phenotypic_abnormality	5
HP:0010967	Abnormality of carnitine metabolism	Phenotypic_abnormality	6
HP:0010995	Abnormality of dicarboxylic acid metabolism	Phenotypic_abnormality	4
HP:0011007	Age of onset	Onset_and_clinical_course	3
HP:0011013	Abnormality of carbohydrate metabolism/homeostasis	Phenotypic_abnormality	3
HP:0011014	Abnormal glucose homeostasis	Phenotypic_abnormality	4
HP:0011015	Abnormality of blood glucose concentration	Phenotypic_abnormality	5
HP:0011017	Abnormality of cell physiology	Phenotypic_abnormality	3
HP:0011277	Abnormality of the urinary system physiology	Phenotypic_abnormality	4
HP:0011446	Abnormality of higher mental function	Phenotypic_abnormality	4
HP:0012072	Aciduria	Phenotypic_abnormality	6
HP:0012103	Abnormality of the mitochondrion	Phenotypic_abnormality	4
HP:0000284	Abnormality of the ocular region	Phenotypic_abnormality	5
HP:0000492	Abnormality of the eyelid	Phenotypic_abnormality	6
HP:0000499	Abnormality of the eyelashes	Phenotypic_abnormality	5
HP:0000534	Abnormality of the eyebrow	Phenotypic_abnormality	5
HP:0000606	Abnormality of the periorbital region	Phenotypic_abnormality	5
HP:0000750	Delayed speech and language development	Phenotypic_abnormality	6
HP:0000998	Hypertrichosis	Phenotypic_abnormality	6
HP:0001217	Clubbing	Phenotypic_abnormality	7
HP:0001595	Abnormality of the hair	Phenotypic_abnormality	4
HP:0001760	Abnormality of the foot	Phenotypic_abnormality	7
HP:0001780	Abnormality of toe	Phenotypic_abnormality	7
HP:0010161	Abnormality of the phalanges of the toes	Phenotypic_abnormality	9
HP:0011138	Abnormality of skin adnexa	Phenotypic_abnormality	3
HP:0011362	Abnormal hair quantity	Phenotypic_abnormality	5
HP:0012758	Neurodevelopmental delay	Phenotypic_abnormality	5
HP:0100760	Clubbing of toes	Phenotypic_abnormality	8
HP:0000269	Prominent occiput	Phenotypic_abnormality	9
HP:0000929	Abnormality of the skull	Phenotypic_abnormality	4
HP:0002648	Abnormality of calvarial morphology	Phenotypic_abnormality	7
HP:0002683	Abnormality of the calvaria	Phenotypic_abnormality	6
HP:0009121	Abnormal axial skeleton morphology	Phenotypic_abnormality	4
HP:0011217	Abnormal shape of the occiput	Phenotypic_abnormality	8
HP:0010876	Abnormality of circulating protein level	Phenotypic_abnormality	3
HP:0011021	Abnormality of circulating enzyme level	Phenotypic_abnormality	4
HP:0010978	Abnormality of immune system physiology	Phenotypic_abnormality	3
HP:0000002	Abnormality of body height	Phenotypic_abnormality	3
HP:0000240	Abnormality of skull size	Phenotypic_abnormality	6
HP:0001507	Growth abnormality	Phenotypic_abnormality	2
HP:0001510	Growth delay	Phenotypic_abnormality	3
HP:0004322	Short stature	Phenotypic_abnormality	4
HP:0002088	Abnormality of the lung	Phenotypic_abnormality	4
HP:0002093	Respiratory insufficiency	Phenotypic_abnormality	4
HP:0012252	Abnormal respiratory system morphology	Phenotypic_abnormality	3
HP:0001367	Abnormal joint morphology	Phenotypic_abnormality	4
HP:0001626	Abnormality of the cardiovascular system	Phenotypic_abnormality	2
HP:0001627	Abnormality of cardiac morphology	Phenotypic_abnormality	3
HP:0001697	Abnormality of the pericardium	Phenotypic_abnormality	5
HP:0001744	Splenomegaly	Phenotypic_abnormality	5
HP:0001881	Abnormality of leukocytes	Phenotypic_abnormality	3
HP:0001945	Fever	Phenotypic_abnormality	4
HP:0001954	Episodic fever	Phenotypic_abnormality	5
HP:0001974	Leukocytosis	Phenotypic_abnormality	6
HP:0002564	Malformation of the heart and great vessels	Phenotypic_abnormality	4
HP:0002585	Abnormality of the peritoneum	Phenotypic_abnormality	4
HP:0002597	Abnormality of the vasculature	Phenotypic_abnormality	3
HP:0002633	Vasculitis	Phenotypic_abnormality	4
HP:0002716	Lymphadenopathy	Phenotypic_abnormality	5
HP:0002733	Abnormality of the lymph nodes	Phenotypic_abnormality	4
HP:0002829	Arthralgia	Phenotypic_abnormality	5
HP:0002843	Abnormality of T cells	Phenotypic_abnormality	6
HP:0002846	Abnormality of B cells	Phenotypic_abnormality	6
HP:0003271	Visceromegaly	Phenotypic_abnormality	4
HP:0003496	Increased IgM level	Phenotypic_abnormality	10
HP:0003565	Elevated erythrocyte sedimentation rate	Phenotypic_abnormality	3
HP:0004332	Abnormality of lymphocytes	Phenotypic_abnormality	5
HP:0004370	Abnormality of temperature regulation	Phenotypic_abnormality	3
HP:0005368	Abnormality of humoral immunity	Phenotypic_abnormality	4
HP:0005372	Abnormality of B cell physiology	Phenotypic_abnormality	7
HP:0010701	Abnormal immunoglobulin level	Phenotypic_abnormality	5
HP:0010702	Hypergammaglobulinemia	Phenotypic_abnormality	9
HP:0010987	Abnormality of cellular immune system	Phenotypic_abnormality	3
HP:0011034	Amyloidosis	Phenotypic_abnormality	3
HP:0011840	Abnormality of T cell physiology	Phenotypic_abnormality	7
HP:0011893	Abnormal leukocyte count	Phenotypic_abnormality	5
HP:0000818	Abnormality of the endocrine system	Phenotypic_abnormality	2
HP:0000840	Adrenogenital syndrome	Phenotypic_abnormality	4
HP:0003623	Neonatal onset	Onset_and_clinical_course	4
HP:0008373	Puberty and gonadal disorders	Phenotypic_abnormality	3
HP:0000708	Behavioral abnormality	Phenotypic_abnormality	4
HP:0000736	Short attention span	Phenotypic_abnormality	5
HP:0000752	Hyperactivity	Phenotypic_abnormality	5
HP:0001428	Somatic mutation	Mode_of_inheritance	2
HP:0007018	Attention deficit hyperactivity disorder	Phenotypic_abnormality	6
HP:0100022	Abnormality of movement	Phenotypic_abnormality	4
HP:0002664	Neoplasm	Phenotypic_abnormality	2
HP:0004375	Neoplasm of the nervous system	Phenotypic_abnormality	4
HP:0009592	Astrocytoma	Phenotypic_abnormality	7
HP:0009733	Glioma	Phenotypic_abnormality	6
HP:0011793	Neoplasm by anatomical site	Phenotypic_abnormality	3
HP:0100006	Neoplasm of the central nervous system	Phenotypic_abnormality	5
HP:0100705	Abnormality of the glial cells	Phenotypic_abnormality	5
HP:0100707	Abnormality of the astrocytes	Phenotypic_abnormality	6
HP:0100836	Malignant neoplasm of the central nervous system	Phenotypic_abnormality	6
HP:0000032	Abnormality of male external genitalia	Phenotypic_abnormality	6
HP:0000078	Abnormality of the genital system	Phenotypic_abnormality	3
HP:0000479	Abnormality of the retina	Phenotypic_abnormality	7
HP:0000517	Abnormality of the lens	Phenotypic_abnormality	6
HP:0000518	Cataract	Phenotypic_abnormality	7
HP:0000811	Abnormal external genitalia	Phenotypic_abnormality	5
HP:0002118	Abnormality of the cerebral ventricles	Phenotypic_abnormality	6
HP:0002119	Ventriculomegaly	Phenotypic_abnormality	7
HP:0004328	Abnormality of the anterior segment of the eye	Phenotypic_abnormality	5
HP:0007703	Abnormal retinal pigmentation	Phenotypic_abnormality	9
HP:0008051	Abnormality of the retinal pigment epithelium	Phenotypic_abnormality	8
HP:0010442	Polydactyly	Phenotypic_abnormality	7
HP:0010461	Abnormality of the male genitalia	Phenotypic_abnormality	5
HP:0012243	Abnormal genital system morphology	Phenotypic_abnormality	4
HP:0100259	Postaxial polydactyly	Phenotypic_abnormality	8
HP:0000008	Abnormality of female internal genitalia	Phenotypic_abnormality	6
HP:0000140	Abnormality of the menstrual cycle	Phenotypic_abnormality	4
HP:0000141	Amenorrhea	Phenotypic_abnormality	8
HP:0000786	Primary amenorrhea	Phenotypic_abnormality	9
HP:0000812	Abnormal internal genitalia	Phenotypic_abnormality	5
HP:0010460	Abnormality of the female genitalia	Phenotypic_abnormality	5
HP:0001250	Seizures	Phenotypic_abnormality	4
HP:0001263	Global developmental delay	Phenotypic_abnormality	6
HP:0002151	Increased serum lactate	Phenotypic_abnormality	5
HP:0000003	Multicystic kidney dysplasia	Phenotypic_abnormality	8
HP:0000035	Abnormality of the testis	Phenotypic_abnormality	7
HP:0000036	Abnormality of the penis	Phenotypic_abnormality	7
HP:0000050	Hypoplastic male external genitalia	Phenotypic_abnormality	7
HP:0000054	Micropenis	Phenotypic_abnormality	9
HP:0000077	Abnormality of the kidney	Phenotypic_abnormality	5
HP:0000080	Abnormality of genital physiology	Phenotypic_abnormality	4
HP:0000100	Nephrotic syndrome	Phenotypic_abnormality	7
HP:0000107	Renal cyst	Phenotypic_abnormality	7
HP:0000135	Hypogonadism	Phenotypic_abnormality	4
HP:0000137	Abnormality of the ovary	Phenotypic_abnormality	7
HP:0000138	Ovarian cysts	Phenotypic_abnormality	8
HP:0000142	Abnormality of the vagina	Phenotypic_abnormality	7
HP:0000147	Polycystic ovaries	Phenotypic_abnormality	9
HP:0000148	Vaginal atresia	Phenotypic_abnormality	6
HP:0000163	Abnormality of the oral cavity	Phenotypic_abnormality	6
HP:0000164	Abnormality of the teeth	Phenotypic_abnormality	7
HP:0000366	Abnormality of the nose	Phenotypic_abnormality	5
HP:0000422	Abnormality of the nasal bridge	Phenotypic_abnormality	6
HP:0000426	Prominent nasal bridge	Phenotypic_abnormality	7
HP:0000464	Abnormality of the neck	Phenotypic_abnormality	3
HP:0000470	Short neck	Phenotypic_abnormality	4
HP:0000481	Abnormality of the cornea	Phenotypic_abnormality	6
HP:0000483	Astigmatism	Phenotypic_abnormality	5
HP:0000486	Strabismus	Phenotypic_abnormality	6
HP:0000494	Downslanted palpebral fissures	Phenotypic_abnormality	9
HP:0000496	Abnormality of eye movement	Phenotypic_abnormality	4
HP:0000510	Retinitis pigmentosa	Phenotypic_abnormality	10
HP:0000512	Abnormal electroretinogram	Phenotypic_abnormality	8
HP:0000539	Abnormality of refraction	Phenotypic_abnormality	4
HP:0000549	Abnormal conjugate eye movement	Phenotypic_abnormality	5
HP:0000556	Retinal dystrophy	Phenotypic_abnormality	8
HP:0000668	Hypodontia	Phenotypic_abnormality	10
HP:0000678	Dental crowding	Phenotypic_abnormality	9
HP:0000692	Misalignment of teeth	Phenotypic_abnormality	8
HP:0000873	Diabetes insipidus	Phenotypic_abnormality	3
HP:0000925	Abnormality of the vertebral column	Phenotypic_abnormality	5
HP:0001007	Hirsutism	Phenotypic_abnormality	6
HP:0001080	Biliary tract abnormality	Phenotypic_abnormality	6
HP:0001159	Syndactyly	Phenotypic_abnormality	7
HP:0001161	Hand polydactyly	Phenotypic_abnormality	8
HP:0001162	Postaxial hand polydactyly	Phenotypic_abnormality	9
HP:0001288	Gait disturbance	Phenotypic_abnormality	5
HP:0001328	Specific learning disability	Phenotypic_abnormality	5
HP:0001395	Hepatic fibrosis	Phenotypic_abnormality	5
HP:0001399	Hepatic failure	Phenotypic_abnormality	6
HP:0001410	Decreased liver function	Phenotypic_abnormality	5
HP:0001711	Abnormality of the left ventricle	Phenotypic_abnormality	6
HP:0001712	Left ventricular hypertrophy	Phenotypic_abnormality	7
HP:0001713	Abnormality of cardiac ventricle	Phenotypic_abnormality	5
HP:0001714	Ventricular hypertrophy	Phenotypic_abnormality	6
HP:0001769	Broad foot	Phenotypic_abnormality	8
HP:0001772	Talipes equinovalgus	Phenotypic_abnormality	10
HP:0001773	Short foot	Phenotypic_abnormality	9
HP:0001827	Genital tract atresia	Phenotypic_abnormality	5
HP:0001829	Foot polydactyly	Phenotypic_abnormality	8
HP:0001883	Talipes	Phenotypic_abnormality	9
HP:0002099	Asthma	Phenotypic_abnormality	5
HP:0002141	Gait imbalance	Phenotypic_abnormality	6
HP:0002242	Abnormality of the intestine	Phenotypic_abnormality	6
HP:0002270	Abnormality of the autonomic nervous system	Phenotypic_abnormality	4
HP:0002311	Incoordination	Phenotypic_abnormality	6
HP:0002370	Poor coordination	Phenotypic_abnormality	7
HP:0003241	External genital hypoplasia	Phenotypic_abnormality	6
HP:0003319	Abnormality of the cervical spine	Phenotypic_abnormality	6
HP:0004207	Abnormality of the 5th finger	Phenotypic_abnormality	9
HP:0004275	Duplication of hand bones	Phenotypic_abnormality	8
HP:0004362	Abnormality of the enteric ganglia	Phenotypic_abnormality	6
HP:0005656	Positional foot deformity	Phenotypic_abnormality	8
HP:0006101	Finger syndactyly	Phenotypic_abnormality	8
HP:0006483	Abnormal number of teeth	Phenotypic_abnormality	8
HP:0006494	Aplasia/Hypoplasia involving bones of the feet	Phenotypic_abnormality	8
HP:0007707	Congenital primary aphakia	Phenotypic_abnormality	8
HP:0008050	Abnormality of the palpebral fissures	Phenotypic_abnormality	7
HP:0008062	Aplasia/Hypoplasia affecting the anterior segment of the eye	Phenotypic_abnormality	6
HP:0008063	Aplasia/Hypoplasia of the lens	Phenotypic_abnormality	7
HP:0008734	Decreased testicular size	Phenotypic_abnormality	8
HP:0008736	Hypoplasia of penis	Phenotypic_abnormality	8
HP:0009136	Duplication involving bones of the feet	Phenotypic_abnormality	8
HP:0009142	Duplication of bones involving the upper extremities	Phenotypic_abnormality	7
HP:0009804	Reduced number of teeth	Phenotypic_abnormality	9
HP:0009806	Nephrogenic diabetes insipidus	Phenotypic_abnormality	4
HP:0009997	Duplication of phalanx of hand	Phenotypic_abnormality	9
HP:0010468	Aplasia/Hypoplasia of the testes	Phenotypic_abnormality	8
HP:0010747	Medial flaring of the eyebrow	Phenotypic_abnormality	7
HP:0010935	Abnormality of the upper urinary tract	Phenotypic_abnormality	4
HP:0011024	Abnormality of the gastrointestinal tract	Phenotypic_abnormality	4
HP:0012210	Abnormal renal morphology	Phenotypic_abnormality	6
HP:0012211	Abnormal renal physiology	Phenotypic_abnormality	5
HP:0012331	Abnormal autonomic nervous system morphology	Phenotypic_abnormality	5
HP:0012373	Abnormal eye physiology	Phenotypic_abnormality	3
HP:0012718	Morphological abnormality of the gastrointestinal tract	Phenotypic_abnormality	5
HP:0100326	Immunologic hypersensitivity	Phenotypic_abnormality	4
HP:0100691	Abnormality of the curvature of the cornea	Phenotypic_abnormality	7
HP:0200006	Slanting of the palpebral fissure	Phenotypic_abnormality	8
HP:0001831	Short toe	Phenotypic_abnormality	8
HP:0001991	Aplasia/Hypoplasia of toe	Phenotypic_abnormality	9
HP:0002410	Aqueductal stenosis	Phenotypic_abnormality	7
HP:0002676	Cloverleaf skull	Phenotypic_abnormality	8
HP:0003795	Short middle phalanx of toe	Phenotypic_abnormality	11
HP:0002754	Osteomyelitis	Phenotypic_abnormality	4
HP:0005661	Salmonella osteomyelitis	Phenotypic_abnormality	5
HP:0011843	Abnormality of skeletal physiology	Phenotypic_abnormality	3
HP:0000172	Abnormality of the uvula	Phenotypic_abnormality	9
HP:0000174	Abnormality of the palate	Phenotypic_abnormality	7
HP:0000175	Cleft palate	Phenotypic_abnormality	7
HP:0000193	Bifid uvula	Phenotypic_abnormality	10
HP:0000202	Oral cleft	Phenotypic_abnormality	6
HP:0001454	Abnormality of the upper arm	Phenotypic_abnormality	7
HP:0003063	Abnormality of the humerus	Phenotypic_abnormality	8
HP:0004050	Absent hand	Phenotypic_abnormality	9
HP:0100736	Abnormality of the soft palate	Phenotypic_abnormality	8
HP:0100737	Abnormality of the hard palate	Phenotypic_abnormality	8
HP:0010920	Zonular cataract	Phenotypic_abnormality	8
HP:0001265	Hyporeflexia	Phenotypic_abnormality	5
HP:0001284	Areflexia	Phenotypic_abnormality	5
HP:0001315	Reduced tendon reflexes	Phenotypic_abnormality	4
HP:0002460	Distal muscle weakness	Phenotypic_abnormality	5
HP:0002522	Areflexia of lower limbs	Phenotypic_abnormality	6
HP:0002600	Hyporeflexia of lower limbs	Phenotypic_abnormality	6
HP:0003457	EMG abnormality	Phenotypic_abnormality	4
HP:0003677	Slow progression	Onset_and_clinical_course	3
HP:0003679	Pace of progression	Onset_and_clinical_course	2
HP:0001646	Abnormality of the aortic valve	Phenotypic_abnormality	6
HP:0001654	Abnormality of the heart valves	Phenotypic_abnormality	5
HP:0000546	Retinal degeneration	Phenotypic_abnormality	8
HP:0000655	Vitreoretinal degeneration	Phenotypic_abnormality	9
HP:0002823	Abnormality of the femur	Phenotypic_abnormality	7
HP:0006499	Abnormality of femoral epiphyses	Phenotypic_abnormality	8
HP:0006500	Abnormality involving the epiphyses of the lower limbs	Phenotypic_abnormality	7
HP:0006505	Abnormality involving the epiphyses of the limbs	Phenotypic_abnormality	6
HP:0001287	Meningitis	Phenotypic_abnormality	6
HP:0001581	Recurrent skin infections	Phenotypic_abnormality	7
HP:0002718	Recurrent bacterial infections	Phenotypic_abnormality	5
HP:0002719	Recurrent infections	Phenotypic_abnormality	4
HP:0002722	Recurrent abscess formation	Phenotypic_abnormality	5
HP:0003549	Abnormality of connective tissue	Phenotypic_abnormality	2
HP:0005406	Recurrent bacterial skin infections	Phenotypic_abnormality	6
HP:0006536	Obstructive lung disease	Phenotypic_abnormality	5
HP:0011122	Abnormality of skin physiology	Phenotypic_abnormality	5
HP:0011123	Inflammatory abnormality of the skin	Phenotypic_abnormality	6
HP:0011450	CNS infection	Phenotypic_abnormality	5
HP:0100523	Liver abscess	Phenotypic_abnormality	5
HP:0100658	Cellulitis	Phenotypic_abnormality	3
HP:0002059	Cerebral atrophy	Phenotypic_abnormality	9
HP:0002060	Abnormality of the cerebrum	Phenotypic_abnormality	7
HP:0002120	Cerebral cortical atrophy	Phenotypic_abnormality	10
HP:0007367	Atrophy/Degeneration affecting the central nervous system	Phenotypic_abnormality	5
HP:0007369	Atrophy/Degeneration affecting the cerebrum	Phenotypic_abnormality	6
HP:0012444	Brain atrophy	Phenotypic_abnormality	6
HP:0000421	Epistaxis	Phenotypic_abnormality	4
HP:0001892	Abnormal bleeding	Phenotypic_abnormality	3
HP:0001928	Abnormality of coagulation	Phenotypic_abnormality	3
HP:0001977	Abnormal thrombosis	Phenotypic_abnormality	3
HP:0002625	Deep venous thrombosis	Phenotypic_abnormality	5
HP:0003645	Prolonged partial thromboplastin time	Phenotypic_abnormality	4
HP:0004936	Venous thrombosis	Phenotypic_abnormality	4
HP:0005261	Joint hemorrhage	Phenotypic_abnormality	5
HP:0011025	Abnormality of cardiovascular system physiology	Phenotypic_abnormality	3
HP:0011028	Abnormality of blood circulation	Phenotypic_abnormality	4
HP:0011029	Internal hemorrhage	Phenotypic_abnormality	4
HP:0002037	Inflammation of the large intestine	Phenotypic_abnormality	7
HP:0004386	Gastrointestinal inflammation	Phenotypic_abnormality	6
HP:0012719	Functional abnormality of the gastrointestinal tract	Phenotypic_abnormality	5
HP:0001376	Limitation of joint mobility	Phenotypic_abnormality	6
HP:0002644	Abnormality of pelvic girdle bone morphology	Phenotypic_abnormality	5
HP:0003366	Abnormality of the femoral neck and head region	Phenotypic_abnormality	8
HP:0003367	Abnormality of the femoral neck	Phenotypic_abnormality	9
HP:0011729	Abnormality of joint mobility	Phenotypic_abnormality	5
HP:0001651	Dextrocardia	Phenotypic_abnormality	6
HP:0001696	Situs inversus totalis	Phenotypic_abnormality	5
HP:0003363	Abdominal situs inversus	Phenotypic_abnormality	4
HP:0004307	Abnormal anatomic location of the heart	Phenotypic_abnormality	5
HP:0011534	Abnormal spatial orientation of the cardiac segments	Phenotypic_abnormality	5
HP:0011620	Abnormality of abdominal situs	Phenotypic_abnormality	3
HP:0000159	Abnormality of the lip	Phenotypic_abnormality	6
HP:0000178	Abnormality of lower lip	Phenotypic_abnormality	7
HP:0000759	Abnormality of the peripheral nervous system	Phenotypic_abnormality	4
HP:0000763	Sensory neuropathy	Phenotypic_abnormality	6
HP:0000969	Edema	Phenotypic_abnormality	4
HP:0001633	Abnormality of the mitral valve	Phenotypic_abnormality	6
HP:0001637	Abnormality of the myocardium	Phenotypic_abnormality	5
HP:0002376	Developmental regression	Phenotypic_abnormality	5
HP:0006705	Abnormality of the atrioventricular valves	Phenotypic_abnormality	5
HP:0009830	Peripheral neuropathy	Phenotypic_abnormality	5
HP:0010549	Paralysis due to lesions of the principle motor tracts	Phenotypic_abnormality	6
HP:0011004	Abnormality of the systemic arterial tree	Phenotypic_abnormality	4
HP:0011032	Abnormality of fluid regulation	Phenotypic_abnormality	3
HP:0000504	Abnormality of vision	Phenotypic_abnormality	4
HP:0000551	Abnormality of color vision	Phenotypic_abnormality	5
HP:0000613	Photophobia	Phenotypic_abnormality	5
HP:0007803	Monochromacy	Phenotypic_abnormality	6
HP:0004337	Abnormality of amino acid metabolism	Phenotypic_abnormality	4
HP:0000364	Hearing abnormality	Phenotypic_abnormality	3
HP:0000365	Hearing impairment	Phenotypic_abnormality	4
HP:0000502	Abnormality of the conjunctiva	Phenotypic_abnormality	4
HP:0000943	Dysostosis multiplex	Phenotypic_abnormality	4
HP:0001014	Angiokeratoma	Phenotypic_abnormality	6
HP:0001640	Cardiomegaly	Phenotypic_abnormality	4
HP:0003541	Urinary glycosaminoglycan excretion	Phenotypic_abnormality	6
HP:0004298	Abnormality of the abdominal wall	Phenotypic_abnormality	3
HP:0004371	Abnormality of glycosaminoglycan metabolism	Phenotypic_abnormality	5
HP:0008047	Abnormality of the vasculature of the eye	Phenotypic_abnormality	4
HP:0008054	Abnormality of the vasculature of the conjunctiva	Phenotypic_abnormality	5
HP:0010318	Aplasia/Hypoplasia of the abdominal wall musculature	Phenotypic_abnormality	5
HP:0010991	Abnormality of the abdominal musculature	Phenotypic_abnormality	4
HP:0011012	Abnormality of polysaccharide metabolism	Phenotypic_abnormality	4
HP:0011276	Vascular skin abnormality	Phenotypic_abnormality	5
HP:0011947	Respiratory tract infection	Phenotypic_abnormality	5
HP:0002171	Gliosis	Phenotypic_abnormality	6
HP:0002490	Increased CSF lactate	Phenotypic_abnormality	6
HP:0002605	Hepatic necrosis	Phenotypic_abnormality	5
HP:0002921	Abnormality of the cerebrospinal fluid	Phenotypic_abnormality	5
HP:0007305	CNS demyelination	Phenotypic_abnormality	6
HP:0011400	Abnormal CNS myelination	Phenotypic_abnormality	5
HP:0012447	Abnormal myelination	Phenotypic_abnormality	4
HP:0000864	Abnormality of the hypothalamus-pituitary axis	Phenotypic_abnormality	3
HP:0010514	Hyperpituitarism	Phenotypic_abnormality	6
HP:0011747	Abnormality of the anterior pituitary	Phenotypic_abnormality	5
HP:0012503	Abnormality of the pituitary gland	Phenotypic_abnormality	4
HP:0001987	Hyperammonemia	Phenotypic_abnormality	5
HP:0002157	Azotemia	Phenotypic_abnormality	4
HP:0004364	Abnormality of nitrogen compound homeostasis	Phenotypic_abnormality	3
HP:0001259	Coma	Phenotypic_abnormality	6
HP:0002013	Vomiting	Phenotypic_abnormality	5
HP:0002017	Nausea and vomiting	Phenotypic_abnormality	4
HP:0011458	Abdominal symptom	Phenotypic_abnormality	3
HP:0000252	Microcephaly	Phenotypic_abnormality	7
HP:0001273	Abnormality of the corpus callosum	Phenotypic_abnormality	10
HP:0001274	Agenesis of corpus callosum	Phenotypic_abnormality	12
HP:0002126	Polymicrogyria	Phenotypic_abnormality	10
HP:0002269	Abnormality of neuronal migration	Phenotypic_abnormality	5
HP:0002363	Abnormality of brainstem morphology	Phenotypic_abnormality	6
HP:0002500	Abnormality of the cerebral white matter	Phenotypic_abnormality	9
HP:0002536	Abnormal cortical gyration	Phenotypic_abnormality	6
HP:0002538	Abnormality of the cerebral cortex	Phenotypic_abnormality	8
HP:0007362	Aplasia/Hypoplasia of the brainstem	Phenotypic_abnormality	6
HP:0007364	Aplasia/Hypoplasia of the cerebrum	Phenotypic_abnormality	6
HP:0007370	Aplasia/Hypoplasia of the corpus callosum	Phenotypic_abnormality	9
HP:0010993	Abnormality of the cerebral subcortex	Phenotypic_abnormality	8
HP:0001276	Hypertonia	Phenotypic_abnormality	6
HP:0100851	Abnormal emotion/affect behavior	Phenotypic_abnormality	5
HP:0008872	Feeding difficulties in infancy	Phenotypic_abnormality	5
HP:0011968	Feeding difficulties	Phenotypic_abnormality	4
HP:0000235	Abnormality of the fontanelles and cranial sutures	Phenotypic_abnormality	7
HP:0000290	Abnormality of the forehead	Phenotypic_abnormality	5
HP:0005487	Prominent metopic ridge	Phenotypic_abnormality	10
HP:0005556	Abnormality of the metopic suture	Phenotypic_abnormality	6
HP:0009145	Abnormality of cerebral artery	Phenotypic_abnormality	5
HP:0011329	Abnormality of cranial sutures	Phenotypic_abnormality	8
HP:0100659	Abnormality of the cerebral vasculature	Phenotypic_abnormality	4
HP:0002910	Elevated hepatic transaminases	Phenotypic_abnormality	5
HP:0000083	Renal insufficiency	Phenotypic_abnormality	7
HP:0000098	Tall stature	Phenotypic_abnormality	4
HP:0000473	Torticollis	Phenotypic_abnormality	5
HP:0001332	Dystonia	Phenotypic_abnormality	5
HP:0001371	Flexion contracture	Phenotypic_abnormality	3
HP:0001382	Joint hypermobility	Phenotypic_abnormality	6
HP:0001533	Slender build	Phenotypic_abnormality	5
HP:0001872	Abnormality of thrombocytes	Phenotypic_abnormality	3
HP:0002791	Hypoventilation	Phenotypic_abnormality	5
HP:0002793	Abnormal pattern of respiration	Phenotypic_abnormality	4
HP:0002877	Nocturnal hypoventilation	Phenotypic_abnormality	6
HP:0003010	Prolonged bleeding time	Phenotypic_abnormality	4
HP:0003028	Abnormality of the ankles	Phenotypic_abnormality	8
HP:0003121	Limb joint contracture	Phenotypic_abnormality	7
HP:0003236	Elevated serum creatine phosphokinase	Phenotypic_abnormality	5
HP:0003306	Spinal rigidity	Phenotypic_abnormality	6
HP:0003325	Limb-girdle muscle weakness	Phenotypic_abnormality	5
HP:0003557	Increased variability in muscle fiber diameter	Phenotypic_abnormality	6
HP:0003713	Muscle fiber necrosis	Phenotypic_abnormality	5
HP:0003803	Type 1 muscle fiber predominance	Phenotypic_abnormality	5
HP:0004303	Abnormality of muscle fibers	Phenotypic_abnormality	4
HP:0004323	Abnormality of body weight	Phenotypic_abnormality	3
HP:0004325	Decreased body weight	Phenotypic_abnormality	4
HP:0004373	Focal dystonia	Phenotypic_abnormality	6
HP:0005072	Hyperextensibility at wrists	Phenotypic_abnormality	7
HP:0005750	Contractures of the joints of the lower limbs	Phenotypic_abnormality	8
HP:0005988	Congenital muscular torticollis	Phenotypic_abnormality	5
HP:0006094	Finger joint hypermobility	Phenotypic_abnormality	9
HP:0006149	Increased laxity of fingers	Phenotypic_abnormality	10
HP:0006256	Abnormality of hand joint mobility	Phenotypic_abnormality	8
HP:0006460	Increased laxity of ankles	Phenotypic_abnormality	9
HP:0006466	Ankle contracture	Phenotypic_abnormality	9
HP:0008180	Mildly elevated creatine phosphokinase	Phenotypic_abnormality	6
HP:0011006	Abnormality of the musculature of the neck	Phenotypic_abnormality	3
HP:0012084	Abnormality of skeletal muscle fiber size	Phenotypic_abnormality	5
HP:0012179	Craniofacial dystonia	Phenotypic_abnormality	7
HP:0100491	Abnormality of the joints of the lower limbs	Phenotypic_abnormality	5
HP:0000322	Short philtrum	Phenotypic_abnormality	7
HP:0000737	Irritability	Phenotypic_abnormality	6
HP:0000482	Microcornea	Phenotypic_abnormality	8
HP:0001120	Abnormality of corneal size	Phenotypic_abnormality	7
HP:0001388	Joint laxity	Phenotypic_abnormality	7
HP:0000989	Pruritus	Phenotypic_abnormality	6
HP:0000991	Xanthomatosis	Phenotypic_abnormality	5
HP:0002024	Malabsorption	Phenotypic_abnormality	7
HP:0002244	Abnormality of the small intestine	Phenotypic_abnormality	7
HP:0002570	Steatorrhea	Phenotypic_abnormality	9
HP:0002621	Atherosclerosis	Phenotypic_abnormality	5
HP:0002630	Fat malabsorption	Phenotypic_abnormality	8
HP:0002634	Arteriosclerosis	Phenotypic_abnormality	4
HP:0003107	Abnormality of cholesterol metabolism	Phenotypic_abnormality	4
HP:0006704	Abnormality of the coronary arteries	Phenotypic_abnormality	5
HP:0011355	Localized skin lesion	Phenotypic_abnormality	4
HP:0000280	Coarse facial features	Phenotypic_abnormality	6
HP:0000765	Abnormality of the thorax	Phenotypic_abnormality	5
HP:0000772	Abnormality of the ribs	Phenotypic_abnormality	7
HP:0001547	Abnormality of the rib cage	Phenotypic_abnormality	6
HP:0001999	Abnormal facial shape	Phenotypic_abnormality	5
HP:0002143	Abnormality of the spinal cord	Phenotypic_abnormality	5
HP:0002196	Myelopathy	Phenotypic_abnormality	6
HP:0003312	Abnormal form of the vertebral bodies	Phenotypic_abnormality	7
HP:0003468	Abnormality of the vertebrae	Phenotypic_abnormality	6
HP:0002861	Melanoma	Phenotypic_abnormality	4
HP:0011792	Neoplasm by histology	Phenotypic_abnormality	3
HP:0000130	Abnormality of the uterus	Phenotypic_abnormality	7
HP:0002076	Migraine	Phenotypic_abnormality	5
HP:0002239	Gastrointestinal hemorrhage	Phenotypic_abnormality	6
HP:0002250	Abnormality of the large intestine	Phenotypic_abnormality	7
HP:0002315	Headache	Phenotypic_abnormality	4
HP:0007378	Neoplasm of the gastrointestinal tract	Phenotypic_abnormality	4
HP:0007379	Neoplasm of the genitourinary tract	Phenotypic_abnormality	3
HP:0010784	Uterine neoplasm	Phenotypic_abnormality	6
HP:0010786	Urinary tract neoplasm	Phenotypic_abnormality	5
HP:0010787	Genital neoplasm	Phenotypic_abnormality	4
HP:0100242	Sarcoma	Phenotypic_abnormality	4
HP:0100834	Neoplasm of the large intestine	Phenotypic_abnormality	6
HP:0006519	Alveolar cell carcinoma	Phenotypic_abnormality	7
HP:0100526	Neoplasm of the lungs	Phenotypic_abnormality	5
HP:0100552	Neoplasm of the tracheobronchial system	Phenotypic_abnormality	6
HP:0100606	Neoplasm of the respiratory system	Phenotypic_abnormality	4
HP:0001695	Cardiac arrest	Phenotypic_abnormality	5
HP:0011675	Arrhythmia	Phenotypic_abnormality	4
HP:0002808	Kyphosis	Phenotypic_abnormality	7
HP:0003330	Abnormal bone structure	Phenotypic_abnormality	4
HP:0004348	Abnormality of bone mineral density	Phenotypic_abnormality	5
HP:0004349	Reduced bone mineral density	Phenotypic_abnormality	6
HP:0010674	Abnormality of the curvature of the vertebral column	Phenotypic_abnormality	6
HP:0002659	Increased susceptibility to fractures	Phenotypic_abnormality	4
HP:0002757	Recurrent fractures	Phenotypic_abnormality	5
HP:0003111	Abnormality of ion homeostasis	Phenotypic_abnormality	3
HP:0004363	Abnormality of calcium homeostasis	Phenotypic_abnormality	6
HP:0010927	Abnormality of divalent inorganic cation homeostasis	Phenotypic_abnormality	5
HP:0010929	Abnormality of cation homeostasis	Phenotypic_abnormality	4
HP:0100026	Arteriovenous malformation	Phenotypic_abnormality	4
HP:0000819	Diabetes mellitus	Phenotypic_abnormality	3
HP:0001513	Obesity	Phenotypic_abnormality	5
HP:0003117	Abnormality of circulating hormone level	Phenotypic_abnormality	3
HP:0004324	Increased body weight	Phenotypic_abnormality	4
HP:0001844	Abnormality of the hallux	Phenotypic_abnormality	9
HP:0000790	Hematuria	Phenotypic_abnormality	7
HP:0001142	Lenticonus	Phenotypic_abnormality	8
HP:0011501	Anterior lenticonus	Phenotypic_abnormality	9
HP:0011526	Abnormality of lens shape	Phenotypic_abnormality	7
HP:0012614	Abnormal urine cytology	Phenotypic_abnormality	6
HP:0001166	Arachnodactyly	Phenotypic_abnormality	10
HP:0001238	Slender finger	Phenotypic_abnormality	9
HP:0001679	Abnormality of the aorta	Phenotypic_abnormality	5
HP:0001724	Aortic dilatation	Phenotypic_abnormality	6
HP:0005111	Dilatation of the ascending aorta	Phenotypic_abnormality	7
HP:0100807	Long fingers	Phenotypic_abnormality	9
HP:0000014	Abnormality of the bladder	Phenotypic_abnormality	5
HP:0000593	Abnormality of the anterior chamber	Phenotypic_abnormality	6
HP:0000971	Abnormality of the sweat gland	Phenotypic_abnormality	4
HP:0000975	Hyperhidrosis	Phenotypic_abnormality	5
HP:0001056	Milia	Phenotypic_abnormality	5
HP:0001597	Abnormality of the nail	Phenotypic_abnormality	4
HP:0001600	Abnormality of the larynx	Phenotypic_abnormality	5
HP:0001806	Onycholysis	Phenotypic_abnormality	5
HP:0001808	Fragile nails	Phenotypic_abnormality	5
HP:0002087	Abnormality of the upper respiratory tract	Phenotypic_abnormality	4
HP:0003341	Junctional split	Phenotypic_abnormality	7
HP:0006089	Palmar hyperhidrosis	Phenotypic_abnormality	6
HP:0008066	Abnormal blistering of the skin	Phenotypic_abnormality	6
HP:0010936	Abnormality of the lower urinary tract	Phenotypic_abnormality	4
HP:0100577	Urinary bladder inflammation	Phenotypic_abnormality	6
HP:0100640	Laryngeal cyst	Phenotypic_abnormality	6
HP:0000023	Inguinal hernia	Phenotypic_abnormality	6
HP:0004299	Hernia of the abdominal wall	Phenotypic_abnormality	4
HP:0004414	Abnormality of the pulmonary artery	Phenotypic_abnormality	5
HP:0004930	Abnormality of the pulmonary vasculature	Phenotypic_abnormality	4
HP:0010866	Abdominal wall defect	Phenotypic_abnormality	4
HP:0100790	Hernia	Phenotypic_abnormality	3
HP:0004431	Complement deficiency	Phenotypic_abnormality	6
HP:0005339	Abnormality of complement system	Phenotypic_abnormality	5
HP:0005420	Recurrent gram-negative bacterial infections	Phenotypic_abnormality	6
HP:0005430	Recurrent Neisserial infections	Phenotypic_abnormality	7
HP:0000168	Abnormality of the gingiva	Phenotypic_abnormality	7
HP:0000324	Facial asymmetry	Phenotypic_abnormality	6
HP:0001426	Multifactorial inheritance	Mode_of_inheritance	2
HP:0001837	Broad toe	Phenotypic_abnormality	9
HP:0004213	Abnormality of the phalanges of the 5th finger	Phenotypic_abnormality	10
HP:0004219	Abnormality of the middle phalanx of the 5th finger	Phenotypic_abnormality	11
HP:0008362	Aplasia/Hypoplasia of the hallux	Phenotypic_abnormality	10
HP:0009833	Abnormality of the middle phalanges of the hand	Phenotypic_abnormality	10
HP:0010055	Broad hallux	Phenotypic_abnormality	10
HP:0010173	Aplasia/Hypoplasia of the phalanges of the toes	Phenotypic_abnormality	10
HP:0010183	Abnormality of the middle phalanges of the toes	Phenotypic_abnormality	10
HP:0010194	Aplasia/Hypoplasia of the middle phalanges of the toes	Phenotypic_abnormality	11
HP:0010760	Absent toe	Phenotypic_abnormality	10
HP:0005381	Recurrent meningococcal disease	Phenotypic_abnormality	8
HP:0000277	Abnormality of the mandible	Phenotypic_abnormality	7
HP:0001083	Ectopia lentis	Phenotypic_abnormality	7
HP:0001629	Ventricular septal defect	Phenotypic_abnormality	7
HP:0001631	Defect in the atrial septum	Phenotypic_abnormality	6
HP:0001671	Abnormality of the cardiac septa	Phenotypic_abnormality	5
HP:0002778	Abnormality of the trachea	Phenotypic_abnormality	6
HP:0005120	Abnormality of cardiac atrium	Phenotypic_abnormality	5
HP:0005607	Abnormality of the tracheobronchial system	Phenotypic_abnormality	5
HP:0009116	Aplasia/Hypoplasia involving bones of the skull	Phenotypic_abnormality	6
HP:0009118	Aplasia/Hypoplasia of the mandible	Phenotypic_abnormality	7
HP:0009122	Aplasia/hypoplasia affecting bones of the axial skeleton	Phenotypic_abnormality	5
HP:0010438	Abnormality of the ventricular septum	Phenotypic_abnormality	6
HP:0011821	Abnormality of facial skeleton	Phenotypic_abnormality	6
HP:0011994	Abnormality of the atrial septum	Phenotypic_abnormality	6
HP:0000245	Abnormality of the sinuses	Phenotypic_abnormality	7
HP:0000246	Sinusitis	Phenotypic_abnormality	8
HP:0000600	Abnormality of the pharynx	Phenotypic_abnormality	4
HP:0001739	Abnormality of the nasopharynx	Phenotypic_abnormality	5
HP:0002090	Pneumonia	Phenotypic_abnormality	6
HP:0002205	Recurrent respiratory infections	Phenotypic_abnormality	5
HP:0002783	Recurrent lower respiratory tract infections	Phenotypic_abnormality	7
HP:0006532	Recurrent pneumonia	Phenotypic_abnormality	7
HP:0000591	Abnormality of the sclera	Phenotypic_abnormality	5
HP:0000592	Blue sclerae	Phenotypic_abnormality	6
HP:0000977	Soft skin	Phenotypic_abnormality	7
HP:0000978	Bruising susceptibility	Phenotypic_abnormality	7
HP:0000987	Atypical scarring of skin	Phenotypic_abnormality	4
HP:0000993	Molluscoid pseudotumors	Phenotypic_abnormality	5
HP:0001030	Fragile skin	Phenotypic_abnormality	5
HP:0001073	Cigarette-paper scars	Phenotypic_abnormality	8
HP:0001075	Atrophic scars	Phenotypic_abnormality	6
HP:0001369	Arthritis	Phenotypic_abnormality	5
HP:0001634	Mitral valve prolapse	Phenotypic_abnormality	7
HP:0001933	Subcutaneous hemorrhage	Phenotypic_abnormality	4
HP:0002624	Venous abnormality	Phenotypic_abnormality	4
HP:0004334	Dermal atrophy	Phenotypic_abnormality	6
HP:0005293	Venous insufficiency	Phenotypic_abnormality	5
HP:0008065	Aplasia/Hypoplasia of the skin	Phenotypic_abnormality	5
HP:0010647	Abnormal elasticity of skin	Phenotypic_abnormality	6
HP:0100699	Scarring	Phenotypic_abnormality	3
HP:0002204	Pulmonary embolism	Phenotypic_abnormality	5
HP:0003256	Abnormality of the coagulation cascade	Phenotypic_abnormality	4
HP:0003812	Phenotypic variability	Onset_and_clinical_course	2
HP:0003828	Variable expressivity	Onset_and_clinical_course	3
HP:0010785	Gonadal neoplasm	Phenotypic_abnormality	6
HP:0010788	Testicular neoplasm	Phenotypic_abnormality	7
HP:0000525	Abnormality of the iris	Phenotypic_abnormality	6
HP:0000553	Abnormality of the uvea	Phenotypic_abnormality	5
HP:0001088	Brushfield spots	Phenotypic_abnormality	8
HP:0001319	Neonatal hypotonia	Phenotypic_abnormality	6
HP:0008034	Abnormal iris pigmentation	Phenotypic_abnormality	7
HP:0008935	Generalized neonatal hypotonia	Phenotypic_abnormality	7
HP:0000465	Webbed neck	Phenotypic_abnormality	4
HP:0000953	Hyperpigmentation of the skin	Phenotypic_abnormality	7
HP:0001000	Abnormality of skin pigmentation	Phenotypic_abnormality	6
HP:0001965	Abnormality of the scalp	Phenotypic_abnormality	4
HP:0002162	Low posterior hairline	Phenotypic_abnormality	4
HP:0002414	Spina bifida	Phenotypic_abnormality	7
HP:0003298	Spina bifida occulta	Phenotypic_abnormality	8
HP:0007400	Irregular hyperpigmentation	Phenotypic_abnormality	8
HP:0009553	Abnormality of the hairline	Phenotypic_abnormality	6
HP:0010301	Spinal dysraphism	Phenotypic_abnormality	6
HP:0010720	Abnormal hair pattern	Phenotypic_abnormality	5
HP:0011361	Congenital abnormal hair pattern	Phenotypic_abnormality	6
HP:0100037	Abnormality of the scalp hair	Phenotypic_abnormality	5
HP:0001176	Large hands	Phenotypic_abnormality	9
HP:0001909	Leukemia	Phenotypic_abnormality	5
HP:0002488	Acute leukemia	Phenotypic_abnormality	6
HP:0004377	Hematological neoplasm	Phenotypic_abnormality	3
HP:0005922	Abnormal hand morphology	Phenotypic_abnormality	8
HP:0000211	Trismus	Phenotypic_abnormality	8
HP:0000275	Narrow face	Phenotypic_abnormality	6
HP:0001373	Joint dislocation	Phenotypic_abnormality	5
HP:0001384	Abnormality of the hip joint	Phenotypic_abnormality	9
HP:0001638	Cardiomyopathy	Phenotypic_abnormality	6
HP:0001644	Dilated cardiomyopathy	Phenotypic_abnormality	7
HP:0001832	Abnormality of the metatarsal bones	Phenotypic_abnormality	8
HP:0001840	Metatarsus adductus	Phenotypic_abnormality	9
HP:0002803	Congenital contracture	Phenotypic_abnormality	7
HP:0002827	Hip dislocation	Phenotypic_abnormality	6
HP:0003272	Abnormality of the hip bone	Phenotypic_abnormality	6
HP:0005684	Distal arthrogryposis	Phenotypic_abnormality	8
HP:0100299	Muscle fiber inclusion bodies	Phenotypic_abnormality	5
HP:0001197	Abnormality of prenatal development or birth	Phenotypic_abnormality	2
HP:0001557	Prenatal movement abnormality	Phenotypic_abnormality	3
HP:0001558	Decreased fetal movement	Phenotypic_abnormality	4
HP:0001608	Abnormality of the voice	Phenotypic_abnormality	2
HP:0001612	Weak cry	Phenotypic_abnormality	3
HP:0002374	Diminished movement	Phenotypic_abnormality	5
HP:0002747	Respiratory insufficiency due to muscle weakness	Phenotypic_abnormality	6
HP:0002804	Arthrogryposis multiplex congenita	Phenotypic_abnormality	8
HP:0003324	Generalized muscle weakness	Phenotypic_abnormality	5
HP:0003388	Easy fatigability	Phenotypic_abnormality	4
HP:0003391	Gowers sign	Phenotypic_abnormality	6
HP:0003398	Abnormality of the neuromuscular junction	Phenotypic_abnormality	5
HP:0003436	Prolonged miniature endplate currents	Phenotypic_abnormality	6
HP:0003443	Decreased size of nerve terminals	Phenotypic_abnormality	5
HP:0003473	Fatigable weakness	Phenotypic_abnormality	5
HP:0004302	Functional motor problems.	Phenotypic_abnormality	4
HP:0004347	Weakness of muscles of respiration	Phenotypic_abnormality	4
HP:0004889	Intermittent episodes of respiratory insufficiency due to muscle weakness	Phenotypic_abnormality	7
HP:0100295	Muscle fiber atrophy	Phenotypic_abnormality	5
HP:0000272	Malar flattening	Phenotypic_abnormality	6
HP:0000309	Abnormality of the midface	Phenotypic_abnormality	5
HP:0001852	Sandal gap	Phenotypic_abnormality	9
HP:0005557	Abnormality of the zygomatic arch	Phenotypic_abnormality	6
HP:0012369	Malar anomaly	Phenotypic_abnormality	6
HP:0000695	Natal tooth	Phenotypic_abnormality	10
HP:0001131	Corneal dystrophy	Phenotypic_abnormality	7
HP:0001425	Heterogeneous	Mode_of_inheritance	2
HP:0001596	Alopecia	Phenotypic_abnormality	6
HP:0001601	Laryngomalacia	Phenotypic_abnormality	6
HP:0002745	Oral leukoplakia	Phenotypic_abnormality	8
HP:0006288	Advanced eruption of teeth	Phenotypic_abnormality	9
HP:0006292	Abnormality of dental eruption	Phenotypic_abnormality	8
HP:0007431	Congenital ichthyosiform erythroderma	Phenotypic_abnormality	9
HP:0007475	Congenital bullous ichthyosiform erythroderma	Phenotypic_abnormality	10
HP:0008069	Neoplasm of the skin	Phenotypic_abnormality	4
HP:0011363	Abnormality of hair growth rate	Phenotypic_abnormality	5
HP:0011830	Abnormality of oral mucosa	Phenotypic_abnormality	7
HP:0000407	Sensorineural hearing impairment	Phenotypic_abnormality	5
HP:0000822	Hypertension	Phenotypic_abnormality	4
HP:0001409	Portal hypertension	Phenotypic_abnormality	5
HP:0001541	Ascites	Phenotypic_abnormality	4
HP:0001964	Aplasia/Hypoplasia of metatarsal bones	Phenotypic_abnormality	9
HP:0002031	Abnormality of the esophagus	Phenotypic_abnormality	6
HP:0002040	Esophageal varix	Phenotypic_abnormality	7
HP:0003026	Short long bones	Phenotypic_abnormality	5
HP:0006707	Abnormality of the hepatic vasculature	Phenotypic_abnormality	5
HP:0010743	Short metatarsal	Phenotypic_abnormality	6
HP:0001279	Syncope	Phenotypic_abnormality	4
HP:0001649	Tachycardia	Phenotypic_abnormality	5
HP:0001692	Primary atrial arrhythmia	Phenotypic_abnormality	7
HP:0001962	Palpitations	Phenotypic_abnormality	5
HP:0002069	Generalized tonic-clonic seizures	Phenotypic_abnormality	6
HP:0002197	Generalized seizures	Phenotypic_abnormality	5
HP:0002900	Hypokalemia	Phenotypic_abnormality	7
HP:0003401	Paresthesia	Phenotypic_abnormality	7
HP:0003470	Paralysis	Phenotypic_abnormality	5
HP:0003768	Periodic paralysis	Phenotypic_abnormality	6
HP:0004755	Supraventricular tachycardia	Phenotypic_abnormality	6
HP:0005110	Atrial fibrillation	Phenotypic_abnormality	8
HP:0005115	Supraventricular arrhythmia	Phenotypic_abnormality	5
HP:0007359	Focal seizures	Phenotypic_abnormality	5
HP:0010930	Abnormality of monovalent inorganic cation homeostasis	Phenotypic_abnormality	5
HP:0011042	Abnormality of potassium homeostasis	Phenotypic_abnormality	6
HP:0011146	Dialeptic seizures	Phenotypic_abnormality	5
HP:0012591	Abnormal urinary electrolyte concentration	Phenotypic_abnormality	6
HP:0001873	Thrombocytopenia	Phenotypic_abnormality	5
HP:0011873	Abnormal platelet count	Phenotypic_abnormality	4
HP:0000301	Abnormality of facial musculature	Phenotypic_abnormality	3
HP:0001270	Motor delay	Phenotypic_abnormality	6
HP:0001291	Abnormality of the cranial nerves	Phenotypic_abnormality	5
HP:0002334	Abnormality of the cerebellar vermis	Phenotypic_abnormality	10
HP:0002438	Cerebellar malformation	Phenotypic_abnormality	9
HP:0003198	Myopathy	Phenotypic_abnormality	4
HP:0006824	Cranial nerve paralysis	Phenotypic_abnormality	6
HP:0010628	Facial palsy	Phenotypic_abnormality	5
HP:0010827	Abnormality of the seventh cranial nerve	Phenotypic_abnormality	6
HP:0011799	Abnormality of facial soft tissue	Phenotypic_abnormality	5
HP:0000069	Abnormality of the ureter	Phenotypic_abnormality	5
HP:0000303	Mandibular prognathia	Phenotypic_abnormality	6
HP:0000306	Abnormality of the chin	Phenotypic_abnormality	5
HP:0000337	Broad forehead	Phenotypic_abnormality	6
HP:0002650	Scoliosis	Phenotypic_abnormality	7
HP:0004808	Acute myeloid leukemia	Phenotypic_abnormality	7
HP:0000639	Nystagmus	Phenotypic_abnormality	6
HP:0012547	Abnormal involuntary eye movements	Phenotypic_abnormality	5
HP:0002109	Abnormality of the bronchi	Phenotypic_abnormality	6
HP:0002110	Bronchiectasis	Phenotypic_abnormality	7
HP:0100360	Contractures of the joints of the upper limbs	Phenotypic_abnormality	8
HP:0001677	Coronary artery disease	Phenotypic_abnormality	6
HP:0005114	Abnormalities of the peripheral arteries	Phenotypic_abnormality	5
HP:0009124	Abnormality of adipose tissue	Phenotypic_abnormality	3
HP:0009125	Lipodystrophy	Phenotypic_abnormality	4
HP:0100545	Arterial stenosis	Phenotypic_abnormality	6
HP:0100578	Lipoatrophy	Phenotypic_abnormality	5
HP:0002577	Abnormality of the stomach	Phenotypic_abnormality	6
HP:0004295	Abnormality of the gastric mucosa	Phenotypic_abnormality	7
HP:0002352	Leukoencephalopathy	Phenotypic_abnormality	8
HP:0002540	Inability to walk	Phenotypic_abnormality	6
HP:0002904	Hyperbilirubinemia	Phenotypic_abnormality	3
HP:0002908	Conjugated hyperbilirubinemia	Phenotypic_abnormality	4
HP:0003537	Hypouricemia	Phenotypic_abnormality	6
HP:0004352	Abnormality of purine metabolism	Phenotypic_abnormality	4
HP:0004369	Decreased purine levels	Phenotypic_abnormality	5
HP:0010932	Abnormality of nucleobase metabolism	Phenotypic_abnormality	3
HP:0001417	X-linked inheritance	Mode_of_inheritance	3
HP:0010985	Gonosomal inheritance	Mode_of_inheritance	2
HP:0000315	Abnormality of the orbital region	Phenotypic_abnormality	5
HP:0000528	Anophthalmia	Phenotypic_abnormality	6
HP:0000568	Microphthalmos	Phenotypic_abnormality	6
HP:0000589	Coloboma	Phenotypic_abnormality	4
HP:0000614	Abnormality of the nasolacrimal system	Phenotypic_abnormality	4
HP:0000625	Cleft eyelid	Phenotypic_abnormality	5
HP:0001539	Omphalocele	Phenotypic_abnormality	6
HP:0004122	Midline defect of the nose	Phenotypic_abnormality	7
HP:0004378	Abnormality of the anus	Phenotypic_abnormality	7
HP:0004397	Ectopic anus	Phenotypic_abnormality	8
HP:0005105	Abnormal nasal morphology	Phenotypic_abnormality	6
HP:0011481	Abnormality of the lacrimal duct	Phenotypic_abnormality	5
HP:0012732	Anorectal anomaly	Phenotypic_abnormality	6
HP:0100589	Urogenital fistula	Phenotypic_abnormality	3
HP:0100887	Abnormality of globe size	Phenotypic_abnormality	5
HP:0000028	Cryptorchidism	Phenotypic_abnormality	8
HP:0001511	Intrauterine growth retardation	Phenotypic_abnormality	4
HP:0011337	Abnormality of mouth size	Phenotypic_abnormality	6