name	term_id	term_name	term_namespace	term_distance
MP:0000001	MP:0000001	mammalian phenotype	root	0
MP:0001186	MP:0001186	pigmentation phenotype	Mammalian_phenotype	1
MP:0002006	MP:0002006	tumorigenesis	Mammalian_phenotype	1
MP:0002873	MP:0002873	normal phenotype	Mammalian_phenotype	1
MP:0003012	MP:0003012	no phenotypic analysis	Mammalian_phenotype	1
MP:0003631	MP:0003631	nervous system phenotype	Mammalian_phenotype	1
MP:0005367	MP:0005367	renal/urinary system phenotype	Mammalian_phenotype	1
MP:0005369	MP:0005369	muscle phenotype	Mammalian_phenotype	1
MP:0005370	MP:0005370	liver/biliary system phenotype	Mammalian_phenotype	1
MP:0005371	MP:0005371	limbs/digits/tail phenotype	Mammalian_phenotype	1
MP:0005375	MP:0005375	adipose tissue phenotype	Mammalian_phenotype	1
MP:0005376	MP:0005376	homeostasis/metabolism phenotype	Mammalian_phenotype	1
MP:0005377	MP:0005377	hearing/vestibular/ear phenotype	Mammalian_phenotype	1
MP:0005378	MP:0005378	growth/size/body phenotype	Mammalian_phenotype	1
MP:0005379	MP:0005379	endocrine/exocrine gland phenotype	Mammalian_phenotype	1
MP:0005380	MP:0005380	embryogenesis phenotype	Mammalian_phenotype	1
MP:0005381	MP:0005381	digestive/alimentary phenotype	Mammalian_phenotype	1
MP:0005382	MP:0005382	craniofacial phenotype	Mammalian_phenotype	1
MP:0005384	MP:0005384	cellular phenotype	Mammalian_phenotype	1
MP:0005385	MP:0005385	cardiovascular system phenotype	Mammalian_phenotype	1
MP:0005386	MP:0005386	behavior/neurological phenotype	Mammalian_phenotype	1
MP:0005387	MP:0005387	immune system phenotype	Mammalian_phenotype	1
MP:0005388	MP:0005388	respiratory system phenotype	Mammalian_phenotype	1
MP:0005389	MP:0005389	reproductive system phenotype	Mammalian_phenotype	1
MP:0005390	MP:0005390	skeleton phenotype	Mammalian_phenotype	1
MP:0005391	MP:0005391	vision/eye phenotype	Mammalian_phenotype	1
MP:0005394	MP:0005394	taste/olfaction phenotype	Mammalian_phenotype	1
MP:0005395	MP:0005395	other phenotype	Mammalian_phenotype	1
MP:0005397	MP:0005397	hematopoietic system phenotype	Mammalian_phenotype	1
MP:0010768	MP:0010768	mortality/aging	Mammalian_phenotype	1
MP:0010771	MP:0010771	integument phenotype	Mammalian_phenotype	1
MP:0009389	MP:0009389	abnormal extracutaneous pigmentation	Mammalian_phenotype	2
MP:0009701	MP:0009701	abnormal birth body size	Mammalian_phenotype	2
MP:0009847	MP:0009847	abnormal scrotum pigmentation	Mammalian_phenotype	2
MP:0010639	MP:0010639	altered tumor pathology	Mammalian_phenotype	2
MP:0010678	MP:0010678	abnormal skin adnexa morphology	Mammalian_phenotype	2
MP:0010680	MP:0010680	abnormal skin adnexa physiology	Mammalian_phenotype	2
MP:0010723	MP:0010723	paternal effect	Mammalian_phenotype	2
MP:0010741	MP:0010741	abnormal melanocyte proliferation	Mammalian_phenotype	2
MP:0010769	MP:0010769	abnormal survival	Mammalian_phenotype	2
MP:0011494	MP:0011494	abnormal pigmentation pattern	Mammalian_phenotype	2
MP:0011614	MP:0011614	slow aging	Mammalian_phenotype	2
MP:0000003	MP:0000003	abnormal adipose tissue morphology	Mammalian_phenotype	2
MP:0000358	MP:0000358	abnormal cell morphology	Mammalian_phenotype	2
MP:0000428	MP:0000428	abnormal craniofacial morphology	Mammalian_phenotype	2
MP:0000462	MP:0000462	abnormal digestive system morphology	Mammalian_phenotype	2
MP:0000516	MP:0000516	abnormal renal/urinary system morphology	Mammalian_phenotype	2
MP:0000569	MP:0000569	abnormal digit pigmentation	Mammalian_phenotype	2
MP:0000685	MP:0000685	abnormal immune system morphology	Mammalian_phenotype	2
MP:0001188	MP:0001188	hyperpigmentation	Mammalian_phenotype	2
MP:0001270	MP:0001270	distended abdomen	Mammalian_phenotype	2
MP:0001533	MP:0001533	abnormal skeleton physiology	Mammalian_phenotype	2
MP:0001544	MP:0001544	abnormal cardiovascular system physiology	Mammalian_phenotype	2
MP:0001545	MP:0001545	abnormal hematopoietic system physiology	Mammalian_phenotype	2
MP:0001657	MP:0001657	abnormal induced morbidity/mortality	Mammalian_phenotype	2
MP:0001663	MP:0001663	abnormal digestive system physiology	Mammalian_phenotype	2
MP:0001672	MP:0001672	abnormal embryogenesis/ development	Mammalian_phenotype	2
MP:0001764	MP:0001764	abnormal homeostasis	Mammalian_phenotype	2
MP:0001790	MP:0001790	abnormal immune system physiology	Mammalian_phenotype	2
MP:0001919	MP:0001919	abnormal reproductive system physiology	Mammalian_phenotype	2
MP:0001968	MP:0001968	abnormal touch/ nociception	Mammalian_phenotype	2
MP:0001983	MP:0001983	abnormal olfactory system physiology	Mammalian_phenotype	2
MP:0001985	MP:0001985	abnormal gustatory system physiology	Mammalian_phenotype	2
MP:0002060	MP:0002060	abnormal skin morphology	Mammalian_phenotype	2
MP:0002075	MP:0002075	abnormal coat/hair pigmentation	Mammalian_phenotype	2
MP:0002089	MP:0002089	abnormal postnatal growth/weight/body size	Mammalian_phenotype	2
MP:0002092	MP:0002092	abnormal eye morphology	Mammalian_phenotype	2
MP:0002095	MP:0002095	abnormal skin pigmentation	Mammalian_phenotype	2
MP:0002102	MP:0002102	abnormal ear morphology	Mammalian_phenotype	2
MP:0002106	MP:0002106	abnormal muscle physiology	Mammalian_phenotype	2
MP:0002108	MP:0002108	abnormal muscle morphology	Mammalian_phenotype	2
MP:0002109	MP:0002109	abnormal limb morphology	Mammalian_phenotype	2
MP:0002111	MP:0002111	abnormal tail morphology	Mammalian_phenotype	2
MP:0002127	MP:0002127	abnormal cardiovascular system morphology	Mammalian_phenotype	2
MP:0002132	MP:0002132	abnormal respiratory system morphology	Mammalian_phenotype	2
MP:0002133	MP:0002133	abnormal respiratory system physiology	Mammalian_phenotype	2
MP:0002138	MP:0002138	abnormal hepatobiliary system morphology	Mammalian_phenotype	2
MP:0002139	MP:0002139	abnormal hepatobiliary system physiology	Mammalian_phenotype	2
MP:0002160	MP:0002160	abnormal reproductive system morphology	Mammalian_phenotype	2
MP:0002163	MP:0002163	abnormal gland morphology	Mammalian_phenotype	2
MP:0002164	MP:0002164	abnormal gland physiology	Mammalian_phenotype	2
MP:0002166	MP:0002166	altered tumor susceptibility	Mammalian_phenotype	2
MP:0002168	MP:0002168	other aberrant phenotype	Mammalian_phenotype	2
MP:0002169	MP:0002169	no abnormal phenotype detected	Mammalian_phenotype	2
MP:0002396	MP:0002396	abnormal hematopoietic system morphology/development	Mammalian_phenotype	2
MP:0002877	MP:0002877	abnormal melanocyte morphology	Mammalian_phenotype	2
MP:0003121	MP:0003121	genetic imprinting	Mammalian_phenotype	2
MP:0003171	MP:0003171	phenotypic reversion	Mammalian_phenotype	2
MP:0003385	MP:0003385	abnormal body wall morphology	Mammalian_phenotype	2
MP:0003632	MP:0003632	abnormal nervous system morphology	Mammalian_phenotype	2
MP:0003633	MP:0003633	abnormal nervous system physiology	Mammalian_phenotype	2
MP:0003718	MP:0003718	maternal effect	Mammalian_phenotype	2
MP:0003786	MP:0003786	premature aging	Mammalian_phenotype	2
MP:0003878	MP:0003878	abnormal ear physiology	Mammalian_phenotype	2
MP:0012719	MP:0012719	abnormal neck morphology	Mammalian_phenotype	2
MP:0013027	MP:0013027	wounding	Mammalian_phenotype	2
MP:0004133	MP:0004133	heterotaxia	Mammalian_phenotype	2
MP:0004134	MP:0004134	abnormal chest morphology	Mammalian_phenotype	2
MP:0004196	MP:0004196	abnormal prenatal growth/weight/body size	Mammalian_phenotype	2
MP:0004924	MP:0004924	abnormal behavior	Mammalian_phenotype	2
MP:0005077	MP:0005077	abnormal melanogenesis	Mammalian_phenotype	2
MP:0005164	MP:0005164	abnormal response to injury	Mammalian_phenotype	2
MP:0005253	MP:0005253	abnormal eye physiology	Mammalian_phenotype	2
MP:0005266	MP:0005266	abnormal metabolism	Mammalian_phenotype	2
MP:0005408	MP:0005408	hypopigmentation	Mammalian_phenotype	2
MP:0005451	MP:0005451	abnormal body composition	Mammalian_phenotype	2
MP:0005499	MP:0005499	abnormal olfactory system morphology	Mammalian_phenotype	2
MP:0005500	MP:0005500	abnormal gustatory system morphology	Mammalian_phenotype	2
MP:0005501	MP:0005501	abnormal skin physiology	Mammalian_phenotype	2
MP:0005502	MP:0005502	abnormal renal/urinary system physiology	Mammalian_phenotype	2
MP:0005508	MP:0005508	abnormal skeleton morphology	Mammalian_phenotype	2
MP:0005621	MP:0005621	abnormal cell physiology	Mammalian_phenotype	2
MP:0005666	MP:0005666	abnormal adipose tissue physiology	Mammalian_phenotype	2
MP:0008834	MP:0008834	abnormal melanosome transport	Mammalian_phenotype	2
MP:0008842	MP:0008842	lipofuscinosis	Mammalian_phenotype	2
MP:0008872	MP:0008872	abnormal physiological response to xenobiotic	Mammalian_phenotype	2
MP:0003936	MP:0003936	abnormal reproductive system development	Mammalian_phenotype	3
MP:0003938	MP:0003938	abnormal ear development	Mammalian_phenotype	3
MP:0003941	MP:0003941	abnormal skin development	Mammalian_phenotype	3
MP:0003942	MP:0003942	abnormal urinary system development	Mammalian_phenotype	3
MP:0003943	MP:0003943	abnormal hepatobiliary system development	Mammalian_phenotype	3
MP:0003948	MP:0003948	abnormal gas homeostasis	Mammalian_phenotype	3
MP:0003950	MP:0003950	abnormal plasma membrane morphology	Mammalian_phenotype	3
MP:0003953	MP:0003953	abnormal hormone level	Mammalian_phenotype	3
MP:0003956	MP:0003956	abnormal body size	Mammalian_phenotype	3
MP:0003959	MP:0003959	abnormal lean body mass	Mammalian_phenotype	3
MP:0003984	MP:0003984	embryonic growth retardation	Mammalian_phenotype	3
MP:0004018	MP:0004018	abnormal galactose homeostasis	Mammalian_phenotype	3
MP:0004019	MP:0004019	abnormal vitamin homeostasis	Mammalian_phenotype	3
MP:0004036	MP:0004036	abnormal muscle relaxation	Mammalian_phenotype	3
MP:0004039	MP:0004039	abnormal cardiac cell glucose uptake	Mammalian_phenotype	3
MP:0004040	MP:0004040	altered susceptibility to kidney reperfusion injury	Mammalian_phenotype	3
MP:0004043	MP:0004043	abnormal pH regulation	Mammalian_phenotype	3
MP:0004084	MP:0004084	abnormal cardiac muscle relaxation	Mammalian_phenotype	3
MP:0004085	MP:0004085	abnormal heartbeat	Mammalian_phenotype	3
MP:0004087	MP:0004087	abnormal muscle fiber morphology	Mammalian_phenotype	3
MP:0004130	MP:0004130	abnormal muscle cell glucose uptake	Mammalian_phenotype	3
MP:0004141	MP:0004141	abnormal enteroendocrine cell morphology	Mammalian_phenotype	3
MP:0004142	MP:0004142	abnormal muscle tone	Mammalian_phenotype	3
MP:0004145	MP:0004145	abnormal muscle electrophysiology	Mammalian_phenotype	3
MP:0004185	MP:0004185	abnormal adipocyte glucose uptake	Mammalian_phenotype	3
MP:0004197	MP:0004197	abnormal fetal growth/weight/body size	Mammalian_phenotype	3
MP:0004215	MP:0004215	abnormal myocardial fiber physiology	Mammalian_phenotype	3
MP:0004233	MP:0004233	abnormal muscle weight	Mammalian_phenotype	3
MP:0004245	MP:0004245	genital hemorrhage	Mammalian_phenotype	3
MP:0004264	MP:0004264	abnormal extraembryonic tissue physiology	Mammalian_phenotype	3
MP:0004272	MP:0004272	abnormal basement membrane morphology	Mammalian_phenotype	3
MP:0004367	MP:0004367	abnormal strial intermediate cell morphology	Mammalian_phenotype	3
MP:0004381	MP:0004381	abnormal hair follicle melanocyte morphology	Mammalian_phenotype	3
MP:0004382	MP:0004382	abnormal hair follicle melanogenesis	Mammalian_phenotype	3
MP:0004484	MP:0004484	altered response of heart to induced stress	Mammalian_phenotype	3
MP:0004510	MP:0004510	myositis	Mammalian_phenotype	3
MP:0004733	MP:0004733	abnormal thoracic cavity morphology	Mammalian_phenotype	3
MP:0004742	MP:0004742	abnormal vestibular system physiology	Mammalian_phenotype	3
MP:0004782	MP:0004782	abnormal surfactant physiology	Mammalian_phenotype	3
MP:0004808	MP:0004808	abnormal hematopoietic stem cell morphology	Mammalian_phenotype	3
MP:0004811	MP:0004811	abnormal neuron physiology	Mammalian_phenotype	3
MP:0004858	MP:0004858	abnormal nervous system regeneration	Mammalian_phenotype	3
MP:0004859	MP:0004859	abnormal synaptic plasticity	Mammalian_phenotype	3
MP:0004885	MP:0004885	abnormal endolymph	Mammalian_phenotype	3
MP:0004888	MP:0004888	abnormal perilymph	Mammalian_phenotype	3
MP:0004947	MP:0004947	skin inflammation	Mammalian_phenotype	3
MP:0004966	MP:0004966	abnormal inner cell mass proliferation	Mammalian_phenotype	3
MP:0004999	MP:0004999	abnormal blood-inner ear barrier function	Mammalian_phenotype	3
MP:0005000	MP:0005000	abnormal immune tolerance	Mammalian_phenotype	3
MP:0005023	MP:0005023	abnormal wound healing	Mammalian_phenotype	3
MP:0005025	MP:0005025	abnormal response to infection	Mammalian_phenotype	3
MP:0005058	MP:0005058	abnormal lysosome morphology	Mammalian_phenotype	3
MP:0005075	MP:0005075	abnormal melanosome morphology	Mammalian_phenotype	3
MP:0005076	MP:0005076	abnormal cell differentiation	Mammalian_phenotype	3
MP:0005083	MP:0005083	abnormal biliary tract morphology	Mammalian_phenotype	3
MP:0005084	MP:0005084	abnormal gallbladder morphology	Mammalian_phenotype	3
MP:0005085	MP:0005085	abnormal gallbladder physiology	Mammalian_phenotype	3
MP:0005149	MP:0005149	abnormal gubernaculum morphology	Mammalian_phenotype	3
MP:0005165	MP:0005165	increased susceptibility to injury	Mammalian_phenotype	3
MP:0005166	MP:0005166	decreased susceptibility to injury	Mammalian_phenotype	3
MP:0005167	MP:0005167	abnormal blood-brain barrier function	Mammalian_phenotype	3
MP:0005172	MP:0005172	decreased eye pigmentation	Mammalian_phenotype	3
MP:0005174	MP:0005174	abnormal tail pigmentation	Mammalian_phenotype	3
MP:0005187	MP:0005187	abnormal penis morphology	Mammalian_phenotype	3
MP:0005190	MP:0005190	osteomyelitis	Mammalian_phenotype	3
MP:0005193	MP:0005193	abnormal anterior eye segment morphology	Mammalian_phenotype	3
MP:0005195	MP:0005195	abnormal posterior eye segment morphology	Mammalian_phenotype	3
MP:0005197	MP:0005197	abnormal uvea morphology	Mammalian_phenotype	3
MP:0005220	MP:0005220	abnormal exocrine pancreas morphology	Mammalian_phenotype	3
MP:0005248	MP:0005248	abnormal Harderian gland morphology	Mammalian_phenotype	3
MP:0005254	MP:0005254	strabismus	Mammalian_phenotype	3
MP:0005257	MP:0005257	abnormal intraocular pressure	Mammalian_phenotype	3
MP:0005275	MP:0005275	abnormal skin tensile strength	Mammalian_phenotype	3
MP:0005310	MP:0005310	abnormal salivary gland physiology	Mammalian_phenotype	3
MP:0005319	MP:0005319	abnormal enzyme/ coenzyme level	Mammalian_phenotype	3
MP:0005330	MP:0005330	cardiomyopathy	Mammalian_phenotype	3
MP:0005332	MP:0005332	abnormal amino acid level	Mammalian_phenotype	3
MP:0005334	MP:0005334	abnormal fat pad morphology	Mammalian_phenotype	3
MP:0005360	MP:0005360	urolithiasis	Mammalian_phenotype	3
MP:0005410	MP:0005410	abnormal fertilization	Mammalian_phenotype	3
MP:0005423	MP:0005423	abnormal somatic nervous system physiology	Mammalian_phenotype	3
MP:0005448	MP:0005448	abnormal energy balance	Mammalian_phenotype	3
MP:0005452	MP:0005452	abnormal adipose tissue amount	Mammalian_phenotype	3
MP:0005503	MP:0005503	abnormal tendon morphology	Mammalian_phenotype	3
MP:0005504	MP:0005504	abnormal ligament morphology	Mammalian_phenotype	3
MP:0005535	MP:0005535	abnormal body temperature	Mammalian_phenotype	3
MP:0005551	MP:0005551	abnormal eye electrophysiology	Mammalian_phenotype	3
MP:0005584	MP:0005584	abnormal enzyme/coenzyme activity	Mammalian_phenotype	3
MP:0005595	MP:0005595	abnormal vascular smooth muscle physiology	Mammalian_phenotype	3
MP:0005620	MP:0005620	abnormal muscle contractility	Mammalian_phenotype	3
MP:0005623	MP:0005623	abnormal meninges morphology	Mammalian_phenotype	3
MP:0005636	MP:0005636	abnormal mineral homeostasis	Mammalian_phenotype	3
MP:0005645	MP:0005645	abnormal hypothalamus physiology	Mammalian_phenotype	3
MP:0005646	MP:0005646	abnormal pituitary gland physiology	Mammalian_phenotype	3
MP:0005647	MP:0005647	abnormal sex gland physiology	Mammalian_phenotype	3
MP:0005653	MP:0005653	phototoxicity	Mammalian_phenotype	3
MP:0005670	MP:0005670	abnormal white adipose tissue physiology	Mammalian_phenotype	3
MP:0005671	MP:0005671	abnormal response to transplant	Mammalian_phenotype	3
MP:0006035	MP:0006035	abnormal mitochondrion morphology	Mammalian_phenotype	3
MP:0006036	MP:0006036	abnormal mitochondrial physiology	Mammalian_phenotype	3
MP:0006054	MP:0006054	spinal hemorrhage	Mammalian_phenotype	3
MP:0006072	MP:0006072	abnormal retinal apoptosis	Mammalian_phenotype	3
MP:0006080	MP:0006080	CNS ischemia	Mammalian_phenotype	3
MP:0006082	MP:0006082	CNS inflammation	Mammalian_phenotype	3
MP:0006088	MP:0006088	abnormal blood-cerebrospinal fluid barrier function	Mammalian_phenotype	3
MP:0006138	MP:0006138	congestive heart failure	Mammalian_phenotype	3
MP:0006190	MP:0006190	retinal ischemia	Mammalian_phenotype	3
MP:0006209	MP:0006209	calcified intraocular region	Mammalian_phenotype	3
MP:0006225	MP:0006225	ocular rupture	Mammalian_phenotype	3
MP:0006244	MP:0006244	involuntary contraction of eyelids	Mammalian_phenotype	3
MP:0006248	MP:0006248	lagophthalmos	Mammalian_phenotype	3
MP:0006251	MP:0006251	eyelid apraxia	Mammalian_phenotype	3
MP:0006276	MP:0006276	abnormal autonomic nervous system physiology	Mammalian_phenotype	3
MP:0006279	MP:0006279	abnormal limb development	Mammalian_phenotype	3
MP:0006281	MP:0006281	abnormal tail development	Mammalian_phenotype	3
MP:0006292	MP:0006292	abnormal nasal placode morphology	Mammalian_phenotype	3
MP:0006322	MP:0006322	abnormal perichondrium morphology	Mammalian_phenotype	3
MP:0008004	MP:0008004	abnormal stomach pH	Mammalian_phenotype	3
MP:0008007	MP:0008007	abnormal cellular replicative senescence	Mammalian_phenotype	3
MP:0008052	MP:0008052	abnormal serous gland morphology	Mammalian_phenotype	3
MP:0008057	MP:0008057	abnormal DNA replication	Mammalian_phenotype	3
MP:0008058	MP:0008058	abnormal DNA repair	Mammalian_phenotype	3
MP:0008069	MP:0008069	abnormal joint mobility	Mammalian_phenotype	3
MP:0008260	MP:0008260	abnormal autophagy	Mammalian_phenotype	3
MP:0008271	MP:0008271	abnormal bone ossification	Mammalian_phenotype	3
MP:0008305	MP:0008305	abnormal organ of Corti supporting cell physiology	Mammalian_phenotype	3
MP:0008390	MP:0008390	abnormal primordial germ cell proliferation	Mammalian_phenotype	3
MP:0008418	MP:0008418	abnormal cutaneous elastic fiber morphology	Mammalian_phenotype	3
MP:0008438	MP:0008438	abnormal cutaneous collagen fibril morphology	Mammalian_phenotype	3
MP:0008469	MP:0008469	abnormal protein level	Mammalian_phenotype	3
MP:0008493	MP:0008493	alpha-synuclein inclusion body	Mammalian_phenotype	3
MP:0008546	MP:0008546	abnormal vesicle-mediated transport	Mammalian_phenotype	3
MP:0008569	MP:0008569	lethality at weaning	Mammalian_phenotype	3
MP:0008775	MP:0008775	abnormal heart ventricle pressure	Mammalian_phenotype	3
MP:0008789	MP:0008789	abnormal olfactory epithelium morphology	Mammalian_phenotype	3
MP:0008793	MP:0008793	abnormal lens epithelium apoptosis	Mammalian_phenotype	3
MP:0008795	MP:0008795	abnormal lens fiber apoptosis	Mammalian_phenotype	3
MP:0008873	MP:0008873	increased physiological sensitivity to xenobiotic	Mammalian_phenotype	3
MP:0008874	MP:0008874	decreased physiological sensitivity to xenobiotic	Mammalian_phenotype	3
MP:0008875	MP:0008875	abnormal xenobiotic pharmacokinetics	Mammalian_phenotype	3
MP:0008923	MP:0008923	thoracoschisis	Mammalian_phenotype	3
MP:0008932	MP:0008932	abnormal embryonic tissue physiology	Mammalian_phenotype	3
MP:0008961	MP:0008961	abnormal basal metabolism	Mammalian_phenotype	3
MP:0008968	MP:0008968	abnormal lacrimal apparatus morphology	Mammalian_phenotype	3
MP:0008985	MP:0008985	hemimelia	Mammalian_phenotype	3
MP:0008995	MP:0008995	early reproductive senescence	Mammalian_phenotype	3
MP:0000013	MP:0000013	abnormal adipose tissue distribution	Mammalian_phenotype	3
MP:0000026	MP:0000026	abnormal inner ear morphology	Mammalian_phenotype	3
MP:0000049	MP:0000049	abnormal middle ear morphology	Mammalian_phenotype	3
MP:0000163	MP:0000163	abnormal cartilage morphology	Mammalian_phenotype	3
MP:0000230	MP:0000230	abnormal systemic arterial blood pressure	Mammalian_phenotype	3
MP:0000249	MP:0000249	abnormal blood vessel physiology	Mammalian_phenotype	3
MP:0000266	MP:0000266	abnormal heart morphology	Mammalian_phenotype	3
MP:0000313	MP:0000313	abnormal cell death	Mammalian_phenotype	3
MP:0000343	MP:0000343	altered response to myocardial infarction	Mammalian_phenotype	3
MP:0000348	MP:0000348	abnormal aerobic fitness	Mammalian_phenotype	3
MP:0000350	MP:0000350	abnormal cell proliferation	Mammalian_phenotype	3
MP:0000367	MP:0000367	abnormal coat/ hair morphology	Mammalian_phenotype	3
MP:0000377	MP:0000377	abnormal hair follicle morphology	Mammalian_phenotype	3
MP:0000383	MP:0000383	abnormal hair follicle orientation	Mammalian_phenotype	3
MP:0000427	MP:0000427	abnormal hair cycle	Mammalian_phenotype	3
MP:0000432	MP:0000432	abnormal head morphology	Mammalian_phenotype	3
MP:0000465	MP:0000465	gastrointestinal hemorrhage	Mammalian_phenotype	3
MP:0000467	MP:0000467	abnormal esophagus morphology	Mammalian_phenotype	3
MP:0000470	MP:0000470	abnormal stomach morphology	Mammalian_phenotype	3
MP:0000477	MP:0000477	abnormal intestine morphology	Mammalian_phenotype	3
MP:0000490	MP:0000490	abnormal crypts of Lieberkuhn morphology	Mammalian_phenotype	3
MP:0000508	MP:0000508	right-sided isomerism	Mammalian_phenotype	3
MP:0000534	MP:0000534	abnormal ureter morphology	Mammalian_phenotype	3
MP:0000537	MP:0000537	abnormal urethra morphology	Mammalian_phenotype	3
MP:0000538	MP:0000538	abnormal urinary bladder morphology	Mammalian_phenotype	3
MP:0000542	MP:0000542	left-sided isomerism	Mammalian_phenotype	3
MP:0000547	MP:0000547	short limbs	Mammalian_phenotype	3
MP:0000548	MP:0000548	long limbs	Mammalian_phenotype	3
MP:0000549	MP:0000549	absent limbs	Mammalian_phenotype	3
MP:0000550	MP:0000550	abnormal forelimb morphology	Mammalian_phenotype	3
MP:0000556	MP:0000556	abnormal hindlimb morphology	Mammalian_phenotype	3
MP:0000566	MP:0000566	synostosis	Mammalian_phenotype	3
MP:0000572	MP:0000572	abnormal autopod morphology	Mammalian_phenotype	3
MP:0000575	MP:0000575	dark foot pads	Mammalian_phenotype	3
MP:0000579	MP:0000579	abnormal nail morphology	Mammalian_phenotype	3
MP:0000585	MP:0000585	kinked tail	Mammalian_phenotype	3
MP:0000588	MP:0000588	thick tail	Mammalian_phenotype	3
MP:0000589	MP:0000589	thin tail	Mammalian_phenotype	3
MP:0000598	MP:0000598	abnormal liver morphology	Mammalian_phenotype	3
MP:0000604	MP:0000604	amyloidosis	Mammalian_phenotype	3
MP:0000609	MP:0000609	abnormal liver physiology	Mammalian_phenotype	3
MP:0000613	MP:0000613	abnormal salivary gland morphology	Mammalian_phenotype	3
MP:0000627	MP:0000627	abnormal mammary gland morphology	Mammalian_phenotype	3
MP:0000631	MP:0000631	abnormal neuroendocrine gland morphology	Mammalian_phenotype	3
MP:0000639	MP:0000639	abnormal adrenal gland morphology	Mammalian_phenotype	3
MP:0000647	MP:0000647	abnormal sebaceous gland morphology	Mammalian_phenotype	3
MP:0000653	MP:0000653	abnormal sex gland morphology	Mammalian_phenotype	3
MP:0000674	MP:0000674	abnormal sweat gland morphology	Mammalian_phenotype	3
MP:0000676	MP:0000676	abnormal water content	Mammalian_phenotype	3
MP:0000678	MP:0000678	abnormal parathyroid gland morphology	Mammalian_phenotype	3
MP:0000681	MP:0000681	abnormal thyroid gland morphology	Mammalian_phenotype	3
MP:0000689	MP:0000689	abnormal spleen morphology	Mammalian_phenotype	3
MP:0000703	MP:0000703	abnormal thymus morphology	Mammalian_phenotype	3
MP:0000716	MP:0000716	abnormal immune system cell morphology	Mammalian_phenotype	3
MP:0000733	MP:0000733	abnormal muscle development	Mammalian_phenotype	3
MP:0000734	MP:0000734	muscle hypoplasia	Mammalian_phenotype	3
MP:0000747	MP:0000747	muscle weakness	Mammalian_phenotype	3
MP:0000749	MP:0000749	muscle degeneration	Mammalian_phenotype	3
MP:0000750	MP:0000750	abnormal muscle regeneration	Mammalian_phenotype	3
MP:0000751	MP:0000751	myopathy	Mammalian_phenotype	3
MP:0000752	MP:0000752	dystrophic muscle	Mammalian_phenotype	3
MP:0000759	MP:0000759	abnormal skeletal muscle morphology	Mammalian_phenotype	3
MP:0000762	MP:0000762	abnormal tongue morphology	Mammalian_phenotype	3
MP:0000767	MP:0000767	abnormal smooth muscle morphology	Mammalian_phenotype	3
MP:0000778	MP:0000778	abnormal nervous system tract morphology	Mammalian_phenotype	3
MP:0000858	MP:0000858	altered metastatic potential	Mammalian_phenotype	3
MP:0000920	MP:0000920	abnormal myelination	Mammalian_phenotype	3
MP:0000955	MP:0000955	abnormal spinal cord morphology	Mammalian_phenotype	3
MP:0001002	MP:0001002	abnormal taste bud morphology	Mammalian_phenotype	3
MP:0001119	MP:0001119	abnormal female reproductive system morphology	Mammalian_phenotype	3
MP:0001145	MP:0001145	abnormal male reproductive system morphology	Mammalian_phenotype	3
MP:0001175	MP:0001175	abnormal lung morphology	Mammalian_phenotype	3
MP:0001177	MP:0001177	atelectasis	Mammalian_phenotype	3
MP:0001191	MP:0001191	abnormal skin condition	Mammalian_phenotype	3
MP:0001202	MP:0001202	skin photosensitivity	Mammalian_phenotype	3
MP:0001203	MP:0001203	increased sensitivity to skin irradiation	Mammalian_phenotype	3
MP:0001204	MP:0001204	decreased sensitivity to skin irradiation	Mammalian_phenotype	3
MP:0001213	MP:0001213	abnormal skin cell number	Mammalian_phenotype	3
MP:0001216	MP:0001216	abnormal epidermal layer morphology	Mammalian_phenotype	3
MP:0001243	MP:0001243	abnormal dermal layer morphology	Mammalian_phenotype	3
MP:0001267	MP:0001267	enlarged chest	Mammalian_phenotype	3
MP:0001268	MP:0001268	barrel chest	Mammalian_phenotype	3
MP:0001286	MP:0001286	abnormal eye development	Mammalian_phenotype	3
MP:0001293	MP:0001293	anophthalmia	Mammalian_phenotype	3
MP:0001299	MP:0001299	abnormal eye distance/ position	Mammalian_phenotype	3
MP:0001324	MP:0001324	abnormal eye pigmentation	Mammalian_phenotype	3
MP:0001337	MP:0001337	dry eyes	Mammalian_phenotype	3
MP:0001340	MP:0001340	abnormal eyelid morphology	Mammalian_phenotype	3
MP:0001346	MP:0001346	abnormal lacrimal gland morphology	Mammalian_phenotype	3
MP:0001348	MP:0001348	abnormal lacrimal gland physiology	Mammalian_phenotype	3
MP:0001349	MP:0001349	excessive tearing	Mammalian_phenotype	3
MP:0001389	MP:0001389	abnormal eye movement	Mammalian_phenotype	3
MP:0001440	MP:0001440	abnormal grooming behavior	Mammalian_phenotype	3
MP:0001502	MP:0001502	abnormal circadian rhythm	Mammalian_phenotype	3
MP:0001529	MP:0001529	abnormal vocalization	Mammalian_phenotype	3
MP:0001542	MP:0001542	abnormal bone strength	Mammalian_phenotype	3
MP:0001614	MP:0001614	abnormal blood vessel morphology	Mammalian_phenotype	3
MP:0001661	MP:0001661	extended life span	Mammalian_phenotype	3
MP:0001664	MP:0001664	abnormal digestion	Mammalian_phenotype	3
MP:0001697	MP:0001697	abnormal embryo size	Mammalian_phenotype	3
MP:0001730	MP:0001730	embryonic growth arrest	Mammalian_phenotype	3
MP:0001731	MP:0001731	abnormal postnatal growth	Mammalian_phenotype	3
MP:0001756	MP:0001756	abnormal urination	Mammalian_phenotype	3
MP:0001765	MP:0001765	abnormal ion homeostasis	Mammalian_phenotype	3
MP:0001777	MP:0001777	abnormal body temperature homeostasis	Mammalian_phenotype	3
MP:0001784	MP:0001784	abnormal fluid regulation	Mammalian_phenotype	3
MP:0001788	MP:0001788	periorbital edema	Mammalian_phenotype	3
MP:0001800	MP:0001800	abnormal humoral immune response	Mammalian_phenotype	3
MP:0001819	MP:0001819	abnormal immune cell physiology	Mammalian_phenotype	3
MP:0001835	MP:0001835	abnormal antigen presentation	Mammalian_phenotype	3
MP:0001845	MP:0001845	abnormal inflammatory response	Mammalian_phenotype	3
MP:0001849	MP:0001849	ear inflammation	Mammalian_phenotype	3
MP:0001851	MP:0001851	eye inflammation	Mammalian_phenotype	3
MP:0001853	MP:0001853	heart inflammation	Mammalian_phenotype	3
MP:0001873	MP:0001873	stomach inflammation	Mammalian_phenotype	3
MP:0001879	MP:0001879	abnormal lymphatic vessel morphology	Mammalian_phenotype	3
MP:0001881	MP:0001881	abnormal mammary gland physiology	Mammalian_phenotype	3
MP:0001905	MP:0001905	abnormal dopamine level	Mammalian_phenotype	3
MP:0001908	MP:0001908	abnormal somatosensory cortex physiology	Mammalian_phenotype	3
MP:0001911	MP:0001911	abnormal cerebrospinal fluid production	Mammalian_phenotype	3
MP:0001915	MP:0001915	intracranial hemorrhage	Mammalian_phenotype	3
MP:0001929	MP:0001929	abnormal gametogenesis	Mammalian_phenotype	3
MP:0001943	MP:0001943	abnormal respiration	Mammalian_phenotype	3
MP:0001944	MP:0001944	abnormal pancreas morphology	Mammalian_phenotype	3
MP:0001947	MP:0001947	abnormal mucociliary clearance	Mammalian_phenotype	3
MP:0001958	MP:0001958	emphysema	Mammalian_phenotype	3
MP:0001963	MP:0001963	abnormal hearing physiology	Mammalian_phenotype	3
MP:0001984	MP:0001984	abnormal olfaction	Mammalian_phenotype	3
MP:0001986	MP:0001986	abnormal taste sensitivity	Mammalian_phenotype	3
MP:0001999	MP:0001999	photosensitivity	Mammalian_phenotype	3
MP:0002009	MP:0002009	preneoplasia	Mammalian_phenotype	3
MP:0002019	MP:0002019	abnormal tumor incidence	Mammalian_phenotype	3
MP:0002063	MP:0002063	abnormal learning/memory/conditioning	Mammalian_phenotype	3
MP:0002064	MP:0002064	seizures	Mammalian_phenotype	3
MP:0002066	MP:0002066	abnormal motor capabilities/coordination/movement	Mammalian_phenotype	3
MP:0002067	MP:0002067	abnormal sensory capabilities/reflexes/nociception	Mammalian_phenotype	3
MP:0002069	MP:0002069	abnormal consumption behavior	Mammalian_phenotype	3
MP:0002078	MP:0002078	abnormal glucose homeostasis	Mammalian_phenotype	3
MP:0002080	MP:0002080	prenatal lethality	Mammalian_phenotype	3
MP:0002081	MP:0002081	perinatal lethality	Mammalian_phenotype	3
MP:0002082	MP:0002082	postnatal lethality	Mammalian_phenotype	3
MP:0002083	MP:0002083	premature death	Mammalian_phenotype	3
MP:0002084	MP:0002084	abnormal developmental patterning	Mammalian_phenotype	3
MP:0002085	MP:0002085	abnormal embryonic tissue morphology	Mammalian_phenotype	3
MP:0002086	MP:0002086	abnormal extraembryonic tissue morphology	Mammalian_phenotype	3
MP:0002088	MP:0002088	abnormal embryonic growth/weight/body size	Mammalian_phenotype	3
MP:0002090	MP:0002090	abnormal vision	Mammalian_phenotype	3
MP:0002098	MP:0002098	abnormal vibrissa morphology	Mammalian_phenotype	3
MP:0002113	MP:0002113	abnormal skeleton development	Mammalian_phenotype	3
MP:0002114	MP:0002114	abnormal axial skeleton morphology	Mammalian_phenotype	3
MP:0002115	MP:0002115	abnormal limb bone morphology	Mammalian_phenotype	3
MP:0002116	MP:0002116	abnormal craniofacial bone morphology	Mammalian_phenotype	3
MP:0002118	MP:0002118	abnormal lipid homeostasis	Mammalian_phenotype	3
MP:0002128	MP:0002128	abnormal blood circulation	Mammalian_phenotype	3
MP:0002135	MP:0002135	abnormal kidney morphology	Mammalian_phenotype	3
MP:0002136	MP:0002136	abnormal kidney physiology	Mammalian_phenotype	3
MP:0002148	MP:0002148	abnormal hypersensitivity reaction	Mammalian_phenotype	3
MP:0002152	MP:0002152	abnormal brain morphology	Mammalian_phenotype	3
MP:0002161	MP:0002161	abnormal fertility/fecundity	Mammalian_phenotype	3
MP:0002177	MP:0002177	abnormal outer ear morphology	Mammalian_phenotype	3
MP:0002184	MP:0002184	abnormal innervation	Mammalian_phenotype	3
MP:0002210	MP:0002210	abnormal sex determination	Mammalian_phenotype	3
MP:0002229	MP:0002229	neurodegeneration	Mammalian_phenotype	3
MP:0002233	MP:0002233	abnormal nose morphology	Mammalian_phenotype	3
MP:0002234	MP:0002234	abnormal pharynx morphology	Mammalian_phenotype	3
MP:0002240	MP:0002240	abnormal paranasal sinus morphology	Mammalian_phenotype	3
MP:0002249	MP:0002249	abnormal larynx morphology	Mammalian_phenotype	3
MP:0002254	MP:0002254	reproductive system inflammation	Mammalian_phenotype	3
MP:0002269	MP:0002269	muscular atrophy	Mammalian_phenotype	3
MP:0002272	MP:0002272	abnormal nervous system electrophysiology	Mammalian_phenotype	3
MP:0002282	MP:0002282	abnormal trachea morphology	Mammalian_phenotype	3
MP:0002295	MP:0002295	abnormal pulmonary circulation	Mammalian_phenotype	3
MP:0002332	MP:0002332	abnormal exercise endurance	Mammalian_phenotype	3
MP:0002398	MP:0002398	abnormal bone marrow cell morphology/development	Mammalian_phenotype	3
MP:0002405	MP:0002405	respiratory system inflammation	Mammalian_phenotype	3
MP:0002419	MP:0002419	abnormal innate immunity	Mammalian_phenotype	3
MP:0002420	MP:0002420	abnormal adaptive immunity	Mammalian_phenotype	3
MP:0002421	MP:0002421	abnormal cell-mediated immunity	Mammalian_phenotype	3
MP:0002429	MP:0002429	abnormal blood cell morphology/development	Mammalian_phenotype	3
MP:0002503	MP:0002503	abnormal histamine physiology	Mammalian_phenotype	3
MP:0002557	MP:0002557	abnormal social/conspecific interaction	Mammalian_phenotype	3
MP:0002572	MP:0002572	abnormal emotion/affect behavior	Mammalian_phenotype	3
MP:0002632	MP:0002632	vestigial tail	Mammalian_phenotype	3
MP:0002634	MP:0002634	abnormal sensorimotor gating	Mammalian_phenotype	3
MP:0002638	MP:0002638	abnormal pupillary reflex	Mammalian_phenotype	3
MP:0002653	MP:0002653	abnormal ependyma morphology	Mammalian_phenotype	3
MP:0002693	MP:0002693	abnormal pancreas physiology	Mammalian_phenotype	3
MP:0002697	MP:0002697	abnormal eye size	Mammalian_phenotype	3
MP:0002698	MP:0002698	abnormal sclera morphology	Mammalian_phenotype	3
MP:0002722	MP:0002722	abnormal immune system organ morphology	Mammalian_phenotype	3
MP:0002723	MP:0002723	abnormal immune serum protein physiology	Mammalian_phenotype	3
MP:0002751	MP:0002751	abnormal autonomic nervous system morphology	Mammalian_phenotype	3
MP:0002752	MP:0002752	abnormal somatic nervous system morphology	Mammalian_phenotype	3
MP:0002759	MP:0002759	abnormal caudal vertebrae morphology	Mammalian_phenotype	3
MP:0002766	MP:0002766	situs inversus	Mammalian_phenotype	3
MP:0002767	MP:0002767	situs ambiguus	Mammalian_phenotype	3
MP:0002796	MP:0002796	impaired skin barrier function	Mammalian_phenotype	3
MP:0002822	MP:0002822	catalepsy	Mammalian_phenotype	3
MP:0002876	MP:0002876	abnormal thyroid physiology	Mammalian_phenotype	3
MP:0002882	MP:0002882	abnormal neuron morphology	Mammalian_phenotype	3
MP:0002899	MP:0002899	fatigue	Mammalian_phenotype	3
MP:0002909	MP:0002909	abnormal adrenal gland physiology	Mammalian_phenotype	3
MP:0002925	MP:0002925	abnormal cardiovascular development	Mammalian_phenotype	3
MP:0002928	MP:0002928	abnormal bile duct morphology	Mammalian_phenotype	3
MP:0002932	MP:0002932	abnormal joint morphology	Mammalian_phenotype	3
MP:0002933	MP:0002933	joint inflammation	Mammalian_phenotype	3
MP:0002970	MP:0002970	abnormal white adipose tissue morphology	Mammalian_phenotype	3
MP:0002971	MP:0002971	abnormal brown adipose tissue morphology	Mammalian_phenotype	3
MP:0002972	MP:0002972	abnormal cardiac muscle contractility	Mammalian_phenotype	3
MP:0002982	MP:0002982	abnormal primordial germ cell migration	Mammalian_phenotype	3
MP:0002991	MP:0002991	abnormal sebaceous gland physiology	Mammalian_phenotype	3
MP:0002998	MP:0002998	abnormal bone remodeling	Mammalian_phenotype	3
MP:0002999	MP:0002999	abnormal bone healing	Mammalian_phenotype	3
MP:0003011	MP:0003011	delayed dark adaptation	Mammalian_phenotype	3
MP:0003045	MP:0003045	fibrosis	Mammalian_phenotype	3
MP:0003051	MP:0003051	curly tail	Mammalian_phenotype	3
MP:0003075	MP:0003075	altered response to CNS ischemic injury	Mammalian_phenotype	3
MP:0003077	MP:0003077	abnormal cell cycle	Mammalian_phenotype	3
MP:0003091	MP:0003091	abnormal cell migration	Mammalian_phenotype	3
MP:0003096	MP:0003096	increased corneal light-scattering	Mammalian_phenotype	3
MP:0003097	MP:0003097	abnormal tendon stiffness	Mammalian_phenotype	3
MP:0003111	MP:0003111	abnormal cell nucleus morphology	Mammalian_phenotype	3
MP:0003115	MP:0003115	abnormal respiratory system development	Mammalian_phenotype	3
MP:0003119	MP:0003119	abnormal digestive system development	Mammalian_phenotype	3
MP:0003122	MP:0003122	maternal imprinting	Mammalian_phenotype	3
MP:0003123	MP:0003123	paternal imprinting	Mammalian_phenotype	3
MP:0003129	MP:0003129	persistent cloaca	Mammalian_phenotype	3
MP:0003137	MP:0003137	abnormal impulse conducting system conduction	Mammalian_phenotype	3
MP:0003158	MP:0003158	dysphagia	Mammalian_phenotype	3
MP:0003172	MP:0003172	abnormal lysosome physiology	Mammalian_phenotype	3
MP:0003175	MP:0003175	reversion by mitotic recombination	Mammalian_phenotype	3
MP:0003176	MP:0003176	reversion by viral sequence excision	Mammalian_phenotype	3
MP:0003183	MP:0003183	abnormal peptide metabolism	Mammalian_phenotype	3
MP:0003186	MP:0003186	abnormal redox activity	Mammalian_phenotype	3
MP:0003191	MP:0003191	abnormal cellular cholesterol metabolism	Mammalian_phenotype	3
MP:0003195	MP:0003195	calcinosis	Mammalian_phenotype	3
MP:0003196	MP:0003196	calcified skin	Mammalian_phenotype	3
MP:0003199	MP:0003199	calcified muscle	Mammalian_phenotype	3
MP:0003221	MP:0003221	abnormal cardiomyocyte apoptosis	Mammalian_phenotype	3
MP:0003249	MP:0003249	increased muscle free fatty acid level	Mammalian_phenotype	3
MP:0003252	MP:0003252	abnormal bile duct physiology	Mammalian_phenotype	3
MP:0003257	MP:0003257	abnormal abdominal wall morphology	Mammalian_phenotype	3
MP:0003278	MP:0003278	esophageal inflammation	Mammalian_phenotype	3
MP:0003279	MP:0003279	aneurysm	Mammalian_phenotype	3
MP:0003283	MP:0003283	abnormal digestive organ placement	Mammalian_phenotype	3
MP:0003295	MP:0003295	lymphomesenteric cysts	Mammalian_phenotype	3
MP:0003298	MP:0003298	choking	Mammalian_phenotype	3
MP:0003300	MP:0003300	gastrointestinal ulcer	Mammalian_phenotype	3
MP:0003303	MP:0003303	peritoneal inflammation	Mammalian_phenotype	3
MP:0003315	MP:0003315	abnormal perineum morphology	Mammalian_phenotype	3
MP:0003328	MP:0003328	portal hypertension	Mammalian_phenotype	3
MP:0003329	MP:0003329	amyloid beta deposits	Mammalian_phenotype	3
MP:0003384	MP:0003384	abnormal ventral body wall morphology	Mammalian_phenotype	3
MP:0003431	MP:0003431	abnormal parathyroid gland physiology	Mammalian_phenotype	3
MP:0003448	MP:0003448	altered tumor morphology	Mammalian_phenotype	3
MP:0003453	MP:0003453	abnormal keratinocyte physiology	Mammalian_phenotype	3
MP:0003456	MP:0003456	absent tail	Mammalian_phenotype	3
MP:0003547	MP:0003547	abnormal pulmonary pressure	Mammalian_phenotype	3
MP:0003566	MP:0003566	abnormal cell adhesion	Mammalian_phenotype	3
MP:0003567	MP:0003567	abnormal fetal cardiomyocyte proliferation	Mammalian_phenotype	3
MP:0003589	MP:0003589	abnormal ureter physiology	Mammalian_phenotype	3
MP:0003630	MP:0003630	abnormal urothelium morphology	Mammalian_phenotype	3
MP:0003634	MP:0003634	abnormal glial cell morphology	Mammalian_phenotype	3
MP:0003635	MP:0003635	abnormal synaptic transmission	Mammalian_phenotype	3
MP:0003638	MP:0003638	abnormal response/metabolism to endogenous compounds	Mammalian_phenotype	3
MP:0003646	MP:0003646	muscle fatigue	Mammalian_phenotype	3
MP:0003673	MP:0003673	abnormal inguinal canal morphology	Mammalian_phenotype	3
MP:0003686	MP:0003686	abnormal eye muscle morphology	Mammalian_phenotype	3
MP:0003689	MP:0003689	ophthalmoplegia	Mammalian_phenotype	3
MP:0003690	MP:0003690	abnormal glial cell physiology	Mammalian_phenotype	3
MP:0003698	MP:0003698	abnormal male reproductive system physiology	Mammalian_phenotype	3
MP:0003699	MP:0003699	abnormal female reproductive system physiology	Mammalian_phenotype	3
MP:0003705	MP:0003705	abnormal hypodermis morphology	Mammalian_phenotype	3
MP:0003745	MP:0003745	abnormal mucosal lining of the mouth	Mammalian_phenotype	3
MP:0003746	MP:0003746	stomatitis	Mammalian_phenotype	3
MP:0003755	MP:0003755	abnormal palate morphology	Mammalian_phenotype	3
MP:0003762	MP:0003762	abnormal immune organ physiology	Mammalian_phenotype	3
MP:0003763	MP:0003763	abnormal thymus physiology	Mammalian_phenotype	3
MP:0003767	MP:0003767	palate inflammation	Mammalian_phenotype	3
MP:0003787	MP:0003787	abnormal imprinting	Mammalian_phenotype	3
MP:0003795	MP:0003795	abnormal bone structure	Mammalian_phenotype	3
MP:0003798	MP:0003798	abnormal Harderian gland pigmentation	Mammalian_phenotype	3
MP:0003806	MP:0003806	abnormal nucleotide metabolism	Mammalian_phenotype	3
MP:0003828	MP:0003828	pulmonary edema	Mammalian_phenotype	3
MP:0003859	MP:0003859	abnormal Harderian gland physiology	Mammalian_phenotype	3
MP:0003861	MP:0003861	abnormal nervous system development	Mammalian_phenotype	3
MP:0003866	MP:0003866	abnormal defecation	Mammalian_phenotype	3
MP:0003868	MP:0003868	abnormal feces composition	Mammalian_phenotype	3
MP:0003879	MP:0003879	abnormal hair cell physiology	Mammalian_phenotype	3
MP:0003880	MP:0003880	abnormal central pattern generator function	Mammalian_phenotype	3
MP:0003890	MP:0003890	abnormal embryonic-extraembryonic boundary morphology	Mammalian_phenotype	3
MP:0003902	MP:0003902	abnormal cell mass	Mammalian_phenotype	3
MP:0003925	MP:0003925	abnormal cellular glucose import	Mammalian_phenotype	3
MP:0003935	MP:0003935	abnormal craniofacial development	Mammalian_phenotype	3
MP:0009046	MP:0009046	muscle twitch	Mammalian_phenotype	3
MP:0009053	MP:0009053	abnormal anal canal morphology	Mammalian_phenotype	3
MP:0009115	MP:0009115	abnormal fat cell morphology	Mammalian_phenotype	3
MP:0009247	MP:0009247	meteorism	Mammalian_phenotype	3
MP:0009250	MP:0009250	abnormal appendicular skeleton morphology	Mammalian_phenotype	3
MP:0009278	MP:0009278	abnormal bone marrow cell physiology	Mammalian_phenotype	3
MP:0009333	MP:0009333	abnormal splenocyte physiology	Mammalian_phenotype	3
MP:0009378	MP:0009378	abnormal endoplasmic reticulum morphology	Mammalian_phenotype	3
MP:0009386	MP:0009386	abnormal dermal melanocyte morphology	Mammalian_phenotype	3
MP:0009388	MP:0009388	abnormal epidermal melanocyte morphology	Mammalian_phenotype	3
MP:0009390	MP:0009390	abnormal otic pigmentation	Mammalian_phenotype	3
MP:0009391	MP:0009391	abnormal leptomeninges pigmentation	Mammalian_phenotype	3
MP:0009410	MP:0009410	abnormal skeletal muscle satellite cell proliferation	Mammalian_phenotype	3
MP:0009473	MP:0009473	abnormal skin exfoliation	Mammalian_phenotype	3
MP:0009536	MP:0009536	abnormal interstitial cell of Cajal morphology	Mammalian_phenotype	3
MP:0009563	MP:0009563	dyskeratosis	Mammalian_phenotype	3
MP:0009642	MP:0009642	abnormal blood homeostasis	Mammalian_phenotype	3
MP:0009643	MP:0009643	abnormal urine homeostasis	Mammalian_phenotype	3
MP:0009672	MP:0009672	abnormal birth weight	Mammalian_phenotype	3
MP:0009697	MP:0009697	abnormal copulation	Mammalian_phenotype	3
MP:0009702	MP:0009702	increased birth body size	Mammalian_phenotype	3
MP:0009703	MP:0009703	decreased birth body size	Mammalian_phenotype	3
MP:0009745	MP:0009745	abnormal behavioral response to xenobiotic	Mammalian_phenotype	3
MP:0009765	MP:0009765	abnormal xenobiotic induced morbidity/mortality	Mammalian_phenotype	3
MP:0009780	MP:0009780	abnormal chondrocyte physiology	Mammalian_phenotype	3
MP:0009781	MP:0009781	abnormal preimplantation embryo development	Mammalian_phenotype	3
MP:0009785	MP:0009785	altered susceptibility to infection induced morbidity/mortality	Mammalian_phenotype	3
MP:0009840	MP:0009840	abnormal foam cell morphology	Mammalian_phenotype	3
MP:0009859	MP:0009859	eye opacity	Mammalian_phenotype	3
MP:0009931	MP:0009931	abnormal skin appearance	Mammalian_phenotype	3
MP:0009932	MP:0009932	skin fibrosis	Mammalian_phenotype	3
MP:0010030	MP:0010030	abnormal orbit morphology	Mammalian_phenotype	3
MP:0010037	MP:0010037	ectopic melanocytes	Mammalian_phenotype	3
MP:0010040	MP:0010040	abnormal oval cell morphology	Mammalian_phenotype	3
MP:0010071	MP:0010071	abnormal pruritus	Mammalian_phenotype	3
MP:0010094	MP:0010094	abnormal chromosome stability	Mammalian_phenotype	3
MP:0010144	MP:0010144	abnormal tumor vascularization	Mammalian_phenotype	3
MP:0010148	MP:0010148	abnormal exocrine pancreas physiology	Mammalian_phenotype	3
MP:0010154	MP:0010154	abnormal gastroesophageal sphincter physiology	Mammalian_phenotype	3
MP:0010155	MP:0010155	abnormal intestine physiology	Mammalian_phenotype	3
MP:0010190	MP:0010190	abnormal retinal melanocyte morphology	Mammalian_phenotype	3
MP:0010191	MP:0010191	abnormal choroid melanocyte morphology	Mammalian_phenotype	3
MP:0010223	MP:0010223	abnormal immunoglobulin transcytosis	Mammalian_phenotype	3
MP:0010233	MP:0010233	hairless tail	Mammalian_phenotype	3
MP:0010234	MP:0010234	abnormal vibrissa follicle morphology	Mammalian_phenotype	3
MP:0010307	MP:0010307	abnormal tumor latency	Mammalian_phenotype	3
MP:0010329	MP:0010329	abnormal lipoprotein level	Mammalian_phenotype	3
MP:0010334	MP:0010334	pleural effusion	Mammalian_phenotype	3
MP:0010352	MP:0010352	gastrointestinal tract polyps	Mammalian_phenotype	3
MP:0010368	MP:0010368	abnormal lymphatic system physiology	Mammalian_phenotype	3
MP:0010370	MP:0010370	abnormal throat morphology	Mammalian_phenotype	3
MP:0010377	MP:0010377	abnormal gut flora balance	Mammalian_phenotype	3
MP:0010386	MP:0010386	abnormal urinary bladder physiology	Mammalian_phenotype	3
MP:0010399	MP:0010399	decreased skeletal muscle glycogen level	Mammalian_phenotype	3
MP:0010401	MP:0010401	increased skeletal muscle glycogen level	Mammalian_phenotype	3
MP:0010431	MP:0010431	atrial situs inversus	Mammalian_phenotype	3
MP:0010531	MP:0010531	gastrointestinal arteriovenous malformation	Mammalian_phenotype	3
MP:0010537	MP:0010537	tumor regression	Mammalian_phenotype	3
MP:0010630	MP:0010630	abnormal cardiac muscle tissue morphology	Mammalian_phenotype	3
MP:0010653	MP:0010653	abnormal Wallerian degeneration	Mammalian_phenotype	3
MP:0010679	MP:0010679	abnormal arrector pilli muscle morphology	Mammalian_phenotype	3
MP:0010695	MP:0010695	abnormal blood pressure regulation	Mammalian_phenotype	3
MP:0010698	MP:0010698	abnormal impulsive behavior control	Mammalian_phenotype	3
MP:0010763	MP:0010763	abnormal hematopoietic stem cell physiology	Mammalian_phenotype	3
MP:0010770	MP:0010770	preweaning lethality	Mammalian_phenotype	3
MP:0010808	MP:0010808	right-sided stomach	Mammalian_phenotype	3
MP:0010820	MP:0010820	abnormal pleura morphology	Mammalian_phenotype	3
MP:0010822	MP:0010822	pneumothorax	Mammalian_phenotype	3
MP:0010831	MP:0010831	partial lethality	Mammalian_phenotype	3
MP:0010854	MP:0010854	lung situs inversus	Mammalian_phenotype	3
MP:0010865	MP:0010865	prenatal growth retardation	Mammalian_phenotype	3
MP:0010866	MP:0010866	abnormal prenatal body size	Mammalian_phenotype	3
MP:0010942	MP:0010942	abnormal respiratory epithelium morphology	Mammalian_phenotype	3
MP:0010950	MP:0010950	abnormal lung hysteresivity	Mammalian_phenotype	3
MP:0010951	MP:0010951	abnormal lipid oxidation	Mammalian_phenotype	3
MP:0010954	MP:0010954	abnormal cellular respiration	Mammalian_phenotype	3
MP:0010994	MP:0010994	aerophagia	Mammalian_phenotype	3
MP:0011005	MP:0011005	abnormal epidermal stem cell physiology	Mammalian_phenotype	3
MP:0011018	MP:0011018	pulmonary hyaline membrane formation	Mammalian_phenotype	3
MP:0011019	MP:0011019	abnormal adaptive thermogenesis	Mammalian_phenotype	3
MP:0011043	MP:0011043	abnormal lung elastance	Mammalian_phenotype	3
MP:0011046	MP:0011046	abnormal lung tissue damping	Mammalian_phenotype	3
MP:0011055	MP:0011055	abnormal respiratory motile cilium physiology	Mammalian_phenotype	3
MP:0011068	MP:0011068	abnormal ependyma motile cilium physiology	Mammalian_phenotype	3
MP:0011082	MP:0011082	abnormal gastrointestinal motility	Mammalian_phenotype	3
MP:0011131	MP:0011131	abnormal lung endothelial cell physiology	Mammalian_phenotype	3
MP:0011159	MP:0011159	abnormal epidermal-dermal junction morphology	Mammalian_phenotype	3
MP:0011164	MP:0011164	panniculitis	Mammalian_phenotype	3
MP:0011167	MP:0011167	abnormal adipose tissue development	Mammalian_phenotype	3
MP:0011186	MP:0011186	abnormal visceral endoderm morphology	Mammalian_phenotype	3
MP:0011194	MP:0011194	abnormal hair follicle physiology	Mammalian_phenotype	3
MP:0011239	MP:0011239	abnormal skin coloration	Mammalian_phenotype	3
MP:0011248	MP:0011248	visceral organ asymmetry	Mammalian_phenotype	3
MP:0011249	MP:0011249	abdominal situs inversus	Mammalian_phenotype	3
MP:0011250	MP:0011250	abdominal situs ambiguus	Mammalian_phenotype	3
MP:0011275	MP:0011275	abnormal behavioral response to light	Mammalian_phenotype	3
MP:0011276	MP:0011276	increased tail pigmentation	Mammalian_phenotype	3
MP:0011277	MP:0011277	decreased tail pigmentation	Mammalian_phenotype	3
MP:0011278	MP:0011278	increased ear pigmentation	Mammalian_phenotype	3
MP:0011279	MP:0011279	decreased ear pigmentation	Mammalian_phenotype	3
MP:0011390	MP:0011390	abnormal fetal cardiomyocyte physiology	Mammalian_phenotype	3
MP:0011396	MP:0011396	abnormal sleep behavior	Mammalian_phenotype	3
MP:0011397	MP:0011397	endoneurial edema	Mammalian_phenotype	3
MP:0011398	MP:0011398	abnormal endoneurial fluid pressure	Mammalian_phenotype	3
MP:0011400	MP:0011400	complete lethality	Mammalian_phenotype	3
MP:0011475	MP:0011475	abnormal glycosaminoglycan level	Mammalian_phenotype	3
MP:0011479	MP:0011479	abnormal catecholamine level	Mammalian_phenotype	3
MP:0011487	MP:0011487	abnormal ureteropelvic junction morphology	Mammalian_phenotype	3
MP:0011488	MP:0011488	abnormal ureterovesical junction morphology	Mammalian_phenotype	3
MP:0011514	MP:0011514	skin hemorrhage	Mammalian_phenotype	3
MP:0011568	MP:0011568	decreased foot pigmentation	Mammalian_phenotype	3
MP:0011610	MP:0011610	abnormal primordial germ cell apoptosis	Mammalian_phenotype	3
MP:0011627	MP:0011627	decreased skin pigmentation	Mammalian_phenotype	3
MP:0011677	MP:0011677	abnormal olfactory sensory neuron physiology	Mammalian_phenotype	3
MP:0011698	MP:0011698	abnormal brown adipose tissue physiology	Mammalian_phenotype	3
MP:0011728	MP:0011728	abnormal pineal gland physiology	Mammalian_phenotype	3
MP:0011743	MP:0011743	abnormal Golgi apparatus morphology	Mammalian_phenotype	3
MP:0011762	MP:0011762	renal/urinary system inflammation	Mammalian_phenotype	3
MP:0011782	MP:0011782	abnormal internal urethral orifice morphology	Mammalian_phenotype	3
MP:0011849	MP:0011849	abnormal clitoral bone morphology	Mammalian_phenotype	3
MP:0011925	MP:0011925	abnormal heart echocardiography feature	Mammalian_phenotype	3
MP:0011926	MP:0011926	abnormal cardiac valve physiology	Mammalian_phenotype	3
MP:0011955	MP:0011955	phenotypic reversion by gene product interaction	Mammalian_phenotype	3
MP:0011989	MP:0011989	abnormal porphyrin level	Mammalian_phenotype	3
MP:0011999	MP:0011999	abnormal tail length	Mammalian_phenotype	3
MP:0012000	MP:0012000	abnormal limb position	Mammalian_phenotype	3
MP:0012006	MP:0012006	abnormal hippocampus physiology	Mammalian_phenotype	3
MP:0012015	MP:0012015	abnormal melanocyte eumelanin content	Mammalian_phenotype	3
MP:0012020	MP:0012020	abnormal olfactory epithelium physiology	Mammalian_phenotype	3
MP:0012021	MP:0012021	abnormal melanocyte number	Mammalian_phenotype	3
MP:0012028	MP:0012028	abnormal visceral endoderm physiology	Mammalian_phenotype	3
MP:0012029	MP:0012029	abnormal electroretinogram waveform feature	Mammalian_phenotype	3
MP:0012048	MP:0012048	altered response to retinal ischemic injury	Mammalian_phenotype	3
MP:0012067	MP:0012067	abnormal olfactory gland morphology	Mammalian_phenotype	3
MP:0012077	MP:0012077	webbed neck	Mammalian_phenotype	3
MP:0012123	MP:0012123	abnormal bronchoconstrictive response	Mammalian_phenotype	3
MP:0012167	MP:0012167	abnormal epigenetic regulation of gene expression	Mammalian_phenotype	3
MP:0012186	MP:0012186	abnormal muscle precursor cell physiology	Mammalian_phenotype	3
MP:0012204	MP:0012204	abnormal neuronal stem cell physiology	Mammalian_phenotype	3
MP:0012241	MP:0012241	abnormal hepatoblast physiology	Mammalian_phenotype	3
MP:0012260	MP:0012260	encephalomeningocele	Mammalian_phenotype	3
MP:0012261	MP:0012261	increased hindbrain apoptosis	Mammalian_phenotype	3
MP:0012320	MP:0012320	abnormal body fat mass	Mammalian_phenotype	3
MP:0012321	MP:0012321	abnormal total tissue mass	Mammalian_phenotype	3
MP:0012382	MP:0012382	abnormal blood cell physiology	Mammalian_phenotype	3
MP:0012502	MP:0012502	decreased hindbrain apoptosis	Mammalian_phenotype	3
MP:0012503	MP:0012503	increased midbrain apoptosis	Mammalian_phenotype	3
MP:0012504	MP:0012504	increased forebrain apoptosis	Mammalian_phenotype	3
MP:0012505	MP:0012505	increased neural tube apoptosis	Mammalian_phenotype	3
MP:0012514	MP:0012514	pectus excavatum	Mammalian_phenotype	3
MP:0012518	MP:0012518	abnormal Brunner's gland morphology	Mammalian_phenotype	3
MP:0012550	MP:0012550	respiratory acidosis	Mammalian_phenotype	3
MP:0012684	MP:0012684	abnormal pleural cavity morphology	Mammalian_phenotype	3
MP:0012704	MP:0012704	abnormal embryonic neuroepithelial cell proliferation	Mammalian_phenotype	3
MP:0012720	MP:0012720	elongated neck	Mammalian_phenotype	3
MP:0012721	MP:0012721	short neck	Mammalian_phenotype	3
MP:0012722	MP:0012722	absent neck	Mammalian_phenotype	3
MP:0012723	MP:0012723	abnormal nuchal region morphology	Mammalian_phenotype	3
MP:0012734	MP:0012734	abnormal response to radiation	Mammalian_phenotype	3
MP:0012735	MP:0012735	abnormal response to exercise	Mammalian_phenotype	3
MP:0013028	MP:0013028	open abrasion	Mammalian_phenotype	3
MP:0013029	MP:0013029	open avulsion	Mammalian_phenotype	3
MP:0013030	MP:0013030	open incision	Mammalian_phenotype	3
MP:0013031	MP:0013031	open laceration	Mammalian_phenotype	3
MP:0013032	MP:0013032	open puncture	Mammalian_phenotype	3
MP:0013033	MP:0013033	closed contusion	Mammalian_phenotype	3
MP:0013034	MP:0013034	entire body wounds	Mammalian_phenotype	3
MP:0013041	MP:0013041	thorax wound	Mammalian_phenotype	3
MP:0013048	MP:0013048	abdomen wound	Mammalian_phenotype	3
MP:0013055	MP:0013055	genital wound	Mammalian_phenotype	3
MP:0013062	MP:0013062	teat wound	Mammalian_phenotype	3
MP:0013069	MP:0013069	limb wound	Mammalian_phenotype	3
MP:0013076	MP:0013076	autopod wound	Mammalian_phenotype	3
MP:0013083	MP:0013083	tail wound	Mammalian_phenotype	3
MP:0013090	MP:0013090	head or neck wound	Mammalian_phenotype	3
MP:0013097	MP:0013097	ear wound	Mammalian_phenotype	3
MP:0013104	MP:0013104	nose wound	Mammalian_phenotype	3
MP:0013113	MP:0013113	greasy tail	Mammalian_phenotype	3
MP:0013114	MP:0013114	greasy head/neck	Mammalian_phenotype	3
MP:0013118	MP:0013118	swellings	Mammalian_phenotype	3
MP:0013133	MP:0013133	pale limbs	Mammalian_phenotype	3
MP:0013136	MP:0013136	genital discharge	Mammalian_phenotype	3
MP:0013139	MP:0013139	moribund	Mammalian_phenotype	3
MP:0013145	MP:0013145	eye discharge	Mammalian_phenotype	3
MP:0013146	MP:0013146	eye lesions	Mammalian_phenotype	3
MP:0020000	MP:0020000	abnormal response to antigen	Mammalian_phenotype	3
MP:0020041	MP:0020041	resistant to pulmonary hyaline membrane formation	Mammalian_phenotype	3
MP:0020086	MP:0020086	abnormal susceptibility to non-insulin-dependent diabetes	Mammalian_phenotype	3
MP:0020092	MP:0020092	abnormal susceptibility to aortic cartilaginous metaplasia	Mammalian_phenotype	3
MP:0020095	MP:0020095	abnormal mean heart rate adaptation	Mammalian_phenotype	3
MP:0020098	MP:0020098	abnormal susceptibility to diet-induced aortic fatty streak lesions	Mammalian_phenotype	3
MP:0020148	MP:0020148	abnormal sensitivity to induced morbidity/mortality	Mammalian_phenotype	3
MP:0012103	MP:0012103	abnormal embryonic disc morphology	Mammalian_phenotype	4
MP:0012106	MP:0012106	impaired exercise endurance	Mammalian_phenotype	4
MP:0012107	MP:0012107	enhanced exercise endurance	Mammalian_phenotype	4
MP:0012110	MP:0012110	increased hair follicle number	Mammalian_phenotype	4
MP:0012111	MP:0012111	failure of morula compaction	Mammalian_phenotype	4
MP:0012115	MP:0012115	abnormal trophectoderm cell proliferation	Mammalian_phenotype	4
MP:0012119	MP:0012119	increased trophectoderm apoptosis	Mammalian_phenotype	4
MP:0012120	MP:0012120	trophectoderm cell degeneration	Mammalian_phenotype	4
MP:0012124	MP:0012124	increased bronchoconstrictive response	Mammalian_phenotype	4
MP:0012125	MP:0012125	decreased bronchoconstrictive response	Mammalian_phenotype	4
MP:0012135	MP:0012135	embryonic-extraembryonic boundary constriction	Mammalian_phenotype	4
MP:0012155	MP:0012155	abnormal optic pit morphology	Mammalian_phenotype	4
MP:0012158	MP:0012158	absent visceral endoderm	Mammalian_phenotype	4
MP:0012171	MP:0012171	oligohydramnios	Mammalian_phenotype	4
MP:0012172	MP:0012172	abnormal amniotic fluid composition	Mammalian_phenotype	4
MP:0012176	MP:0012176	abnormal head development	Mammalian_phenotype	4
MP:0012187	MP:0012187	abnormal intraembryonic coelom morphology	Mammalian_phenotype	4
MP:0012192	MP:0012192	abnormal keratinocyte migration	Mammalian_phenotype	4
MP:0012195	MP:0012195	impaired neural crest cell differentiation	Mammalian_phenotype	4
MP:0012196	MP:0012196	abnormal myofibroblast differentiation	Mammalian_phenotype	4
MP:0012199	MP:0012199	abnormal interphalangeal joint	Mammalian_phenotype	4
MP:0012202	MP:0012202	abnormal endothelial cell proliferation	Mammalian_phenotype	4
MP:0012203	MP:0012203	abnormal neuronal stem cell morphology	Mammalian_phenotype	4
MP:0012205	MP:0012205	abnormal neuronal stem cell self-renewal	Mammalian_phenotype	4
MP:0012208	MP:0012208	abnormal hypoxanthine-guanine phosphoribosyltransferase level	Mammalian_phenotype	4
MP:0012218	MP:0012218	decreased brain plasmalogen level	Mammalian_phenotype	4
MP:0012219	MP:0012219	increased brain plasmalogen level	Mammalian_phenotype	4
MP:0012221	MP:0012221	abnormal prothrombin level	Mammalian_phenotype	4
MP:0012234	MP:0012234	abnormal hepatic diverticulum morphology	Mammalian_phenotype	4
MP:0012237	MP:0012237	increased cholangiocyte apoptosis	Mammalian_phenotype	4
MP:0012239	MP:0012239	abnormal cholangiocyte primary cilium physiology	Mammalian_phenotype	4
MP:0012240	MP:0012240	abnormal hepatoblast morphology	Mammalian_phenotype	4
MP:0012244	MP:0012244	increased hepatoblast apoptosis	Mammalian_phenotype	4
MP:0012245	MP:0012245	abnormal hepatoblast migration	Mammalian_phenotype	4
MP:0012246	MP:0012246	abnormal hepatic cord morphology	Mammalian_phenotype	4
MP:0012252	MP:0012252	abnormal septum transversum morphology	Mammalian_phenotype	4
MP:0012253	MP:0012253	abnormal intersomitic vessel morphology	Mammalian_phenotype	4
MP:0012269	MP:0012269	nuchal edema	Mammalian_phenotype	4
MP:0012278	MP:0012278	abnormal cardiogenic mesoderm morphology	Mammalian_phenotype	4
MP:0012299	MP:0012299	hydropic allantois	Mammalian_phenotype	4
MP:0012314	MP:0012314	enhanced learning	Mammalian_phenotype	4
MP:0012315	MP:0012315	impaired learning	Mammalian_phenotype	4
MP:0012316	MP:0012316	enhanced conditioning behavior	Mammalian_phenotype	4
MP:0012317	MP:0012317	impaired conditioning behavior	Mammalian_phenotype	4
MP:0012322	MP:0012322	decreased total tissue mass	Mammalian_phenotype	4
MP:0012323	MP:0012323	increased total tissue mass	Mammalian_phenotype	4
MP:0012360	MP:0012360	abnormal large unstained cell number	Mammalian_phenotype	4
MP:0012384	MP:0012384	abnormal erythrocyte ion transport	Mammalian_phenotype	4
MP:0012399	MP:0012399	short nails	Mammalian_phenotype	4
MP:0012400	MP:0012400	nail dystrophy	Mammalian_phenotype	4
MP:0012401	MP:0012401	long nails	Mammalian_phenotype	4
MP:0012402	MP:0012402	abnormal nail bed morphology	Mammalian_phenotype	4
MP:0012403	MP:0012403	abnormal nail plate morphology	Mammalian_phenotype	4
MP:0012404	MP:0012404	abnormal nail color	Mammalian_phenotype	4
MP:0012405	MP:0012405	abnormal nail matrix morphology	Mammalian_phenotype	4
MP:0012454	MP:0012454	abnormal mammillothalamic tract morphology	Mammalian_phenotype	4
MP:0012491	MP:0012491	larynx stenosis	Mammalian_phenotype	4
MP:0012496	MP:0012496	abnormal pleuropericardial membrane morphology	Mammalian_phenotype	4
MP:0012498	MP:0012498	abnormal cardiogenic plate morphology	Mammalian_phenotype	4
MP:0012500	MP:0012500	abnormal angioblastic cord morphology	Mammalian_phenotype	4
MP:0012501	MP:0012501	abnormal pericardial cavity morphology	Mammalian_phenotype	4
MP:0012506	MP:0012506	brain atrophy	Mammalian_phenotype	4
MP:0012510	MP:0012510	abnormal aortic sac morphology	Mammalian_phenotype	4
MP:0012515	MP:0012515	abnormal heart apex morphology	Mammalian_phenotype	4
MP:0012521	MP:0012521	abnormal buccopharyngeal membrane morphology	Mammalian_phenotype	4
MP:0012522	MP:0012522	abnormal stomodeum morphology	Mammalian_phenotype	4
MP:0012531	MP:0012531	delayed limb development	Mammalian_phenotype	4
MP:0012533	MP:0012533	uveal coloboma	Mammalian_phenotype	4
MP:0012534	MP:0012534	abnormal optic fissure morphology	Mammalian_phenotype	4
MP:0012535	MP:0012535	abnormal optic fissure closure	Mammalian_phenotype	4
MP:0012537	MP:0012537	abnormal hyaloid artery morphology	Mammalian_phenotype	4
MP:0012538	MP:0012538	persistent hyaloid artery	Mammalian_phenotype	4
MP:0012545	MP:0012545	syringomyelia	Mammalian_phenotype	4
MP:0012555	MP:0012555	decreased cell death	Mammalian_phenotype	4
MP:0012556	MP:0012556	increased cell death	Mammalian_phenotype	4
MP:0012557	MP:0012557	decreased calcium uptake by cardiac muscle	Mammalian_phenotype	4
MP:0012558	MP:0012558	increased calcium uptake by cardiac muscle	Mammalian_phenotype	4
MP:0012562	MP:0012562	vasculature degeneration	Mammalian_phenotype	4
MP:0012576	MP:0012576	abnormal kidney glutathione peroxidase activity	Mammalian_phenotype	4
MP:0012579	MP:0012579	abnormal peroxidase activity	Mammalian_phenotype	4
MP:0012584	MP:0012584	abnormal catechol O-methyltransferase activity	Mammalian_phenotype	4
MP:0012589	MP:0012589	abnormal choline acetyltransferase activity	Mammalian_phenotype	4
MP:0012594	MP:0012594	abnormal glutamate decarboxylase activity	Mammalian_phenotype	4
MP:0012597	MP:0012597	abnormal nicotinamide N-methyltransferase activity	Mammalian_phenotype	4
MP:0012600	MP:0012600	abnormal alpha-fetoprotein level	Mammalian_phenotype	4
MP:0012603	MP:0012603	abnormal glutathione level	Mammalian_phenotype	4
MP:0012611	MP:0012611	abnormal ceruloplasmin level	Mammalian_phenotype	4
MP:0012623	MP:0012623	abnormal acetylcholinesterase activity	Mammalian_phenotype	4
MP:0012628	MP:0012628	abnormal glutathione reductase level	Mammalian_phenotype	4
MP:0012635	MP:0012635	abnormal monoamine oxidase activity	Mammalian_phenotype	4
MP:0012640	MP:0012640	abnormal benz (alpha) pyrene hydroxylase activity	Mammalian_phenotype	4
MP:0012643	MP:0012643	abnormal 3 aminolaevulinic acid synthetase activity	Mammalian_phenotype	4
MP:0012646	MP:0012646	abnormal urokinase activity	Mammalian_phenotype	4
MP:0012649	MP:0012649	abnormal catalase level	Mammalian_phenotype	4
MP:0012658	MP:0012658	abnormal superoxide dismutase level	Mammalian_phenotype	4
MP:0012672	MP:0012672	enlarged trachea	Mammalian_phenotype	4
MP:0012689	MP:0012689	abnormal adrenal gland weight	Mammalian_phenotype	4
MP:0012691	MP:0012691	abnormal acetaminophen metabolism	Mammalian_phenotype	4
MP:0012692	MP:0012692	abnormal fluoxetine metabolism	Mammalian_phenotype	4
MP:0012693	MP:0012693	abnormal haloperidol metabolism	Mammalian_phenotype	4
MP:0012694	MP:0012694	abnormal lithium metabolism	Mammalian_phenotype	4
MP:0012695	MP:0012695	abnormal nicotine metabolism	Mammalian_phenotype	4
MP:0012696	MP:0012696	abnormal trichloroethylene metabolism	Mammalian_phenotype	4
MP:0012701	MP:0012701	increased embryonic neuroepithelium apoptosis	Mammalian_phenotype	4
MP:0012705	MP:0012705	increased embryonic neuroepithelial cell proliferation	Mammalian_phenotype	4
MP:0012706	MP:0012706	decreased embryonic neuroepithelial cell proliferation	Mammalian_phenotype	4
MP:0012710	MP:0012710	diastematomyelia	Mammalian_phenotype	4
MP:0012711	MP:0012711	diplomyelia	Mammalian_phenotype	4
MP:0012712	MP:0012712	spinal cord degeneration	Mammalian_phenotype	4
MP:0012725	MP:0012725	small sebaceous gland	Mammalian_phenotype	4
MP:0012745	MP:0012745	abnormal neural crest cell physiology	Mammalian_phenotype	4
MP:0012747	MP:0012747	abnormal cardiac neural crest cell morphology	Mammalian_phenotype	4
MP:0012776	MP:0012776	abnormal liver cholesterol level	Mammalian_phenotype	4
MP:0012777	MP:0012777	abnormal liver glycogen level	Mammalian_phenotype	4
MP:0012778	MP:0012778	abnormal liver triglyceride level	Mammalian_phenotype	4
MP:0012779	MP:0012779	abnormal brain cholesterol level	Mammalian_phenotype	4
MP:0012780	MP:0012780	abnormal phospholipid transfer protein activity	Mammalian_phenotype	4
MP:0013035	MP:0013035	entire body open abrasion	Mammalian_phenotype	4
MP:0013036	MP:0013036	entire body open avulsion	Mammalian_phenotype	4
MP:0013037	MP:0013037	entire body open incision	Mammalian_phenotype	4
MP:0013038	MP:0013038	entire body open laceration	Mammalian_phenotype	4
MP:0013039	MP:0013039	entire body open puncture	Mammalian_phenotype	4
MP:0013040	MP:0013040	entire body closed contusion	Mammalian_phenotype	4
MP:0013042	MP:0013042	thorax open abrasion	Mammalian_phenotype	4
MP:0013043	MP:0013043	thorax open avulsion	Mammalian_phenotype	4
MP:0013044	MP:0013044	thorax open incision	Mammalian_phenotype	4
MP:0013045	MP:0013045	thorax open laceration	Mammalian_phenotype	4
MP:0013046	MP:0013046	thorax open puncture	Mammalian_phenotype	4
MP:0013047	MP:0013047	thorax closed contusion	Mammalian_phenotype	4
MP:0013049	MP:0013049	abdomen open abrasion	Mammalian_phenotype	4
MP:0013050	MP:0013050	abdomen open avulsion	Mammalian_phenotype	4
MP:0013051	MP:0013051	abdomen open incision	Mammalian_phenotype	4
MP:0013052	MP:0013052	abdomen open laceration	Mammalian_phenotype	4
MP:0013053	MP:0013053	abdomen open puncture	Mammalian_phenotype	4
MP:0013054	MP:0013054	abdomen closed contusion	Mammalian_phenotype	4
MP:0013056	MP:0013056	genital open abrasion	Mammalian_phenotype	4
MP:0013057	MP:0013057	genital open avulsion	Mammalian_phenotype	4
MP:0013058	MP:0013058	genital open incision	Mammalian_phenotype	4
MP:0013059	MP:0013059	genital open laceration	Mammalian_phenotype	4
MP:0013060	MP:0013060	genital open puncture	Mammalian_phenotype	4
MP:0013061	MP:0013061	genital closed contusion	Mammalian_phenotype	4
MP:0013063	MP:0013063	teat open abrasion	Mammalian_phenotype	4
MP:0013064	MP:0013064	teat open avulsion	Mammalian_phenotype	4
MP:0013065	MP:0013065	teat open incision	Mammalian_phenotype	4
MP:0013066	MP:0013066	teat open laceration	Mammalian_phenotype	4
MP:0013067	MP:0013067	teat open puncture	Mammalian_phenotype	4
MP:0013068	MP:0013068	teat closed contusion	Mammalian_phenotype	4
MP:0013070	MP:0013070	limb open abrasion	Mammalian_phenotype	4
MP:0013071	MP:0013071	limb open avulsion	Mammalian_phenotype	4
MP:0013072	MP:0013072	limb open incision	Mammalian_phenotype	4
MP:0013073	MP:0013073	limb open laceration	Mammalian_phenotype	4
MP:0013074	MP:0013074	limb open puncture	Mammalian_phenotype	4
MP:0013075	MP:0013075	limb closed contusion	Mammalian_phenotype	4
MP:0013077	MP:0013077	autopod open abrasion	Mammalian_phenotype	4
MP:0013078	MP:0013078	autopod open avulsion	Mammalian_phenotype	4
MP:0013079	MP:0013079	autopod open incision	Mammalian_phenotype	4
MP:0013080	MP:0013080	autopod open laceration	Mammalian_phenotype	4
MP:0013081	MP:0013081	autopod open puncture	Mammalian_phenotype	4
MP:0013082	MP:0013082	autopod closed contusion	Mammalian_phenotype	4
MP:0013084	MP:0013084	tail open abrasion	Mammalian_phenotype	4
MP:0013085	MP:0013085	tail open avulsion	Mammalian_phenotype	4
MP:0013086	MP:0013086	tail open incision	Mammalian_phenotype	4
MP:0013087	MP:0013087	tail open laceration	Mammalian_phenotype	4
MP:0013088	MP:0013088	tail open puncture	Mammalian_phenotype	4
MP:0013089	MP:0013089	tail closed contusion	Mammalian_phenotype	4
MP:0013091	MP:0013091	head or neck open abrasion	Mammalian_phenotype	4
MP:0013092	MP:0013092	head or neck open avulsion	Mammalian_phenotype	4
MP:0013093	MP:0013093	head or neck open incision	Mammalian_phenotype	4
MP:0013094	MP:0013094	head or neck open laceration	Mammalian_phenotype	4
MP:0013095	MP:0013095	head or neck open puncture	Mammalian_phenotype	4
MP:0013096	MP:0013096	head or neck closed contusion	Mammalian_phenotype	4
MP:0013098	MP:0013098	ear open abrasion	Mammalian_phenotype	4
MP:0013099	MP:0013099	ear open avulsion	Mammalian_phenotype	4
MP:0013100	MP:0013100	ear open incision	Mammalian_phenotype	4
MP:0013101	MP:0013101	ear open laceration	Mammalian_phenotype	4
MP:0013102	MP:0013102	ear open puncture	Mammalian_phenotype	4
MP:0013103	MP:0013103	ear closed contusion	Mammalian_phenotype	4
MP:0013105	MP:0013105	nose open abrasion	Mammalian_phenotype	4
MP:0013106	MP:0013106	nose open avulsion	Mammalian_phenotype	4
MP:0013107	MP:0013107	nose open incision	Mammalian_phenotype	4
MP:0013108	MP:0013108	nose open laceration	Mammalian_phenotype	4
MP:0013109	MP:0013109	nose open puncture	Mammalian_phenotype	4
MP:0013110	MP:0013110	nose closed contusion	Mammalian_phenotype	4
MP:0013119	MP:0013119	abdomen swellings	Mammalian_phenotype	4
MP:0013120	MP:0013120	urogenital swellings	Mammalian_phenotype	4
MP:0013121	MP:0013121	testicular swellings	Mammalian_phenotype	4
MP:0013122	MP:0013122	tail swellings	Mammalian_phenotype	4
MP:0013123	MP:0013123	head/neck swellings	Mammalian_phenotype	4
MP:0013124	MP:0013124	mouth swellings	Mammalian_phenotype	4
MP:0013125	MP:0013125	thorax swellings	Mammalian_phenotype	4
MP:0013126	MP:0013126	teat swellings	Mammalian_phenotype	4
MP:0013140	MP:0013140	excessive vocalization	Mammalian_phenotype	4
MP:0013143	MP:0013143	penis inflammation	Mammalian_phenotype	4
MP:0013144	MP:0013144	greasy skin	Mammalian_phenotype	4
MP:0013148	MP:0013148	mastitis	Mammalian_phenotype	4
MP:0013151	MP:0013151	abnormal incidence of induced tumors	Mammalian_phenotype	4
MP:0013152	MP:0013152	abnormal organ/body region tumor incidence	Mammalian_phenotype	4
MP:0013160	MP:0013160	impaired muscle regeneration	Mammalian_phenotype	4
MP:0013161	MP:0013161	improved muscle regeneration	Mammalian_phenotype	4
MP:0013162	MP:0013162	abnormal thyroid gland isthmus morphology	Mammalian_phenotype	4
MP:0020001	MP:0020001	decreased response to antigen	Mammalian_phenotype	4
MP:0020002	MP:0020002	increased response to antigen	Mammalian_phenotype	4
MP:0020012	MP:0020012	abnormal arylsulphatase activity	Mammalian_phenotype	4
MP:0020015	MP:0020015	abnormal aldehyde dehydrogenase activity	Mammalian_phenotype	4
MP:0020018	MP:0020018	abnormal phenylalanine decarboxylase activity	Mammalian_phenotype	4
MP:0020021	MP:0020021	abnormal delta-aminolaevulinate dehydratase activity	Mammalian_phenotype	4
MP:0020026	MP:0020026	abnormal aldehyde oxidase activity	Mammalian_phenotype	4
MP:0020029	MP:0020029	abnormal cholinesterase activity	Mammalian_phenotype	4
MP:0020035	MP:0020035	abnormal coumarin hydroxylase activity	Mammalian_phenotype	4
MP:0020042	MP:0020042	abnormal glucose-6-phosphate dehydrogenase activity	Mammalian_phenotype	4
MP:0020045	MP:0020045	abnormal tyrosine aminotransferase activity	Mammalian_phenotype	4
MP:0020048	MP:0020048	abnormal maltase activity	Mammalian_phenotype	4
MP:0020051	MP:0020051	abnormal procollagen-proline 4-dioxygenase activity	Mammalian_phenotype	4
MP:0020054	MP:0020054	abnormal beta-glucuronidase activity	Mammalian_phenotype	4
MP:0020060	MP:0020060	abnormal hypoxanthine phosphoribosyltransferase activity	Mammalian_phenotype	4
MP:0020063	MP:0020063	abnormal thiopurine S-methyltransferase activity	Mammalian_phenotype	4
MP:0020073	MP:0020073	abnormal tyrosine hydroxylase activity	Mammalian_phenotype	4
MP:0020081	MP:0020081	degenerative myocardium	Mammalian_phenotype	4
MP:0020087	MP:0020087	increased susceptibility to non-insulin-dependent diabetes	Mammalian_phenotype	4
MP:0020088	MP:0020088	decreased susceptibility to non-insulin-dependent diabetes	Mammalian_phenotype	4
MP:0020091	MP:0020091	abnormal susceptibility to diet-induced non-insulin dependent diabetes	Mammalian_phenotype	4
MP:0020093	MP:0020093	decreased susceptibility to aortic cartilaginous metaplasia	Mammalian_phenotype	4
MP:0020094	MP:0020094	increased susceptibility to aortic cartilaginous metaplasia	Mammalian_phenotype	4
MP:0020096	MP:0020096	high mean heart rate adaptation	Mammalian_phenotype	4
MP:0020097	MP:0020097	low mean heart rate adaptation	Mammalian_phenotype	4
MP:0020099	MP:0020099	increased susceptibility to diet-induced aortic fatty streak lesions	Mammalian_phenotype	4
MP:0020100	MP:0020100	decreased susceptibility to diet-induced aortic fatty streak lesions	Mammalian_phenotype	4
MP:0020101	MP:0020101	abnormal hepatic glucose production	Mammalian_phenotype	4
MP:0020104	MP:0020104	abnormal nitrate level	Mammalian_phenotype	4
MP:0020107	MP:0020107	abnormal nitrite level	Mammalian_phenotype	4
MP:0020118	MP:0020118	abnormal alcohol dehydrogenase activity	Mammalian_phenotype	4
MP:0020121	MP:0020121	abnormal tyrosine 3-monooxygenase activity	Mammalian_phenotype	4
MP:0020130	MP:0020130	abnormal total fat pad weight	Mammalian_phenotype	4
MP:0020147	MP:0020147	abnormal defecation amount	Mammalian_phenotype	4
MP:0020149	MP:0020149	abnormal mortality induced by ionizing radiation	Mammalian_phenotype	4
MP:0020154	MP:0020154	impaired humoral immune response	Mammalian_phenotype	4
MP:0020155	MP:0020155	enhanced humoral immune response	Mammalian_phenotype	4
MP:0020181	MP:0020181	abnormal body weight	Mammalian_phenotype	4
MP:0020188	MP:0020188	abnormal classified tumor incidence	Mammalian_phenotype	4
MP:0000010	MP:0000010	abnormal abdominal fat pad morphology	Mammalian_phenotype	4
MP:0000028	MP:0000028	abnormal pars superior vestibularis morphology	Mammalian_phenotype	4
MP:0000030	MP:0000030	abnormal tympanic ring morphology	Mammalian_phenotype	4
MP:0000031	MP:0000031	abnormal cochlea morphology	Mammalian_phenotype	4
MP:0000034	MP:0000034	abnormal inner ear vestibule morphology	Mammalian_phenotype	4
MP:0000035	MP:0000035	abnormal membranous labyrinth morphology	Mammalian_phenotype	4
MP:0000039	MP:0000039	abnormal otic capsule morphology	Mammalian_phenotype	4
MP:0000045	MP:0000045	abnormal hair cell morphology	Mammalian_phenotype	4
MP:0000046	MP:0000046	abnormal sulcus ampullaris morphology	Mammalian_phenotype	4
MP:0000060	MP:0000060	delayed bone ossification	Mammalian_phenotype	4
MP:0000061	MP:0000061	fragile skeleton	Mammalian_phenotype	4
MP:0000065	MP:0000065	abnormal bone marrow cavity morphology	Mammalian_phenotype	4
MP:0000071	MP:0000071	axial skeleton hypoplasia	Mammalian_phenotype	4
MP:0000084	MP:0000084	abnormal fontanelle morphology	Mammalian_phenotype	4
MP:0000116	MP:0000116	abnormal tooth development	Mammalian_phenotype	4
MP:0000130	MP:0000130	abnormal trabecular bone morphology	Mammalian_phenotype	4
MP:0000131	MP:0000131	abnormal long bone epiphysis morphology	Mammalian_phenotype	4
MP:0000164	MP:0000164	abnormal cartilage development	Mammalian_phenotype	4
MP:0000166	MP:0000166	abnormal chondrocyte morphology	Mammalian_phenotype	4
MP:0000168	MP:0000168	abnormal bone marrow development	Mammalian_phenotype	4
MP:0000172	MP:0000172	abnormal bone marrow cell number	Mammalian_phenotype	4
MP:0000188	MP:0000188	abnormal circulating glucose level	Mammalian_phenotype	4
MP:0000192	MP:0000192	abnormal mineral level	Mammalian_phenotype	4
MP:0000229	MP:0000229	abnormal megakaryocyte differentiation	Mammalian_phenotype	4
MP:0000233	MP:0000233	abnormal blood flow velocity	Mammalian_phenotype	4
MP:0000242	MP:0000242	impaired fertilization	Mammalian_phenotype	4
MP:0000250	MP:0000250	abnormal vasoconstriction	Mammalian_phenotype	4
MP:0000255	MP:0000255	vasculature congestion	Mammalian_phenotype	4
MP:0000259	MP:0000259	abnormal vascular development	Mammalian_phenotype	4
MP:0000265	MP:0000265	atretic vasculature	Mammalian_phenotype	4
MP:0000267	MP:0000267	abnormal heart development	Mammalian_phenotype	4
MP:0000277	MP:0000277	abnormal heart shape	Mammalian_phenotype	4
MP:0000278	MP:0000278	abnormal myocardial fiber morphology	Mammalian_phenotype	4
MP:0000285	MP:0000285	abnormal heart valve morphology	Mammalian_phenotype	4
MP:0000288	MP:0000288	abnormal pericardium morphology	Mammalian_phenotype	4
MP:0000304	MP:0000304	abnormal cardiac stroke volume	Mammalian_phenotype	4
MP:0000327	MP:0000327	hemosiderinuria	Mammalian_phenotype	4
MP:0000341	MP:0000341	abnormal bile color	Mammalian_phenotype	4
MP:0000351	MP:0000351	increased cell proliferation	Mammalian_phenotype	4
MP:0000352	MP:0000352	decreased cell proliferation	Mammalian_phenotype	4
MP:0000376	MP:0000376	folliculitis	Mammalian_phenotype	4
MP:0000378	MP:0000378	absent hair follicles	Mammalian_phenotype	4
MP:0000379	MP:0000379	decreased hair follicle number	Mammalian_phenotype	4
MP:0000380	MP:0000380	small hair follicles	Mammalian_phenotype	4
MP:0000381	MP:0000381	enlarged hair follicles	Mammalian_phenotype	4
MP:0000384	MP:0000384	distorted hair follicle pattern	Mammalian_phenotype	4
MP:0000385	MP:0000385	distended hair follicles	Mammalian_phenotype	4
MP:0000393	MP:0000393	persistent hair follicle morphogenesis	Mammalian_phenotype	4
MP:0000397	MP:0000397	abnormal guard hair morphology	Mammalian_phenotype	4
MP:0000400	MP:0000400	abnormal awl hair morphology	Mammalian_phenotype	4
MP:0000402	MP:0000402	abnormal zigzag hair morphology	Mammalian_phenotype	4
MP:0000405	MP:0000405	abnormal auchene hair morphology	Mammalian_phenotype	4
MP:0000407	MP:0000407	abnormal duvet hair morphology	Mammalian_phenotype	4
MP:0000423	MP:0000423	delayed hair regrowth	Mammalian_phenotype	4
MP:0000425	MP:0000425	loss of eyelid cilia	Mammalian_phenotype	4
MP:0000468	MP:0000468	abnormal esophageal epithelium morphology	Mammalian_phenotype	4
MP:0000474	MP:0000474	abnormal foregut morphology	Mammalian_phenotype	4
MP:0000488	MP:0000488	abnormal intestinal epithelium morphology	Mammalian_phenotype	4
MP:0000489	MP:0000489	abnormal large intestine morphology	Mammalian_phenotype	4
MP:0000496	MP:0000496	abnormal small intestine morphology	Mammalian_phenotype	4
MP:0000497	MP:0000497	abnormal small intestine placement	Mammalian_phenotype	4
MP:0000501	MP:0000501	abnormal digestive secretion	Mammalian_phenotype	4
MP:0000512	MP:0000512	intestinal ulcer	Mammalian_phenotype	4
MP:0000520	MP:0000520	absent kidney	Mammalian_phenotype	4
MP:0000521	MP:0000521	abnormal kidney cortex morphology	Mammalian_phenotype	4
MP:0000525	MP:0000525	renal tubular acidosis	Mammalian_phenotype	4
MP:0000527	MP:0000527	abnormal kidney development	Mammalian_phenotype	4
MP:0000530	MP:0000530	abnormal kidney blood vessel morphology	Mammalian_phenotype	4
MP:0000531	MP:0000531	right pulmonary isomerism	Mammalian_phenotype	4
MP:0000533	MP:0000533	kidney hemorrhage	Mammalian_phenotype	4
MP:0000536	MP:0000536	hydroureter	Mammalian_phenotype	4
MP:0000539	MP:0000539	distended urinary bladder	Mammalian_phenotype	4
MP:0000540	MP:0000540	abnormal urinary bladder urothelium morphology	Mammalian_phenotype	4
MP:0000551	MP:0000551	absent forelimb	Mammalian_phenotype	4
MP:0000557	MP:0000557	absent hindlimb	Mammalian_phenotype	4
MP:0000573	MP:0000573	enlarged hind paws	Mammalian_phenotype	4
MP:0000574	MP:0000574	abnormal foot pad morphology	Mammalian_phenotype	4
MP:0000576	MP:0000576	clubfoot	Mammalian_phenotype	4
MP:0000578	MP:0000578	ulcerated paws	Mammalian_phenotype	4
MP:0000580	MP:0000580	deformed nails	Mammalian_phenotype	4
MP:0000582	MP:0000582	toenail hyperkeratosis	Mammalian_phenotype	4
MP:0000592	MP:0000592	short tail	Mammalian_phenotype	4
MP:0000596	MP:0000596	abnormal liver development	Mammalian_phenotype	4
MP:0000603	MP:0000603	pale liver	Mammalian_phenotype	4
MP:0000610	MP:0000610	cholestasis	Mammalian_phenotype	4
MP:0000611	MP:0000611	jaundice	Mammalian_phenotype	4
MP:0000614	MP:0000614	absent salivary gland	Mammalian_phenotype	4
MP:0000617	MP:0000617	increased salivary gland mucosal cell number	Mammalian_phenotype	4
MP:0000618	MP:0000618	small salivary gland	Mammalian_phenotype	4
MP:0000619	MP:0000619	salivary gland epithelial hyperplasia	Mammalian_phenotype	4
MP:0000622	MP:0000622	increased salivation	Mammalian_phenotype	4
MP:0000623	MP:0000623	decreased salivation	Mammalian_phenotype	4
MP:0000628	MP:0000628	abnormal mammary gland development	Mammalian_phenotype	4
MP:0000630	MP:0000630	mammary gland hyperplasia	Mammalian_phenotype	4
MP:0000632	MP:0000632	abnormal pineal gland morphology	Mammalian_phenotype	4
MP:0000633	MP:0000633	abnormal pituitary gland morphology	Mammalian_phenotype	4
MP:0000642	MP:0000642	enlarged adrenal glands	Mammalian_phenotype	4
MP:0000648	MP:0000648	absent sebaceous gland	Mammalian_phenotype	4
MP:0000649	MP:0000649	sebaceous gland atrophy	Mammalian_phenotype	4
MP:0000652	MP:0000652	enlarged sebaceous gland	Mammalian_phenotype	4
MP:0000654	MP:0000654	absent sex gland	Mammalian_phenotype	4
MP:0000655	MP:0000655	dilated sex gland	Mammalian_phenotype	4
MP:0000675	MP:0000675	abnormal eccrine gland morphology	Mammalian_phenotype	4
MP:0000679	MP:0000679	increased percent water in carcass	Mammalian_phenotype	4
MP:0000680	MP:0000680	absent parathyroid glands	Mammalian_phenotype	4
MP:0000683	MP:0000683	decreased percent water in carcass	Mammalian_phenotype	4
MP:0000729	MP:0000729	abnormal myogenesis	Mammalian_phenotype	4
MP:0000730	MP:0000730	increased satellite cell number	Mammalian_phenotype	4
MP:0000731	MP:0000731	increased collagen deposition in the muscles	Mammalian_phenotype	4
MP:0000736	MP:0000736	delayed muscle development	Mammalian_phenotype	4
MP:0000738	MP:0000738	impaired muscle contractility	Mammalian_phenotype	4
MP:0000741	MP:0000741	impaired contractility of urinary bladder detrusor smooth muscle	Mammalian_phenotype	4
MP:0000743	MP:0000743	muscle spasm	Mammalian_phenotype	4
MP:0000748	MP:0000748	progressive muscle weakness	Mammalian_phenotype	4
MP:0000757	MP:0000757	herniated abdominal wall	Mammalian_phenotype	4
MP:0000771	MP:0000771	abnormal brain size	Mammalian_phenotype	4
MP:0000783	MP:0000783	abnormal forebrain morphology	Mammalian_phenotype	4
MP:0000841	MP:0000841	abnormal hindbrain morphology	Mammalian_phenotype	4
MP:0000877	MP:0000877	abnormal Purkinje cell morphology	Mammalian_phenotype	4
MP:0000897	MP:0000897	abnormal midbrain morphology	Mammalian_phenotype	4
MP:0000913	MP:0000913	abnormal brain development	Mammalian_phenotype	4
MP:0000921	MP:0000921	demyelination	Mammalian_phenotype	4
MP:0000937	MP:0000937	abnormal motor neuron morphology	Mammalian_phenotype	4
MP:0000940	MP:0000940	abnormal motor neuron innervation pattern	Mammalian_phenotype	4
MP:0000947	MP:0000947	convulsive seizures	Mammalian_phenotype	4
MP:0000948	MP:0000948	nonconvulsive seizures	Mammalian_phenotype	4
MP:0000950	MP:0000950	abnormal seizure response to pharmacological agent	Mammalian_phenotype	4
MP:0000951	MP:0000951	sporadic seizures	Mammalian_phenotype	4
MP:0000952	MP:0000952	abnormal CNS glial cell morphology	Mammalian_phenotype	4
MP:0000956	MP:0000956	decreased spinal cord size	Mammalian_phenotype	4
MP:0000958	MP:0000958	peripheral nervous system degeneration	Mammalian_phenotype	4
MP:0000959	MP:0000959	abnormal somatic sensory system morphology	Mammalian_phenotype	4
MP:0000965	MP:0000965	abnormal sensory neuron morphology	Mammalian_phenotype	4
MP:0000968	MP:0000968	abnormal sensory neuron innervation pattern	Mammalian_phenotype	4
MP:0000990	MP:0000990	abnormal skeletal muscle mechanoreceptor morphology	Mammalian_phenotype	4
MP:0000997	MP:0000997	abnormal joint capsule morphology	Mammalian_phenotype	4
MP:0001007	MP:0001007	abnormal sympathetic system morphology	Mammalian_phenotype	4
MP:0001026	MP:0001026	abnormal adrenergic neuron morphology	Mammalian_phenotype	4
MP:0001032	MP:0001032	abnormal peptidergic neuron morphology	Mammalian_phenotype	4
MP:0001033	MP:0001033	abnormal parasympathetic system morphology	Mammalian_phenotype	4
MP:0001038	MP:0001038	abnormal cholinergic neuron morphology	Mammalian_phenotype	4
MP:0001044	MP:0001044	abnormal enteric nervous system morphology	Mammalian_phenotype	4
MP:0001046	MP:0001046	abnormal enteric neuron morphology	Mammalian_phenotype	4
MP:0001051	MP:0001051	abnormal somatic motor system morphology	Mammalian_phenotype	4
MP:0001052	MP:0001052	abnormal innervation pattern to muscle	Mammalian_phenotype	4
MP:0001056	MP:0001056	abnormal cranial nerve morphology	Mammalian_phenotype	4
MP:0001077	MP:0001077	abnormal spinal nerve morphology	Mammalian_phenotype	4
MP:0001081	MP:0001081	abnormal cranial ganglia morphology	Mammalian_phenotype	4
MP:0001105	MP:0001105	abnormal PNS glial cell morphology	Mammalian_phenotype	4
MP:0001126	MP:0001126	abnormal ovary morphology	Mammalian_phenotype	4
MP:0001133	MP:0001133	impaired luteal cell differentiation	Mammalian_phenotype	4
MP:0001146	MP:0001146	abnormal testis morphology	Mammalian_phenotype	4
MP:0001156	MP:0001156	abnormal spermatogenesis	Mammalian_phenotype	4
MP:0001158	MP:0001158	abnormal prostate gland morphology	Mammalian_phenotype	4
MP:0001169	MP:0001169	abnormal bulbourethral gland morphology	Mammalian_phenotype	4
MP:0001176	MP:0001176	abnormal lung development	Mammalian_phenotype	4
MP:0001181	MP:0001181	absent lungs	Mammalian_phenotype	4
MP:0001190	MP:0001190	reddish skin	Mammalian_phenotype	4
MP:0001192	MP:0001192	scaly skin	Mammalian_phenotype	4
MP:0001193	MP:0001193	psoriasis	Mammalian_phenotype	4
MP:0001195	MP:0001195	flaky skin	Mammalian_phenotype	4
MP:0001196	MP:0001196	shiny skin	Mammalian_phenotype	4
MP:0001198	MP:0001198	tight skin	Mammalian_phenotype	4
MP:0001199	MP:0001199	thin skin	Mammalian_phenotype	4
MP:0001200	MP:0001200	thick skin	Mammalian_phenotype	4
MP:0001201	MP:0001201	translucent skin	Mammalian_phenotype	4
MP:0001208	MP:0001208	blistering	Mammalian_phenotype	4
MP:0001210	MP:0001210	skin ridges	Mammalian_phenotype	4
MP:0001211	MP:0001211	wrinkled skin	Mammalian_phenotype	4
MP:0001212	MP:0001212	skin lesions	Mammalian_phenotype	4
MP:0001214	MP:0001214	skin hyperplasia	Mammalian_phenotype	4
MP:0001215	MP:0001215	skin hypoplasia	Mammalian_phenotype	4
MP:0001217	MP:0001217	absent epidermis	Mammalian_phenotype	4
MP:0001218	MP:0001218	thin epidermis	Mammalian_phenotype	4
MP:0001219	MP:0001219	thick epidermis	Mammalian_phenotype	4
MP:0001220	MP:0001220	epidermal necrosis	Mammalian_phenotype	4
MP:0001221	MP:0001221	epidermal atrophy	Mammalian_phenotype	4
MP:0001222	MP:0001222	epidermal hyperplasia	Mammalian_phenotype	4
MP:0001224	MP:0001224	abnormal keratinocyte apoptosis	Mammalian_phenotype	4
MP:0001230	MP:0001230	epidermal desquamation	Mammalian_phenotype	4
MP:0001231	MP:0001231	abnormal epidermis stratum basale morphology	Mammalian_phenotype	4
MP:0001233	MP:0001233	abnormal epidermis suprabasal layer morphology	Mammalian_phenotype	4
MP:0001236	MP:0001236	abnormal epidermis stratum spinosum morphology	Mammalian_phenotype	4
MP:0001239	MP:0001239	abnormal epidermis stratum granulosum morphology	Mammalian_phenotype	4
MP:0001240	MP:0001240	abnormal epidermis stratum corneum morphology	Mammalian_phenotype	4
MP:0001244	MP:0001244	thin dermal layer	Mammalian_phenotype	4
MP:0001245	MP:0001245	thick dermal layer	Mammalian_phenotype	4
MP:0001246	MP:0001246	mixed cellular infiltration to dermis	Mammalian_phenotype	4
MP:0001247	MP:0001247	dermal cysts	Mammalian_phenotype	4
MP:0001253	MP:0001253	abnormal body height	Mammalian_phenotype	4
MP:0001256	MP:0001256	abnormal body length	Mammalian_phenotype	4
MP:0001259	MP:0001259	abnormal body weight	Mammalian_phenotype	4
MP:0001264	MP:0001264	increased body size	Mammalian_phenotype	4
MP:0001265	MP:0001265	decreased body size	Mammalian_phenotype	4
MP:0001272	MP:0001272	increased metastatic potential	Mammalian_phenotype	4
MP:0001273	MP:0001273	decreased metastatic potential	Mammalian_phenotype	4
MP:0001274	MP:0001274	curly vibrissae	Mammalian_phenotype	4
MP:0001277	MP:0001277	tangled vibrissae	Mammalian_phenotype	4
MP:0001278	MP:0001278	kinked vibrissae	Mammalian_phenotype	4
MP:0001279	MP:0001279	wavy vibrissae	Mammalian_phenotype	4
MP:0001280	MP:0001280	loss of vibrissae	Mammalian_phenotype	4
MP:0001281	MP:0001281	increased vibrissae length	Mammalian_phenotype	4
MP:0001282	MP:0001282	short vibrissae	Mammalian_phenotype	4
MP:0001283	MP:0001283	sparse vibrissae	Mammalian_phenotype	4
MP:0001284	MP:0001284	absent vibrissae	Mammalian_phenotype	4
MP:0001289	MP:0001289	persistence of hyaloid vascular system	Mammalian_phenotype	4
MP:0001296	MP:0001296	macrophthalmia	Mammalian_phenotype	4
MP:0001297	MP:0001297	microphthalmia	Mammalian_phenotype	4
MP:0001300	MP:0001300	ocular hypertelorism	Mammalian_phenotype	4
MP:0001302	MP:0001302	eyelids open at birth	Mammalian_phenotype	4
MP:0001303	MP:0001303	abnormal lens morphology	Mammalian_phenotype	4
MP:0001310	MP:0001310	abnormal conjunctiva morphology	Mammalian_phenotype	4
MP:0001312	MP:0001312	abnormal cornea morphology	Mammalian_phenotype	4
MP:0001330	MP:0001330	abnormal optic nerve morphology	Mammalian_phenotype	4
MP:0001341	MP:0001341	absent eyelids	Mammalian_phenotype	4
MP:0001343	MP:0001343	pronounced eyelids	Mammalian_phenotype	4
MP:0001344	MP:0001344	blepharoptosis	Mammalian_phenotype	4
MP:0001353	MP:0001353	increased aggression towards mice	Mammalian_phenotype	4
MP:0001355	MP:0001355	submission towards male mice	Mammalian_phenotype	4
MP:0001360	MP:0001360	abnormal social investigation	Mammalian_phenotype	4
MP:0001378	MP:0001378	abnormal ejaculation	Mammalian_phenotype	4
MP:0001379	MP:0001379	abnormal penile erection	Mammalian_phenotype	4
MP:0001400	MP:0001400	hyperresponsive	Mammalian_phenotype	4
MP:0001408	MP:0001408	stereotypic behavior	Mammalian_phenotype	4
MP:0001412	MP:0001412	excessive scratching	Mammalian_phenotype	4
MP:0001413	MP:0001413	abnormal response to new environment	Mammalian_phenotype	4
MP:0001422	MP:0001422	abnormal drinking behavior	Mammalian_phenotype	4
MP:0001425	MP:0001425	abnormal alcohol consumption	Mammalian_phenotype	4
MP:0001429	MP:0001429	dehydration	Mammalian_phenotype	4
MP:0001431	MP:0001431	abnormal eating behavior	Mammalian_phenotype	4
MP:0001441	MP:0001441	increased grooming behavior	Mammalian_phenotype	4
MP:0001442	MP:0001442	decreased grooming behavior	Mammalian_phenotype	4
MP:0001443	MP:0001443	poor grooming	Mammalian_phenotype	4
MP:0001448	MP:0001448	abnormal huddling behavior	Mammalian_phenotype	4
MP:0001458	MP:0001458	abnormal object recognition memory	Mammalian_phenotype	4
MP:0001463	MP:0001463	abnormal spatial learning	Mammalian_phenotype	4
MP:0001468	MP:0001468	abnormal temporal memory	Mammalian_phenotype	4
MP:0001501	MP:0001501	abnormal sleep pattern	Mammalian_phenotype	4
MP:0001504	MP:0001504	abnormal posture	Mammalian_phenotype	4
MP:0001510	MP:0001510	abnormal coat appearance	Mammalian_phenotype	4
MP:0001516	MP:0001516	abnormal motor coordination/ balance	Mammalian_phenotype	4
MP:0001541	MP:0001541	abnormal osteoclast physiology	Mammalian_phenotype	4
MP:0001547	MP:0001547	abnormal lipid level	Mammalian_phenotype	4
MP:0001560	MP:0001560	abnormal circulating insulin level	Mammalian_phenotype	4
MP:0001565	MP:0001565	abnormal circulating phosphate level	Mammalian_phenotype	4
MP:0001569	MP:0001569	abnormal circulating bilirubin level	Mammalian_phenotype	4
MP:0001570	MP:0001570	abnormal circulating enzyme level	Mammalian_phenotype	4
MP:0001574	MP:0001574	abnormal oxygen level	Mammalian_phenotype	4
MP:0001575	MP:0001575	cyanosis	Mammalian_phenotype	4
MP:0001598	MP:0001598	abnormal blood viscosity	Mammalian_phenotype	4
MP:0001599	MP:0001599	abnormal blood volume	Mammalian_phenotype	4
MP:0001619	MP:0001619	abnormal vascular permeability	Mammalian_phenotype	4
MP:0001627	MP:0001627	abnormal cardiac output	Mammalian_phenotype	4
MP:0001629	MP:0001629	abnormal heart rate	Mammalian_phenotype	4
MP:0001633	MP:0001633	poor circulation	Mammalian_phenotype	4
MP:0001636	MP:0001636	irregular heartbeat	Mammalian_phenotype	4
MP:0001648	MP:0001648	abnormal apoptosis	Mammalian_phenotype	4
MP:0001651	MP:0001651	necrosis	Mammalian_phenotype	4
MP:0001653	MP:0001653	gastric necrosis	Mammalian_phenotype	4
MP:0001654	MP:0001654	hepatic necrosis	Mammalian_phenotype	4
MP:0001666	MP:0001666	abnormal intestinal absorption	Mammalian_phenotype	4
MP:0001671	MP:0001671	abnormal vitamin absorption	Mammalian_phenotype	4
MP:0001674	MP:0001674	abnormal triploblastic development	Mammalian_phenotype	4
MP:0001688	MP:0001688	abnormal somite development	Mammalian_phenotype	4
MP:0001695	MP:0001695	abnormal gastrulation	Mammalian_phenotype	4
MP:0001704	MP:0001704	abnormal dorsal-ventral axis patterning	Mammalian_phenotype	4
MP:0001705	MP:0001705	abnormal proximal-distal axis patterning	Mammalian_phenotype	4
MP:0001706	MP:0001706	abnormal left-right axis patterning	Mammalian_phenotype	4
MP:0001711	MP:0001711	abnormal placenta morphology	Mammalian_phenotype	4
MP:0001718	MP:0001718	abnormal visceral yolk sac morphology	Mammalian_phenotype	4
MP:0001724	MP:0001724	abnormal extraembryonic endoderm formation	Mammalian_phenotype	4
MP:0001725	MP:0001725	abnormal umbilical cord morphology	Mammalian_phenotype	4
MP:0001726	MP:0001726	abnormal allantois morphology	Mammalian_phenotype	4
MP:0001732	MP:0001732	postnatal growth retardation	Mammalian_phenotype	4
MP:0001739	MP:0001739	abnormal adrenal gland secretion	Mammalian_phenotype	4
MP:0001746	MP:0001746	abnormal pituitary secretion	Mammalian_phenotype	4
MP:0001752	MP:0001752	abnormal hypothalamus secretion	Mammalian_phenotype	4
MP:0001758	MP:0001758	abnormal urine glucose level	Mammalian_phenotype	4
MP:0001760	MP:0001760	abnormal urine enzyme level	Mammalian_phenotype	4
MP:0001761	MP:0001761	abnormal urination pattern	Mammalian_phenotype	4
MP:0001762	MP:0001762	polyuria	Mammalian_phenotype	4
MP:0001778	MP:0001778	abnormal brown adipose tissue amount	Mammalian_phenotype	4
MP:0001781	MP:0001781	abnormal white adipose tissue amount	Mammalian_phenotype	4
MP:0001785	MP:0001785	edema	Mammalian_phenotype	4
MP:0001786	MP:0001786	skin edema	Mammalian_phenotype	4
MP:0001792	MP:0001792	impaired wound healing	Mammalian_phenotype	4
MP:0001793	MP:0001793	altered susceptibility to infection	Mammalian_phenotype	4
MP:0001836	MP:0001836	abnormal antigen presentation via MHC class I	Mammalian_phenotype	4
MP:0001846	MP:0001846	increased inflammatory response	Mammalian_phenotype	4
MP:0001858	MP:0001858	intestinal inflammation	Mammalian_phenotype	4
MP:0001859	MP:0001859	kidney inflammation	Mammalian_phenotype	4
MP:0001860	MP:0001860	liver inflammation	Mammalian_phenotype	4
MP:0001863	MP:0001863	vascular inflammation	Mammalian_phenotype	4
MP:0001868	MP:0001868	ovary inflammation	Mammalian_phenotype	4
MP:0001869	MP:0001869	pancreas inflammation	Mammalian_phenotype	4
MP:0001870	MP:0001870	salivary gland inflammation	Mammalian_phenotype	4
MP:0001875	MP:0001875	testis inflammation	Mammalian_phenotype	4
MP:0001876	MP:0001876	decreased inflammatory response	Mammalian_phenotype	4
MP:0001882	MP:0001882	abnormal lactation	Mammalian_phenotype	4
MP:0001890	MP:0001890	anencephaly	Mammalian_phenotype	4
MP:0001900	MP:0001900	impaired synaptic plasticity	Mammalian_phenotype	4
MP:0001909	MP:0001909	reduced NMDA receptor mediated synaptic activity in barrel cortex	Mammalian_phenotype	4
MP:0001912	MP:0001912	increased cerebrospinal fluid production	Mammalian_phenotype	4
MP:0001913	MP:0001913	decreased cerebrospinal fluid production	Mammalian_phenotype	4
MP:0001914	MP:0001914	hemorrhage	Mammalian_phenotype	4
MP:0001921	MP:0001921	reduced fertility	Mammalian_phenotype	4
MP:0001922	MP:0001922	reduced male fertility	Mammalian_phenotype	4
MP:0001923	MP:0001923	reduced female fertility	Mammalian_phenotype	4
MP:0001924	MP:0001924	infertility	Mammalian_phenotype	4
MP:0001925	MP:0001925	male infertility	Mammalian_phenotype	4
MP:0001926	MP:0001926	female infertility	Mammalian_phenotype	4
MP:0001928	MP:0001928	abnormal ovulation	Mammalian_phenotype	4
MP:0001930	MP:0001930	abnormal meiosis	Mammalian_phenotype	4
MP:0001931	MP:0001931	abnormal oogenesis	Mammalian_phenotype	4
MP:0001933	MP:0001933	abnormal litter size	Mammalian_phenotype	4
MP:0001942	MP:0001942	abnormal lung volume	Mammalian_phenotype	4
MP:0001948	MP:0001948	vesicoureteral reflux	Mammalian_phenotype	4
MP:0001950	MP:0001950	abnormal respiratory sounds	Mammalian_phenotype	4
MP:0001953	MP:0001953	respiratory failure	Mammalian_phenotype	4
MP:0001961	MP:0001961	abnormal reflex	Mammalian_phenotype	4
MP:0002001	MP:0002001	blindness	Mammalian_phenotype	4
MP:0002015	MP:0002015	epithelioid cysts	Mammalian_phenotype	4
MP:0002020	MP:0002020	increased tumor incidence	Mammalian_phenotype	4
MP:0002052	MP:0002052	decreased tumor incidence	Mammalian_phenotype	4
MP:0002059	MP:0002059	abnormal seminal vesicle morphology	Mammalian_phenotype	4
MP:0002061	MP:0002061	abnormal aggression-related behavior	Mammalian_phenotype	4
MP:0002062	MP:0002062	abnormal associative learning	Mammalian_phenotype	4
MP:0002065	MP:0002065	abnormal fear/anxiety-related behavior	Mammalian_phenotype	4
MP:0002068	MP:0002068	abnormal parental behavior	Mammalian_phenotype	4
MP:0002110	MP:0002110	abnormal digit morphology	Mammalian_phenotype	4
MP:0002123	MP:0002123	abnormal hematopoiesis	Mammalian_phenotype	4
MP:0002151	MP:0002151	abnormal neural tube morphology/development	Mammalian_phenotype	4
MP:0002183	MP:0002183	gliosis	Mammalian_phenotype	4
MP:0002189	MP:0002189	abnormal myocardial trabeculae morphology	Mammalian_phenotype	4
MP:0002191	MP:0002191	abnormal artery morphology	Mammalian_phenotype	4
MP:0002199	MP:0002199	abnormal brain commissure morphology	Mammalian_phenotype	4
MP:0002200	MP:0002200	abnormal brain ventricular system morphology	Mammalian_phenotype	4
MP:0002204	MP:0002204	abnormal neurotransmitter level	Mammalian_phenotype	4
MP:0002206	MP:0002206	abnormal CNS synaptic transmission	Mammalian_phenotype	4
MP:0002208	MP:0002208	abnormal germ cell morphology	Mammalian_phenotype	4
MP:0002211	MP:0002211	abnormal primary sex determination	Mammalian_phenotype	4
MP:0002212	MP:0002212	abnormal secondary sex determination	Mammalian_phenotype	4
MP:0002214	MP:0002214	streak gonad	Mammalian_phenotype	4
MP:0002221	MP:0002221	abnormal lymph organ size	Mammalian_phenotype	4
MP:0002250	MP:0002250	abnormal hypopharynx morphology	Mammalian_phenotype	4
MP:0002251	MP:0002251	abnormal nasopharynx morphology	Mammalian_phenotype	4
MP:0002252	MP:0002252	abnormal oropharynx morphology	Mammalian_phenotype	4
MP:0002253	MP:0002253	abnormal pharyngeal muscle morphology	Mammalian_phenotype	4
MP:0002255	MP:0002255	abnormal glottis morphology	Mammalian_phenotype	4
MP:0002256	MP:0002256	abnormal laryngeal cartilage morphology	Mammalian_phenotype	4
MP:0002261	MP:0002261	abnormal laryngeal mucosa morphology	Mammalian_phenotype	4
MP:0002263	MP:0002263	abnormal laryngeal muscle morphology	Mammalian_phenotype	4
MP:0002276	MP:0002276	abnormal lung interstitium morphology	Mammalian_phenotype	4
MP:0002277	MP:0002277	abnormal respiratory mucosa morphology	Mammalian_phenotype	4
MP:0002284	MP:0002284	abnormal tracheal smooth muscle morphology	Mammalian_phenotype	4
MP:0002285	MP:0002285	abnormal tracheal ciliated epithelium morphology	Mammalian_phenotype	4
MP:0002292	MP:0002292	abnormal gestational length	Mammalian_phenotype	4
MP:0002310	MP:0002310	decreased susceptibility to hepatic steatosis	Mammalian_phenotype	4
MP:0002314	MP:0002314	abnormal respiratory mechanics	Mammalian_phenotype	4
MP:0002322	MP:0002322	abnormal respiratory transport	Mammalian_phenotype	4
MP:0002323	MP:0002323	decreased susceptibility to hyperlipidemia	Mammalian_phenotype	4
MP:0002327	MP:0002327	abnormal respiratory function	Mammalian_phenotype	4
MP:0002329	MP:0002329	abnormal blood gas level	Mammalian_phenotype	4
MP:0002339	MP:0002339	abnormal lymph node morphology	Mammalian_phenotype	4
MP:0002349	MP:0002349	abnormal afferent lymphatic vessel morphology	Mammalian_phenotype	4
MP:0002350	MP:0002350	abnormal efferent lymphatic vessel morphology	Mammalian_phenotype	4
MP:0002377	MP:0002377	abnormal mucosa-associated lymphoid tissue morphology	Mammalian_phenotype	4
MP:0002378	MP:0002378	abnormal gut-associated lymphoid tissue morphology	Mammalian_phenotype	4
MP:0002393	MP:0002393	abnormal bronchus-associated lymphoid tissue morphology	Mammalian_phenotype	4
MP:0002397	MP:0002397	abnormal bone marrow morphology	Mammalian_phenotype	4
MP:0002399	MP:0002399	abnormal pluripotent precursor cell morphology/development	Mammalian_phenotype	4
MP:0002413	MP:0002413	abnormal megakaryocyte progenitor cell morphology	Mammalian_phenotype	4
MP:0002414	MP:0002414	abnormal myeloblast morphology/development	Mammalian_phenotype	4
MP:0002416	MP:0002416	abnormal proerythroblast morphology	Mammalian_phenotype	4
MP:0002442	MP:0002442	abnormal leukocyte physiology	Mammalian_phenotype	4
MP:0002445	MP:0002445	abnormal mononuclear cell differentiation	Mammalian_phenotype	4
MP:0002450	MP:0002450	abnormal lymph organ development	Mammalian_phenotype	4
MP:0002451	MP:0002451	abnormal macrophage physiology	Mammalian_phenotype	4
MP:0002452	MP:0002452	abnormal professional antigen presenting cell physiology	Mammalian_phenotype	4
MP:0002453	MP:0002453	abnormal B lymphocyte antigen presentation	Mammalian_phenotype	4
MP:0002454	MP:0002454	abnormal macrophage antigen presentation	Mammalian_phenotype	4
MP:0002455	MP:0002455	abnormal dendritic cell antigen presentation	Mammalian_phenotype	4
MP:0002463	MP:0002463	abnormal neutrophil physiology	Mammalian_phenotype	4
MP:0002471	MP:0002471	abnormal complement pathway	Mammalian_phenotype	4
MP:0002490	MP:0002490	abnormal immunoglobulin level	Mammalian_phenotype	4
MP:0002498	MP:0002498	abnormal acute inflammation	Mammalian_phenotype	4
MP:0002499	MP:0002499	chronic inflammation	Mammalian_phenotype	4
MP:0002531	MP:0002531	abnormal type I hypersensitivity reaction	Mammalian_phenotype	4
MP:0002532	MP:0002532	abnormal type II hypersensitivity reaction	Mammalian_phenotype	4
MP:0002533	MP:0002533	abnormal type III hypersensitivity reaction	Mammalian_phenotype	4
MP:0002534	MP:0002534	abnormal type IV hypersensitivity reaction	Mammalian_phenotype	4
MP:0002553	MP:0002553	preference for addictive substance	Mammalian_phenotype	4
MP:0002554	MP:0002554	aversion to addictive substance	Mammalian_phenotype	4
MP:0002556	MP:0002556	abnormal cocaine consumption	Mammalian_phenotype	4
MP:0002558	MP:0002558	abnormal circadian period	Mammalian_phenotype	4
MP:0002559	MP:0002559	abnormal circadian persistence	Mammalian_phenotype	4
MP:0002561	MP:0002561	abnormal circadian phase	Mammalian_phenotype	4
MP:0002566	MP:0002566	abnormal sexual interaction	Mammalian_phenotype	4
MP:0002571	MP:0002571	senility	Mammalian_phenotype	4
MP:0002582	MP:0002582	disorganized extraembryonic tissue	Mammalian_phenotype	4
MP:0002628	MP:0002628	hepatic steatosis	Mammalian_phenotype	4
MP:0002635	MP:0002635	reduced sensorimotor gating	Mammalian_phenotype	4
MP:0002654	MP:0002654	spongiform encephalopathy	Mammalian_phenotype	4
MP:0002655	MP:0002655	abnormal keratinocyte morphology	Mammalian_phenotype	4
MP:0002656	MP:0002656	abnormal keratinocyte differentiation	Mammalian_phenotype	4
MP:0002657	MP:0002657	chondrodystrophy	Mammalian_phenotype	4
MP:0002658	MP:0002658	abnormal liver regeneration	Mammalian_phenotype	4
MP:0002673	MP:0002673	abnormal sperm number	Mammalian_phenotype	4
MP:0002683	MP:0002683	delayed fertility	Mammalian_phenotype	4
MP:0002685	MP:0002685	abnormal spermatogonia proliferation	Mammalian_phenotype	4
MP:0002691	MP:0002691	small stomach	Mammalian_phenotype	4
MP:0002694	MP:0002694	abnormal pancreas secretion	Mammalian_phenotype	4
MP:0002695	MP:0002695	abnormal circulating glucagon level	Mammalian_phenotype	4
MP:0002699	MP:0002699	abnormal vitreous body morphology	Mammalian_phenotype	4
MP:0002706	MP:0002706	abnormal kidney size	Mammalian_phenotype	4
MP:0002708	MP:0002708	nephrolithiasis	Mammalian_phenotype	4
MP:0002717	MP:0002717	abnormal male preputial gland morphology	Mammalian_phenotype	4
MP:0002724	MP:0002724	enhanced wound healing	Mammalian_phenotype	4
MP:0002725	MP:0002725	abnormal vein morphology	Mammalian_phenotype	4
MP:0002729	MP:0002729	abnormal inner ear canal morphology	Mammalian_phenotype	4
MP:0002750	MP:0002750	exophthalmos	Mammalian_phenotype	4
MP:0002758	MP:0002758	long tail	Mammalian_phenotype	4
MP:0002768	MP:0002768	small adrenal glands	Mammalian_phenotype	4
MP:0002772	MP:0002772	brachypodia	Mammalian_phenotype	4
MP:0002779	MP:0002779	abnormal sex gland secretion	Mammalian_phenotype	4
MP:0002791	MP:0002791	steatorrhea	Mammalian_phenotype	4
MP:0002792	MP:0002792	abnormal retinal vasculature morphology	Mammalian_phenotype	4
MP:0002794	MP:0002794	lenticonus	Mammalian_phenotype	4
MP:0002795	MP:0002795	dilated cardiomyopathy	Mammalian_phenotype	4
MP:0002802	MP:0002802	abnormal discrimination learning	Mammalian_phenotype	4
MP:0002804	MP:0002804	abnormal motor learning	Mammalian_phenotype	4
MP:0002808	MP:0002808	abnormal barbering behavior	Mammalian_phenotype	4
MP:0002809	MP:0002809	increased spinal cord size	Mammalian_phenotype	4
MP:0002823	MP:0002823	abnormal rib development	Mammalian_phenotype	4
MP:0002825	MP:0002825	abnormal notochord morphology	Mammalian_phenotype	4
MP:0002830	MP:0002830	gallstones	Mammalian_phenotype	4
MP:0002836	MP:0002836	abnormal chorion morphology	Mammalian_phenotype	4
MP:0002837	MP:0002837	dystrophic cardiac calcinosis	Mammalian_phenotype	4
MP:0002842	MP:0002842	increased systemic arterial blood pressure	Mammalian_phenotype	4
MP:0002843	MP:0002843	decreased systemic arterial blood pressure	Mammalian_phenotype	4
MP:0002847	MP:0002847	abnormal renal glomerular filtration rate	Mammalian_phenotype	4
MP:0002861	MP:0002861	abnormal tail bud morphology	Mammalian_phenotype	4
MP:0002864	MP:0002864	abnormal ocular fundus morphology	Mammalian_phenotype	4
MP:0002865	MP:0002865	increased growth rate	Mammalian_phenotype	4
MP:0002866	MP:0002866	abnormal glutamic acid decarboxylase level	Mammalian_phenotype	4
MP:0002878	MP:0002878	abnormal corticospinal tract morphology	Mammalian_phenotype	4
MP:0002883	MP:0002883	chromatolysis	Mammalian_phenotype	4
MP:0002884	MP:0002884	abnormal branchial arch morphology	Mammalian_phenotype	4
MP:0002891	MP:0002891	increased insulin sensitivity	Mammalian_phenotype	4
MP:0002896	MP:0002896	abnormal bone mineralization	Mammalian_phenotype	4
MP:0002897	MP:0002897	blotchy skin	Mammalian_phenotype	4
MP:0002898	MP:0002898	absent cartilage	Mammalian_phenotype	4
MP:0002900	MP:0002900	abnormal urine phosphate level	Mammalian_phenotype	4
MP:0002908	MP:0002908	delayed wound healing	Mammalian_phenotype	4
MP:0002913	MP:0002913	abnormal PNS synaptic transmission	Mammalian_phenotype	4
MP:0002918	MP:0002918	abnormal paired-pulse facilitation	Mammalian_phenotype	4
MP:0002929	MP:0002929	abnormal bile duct development	Mammalian_phenotype	4
MP:0002936	MP:0002936	joint swelling	Mammalian_phenotype	4
MP:0002937	MP:0002937	synovial hyperemia	Mammalian_phenotype	4
MP:0002943	MP:0002943	abnormal lactate dehydrogenase level	Mammalian_phenotype	4
MP:0002948	MP:0002948	abnormal neuron specification	Mammalian_phenotype	4
MP:0002950	MP:0002950	abnormal neural crest cell migration	Mammalian_phenotype	4
MP:0002951	MP:0002951	small thyroid gland	Mammalian_phenotype	4
MP:0002952	MP:0002952	ventricular cardiomyopathy	Mammalian_phenotype	4
MP:0002985	MP:0002985	abnormal urine calcium level	Mammalian_phenotype	4
MP:0002987	MP:0002987	abnormal urine osmolality	Mammalian_phenotype	4
MP:0002990	MP:0002990	short ureter	Mammalian_phenotype	4
MP:0002992	MP:0002992	abnormal sebaceous lipid secretion	Mammalian_phenotype	4
MP:0002996	MP:0002996	ovotestis	Mammalian_phenotype	4
MP:0003009	MP:0003009	abnormal cytokine secretion	Mammalian_phenotype	4
MP:0003014	MP:0003014	abnormal kidney medulla morphology	Mammalian_phenotype	4
MP:0003015	MP:0003015	abnormal circulating bicarbonate level	Mammalian_phenotype	4
MP:0003027	MP:0003027	abnormal blood pH regulation	Mammalian_phenotype	4
MP:0003028	MP:0003028	alkalosis	Mammalian_phenotype	4
MP:0003031	MP:0003031	acidosis	Mammalian_phenotype	4
MP:0003037	MP:0003037	increased myocardial infarction size	Mammalian_phenotype	4
MP:0003038	MP:0003038	decreased myocardial infarction size	Mammalian_phenotype	4
MP:0003039	MP:0003039	increased time of peak ischemic contracture	Mammalian_phenotype	4
MP:0003040	MP:0003040	decreased time of peak ischemic contracture	Mammalian_phenotype	4
MP:0003041	MP:0003041	increased time of onset of induced ischemic contracture	Mammalian_phenotype	4
MP:0003042	MP:0003042	decreased time of onset of induced ischemic contracture	Mammalian_phenotype	4
MP:0003044	MP:0003044	impaired basement membrane formation	Mammalian_phenotype	4
MP:0003046	MP:0003046	liver cirrhosis	Mammalian_phenotype	4
MP:0003052	MP:0003052	omphalocele	Mammalian_phenotype	4
MP:0003055	MP:0003055	abnormal long bone epiphyseal plate morphology	Mammalian_phenotype	4
MP:0003060	MP:0003060	increased aerobic running capacity	Mammalian_phenotype	4
MP:0003061	MP:0003061	decreased aerobic running capacity	Mammalian_phenotype	4
MP:0003065	MP:0003065	abnormal liver copper level	Mammalian_phenotype	4
MP:0003076	MP:0003076	increased susceptibility to ischemic brain injury	Mammalian_phenotype	4
MP:0003084	MP:0003084	abnormal skeletal muscle fiber morphology	Mammalian_phenotype	4
MP:0003085	MP:0003085	abnormal egg cylinder morphology	Mammalian_phenotype	4
MP:0003086	MP:0003086	hydromyelia	Mammalian_phenotype	4
MP:0003089	MP:0003089	decreased skin tensile strength	Mammalian_phenotype	4
MP:0003090	MP:0003090	abnormal muscle precursor cell migration	Mammalian_phenotype	4
MP:0003095	MP:0003095	abnormal corneal stroma development	Mammalian_phenotype	4
MP:0003098	MP:0003098	decreased tendon stiffness	Mammalian_phenotype	4
MP:0003100	MP:0003100	myopia	Mammalian_phenotype	4
MP:0003102	MP:0003102	sclera thinning	Mammalian_phenotype	4
MP:0003103	MP:0003103	liver degeneration	Mammalian_phenotype	4
MP:0003105	MP:0003105	abnormal heart atrium morphology	Mammalian_phenotype	4
MP:0003107	MP:0003107	abnormal response to novelty	Mammalian_phenotype	4
MP:0003112	MP:0003112	enlarged parathyroid gland	Mammalian_phenotype	4
MP:0003113	MP:0003113	small parathyroid gland	Mammalian_phenotype	4
MP:0003114	MP:0003114	pigmented parathyroid gland	Mammalian_phenotype	4
MP:0003120	MP:0003120	abnormal tracheal cartilage morphology	Mammalian_phenotype	4
MP:0003141	MP:0003141	cardiac fibrosis	Mammalian_phenotype	4
MP:0003156	MP:0003156	abnormal leukocyte migration	Mammalian_phenotype	4
MP:0003157	MP:0003157	impaired muscle relaxation	Mammalian_phenotype	4
MP:0003159	MP:0003159	abnormal esophageal smooth muscle morphology	Mammalian_phenotype	4
MP:0003160	MP:0003160	abnormal esophageal development	Mammalian_phenotype	4
MP:0003173	MP:0003173	decreased lysosomal enzyme secretion	Mammalian_phenotype	4
MP:0003174	MP:0003174	increased lysosomal enzyme secretion	Mammalian_phenotype	4
MP:0003178	MP:0003178	left pulmonary isomerism	Mammalian_phenotype	4
MP:0003184	MP:0003184	increased angiotensin I-converting enzyme activity	Mammalian_phenotype	4
MP:0003185	MP:0003185	decreased angiotensin I-converting enzyme activity	Mammalian_phenotype	4
MP:0003189	MP:0003189	fused joints	Mammalian_phenotype	4
MP:0003192	MP:0003192	increased cholesterol efflux	Mammalian_phenotype	4
MP:0003193	MP:0003193	decreased cholesterol efflux	Mammalian_phenotype	4
MP:0003197	MP:0003197	nephrocalcinosis	Mammalian_phenotype	4
MP:0003198	MP:0003198	calcified tendon	Mammalian_phenotype	4
MP:0003200	MP:0003200	calcified joint	Mammalian_phenotype	4
MP:0003202	MP:0003202	abnormal neuron apoptosis	Mammalian_phenotype	4
MP:0003209	MP:0003209	abnormal pulmonary elastic fiber morphology	Mammalian_phenotype	4
MP:0003214	MP:0003214	neurofibrillary tangles	Mammalian_phenotype	4
MP:0003224	MP:0003224	neuron degeneration	Mammalian_phenotype	4
MP:0003229	MP:0003229	abnormal vitelline vasculature morphology	Mammalian_phenotype	4
MP:0003231	MP:0003231	abnormal placenta vasculature	Mammalian_phenotype	4
MP:0003243	MP:0003243	abnormal dopaminergic neuron morphology	Mammalian_phenotype	4
MP:0003245	MP:0003245	abnormal GABAergic neuron morphology	Mammalian_phenotype	4
MP:0003247	MP:0003247	abnormal glutaminergic neuron morphology	Mammalian_phenotype	4
MP:0003251	MP:0003251	gallbladder inflammation	Mammalian_phenotype	4
MP:0003254	MP:0003254	bile duct inflammation	Mammalian_phenotype	4
MP:0003255	MP:0003255	bile duct proliferation	Mammalian_phenotype	4
MP:0003256	MP:0003256	biliary cirrhosis	Mammalian_phenotype	4
MP:0003258	MP:0003258	hiatal hernia	Mammalian_phenotype	4
MP:0003259	MP:0003259	nausea	Mammalian_phenotype	4
MP:0003260	MP:0003260	vomiting	Mammalian_phenotype	4
MP:0003262	MP:0003262	intestinal/bowel diverticulum	Mammalian_phenotype	4
MP:0003267	MP:0003267	constipation	Mammalian_phenotype	4
MP:0003270	MP:0003270	intestinal obstruction	Mammalian_phenotype	4
MP:0003274	MP:0003274	intestinal microaneurysm	Mammalian_phenotype	4
MP:0003275	MP:0003275	gastric microaneurysm	Mammalian_phenotype	4
MP:0003276	MP:0003276	esophageal atresia	Mammalian_phenotype	4
MP:0003280	MP:0003280	urinary incontinence	Mammalian_phenotype	4
MP:0003281	MP:0003281	fecal incontinence	Mammalian_phenotype	4
MP:0003284	MP:0003284	abnormal large intestine placement	Mammalian_phenotype	4
MP:0003286	MP:0003286	gastroesophageal reflux	Mammalian_phenotype	4
MP:0003288	MP:0003288	intestinal edema	Mammalian_phenotype	4
MP:0003289	MP:0003289	abnormal intestinal peristalsis	Mammalian_phenotype	4
MP:0003292	MP:0003292	melena	Mammalian_phenotype	4
MP:0003294	MP:0003294	intussusception	Mammalian_phenotype	4
MP:0003299	MP:0003299	gastric polyps	Mammalian_phenotype	4
MP:0003301	MP:0003301	peptic ulcer	Mammalian_phenotype	4
MP:0003316	MP:0003316	perineal fistula	Mammalian_phenotype	4
MP:0003321	MP:0003321	tracheoesophageal fistula	Mammalian_phenotype	4
MP:0003322	MP:0003322	biliary fistula	Mammalian_phenotype	4
MP:0003323	MP:0003323	gastrocolic fistula	Mammalian_phenotype	4
MP:0003325	MP:0003325	decreased liver function	Mammalian_phenotype	4
MP:0003326	MP:0003326	liver failure	Mammalian_phenotype	4
MP:0003327	MP:0003327	liver cysts	Mammalian_phenotype	4
MP:0003330	MP:0003330	abnormal auditory tube	Mammalian_phenotype	4
MP:0003332	MP:0003332	liver abscess	Mammalian_phenotype	4
MP:0003333	MP:0003333	liver fibrosis	Mammalian_phenotype	4
MP:0003334	MP:0003334	pancreas fibrosis	Mammalian_phenotype	4
MP:0003336	MP:0003336	pancreas cysts	Mammalian_phenotype	4
MP:0003338	MP:0003338	pancreas lipomatosis	Mammalian_phenotype	4
MP:0003344	MP:0003344	mammary gland hypoplasia	Mammalian_phenotype	4
MP:0003356	MP:0003356	impaired luteinization	Mammalian_phenotype	4
MP:0003357	MP:0003357	impaired granulosa cell differentiation	Mammalian_phenotype	4
MP:0003358	MP:0003358	abnormal hypaxial muscle morphology	Mammalian_phenotype	4
MP:0003359	MP:0003359	hypaxial muscle hypoplasia	Mammalian_phenotype	4
MP:0003360	MP:0003360	abnormal depression-related behavior	Mammalian_phenotype	4
MP:0003380	MP:0003380	abnormal intestine regeneration	Mammalian_phenotype	4
MP:0003383	MP:0003383	abnormal gluconeogenesis	Mammalian_phenotype	4
MP:0003396	MP:0003396	abnormal embryonic hematopoiesis	Mammalian_phenotype	4
MP:0003397	MP:0003397	increased muscle weight	Mammalian_phenotype	4
MP:0003406	MP:0003406	failure of zygotic cell division	Mammalian_phenotype	4
MP:0003407	MP:0003407	abnormal central nervous system regeneration	Mammalian_phenotype	4
MP:0003412	MP:0003412	abnormal afterhyperpolarization	Mammalian_phenotype	4
MP:0003413	MP:0003413	hair follicle degeneration	Mammalian_phenotype	4
MP:0003414	MP:0003414	epidermal cyst	Mammalian_phenotype	4
MP:0003416	MP:0003416	premature bone ossification	Mammalian_phenotype	4
MP:0003421	MP:0003421	abnormal thyroid gland development	Mammalian_phenotype	4
MP:0003425	MP:0003425	abnormal optic vesicle formation	Mammalian_phenotype	4
MP:0003429	MP:0003429	insensitivity to growth hormone	Mammalian_phenotype	4
MP:0003432	MP:0003432	increased activity of parathyroid	Mammalian_phenotype	4
MP:0003433	MP:0003433	decreased activity of parathyroid	Mammalian_phenotype	4
MP:0003438	MP:0003438	abnormal carotid body physiology	Mammalian_phenotype	4
MP:0003445	MP:0003445	sirenomelia	Mammalian_phenotype	4
MP:0003447	MP:0003447	decreased tumor growth/size	Mammalian_phenotype	4
MP:0003457	MP:0003457	abnormal circulating ketone body level	Mammalian_phenotype	4
MP:0003463	MP:0003463	abnormal single cell response	Mammalian_phenotype	4
MP:0003470	MP:0003470	abnormal summary potential	Mammalian_phenotype	4
MP:0003477	MP:0003477	abnormal nerve fiber response	Mammalian_phenotype	4
MP:0003484	MP:0003484	abnormal channel response	Mammalian_phenotype	4
MP:0003491	MP:0003491	abnormal voluntary movement	Mammalian_phenotype	4
MP:0003492	MP:0003492	abnormal involuntary movement	Mammalian_phenotype	4
MP:0003497	MP:0003497	insensitivity to parathyroid hormone	Mammalian_phenotype	4
MP:0003501	MP:0003501	iodide oxidation defect	Mammalian_phenotype	4
MP:0003502	MP:0003502	increased activity of thyroid	Mammalian_phenotype	4
MP:0003503	MP:0003503	decreased activity of thyroid	Mammalian_phenotype	4
MP:0003504	MP:0003504	thyroid inflammation	Mammalian_phenotype	4
MP:0003507	MP:0003507	abnormal ovary physiology	Mammalian_phenotype	4
MP:0003531	MP:0003531	abnormal vagina development	Mammalian_phenotype	4
MP:0003543	MP:0003543	abnormal vascular endothelial cell differentiation	Mammalian_phenotype	4
MP:0003544	MP:0003544	abnormal vascular endothelial cell migration	Mammalian_phenotype	4
MP:0003551	MP:0003551	blind perineal pouch	Mammalian_phenotype	4
MP:0003555	MP:0003555	chordee	Mammalian_phenotype	4
MP:0003564	MP:0003564	abnormal insulin secretion	Mammalian_phenotype	4
MP:0003565	MP:0003565	abnormal glucagon secretion	Mammalian_phenotype	4
MP:0003572	MP:0003572	abnormal uterus development	Mammalian_phenotype	4
MP:0003582	MP:0003582	abnormal ovary development	Mammalian_phenotype	4
MP:0003584	MP:0003584	bifid ureter	Mammalian_phenotype	4
MP:0003585	MP:0003585	large ureter	Mammalian_phenotype	4
MP:0003586	MP:0003586	dilated ureter	Mammalian_phenotype	4
MP:0003587	MP:0003587	ureter obstruction	Mammalian_phenotype	4
MP:0003588	MP:0003588	ureter stenosis	Mammalian_phenotype	4
MP:0003590	MP:0003590	ureteral reflux	Mammalian_phenotype	4
MP:0003591	MP:0003591	urethra atresia	Mammalian_phenotype	4
MP:0003592	MP:0003592	urethra stricture	Mammalian_phenotype	4
MP:0003593	MP:0003593	urethrovaginal fistula	Mammalian_phenotype	4
MP:0003594	MP:0003594	small urethra	Mammalian_phenotype	4
MP:0003600	MP:0003600	ectopic kidney	Mammalian_phenotype	4
MP:0003601	MP:0003601	bifid kidney	Mammalian_phenotype	4
MP:0003604	MP:0003604	single kidney	Mammalian_phenotype	4
MP:0003605	MP:0003605	fused kidneys	Mammalian_phenotype	4
MP:0003606	MP:0003606	kidney failure	Mammalian_phenotype	4
MP:0003607	MP:0003607	abnormal prostate gland physiology	Mammalian_phenotype	4
MP:0003614	MP:0003614	urinary bladder prolapse	Mammalian_phenotype	4
MP:0003615	MP:0003615	urinary bladder diverticulum	Mammalian_phenotype	4
MP:0003616	MP:0003616	abnormal urachus morphology	Mammalian_phenotype	4
MP:0003617	MP:0003617	urinary bladder hypoplasia	Mammalian_phenotype	4
MP:0003619	MP:0003619	abnormal urine color	Mammalian_phenotype	4
MP:0003620	MP:0003620	oliguria	Mammalian_phenotype	4
MP:0003621	MP:0003621	dysuria	Mammalian_phenotype	4
MP:0003622	MP:0003622	ischuria	Mammalian_phenotype	4
MP:0003624	MP:0003624	anuria	Mammalian_phenotype	4
MP:0003639	MP:0003639	abnormal response to vitamins	Mammalian_phenotype	4
MP:0003652	MP:0003652	abnormal skin turgor	Mammalian_phenotype	4
MP:0003655	MP:0003655	absent pancreas	Mammalian_phenotype	4
MP:0003656	MP:0003656	abnormal erythrocyte physiology	Mammalian_phenotype	4
MP:0003658	MP:0003658	abnormal capillary morphology	Mammalian_phenotype	4
MP:0003659	MP:0003659	abnormal lymph circulation	Mammalian_phenotype	4
MP:0003663	MP:0003663	abnormal thermosensation	Mammalian_phenotype	4
MP:0003665	MP:0003665	endophthalmitis	Mammalian_phenotype	4
MP:0003668	MP:0003668	abnormal periodontal ligament morphology	Mammalian_phenotype	4
MP:0003671	MP:0003671	abnormal eyelid aperture	Mammalian_phenotype	4
MP:0003672	MP:0003672	abnormal ureter development	Mammalian_phenotype	4
MP:0003674	MP:0003674	oxidative stress	Mammalian_phenotype	4
MP:0003675	MP:0003675	kidney cysts	Mammalian_phenotype	4
MP:0003687	MP:0003687	abnormal intraocular muscle morphology	Mammalian_phenotype	4
MP:0003688	MP:0003688	ophthalmoparesis	Mammalian_phenotype	4
MP:0003691	MP:0003691	abnormal microglial cell physiology	Mammalian_phenotype	4
MP:0003692	MP:0003692	xanthoma	Mammalian_phenotype	4
MP:0003693	MP:0003693	abnormal blastocyst hatching	Mammalian_phenotype	4
MP:0003702	MP:0003702	abnormal chromosome morphology	Mammalian_phenotype	4
MP:0003703	MP:0003703	abnormal vestibulocochlear ganglion morphology	Mammalian_phenotype	4
MP:0003704	MP:0003704	abnormal hair follicle development	Mammalian_phenotype	4
MP:0003706	MP:0003706	abnormal cell nucleus count	Mammalian_phenotype	4
MP:0003717	MP:0003717	pallor	Mammalian_phenotype	4
MP:0003719	MP:0003719	abnormal pericyte morphology	Mammalian_phenotype	4
MP:0003721	MP:0003721	increased tumor growth/size	Mammalian_phenotype	4
MP:0003722	MP:0003722	absent ureter	Mammalian_phenotype	4
MP:0003723	MP:0003723	abnormal long bone morphology	Mammalian_phenotype	4
MP:0003741	MP:0003741	tinnitus	Mammalian_phenotype	4
MP:0003743	MP:0003743	abnormal facial morphology	Mammalian_phenotype	4
MP:0003791	MP:0003791	abnormal minor salivary gland morphology	Mammalian_phenotype	4
MP:0003792	MP:0003792	abnormal major salivary gland morphology	Mammalian_phenotype	4
MP:0003797	MP:0003797	abnormal compact bone morphology	Mammalian_phenotype	4
MP:0003809	MP:0003809	abnormal hair shaft morphology	Mammalian_phenotype	4
MP:0003818	MP:0003818	abnormal eye muscle development	Mammalian_phenotype	4
MP:0003829	MP:0003829	impaired febrile response	Mammalian_phenotype	4
MP:0003830	MP:0003830	abnormal testis development	Mammalian_phenotype	4
MP:0003833	MP:0003833	decreased satellite cell number	Mammalian_phenotype	4
MP:0003839	MP:0003839	abnormal insulin clearance	Mammalian_phenotype	4
MP:0003852	MP:0003852	skeletal muscle necrosis	Mammalian_phenotype	4
MP:0003853	MP:0003853	dry skin	Mammalian_phenotype	4
MP:0003854	MP:0003854	abnormal forelimb stylopod morphology	Mammalian_phenotype	4
MP:0003855	MP:0003855	abnormal forelimb zeugopod morphology	Mammalian_phenotype	4
MP:0003856	MP:0003856	abnormal hindlimb stylopod morphology	Mammalian_phenotype	4
MP:0003857	MP:0003857	abnormal hindlimb zeugopod morphology	Mammalian_phenotype	4
MP:0003860	MP:0003860	abnormal carbon dioxide level	Mammalian_phenotype	4
MP:0003863	MP:0003863	decreased aggression towards mice	Mammalian_phenotype	4
MP:0003865	MP:0003865	lymph node inflammation	Mammalian_phenotype	4
MP:0003869	MP:0003869	ectopic cartilage	Mammalian_phenotype	4
MP:0003875	MP:0003875	abnormal hair follicle regression	Mammalian_phenotype	4
MP:0003877	MP:0003877	abnormal serotonergic neuron morphology	Mammalian_phenotype	4
MP:0003881	MP:0003881	abnormal nephron morphology	Mammalian_phenotype	4
MP:0003882	MP:0003882	abnormal pulse pressure	Mammalian_phenotype	4
MP:0003883	MP:0003883	enlarged stomach	Mammalian_phenotype	4
MP:0003885	MP:0003885	abnormal rostral-caudal body axis extension	Mammalian_phenotype	4
MP:0003888	MP:0003888	liver hemorrhage	Mammalian_phenotype	4
MP:0003889	MP:0003889	enhanced sensorimotor gating	Mammalian_phenotype	4
MP:0003894	MP:0003894	abnormal Purkinje cell innervation	Mammalian_phenotype	4
MP:0003903	MP:0003903	increased cell mass	Mammalian_phenotype	4
MP:0003904	MP:0003904	decreased cell mass	Mammalian_phenotype	4
MP:0003926	MP:0003926	impaired cellular glucose import	Mammalian_phenotype	4
MP:0003927	MP:0003927	enhanced cellular glucose import	Mammalian_phenotype	4
MP:0003934	MP:0003934	abnormal pancreas development	Mammalian_phenotype	4
MP:0003939	MP:0003939	abnormal myotome morphology	Mammalian_phenotype	4
MP:0003940	MP:0003940	abnormal dermatome morphology	Mammalian_phenotype	4
MP:0003949	MP:0003949	abnormal circulating lipid level	Mammalian_phenotype	4
MP:0003951	MP:0003951	abnormal copper homeostasis	Mammalian_phenotype	4
MP:0003957	MP:0003957	abnormal nitric oxide homeostasis	Mammalian_phenotype	4
MP:0003960	MP:0003960	increased lean body mass	Mammalian_phenotype	4
MP:0003961	MP:0003961	decreased lean body mass	Mammalian_phenotype	4
MP:0003962	MP:0003962	abnormal adrenaline level	Mammalian_phenotype	4
MP:0003963	MP:0003963	abnormal corticosterone level	Mammalian_phenotype	4
MP:0003964	MP:0003964	abnormal noradrenaline level	Mammalian_phenotype	4
MP:0003965	MP:0003965	abnormal pituitary hormone level	Mammalian_phenotype	4
MP:0003985	MP:0003985	renal fibrosis	Mammalian_phenotype	4
MP:0003988	MP:0003988	disorganized embryonic tissue	Mammalian_phenotype	4
MP:0004003	MP:0004003	abnormal vascular endothelial cell physiology	Mammalian_phenotype	4
MP:0004007	MP:0004007	abnormal lung vasculature morphology	Mammalian_phenotype	4
MP:0004009	MP:0004009	abnormal diastolic filling velocity	Mammalian_phenotype	4
MP:0004012	MP:0004012	increased pulmonary artery pressure	Mammalian_phenotype	4
MP:0004013	MP:0004013	decreased pulmonary artery pressure	Mammalian_phenotype	4
MP:0004016	MP:0004016	decreased bone mass	Mammalian_phenotype	4
MP:0004017	MP:0004017	duplex kidney	Mammalian_phenotype	4
MP:0004020	MP:0004020	polyhydramnios	Mammalian_phenotype	4
MP:0004021	MP:0004021	abnormal rod electrophysiology	Mammalian_phenotype	4
MP:0004022	MP:0004022	abnormal cone electrophysiology	Mammalian_phenotype	4
MP:0004023	MP:0004023	abnormal chromosome number	Mammalian_phenotype	4
MP:0004037	MP:0004037	increased muscle relaxation	Mammalian_phenotype	4
MP:0004042	MP:0004042	decreased susceptibility to kidney reperfusion injury	Mammalian_phenotype	4
MP:0004045	MP:0004045	abnormal cell cycle checkpoint function	Mammalian_phenotype	4
MP:0004046	MP:0004046	abnormal mitosis	Mammalian_phenotype	4
MP:0004050	MP:0004050	abnormal renal sympathetic nerve activity	Mammalian_phenotype	4
MP:0004054	MP:0004054	abnormal periocular mesenchyme morphology	Mammalian_phenotype	4
MP:0004064	MP:0004064	decreased susceptibility to induced muscular atrophy	Mammalian_phenotype	4
MP:0004065	MP:0004065	increased susceptibility to induced muscular atrophy	Mammalian_phenotype	4
MP:0004072	MP:0004072	abnormal frontal plane axis	Mammalian_phenotype	4
MP:0004086	MP:0004086	absent heartbeat	Mammalian_phenotype	4
MP:0004088	MP:0004088	abnormal sarcoplasmic reticulum morphology	Mammalian_phenotype	4
MP:0004090	MP:0004090	abnormal sarcomere morphology	Mammalian_phenotype	4
MP:0004095	MP:0004095	ocular distichiasis	Mammalian_phenotype	4
MP:0004101	MP:0004101	abnormal brain interneuron morphology	Mammalian_phenotype	4
MP:0004107	MP:0004107	abnormal thoracic duct morphology	Mammalian_phenotype	4
MP:0004108	MP:0004108	abnormal esophageal peristalsis	Mammalian_phenotype	4
MP:0004116	MP:0004116	abnormal atrioventricular bundle conduction	Mammalian_phenotype	4
MP:0004121	MP:0004121	abnormal sarcolemma morphology	Mammalian_phenotype	4
MP:0004123	MP:0004123	abnormal impulse conducting system morphology	Mammalian_phenotype	4
MP:0004126	MP:0004126	thin hypodermis	Mammalian_phenotype	4
MP:0004127	MP:0004127	thick hypodermis	Mammalian_phenotype	4
MP:0004129	MP:0004129	abnormal respiratory quotient	Mammalian_phenotype	4
MP:0004136	MP:0004136	abnormal tongue muscle morphology	Mammalian_phenotype	4
MP:0004143	MP:0004143	muscle hypertonia	Mammalian_phenotype	4
MP:0004144	MP:0004144	hypotonia	Mammalian_phenotype	4
MP:0004147	MP:0004147	increased porphyrin level	Mammalian_phenotype	4
MP:0004149	MP:0004149	increased bone strength	Mammalian_phenotype	4
MP:0004150	MP:0004150	absent caveolae	Mammalian_phenotype	4
MP:0004155	MP:0004155	decreased susceptibility to induced pancreatitis	Mammalian_phenotype	4
MP:0004173	MP:0004173	abnormal intervertebral disk morphology	Mammalian_phenotype	4
MP:0004179	MP:0004179	transmission ratio distortion	Mammalian_phenotype	4
MP:0004183	MP:0004183	abnormal sympathetic nervous system physiology	Mammalian_phenotype	4
MP:0004191	MP:0004191	neuronal intranuclear inclusions	Mammalian_phenotype	4
MP:0004194	MP:0004194	abnormal kidney pelvis morphology	Mammalian_phenotype	4
MP:0004198	MP:0004198	abnormal fetal size	Mammalian_phenotype	4
MP:0004201	MP:0004201	fetal growth retardation	Mammalian_phenotype	4
MP:0004209	MP:0004209	abnormal sweet taste sensitivity	Mammalian_phenotype	4
MP:0004210	MP:0004210	abnormal bitter taste sensitivity	Mammalian_phenotype	4
MP:0004211	MP:0004211	abnormal sour taste sensitivity	Mammalian_phenotype	4
MP:0004212	MP:0004212	abnormal salty taste sensitivity	Mammalian_phenotype	4
MP:0004213	MP:0004213	abnormal umami taste sensitivity	Mammalian_phenotype	4
MP:0004220	MP:0004220	abnormal peripheral nervous system regeneration	Mammalian_phenotype	4
MP:0004231	MP:0004231	abnormal calcium ion homeostasis	Mammalian_phenotype	4
MP:0004232	MP:0004232	decreased muscle weight	Mammalian_phenotype	4
MP:0004234	MP:0004234	abnormal masticatory muscle morphology	Mammalian_phenotype	4
MP:0004244	MP:0004244	abnormal spontaneous abortion rate	Mammalian_phenotype	4
MP:0004248	MP:0004248	abnormal epaxial muscle morphology	Mammalian_phenotype	4
MP:0004250	MP:0004250	tau protein deposits	Mammalian_phenotype	4
MP:0004254	MP:0004254	cerebral amyloid angiopathy	Mammalian_phenotype	4
MP:0004262	MP:0004262	abnormal physical strength	Mammalian_phenotype	4
MP:0004267	MP:0004267	abnormal optic tract morphology	Mammalian_phenotype	4
MP:0004268	MP:0004268	abnormal optic stalk morphology	Mammalian_phenotype	4
MP:0004269	MP:0004269	abnormal optic cup morphology	Mammalian_phenotype	4
MP:0004273	MP:0004273	abnormal basal lamina morphology	Mammalian_phenotype	4
MP:0004274	MP:0004274	abnormal embryonic/fetal subventricular zone morphology	Mammalian_phenotype	4
MP:0004275	MP:0004275	abnormal postnatal subventricular zone morphology	Mammalian_phenotype	4
MP:0004286	MP:0004286	abnormal internal auditory canal morphology	Mammalian_phenotype	4
MP:0004288	MP:0004288	abnormal spiral ligament morphology	Mammalian_phenotype	4
MP:0004289	MP:0004289	abnormal bony labyrinth	Mammalian_phenotype	4
MP:0004368	MP:0004368	abnormal stria vascularis vasculature morphology	Mammalian_phenotype	4
MP:0004387	MP:0004387	abnormal prechordal plate morphology	Mammalian_phenotype	4
MP:0004391	MP:0004391	abnormal respiratory conducting tube morphology	Mammalian_phenotype	4
MP:0004479	MP:0004479	abnormal oval window morphology	Mammalian_phenotype	4
MP:0004480	MP:0004480	abnormal round window morphology	Mammalian_phenotype	4
MP:0004485	MP:0004485	increased response of heart to induced stress	Mammalian_phenotype	4
MP:0004486	MP:0004486	decreased response of heart to induced stress	Mammalian_phenotype	4
MP:0004499	MP:0004499	increased incidence of tumors by chemical induction	Mammalian_phenotype	4
MP:0004502	MP:0004502	decreased incidence of tumors by chemical induction	Mammalian_phenotype	4
MP:0004508	MP:0004508	abnormal pectoral girdle bone morphology	Mammalian_phenotype	4
MP:0004509	MP:0004509	abnormal pelvic girdle bone morphology	Mammalian_phenotype	4
MP:0004512	MP:0004512	anosmia	Mammalian_phenotype	4
MP:0004513	MP:0004513	avnosmia	Mammalian_phenotype	4
MP:0004542	MP:0004542	impaired acrosome reaction	Mammalian_phenotype	4
MP:0004543	MP:0004543	abnormal sperm physiology	Mammalian_phenotype	4
MP:0004544	MP:0004544	absent esophagus	Mammalian_phenotype	4
MP:0004545	MP:0004545	enlarged esophagus	Mammalian_phenotype	4
MP:0004547	MP:0004547	esophageal ulcer	Mammalian_phenotype	4
MP:0004548	MP:0004548	dilated esophagus	Mammalian_phenotype	4
MP:0004549	MP:0004549	small trachea	Mammalian_phenotype	4
MP:0004554	MP:0004554	small pharynx	Mammalian_phenotype	4
MP:0004576	MP:0004576	abnormal foot plate morphology	Mammalian_phenotype	4
MP:0004588	MP:0004588	abnormal vestibular hair cell development	Mammalian_phenotype	4
MP:0004589	MP:0004589	abnormal cochlear hair cell development	Mammalian_phenotype	4
MP:0004598	MP:0004598	abnormal cochlear basement membrane morphology	Mammalian_phenotype	4
MP:0004611	MP:0004611	increased susceptibility to ototoxicity-induced hearing loss	Mammalian_phenotype	4
MP:0004624	MP:0004624	abnormal thoracic cage morphology	Mammalian_phenotype	4
MP:0004663	MP:0004663	athyroidism	Mammalian_phenotype	4
MP:0004696	MP:0004696	abnormal thyroid follicle morphology	Mammalian_phenotype	4
MP:0004698	MP:0004698	abnormal thyroid parafollicular C-cell morphology	Mammalian_phenotype	4
MP:0004703	MP:0004703	abnormal vertebral column morphology	Mammalian_phenotype	4
MP:0004726	MP:0004726	abnormal nasal capsule morphology	Mammalian_phenotype	4
MP:0004734	MP:0004734	small thoracic cavity	Mammalian_phenotype	4
MP:0004735	MP:0004735	enlarged thoracic cavity	Mammalian_phenotype	4
MP:0004743	MP:0004743	abnormal vestibular evoked myogenic potential	Mammalian_phenotype	4
MP:0004751	MP:0004751	increased length of allograft survival	Mammalian_phenotype	4
MP:0004752	MP:0004752	decreased length of allograft survival	Mammalian_phenotype	4
MP:0004754	MP:0004754	abnormal kidney collecting duct morphology	Mammalian_phenotype	4
MP:0004768	MP:0004768	abnormal axonal transport	Mammalian_phenotype	4
MP:0004770	MP:0004770	abnormal synaptic vesicle recycling	Mammalian_phenotype	4
MP:0004772	MP:0004772	abnormal bile secretion	Mammalian_phenotype	4
MP:0004773	MP:0004773	abnormal bile composition	Mammalian_phenotype	4
MP:0004780	MP:0004780	abnormal surfactant secretion	Mammalian_phenotype	4
MP:0004781	MP:0004781	abnormal surfactant composition	Mammalian_phenotype	4
MP:0004793	MP:0004793	abnormal synaptic vesicle clustering	Mammalian_phenotype	4
MP:0004807	MP:0004807	abnormal paired-pulse inhibition	Mammalian_phenotype	4
MP:0004809	MP:0004809	increased hematopoietic stem cell number	Mammalian_phenotype	4
MP:0004810	MP:0004810	decreased hematopoietic stem cell number	Mammalian_phenotype	4
MP:0004812	MP:0004812	abnormal linear vestibular evoked potential	Mammalian_phenotype	4
MP:0004815	MP:0004815	abnormal somatic hypermutation frequency	Mammalian_phenotype	4
MP:0004816	MP:0004816	abnormal class switch recombination	Mammalian_phenotype	4
MP:0004817	MP:0004817	abnormal skeletal muscle mass	Mammalian_phenotype	4
MP:0004820	MP:0004820	abnormal urine potassium level	Mammalian_phenotype	4
MP:0004844	MP:0004844	abnormal vestibuloocular reflex	Mammalian_phenotype	4
MP:0004846	MP:0004846	absent skeletal muscle	Mammalian_phenotype	4
MP:0004848	MP:0004848	abnormal liver size	Mammalian_phenotype	4
MP:0004874	MP:0004874	abnormal timing of postnatal eyelid opening	Mammalian_phenotype	4
MP:0004880	MP:0004880	lung cysts	Mammalian_phenotype	4
MP:0004881	MP:0004881	abnormal lung size	Mammalian_phenotype	4
MP:0004883	MP:0004883	abnormal vascular wound healing	Mammalian_phenotype	4
MP:0004884	MP:0004884	abnormal testis physiology	Mammalian_phenotype	4
MP:0004886	MP:0004886	increased endolymph production	Mammalian_phenotype	4
MP:0004887	MP:0004887	decreased endolymph production	Mammalian_phenotype	4
MP:0004891	MP:0004891	abnormal adiponectin level	Mammalian_phenotype	4
MP:0004915	MP:0004915	abnormal Reichert's cartilage morphology	Mammalian_phenotype	4
MP:0004937	MP:0004937	dilated heart	Mammalian_phenotype	4
MP:0004938	MP:0004938	dilated vasculature	Mammalian_phenotype	4
MP:0004945	MP:0004945	abnormal bone resorption	Mammalian_phenotype	4
MP:0004950	MP:0004950	abnormal brain vasculature morphology	Mammalian_phenotype	4
MP:0004957	MP:0004957	abnormal blastocyst morphology	Mammalian_phenotype	4
MP:0004967	MP:0004967	abnormal kidney epithelium morphology	Mammalian_phenotype	4
MP:0004969	MP:0004969	pale kidney	Mammalian_phenotype	4
MP:0004971	MP:0004971	dermal hyperplasia	Mammalian_phenotype	4
MP:0004982	MP:0004982	abnormal osteoclast morphology	Mammalian_phenotype	4
MP:0004986	MP:0004986	abnormal osteoblast morphology	Mammalian_phenotype	4
MP:0004991	MP:0004991	decreased bone strength	Mammalian_phenotype	4
MP:0004994	MP:0004994	abnormal brain wave pattern	Mammalian_phenotype	4
MP:0004996	MP:0004996	abnormal CNS synapse formation	Mammalian_phenotype	4
MP:0005001	MP:0005001	abnormal clonal deletion	Mammalian_phenotype	4
MP:0005004	MP:0005004	abnormal lymphocyte anergy	Mammalian_phenotype	4
MP:0005005	MP:0005005	abnormal self tolerance	Mammalian_phenotype	4
MP:0005006	MP:0005006	abnormal osteoblast physiology	Mammalian_phenotype	4
MP:0005029	MP:0005029	abnormal amnion morphology	Mammalian_phenotype	4
MP:0005034	MP:0005034	abnormal anus morphology	Mammalian_phenotype	4
MP:0005036	MP:0005036	diarrhea	Mammalian_phenotype	4
MP:0005041	MP:0005041	abnormal antigen presentation via MHC class II	Mammalian_phenotype	4
MP:0005044	MP:0005044	sepsis	Mammalian_phenotype	4
MP:0005059	MP:0005059	lysosomal protein accumulation	Mammalian_phenotype	4
MP:0005060	MP:0005060	accumulation of giant lysosomes in kidney/renal tubule cells	Mammalian_phenotype	4
MP:0005072	MP:0005072	abnormal hair follicle melanin granule morphology	Mammalian_phenotype	4
MP:0005081	MP:0005081	abnormal dermis reticular layer morphology	Mammalian_phenotype	4
MP:0005100	MP:0005100	abnormal choroid pigmentation	Mammalian_phenotype	4
MP:0005102	MP:0005102	abnormal iris pigmentation	Mammalian_phenotype	4
MP:0005104	MP:0005104	abnormal tarsal bone morphology	Mammalian_phenotype	4
MP:0005105	MP:0005105	abnormal middle ear ossicle morphology	Mammalian_phenotype	4
MP:0005155	MP:0005155	herniated intestine	Mammalian_phenotype	4
MP:0005161	MP:0005161	hematuria	Mammalian_phenotype	4
MP:0005163	MP:0005163	cyclopia	Mammalian_phenotype	4
MP:0005189	MP:0005189	abnormal anogenital distance	Mammalian_phenotype	4
MP:0005194	MP:0005194	abnormal anterior uvea morphology	Mammalian_phenotype	4
MP:0005196	MP:0005196	abnormal posterior uvea morphology	Mammalian_phenotype	4
MP:0005200	MP:0005200	abnormal eye pigment epithelium morphology	Mammalian_phenotype	4
MP:0005205	MP:0005205	abnormal eye anterior chamber morphology	Mammalian_phenotype	4
MP:0005213	MP:0005213	gastric metaplasia	Mammalian_phenotype	4
MP:0005221	MP:0005221	abnormal rostral-caudal axis patterning	Mammalian_phenotype	4
MP:0005225	MP:0005225	abnormal vertebrae development	Mammalian_phenotype	4
MP:0005245	MP:0005245	hemarthrosis	Mammalian_phenotype	4
MP:0005247	MP:0005247	abnormal extraocular muscle morphology	Mammalian_phenotype	4
MP:0005251	MP:0005251	blepharitis	Mammalian_phenotype	4
MP:0005252	MP:0005252	abnormal meibomian gland morphology	Mammalian_phenotype	4
MP:0005255	MP:0005255	exotropia	Mammalian_phenotype	4
MP:0005256	MP:0005256	esotropia	Mammalian_phenotype	4
MP:0005258	MP:0005258	ocular hypertension	Mammalian_phenotype	4
MP:0005260	MP:0005260	ocular hypotension	Mammalian_phenotype	4
MP:0005261	MP:0005261	aniridia	Mammalian_phenotype	4
MP:0005262	MP:0005262	coloboma	Mammalian_phenotype	4
MP:0005263	MP:0005263	ectopia lentis	Mammalian_phenotype	4
MP:0005265	MP:0005265	abnormal blood urea nitrogen level	Mammalian_phenotype	4
MP:0005277	MP:0005277	abnormal brainstem morphology	Mammalian_phenotype	4
MP:0005278	MP:0005278	abnormal cholesterol homeostasis	Mammalian_phenotype	4
MP:0005288	MP:0005288	abnormal oxygen consumption	Mammalian_phenotype	4
MP:0005291	MP:0005291	abnormal glucose tolerance	Mammalian_phenotype	4
MP:0005294	MP:0005294	abnormal heart ventricle morphology	Mammalian_phenotype	4
MP:0005299	MP:0005299	abnormal eye posterior chamber morphology	Mammalian_phenotype	4
MP:0005302	MP:0005302	neurogenic bladder	Mammalian_phenotype	4
MP:0005308	MP:0005308	abnormal circulating ammonia level	Mammalian_phenotype	4
MP:0005311	MP:0005311	abnormal circulating amino acid level	Mammalian_phenotype	4
MP:0005312	MP:0005312	pericardial effusion	Mammalian_phenotype	4
MP:0005313	MP:0005313	absent adrenal gland	Mammalian_phenotype	4
MP:0005320	MP:0005320	abnormal biopterin level	Mammalian_phenotype	4
MP:0005322	MP:0005322	abnormal serotonin level	Mammalian_phenotype	4
MP:0005323	MP:0005323	dystonia	Mammalian_phenotype	4
MP:0005324	MP:0005324	ascites	Mammalian_phenotype	4
MP:0005331	MP:0005331	insulin resistance	Mammalian_phenotype	4
MP:0005342	MP:0005342	abnormal intestinal lipid absorption	Mammalian_phenotype	4
MP:0005355	MP:0005355	enlarged thyroid gland	Mammalian_phenotype	4
MP:0005365	MP:0005365	abnormal bile salt homeostasis	Mammalian_phenotype	4
MP:0005400	MP:0005400	abnormal vitamin level	Mammalian_phenotype	4
MP:0005402	MP:0005402	abnormal action potential	Mammalian_phenotype	4
MP:0005403	MP:0005403	abnormal nerve conduction	Mammalian_phenotype	4
MP:0005405	MP:0005405	axon degeneration	Mammalian_phenotype	4
MP:0005406	MP:0005406	abnormal heart size	Mammalian_phenotype	4
MP:0005411	MP:0005411	delayed fertilization	Mammalian_phenotype	4
MP:0005412	MP:0005412	vascular stenosis	Mammalian_phenotype	4
MP:0005415	MP:0005415	intrahepatic cholestasis	Mammalian_phenotype	4
MP:0005416	MP:0005416	abnormal circulating protein level	Mammalian_phenotype	4
MP:0005418	MP:0005418	abnormal circulating hormone level	Mammalian_phenotype	4
MP:0005421	MP:0005421	loose skin	Mammalian_phenotype	4
MP:0005422	MP:0005422	osteosclerosis	Mammalian_phenotype	4
MP:0005438	MP:0005438	abnormal glycogen homeostasis	Mammalian_phenotype	4
MP:0005443	MP:0005443	abnormal ethanol metabolism	Mammalian_phenotype	4
MP:0005450	MP:0005450	abnormal energy expenditure	Mammalian_phenotype	4
MP:0005457	MP:0005457	abnormal percent body fat	Mammalian_phenotype	4
MP:0005460	MP:0005460	abnormal leukopoiesis	Mammalian_phenotype	4
MP:0005464	MP:0005464	abnormal platelet physiology	Mammalian_phenotype	4
MP:0005468	MP:0005468	abnormal thyroid hormone level	Mammalian_phenotype	4
MP:0005494	MP:0005494	esophagogastric junction metaplasia	Mammalian_phenotype	4
MP:0005515	MP:0005515	uveitis	Mammalian_phenotype	4
MP:0005518	MP:0005518	abnormal pancreas regeneration	Mammalian_phenotype	4
MP:0005524	MP:0005524	abnormal renal plasma flow rate	Mammalian_phenotype	4
MP:0005529	MP:0005529	abnormal renal vascular resistance	Mammalian_phenotype	4
MP:0005532	MP:0005532	abnormal vascular resistance	Mammalian_phenotype	4
MP:0005533	MP:0005533	increased body temperature	Mammalian_phenotype	4
MP:0005534	MP:0005534	decreased body temperature	Mammalian_phenotype	4
MP:0005545	MP:0005545	abnormal lens development	Mammalian_phenotype	4
MP:0005556	MP:0005556	abnormal kidney clearance	Mammalian_phenotype	4
MP:0005581	MP:0005581	abnormal renin activity	Mammalian_phenotype	4
MP:0005587	MP:0005587	abnormal Meckel's cartilage morphology	Mammalian_phenotype	4
MP:0005592	MP:0005592	abnormal vascular smooth muscle morphology	Mammalian_phenotype	4
MP:0005603	MP:0005603	neuron hypertrophy	Mammalian_phenotype	4
MP:0005605	MP:0005605	increased bone mass	Mammalian_phenotype	4
MP:0005624	MP:0005624	abnormal plasma anion gap	Mammalian_phenotype	4
MP:0005637	MP:0005637	abnormal iron homeostasis	Mammalian_phenotype	4
MP:0005650	MP:0005650	abnormal limb bud morphology	Mammalian_phenotype	4
MP:0005651	MP:0005651	abnormal gonad rudiment morphology	Mammalian_phenotype	4
MP:0005652	MP:0005652	sex reversal	Mammalian_phenotype	4
MP:0005657	MP:0005657	abnormal neural plate morphology	Mammalian_phenotype	4
MP:0005672	MP:0005672	increased susceptibility to graft versus host disease	Mammalian_phenotype	4
MP:0005673	MP:0005673	decreased susceptibility to graft versus host disease	Mammalian_phenotype	4
MP:0006001	MP:0006001	abnormal intestinal transit time	Mammalian_phenotype	4
MP:0006009	MP:0006009	abnormal neuronal migration	Mammalian_phenotype	4
MP:0006018	MP:0006018	abnormal tympanic membrane morphology	Mammalian_phenotype	4
MP:0006029	MP:0006029	abnormal sclerotome morphology	Mammalian_phenotype	4
MP:0006031	MP:0006031	abnormal branchial pouch morphology	Mammalian_phenotype	4
MP:0006032	MP:0006032	abnormal ureteric bud morphology	Mammalian_phenotype	4
MP:0006037	MP:0006037	abnormal mitochondrial proliferation	Mammalian_phenotype	4
MP:0006050	MP:0006050	pulmonary fibrosis	Mammalian_phenotype	4
MP:0006059	MP:0006059	decreased susceptibility to ischemic brain injury	Mammalian_phenotype	4
MP:0006061	MP:0006061	right atrial isomerism	Mammalian_phenotype	4
MP:0006065	MP:0006065	abnormal heart position or orientation	Mammalian_phenotype	4
MP:0006078	MP:0006078	abnormal nipple morphology	Mammalian_phenotype	4
MP:0006083	MP:0006083	abnormal blood vessel elastic tissue morphology	Mammalian_phenotype	4
MP:0006093	MP:0006093	arteriovenous malformation	Mammalian_phenotype	4
MP:0006094	MP:0006094	increased fat cell size	Mammalian_phenotype	4
MP:0006111	MP:0006111	abnormal coronary circulation	Mammalian_phenotype	4
MP:0006113	MP:0006113	abnormal heart septum morphology	Mammalian_phenotype	4
MP:0006114	MP:0006114	cardiac murmur	Mammalian_phenotype	4
MP:0006126	MP:0006126	abnormal outflow tract development	Mammalian_phenotype	4
MP:0006141	MP:0006141	abnormal atrioventricular node conduction	Mammalian_phenotype	4
MP:0006142	MP:0006142	abnormal sinoatrial node conduction	Mammalian_phenotype	4
MP:0006150	MP:0006150	double vision	Mammalian_phenotype	4
MP:0006152	MP:0006152	tunnel vision	Mammalian_phenotype	4
MP:0006153	MP:0006153	hypermetropia	Mammalian_phenotype	4
MP:0006162	MP:0006162	thick eyelids	Mammalian_phenotype	4
MP:0006163	MP:0006163	ankyloblepharon filiform	Mammalian_phenotype	4
MP:0006164	MP:0006164	ectropion	Mammalian_phenotype	4
MP:0006165	MP:0006165	entropion	Mammalian_phenotype	4
MP:0006167	MP:0006167	eyelid edema	Mammalian_phenotype	4
MP:0006168	MP:0006168	epicanthus inversus	Mammalian_phenotype	4
MP:0006188	MP:0006188	calcified retina	Mammalian_phenotype	4
MP:0006192	MP:0006192	abnormal conjunctival vasculature morphology	Mammalian_phenotype	4
MP:0006197	MP:0006197	ocular hypotelorism	Mammalian_phenotype	4
MP:0006198	MP:0006198	enophthalmos	Mammalian_phenotype	4
MP:0006199	MP:0006199	hypertropia	Mammalian_phenotype	4
MP:0006237	MP:0006237	abnormal choroid vasculature morphology	Mammalian_phenotype	4
MP:0006249	MP:0006249	phthisis bulbi	Mammalian_phenotype	4
MP:0006260	MP:0006260	abnormal gustatory papillae taste bud morphology	Mammalian_phenotype	4
MP:0006261	MP:0006261	annular pancreas	Mammalian_phenotype	4
MP:0006272	MP:0006272	abnormal urine organic anion level	Mammalian_phenotype	4
MP:0006273	MP:0006273	abnormal urine organic cation level	Mammalian_phenotype	4
MP:0006274	MP:0006274	abnormal urine sodium level	Mammalian_phenotype	4
MP:0006277	MP:0006277	abnormal parasympathetic nervous system physiology	Mammalian_phenotype	4
MP:0006278	MP:0006278	aortic aneurysm	Mammalian_phenotype	4
MP:0006280	MP:0006280	abnormal digit development	Mammalian_phenotype	4
MP:0006285	MP:0006285	absent inner ear	Mammalian_phenotype	4
MP:0006286	MP:0006286	inner ear hypoplasia	Mammalian_phenotype	4
MP:0006287	MP:0006287	inner ear cysts	Mammalian_phenotype	4
MP:0006301	MP:0006301	abnormal mesenchyme morphology	Mammalian_phenotype	4
MP:0006305	MP:0006305	abnormal optic eminence morphology	Mammalian_phenotype	4
MP:0006306	MP:0006306	abnormal nasal pit morphology	Mammalian_phenotype	4
MP:0006315	MP:0006315	abnormal urine protein level	Mammalian_phenotype	4
MP:0006320	MP:0006320	abnormal interscapular fat pad morphology	Mammalian_phenotype	4
MP:0006323	MP:0006323	abnormal extraembryonic mesoderm development	Mammalian_phenotype	4
MP:0006325	MP:0006325	impaired hearing	Mammalian_phenotype	4
MP:0006334	MP:0006334	abnormal susceptibility to hearing loss	Mammalian_phenotype	4
MP:0006335	MP:0006335	abnormal hearing electrophysiology	Mammalian_phenotype	4
MP:0006336	MP:0006336	abnormal otoacoustic response	Mammalian_phenotype	4
MP:0006357	MP:0006357	abnormal circulating mineral level	Mammalian_phenotype	4
MP:0006367	MP:0006367	absent sweat gland	Mammalian_phenotype	4
MP:0006377	MP:0006377	abnormal vestibulocollic reflex	Mammalian_phenotype	4
MP:0006382	MP:0006382	abnormal lung epithelium morphology	Mammalian_phenotype	4
MP:0006389	MP:0006389	abnormal vestibular endolymph	Mammalian_phenotype	4
MP:0006390	MP:0006390	abnormal cochlear endolymph	Mammalian_phenotype	4
MP:0006395	MP:0006395	abnormal epiphyseal plate morphology	Mammalian_phenotype	4
MP:0006410	MP:0006410	abnormal common myeloid progenitor cell morphology	Mammalian_phenotype	4
MP:0006429	MP:0006429	abnormal hyaline cartilage morphology	Mammalian_phenotype	4
MP:0006430	MP:0006430	abnormal elastic cartilage morphology	Mammalian_phenotype	4
MP:0006431	MP:0006431	abnormal fibrocartilage morphology	Mammalian_phenotype	4
MP:0006432	MP:0006432	abnormal costal cartilage morphology	Mammalian_phenotype	4
MP:0008005	MP:0008005	decreased stomach pH	Mammalian_phenotype	4
MP:0008006	MP:0008006	increased stomach pH	Mammalian_phenotype	4
MP:0008008	MP:0008008	early cellular replicative senescence	Mammalian_phenotype	4
MP:0008009	MP:0008009	delayed cellular replicative senescence	Mammalian_phenotype	4
MP:0008011	MP:0008011	intestine polyps	Mammalian_phenotype	4
MP:0008015	MP:0008015	abnormal female inguinal canal morphology	Mammalian_phenotype	4
MP:0008016	MP:0008016	abnormal male inguinal canal morphology	Mammalian_phenotype	4
MP:0008017	MP:0008017	inguinal cysts	Mammalian_phenotype	4
MP:0008020	MP:0008020	abnormal dermal mast cell morphology	Mammalian_phenotype	4
MP:0008025	MP:0008025	brain vacuoles	Mammalian_phenotype	4
MP:0008026	MP:0008026	abnormal brain white matter morphology	Mammalian_phenotype	4
MP:0008027	MP:0008027	abnormal spinal cord white matter morphology	Mammalian_phenotype	4
MP:0008028	MP:0008028	pregnancy-related premature death	Mammalian_phenotype	4
MP:0008030	MP:0008030	abnormal Cajal-Retzius cell morphology	Mammalian_phenotype	4
MP:0008032	MP:0008032	abnormal lipolysis	Mammalian_phenotype	4
MP:0008111	MP:0008111	abnormal granulocyte differentiation	Mammalian_phenotype	4
MP:0008115	MP:0008115	abnormal dendritic cell differentiation	Mammalian_phenotype	4
MP:0008145	MP:0008145	hemeralopia	Mammalian_phenotype	4
MP:0008195	MP:0008195	abnormal professional antigen presenting cell morphology	Mammalian_phenotype	4
MP:0008196	MP:0008196	abnormal follicular dendritic cell morphology	Mammalian_phenotype	4
MP:0008197	MP:0008197	abnormal follicular dendritic cell physiology	Mammalian_phenotype	4
MP:0008198	MP:0008198	abnormal follicular dendritic cell antigen presentation	Mammalian_phenotype	4
MP:0008218	MP:0008218	delayed emergence of vibrissae	Mammalian_phenotype	4
MP:0008232	MP:0008232	abnormal cingulum morphology	Mammalian_phenotype	4
MP:0008235	MP:0008235	increased susceptibility to neuronal excitotoxicity	Mammalian_phenotype	4
MP:0008236	MP:0008236	decreased susceptibility to neuronal excitotoxicity	Mammalian_phenotype	4
MP:0008242	MP:0008242	abnormal perivascular macrophage morphology	Mammalian_phenotype	4
MP:0008243	MP:0008243	abnormal macrophage derived foam cell morphology	Mammalian_phenotype	4
MP:0008246	MP:0008246	abnormal leukocyte morphology	Mammalian_phenotype	4
MP:0008249	MP:0008249	abnormal common lymphocyte progenitor cell morphology	Mammalian_phenotype	4
MP:0008272	MP:0008272	abnormal endochondral bone ossification	Mammalian_phenotype	4
MP:0008273	MP:0008273	abnormal intramembranous bone ossification	Mammalian_phenotype	4
MP:0008274	MP:0008274	failure of bone ossification	Mammalian_phenotype	4
MP:0008280	MP:0008280	abnormal male germ cell apoptosis	Mammalian_phenotype	4
MP:0008288	MP:0008288	abnormal adrenal cortex morphology	Mammalian_phenotype	4
MP:0008289	MP:0008289	abnormal adrenal medulla morphology	Mammalian_phenotype	4
MP:0008304	MP:0008304	abnormal organ of Corti supporting cell differentiation	Mammalian_phenotype	4
MP:0008306	MP:0008306	abnormal organ of Corti supporting cell proliferation	Mammalian_phenotype	4
MP:0008395	MP:0008395	abnormal osteoblast differentiation	Mammalian_phenotype	4
MP:0008396	MP:0008396	abnormal osteoclast differentiation	Mammalian_phenotype	4
MP:0008414	MP:0008414	abnormal spatial reference memory	Mammalian_phenotype	4
MP:0008415	MP:0008415	abnormal neurite morphology	Mammalian_phenotype	4
MP:0008419	MP:0008419	abnormal cutaneous microfibril morphology	Mammalian_phenotype	4
MP:0008428	MP:0008428	abnormal spatial working memory	Mammalian_phenotype	4
MP:0008461	MP:0008461	left atrial isomerism	Mammalian_phenotype	4
MP:0008462	MP:0008462	abnormal medium spiny neuron morphology	Mammalian_phenotype	4
MP:0008480	MP:0008480	absent eye pigmentation	Mammalian_phenotype	4
MP:0008487	MP:0008487	abnormal mesonephros morphology	Mammalian_phenotype	4
MP:0008494	MP:0008494	absence of all nails	Mammalian_phenotype	4
MP:0008503	MP:0008503	abnormal spinal cord grey matter morphology	Mammalian_phenotype	4
MP:0008533	MP:0008533	abnormal anterior visceral endoderm morphology	Mammalian_phenotype	4
MP:0008544	MP:0008544	impaired olfaction	Mammalian_phenotype	4
MP:0008713	MP:0008713	abnormal cytokine level	Mammalian_phenotype	4
MP:0008731	MP:0008731	abnormal hair shaft melanin granule morphology	Mammalian_phenotype	4
MP:0008736	MP:0008736	micromelia	Mammalian_phenotype	4
MP:0008737	MP:0008737	abnormal spleen physiology	Mammalian_phenotype	4
MP:0008738	MP:0008738	abnormal liver iron level	Mammalian_phenotype	4
MP:0008740	MP:0008740	abnormal intestinal iron level	Mammalian_phenotype	4
MP:0008741	MP:0008741	abnormal heart iron level	Mammalian_phenotype	4
MP:0008742	MP:0008742	abnormal kidney iron level	Mammalian_phenotype	4
MP:0008770	MP:0008770	decreased survivor rate	Mammalian_phenotype	4
MP:0008778	MP:0008778	abnormal lymphangiogenesis	Mammalian_phenotype	4
MP:0008786	MP:0008786	abnormal hindgut morphology	Mammalian_phenotype	4
MP:0008787	MP:0008787	abnormal tailgut morphology	Mammalian_phenotype	4
MP:0008801	MP:0008801	abnormal erythroid progenitor cell morphology	Mammalian_phenotype	4
MP:0008802	MP:0008802	abnormal intestinal smooth muscle morphology	Mammalian_phenotype	4
MP:0008811	MP:0008811	abnormal brain iron level	Mammalian_phenotype	4
MP:0008815	MP:0008815	anterior staphyloma	Mammalian_phenotype	4
MP:0008820	MP:0008820	abnormal blood uric acid level	Mammalian_phenotype	4
MP:0008825	MP:0008825	abnormal cardiac epithelial to mesenchymal transition	Mammalian_phenotype	4
MP:0008830	MP:0008830	abnormal nucleolus morphology	Mammalian_phenotype	4
MP:0008831	MP:0008831	abnormal insulin-like growth factor I level	Mammalian_phenotype	4
MP:0008835	MP:0008835	abnormal intercellular signaling peptide or protein level	Mammalian_phenotype	4
MP:0008854	MP:0008854	bleb	Mammalian_phenotype	4
MP:0008855	MP:0008855	eye bleb	Mammalian_phenotype	4
MP:0008856	MP:0008856	fetal bleb	Mammalian_phenotype	4
MP:0008858	MP:0008858	abnormal hair cycle anagen phase	Mammalian_phenotype	4
MP:0008859	MP:0008859	abnormal hair cycle catagen phase	Mammalian_phenotype	4
MP:0008860	MP:0008860	abnormal hair cycle telogen phase	Mammalian_phenotype	4
MP:0008861	MP:0008861	abnormal hair shedding	Mammalian_phenotype	4
MP:0008863	MP:0008863	craniofacial asymmetry	Mammalian_phenotype	4
MP:0008866	MP:0008866	chromosomal instability	Mammalian_phenotype	4
MP:0008877	MP:0008877	abnormal DNA methylation	Mammalian_phenotype	4
MP:0008878	MP:0008878	abnormal DNA methylation during gametogenesis	Mammalian_phenotype	4
MP:0008880	MP:0008880	lacrimal gland inflammation	Mammalian_phenotype	4
MP:0008881	MP:0008881	absent Harderian gland	Mammalian_phenotype	4
MP:0008882	MP:0008882	abnormal enterocyte physiology	Mammalian_phenotype	4
MP:0008883	MP:0008883	abnormal enterocyte proliferation	Mammalian_phenotype	4
MP:0008886	MP:0008886	abnormal PML bodies	Mammalian_phenotype	4
MP:0008887	MP:0008887	abnormal splicing factor domain morphology	Mammalian_phenotype	4
MP:0008888	MP:0008888	abnormal Cajal body morphology	Mammalian_phenotype	4
MP:0008889	MP:0008889	abnormal Gem morphology	Mammalian_phenotype	4
MP:0008890	MP:0008890	abnormal nuclear lamina morphology	Mammalian_phenotype	4
MP:0008902	MP:0008902	abnormal renal fat pad morphology	Mammalian_phenotype	4
MP:0008904	MP:0008904	abnormal mammary fat pad morphology	Mammalian_phenotype	4
MP:0008905	MP:0008905	abnormal femoral fat pad morphology	Mammalian_phenotype	4
MP:0008909	MP:0008909	supination	Mammalian_phenotype	4
MP:0008916	MP:0008916	abnormal astrocyte physiology	Mammalian_phenotype	4
MP:0008917	MP:0008917	abnormal oligodendrocyte physiology	Mammalian_phenotype	4
MP:0008926	MP:0008926	abnormal anterior definitive endoderm morphology	Mammalian_phenotype	4
MP:0008933	MP:0008933	abnormal embryonic cilium physiology	Mammalian_phenotype	4
MP:0008942	MP:0008942	abnormal induced cell death	Mammalian_phenotype	4
MP:0008946	MP:0008946	abnormal neuron number	Mammalian_phenotype	4
MP:0008962	MP:0008962	abnormal carbon dioxide production	Mammalian_phenotype	4
MP:0008965	MP:0008965	increased basal metabolism	Mammalian_phenotype	4
MP:0008969	MP:0008969	abnormal nasolacrimal duct morphology	Mammalian_phenotype	4
MP:0008986	MP:0008986	abnormal liver parenchyma morphology	Mammalian_phenotype	4
MP:0008996	MP:0008996	abnormal blood osmolality	Mammalian_phenotype	4
MP:0009003	MP:0009003	abnormal vibrissa number	Mammalian_phenotype	4
MP:0009022	MP:0009022	abnormal brain meninges morphology	Mammalian_phenotype	4
MP:0009023	MP:0009023	abnormal spinal cord meninges morphology	Mammalian_phenotype	4
MP:0009027	MP:0009027	abnormal subarachnoid space morphology	Mammalian_phenotype	4
MP:0009042	MP:0009042	pilar cyst	Mammalian_phenotype	4
MP:0009054	MP:0009054	absent anal canal	Mammalian_phenotype	4
MP:0009055	MP:0009055	abnormal internal anal sphincter morphology	Mammalian_phenotype	4
MP:0009106	MP:0009106	abnormal pancreas size	Mammalian_phenotype	4
MP:0009116	MP:0009116	abnormal brown fat cell morphology	Mammalian_phenotype	4
MP:0009117	MP:0009117	abnormal white fat cell morphology	Mammalian_phenotype	4
MP:0009148	MP:0009148	pancreas necrosis	Mammalian_phenotype	4
MP:0009165	MP:0009165	abnormal endocrine pancreas morphology	Mammalian_phenotype	4
MP:0009175	MP:0009175	abnormal pancreatic beta cell differentiation	Mammalian_phenotype	4
MP:0009179	MP:0009179	abnormal pancreatic alpha cell differentiation	Mammalian_phenotype	4
MP:0009183	MP:0009183	abnormal pancreatic delta cell differentiation	Mammalian_phenotype	4
MP:0009188	MP:0009188	abnormal PP cell differentiation	Mammalian_phenotype	4
MP:0009193	MP:0009193	abnormal pancreatic epsilon cell differentiation	Mammalian_phenotype	4
MP:0009198	MP:0009198	abnormal male genitalia morphology	Mammalian_phenotype	4
MP:0009208	MP:0009208	abnormal female genitalia morphology	Mammalian_phenotype	4
MP:0009216	MP:0009216	abnormal peritoneum morphology	Mammalian_phenotype	4
MP:0009252	MP:0009252	absent urinary bladder	Mammalian_phenotype	4
MP:0009269	MP:0009269	decreased fat cell size	Mammalian_phenotype	4
MP:0009284	MP:0009284	abnormal sympathetic neuron innervation pattern	Mammalian_phenotype	4
MP:0009334	MP:0009334	abnormal splenocyte proliferation	Mammalian_phenotype	4
MP:0009344	MP:0009344	abnormal ovulation cycle	Mammalian_phenotype	4
MP:0009348	MP:0009348	abnormal urine pH	Mammalian_phenotype	4
MP:0009357	MP:0009357	abnormal seizure response to inducing agent	Mammalian_phenotype	4
MP:0009384	MP:0009384	cardiac valve regurgitation	Mammalian_phenotype	4
MP:0009407	MP:0009407	increased skeletal muscle fiber density	Mammalian_phenotype	4
MP:0009408	MP:0009408	decreased skeletal muscle fiber density	Mammalian_phenotype	4
MP:0009409	MP:0009409	abnormal skeletal muscle fiber type ratio	Mammalian_phenotype	4
MP:0009415	MP:0009415	skeletal muscle degeneration	Mammalian_phenotype	4
MP:0009416	MP:0009416	cardiac muscle degeneration	Mammalian_phenotype	4
MP:0009417	MP:0009417	skeletal muscle atrophy	Mammalian_phenotype	4
MP:0009418	MP:0009418	cardiac muscle atrophy	Mammalian_phenotype	4
MP:0009419	MP:0009419	skeletal muscle fibrosis	Mammalian_phenotype	4
MP:0009441	MP:0009441	delayed skin barrier formation	Mammalian_phenotype	4
MP:0009470	MP:0009470	mirror image duplication	Mammalian_phenotype	4
MP:0009471	MP:0009471	abnormal urine sulfate level	Mammalian_phenotype	4
MP:0009488	MP:0009488	abnormal pancreatic islet cell apoptosis	Mammalian_phenotype	4
MP:0009489	MP:0009489	abnormal blood vessel endothelium morphology	Mammalian_phenotype	4
MP:0009497	MP:0009497	abnormal intrahepatic bile duct morphology	Mammalian_phenotype	4
MP:0009502	MP:0009502	abnormal areola morphology	Mammalian_phenotype	4
MP:0009503	MP:0009503	abnormal mammary gland duct morphology	Mammalian_phenotype	4
MP:0009504	MP:0009504	abnormal mammary gland epithelium morphology	Mammalian_phenotype	4
MP:0009505	MP:0009505	abnormal mammary gland lobule morphology	Mammalian_phenotype	4
MP:0009507	MP:0009507	abnormal mammary gland connective tissue morphology	Mammalian_phenotype	4
MP:0009511	MP:0009511	distended stomach	Mammalian_phenotype	4
MP:0009516	MP:0009516	enlarged salivary gland	Mammalian_phenotype	4
MP:0009517	MP:0009517	abnormal salivary gland duct morphology	Mammalian_phenotype	4
MP:0009535	MP:0009535	abnormal skin sebaceous gland morphology	Mammalian_phenotype	4
MP:0009537	MP:0009537	interstitial cells of Cajal hyperplasia	Mammalian_phenotype	4
MP:0009538	MP:0009538	abnormal synapse morphology	Mammalian_phenotype	4
MP:0009545	MP:0009545	abnormal dermis papillary layer morphology	Mammalian_phenotype	4
MP:0009552	MP:0009552	urinary bladder obstruction	Mammalian_phenotype	4
MP:0009562	MP:0009562	abnormal odor adaptation	Mammalian_phenotype	4
MP:0009569	MP:0009569	abnormal left lung morphology	Mammalian_phenotype	4
MP:0009570	MP:0009570	abnormal right lung morphology	Mammalian_phenotype	4
MP:0009579	MP:0009579	acephaly	Mammalian_phenotype	4
MP:0009582	MP:0009582	abnormal keratinocyte proliferation	Mammalian_phenotype	4
MP:0009585	MP:0009585	ectopic bone formation	Mammalian_phenotype	4
MP:0009587	MP:0009587	abnormal plasma membrane sphingolipid content	Mammalian_phenotype	4
MP:0009610	MP:0009610	abnormal epidermis stratum lucidum morphology	Mammalian_phenotype	4
MP:0009615	MP:0009615	abnormal zinc homeostasis	Mammalian_phenotype	4
MP:0009620	MP:0009620	abnormal primary vitreous morphology	Mammalian_phenotype	4
MP:0009641	MP:0009641	kidney degeneration	Mammalian_phenotype	4
MP:0009644	MP:0009644	uremia	Mammalian_phenotype	4
MP:0009645	MP:0009645	crystalluria	Mammalian_phenotype	4
MP:0009646	MP:0009646	urinary bladder inflammation	Mammalian_phenotype	4
MP:0009647	MP:0009647	decreased fertilization frequency	Mammalian_phenotype	4
MP:0009651	MP:0009651	abnormal eyelid development	Mammalian_phenotype	4
MP:0009653	MP:0009653	abnormal palate development	Mammalian_phenotype	4
MP:0009661	MP:0009661	abnormal pregnancy	Mammalian_phenotype	4
MP:0009671	MP:0009671	abnormal uterus physiology	Mammalian_phenotype	4
MP:0009673	MP:0009673	increased birth weight	Mammalian_phenotype	4
MP:0009674	MP:0009674	decreased birth weight	Mammalian_phenotype	4
MP:0009676	MP:0009676	abnormal hemostasis	Mammalian_phenotype	4
MP:0009682	MP:0009682	abnormal anterior corticospinal tract morphology	Mammalian_phenotype	4
MP:0009683	MP:0009683	abnormal lateral corticospinal tract morphology	Mammalian_phenotype	4
MP:0009685	MP:0009685	abnormal spinal cord motor column morphology	Mammalian_phenotype	4
MP:0009688	MP:0009688	abnormal spinal cord central canal morphology	Mammalian_phenotype	4
MP:0009694	MP:0009694	abnormal spinal cord commissure morphology	Mammalian_phenotype	4
MP:0009705	MP:0009705	abnormal midgut morphology	Mammalian_phenotype	4
MP:0009716	MP:0009716	abnormal subcommissural organ morphology	Mammalian_phenotype	4
MP:0009746	MP:0009746	enhanced behavioral response to xenobiotic	Mammalian_phenotype	4
MP:0009747	MP:0009747	impaired behavioral response to xenobiotic	Mammalian_phenotype	4
MP:0009748	MP:0009748	abnormal behavioral response to addictive substance	Mammalian_phenotype	4
MP:0009763	MP:0009763	increased sensitivity to induced morbidity/mortality	Mammalian_phenotype	4
MP:0009764	MP:0009764	decreased sensitivity to induced morbidity/mortality	Mammalian_phenotype	4
MP:0009766	MP:0009766	increased sensitivity to xenobiotic induced morbidity/mortality	Mammalian_phenotype	4
MP:0009767	MP:0009767	decreased sensitivity to xenobiotic induced morbidity/mortality	Mammalian_phenotype	4
MP:0009772	MP:0009772	abnormal retinal development	Mammalian_phenotype	4
MP:0009777	MP:0009777	abnormal behavioral response to anesthetic	Mammalian_phenotype	4
MP:0009796	MP:0009796	abnormal base-excision repair	Mammalian_phenotype	4
MP:0009797	MP:0009797	abnormal mismatch repair	Mammalian_phenotype	4
MP:0009806	MP:0009806	abnormal otic vesicle morphology	Mammalian_phenotype	4
MP:0009807	MP:0009807	abnormal pelvic ligament morphology	Mammalian_phenotype	4
MP:0009809	MP:0009809	abnormal urine uric acid level	Mammalian_phenotype	4
MP:0009820	MP:0009820	abnormal liver vasculature morphology	Mammalian_phenotype	4
MP:0009821	MP:0009821	abnormal vestibular aqueduct morphology	Mammalian_phenotype	4
MP:0009827	MP:0009827	skin detachment	Mammalian_phenotype	4
MP:0009828	MP:0009828	increased tumor latency	Mammalian_phenotype	4
MP:0009841	MP:0009841	foam cell reticulosis	Mammalian_phenotype	4
MP:0009842	MP:0009842	abnormal neural crest cell proliferation	Mammalian_phenotype	4
MP:0009854	MP:0009854	impaired gastric peristalsis	Mammalian_phenotype	4
MP:0009860	MP:0009860	nephrosclerosis	Mammalian_phenotype	4
MP:0009861	MP:0009861	abnormal pyloric sphincter morphology	Mammalian_phenotype	4
MP:0009877	MP:0009877	exostosis	Mammalian_phenotype	4
MP:0009901	MP:0009901	abnormal frontonasal prominence morphology	Mammalian_phenotype	4
MP:0009902	MP:0009902	abnormal lateral nasal prominence morphology	Mammalian_phenotype	4
MP:0009903	MP:0009903	abnormal medial nasal prominence morphology	Mammalian_phenotype	4
MP:0009918	MP:0009918	abnormal stylohyoid ligament morphology	Mammalian_phenotype	4
MP:0009937	MP:0009937	abnormal neuron differentiation	Mammalian_phenotype	4
MP:0009939	MP:0009939	abnormal hippocampus neuron morphology	Mammalian_phenotype	4
MP:0009967	MP:0009967	abnormal neuron proliferation	Mammalian_phenotype	4
MP:0009969	MP:0009969	abnormal cerebral cortex pyramidal cell morphology	Mammalian_phenotype	4
MP:0010021	MP:0010021	heart vascular congestion	Mammalian_phenotype	4
MP:0010024	MP:0010024	increased total body fat amount	Mammalian_phenotype	4
MP:0010025	MP:0010025	decreased total body fat amount	Mammalian_phenotype	4
MP:0010028	MP:0010028	aciduria	Mammalian_phenotype	4
MP:0010038	MP:0010038	abnormal placenta physiology	Mammalian_phenotype	4
MP:0010039	MP:0010039	abnormal trophoblast giant cell proliferation	Mammalian_phenotype	4
MP:0010041	MP:0010041	absent oval cells	Mammalian_phenotype	4
MP:0010042	MP:0010042	abnormal oval cell physiology	Mammalian_phenotype	4
MP:0010050	MP:0010050	hypermyelination	Mammalian_phenotype	4
MP:0010055	MP:0010055	abnormal sensory neuron physiology	Mammalian_phenotype	4
MP:0010056	MP:0010056	ectopic skeletal muscle	Mammalian_phenotype	4
MP:0010060	MP:0010060	abnormal creatine level	Mammalian_phenotype	4
MP:0010072	MP:0010072	increased pruritus	Mammalian_phenotype	4
MP:0010073	MP:0010073	decreased pruritus	Mammalian_phenotype	4
MP:0010080	MP:0010080	abnormal hepatocyte physiology	Mammalian_phenotype	4
MP:0010086	MP:0010086	abnormal circulating fructosamine level	Mammalian_phenotype	4
MP:0010095	MP:0010095	increased chromosomal stability	Mammalian_phenotype	4
MP:0010107	MP:0010107	abnormal renal reabsorbtion	Mammalian_phenotype	4
MP:0010108	MP:0010108	abnormal renal water reabsorbtion	Mammalian_phenotype	4
MP:0010109	MP:0010109	abnormal renal sodium reabsorbtion	Mammalian_phenotype	4
MP:0010110	MP:0010110	abnormal renal phosphate reabsorbtion	Mammalian_phenotype	4
MP:0010115	MP:0010115	abnormal embryonic cloaca morphology	Mammalian_phenotype	4
MP:0010119	MP:0010119	abnormal bone mineral density	Mammalian_phenotype	4
MP:0010122	MP:0010122	abnormal bone mineral content	Mammalian_phenotype	4
MP:0010126	MP:0010126	abnormal distal visceral endoderm morphology	Mammalian_phenotype	4
MP:0010143	MP:0010143	enhanced fertility	Mammalian_phenotype	4
MP:0010147	MP:0010147	abnormal endocrine pancreas physiology	Mammalian_phenotype	4
MP:0010151	MP:0010151	abnormal spinal cord ependymal layer morphology	Mammalian_phenotype	4
MP:0010152	MP:0010152	abnormal brain ependyma morphology	Mammalian_phenotype	4
MP:0010153	MP:0010153	abnormal gastroesophageal sphincter morphology	Mammalian_phenotype	4
MP:0010156	MP:0010156	abnormal small intestinal crypt cell physiology	Mammalian_phenotype	4
MP:0010157	MP:0010157	abnormal small intestinal crypt cell proliferation	Mammalian_phenotype	4
MP:0010158	MP:0010158	abnormal intestine development	Mammalian_phenotype	4
MP:0010159	MP:0010159	abnormal enterocyte differentiation	Mammalian_phenotype	4
MP:0010165	MP:0010165	abnormal response to stress-induced hyperthermia	Mammalian_phenotype	4
MP:0010170	MP:0010170	abnormal glial cell apoptosis	Mammalian_phenotype	4
MP:0010172	MP:0010172	abnormal mammary gland epithelium physiology	Mammalian_phenotype	4
MP:0010192	MP:0010192	abnormal retinal melanin granule morphology	Mammalian_phenotype	4
MP:0010193	MP:0010193	abnormal choroid melanin granule morphology	Mammalian_phenotype	4
MP:0010194	MP:0010194	absent lymphatic vessels	Mammalian_phenotype	4
MP:0010195	MP:0010195	abnormal lymphatic vessel endothelium morphology	Mammalian_phenotype	4
MP:0010196	MP:0010196	abnormal lymphatic vessel smooth muscle morphology	Mammalian_phenotype	4
MP:0010200	MP:0010200	enlarged lymphatic vessel	Mammalian_phenotype	4
MP:0010211	MP:0010211	abnormal acute phase protein level	Mammalian_phenotype	4
MP:0010237	MP:0010237	abnormal skeletal muscle weight	Mammalian_phenotype	4
MP:0010300	MP:0010300	increased skin tumor incidence	Mammalian_phenotype	4
MP:0010308	MP:0010308	decreased tumor latency	Mammalian_phenotype	4
MP:0010330	MP:0010330	abnormal circulating lipoprotein level	Mammalian_phenotype	4
MP:0010331	MP:0010331	abnormal apolipoprotein level	Mammalian_phenotype	4
MP:0010347	MP:0010347	osseous metaplasia	Mammalian_phenotype	4
MP:0010359	MP:0010359	increased liver free fatty acids level	Mammalian_phenotype	4
MP:0010360	MP:0010360	decreased liver free fatty acids level	Mammalian_phenotype	4
MP:0010369	MP:0010369	abnormal thalamus neuron morphology	Mammalian_phenotype	4
MP:0010371	MP:0010371	abnormal epiglottis morphology	Mammalian_phenotype	4
MP:0010372	MP:0010372	throat cyst	Mammalian_phenotype	4
MP:0010380	MP:0010380	abnormal inner cell mass apoptosis	Mammalian_phenotype	4
MP:0010381	MP:0010381	abnormal dosage compensation	Mammalian_phenotype	4
MP:0010385	MP:0010385	abnormal glycinergic neuron morphology	Mammalian_phenotype	4
MP:0010388	MP:0010388	abnormal Bergmann glial cell differentiation	Mammalian_phenotype	4
MP:0010421	MP:0010421	ventricular aneurysm	Mammalian_phenotype	4
MP:0010425	MP:0010425	abnormal heart and great vessel attachment	Mammalian_phenotype	4
MP:0010435	MP:0010435	abnormal heart atrium and ventricle connection	Mammalian_phenotype	4
MP:0010450	MP:0010450	atrial septal aneurysm	Mammalian_phenotype	4
MP:0010451	MP:0010451	kidney microaneurysm	Mammalian_phenotype	4
MP:0010452	MP:0010452	retina microaneurysm	Mammalian_phenotype	4
MP:0010462	MP:0010462	pulmonary artery aneurysm	Mammalian_phenotype	4
MP:0010477	MP:0010477	coronary artery aneurysm	Mammalian_phenotype	4
MP:0010478	MP:0010478	intracranial aneurysm	Mammalian_phenotype	4
MP:0010479	MP:0010479	brain aneurysm	Mammalian_phenotype	4
MP:0010508	MP:0010508	abnormal heart electrocardiography waveform feature	Mammalian_phenotype	4
MP:0010545	MP:0010545	abnormal heart layer morphology	Mammalian_phenotype	4
MP:0010551	MP:0010551	abnormal coronary vessel morphology	Mammalian_phenotype	4
MP:0010559	MP:0010559	heart block	Mammalian_phenotype	4
MP:0010632	MP:0010632	cardiac muscle necrosis	Mammalian_phenotype	4
MP:0010681	MP:0010681	abnormal hair follicle bulb morphology	Mammalian_phenotype	4
MP:0010682	MP:0010682	abnormal hair follicle infundibulum morphology	Mammalian_phenotype	4
MP:0010684	MP:0010684	abnormal hair follicle outer root sheath morphology	Mammalian_phenotype	4
MP:0010685	MP:0010685	abnormal hair follicle inner root sheath morphology	Mammalian_phenotype	4
MP:0010694	MP:0010694	abnormal hair follicle isthmus morphology	Mammalian_phenotype	4
MP:0010697	MP:0010697	abnormal systemic arterial blood pressure regulation	Mammalian_phenotype	4
MP:0010699	MP:0010699	dilated hair follicles	Mammalian_phenotype	4
MP:0010700	MP:0010700	hair follicle comedo	Mammalian_phenotype	4
MP:0010710	MP:0010710	absent sclera	Mammalian_phenotype	4
MP:0010726	MP:0010726	abnormal collateral sprouting	Mammalian_phenotype	4
MP:0010736	MP:0010736	abnormal extraembryonic ectoderm morphology	Mammalian_phenotype	4
MP:0010746	MP:0010746	abnormal pre-Botzinger complex physiology	Mammalian_phenotype	4
MP:0010748	MP:0010748	abnormal visual evoked potential	Mammalian_phenotype	4
MP:0010752	MP:0010752	impaired mucociliary clearance	Mammalian_phenotype	4
MP:0010753	MP:0010753	improved mucociliary clearance	Mammalian_phenotype	4
MP:0010754	MP:0010754	abnormal heart left ventricle pressure	Mammalian_phenotype	4
MP:0010755	MP:0010755	abnormal heart right ventricle pressure	Mammalian_phenotype	4
MP:0010766	MP:0010766	abnormal NK cell physiology	Mammalian_phenotype	4
MP:0010778	MP:0010778	abnormal stomach fundus morphology	Mammalian_phenotype	4
MP:0010779	MP:0010779	abnormal stomach muscularis externa morphology	Mammalian_phenotype	4
MP:0010783	MP:0010783	abnormal stomach wall morphology	Mammalian_phenotype	4
MP:0010784	MP:0010784	abnormal forestomach morphology	Mammalian_phenotype	4
MP:0010785	MP:0010785	abnormal stomach pyloric region morphology	Mammalian_phenotype	4
MP:0010787	MP:0010787	gastric cysts	Mammalian_phenotype	4
MP:0010789	MP:0010789	abnormal stomach mesentery morphology	Mammalian_phenotype	4
MP:0010798	MP:0010798	abnormal stomach cardiac region morphology	Mammalian_phenotype	4
MP:0010802	MP:0010802	abnormal intestinal enteroendocrine cell morphology	Mammalian_phenotype	4
MP:0010803	MP:0010803	abnormal stomach enteroendocrine cell morphology	Mammalian_phenotype	4
MP:0010806	MP:0010806	abnormal stomach muscularis mucosa morphology	Mammalian_phenotype	4
MP:0010807	MP:0010807	abnormal stomach position or orientation	Mammalian_phenotype	4
MP:0010818	MP:0010818	adhesive atelectasis	Mammalian_phenotype	4
MP:0010819	MP:0010819	primary atelectasis	Mammalian_phenotype	4
MP:0010821	MP:0010821	abnormal visceral pleura morphology	Mammalian_phenotype	4
MP:0010823	MP:0010823	abnormal parietal pleura morphology	Mammalian_phenotype	4
MP:0010832	MP:0010832	lethality during fetal growth through weaning	Mammalian_phenotype	4
MP:0010853	MP:0010853	abnormal lung position or orientation	Mammalian_phenotype	4
MP:0010857	MP:0010857	pulmonary necrosis	Mammalian_phenotype	4
MP:0010874	MP:0010874	abnormal bone volume	Mammalian_phenotype	4
MP:0010880	MP:0010880	small esophagus	Mammalian_phenotype	4
MP:0010883	MP:0010883	trachea stenosis	Mammalian_phenotype	4
MP:0010884	MP:0010884	esophagus stenosis	Mammalian_phenotype	4
MP:0010885	MP:0010885	absent trachea	Mammalian_phenotype	4
MP:0010887	MP:0010887	pale lung	Mammalian_phenotype	4
MP:0010899	MP:0010899	abnormal pulmonary alveolar system morphology	Mammalian_phenotype	4
MP:0010912	MP:0010912	herniated liver	Mammalian_phenotype	4
MP:0010913	MP:0010913	abnormal neuroendocrine cell morphology	Mammalian_phenotype	4
MP:0010924	MP:0010924	abnormal osteoid morphology	Mammalian_phenotype	4
MP:0010939	MP:0010939	abnormal mandibular prominence morphology	Mammalian_phenotype	4
MP:0010940	MP:0010940	abnormal maxillary prominence morphology	Mammalian_phenotype	4
MP:0010944	MP:0010944	respiratory epithelium hypertrophy	Mammalian_phenotype	4
MP:0010945	MP:0010945	lung epithelium hyperplasia	Mammalian_phenotype	4
MP:0010947	MP:0010947	abnormal single-strand DNA break repair	Mammalian_phenotype	4
MP:0010948	MP:0010948	abnormal double-strand DNA break repair	Mammalian_phenotype	4
MP:0010955	MP:0010955	abnormal respiratory electron transport chain	Mammalian_phenotype	4
MP:0010957	MP:0010957	abnormal aerobic respiration	Mammalian_phenotype	4
MP:0010958	MP:0010958	abnormal tricarboxylic acid cycle	Mammalian_phenotype	4
MP:0010959	MP:0010959	abnormal oxidative phosphorylation	Mammalian_phenotype	4
MP:0010971	MP:0010971	abnormal periosteum morphology	Mammalian_phenotype	4
MP:0010975	MP:0010975	abnormal lung lobe morphology	Mammalian_phenotype	4
MP:0010999	MP:0010999	proteinosis	Mammalian_phenotype	4
MP:0011000	MP:0011000	abnormal allogrooming behavior	Mammalian_phenotype	4
MP:0011004	MP:0011004	abnormal epidermal stem cell morphology	Mammalian_phenotype	4
MP:0011006	MP:0011006	abnormal epidermal stem cell proliferation	Mammalian_phenotype	4
MP:0011007	MP:0011007	abnormal epidermal stem cell apoptosis	Mammalian_phenotype	4
MP:0011020	MP:0011020	abnormal circadian temperature homeostasis	Mammalian_phenotype	4
MP:0011021	MP:0011021	abnormal circadian regulation of heart rate	Mammalian_phenotype	4
MP:0011022	MP:0011022	abnormal circadian regulation of systemic arterial blood pressure	Mammalian_phenotype	4
MP:0011044	MP:0011044	increased lung elastance	Mammalian_phenotype	4
MP:0011045	MP:0011045	decreased lung elastance	Mammalian_phenotype	4
MP:0011047	MP:0011047	increased lung tissue damping	Mammalian_phenotype	4
MP:0011048	MP:0011048	decreased lung tissue damping	Mammalian_phenotype	4
MP:0011049	MP:0011049	impaired adaptive thermogenesis	Mammalian_phenotype	4
MP:0011050	MP:0011050	abnormal respiratory motile cilium morphology	Mammalian_phenotype	4
MP:0011059	MP:0011059	abnormal ependyma motile cilium morphology	Mammalian_phenotype	4
MP:0011067	MP:0011067	abnormal somatostatin level	Mammalian_phenotype	4
MP:0011069	MP:0011069	abnormal brain ependyma motile cilium physiology	Mammalian_phenotype	4
MP:0011070	MP:0011070	abnormal spinal cord motile cilium physiology	Mammalian_phenotype	4
MP:0011083	MP:0011083	complete lethality at weaning	Mammalian_phenotype	4
MP:0011084	MP:0011084	partial lethality at weaning	Mammalian_phenotype	4
MP:0011100	MP:0011100	complete preweaning lethality	Mammalian_phenotype	4
MP:0011110	MP:0011110	partial preweaning lethality	Mammalian_phenotype	4
MP:0011113	MP:0011113	abnormal airway basal cell morphology	Mammalian_phenotype	4
MP:0011114	MP:0011114	abnormal airway basal cell differentiation	Mammalian_phenotype	4
MP:0011132	MP:0011132	abnormal lung endothelial cell migration	Mammalian_phenotype	4
MP:0011135	MP:0011135	abnormal lung endothelial cell adhesion	Mammalian_phenotype	4
MP:0011138	MP:0011138	abnormal lung endothelial cell proliferation	Mammalian_phenotype	4
MP:0011141	MP:0011141	increased lung endothelial cell apoptosis	Mammalian_phenotype	4
MP:0011145	MP:0011145	abnormal mesenchymal cell differentiation involved in lung development	Mammalian_phenotype	4
MP:0011146	MP:0011146	abnormal mesenchymal cell proliferation involved in lung development	Mammalian_phenotype	4
MP:0011156	MP:0011156	abnormal hypodermis fat layer morphology	Mammalian_phenotype	4
MP:0011157	MP:0011157	abnormal hypodermis muscle layer morphology	Mammalian_phenotype	4
MP:0011160	MP:0011160	dermal-epidermal separation	Mammalian_phenotype	4
MP:0011161	MP:0011161	increased hypodermis neovascularization	Mammalian_phenotype	4
MP:0011168	MP:0011168	abnormal fat cell differentiation	Mammalian_phenotype	4
MP:0011172	MP:0011172	abnormal otic pit morphology	Mammalian_phenotype	4
MP:0011173	MP:0011173	abnormal otic placode morphology	Mammalian_phenotype	4
MP:0011195	MP:0011195	increased hair follicle apoptosis	Mammalian_phenotype	4
MP:0011196	MP:0011196	decreased hair follicle apoptosis	Mammalian_phenotype	4
MP:0011197	MP:0011197	abnormal proamniotic cavity morphology	Mammalian_phenotype	4
MP:0011199	MP:0011199	abnormal amniotic cavity morphology	Mammalian_phenotype	4
MP:0011200	MP:0011200	abnormal extraembryonic coelom morphology	Mammalian_phenotype	4
MP:0011201	MP:0011201	abnormal visceral yolk sac cavity morphology	Mammalian_phenotype	4
MP:0011202	MP:0011202	abnormal ectoplacental cavity morphology	Mammalian_phenotype	4
MP:0011203	MP:0011203	abnormal parietal yolk sac morphology	Mammalian_phenotype	4
MP:0011210	MP:0011210	abnormal temporomandibular joint morphology	Mammalian_phenotype	4
MP:0011211	MP:0011211	abnormal common peroneal nerve morphology	Mammalian_phenotype	4
MP:0011213	MP:0011213	abnormal brain copper level	Mammalian_phenotype	4
MP:0011233	MP:0011233	abnormal vitamin A metabolism	Mammalian_phenotype	4
MP:0011235	MP:0011235	abnormal blood oxygen capacity	Mammalian_phenotype	4
MP:0011238	MP:0011238	abnormal inner ear development	Mammalian_phenotype	4
MP:0011246	MP:0011246	abnormal fetal liver hematopoietic progenitor cell morphology	Mammalian_phenotype	4
MP:0011247	MP:0011247	abnormal yolk sac hematopoietic stem cell morphology	Mammalian_phenotype	4
MP:0011252	MP:0011252	situs inversus totalis	Mammalian_phenotype	4
MP:0011253	MP:0011253	situs inversus with levocardia	Mammalian_phenotype	4
MP:0011255	MP:0011255	abnormal anterior visceral endoderm cell migration	Mammalian_phenotype	4
MP:0011256	MP:0011256	abnormal neural fold morphology	Mammalian_phenotype	4
MP:0011257	MP:0011257	abnormal head fold morphology	Mammalian_phenotype	4
MP:0011258	MP:0011258	abnormal tail fold morphology	Mammalian_phenotype	4
MP:0011260	MP:0011260	abnormal head mesenchyme morphology	Mammalian_phenotype	4
MP:0011264	MP:0011264	abnormal cardiac mesenchyme morphology	Mammalian_phenotype	4
MP:0011283	MP:0011283	abnormal erythropoietin level	Mammalian_phenotype	4
MP:0011295	MP:0011295	abnormal tubuloglomerular feedback response	Mammalian_phenotype	4
MP:0011298	MP:0011298	ureter hypoplasia	Mammalian_phenotype	4
MP:0011336	MP:0011336	abnormal kidney pelvis urothelium morphology	Mammalian_phenotype	4
MP:0011358	MP:0011358	renal artery aneurysm	Mammalian_phenotype	4
MP:0011362	MP:0011362	ectopic adrenal gland	Mammalian_phenotype	4
MP:0011367	MP:0011367	abnormal kidney apoptosis	Mammalian_phenotype	4
MP:0011376	MP:0011376	abnormal kidney corticomedullary boundary morphology	Mammalian_phenotype	4
MP:0011381	MP:0011381	abnormal kidney lobe morphology	Mammalian_phenotype	4
MP:0011382	MP:0011382	abnormal kidney lobule morphology	Mammalian_phenotype	4
MP:0011383	MP:0011383	abnormal kidney capsule morphology	Mammalian_phenotype	4
MP:0011384	MP:0011384	abnormal progesterone level	Mammalian_phenotype	4
MP:0011385	MP:0011385	abnormal testosterone level	Mammalian_phenotype	4
MP:0011388	MP:0011388	absent heart	Mammalian_phenotype	4
MP:0011391	MP:0011391	abnormal fetal cardiomyocyte apoptosis	Mammalian_phenotype	4
MP:0011399	MP:0011399	increased endoneurial fluid pressure	Mammalian_phenotype	4
MP:0011401	MP:0011401	abnormal vascular smooth muscle development	Mammalian_phenotype	4
MP:0011411	MP:0011411	abnormal gonadal ridge morphology	Mammalian_phenotype	4
MP:0011415	MP:0011415	abnormal aldosterone level	Mammalian_phenotype	4
MP:0011417	MP:0011417	abnormal renal transport	Mammalian_phenotype	4
MP:0011418	MP:0011418	leukocyturia	Mammalian_phenotype	4
MP:0011420	MP:0011420	pyuria	Mammalian_phenotype	4
MP:0011421	MP:0011421	cylindruria	Mammalian_phenotype	4
MP:0011425	MP:0011425	abnormal kidney interstitium morphology	Mammalian_phenotype	4
MP:0011426	MP:0011426	abnormal ureter smooth muscle morphology	Mammalian_phenotype	4
MP:0011431	MP:0011431	increased urine flow rate	Mammalian_phenotype	4
MP:0011432	MP:0011432	decreased urine flow rate	Mammalian_phenotype	4
MP:0011434	MP:0011434	abnormal urine magnesium level	Mammalian_phenotype	4
MP:0011439	MP:0011439	abnormal kidney cell proliferation	Mammalian_phenotype	4
MP:0011444	MP:0011444	abnormal renal water homeostasis	Mammalian_phenotype	4
MP:0011445	MP:0011445	abnormal renal protein reabsorption	Mammalian_phenotype	4
MP:0011447	MP:0011447	abnormal renal glucose reabsorption	Mammalian_phenotype	4
MP:0011458	MP:0011458	abnormal urine chloride ion level	Mammalian_phenotype	4
MP:0011461	MP:0011461	abnormal urine bicarbonate level	Mammalian_phenotype	4
MP:0011465	MP:0011465	abnormal urine urea nitrogen level	Mammalian_phenotype	4
MP:0011468	MP:0011468	abnormal urine amino acid level	Mammalian_phenotype	4
MP:0011472	MP:0011472	abnormal urine glycosaminoglycan level	Mammalian_phenotype	4
MP:0011476	MP:0011476	abnormal urine nucleotide level	Mammalian_phenotype	4
MP:0011477	MP:0011477	abnormal urine nucleoside level	Mammalian_phenotype	4
MP:0011478	MP:0011478	abnormal urine catecholamine level	Mammalian_phenotype	4
MP:0011480	MP:0011480	impaired ureteric peristalsis	Mammalian_phenotype	4
MP:0011484	MP:0011484	abnormal ureter urothelium morphology	Mammalian_phenotype	4
MP:0011485	MP:0011485	abnormal urethra urothelium morphology	Mammalian_phenotype	4
MP:0011486	MP:0011486	ectopic ureter	Mammalian_phenotype	4
MP:0011489	MP:0011489	ureteropelvic junction atresia	Mammalian_phenotype	4
MP:0011490	MP:0011490	ureteropelvic junction stenosis	Mammalian_phenotype	4
MP:0011491	MP:0011491	ureteropelvic junction obstruction	Mammalian_phenotype	4
MP:0011492	MP:0011492	ureterovesical junction obstruction	Mammalian_phenotype	4
MP:0011493	MP:0011493	double ureter	Mammalian_phenotype	4
MP:0011495	MP:0011495	abnormal head shape	Mammalian_phenotype	4
MP:0011496	MP:0011496	abnormal head size	Mammalian_phenotype	4
MP:0011517	MP:0011517	hyperoxaluria	Mammalian_phenotype	4
MP:0011518	MP:0011518	abnormal cell chemotaxis	Mammalian_phenotype	4
MP:0011534	MP:0011534	granular kidney	Mammalian_phenotype	4
MP:0011538	MP:0011538	abnormal urine hormone level	Mammalian_phenotype	4
MP:0011551	MP:0011551	variegated eye pigmentation pattern	Mammalian_phenotype	4
MP:0011552	MP:0011552	abnormal urine deoxycorticosterone level	Mammalian_phenotype	4
MP:0011558	MP:0011558	abnormal urine insulin level	Mammalian_phenotype	4
MP:0011562	MP:0011562	abnormal urine prostaglandin level	Mammalian_phenotype	4
MP:0011566	MP:0011566	abnormal complement protein level	Mammalian_phenotype	4
MP:0011570	MP:0011570	esophageal achalasia	Mammalian_phenotype	4
MP:0011577	MP:0011577	abnormal lipoprotein lipase activity	Mammalian_phenotype	4
MP:0011580	MP:0011580	abnormal triglyceride lipase activity	Mammalian_phenotype	4
MP:0011583	MP:0011583	abnormal alkaline phosphatase activity	Mammalian_phenotype	4
MP:0011586	MP:0011586	abnormal ornithine carbamoyltransferase activity	Mammalian_phenotype	4
MP:0011589	MP:0011589	abnormal hormone-sensitive lipase activity	Mammalian_phenotype	4
MP:0011592	MP:0011592	abnormal catalase activity	Mammalian_phenotype	4
MP:0011595	MP:0011595	abnormal purine-nucleoside phosphorylase activity	Mammalian_phenotype	4
MP:0011598	MP:0011598	abnormal phosphatidylcholine-sterol O-acyltransferase activity	Mammalian_phenotype	4
MP:0011604	MP:0011604	abnormal glucokinase activity	Mammalian_phenotype	4
MP:0011607	MP:0011607	abnormal glyceraldehyde-3-phosphate dehydrogenase (NAD+) (phosphorylating) activity	Mammalian_phenotype	4
MP:0011616	MP:0011616	abnormal nonassociative learning	Mammalian_phenotype	4
MP:0011623	MP:0011623	abnormal habituation to xenobiotic	Mammalian_phenotype	4
MP:0011624	MP:0011624	abnormal sensitization to xenobiotic	Mammalian_phenotype	4
MP:0011625	MP:0011625	cystolithiasis	Mammalian_phenotype	4
MP:0011628	MP:0011628	increased mitochondria number	Mammalian_phenotype	4
MP:0011629	MP:0011629	decreased mitochondria number	Mammalian_phenotype	4
MP:0011630	MP:0011630	increased mitochondria size	Mammalian_phenotype	4
MP:0011631	MP:0011631	decreased mitochondria size	Mammalian_phenotype	4
MP:0011633	MP:0011633	abnormal mitochondrial shape	Mammalian_phenotype	4
MP:0011634	MP:0011634	abnormal mitochondrial inner membrane morphology	Mammalian_phenotype	4
MP:0011637	MP:0011637	abnormal mitochondrial matrix morphology	Mammalian_phenotype	4
MP:0011638	MP:0011638	abnormal mitochondrial chromosome morphology	Mammalian_phenotype	4
MP:0011641	MP:0011641	abnormal pulmonary collagen fibril morphology	Mammalian_phenotype	4
MP:0011642	MP:0011642	abnormal bone collagen fibril morphology	Mammalian_phenotype	4
MP:0011643	MP:0011643	abnormal tendon collagen fibril morphology	Mammalian_phenotype	4
MP:0011649	MP:0011649	immotile respiratory cilia	Mammalian_phenotype	4
MP:0011685	MP:0011685	abnormal limb paddle morphology	Mammalian_phenotype	4
MP:0011699	MP:0011699	abnormal brown adipose tissue thermogenesis	Mammalian_phenotype	4
MP:0011702	MP:0011702	abnormal fibroblast proliferation	Mammalian_phenotype	4
MP:0011706	MP:0011706	abnormal fibroblast migration	Mammalian_phenotype	4
MP:0011720	MP:0011720	abnormal ossification involved in bone remodeling	Mammalian_phenotype	4
MP:0011722	MP:0011722	abnormal ossification involved in bone maturation	Mammalian_phenotype	4
MP:0011723	MP:0011723	ectopic neuron	Mammalian_phenotype	4
MP:0011729	MP:0011729	abnormal pineal gland melatonin secretion	Mammalian_phenotype	4
MP:0011734	MP:0011734	abnormal urine ammonia level	Mammalian_phenotype	4
MP:0011740	MP:0011740	abnormal urine nitrite level	Mammalian_phenotype	4
MP:0011744	MP:0011744	abnormal kidney epithelial cell primary cilium physiology	Mammalian_phenotype	4
MP:0011748	MP:0011748	intestinal fibrosis	Mammalian_phenotype	4
MP:0011749	MP:0011749	perivascular fibrosis	Mammalian_phenotype	4
MP:0011758	MP:0011758	renal ischemia	Mammalian_phenotype	4
MP:0011766	MP:0011766	abnormal urinary bladder mucosa morphology	Mammalian_phenotype	4
MP:0011767	MP:0011767	ureterocele	Mammalian_phenotype	4
MP:0011768	MP:0011768	abnormal urinary bladder trigone morphology	Mammalian_phenotype	4
MP:0011769	MP:0011769	urinary bladder fibrosis	Mammalian_phenotype	4
MP:0011770	MP:0011770	increased urine selenium level	Mammalian_phenotype	4
MP:0011771	MP:0011771	abnormal genital tubercle morphology	Mammalian_phenotype	4
MP:0011773	MP:0011773	abnormal urinary bladder blood vessel morphology	Mammalian_phenotype	4
MP:0011774	MP:0011774	abnormal urinary bladder detrusor smooth muscle morphology	Mammalian_phenotype	4
MP:0011776	MP:0011776	abnormal male urethra morphology	Mammalian_phenotype	4
MP:0011780	MP:0011780	abnormal female urethra morphology	Mammalian_phenotype	4
MP:0011781	MP:0011781	abnormal bulbourethral gland physiology	Mammalian_phenotype	4
MP:0011783	MP:0011783	abnormal ureteral orifice morphology	Mammalian_phenotype	4
MP:0011784	MP:0011784	abnormal urinary bladder neck morphology	Mammalian_phenotype	4
MP:0011785	MP:0011785	abnormal urinary bladder fundus morphology	Mammalian_phenotype	4
MP:0011786	MP:0011786	rectourethral fistula	Mammalian_phenotype	4
MP:0011787	MP:0011787	abnormal Bartholin's gland morphology	Mammalian_phenotype	4
MP:0011788	MP:0011788	absent urethra	Mammalian_phenotype	4
MP:0011792	MP:0011792	abnormal urethral gland morphology	Mammalian_phenotype	4
MP:0011795	MP:0011795	abnormal urinary bladder development	Mammalian_phenotype	4
MP:0011796	MP:0011796	abnormal external urethral orifice morphology	Mammalian_phenotype	4
MP:0011797	MP:0011797	blind ureter	Mammalian_phenotype	4
MP:0011798	MP:0011798	abnormal urinary bladder weight	Mammalian_phenotype	4
MP:0011801	MP:0011801	urethra obstruction	Mammalian_phenotype	4
MP:0011804	MP:0011804	increased cell migration	Mammalian_phenotype	4
MP:0011805	MP:0011805	decreased cell migration	Mammalian_phenotype	4
MP:0011808	MP:0011808	abnormal myoblast differentiation	Mammalian_phenotype	4
MP:0011818	MP:0011818	abnormal pancreatic beta cell proliferation	Mammalian_phenotype	4
MP:0011821	MP:0011821	abnormal CD8-positive, alpha-beta memory T cell proliferation	Mammalian_phenotype	4
MP:0011828	MP:0011828	urinary bladder cysts	Mammalian_phenotype	4
MP:0011829	MP:0011829	vesicovaginal fistula	Mammalian_phenotype	4
MP:0011831	MP:0011831	abnormal visual contrast sensitivity	Mammalian_phenotype	4
MP:0011832	MP:0011832	abnormal visual acuity	Mammalian_phenotype	4
MP:0011833	MP:0011833	abnormal cremaster muscle morphology	Mammalian_phenotype	4
MP:0011834	MP:0011834	abnormal clitoral gland morphology	Mammalian_phenotype	4
MP:0011835	MP:0011835	abnormal urogenital fold morphology	Mammalian_phenotype	4
MP:0011840	MP:0011840	abnormal urethral crest morphology	Mammalian_phenotype	4
MP:0011853	MP:0011853	abnormal urorectal septum morphology	Mammalian_phenotype	4
MP:0011856	MP:0011856	abnormal glomerular filtration barrier function	Mammalian_phenotype	4
MP:0011863	MP:0011863	abnormal podocyte physiology	Mammalian_phenotype	4
MP:0011864	MP:0011864	abnormal podocyte adhesion	Mammalian_phenotype	4
MP:0011865	MP:0011865	abnormal podocyte motility	Mammalian_phenotype	4
MP:0011874	MP:0011874	enlarged urinary bladder	Mammalian_phenotype	4
MP:0011875	MP:0011875	absent stomach	Mammalian_phenotype	4
MP:0011877	MP:0011877	absent liver	Mammalian_phenotype	4
MP:0011900	MP:0011900	podocyturia	Mammalian_phenotype	4
MP:0011901	MP:0011901	abnormal hematopoietic stem cell proliferation	Mammalian_phenotype	4
MP:0011904	MP:0011904	abnormal Schwann cell physiology	Mammalian_phenotype	4
MP:0011905	MP:0011905	abnormal Schwann cell proliferation	Mammalian_phenotype	4
MP:0011908	MP:0011908	abnormal pancreatic endocrine progenitor cell proliferation	Mammalian_phenotype	4
MP:0011923	MP:0011923	abnormal bladder urine volume	Mammalian_phenotype	4
MP:0011924	MP:0011924	abnormal liver zinc level	Mammalian_phenotype	4
MP:0011927	MP:0011927	abnormal cardiac valve flow	Mammalian_phenotype	4
MP:0011974	MP:0011974	intestinal stenosis	Mammalian_phenotype	4
MP:0011975	MP:0011975	neuronal cytoplasmic inclusions	Mammalian_phenotype	4
MP:0011977	MP:0011977	abnormal sodium ion homeostasis	Mammalian_phenotype	4
MP:0011978	MP:0011978	abnormal potassium ion homeostasis	Mammalian_phenotype	4
MP:0011979	MP:0011979	abnormal magnesium ion homeostasis	Mammalian_phenotype	4
MP:0011984	MP:0011984	decreased enteroendocrine cell number	Mammalian_phenotype	4
MP:0011985	MP:0011985	abnormal macrophage proliferation	Mammalian_phenotype	4
MP:0011987	MP:0011987	abnormal GABAergic neuron physiology	Mammalian_phenotype	4
MP:0011990	MP:0011990	decreased porphyrin level	Mammalian_phenotype	4
MP:0012001	MP:0012001	abnormal touch escape response	Mammalian_phenotype	4
MP:0012007	MP:0012007	abnormal chloride level	Mammalian_phenotype	4
MP:0012011	MP:0012011	febrile seizures	Mammalian_phenotype	4
MP:0012013	MP:0012013	abnormal innate avoidance response	Mammalian_phenotype	4
MP:0012016	MP:0012016	abnormal hair follicle melanocyte eumelanin content	Mammalian_phenotype	4
MP:0012018	MP:0012018	abnormal oviduct physiology	Mammalian_phenotype	4
MP:0012022	MP:0012022	increased melanocyte number	Mammalian_phenotype	4
MP:0012023	MP:0012023	decreased melanocyte number	Mammalian_phenotype	4
MP:0012032	MP:0012032	abnormal ERG latency	Mammalian_phenotype	4
MP:0012033	MP:0012033	abnormal ERG implicit time	Mammalian_phenotype	4
MP:0012034	MP:0012034	abnormal a wave shape	Mammalian_phenotype	4
MP:0012035	MP:0012035	abnormal b-wave shape	Mammalian_phenotype	4
MP:0012040	MP:0012040	abnormal c wave shape	Mammalian_phenotype	4
MP:0012041	MP:0012041	susceptible to pulmonary hyaline membrane formation	Mammalian_phenotype	4
MP:0012044	MP:0012044	abnormal phospholipase A2 level	Mammalian_phenotype	4
MP:0012047	MP:0012047	abnormal cholinesterase level	Mammalian_phenotype	4
MP:0012049	MP:0012049	increased susceptilbility to retinal ischemic injury	Mammalian_phenotype	4
MP:0012050	MP:0012050	decreased susceptilbility to retinal ischemic injury	Mammalian_phenotype	4
MP:0012054	MP:0012054	abnormal phrenic nerve innervation pattern	Mammalian_phenotype	4
MP:0012058	MP:0012058	abnormal morula morphology	Mammalian_phenotype	4
MP:0012061	MP:0012061	abnormal central tendon morphology	Mammalian_phenotype	4
MP:0012070	MP:0012070	altered susceptibility to osteoporosis	Mammalian_phenotype	4
MP:0012078	MP:0012078	abnormal tail ring morphology	Mammalian_phenotype	4
MP:0009026	MP:0009026	abnormal brain pia mater morphology	Mammalian_phenotype	5
MP:0009032	MP:0009032	abnormal subarachnoid cistern morphology	Mammalian_phenotype	5
MP:0009037	MP:0009037	abnormal subarachnoid space development	Mammalian_phenotype	5
MP:0009045	MP:0009045	muscle tetany	Mammalian_phenotype	5
MP:0009049	MP:0009049	abnormal hallux morphology	Mammalian_phenotype	5
MP:0009052	MP:0009052	anal stenosis	Mammalian_phenotype	5
MP:0009062	MP:0009062	impaired lectin complement pathway	Mammalian_phenotype	5
MP:0009078	MP:0009078	adrenal gland hyperplasia	Mammalian_phenotype	5
MP:0009099	MP:0009099	abnormal uterine NK cell physiology	Mammalian_phenotype	5
MP:0009107	MP:0009107	abnormal pancreas weight	Mammalian_phenotype	5
MP:0009118	MP:0009118	increased white fat cell size	Mammalian_phenotype	5
MP:0009119	MP:0009119	increased brown fat cell size	Mammalian_phenotype	5
MP:0009120	MP:0009120	abnormal white fat cell lipid droplet size	Mammalian_phenotype	5
MP:0009123	MP:0009123	abnormal brown fat cell lipid droplet size	Mammalian_phenotype	5
MP:0009126	MP:0009126	abnormal brown fat cell number	Mammalian_phenotype	5
MP:0009129	MP:0009129	abnormal white fat cell number	Mammalian_phenotype	5
MP:0009132	MP:0009132	abnormal white fat cell size	Mammalian_phenotype	5
MP:0009133	MP:0009133	decreased white fat cell size	Mammalian_phenotype	5
MP:0009134	MP:0009134	abnormal brown fat lipid droplet number	Mammalian_phenotype	5
MP:0009135	MP:0009135	abnormal brown fat cell size	Mammalian_phenotype	5
MP:0009136	MP:0009136	decreased brown fat cell size	Mammalian_phenotype	5
MP:0009143	MP:0009143	abnormal pancreatic duct morphology	Mammalian_phenotype	5
MP:0009145	MP:0009145	abnormal pancreatic acinus morphology	Mammalian_phenotype	5
MP:0009147	MP:0009147	abnormal pancreatic acinar cell physiology	Mammalian_phenotype	5
MP:0009164	MP:0009164	exocrine pancreas atrophy	Mammalian_phenotype	5
MP:0009194	MP:0009194	abnormal pancreatic epsilon cell physiology	Mammalian_phenotype	5
MP:0009195	MP:0009195	abnormal PP cell physiology	Mammalian_phenotype	5
MP:0009196	MP:0009196	abnormal pancreatic ghrelin secretion	Mammalian_phenotype	5
MP:0009197	MP:0009197	abnormal pancreatic polypeptide secretion	Mammalian_phenotype	5
MP:0009199	MP:0009199	abnormal external male genitalia morphology	Mammalian_phenotype	5
MP:0009205	MP:0009205	abnormal internal male genitalia morphology	Mammalian_phenotype	5
MP:0009209	MP:0009209	abnormal internal female genitalia morphology	Mammalian_phenotype	5
MP:0009213	MP:0009213	absent male inguinal canal	Mammalian_phenotype	5
MP:0009217	MP:0009217	abnormal peritoneal vaginal process morphology	Mammalian_phenotype	5
MP:0009228	MP:0009228	uterine cervix inflammation	Mammalian_phenotype	5
MP:0009244	MP:0009244	abnormal acid-activated cation-mediated receptor currents	Mammalian_phenotype	5
MP:0009245	MP:0009245	caudal rachischisis	Mammalian_phenotype	5
MP:0009246	MP:0009246	pale spleen	Mammalian_phenotype	5
MP:0009253	MP:0009253	abnormal sympathetic neuron physiology	Mammalian_phenotype	5
MP:0009258	MP:0009258	abnormal thymocyte apoptosis	Mammalian_phenotype	5
MP:0009263	MP:0009263	abnormal eyelid fusion	Mammalian_phenotype	5
MP:0009270	MP:0009270	abnormal guard hair length	Mammalian_phenotype	5
MP:0009274	MP:0009274	buphthalmos	Mammalian_phenotype	5
MP:0009286	MP:0009286	increased abdominal fat pad weight	Mammalian_phenotype	5
MP:0009287	MP:0009287	decreased abdominal fat pad weight	Mammalian_phenotype	5
MP:0009290	MP:0009290	increased femoral fat pad weight	Mammalian_phenotype	5
MP:0009291	MP:0009291	decreased femoral fat pad weight	Mammalian_phenotype	5
MP:0009294	MP:0009294	increased interscapular fat pad weight	Mammalian_phenotype	5
MP:0009295	MP:0009295	decreased interscapular fat pad weight	Mammalian_phenotype	5
MP:0009296	MP:0009296	increased mammary fat pad weight	Mammalian_phenotype	5
MP:0009297	MP:0009297	decreased mammary fat pad weight	Mammalian_phenotype	5
MP:0009302	MP:0009302	increased renal fat pad weight	Mammalian_phenotype	5
MP:0009303	MP:0009303	decreased renal fat pad weight	Mammalian_phenotype	5
MP:0009323	MP:0009323	abnormal spleen development	Mammalian_phenotype	5
MP:0009325	MP:0009325	necrospermia	Mammalian_phenotype	5
MP:0009332	MP:0009332	abnormal splenocyte morphology	Mammalian_phenotype	5
MP:0009335	MP:0009335	decreased splenocyte proliferation	Mammalian_phenotype	5
MP:0009336	MP:0009336	increased splenocyte proliferation	Mammalian_phenotype	5
MP:0009340	MP:0009340	abnormal splenocyte apoptosis	Mammalian_phenotype	5
MP:0009342	MP:0009342	enlarged gallbladder	Mammalian_phenotype	5
MP:0009343	MP:0009343	dilated gallbladder	Mammalian_phenotype	5
MP:0009345	MP:0009345	abnormal trabecular bone thickness	Mammalian_phenotype	5
MP:0009349	MP:0009349	increased urine pH	Mammalian_phenotype	5
MP:0009350	MP:0009350	decreased urine pH	Mammalian_phenotype	5
MP:0009351	MP:0009351	thin hair shaft	Mammalian_phenotype	5
MP:0009354	MP:0009354	emprosthotonos	Mammalian_phenotype	5
MP:0009358	MP:0009358	environmentally induced seizures	Mammalian_phenotype	5
MP:0009360	MP:0009360	endometrium inflammation	Mammalian_phenotype	5
MP:0009379	MP:0009379	abnormal foot pigmentation	Mammalian_phenotype	5
MP:0009382	MP:0009382	abnormal cardiac jelly morphology	Mammalian_phenotype	5
MP:0009385	MP:0009385	abnormal dermal pigmentation	Mammalian_phenotype	5
MP:0009387	MP:0009387	abnormal epidermal pigmentation	Mammalian_phenotype	5
MP:0009393	MP:0009393	abnormal resting posture	Mammalian_phenotype	5
MP:0009398	MP:0009398	abnormal skeletal muscle fiber size	Mammalian_phenotype	5
MP:0009404	MP:0009404	centrally nucleated skeletal muscle fibers	Mammalian_phenotype	5
MP:0009405	MP:0009405	increased skeletal muscle fiber number	Mammalian_phenotype	5
MP:0009406	MP:0009406	decreased skeletal muscle fiber number	Mammalian_phenotype	5
MP:0009411	MP:0009411	abnormal skeletal muscle fiber triad morphology	Mammalian_phenotype	5
MP:0009412	MP:0009412	skeletal muscle fiber degeneration	Mammalian_phenotype	5
MP:0009414	MP:0009414	skeletal muscle fiber necrosis	Mammalian_phenotype	5
MP:0009420	MP:0009420	skeletal muscle endomysial fibrosis	Mammalian_phenotype	5
MP:0009435	MP:0009435	abnormal miniature inhibitory postsynaptic currents	Mammalian_phenotype	5
MP:0009436	MP:0009436	fragmentation of sleep/wake states	Mammalian_phenotype	5
MP:0009438	MP:0009438	cricoid and tracheal cartilage fusion	Mammalian_phenotype	5
MP:0009445	MP:0009445	osteomalacia	Mammalian_phenotype	5
MP:0009450	MP:0009450	abnormal axon fasciculation	Mammalian_phenotype	5
MP:0009451	MP:0009451	abnormal chromosome pairing during meiosis	Mammalian_phenotype	5
MP:0009452	MP:0009452	abnormal synaptonemal complex	Mammalian_phenotype	5
MP:0009453	MP:0009453	enhanced contextual conditioning behavior	Mammalian_phenotype	5
MP:0009454	MP:0009454	impaired contextual conditioning behavior	Mammalian_phenotype	5
MP:0009455	MP:0009455	enhanced cued conditioning behavior	Mammalian_phenotype	5
MP:0009456	MP:0009456	impaired cued conditioning behavior	Mammalian_phenotype	5
MP:0009457	MP:0009457	whorled hair	Mammalian_phenotype	5
MP:0009458	MP:0009458	abnormal skeletal muscle size	Mammalian_phenotype	5
MP:0009465	MP:0009465	abnormal gallbladder infundibulum morphology	Mammalian_phenotype	5
MP:0009467	MP:0009467	abnormal magnocellular neurosecretory cell morphology	Mammalian_phenotype	5
MP:0009472	MP:0009472	increased urine sulfate level	Mammalian_phenotype	5
MP:0009474	MP:0009474	thick epidermis stratum spinosum	Mammalian_phenotype	5
MP:0009475	MP:0009475	abnormal nicotine-mediated receptor currents	Mammalian_phenotype	5
MP:0009492	MP:0009492	abnormal gallbladder epithelium morphology	Mammalian_phenotype	5
MP:0009493	MP:0009493	abnormal cystic duct morphology	Mammalian_phenotype	5
MP:0009498	MP:0009498	abnormal extrahepatic bile duct morphology	Mammalian_phenotype	5
MP:0009501	MP:0009501	abnormal hepatic duct morphology	Mammalian_phenotype	5
MP:0009506	MP:0009506	abnormal mammary gland alveolus morphology	Mammalian_phenotype	5
MP:0009514	MP:0009514	titubation	Mammalian_phenotype	5
MP:0009518	MP:0009518	abnormal anterior lingual gland morphology	Mammalian_phenotype	5
MP:0009519	MP:0009519	abnormal anterior buccal gland morphology	Mammalian_phenotype	5
MP:0009525	MP:0009525	abnormal submandibular duct morphology	Mammalian_phenotype	5
MP:0009527	MP:0009527	abnormal sublingual duct morphology	Mammalian_phenotype	5
MP:0009530	MP:0009530	abnormal parotid duct morphology	Mammalian_phenotype	5
MP:0009544	MP:0009544	abnormal thymus epithelium morphology	Mammalian_phenotype	5
MP:0009560	MP:0009560	absent epidermis stratum granulosum	Mammalian_phenotype	5
MP:0009564	MP:0009564	abnormal meiotic configurations	Mammalian_phenotype	5
MP:0009566	MP:0009566	meiotic nondisjunction	Mammalian_phenotype	5
MP:0009567	MP:0009567	mitotic nondisjuction	Mammalian_phenotype	5
MP:0009571	MP:0009571	abnormal right lung accessory lobe morphology	Mammalian_phenotype	5
MP:0009572	MP:0009572	abnormal right lung cranial lobe morphology	Mammalian_phenotype	5
MP:0009573	MP:0009573	abnormal right lung middle lobe morphology	Mammalian_phenotype	5
MP:0009574	MP:0009574	abnormal right lung caudal lobe morphology	Mammalian_phenotype	5
MP:0009578	MP:0009578	otocephaly	Mammalian_phenotype	5
MP:0009583	MP:0009583	increased keratinocyte proliferation	Mammalian_phenotype	5
MP:0009584	MP:0009584	decreased keratinocyte proliferation	Mammalian_phenotype	5
MP:0009588	MP:0009588	increased plasma membrane sphingolipid content	Mammalian_phenotype	5
MP:0009589	MP:0009589	sphingomyelinosis	Mammalian_phenotype	5
MP:0009593	MP:0009593	absent chorion	Mammalian_phenotype	5
MP:0009594	MP:0009594	abnormal corneocyte envelope morphology	Mammalian_phenotype	5
MP:0009596	MP:0009596	abnormal stratum corneum lipid matrix formation	Mammalian_phenotype	5
MP:0009597	MP:0009597	impaired stratum corneum desquamation	Mammalian_phenotype	5
MP:0009598	MP:0009598	thin epidermis stratum granulosum	Mammalian_phenotype	5
MP:0009599	MP:0009599	thick epidermis stratum granulosum	Mammalian_phenotype	5
MP:0009601	MP:0009601	epidermis stratum granulosum hyperplasia	Mammalian_phenotype	5
MP:0009602	MP:0009602	abnormal keratohyalin granule morphology	Mammalian_phenotype	5
MP:0009608	MP:0009608	abnormal epidermal lamellar body morphology	Mammalian_phenotype	5
MP:0009611	MP:0009611	epidermis stratum spinosum hyperplasia	Mammalian_phenotype	5
MP:0009612	MP:0009612	thick epidermis suprabasal layer	Mammalian_phenotype	5
MP:0009613	MP:0009613	thin epidermis suprabasal layer	Mammalian_phenotype	5
MP:0009614	MP:0009614	absent epidermis stratum spinosum	Mammalian_phenotype	5
MP:0009616	MP:0009616	abnormal brain zinc level	Mammalian_phenotype	5
MP:0009625	MP:0009625	abnormal abdominal lymph node morphology	Mammalian_phenotype	5
MP:0009640	MP:0009640	abnormal renal tubule epithelium morphology	Mammalian_phenotype	5
MP:0009648	MP:0009648	abnormal superovulation	Mammalian_phenotype	5
MP:0009658	MP:0009658	increased placenta apoptosis	Mammalian_phenotype	5
MP:0009659	MP:0009659	striated fur	Mammalian_phenotype	5
MP:0009668	MP:0009668	ectopic pregnancy	Mammalian_phenotype	5
MP:0009669	MP:0009669	abnormal postimplantation uterine environment	Mammalian_phenotype	5
MP:0009677	MP:0009677	abnormal spinal cord dorsal column morphology	Mammalian_phenotype	5
MP:0009678	MP:0009678	abnormal spinal cord lateral column morphology	Mammalian_phenotype	5
MP:0009679	MP:0009679	abnormal spinal cord ventral column morphology	Mammalian_phenotype	5
MP:0009684	MP:0009684	abnormal spinal cord lateral motor column morphology	Mammalian_phenotype	5
MP:0009686	MP:0009686	abnormal spinal cord medial motor column morphology	Mammalian_phenotype	5
MP:0009689	MP:0009689	abnormal neural tube ventricular layer morphology	Mammalian_phenotype	5
MP:0009690	MP:0009690	abnormal neural tube mantle layer morphology	Mammalian_phenotype	5
MP:0009691	MP:0009691	abnormal neural tube marginal layer morphology	Mammalian_phenotype	5
MP:0009695	MP:0009695	abnormal spinal cord ventral commissure morphology	Mammalian_phenotype	5
MP:0009696	MP:0009696	abnormal spinal cord grey commissure morphology	Mammalian_phenotype	5
MP:0009699	MP:0009699	hyperchylomicronemia	Mammalian_phenotype	5
MP:0009706	MP:0009706	absent midgut	Mammalian_phenotype	5
MP:0009710	MP:0009710	anhedonia	Mammalian_phenotype	5
MP:0009711	MP:0009711	abnormal conditioned place preference behavior	Mammalian_phenotype	5
MP:0009712	MP:0009712	impaired conditioned place preference behavior	Mammalian_phenotype	5
MP:0009713	MP:0009713	enhanced conditioned place preference behavior	Mammalian_phenotype	5
MP:0009714	MP:0009714	thin epidermis stratum basale	Mammalian_phenotype	5
MP:0009715	MP:0009715	thick epidermis stratum basale	Mammalian_phenotype	5
MP:0009717	MP:0009717	absent subcommissural organ	Mammalian_phenotype	5
MP:0009720	MP:0009720	abnormal mammary gland pattern	Mammalian_phenotype	5
MP:0009722	MP:0009722	abnormal nipple development	Mammalian_phenotype	5
MP:0009723	MP:0009723	supernumerary nipples	Mammalian_phenotype	5
MP:0009724	MP:0009724	ectopic nipples	Mammalian_phenotype	5
MP:0009726	MP:0009726	abnormal primordial meninx morphology	Mammalian_phenotype	5
MP:0009732	MP:0009732	ventricular premature beat	Mammalian_phenotype	5
MP:0009733	MP:0009733	absent nipple	Mammalian_phenotype	5
MP:0009749	MP:0009749	enhanced behavioral response to addictive substance	Mammalian_phenotype	5
MP:0009750	MP:0009750	impaired behavioral response to addictive substance	Mammalian_phenotype	5
MP:0009759	MP:0009759	abnormal hair follicle bulge morphology	Mammalian_phenotype	5
MP:0009760	MP:0009760	abnormal mitotic spindle morphology	Mammalian_phenotype	5
MP:0009761	MP:0009761	abnormal meiotic spindle morphology	Mammalian_phenotype	5
MP:0009762	MP:0009762	abnormal mitotic spindle assembly checkpoint	Mammalian_phenotype	5
MP:0009768	MP:0009768	impaired somite development	Mammalian_phenotype	5
MP:0009769	MP:0009769	abnormal meiotic spindle assembly checkpoint	Mammalian_phenotype	5
MP:0009774	MP:0009774	abnormal behavioral withdrawal response	Mammalian_phenotype	5
MP:0009778	MP:0009778	impaired behavioral response to anesthetic	Mammalian_phenotype	5
MP:0009779	MP:0009779	enhanced behavioral response to anesthetic	Mammalian_phenotype	5
MP:0009793	MP:0009793	sebaceous gland hypertrophy	Mammalian_phenotype	5
MP:0009794	MP:0009794	sebaceous gland hyperplasia	Mammalian_phenotype	5
MP:0009802	MP:0009802	abnormal median aperture morphology	Mammalian_phenotype	5
MP:0009803	MP:0009803	abnormal lateral aperture morphology	Mammalian_phenotype	5
MP:0009804	MP:0009804	abnormal interventricular foramen morphology	Mammalian_phenotype	5
MP:0009810	MP:0009810	increased urine uric acid level	Mammalian_phenotype	5
MP:0009811	MP:0009811	abnormal prostaglandin level	Mammalian_phenotype	5
MP:0009812	MP:0009812	abnormal bradykinin level	Mammalian_phenotype	5
MP:0009813	MP:0009813	abnormal leukotriene level	Mammalian_phenotype	5
MP:0009818	MP:0009818	abnormal thromboxane level	Mammalian_phenotype	5
MP:0009819	MP:0009819	abnormal circulating androgen level	Mammalian_phenotype	5
MP:0009825	MP:0009825	cornea ulcer	Mammalian_phenotype	5
MP:0009826	MP:0009826	abnormal dermis reticular layer collagen network	Mammalian_phenotype	5
MP:0009829	MP:0009829	enlarged eye anterior chamber	Mammalian_phenotype	5
MP:0009844	MP:0009844	abnormal neural crest cell apoptosis	Mammalian_phenotype	5
MP:0009846	MP:0009846	abnormal neural crest morphology	Mammalian_phenotype	5
MP:0009855	MP:0009855	midface retrusion	Mammalian_phenotype	5
MP:0009856	MP:0009856	failure of ejaculation	Mammalian_phenotype	5
MP:0009857	MP:0009857	absent kidney cortex	Mammalian_phenotype	5
MP:0009862	MP:0009862	abnormal aorta elastic tissue morphology	Mammalian_phenotype	5
MP:0009864	MP:0009864	abnormal aorta endothelium morphology	Mammalian_phenotype	5
MP:0009865	MP:0009865	abnormal aorta smooth muscle morphology	Mammalian_phenotype	5
MP:0009874	MP:0009874	abnormal interdigital cell death	Mammalian_phenotype	5
MP:0009878	MP:0009878	decreased susceptibility to bone fracture	Mammalian_phenotype	5
MP:0009929	MP:0009929	meningomyelocele	Mammalian_phenotype	5
MP:0009935	MP:0009935	abnormal meibomian gland acinus morphology	Mammalian_phenotype	5
MP:0009952	MP:0009952	abnormal olfactory bulb subventricular zone morphology	Mammalian_phenotype	5
MP:0009968	MP:0009968	abnormal cerebellar granule cell proliferation	Mammalian_phenotype	5
MP:0009977	MP:0009977	abnormal cerebellar granule cell migration	Mammalian_phenotype	5
MP:0009978	MP:0009978	abnormal cerebellum white matter morphology	Mammalian_phenotype	5
MP:0010008	MP:0010008	abnormal Purkinje cell migration	Mammalian_phenotype	5
MP:0010011	MP:0010011	ectopic hippocampus pyramidal cells	Mammalian_phenotype	5
MP:0010012	MP:0010012	ectopic cerebral cortex pyramidal cells	Mammalian_phenotype	5
MP:0010016	MP:0010016	variable depigmentation	Mammalian_phenotype	5
MP:0010017	MP:0010017	visceral vascular congestion	Mammalian_phenotype	5
MP:0010018	MP:0010018	pulmonary vascular congestion	Mammalian_phenotype	5
MP:0010019	MP:0010019	liver vascular congestion	Mammalian_phenotype	5
MP:0010020	MP:0010020	spleen vascular congestion	Mammalian_phenotype	5
MP:0010022	MP:0010022	brain vascular congestion	Mammalian_phenotype	5
MP:0010032	MP:0010032	meiotic drive	Mammalian_phenotype	5
MP:0010034	MP:0010034	abnormal erythrocyte clearance	Mammalian_phenotype	5
MP:0010044	MP:0010044	abnormal omental fat pad morphology	Mammalian_phenotype	5
MP:0010047	MP:0010047	axonal spheroids	Mammalian_phenotype	5
MP:0010061	MP:0010061	increased creatine level	Mammalian_phenotype	5
MP:0010062	MP:0010062	decreased creatine level	Mammalian_phenotype	5
MP:0010063	MP:0010063	abnormal circulating creatine level	Mammalian_phenotype	5
MP:0010069	MP:0010069	increased serotonin level	Mammalian_phenotype	5
MP:0010070	MP:0010070	decreased serotonin level	Mammalian_phenotype	5
MP:0010081	MP:0010081	posterior microphthalmia	Mammalian_phenotype	5
MP:0010087	MP:0010087	increased circulating fructosamine level	Mammalian_phenotype	5
MP:0010088	MP:0010088	decreased circulating fructosamine level	Mammalian_phenotype	5
MP:0010099	MP:0010099	abnormal thoracic cage shape	Mammalian_phenotype	5
MP:0010103	MP:0010103	small thoracic cage	Mammalian_phenotype	5
MP:0010104	MP:0010104	enlarged thoracic cage	Mammalian_phenotype	5
MP:0010111	MP:0010111	abnormal renal calcium reabsorbtion	Mammalian_phenotype	5
MP:0010113	MP:0010113	abnormal sacrum morphology	Mammalian_phenotype	5
MP:0010114	MP:0010114	abnormal coccyx morphology	Mammalian_phenotype	5
MP:0010116	MP:0010116	abnormal primitive urogenital sinus morphology	Mammalian_phenotype	5
MP:0010123	MP:0010123	increased bone mineral content	Mammalian_phenotype	5
MP:0010124	MP:0010124	decreased bone mineral content	Mammalian_phenotype	5
MP:0010125	MP:0010125	abnormal parvocellular neurosecretory cell morphology	Mammalian_phenotype	5
MP:0010127	MP:0010127	hypervolemia	Mammalian_phenotype	5
MP:0010128	MP:0010128	hypovolemia	Mammalian_phenotype	5
MP:0010137	MP:0010137	delayed exit from anagen phase	Mammalian_phenotype	5
MP:0010142	MP:0010142	disorganized hair shaft	Mammalian_phenotype	5
MP:0010146	MP:0010146	umbilical hernia	Mammalian_phenotype	5
MP:0010163	MP:0010163	hemolysis	Mammalian_phenotype	5
MP:0010166	MP:0010166	increased response to stress-induced hyperthermia	Mammalian_phenotype	5
MP:0010167	MP:0010167	decreased response to stress-induced hyperthermia	Mammalian_phenotype	5
MP:0010173	MP:0010173	increased mammary gland epithelium proliferation	Mammalian_phenotype	5
MP:0010174	MP:0010174	decreased mammary gland epithelium proliferation	Mammalian_phenotype	5
MP:0010197	MP:0010197	abnormal lymphatic vessel endothelial cell morphology	Mammalian_phenotype	5
MP:0010204	MP:0010204	abnormal astrocyte apoptosis	Mammalian_phenotype	5
MP:0010205	MP:0010205	abnormal oligodendrocyte apoptosis	Mammalian_phenotype	5
MP:0010206	MP:0010206	pigment incontinence	Mammalian_phenotype	5
MP:0010207	MP:0010207	abnormal telomere morphology	Mammalian_phenotype	5
MP:0010210	MP:0010210	abnormal circulating cytokine level	Mammalian_phenotype	5
MP:0010212	MP:0010212	abnormal circulating C-reactive protein level	Mammalian_phenotype	5
MP:0010213	MP:0010213	abnormal circulating fibrinogen level	Mammalian_phenotype	5
MP:0010214	MP:0010214	abnormal circulating serum amyloid protein level	Mammalian_phenotype	5
MP:0010215	MP:0010215	abnormal circulating complement protein level	Mammalian_phenotype	5
MP:0010216	MP:0010216	abnormal circulating retinol binding protein level	Mammalian_phenotype	5
MP:0010224	MP:0010224	abnormal heart ventricle outflow tract morphology	Mammalian_phenotype	5
MP:0010225	MP:0010225	abnormal quadriceps morphology	Mammalian_phenotype	5
MP:0010232	MP:0010232	delayed skin pigmentation appearance	Mammalian_phenotype	5
MP:0010238	MP:0010238	increased skeletal muscle weight	Mammalian_phenotype	5
MP:0010239	MP:0010239	decreased skeletal muscle weight	Mammalian_phenotype	5
MP:0010245	MP:0010245	abnormal spleen perifollicular zone morphology	Mammalian_phenotype	5
MP:0010249	MP:0010249	lactation failure	Mammalian_phenotype	5
MP:0010273	MP:0010273	increased classified tumor incidence	Mammalian_phenotype	5
MP:0010274	MP:0010274	increased organ/body region tumor incidence	Mammalian_phenotype	5
MP:0010282	MP:0010282	decreased organ/body region tumor incidence	Mammalian_phenotype	5
MP:0010283	MP:0010283	decreased classified tumor incidence	Mammalian_phenotype	5
MP:0010332	MP:0010332	abnormal circulating apolipoprotein level	Mammalian_phenotype	5
MP:0010374	MP:0010374	bilirubinate stones	Mammalian_phenotype	5
MP:0010378	MP:0010378	increased respiratory quotient	Mammalian_phenotype	5
MP:0010379	MP:0010379	decreased respiratory quotient	Mammalian_phenotype	5
MP:0010382	MP:0010382	abnormal dosage compensation, by inactivation of X chromosome	Mammalian_phenotype	5
MP:0010395	MP:0010395	abnormal branchial arch development	Mammalian_phenotype	5
MP:0010396	MP:0010396	ectopic branchial arch	Mammalian_phenotype	5
MP:0010397	MP:0010397	abnormal otic capsule development	Mammalian_phenotype	5
MP:0010409	MP:0010409	cor triatriatum	Mammalian_phenotype	5
MP:0010426	MP:0010426	abnormal heart and great artery attachment	Mammalian_phenotype	5
MP:0010433	MP:0010433	double inlet heart left ventricle	Mammalian_phenotype	5
MP:0010434	MP:0010434	double inlet heart right ventricle	Mammalian_phenotype	5
MP:0010436	MP:0010436	abnormal coronary sinus morphology	Mammalian_phenotype	5
MP:0010438	MP:0010438	pulmonary vein stenosis	Mammalian_phenotype	5
MP:0010439	MP:0010439	abnormal hepatic vein morphology	Mammalian_phenotype	5
MP:0010440	MP:0010440	anomalous pulmonary venous connection	Mammalian_phenotype	5
MP:0010453	MP:0010453	abnormal coronary vein morphology	Mammalian_phenotype	5
MP:0010454	MP:0010454	abnormal truncus arteriosus septation	Mammalian_phenotype	5
MP:0010480	MP:0010480	pulmonary arteriovenous malformation	Mammalian_phenotype	5
MP:0010489	MP:0010489	abnormal heart atrium auricular region morphology	Mammalian_phenotype	5
MP:0010490	MP:0010490	abnormal inferior vena cava valve morphology	Mammalian_phenotype	5
MP:0010491	MP:0010491	abnormal coronary sinus valve morphology	Mammalian_phenotype	5
MP:0010492	MP:0010492	abnormal atrium endocardium morphology	Mammalian_phenotype	5
MP:0010493	MP:0010493	abnormal atrium myocardium morphology	Mammalian_phenotype	5
MP:0010494	MP:0010494	abnormal ventricle endocardium morphology	Mammalian_phenotype	5
MP:0010499	MP:0010499	abnormal ventricle myocardium morphology	Mammalian_phenotype	5
MP:0010504	MP:0010504	abnormal RR interval	Mammalian_phenotype	5
MP:0010505	MP:0010505	abnormal T wave	Mammalian_phenotype	5
MP:0010517	MP:0010517	abnormal Bachmann's bundle morphology	Mammalian_phenotype	5
MP:0010519	MP:0010519	atrioventricular block	Mammalian_phenotype	5
MP:0010520	MP:0010520	sinoatrial block	Mammalian_phenotype	5
MP:0010529	MP:0010529	hepatic arteriovenous malformation	Mammalian_phenotype	5
MP:0010530	MP:0010530	cerebral arteriovenous malformation	Mammalian_phenotype	5
MP:0010546	MP:0010546	abnormal subendocardium layer morphology	Mammalian_phenotype	5
MP:0010547	MP:0010547	abnormal mesocardium morphology	Mammalian_phenotype	5
MP:0010552	MP:0010552	abnormal HV interval	Mammalian_phenotype	5
MP:0010560	MP:0010560	intraventricular block	Mammalian_phenotype	5
MP:0010561	MP:0010561	absent coronary vessels	Mammalian_phenotype	5
MP:0010564	MP:0010564	abnormal fetal ductus arteriosus morphology	Mammalian_phenotype	5
MP:0010585	MP:0010585	abnormal conotruncal ridge morphology	Mammalian_phenotype	5
MP:0010589	MP:0010589	common truncal valve	Mammalian_phenotype	5
MP:0010592	MP:0010592	abnormal atrioventricular septum morphology	Mammalian_phenotype	5
MP:0010635	MP:0010635	aorta pulmonary collateral arteries	Mammalian_phenotype	5
MP:0010650	MP:0010650	abnormal aorticopulmonary septum morphology	Mammalian_phenotype	5
MP:0010654	MP:0010654	slow Wallerian degeneration	Mammalian_phenotype	5
MP:0010662	MP:0010662	abnormal intersomitic artery morphology	Mammalian_phenotype	5
MP:0010668	MP:0010668	abnormal hepatic portal vein morphology	Mammalian_phenotype	5
MP:0010683	MP:0010683	dilated hair follicle infundibulum	Mammalian_phenotype	5
MP:0010686	MP:0010686	abnormal hair follicle matrix region morphology	Mammalian_phenotype	5
MP:0010688	MP:0010688	hair follicle outer rooth sheath hyperplasia	Mammalian_phenotype	5
MP:0010689	MP:0010689	thin hair follicle outer rooth sheath	Mammalian_phenotype	5
MP:0010690	MP:0010690	thick hair follicle outer rooth sheath	Mammalian_phenotype	5
MP:0010691	MP:0010691	hair follicle inner rooth sheath hyperplasia	Mammalian_phenotype	5
MP:0010692	MP:0010692	thick hair follicle inner rooth sheath	Mammalian_phenotype	5
MP:0010693	MP:0010693	thin hair follicle inner rooth sheath	Mammalian_phenotype	5
MP:0010709	MP:0010709	absent anterior chamber	Mammalian_phenotype	5
MP:0010712	MP:0010712	absent nasolacrimal duct	Mammalian_phenotype	5
MP:0010713	MP:0010713	corneal-lenticular stalk	Mammalian_phenotype	5
MP:0010715	MP:0010715	retina coloboma	Mammalian_phenotype	5
MP:0010716	MP:0010716	optic disc coloboma	Mammalian_phenotype	5
MP:0010717	MP:0010717	optic nerve coloboma	Mammalian_phenotype	5
MP:0010740	MP:0010740	abnormal dendritic cell chemotaxis	Mammalian_phenotype	5
MP:0010744	MP:0010744	abnormal cervical flexure morphology	Mammalian_phenotype	5
MP:0010745	MP:0010745	abnormal pre-Botzinger complex morphology	Mammalian_phenotype	5
MP:0010749	MP:0010749	absent visual evoked potential	Mammalian_phenotype	5
MP:0010756	MP:0010756	decreased right ventricle peak pressure	Mammalian_phenotype	5
MP:0010757	MP:0010757	decreased right ventricle diastolic pressure	Mammalian_phenotype	5
MP:0010758	MP:0010758	increased right ventricle systolic pressure	Mammalian_phenotype	5
MP:0010759	MP:0010759	decreased right ventricle systolic pressure	Mammalian_phenotype	5
MP:0010760	MP:0010760	abnormal macrophage chemotaxis	Mammalian_phenotype	5
MP:0010764	MP:0010764	abnormal granulocyte chemotaxis	Mammalian_phenotype	5
MP:0010772	MP:0010772	abnormal pollex morphology	Mammalian_phenotype	5
MP:0010786	MP:0010786	stomach fundus hypertrophy	Mammalian_phenotype	5
MP:0010788	MP:0010788	stomach hypoplasia	Mammalian_phenotype	5
MP:0010790	MP:0010790	abnormal stomach pyloric antrum morphology	Mammalian_phenotype	5
MP:0010791	MP:0010791	abnormal pyloric canal morphology	Mammalian_phenotype	5
MP:0010792	MP:0010792	abnormal stomach mucosa morphology	Mammalian_phenotype	5
MP:0010793	MP:0010793	abnormal stomach serosa morphology	Mammalian_phenotype	5
MP:0010794	MP:0010794	abnormal stomach submucosa morphology	Mammalian_phenotype	5
MP:0010795	MP:0010795	abnormal cardiac gastric gland morphology	Mammalian_phenotype	5
MP:0010797	MP:0010797	abnormal pyloric gastric gland morphology	Mammalian_phenotype	5
MP:0010800	MP:0010800	abnormal submucous nerve plexus morphology	Mammalian_phenotype	5
MP:0010801	MP:0010801	abnormal myenteric nerve plexus morphology	Mammalian_phenotype	5
MP:0010825	MP:0010825	abnormal lung saccule morphology	Mammalian_phenotype	5
MP:0010828	MP:0010828	abnormal bronchioalveolar stem cell morphology	Mammalian_phenotype	5
MP:0010855	MP:0010855	pulmonary hyperemia	Mammalian_phenotype	5
MP:0010856	MP:0010856	dilated respiratory conducting tubes	Mammalian_phenotype	5
MP:0010858	MP:0010858	pulmonary epithelial necrosis	Mammalian_phenotype	5
MP:0010867	MP:0010867	abnormal bone trabecula morphology	Mammalian_phenotype	5
MP:0010871	MP:0010871	abnormal trabecular bone mass	Mammalian_phenotype	5
MP:0010872	MP:0010872	increased trabecular bone mass	Mammalian_phenotype	5
MP:0010873	MP:0010873	decreased trabecular bone mass	Mammalian_phenotype	5
MP:0010875	MP:0010875	increased bone volume	Mammalian_phenotype	5
MP:0010876	MP:0010876	decreased bone volume	Mammalian_phenotype	5
MP:0010877	MP:0010877	abnormal trabecular bone volume	Mammalian_phenotype	5
MP:0010881	MP:0010881	esophagus hypoplasia	Mammalian_phenotype	5
MP:0010882	MP:0010882	trachea hypoplasia	Mammalian_phenotype	5
MP:0010886	MP:0010886	absent minor salivary glands	Mammalian_phenotype	5
MP:0010892	MP:0010892	increased oligodendrocyte progenitor number	Mammalian_phenotype	5
MP:0010897	MP:0010897	abnormal bronchiole epithelium morphology	Mammalian_phenotype	5
MP:0010898	MP:0010898	abnormal pulmonary alveolus epithelium morphology	Mammalian_phenotype	5
MP:0010901	MP:0010901	abnormal pulmonary alveolar parenchyma morphology	Mammalian_phenotype	5
MP:0010906	MP:0010906	abnormal lung bud morphology	Mammalian_phenotype	5
MP:0010911	MP:0010911	abnormal pulmonary acinus morphology	Mammalian_phenotype	5
MP:0010914	MP:0010914	abnormal solitary pulmonary neuroendocrine cell morphology	Mammalian_phenotype	5
MP:0010918	MP:0010918	abnormal pulmonary neuroendocrine body morphology	Mammalian_phenotype	5
MP:0010925	MP:0010925	abnormal osteoid volume	Mammalian_phenotype	5
MP:0010928	MP:0010928	abnormal osteoid thickness	Mammalian_phenotype	5
MP:0010931	MP:0010931	abnormal trabecular bone connectivity density	Mammalian_phenotype	5
MP:0010934	MP:0010934	increased subcutaneous adipose tissue amount	Mammalian_phenotype	5
MP:0010943	MP:0010943	abnormal bronchus epithelium morphology	Mammalian_phenotype	5
MP:0010953	MP:0010953	abnormal fatty acid oxidation	Mammalian_phenotype	5
MP:0010956	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport	Mammalian_phenotype	5
MP:0010960	MP:0010960	abnormal compact bone mass	Mammalian_phenotype	5
MP:0010961	MP:0010961	increased compact bone mass	Mammalian_phenotype	5
MP:0010962	MP:0010962	decreased compact bone mass	Mammalian_phenotype	5
MP:0010963	MP:0010963	abnormal compact bone volume	Mammalian_phenotype	5
MP:0010966	MP:0010966	abnormal compact bone area	Mammalian_phenotype	5
MP:0010969	MP:0010969	absent compact bone	Mammalian_phenotype	5
MP:0010970	MP:0010970	abnormal compact bone lamellar structure	Mammalian_phenotype	5
MP:0010972	MP:0010972	absent periosteum	Mammalian_phenotype	5
MP:0010973	MP:0010973	increased periosteum thickness	Mammalian_phenotype	5
MP:0010974	MP:0010974	decreased periosteum thickness	Mammalian_phenotype	5
MP:0010976	MP:0010976	small lung lobe	Mammalian_phenotype	5
MP:0010977	MP:0010977	fused right lung lobes	Mammalian_phenotype	5
MP:0010978	MP:0010978	absent ureteric bud	Mammalian_phenotype	5
MP:0010979	MP:0010979	small ureteric bud	Mammalian_phenotype	5
MP:0010980	MP:0010980	ectopic ureteric bud	Mammalian_phenotype	5
MP:0010981	MP:0010981	abnormal branching involved in ureteric bud morphogenesis	Mammalian_phenotype	5
MP:0010982	MP:0010982	abnormal ureteric bud elongation	Mammalian_phenotype	5
MP:0010985	MP:0010985	abnormal kidney mesenchyme morphology	Mammalian_phenotype	5
MP:0010992	MP:0010992	increased surfactant secretion	Mammalian_phenotype	5
MP:0010993	MP:0010993	decreased surfactant secretion	Mammalian_phenotype	5
MP:0010995	MP:0010995	abnormal lung alveolus development	Mammalian_phenotype	5
MP:0010998	MP:0010998	pulmonary alveolar proteinosis	Mammalian_phenotype	5
MP:0011011	MP:0011011	impaired lung lobe morphogenesis	Mammalian_phenotype	5
MP:0011014	MP:0011014	decreased core body temperature	Mammalian_phenotype	5
MP:0011015	MP:0011015	decreased body surface temperature	Mammalian_phenotype	5
MP:0011016	MP:0011016	increased core body temperature	Mammalian_phenotype	5
MP:0011017	MP:0011017	increased body surface temperature	Mammalian_phenotype	5
MP:0011024	MP:0011024	abnormal branching involved in lung morphogenesis	Mammalian_phenotype	5
MP:0011051	MP:0011051	abnormal respiratory motile cilium number	Mammalian_phenotype	5
MP:0011056	MP:0011056	abnormal brain ependyma motile cilium morphology	Mammalian_phenotype	5
MP:0011058	MP:0011058	abnormal spinal cord motile cilium morphology	Mammalian_phenotype	5
MP:0011065	MP:0011065	abnormal kidney epithelial cell primary cilium morphology	Mammalian_phenotype	5
MP:0011073	MP:0011073	abnormal macrophage apoptosis	Mammalian_phenotype	5
MP:0011074	MP:0011074	abnormal macrophage nitric oxide production	Mammalian_phenotype	5
MP:0011091	MP:0011091	complete prenatal lethality	Mammalian_phenotype	5
MP:0011101	MP:0011101	partial prenatal lethality	Mammalian_phenotype	5
MP:0011111	MP:0011111	complete lethality during fetal growth through weaning	Mammalian_phenotype	5
MP:0011112	MP:0011112	partial lethality during fetal growth through weaning	Mammalian_phenotype	5
MP:0011115	MP:0011115	airway basal cell hyperplasia	Mammalian_phenotype	5
MP:0011117	MP:0011117	abnormal susceptibility to weight gain	Mammalian_phenotype	5
MP:0011118	MP:0011118	abnormal susceptibility to weight loss	Mammalian_phenotype	5
MP:0011133	MP:0011133	increased lung endothelial cell migration	Mammalian_phenotype	5
MP:0011134	MP:0011134	decreased lung endothelial cell migration	Mammalian_phenotype	5
MP:0011136	MP:0011136	increased lung endothelial cell adhesion	Mammalian_phenotype	5
MP:0011137	MP:0011137	decreased lung endothelial cell adhesion	Mammalian_phenotype	5
MP:0011139	MP:0011139	increased lung endothelial cell proliferation	Mammalian_phenotype	5
MP:0011140	MP:0011140	decreased lung endothelial cell proliferation	Mammalian_phenotype	5
MP:0011142	MP:0011142	abnormal lung-associated mesenchyme development	Mammalian_phenotype	5
MP:0011143	MP:0011143	thick lung-associated mesenchyme	Mammalian_phenotype	5
MP:0011144	MP:0011144	thin lung-associated mesenchyme	Mammalian_phenotype	5
MP:0011147	MP:0011147	increased mesenchymal cell proliferation involved in lung development	Mammalian_phenotype	5
MP:0011148	MP:0011148	decreased mesenchymal cell proliferation involved in lung development	Mammalian_phenotype	5
MP:0011158	MP:0011158	absent hypodermis muscle layer	Mammalian_phenotype	5
MP:0011169	MP:0011169	abnormal white fat cell differentation	Mammalian_phenotype	5
MP:0011170	MP:0011170	abnormal brown fat cell differentiation	Mammalian_phenotype	5
MP:0011174	MP:0011174	lipodystrophy	Mammalian_phenotype	5
MP:0011180	MP:0011180	abnormal hematopoietic cell number	Mammalian_phenotype	5
MP:0011183	MP:0011183	abnormal primitive endoderm morphology	Mammalian_phenotype	5
MP:0011187	MP:0011187	abnormal parietal endoderm morphology	Mammalian_phenotype	5
MP:0011188	MP:0011188	increased erythrocyte protoporphyrin level	Mammalian_phenotype	5
MP:0011192	MP:0011192	decreased embryonic epiblast cell proliferation	Mammalian_phenotype	5
MP:0011198	MP:0011198	absent proamniotic cavity	Mammalian_phenotype	5
MP:0011204	MP:0011204	abnormal visceral yolk sac blood island morphology	Mammalian_phenotype	5
MP:0011205	MP:0011205	excessive folding of visceral yolk sac	Mammalian_phenotype	5
MP:0011206	MP:0011206	absent visceral yolk sac	Mammalian_phenotype	5
MP:0011207	MP:0011207	absent ectoplacental cavity	Mammalian_phenotype	5
MP:0011208	MP:0011208	small proamniotic cavity	Mammalian_phenotype	5
MP:0011209	MP:0011209	absent extraembryonic coelom	Mammalian_phenotype	5
MP:0011212	MP:0011212	absent common peroneal nerve	Mammalian_phenotype	5
MP:0011216	MP:0011216	abnormal brainstem copper level	Mammalian_phenotype	5
MP:0011226	MP:0011226	abnormal thiamin level	Mammalian_phenotype	5
MP:0011227	MP:0011227	abnormal vitamin B12 level	Mammalian_phenotype	5
MP:0011229	MP:0011229	abnormal vitamin C level	Mammalian_phenotype	5
MP:0011230	MP:0011230	abnormal folic acid level	Mammalian_phenotype	5
MP:0011236	MP:0011236	increased blood oxygen capacity	Mammalian_phenotype	5
MP:0011237	MP:0011237	decreased blood oxygen capacity	Mammalian_phenotype	5
MP:0011245	MP:0011245	abnormal fetal derived definitive erythrocyte physiology	Mammalian_phenotype	5
MP:0011254	MP:0011254	superior-inferior ventricles	Mammalian_phenotype	5
MP:0011259	MP:0011259	abnormal cephalic neural fold morphology	Mammalian_phenotype	5
MP:0011261	MP:0011261	abnormal limb mesenchyme morphology	Mammalian_phenotype	5
MP:0011265	MP:0011265	abnormal pancreas mesenchyme morphology	Mammalian_phenotype	5
MP:0011284	MP:0011284	abnormal circulating erythropoietin level	Mammalian_phenotype	5
MP:0011287	MP:0011287	increased erythropoietin level	Mammalian_phenotype	5
MP:0011288	MP:0011288	decreased erythropoietin level	Mammalian_phenotype	5
MP:0011289	MP:0011289	abnormal nephron number	Mammalian_phenotype	5
MP:0011291	MP:0011291	nephron necrosis	Mammalian_phenotype	5
MP:0011292	MP:0011292	absent nephron	Mammalian_phenotype	5
MP:0011293	MP:0011293	dilated nephron	Mammalian_phenotype	5
MP:0011296	MP:0011296	decreased tubuloglomerular feedback response	Mammalian_phenotype	5
MP:0011297	MP:0011297	absent tubuloglomerular feedback response	Mammalian_phenotype	5
MP:0011306	MP:0011306	absent kidney pelvis	Mammalian_phenotype	5
MP:0011307	MP:0011307	kidney medulla cysts	Mammalian_phenotype	5
MP:0011308	MP:0011308	kidney corticomedullary cysts	Mammalian_phenotype	5
MP:0011309	MP:0011309	abnormal kidney arterial blood vessel morphology	Mammalian_phenotype	5
MP:0011310	MP:0011310	abnormal kidney capillary morphology	Mammalian_phenotype	5
MP:0011311	MP:0011311	abnormal kidney venous blood vessel morphology	Mammalian_phenotype	5
MP:0011314	MP:0011314	abnormal kidney cortex artery morphology	Mammalian_phenotype	5
MP:0011322	MP:0011322	abnormal kidney cortex vein morphology	Mammalian_phenotype	5
MP:0011324	MP:0011324	abnormal kidney vasa recta morphology	Mammalian_phenotype	5
MP:0011331	MP:0011331	abnormal papillary duct morphology	Mammalian_phenotype	5
MP:0011332	MP:0011332	abnormal kidney outer medulla morphology	Mammalian_phenotype	5
MP:0011333	MP:0011333	abnormal kidney inner medulla morphology	Mammalian_phenotype	5
MP:0011334	MP:0011334	abnormal nephrogenic zone morphology	Mammalian_phenotype	5
MP:0011335	MP:0011335	abnormal kidney pelvis smooth muscle morphology	Mammalian_phenotype	5
MP:0011337	MP:0011337	abnormal perihilar interstitium morphology	Mammalian_phenotype	5
MP:0011347	MP:0011347	abnormal kidney medullary ray morphology	Mammalian_phenotype	5
MP:0011360	MP:0011360	kidney cortex hypoplasia	Mammalian_phenotype	5
MP:0011361	MP:0011361	pelvic kidney	Mammalian_phenotype	5
MP:0011364	MP:0011364	abnormal metanephros morphology	Mammalian_phenotype	5
MP:0011377	MP:0011377	renal glomerulus fibrosis	Mammalian_phenotype	5
MP:0011394	MP:0011394	increased fetal cardiomyocyte proliferation	Mammalian_phenotype	5
MP:0011395	MP:0011395	decreased fetal cardiomyocyte proliferation	Mammalian_phenotype	5
MP:0011402	MP:0011402	renal cast	Mammalian_phenotype	5
MP:0011412	MP:0011412	gonadal ridge hypoplasia	Mammalian_phenotype	5
MP:0011413	MP:0011413	colorless urine	Mammalian_phenotype	5
MP:0011414	MP:0011414	erythruria	Mammalian_phenotype	5
MP:0011419	MP:0011419	erythrocyturia	Mammalian_phenotype	5
MP:0011422	MP:0011422	kidney medulla atrophy	Mammalian_phenotype	5
MP:0011423	MP:0011423	kidney cortex atrophy	Mammalian_phenotype	5
MP:0011424	MP:0011424	decreased urine uric acid level	Mammalian_phenotype	5
MP:0011435	MP:0011435	increased urine magnesium level	Mammalian_phenotype	5
MP:0011436	MP:0011436	decreased urine magnesium level	Mammalian_phenotype	5
MP:0011438	MP:0011438	absent kidney medulla	Mammalian_phenotype	5
MP:0011440	MP:0011440	increased kidney cell proliferation	Mammalian_phenotype	5
MP:0011441	MP:0011441	decreased kidney cell proliferation	Mammalian_phenotype	5
MP:0011442	MP:0011442	abnormal renal sodium ion transport	Mammalian_phenotype	5
MP:0011443	MP:0011443	abnormal renal water transport	Mammalian_phenotype	5
MP:0011448	MP:0011448	decreased dopaminergic neuron number	Mammalian_phenotype	5
MP:0011449	MP:0011449	increased dopaminergic neuron number	Mammalian_phenotype	5
MP:0011450	MP:0011450	ectopic dopaminergic neuron	Mammalian_phenotype	5
MP:0011456	MP:0011456	abnormal ureter ureteric bud development	Mammalian_phenotype	5
MP:0011457	MP:0011457	abnormal metanephric ureteric bud development	Mammalian_phenotype	5
MP:0011462	MP:0011462	increased urine bicarbonate level	Mammalian_phenotype	5
MP:0011463	MP:0011463	decreased urine bicarbonate level	Mammalian_phenotype	5
MP:0011466	MP:0011466	increased urine urea nitrogen level	Mammalian_phenotype	5
MP:0011467	MP:0011467	decreased urine urea nitrogen level	Mammalian_phenotype	5
MP:0011469	MP:0011469	abnormal urine creatinine level	Mammalian_phenotype	5
MP:0011473	MP:0011473	increased urine glycosaminoglycan level	Mammalian_phenotype	5
MP:0011474	MP:0011474	decreased urine glycosaminoglycan level	Mammalian_phenotype	5
MP:0011481	MP:0011481	anterior iris synechia	Mammalian_phenotype	5
MP:0011504	MP:0011504	abnormal limb long bone morphology	Mammalian_phenotype	5
MP:0011507	MP:0011507	kidney thrombosis	Mammalian_phenotype	5
MP:0011510	MP:0011510	biventricular, discordant atrioventricular connection	Mammalian_phenotype	5
MP:0011511	MP:0011511	biventricular, ambiguous atrioventricular connection	Mammalian_phenotype	5
MP:0011535	MP:0011535	increased urination frequency	Mammalian_phenotype	5
MP:0011536	MP:0011536	decreased urination frequency	Mammalian_phenotype	5
MP:0011539	MP:0011539	abnormal urine aldosterone level	Mammalian_phenotype	5
MP:0011542	MP:0011542	abnormal urine antidiuretic hormone level	Mammalian_phenotype	5
MP:0011545	MP:0011545	abnormal urine progesterone level	Mammalian_phenotype	5
MP:0011548	MP:0011548	abnormal urine corticosterone level	Mammalian_phenotype	5
MP:0011553	MP:0011553	increased urine deoxycorticosterone level	Mammalian_phenotype	5
MP:0011554	MP:0011554	decreased urine deoxycorticosterone level	Mammalian_phenotype	5
MP:0011559	MP:0011559	increased urine insulin level	Mammalian_phenotype	5
MP:0011560	MP:0011560	decreased urine insulin level	Mammalian_phenotype	5
MP:0011563	MP:0011563	increased urine prostaglandin level	Mammalian_phenotype	5
MP:0011564	MP:0011564	decreased urine prostaglandin level	Mammalian_phenotype	5
MP:0011569	MP:0011569	abnormal azygos vein morphology	Mammalian_phenotype	5
MP:0011578	MP:0011578	increased lipoprotein lipase activity	Mammalian_phenotype	5
MP:0011579	MP:0011579	decreased lipoprotein lipase activity	Mammalian_phenotype	5
MP:0011581	MP:0011581	increased triglyceride lipase activity	Mammalian_phenotype	5
MP:0011582	MP:0011582	decreased triglyceride lipase activity	Mammalian_phenotype	5
MP:0011584	MP:0011584	increased alkaline phosphatase activity	Mammalian_phenotype	5
MP:0011585	MP:0011585	decreased alkaline phosphatase activity	Mammalian_phenotype	5
MP:0011587	MP:0011587	increased ornithine carbamoyltransferase activity	Mammalian_phenotype	5
MP:0011588	MP:0011588	decreased ornithine carbamoyltransferase activity	Mammalian_phenotype	5
MP:0011590	MP:0011590	increased hormone-sensitive lipase activity	Mammalian_phenotype	5
MP:0011591	MP:0011591	decreased hormone-sensitive lipase activity	Mammalian_phenotype	5
MP:0011593	MP:0011593	increased catalase activity	Mammalian_phenotype	5
MP:0011594	MP:0011594	decreased catalase activity	Mammalian_phenotype	5
MP:0011596	MP:0011596	increased purine-nucleoside phosphorylase activity	Mammalian_phenotype	5
MP:0011597	MP:0011597	decreased purine-nucleoside phosphorylase activity	Mammalian_phenotype	5
MP:0011599	MP:0011599	increased phosphatidylcholine-sterol O-acyltransferase activity	Mammalian_phenotype	5
MP:0011600	MP:0011600	decreased phosphatidylcholine-sterol O-acyltransferase activity	Mammalian_phenotype	5
MP:0011601	MP:0011601	abnormal glutathione peroxidase activity	Mammalian_phenotype	5
MP:0011605	MP:0011605	increased glucokinase activity	Mammalian_phenotype	5
MP:0011606	MP:0011606	decreased glucokinase activity	Mammalian_phenotype	5
MP:0011608	MP:0011608	increased glyceraldehyde-3-phosphate dehydrogenase (NAD+) (phosphorylating) activity	Mammalian_phenotype	5
MP:0011609	MP:0011609	decreased glyceraldehyde-3-phosphate dehydrogenase (NAD+) (phosphorylating) activity	Mammalian_phenotype	5
MP:0011611	MP:0011611	abnormal circulating ghrelin level	Mammalian_phenotype	5
MP:0011617	MP:0011617	abnormal habituation	Mammalian_phenotype	5
MP:0011618	MP:0011618	abnormal sensitization	Mammalian_phenotype	5
MP:0011619	MP:0011619	abnormal dishabituation	Mammalian_phenotype	5
MP:0011626	MP:0011626	orotic acid urinary bladder stones	Mammalian_phenotype	5
MP:0011632	MP:0011632	dilated mitochondria	Mammalian_phenotype	5
MP:0011635	MP:0011635	abnormal mitochondrial crista morphology	Mammalian_phenotype	5
MP:0011639	MP:0011639	decreased mitochondrial DNA content	Mammalian_phenotype	5
MP:0011646	MP:0011646	abnormal sinuatrial valve morphology	Mammalian_phenotype	5
MP:0011648	MP:0011648	thick heart valve cusps	Mammalian_phenotype	5
MP:0011651	MP:0011651	abnormal circulating histidine level	Mammalian_phenotype	5
MP:0011655	MP:0011655	abnormal systemic artery morphology	Mammalian_phenotype	5
MP:0011660	MP:0011660	ectopia cordis	Mammalian_phenotype	5
MP:0011678	MP:0011678	abnormal vomeronasal sensory neuron physiology	Mammalian_phenotype	5
MP:0011681	MP:0011681	atrium cysts	Mammalian_phenotype	5
MP:0011682	MP:0011682	renal glomerulus cysts	Mammalian_phenotype	5
MP:0011686	MP:0011686	increased epidermal stem cell number	Mammalian_phenotype	5
MP:0011687	MP:0011687	decreased epidermal stem cell number	Mammalian_phenotype	5
MP:0011692	MP:0011692	increased chondrocyte number	Mammalian_phenotype	5
MP:0011695	MP:0011695	absent hematopoietic stem cells	Mammalian_phenotype	5
MP:0011703	MP:0011703	increased fibroblast proliferation	Mammalian_phenotype	5
MP:0011704	MP:0011704	decreased fibroblast proliferation	Mammalian_phenotype	5
MP:0011708	MP:0011708	decreased fibroblast cell migration	Mammalian_phenotype	5
MP:0011709	MP:0011709	increased fibroblast cell migration	Mammalian_phenotype	5
MP:0011721	MP:0011721	abnormal bone mineralization involved in bone maturation	Mammalian_phenotype	5
MP:0011724	MP:0011724	ectopic cortical neuron	Mammalian_phenotype	5
MP:0011725	MP:0011725	neuronal leptomeningeal ectopia	Mammalian_phenotype	5
MP:0011726	MP:0011726	ectopic Cajal-Retzius cell morphology	Mammalian_phenotype	5
MP:0011733	MP:0011733	fused somites	Mammalian_phenotype	5
MP:0011735	MP:0011735	increased urine ammonia level	Mammalian_phenotype	5
MP:0011736	MP:0011736	decreased urine ammonia level	Mammalian_phenotype	5
MP:0011737	MP:0011737	hypodipsia	Mammalian_phenotype	5
MP:0011738	MP:0011738	anasarca	Mammalian_phenotype	5
MP:0011739	MP:0011739	abnormal Boettcher cell morphology	Mammalian_phenotype	5
MP:0011741	MP:0011741	increased urine nitrite level	Mammalian_phenotype	5
MP:0011742	MP:0011742	decreased urine nitrite level	Mammalian_phenotype	5
MP:0011746	MP:0011746	spleen fibrosis	Mammalian_phenotype	5
MP:0011747	MP:0011747	myelofibrosis	Mammalian_phenotype	5
MP:0011760	MP:0011760	abnormal ureteric bud tip morphology	Mammalian_phenotype	5
MP:0011761	MP:0011761	abnormal ureteric bud trunk morphology	Mammalian_phenotype	5
MP:0011765	MP:0011765	oroticaciduria	Mammalian_phenotype	5
MP:0011772	MP:0011772	genital tubercle hypoplasia	Mammalian_phenotype	5
MP:0011777	MP:0011777	abnormal male prostatic urethra morphology	Mammalian_phenotype	5
MP:0011778	MP:0011778	abnormal male membranous urethra morphology	Mammalian_phenotype	5
MP:0011779	MP:0011779	abnormal male spongy urethra morphology	Mammalian_phenotype	5
MP:0011793	MP:0011793	abnormal female urethral gland morphology	Mammalian_phenotype	5
MP:0011794	MP:0011794	abnormal male urethral gland morphology	Mammalian_phenotype	5
MP:0011799	MP:0011799	increased urinary bladder weight	Mammalian_phenotype	5
MP:0011800	MP:0011800	decreased urinary bladder weight	Mammalian_phenotype	5
MP:0011803	MP:0011803	double kidney pelvis	Mammalian_phenotype	5
MP:0011809	MP:0011809	abnormal anoikis	Mammalian_phenotype	5
MP:0011822	MP:0011822	increased CD8-positive, alpha-beta memory T cell proliferation	Mammalian_phenotype	5
MP:0011823	MP:0011823	decreased CD8-positive, alpha-beta memory T cell proliferation	Mammalian_phenotype	5
MP:0011824	MP:0011824	increased cell chemotaxis	Mammalian_phenotype	5
MP:0011825	MP:0011825	decreased cell chemotaxis	Mammalian_phenotype	5
MP:0011827	MP:0011827	impaired neuron differentiation	Mammalian_phenotype	5
MP:0011836	MP:0011836	abnormal cloacal fold morphology	Mammalian_phenotype	5
MP:0011837	MP:0011837	abnormal cloacal membrane morphology	Mammalian_phenotype	5
MP:0011841	MP:0011841	abnormal male urethral crest morphology	Mammalian_phenotype	5
MP:0011842	MP:0011842	abnormal female urethral crest morphology	Mammalian_phenotype	5
MP:0011843	MP:0011843	abnormal kidney collecting duct epithelium morphology	Mammalian_phenotype	5
MP:0011844	MP:0011844	kidney collecting duct atrophy	Mammalian_phenotype	5
MP:0011845	MP:0011845	abnormal kidney collecting duct number	Mammalian_phenotype	5
MP:0011851	MP:0011851	abnormal embryonic cloaca development	Mammalian_phenotype	5
MP:0011854	MP:0011854	cerebral edema	Mammalian_phenotype	5
MP:0011866	MP:0011866	increased podocyte motility	Mammalian_phenotype	5
MP:0011867	MP:0011867	decreased podocyte motility	Mammalian_phenotype	5
MP:0011888	MP:0011888	abnormal circulating total protein level	Mammalian_phenotype	5
MP:0011889	MP:0011889	abnormal circulating ferritin level	Mammalian_phenotype	5
MP:0011892	MP:0011892	abnormal circulating transferrin level	Mammalian_phenotype	5
MP:0011902	MP:0011902	increased hematopoietic stem cell proliferation	Mammalian_phenotype	5
MP:0011903	MP:0011903	decreased hematopoietic stem cell proliferation	Mammalian_phenotype	5
MP:0011906	MP:0011906	increased Schwann cell proliferation	Mammalian_phenotype	5
MP:0011907	MP:0011907	decreased Schwann cell proliferation	Mammalian_phenotype	5
MP:0011909	MP:0011909	increased pancreatic endocrine progenitor cell proliferation	Mammalian_phenotype	5
MP:0011910	MP:0011910	decreased pancreatic endocrine progenitor cell proliferation	Mammalian_phenotype	5
MP:0011911	MP:0011911	abnormal pancreatic endocrine progenitor cell physiology	Mammalian_phenotype	5
MP:0011912	MP:0011912	abnormal circulating fibronectin level	Mammalian_phenotype	5
MP:0011918	MP:0011918	abnormal PQ interval	Mammalian_phenotype	5
MP:0011919	MP:0011919	abnormal R wave	Mammalian_phenotype	5
MP:0011920	MP:0011920	abnormal S wave	Mammalian_phenotype	5
MP:0011921	MP:0011921	abnormal zona intermedia morphology	Mammalian_phenotype	5
MP:0011922	MP:0011922	abnormal circulating osteocalcin level	Mammalian_phenotype	5
MP:0011928	MP:0011928	abnormal mitral valve flow	Mammalian_phenotype	5
MP:0011929	MP:0011929	abnormal aortic valve flow	Mammalian_phenotype	5
MP:0011930	MP:0011930	abnormal tricuspid valve flow	Mammalian_phenotype	5
MP:0011931	MP:0011931	abnormal pulmonary valve flow	Mammalian_phenotype	5
MP:0011932	MP:0011932	abnormal endocrine pancreas development	Mammalian_phenotype	5
MP:0011933	MP:0011933	abnormal exocrine pancreas development	Mammalian_phenotype	5
MP:0011934	MP:0011934	abnormal branching involved in pancreas development	Mammalian_phenotype	5
MP:0011936	MP:0011936	abnormal PP interval	Mammalian_phenotype	5
MP:0011943	MP:0011943	abnormal circadian feeding behavior	Mammalian_phenotype	5
MP:0011944	MP:0011944	abnormal eating frequency	Mammalian_phenotype	5
MP:0011947	MP:0011947	abnormal fluid intake	Mammalian_phenotype	5
MP:0011948	MP:0011948	abnormal drinking frequency	Mammalian_phenotype	5
MP:0011951	MP:0011951	increased cardiac stroke volume	Mammalian_phenotype	5
MP:0011952	MP:0011952	decreased cardiac stroke volume	Mammalian_phenotype	5
MP:0011956	MP:0011956	abnormal compensatory feeding amount	Mammalian_phenotype	5
MP:0011959	MP:0011959	abnormal eye posterior chamber depth	Mammalian_phenotype	5
MP:0011960	MP:0011960	abnormal eye anterior chamber depth	Mammalian_phenotype	5
MP:0011961	MP:0011961	abnormal cornea thickness	Mammalian_phenotype	5
MP:0011970	MP:0011970	abnormal circulating lactate dehydrogenase level	Mammalian_phenotype	5
MP:0011986	MP:0011986	decreased macrophage proliferation	Mammalian_phenotype	5
MP:0011993	MP:0011993	increased foot pad temperature	Mammalian_phenotype	5
MP:0011994	MP:0011994	increased nerve conduction velocity	Mammalian_phenotype	5
MP:0012002	MP:0012002	impaired touch escape response	Mammalian_phenotype	5
MP:0012012	MP:0012012	abnormal innate olfactory avoidance response	Mammalian_phenotype	5
MP:0012019	MP:0012019	abnormal oviduct epithelium motile cilium physiology	Mammalian_phenotype	5
MP:0012024	MP:0012024	abnormal nephron morphogenesis	Mammalian_phenotype	5
MP:0012030	MP:0012030	abnormal a wave amplitude	Mammalian_phenotype	5
MP:0012031	MP:0012031	abnormal b wave amplitude	Mammalian_phenotype	5
MP:0012036	MP:0012036	abnormal a wave latency	Mammalian_phenotype	5
MP:0012037	MP:0012037	abnormal b wave latency	Mammalian_phenotype	5
MP:0012038	MP:0012038	abnormal a wave implicit time	Mammalian_phenotype	5
MP:0012039	MP:0012039	abnormal b wave implicit time	Mammalian_phenotype	5
MP:0012051	MP:0012051	spasticity	Mammalian_phenotype	5
MP:0012055	MP:0012055	abnormal phrenic nerve innervation pattern to diaphragm	Mammalian_phenotype	5
MP:0012062	MP:0012062	small tail bud	Mammalian_phenotype	5
MP:0012063	MP:0012063	absent tail bud	Mammalian_phenotype	5
MP:0012071	MP:0012071	increased susceptibility to osteoporosis	Mammalian_phenotype	5
MP:0012072	MP:0012072	decreased susceptibility to osteoporosis	Mammalian_phenotype	5
MP:0012080	MP:0012080	chylous ascites	Mammalian_phenotype	5
MP:0000005	MP:0000005	increased brown adipose tissue amount	Mammalian_phenotype	5
MP:0000008	MP:0000008	increased white adipose tissue amount	Mammalian_phenotype	5
MP:0000015	MP:0000015	abnormal ear pigmentation	Mammalian_phenotype	5
MP:0000017	MP:0000017	big ears	Mammalian_phenotype	5
MP:0000018	MP:0000018	small ears	Mammalian_phenotype	5
MP:0000019	MP:0000019	thick ears	Mammalian_phenotype	5
MP:0000020	MP:0000020	scaly ears	Mammalian_phenotype	5
MP:0000021	MP:0000021	prominent ears	Mammalian_phenotype	5
MP:0000022	MP:0000022	abnormal ear shape	Mammalian_phenotype	5
MP:0000023	MP:0000023	abnormal ear distance/ position	Mammalian_phenotype	5
MP:0000032	MP:0000032	cochlear degeneration	Mammalian_phenotype	5
MP:0000052	MP:0000052	early ear unfolding	Mammalian_phenotype	5
MP:0000053	MP:0000053	excessive ear growth	Mammalian_phenotype	5
MP:0000054	MP:0000054	delayed ear emergence	Mammalian_phenotype	5
MP:0000062	MP:0000062	increased bone mineral density	Mammalian_phenotype	5
MP:0000063	MP:0000063	decreased bone mineral density	Mammalian_phenotype	5
MP:0000064	MP:0000064	failure of secondary bone resorption	Mammalian_phenotype	5
MP:0000066	MP:0000066	osteoporosis	Mammalian_phenotype	5
MP:0000067	MP:0000067	osteopetrosis	Mammalian_phenotype	5
MP:0000073	MP:0000073	absent craniofacial bones	Mammalian_phenotype	5
MP:0000083	MP:0000083	ectopic cranial bone growth	Mammalian_phenotype	5
MP:0000105	MP:0000105	impaired ossification of basisphenoid bone	Mammalian_phenotype	5
MP:0000133	MP:0000133	abnormal long bone metaphysis morphology	Mammalian_phenotype	5
MP:0000134	MP:0000134	abnormal compact bone thickness	Mammalian_phenotype	5
MP:0000136	MP:0000136	abnormal microglial cell morphology	Mammalian_phenotype	5
MP:0000137	MP:0000137	abnormal vertebrae morphology	Mammalian_phenotype	5
MP:0000149	MP:0000149	abnormal scapula morphology	Mammalian_phenotype	5
MP:0000150	MP:0000150	abnormal rib morphology	Mammalian_phenotype	5
MP:0000157	MP:0000157	abnormal sternum morphology	Mammalian_phenotype	5
MP:0000165	MP:0000165	abnormal long bone hypertrophic chondrocyte zone	Mammalian_phenotype	5
MP:0000167	MP:0000167	decreased chondrocyte number	Mammalian_phenotype	5
MP:0000181	MP:0000181	abnormal circulating LDL cholesterol level	Mammalian_phenotype	5
MP:0000184	MP:0000184	abnormal circulating HDL cholesterol level	Mammalian_phenotype	5
MP:0000187	MP:0000187	abnormal triglyceride level	Mammalian_phenotype	5
MP:0000199	MP:0000199	abnormal circulating serum albumin level	Mammalian_phenotype	5
MP:0000228	MP:0000228	abnormal thrombopoiesis	Mammalian_phenotype	5
MP:0000231	MP:0000231	hypertension	Mammalian_phenotype	5
MP:0000240	MP:0000240	extramedullary hematopoiesis	Mammalian_phenotype	5
MP:0000243	MP:0000243	myoclonus	Mammalian_phenotype	5
MP:0000245	MP:0000245	abnormal erythropoiesis	Mammalian_phenotype	5
MP:0000260	MP:0000260	abnormal angiogenesis	Mammalian_phenotype	5
MP:0000269	MP:0000269	abnormal heart looping	Mammalian_phenotype	5
MP:0000270	MP:0000270	abnormal heart tube morphology	Mammalian_phenotype	5
MP:0000274	MP:0000274	enlarged heart	Mammalian_phenotype	5
MP:0000279	MP:0000279	ventricular hypoplasia	Mammalian_phenotype	5
MP:0000281	MP:0000281	abnormal interventricular septum morphology	Mammalian_phenotype	5
MP:0000282	MP:0000282	abnormal interatrial septum morphology	Mammalian_phenotype	5
MP:0000287	MP:0000287	heart valve hypoplasia	Mammalian_phenotype	5
MP:0000291	MP:0000291	enlarged pericardium	Mammalian_phenotype	5
MP:0000292	MP:0000292	distended pericardium	Mammalian_phenotype	5
MP:0000316	MP:0000316	cellular necrosis	Mammalian_phenotype	5
MP:0000321	MP:0000321	increased bone marrow cell number	Mammalian_phenotype	5
MP:0000332	MP:0000332	hemoglobinemia	Mammalian_phenotype	5
MP:0000333	MP:0000333	decreased bone marrow cell number	Mammalian_phenotype	5
MP:0000346	MP:0000346	broad head	Mammalian_phenotype	5
MP:0000382	MP:0000382	underdeveloped hair follicles	Mammalian_phenotype	5
MP:0000387	MP:0000387	disorganized inner root sheath cells	Mammalian_phenotype	5
MP:0000388	MP:0000388	absent hair follicle inner root sheath	Mammalian_phenotype	5
MP:0000389	MP:0000389	disorganized outer root sheath cells	Mammalian_phenotype	5
MP:0000391	MP:0000391	premature hair follicle generation	Mammalian_phenotype	5
MP:0000392	MP:0000392	accelerated hair follicle regression	Mammalian_phenotype	5
MP:0000396	MP:0000396	increased curvature of hairs	Mammalian_phenotype	5
MP:0000398	MP:0000398	splitting of guard hairs	Mammalian_phenotype	5
MP:0000399	MP:0000399	increased curvature of guard hairs	Mammalian_phenotype	5
MP:0000401	MP:0000401	increased curvature of awl hairs	Mammalian_phenotype	5
MP:0000403	MP:0000403	increased curvature of zigzag hairs	Mammalian_phenotype	5
MP:0000404	MP:0000404	decreased curvature of zigzag hairs	Mammalian_phenotype	5
MP:0000406	MP:0000406	increased curvature of auchene hairs	Mammalian_phenotype	5
MP:0000408	MP:0000408	absent duvet hair	Mammalian_phenotype	5
MP:0000410	MP:0000410	waved hair	Mammalian_phenotype	5
MP:0000411	MP:0000411	shiny fur	Mammalian_phenotype	5
MP:0000420	MP:0000420	ruffled hair	Mammalian_phenotype	5
MP:0000433	MP:0000433	microcephaly	Mammalian_phenotype	5
MP:0000434	MP:0000434	megacephaly	Mammalian_phenotype	5
MP:0000435	MP:0000435	shortened head	Mammalian_phenotype	5
MP:0000437	MP:0000437	taut facial appearance	Mammalian_phenotype	5
MP:0000438	MP:0000438	abnormal cranium morphology	Mammalian_phenotype	5
MP:0000443	MP:0000443	abnormal snout morphology	Mammalian_phenotype	5
MP:0000466	MP:0000466	esophageal epithelium hyperplasia	Mammalian_phenotype	5
MP:0000469	MP:0000469	abnormal esophageal squamous epithelium morphology	Mammalian_phenotype	5
MP:0000478	MP:0000478	delayed intestine development	Mammalian_phenotype	5
MP:0000479	MP:0000479	abnormal enterocyte morphology	Mammalian_phenotype	5
MP:0000484	MP:0000484	abnormal pulmonary artery morphology	Mammalian_phenotype	5
MP:0000486	MP:0000486	abnormal pulmonary trunk morphology	Mammalian_phenotype	5
MP:0000492	MP:0000492	abnormal rectum morphology	Mammalian_phenotype	5
MP:0000494	MP:0000494	abnormal cecum morphology	Mammalian_phenotype	5
MP:0000495	MP:0000495	abnormal colon morphology	Mammalian_phenotype	5
MP:0000500	MP:0000500	small intestinal prolapse	Mammalian_phenotype	5
MP:0000503	MP:0000503	excessive digestive secretion	Mammalian_phenotype	5
MP:0000505	MP:0000505	decreased digestive secretion	Mammalian_phenotype	5
MP:0000507	MP:0000507	absent digestive secretion	Mammalian_phenotype	5
MP:0000511	MP:0000511	abnormal intestinal mucosa morphology	Mammalian_phenotype	5
MP:0000519	MP:0000519	hydronephrosis	Mammalian_phenotype	5
MP:0000522	MP:0000522	kidney cortex cysts	Mammalian_phenotype	5
MP:0000528	MP:0000528	delayed kidney development	Mammalian_phenotype	5
MP:0000532	MP:0000532	kidney vascular congestion	Mammalian_phenotype	5
MP:0000535	MP:0000535	ureter urothelium hyperplasia	Mammalian_phenotype	5
MP:0000541	MP:0000541	abnormal urinary bladder transitional epithelium morphology	Mammalian_phenotype	5
MP:0000552	MP:0000552	abnormal radius morphology	Mammalian_phenotype	5
MP:0000554	MP:0000554	abnormal carpal bone morphology	Mammalian_phenotype	5
MP:0000558	MP:0000558	abnormal tibia morphology	Mammalian_phenotype	5
MP:0000559	MP:0000559	abnormal femur morphology	Mammalian_phenotype	5
MP:0000561	MP:0000561	adactyly	Mammalian_phenotype	5
MP:0000562	MP:0000562	polydactyly	Mammalian_phenotype	5
MP:0000564	MP:0000564	syndactyly	Mammalian_phenotype	5
MP:0000565	MP:0000565	oligodactyly	Mammalian_phenotype	5
MP:0000567	MP:0000567	truncation of digits	Mammalian_phenotype	5
MP:0000568	MP:0000568	ectopic digits	Mammalian_phenotype	5
MP:0000577	MP:0000577	absent eccrine glands	Mammalian_phenotype	5
MP:0000583	MP:0000583	long toenails	Mammalian_phenotype	5
MP:0000597	MP:0000597	delayed hepatic development	Mammalian_phenotype	5
MP:0000599	MP:0000599	enlarged liver	Mammalian_phenotype	5
MP:0000601	MP:0000601	small liver	Mammalian_phenotype	5
MP:0000615	MP:0000615	abnormal palatine gland morphology	Mammalian_phenotype	5
MP:0000616	MP:0000616	decreased ductal branching in the palatine gland	Mammalian_phenotype	5
MP:0000620	MP:0000620	narrow salivary ducts	Mammalian_phenotype	5
MP:0000624	MP:0000624	xerostomia	Mammalian_phenotype	5
MP:0000640	MP:0000640	adrenal gland hypoplasia	Mammalian_phenotype	5
MP:0000643	MP:0000643	absent adrenal medulla	Mammalian_phenotype	5
MP:0000644	MP:0000644	dextrocardia	Mammalian_phenotype	5
MP:0000650	MP:0000650	mesocardia	Mammalian_phenotype	5
MP:0000662	MP:0000662	abnormal branching of the mammary ductal tree	Mammalian_phenotype	5
MP:0000687	MP:0000687	small lymphoid organs	Mammalian_phenotype	5
MP:0000690	MP:0000690	absent spleen	Mammalian_phenotype	5
MP:0000696	MP:0000696	abnormal Peyer's patch morphology	Mammalian_phenotype	5
MP:0000700	MP:0000700	abnormal lymph node number	Mammalian_phenotype	5
MP:0000701	MP:0000701	abnormal lymph node size	Mammalian_phenotype	5
MP:0000704	MP:0000704	abnormal thymus development	Mammalian_phenotype	5
MP:0000705	MP:0000705	athymia	Mammalian_phenotype	5
MP:0000714	MP:0000714	increased thymocyte number	Mammalian_phenotype	5
MP:0000715	MP:0000715	decreased thymocyte number	Mammalian_phenotype	5
MP:0000732	MP:0000732	delayed primary myocyte appearance	Mammalian_phenotype	5
MP:0000737	MP:0000737	abnormal myotome development	Mammalian_phenotype	5
MP:0000740	MP:0000740	impaired smooth muscle contractility	Mammalian_phenotype	5
MP:0000745	MP:0000745	tremors	Mammalian_phenotype	5
MP:0000746	MP:0000746	weakness	Mammalian_phenotype	5
MP:0000753	MP:0000753	paralysis	Mammalian_phenotype	5
MP:0000754	MP:0000754	paresis	Mammalian_phenotype	5
MP:0000774	MP:0000774	decreased brain size	Mammalian_phenotype	5
MP:0000786	MP:0000786	abnormal embryonic neuroepithelial layer differentiation	Mammalian_phenotype	5
MP:0000787	MP:0000787	abnormal telencephalon morphology	Mammalian_phenotype	5
MP:0000811	MP:0000811	hippocampal neuron degeneration	Mammalian_phenotype	5
MP:0000822	MP:0000822	abnormal brain ventricle morphology	Mammalian_phenotype	5
MP:0000828	MP:0000828	abnormal fourth ventricle morphology	Mammalian_phenotype	5
MP:0000830	MP:0000830	abnormal diencephalon morphology	Mammalian_phenotype	5
MP:0000844	MP:0000844	abnormal pontine flexure morphology	Mammalian_phenotype	5
MP:0000846	MP:0000846	abnormal medulla oblongata morphology	Mammalian_phenotype	5
MP:0000847	MP:0000847	abnormal metencephalon morphology	Mammalian_phenotype	5
MP:0000848	MP:0000848	abnormal pons morphology	Mammalian_phenotype	5
MP:0000876	MP:0000876	Purkinje cell degeneration	Mammalian_phenotype	5
MP:0000885	MP:0000885	ectopic Purkinje cell	Mammalian_phenotype	5
MP:0000914	MP:0000914	exencephaly	Mammalian_phenotype	5
MP:0000923	MP:0000923	abnormal roof plate morphology	Mammalian_phenotype	5
MP:0000925	MP:0000925	abnormal floor plate morphology	Mammalian_phenotype	5
MP:0000930	MP:0000930	wavy neural tube	Mammalian_phenotype	5
MP:0000932	MP:0000932	absent notochord	Mammalian_phenotype	5
MP:0000938	MP:0000938	motor neuron degeneration	Mammalian_phenotype	5
MP:0000953	MP:0000953	abnormal oligodendrocyte morphology	Mammalian_phenotype	5
MP:0000954	MP:0000954	decreased oligodendrocyte progenitor number	Mammalian_phenotype	5
MP:0000960	MP:0000960	abnormal sensory ganglion morphology	Mammalian_phenotype	5
MP:0000998	MP:0000998	absent joint capsule	Mammalian_phenotype	5
MP:0001008	MP:0001008	abnormal sympathetic ganglion morphology	Mammalian_phenotype	5
MP:0001025	MP:0001025	abnormal sympathetic neuron morphology	Mammalian_phenotype	5
MP:0001034	MP:0001034	abnormal parasympathetic ganglion morphology	Mammalian_phenotype	5
MP:0001037	MP:0001037	abnormal parasympathetic neuron morphology	Mammalian_phenotype	5
MP:0001045	MP:0001045	abnormal enteric ganglia morphology	Mammalian_phenotype	5
MP:0001047	MP:0001047	abnormal enteric cholinergic neuron morphology	Mammalian_phenotype	5
MP:0001053	MP:0001053	abnormal neuromuscular synapse morphology	Mammalian_phenotype	5
MP:0001061	MP:0001061	abnormal oculomotor nerve morphology	Mammalian_phenotype	5
MP:0001063	MP:0001063	abnormal trochlear nerve morphology	Mammalian_phenotype	5
MP:0001065	MP:0001065	abnormal trigeminal nerve morphology	Mammalian_phenotype	5
MP:0001070	MP:0001070	abnormal abducens nerve morphology	Mammalian_phenotype	5
MP:0001071	MP:0001071	abnormal facial nerve morphology	Mammalian_phenotype	5
MP:0001072	MP:0001072	abnormal vestibulocochlear nerve morphology	Mammalian_phenotype	5
MP:0001073	MP:0001073	abnormal glossopharyngeal nerve morphology	Mammalian_phenotype	5
MP:0001074	MP:0001074	abnormal vagus nerve morphology	Mammalian_phenotype	5
MP:0001075	MP:0001075	abnormal accessory nerve morphology	Mammalian_phenotype	5
MP:0001076	MP:0001076	abnormal hypoglossal nerve morphology	Mammalian_phenotype	5
MP:0001078	MP:0001078	abnormal phrenic nerve morphology	Mammalian_phenotype	5
MP:0001082	MP:0001082	abnormal geniculate ganglion morphology	Mammalian_phenotype	5
MP:0001092	MP:0001092	abnormal trigeminal ganglion morphology	Mammalian_phenotype	5
MP:0001096	MP:0001096	abnormal glossopharyngeal ganglion morphology	Mammalian_phenotype	5
MP:0001100	MP:0001100	abnormal vagus ganglion morphology	Mammalian_phenotype	5
MP:0001106	MP:0001106	abnormal Schwann cell morphology	Mammalian_phenotype	5
MP:0001116	MP:0001116	small gonad	Mammalian_phenotype	5
MP:0001124	MP:0001124	abnormal gametes	Mammalian_phenotype	5
MP:0001125	MP:0001125	abnormal oocyte morphology	Mammalian_phenotype	5
MP:0001155	MP:0001155	arrest of spermatogenesis	Mammalian_phenotype	5
MP:0001182	MP:0001182	lung hemorrhage	Mammalian_phenotype	5
MP:0001189	MP:0001189	absent skin pigmentation	Mammalian_phenotype	5
MP:0001197	MP:0001197	oily skin	Mammalian_phenotype	5
MP:0001209	MP:0001209	spontaneous skin ulceration	Mammalian_phenotype	5
MP:0001232	MP:0001232	absent epidermis stratum basale	Mammalian_phenotype	5
MP:0001234	MP:0001234	absent suprabasal layer	Mammalian_phenotype	5
MP:0001235	MP:0001235	disorganized suprabasal layer	Mammalian_phenotype	5
MP:0001237	MP:0001237	enlarged spinous cells	Mammalian_phenotype	5
MP:0001238	MP:0001238	thin epidermis stratum spinosum	Mammalian_phenotype	5
MP:0001241	MP:0001241	absent epidermis stratum corneum	Mammalian_phenotype	5
MP:0001242	MP:0001242	hyperkeratosis	Mammalian_phenotype	5
MP:0001251	MP:0001251	dermis papillary layer hypercellularity	Mammalian_phenotype	5
MP:0001254	MP:0001254	increased body height	Mammalian_phenotype	5
MP:0001255	MP:0001255	decreased body height	Mammalian_phenotype	5
MP:0001257	MP:0001257	increased body length	Mammalian_phenotype	5
MP:0001258	MP:0001258	decreased body length	Mammalian_phenotype	5
MP:0001260	MP:0001260	increased body weight	Mammalian_phenotype	5
MP:0001262	MP:0001262	decreased body weight	Mammalian_phenotype	5
MP:0001290	MP:0001290	delayed eyelid opening	Mammalian_phenotype	5
MP:0001304	MP:0001304	cataracts	Mammalian_phenotype	5
MP:0001305	MP:0001305	enlarged lens	Mammalian_phenotype	5
MP:0001306	MP:0001306	small lens	Mammalian_phenotype	5
MP:0001307	MP:0001307	fused cornea and lens	Mammalian_phenotype	5
MP:0001308	MP:0001308	abnormal lens polarity	Mammalian_phenotype	5
MP:0001313	MP:0001313	increased incidence of corneal inflammation	Mammalian_phenotype	5
MP:0001314	MP:0001314	corneal opacity	Mammalian_phenotype	5
MP:0001316	MP:0001316	corneal scarring	Mammalian_phenotype	5
MP:0001322	MP:0001322	abnormal iris morphology	Mammalian_phenotype	5
MP:0001325	MP:0001325	abnormal retina morphology	Mammalian_phenotype	5
MP:0001345	MP:0001345	meibomian gland atrophy	Mammalian_phenotype	5
MP:0001347	MP:0001347	absent lacrimal glands	Mammalian_phenotype	5
MP:0001361	MP:0001361	social withdrawal	Mammalian_phenotype	5
MP:0001362	MP:0001362	abnormal anxiety-related response	Mammalian_phenotype	5
MP:0001375	MP:0001375	abnormal mating preference	Mammalian_phenotype	5
MP:0001376	MP:0001376	abnormal mating receptivity	Mammalian_phenotype	5
MP:0001377	MP:0001377	abnormal mating frequency	Mammalian_phenotype	5
MP:0001388	MP:0001388	abnormal stationary movement	Mammalian_phenotype	5
MP:0001392	MP:0001392	abnormal locomotor behavior	Mammalian_phenotype	5
MP:0001393	MP:0001393	ataxia	Mammalian_phenotype	5
MP:0001394	MP:0001394	circling	Mammalian_phenotype	5
MP:0001401	MP:0001401	jumpy	Mammalian_phenotype	5
MP:0001405	MP:0001405	impaired coordination	Mammalian_phenotype	5
MP:0001409	MP:0001409	increased stereotypic behavior	Mammalian_phenotype	5
MP:0001410	MP:0001410	head bobbing	Mammalian_phenotype	5
MP:0001411	MP:0001411	spinning	Mammalian_phenotype	5
MP:0001423	MP:0001423	abnormal liquid preference	Mammalian_phenotype	5
MP:0001428	MP:0001428	adipsia	Mammalian_phenotype	5
MP:0001432	MP:0001432	abnormal food preference	Mammalian_phenotype	5
MP:0001436	MP:0001436	abnormal suckling behavior	Mammalian_phenotype	5
MP:0001446	MP:0001446	abnormal whisker trimming behavior	Mammalian_phenotype	5
MP:0001447	MP:0001447	abnormal nest building behavior	Mammalian_phenotype	5
MP:0001454	MP:0001454	abnormal cued conditioning behavior	Mammalian_phenotype	5
MP:0001460	MP:0001460	abnormal olfactory -discrimination memory	Mammalian_phenotype	5
MP:0001462	MP:0001462	abnormal avoidance learning behavior	Mammalian_phenotype	5
MP:0001469	MP:0001469	abnormal contextual conditioning behavior	Mammalian_phenotype	5
MP:0001496	MP:0001496	audiogenic seizures	Mammalian_phenotype	5
MP:0001505	MP:0001505	hunched posture	Mammalian_phenotype	5
MP:0001506	MP:0001506	limp posture	Mammalian_phenotype	5
MP:0001511	MP:0001511	disheveled coat	Mammalian_phenotype	5
MP:0001512	MP:0001512	trunk curl	Mammalian_phenotype	5
MP:0001515	MP:0001515	abnormal grip strength	Mammalian_phenotype	5
MP:0001522	MP:0001522	impaired swimming	Mammalian_phenotype	5
MP:0001524	MP:0001524	impaired limb coordination	Mammalian_phenotype	5
MP:0001525	MP:0001525	impaired balance	Mammalian_phenotype	5
MP:0001526	MP:0001526	abnormal placing response	Mammalian_phenotype	5
MP:0001527	MP:0001527	athetotic walking movements	Mammalian_phenotype	5
MP:0001562	MP:0001562	abnormal circulating calcium level	Mammalian_phenotype	5
MP:0001596	MP:0001596	hypotension	Mammalian_phenotype	5
MP:0001606	MP:0001606	impaired hematopoiesis	Mammalian_phenotype	5
MP:0001613	MP:0001613	abnormal vasodilation	Mammalian_phenotype	5
MP:0001622	MP:0001622	abnormal vasculogenesis	Mammalian_phenotype	5
MP:0001634	MP:0001634	internal hemorrhage	Mammalian_phenotype	5
MP:0001650	MP:0001650	abnormal seizure response to electrical stimulation	Mammalian_phenotype	5
MP:0001655	MP:0001655	multifocal hepatic necrosis	Mammalian_phenotype	5
MP:0001656	MP:0001656	focal hepatic necrosis	Mammalian_phenotype	5
MP:0001665	MP:0001665	chronic diarrhea	Mammalian_phenotype	5
MP:0001667	MP:0001667	abnormal carbohydrate absorption	Mammalian_phenotype	5
MP:0001670	MP:0001670	abnormal intestinal mineral absorption	Mammalian_phenotype	5
MP:0001676	MP:0001676	abnormal apical ectodermal ridge morphology	Mammalian_phenotype	5
MP:0001691	MP:0001691	abnormal somite shape	Mammalian_phenotype	5
MP:0001694	MP:0001694	failure to form egg cylinders	Mammalian_phenotype	5
MP:0001696	MP:0001696	failure to gastrulate	Mammalian_phenotype	5
MP:0001698	MP:0001698	decreased embryo size	Mammalian_phenotype	5
MP:0001699	MP:0001699	increased embryo size	Mammalian_phenotype	5
MP:0001700	MP:0001700	abnormal embryo turning	Mammalian_phenotype	5
MP:0001710	MP:0001710	absent amniotic folds	Mammalian_phenotype	5
MP:0001712	MP:0001712	abnormal placenta development	Mammalian_phenotype	5
MP:0001716	MP:0001716	abnormal placenta labyrinth morphology	Mammalian_phenotype	5
MP:0001722	MP:0001722	pale yolk sac	Mammalian_phenotype	5
MP:0001723	MP:0001723	disorganized yolk sac vascular plexus	Mammalian_phenotype	5
MP:0001727	MP:0001727	abnormal embryo implantation	Mammalian_phenotype	5
MP:0001740	MP:0001740	failure of adrenal epinephrine secretion	Mammalian_phenotype	5
MP:0001744	MP:0001744	hypersecretion of corticosterone	Mammalian_phenotype	5
MP:0001753	MP:0001753	hypersecretion of corticotropin-releasing hormone	Mammalian_phenotype	5
MP:0001754	MP:0001754	increased circulating corticotropin-releasing hormone level	Mammalian_phenotype	5
MP:0001759	MP:0001759	increased urine glucose level	Mammalian_phenotype	5
MP:0001770	MP:0001770	abnormal iron level	Mammalian_phenotype	5
MP:0001771	MP:0001771	abnormal circulating magnesium level	Mammalian_phenotype	5
MP:0001775	MP:0001775	abnormal selenium level	Mammalian_phenotype	5
MP:0001776	MP:0001776	abnormal circulating sodium level	Mammalian_phenotype	5
MP:0001780	MP:0001780	decreased brown adipose tissue amount	Mammalian_phenotype	5
MP:0001783	MP:0001783	decreased white adipose tissue amount	Mammalian_phenotype	5
MP:0001787	MP:0001787	pericardial edema	Mammalian_phenotype	5
MP:0001824	MP:0001824	abnormal thymus involution	Mammalian_phenotype	5
MP:0001837	MP:0001837	defective assembly of class I molecules	Mammalian_phenotype	5
MP:0001838	MP:0001838	defective intracellular transport of class I molecules	Mammalian_phenotype	5
MP:0001839	MP:0001839	abnormal level of surface class I molecules	Mammalian_phenotype	5
MP:0001844	MP:0001844	autoimmune response	Mammalian_phenotype	5
MP:0001852	MP:0001852	conjunctivitis	Mammalian_phenotype	5
MP:0001885	MP:0001885	mammary gland duct hyperplasia	Mammalian_phenotype	5
MP:0001889	MP:0001889	delayed brain development	Mammalian_phenotype	5
MP:0001891	MP:0001891	hydroencephaly	Mammalian_phenotype	5
MP:0001906	MP:0001906	increased dopamine level	Mammalian_phenotype	5
MP:0001927	MP:0001927	abnormal estrous cycle	Mammalian_phenotype	5
MP:0001932	MP:0001932	abnormal spermiogenesis	Mammalian_phenotype	5
MP:0001934	MP:0001934	increased litter size	Mammalian_phenotype	5
MP:0001935	MP:0001935	decreased litter size	Mammalian_phenotype	5
MP:0001937	MP:0001937	abnormal sexual maturation	Mammalian_phenotype	5
MP:0001939	MP:0001939	secondary sex reversal	Mammalian_phenotype	5
MP:0001945	MP:0001945	bronchoconstriction	Mammalian_phenotype	5
MP:0001951	MP:0001951	abnormal breathing pattern	Mammalian_phenotype	5
MP:0001967	MP:0001967	deafness	Mammalian_phenotype	5
MP:0001970	MP:0001970	abnormal pain threshold	Mammalian_phenotype	5
MP:0001987	MP:0001987	alcohol preference	Mammalian_phenotype	5
MP:0001988	MP:0001988	cocaine preference	Mammalian_phenotype	5
MP:0002021	MP:0002021	increased incidence of induced tumors	Mammalian_phenotype	5
MP:0002053	MP:0002053	decreased incidence of induced tumors	Mammalian_phenotype	5
MP:0002073	MP:0002073	abnormal hair growth	Mammalian_phenotype	5
MP:0002074	MP:0002074	abnormal hair texture	Mammalian_phenotype	5
MP:0002174	MP:0002174	abnormal gastrulation movements	Mammalian_phenotype	5
MP:0002182	MP:0002182	abnormal astrocyte morphology	Mammalian_phenotype	5
MP:0002187	MP:0002187	abnormal fibula morphology	Mammalian_phenotype	5
MP:0002188	MP:0002188	small heart	Mammalian_phenotype	5
MP:0002192	MP:0002192	hydrops fetalis	Mammalian_phenotype	5
MP:0002207	MP:0002207	abnormal long term potentiation	Mammalian_phenotype	5
MP:0002209	MP:0002209	decreased germ cell number	Mammalian_phenotype	5
MP:0002213	MP:0002213	true hermaphroditism	Mammalian_phenotype	5
MP:0002220	MP:0002220	large lymphoid organs	Mammalian_phenotype	5
MP:0002224	MP:0002224	abnormal spleen size	Mammalian_phenotype	5
MP:0002227	MP:0002227	abnormal spleen capsule morphology	Mammalian_phenotype	5
MP:0002228	MP:0002228	abnormal spleen trabecular vein morphology	Mammalian_phenotype	5
MP:0002231	MP:0002231	abnormal primitive streak morphology	Mammalian_phenotype	5
MP:0002238	MP:0002238	abnormal nasal mucosa morphology	Mammalian_phenotype	5
MP:0002243	MP:0002243	abnormal vomeronasal organ morphology	Mammalian_phenotype	5
MP:0002257	MP:0002257	abnormal arytenoid cartilage morphology	Mammalian_phenotype	5
MP:0002258	MP:0002258	abnormal cricoid cartilage morphology	Mammalian_phenotype	5
MP:0002260	MP:0002260	abnormal thyroid cartilage morphology	Mammalian_phenotype	5
MP:0002264	MP:0002264	abnormal bronchus morphology	Mammalian_phenotype	5
MP:0002267	MP:0002267	abnormal bronchiole morphology	Mammalian_phenotype	5
MP:0002279	MP:0002279	abnormal diaphragm morphology	Mammalian_phenotype	5
MP:0002280	MP:0002280	abnormal intercostal muscle morphology	Mammalian_phenotype	5
MP:0002281	MP:0002281	abnormal respiratory mucosa goblet cell morphology	Mammalian_phenotype	5
MP:0002293	MP:0002293	long gestation period	Mammalian_phenotype	5
MP:0002294	MP:0002294	short gestation period	Mammalian_phenotype	5
MP:0002296	MP:0002296	aspiration	Mammalian_phenotype	5
MP:0002297	MP:0002297	abnormal forced expiratory flow rates	Mammalian_phenotype	5
MP:0002304	MP:0002304	abnormal total lung capacity	Mammalian_phenotype	5
MP:0002306	MP:0002306	abnormal functional residual capacity	Mammalian_phenotype	5
MP:0002308	MP:0002308	abnormal residual volume	Mammalian_phenotype	5
MP:0002309	MP:0002309	abnormal vital capacity	Mammalian_phenotype	5
MP:0002311	MP:0002311	abnormal inspiratory capacity	Mammalian_phenotype	5
MP:0002312	MP:0002312	abnormal inspiratory reserve volume	Mammalian_phenotype	5
MP:0002313	MP:0002313	abnormal tidal volume	Mammalian_phenotype	5
MP:0002316	MP:0002316	anoxia	Mammalian_phenotype	5
MP:0002318	MP:0002318	hypercapnia	Mammalian_phenotype	5
MP:0002319	MP:0002319	hyperoxia	Mammalian_phenotype	5
MP:0002326	MP:0002326	abnormal ventilation-perfusion ratio	Mammalian_phenotype	5
MP:0002328	MP:0002328	abnormal airway resistance	Mammalian_phenotype	5
MP:0002330	MP:0002330	abnormal bronchial provocation	Mammalian_phenotype	5
MP:0002333	MP:0002333	abnormal lung compliance	Mammalian_phenotype	5
MP:0002336	MP:0002336	abnormal pulmonary gas exchange	Mammalian_phenotype	5
MP:0002337	MP:0002337	abnormal whole-body plethysmography	Mammalian_phenotype	5
MP:0002338	MP:0002338	abnormal pulmonary ventilation	Mammalian_phenotype	5
MP:0002342	MP:0002342	abnormal lymph node trabecula morphology	Mammalian_phenotype	5
MP:0002343	MP:0002343	abnormal lymph node cortex morphology	Mammalian_phenotype	5
MP:0002348	MP:0002348	abnormal lymph node medulla morphology	Mammalian_phenotype	5
MP:0002354	MP:0002354	abnormal spleen trabecular artery morphology	Mammalian_phenotype	5
MP:0002356	MP:0002356	abnormal spleen red pulp morphology	Mammalian_phenotype	5
MP:0002357	MP:0002357	abnormal spleen white pulp morphology	Mammalian_phenotype	5
MP:0002364	MP:0002364	abnormal thymus size	Mammalian_phenotype	5
MP:0002367	MP:0002367	abnormal thymus lobule morphology	Mammalian_phenotype	5
MP:0002368	MP:0002368	abnormal thymus capsule morphology	Mammalian_phenotype	5
MP:0002370	MP:0002370	abnormal thymus trabecula morphology	Mammalian_phenotype	5
MP:0002376	MP:0002376	abnormal dendritic cell physiology	Mammalian_phenotype	5
MP:0002379	MP:0002379	abnormal oropharyngeal lymphoid tissue morphology	Mammalian_phenotype	5
MP:0002388	MP:0002388	abnormal Peyer's patch epithelium morphology	Mammalian_phenotype	5
MP:0002400	MP:0002400	abnormal multipotent stem cell morphology	Mammalian_phenotype	5
MP:0002406	MP:0002406	increased susceptibility to infection	Mammalian_phenotype	5
MP:0002409	MP:0002409	decreased susceptibility to infection	Mammalian_phenotype	5
MP:0002415	MP:0002415	abnormal neutrophil differentiation	Mammalian_phenotype	5
MP:0002417	MP:0002417	abnormal megakaryocyte morphology	Mammalian_phenotype	5
MP:0002422	MP:0002422	abnormal basophil morphology	Mammalian_phenotype	5
MP:0002427	MP:0002427	disproportionate dwarf	Mammalian_phenotype	5
MP:0002428	MP:0002428	abnormal semicircular canal morphology	Mammalian_phenotype	5
MP:0002446	MP:0002446	abnormal macrophage morphology	Mammalian_phenotype	5
MP:0002459	MP:0002459	abnormal B cell physiology	Mammalian_phenotype	5
MP:0002462	MP:0002462	abnormal granulocyte physiology	Mammalian_phenotype	5
MP:0002472	MP:0002472	impaired complement alternative pathway	Mammalian_phenotype	5
MP:0002473	MP:0002473	impaired complement classical pathway	Mammalian_phenotype	5
MP:0002500	MP:0002500	granulomatous inflammation	Mammalian_phenotype	5
MP:0002544	MP:0002544	brachydactyly	Mammalian_phenotype	5
MP:0002551	MP:0002551	abnormal blood coagulation	Mammalian_phenotype	5
MP:0002555	MP:0002555	addiction	Mammalian_phenotype	5
MP:0002560	MP:0002560	arrhythmic circadian persistence	Mammalian_phenotype	5
MP:0002562	MP:0002562	prolonged circadian period	Mammalian_phenotype	5
MP:0002563	MP:0002563	shortened circadian period	Mammalian_phenotype	5
MP:0002564	MP:0002564	advanced circadian phase	Mammalian_phenotype	5
MP:0002565	MP:0002565	delayed circadian phase	Mammalian_phenotype	5
MP:0002570	MP:0002570	alcohol aversion	Mammalian_phenotype	5
MP:0002573	MP:0002573	behavioral despair	Mammalian_phenotype	5
MP:0002575	MP:0002575	increased circulating ketone body level	Mammalian_phenotype	5
MP:0002578	MP:0002578	impaired ability to fire action potentials	Mammalian_phenotype	5
MP:0002581	MP:0002581	abnormal ileum morphology	Mammalian_phenotype	5
MP:0002583	MP:0002583	absent extraembryonic ectoderm	Mammalian_phenotype	5
MP:0002623	MP:0002623	abnormal vestibular hair cell morphology	Mammalian_phenotype	5
MP:0002626	MP:0002626	increased heart rate	Mammalian_phenotype	5
MP:0002630	MP:0002630	abnormal endocochlear potential	Mammalian_phenotype	5
MP:0002651	MP:0002651	abnormal sciatic nerve morphology	Mammalian_phenotype	5
MP:0002668	MP:0002668	abnormal circulating potassium level	Mammalian_phenotype	5
MP:0002672	MP:0002672	abnormal branchial arch artery morphology	Mammalian_phenotype	5
MP:0002674	MP:0002674	abnormal sperm motility	Mammalian_phenotype	5
MP:0002687	MP:0002687	oligozoospermia	Mammalian_phenotype	5
MP:0002700	MP:0002700	opacity of vitreous body	Mammalian_phenotype	5
MP:0002703	MP:0002703	abnormal renal tubule morphology	Mammalian_phenotype	5
MP:0002707	MP:0002707	abnormal kidney weight	Mammalian_phenotype	5
MP:0002713	MP:0002713	abnormal glycogen catabolism	Mammalian_phenotype	5
MP:0002718	MP:0002718	abnormal inner cell mass morphology	Mammalian_phenotype	5
MP:0002726	MP:0002726	abnormal pulmonary vein morphology	Mammalian_phenotype	5
MP:0002730	MP:0002730	head shaking	Mammalian_phenotype	5
MP:0002733	MP:0002733	abnormal thermal nociception	Mammalian_phenotype	5
MP:0002734	MP:0002734	abnormal mechanical nociception	Mammalian_phenotype	5
MP:0002735	MP:0002735	abnormal chemical nociception	Mammalian_phenotype	5
MP:0002736	MP:0002736	abnormal nociception after inflammation	Mammalian_phenotype	5
MP:0002739	MP:0002739	abnormal olfactory bulb development	Mammalian_phenotype	5
MP:0002745	MP:0002745	abnormal atrioventricular valve morphology	Mammalian_phenotype	5
MP:0002746	MP:0002746	abnormal semilunar valve morphology	Mammalian_phenotype	5
MP:0002762	MP:0002762	ectopic cerebellar granule cells	Mammalian_phenotype	5
MP:0002763	MP:0002763	ectopic Bergmann glia cells	Mammalian_phenotype	5
MP:0002778	MP:0002778	meroanencephaly	Mammalian_phenotype	5
MP:0002782	MP:0002782	abnormal testes secretion	Mammalian_phenotype	5
MP:0002783	MP:0002783	abnormal ovarian secretion	Mammalian_phenotype	5
MP:0002787	MP:0002787	pseudohermaphroditism	Mammalian_phenotype	5
MP:0002800	MP:0002800	abnormal short term object recognition memory	Mammalian_phenotype	5
MP:0002801	MP:0002801	abnormal long term object recognition memory	Mammalian_phenotype	5
MP:0002803	MP:0002803	abnormal operant conditioning behavior	Mammalian_phenotype	5
MP:0002806	MP:0002806	abnormal conditioned emotional response	Mammalian_phenotype	5
MP:0002807	MP:0002807	abnormal eye blink conditioning behavior	Mammalian_phenotype	5
MP:0002826	MP:0002826	tonic seizures	Mammalian_phenotype	5
MP:0002827	MP:0002827	abnormal renal corpuscle morphology	Mammalian_phenotype	5
MP:0002829	MP:0002829	abnormal juxtaglomerular apparatus morphology	Mammalian_phenotype	5
MP:0002838	MP:0002838	decreased susceptibility to dystrophic cardiac calcinosis	Mammalian_phenotype	5
MP:0002839	MP:0002839	increased susceptibility to dystrophic cardiac calcinosis	Mammalian_phenotype	5
MP:0002840	MP:0002840	abnormal lens fiber morphology	Mammalian_phenotype	5
MP:0002841	MP:0002841	impaired skeletal muscle contractility	Mammalian_phenotype	5
MP:0002855	MP:0002855	abnormal cochlear ganglion morphology	Mammalian_phenotype	5
MP:0002856	MP:0002856	abnormal vestibular ganglion morphology	Mammalian_phenotype	5
MP:0002859	MP:0002859	abnormal inner ear canal fusion	Mammalian_phenotype	5
MP:0002862	MP:0002862	altered righting response	Mammalian_phenotype	5
MP:0002867	MP:0002867	increased glutamic acid decarboxylase level	Mammalian_phenotype	5
MP:0002868	MP:0002868	decreased glutamic acid decarboxylase level	Mammalian_phenotype	5
MP:0002880	MP:0002880	opisthotonus	Mammalian_phenotype	5
MP:0002886	MP:0002886	abnormal glutamate-mediated receptor currents	Mammalian_phenotype	5
MP:0002893	MP:0002893	ketoaciduria	Mammalian_phenotype	5
MP:0002901	MP:0002901	increased urine phosphate level	Mammalian_phenotype	5
MP:0002902	MP:0002902	decreased urine phosphate level	Mammalian_phenotype	5
MP:0002903	MP:0002903	abnormal circulating parathyroid hormone level	Mammalian_phenotype	5
MP:0002907	MP:0002907	abnormal parturition	Mammalian_phenotype	5
MP:0002910	MP:0002910	abnormal excitatory postsynaptic currents	Mammalian_phenotype	5
MP:0002911	MP:0002911	abnormal inhibitory postsynaptic potential	Mammalian_phenotype	5
MP:0002912	MP:0002912	abnormal excitatory postsynaptic potential	Mammalian_phenotype	5
MP:0002914	MP:0002914	abnormal endplate potential	Mammalian_phenotype	5
MP:0002915	MP:0002915	abnormal synaptic depression	Mammalian_phenotype	5
MP:0002919	MP:0002919	enhanced paired-pulse facilitation	Mammalian_phenotype	5
MP:0002920	MP:0002920	decreased paired-pulse facilitation	Mammalian_phenotype	5
MP:0002921	MP:0002921	abnormal post-tetanic potentiation	Mammalian_phenotype	5
MP:0002924	MP:0002924	delayed CNS synapse formation	Mammalian_phenotype	5
MP:0002944	MP:0002944	increased lactate dehydrogenase level	Mammalian_phenotype	5
MP:0002945	MP:0002945	abnormal inhibitory postsynaptic currents	Mammalian_phenotype	5
MP:0002955	MP:0002955	increased compensatory renal growth	Mammalian_phenotype	5
MP:0002956	MP:0002956	decreased compensatory renal growth	Mammalian_phenotype	5
MP:0002961	MP:0002961	abnormal axon guidance	Mammalian_phenotype	5
MP:0002962	MP:0002962	increased urine protein level	Mammalian_phenotype	5
MP:0002963	MP:0002963	decreased urine protein level	Mammalian_phenotype	5
MP:0002975	MP:0002975	vascular smooth muscle hypertrophy	Mammalian_phenotype	5
MP:0002976	MP:0002976	vascular smooth muscle hypotrophy	Mammalian_phenotype	5
MP:0002986	MP:0002986	decreased urine calcium level	Mammalian_phenotype	5
MP:0002988	MP:0002988	decreased urine osmolality	Mammalian_phenotype	5
MP:0002989	MP:0002989	small kidney	Mammalian_phenotype	5
MP:0002995	MP:0002995	primary sex reversal	Mammalian_phenotype	5
MP:0003007	MP:0003007	ectopic thymus	Mammalian_phenotype	5
MP:0003010	MP:0003010	decreased mortality induced by ionizing radiation	Mammalian_phenotype	5
MP:0003016	MP:0003016	increased circulating bicarbonate level	Mammalian_phenotype	5
MP:0003017	MP:0003017	decreased circulating bicarbonate level	Mammalian_phenotype	5
MP:0003018	MP:0003018	abnormal circulating chloride level	Mammalian_phenotype	5
MP:0003021	MP:0003021	abnormal coronary flow rate	Mammalian_phenotype	5
MP:0003029	MP:0003029	alkalemia	Mammalian_phenotype	5
MP:0003030	MP:0003030	acidemia	Mammalian_phenotype	5
MP:0003032	MP:0003032	hypocapnia	Mammalian_phenotype	5
MP:0003033	MP:0003033	abnormal pulmonary vascular resistance	Mammalian_phenotype	5
MP:0003047	MP:0003047	abnormal thoracic vertebrae morphology	Mammalian_phenotype	5
MP:0003057	MP:0003057	abnormal epicardium morphology	Mammalian_phenotype	5
MP:0003062	MP:0003062	abnormal coping response	Mammalian_phenotype	5
MP:0003068	MP:0003068	enlarged kidney	Mammalian_phenotype	5
MP:0003070	MP:0003070	increased vascular permeability	Mammalian_phenotype	5
MP:0003071	MP:0003071	decreased vascular permeability	Mammalian_phenotype	5
MP:0003072	MP:0003072	abnormal metatarsal bone morphology	Mammalian_phenotype	5
MP:0003073	MP:0003073	abnormal metacarpal bone morphology	Mammalian_phenotype	5
MP:0003078	MP:0003078	aphakia	Mammalian_phenotype	5
MP:0003081	MP:0003081	abnormal soleus morphology	Mammalian_phenotype	5
MP:0003082	MP:0003082	abnormal gastrocnemius morphology	Mammalian_phenotype	5
MP:0003083	MP:0003083	abnormal tibialis anterior morphology	Mammalian_phenotype	5
MP:0003087	MP:0003087	absent allantois	Mammalian_phenotype	5
MP:0003088	MP:0003088	abnormal prepulse inhibition	Mammalian_phenotype	5
MP:0003101	MP:0003101	high myopia	Mammalian_phenotype	5
MP:0003106	MP:0003106	abnormal fear-related response	Mammalian_phenotype	5
MP:0003116	MP:0003116	rickets	Mammalian_phenotype	5
MP:0003124	MP:0003124	hypospadia	Mammalian_phenotype	5
MP:0003125	MP:0003125	abnormal septation of the cloaca	Mammalian_phenotype	5
MP:0003126	MP:0003126	abnormal external female genitalia morphology	Mammalian_phenotype	5
MP:0003130	MP:0003130	anal atresia	Mammalian_phenotype	5
MP:0003138	MP:0003138	absent tympanic ring	Mammalian_phenotype	5
MP:0003140	MP:0003140	dilated heart atrium	Mammalian_phenotype	5
MP:0003147	MP:0003147	absent cochlea	Mammalian_phenotype	5
MP:0003148	MP:0003148	decreased cochlear coiling	Mammalian_phenotype	5
MP:0003153	MP:0003153	early eyelid opening	Mammalian_phenotype	5
MP:0003167	MP:0003167	abnormal scala tympani morphology	Mammalian_phenotype	5
MP:0003168	MP:0003168	abnormal scala vestibuli morphology	Mammalian_phenotype	5
MP:0003169	MP:0003169	abnormal scala media morphology	Mammalian_phenotype	5
MP:0003180	MP:0003180	abnormal pulmonary endothelial cell surface	Mammalian_phenotype	5
MP:0003190	MP:0003190	fused synovial joints	Mammalian_phenotype	5
MP:0003201	MP:0003201	extremity edema	Mammalian_phenotype	5
MP:0003208	MP:0003208	abnormal neuromere morphology	Mammalian_phenotype	5
MP:0003215	MP:0003215	renal interstitial fibrosis	Mammalian_phenotype	5
MP:0003216	MP:0003216	absence seizures	Mammalian_phenotype	5
MP:0003225	MP:0003225	axonal dystrophy	Mammalian_phenotype	5
MP:0003228	MP:0003228	abnormal sinus venosus morphology	Mammalian_phenotype	5
MP:0003232	MP:0003232	abnormal forebrain development	Mammalian_phenotype	5
MP:0003236	MP:0003236	abnormal lens capsule morphology	Mammalian_phenotype	5
MP:0003237	MP:0003237	abnormal lens epithelium morphology	Mammalian_phenotype	5
MP:0003244	MP:0003244	loss of dopaminergic neurons	Mammalian_phenotype	5
MP:0003246	MP:0003246	loss of GABAergic neurons	Mammalian_phenotype	5
MP:0003248	MP:0003248	loss of glutamate neurons	Mammalian_phenotype	5
MP:0003250	MP:0003250	absent gallbladder	Mammalian_phenotype	5
MP:0003253	MP:0003253	dilated bile duct	Mammalian_phenotype	5
MP:0003261	MP:0003261	hematemesis	Mammalian_phenotype	5
MP:0003266	MP:0003266	biliary cyst	Mammalian_phenotype	5
MP:0003268	MP:0003268	chronic constipation	Mammalian_phenotype	5
MP:0003269	MP:0003269	colon polyps	Mammalian_phenotype	5
MP:0003271	MP:0003271	abnormal duodenum morphology	Mammalian_phenotype	5
MP:0003273	MP:0003273	duodenal ulcer	Mammalian_phenotype	5
MP:0003282	MP:0003282	gastric ulcer	Mammalian_phenotype	5
MP:0003285	MP:0003285	gastric hypertrophy	Mammalian_phenotype	5
MP:0003290	MP:0003290	intestinal hypoperistalsis	Mammalian_phenotype	5
MP:0003291	MP:0003291	interstinal hyperperistalsis	Mammalian_phenotype	5
MP:0003307	MP:0003307	pyloric stenosis	Mammalian_phenotype	5
MP:0003308	MP:0003308	abnormal cochlear sensory epithelium morphology	Mammalian_phenotype	5
MP:0003309	MP:0003309	abnormal modiolus morphology	Mammalian_phenotype	5
MP:0003311	MP:0003311	aminoaciduria	Mammalian_phenotype	5
MP:0003314	MP:0003314	dysmetria	Mammalian_phenotype	5
MP:0003317	MP:0003317	anoperineal fistula	Mammalian_phenotype	5
MP:0003318	MP:0003318	rectoperineal fistula	Mammalian_phenotype	5
MP:0003319	MP:0003319	anal fistula	Mammalian_phenotype	5
MP:0003335	MP:0003335	exocrine pancreatic insufficiency	Mammalian_phenotype	5
MP:0003337	MP:0003337	exocrine pancreas hyperplasia	Mammalian_phenotype	5
MP:0003342	MP:0003342	accessory spleen	Mammalian_phenotype	5
MP:0003346	MP:0003346	abnormal pectoral muscle morphology	Mammalian_phenotype	5
MP:0003347	MP:0003347	hyperpituitarism	Mammalian_phenotype	5
MP:0003348	MP:0003348	hypopituitarism	Mammalian_phenotype	5
MP:0003350	MP:0003350	increased circulating levels of thyroid hormone	Mammalian_phenotype	5
MP:0003351	MP:0003351	decreased circulating levels of thyroid hormone	Mammalian_phenotype	5
MP:0003354	MP:0003354	astrocytosis	Mammalian_phenotype	5
MP:0003355	MP:0003355	decreased ovulation rate	Mammalian_phenotype	5
MP:0003361	MP:0003361	abnormal circulating gonadotropin level	Mammalian_phenotype	5
MP:0003366	MP:0003366	abnormal circulating glucocorticoid level	Mammalian_phenotype	5
MP:0003369	MP:0003369	abnormal circulating estrogen level	Mammalian_phenotype	5
MP:0003372	MP:0003372	abnormal circulating mineralocorticoid level	Mammalian_phenotype	5
MP:0003375	MP:0003375	abnormal menstrual cycle	Mammalian_phenotype	5
MP:0003381	MP:0003381	vitreal fibroplasia	Mammalian_phenotype	5
MP:0003388	MP:0003388	absent pericardium	Mammalian_phenotype	5
MP:0003389	MP:0003389	constriction of pericardium	Mammalian_phenotype	5
MP:0003390	MP:0003390	lymphedema	Mammalian_phenotype	5
MP:0003393	MP:0003393	decreased cardiac output	Mammalian_phenotype	5
MP:0003394	MP:0003394	increased cardiac output	Mammalian_phenotype	5
MP:0003400	MP:0003400	kinked neural tube	Mammalian_phenotype	5
MP:0003401	MP:0003401	enlarged tail bud	Mammalian_phenotype	5
MP:0003410	MP:0003410	abnormal artery development	Mammalian_phenotype	5
MP:0003411	MP:0003411	abnormal vein development	Mammalian_phenotype	5
MP:0003415	MP:0003415	priapism	Mammalian_phenotype	5
MP:0003417	MP:0003417	premature endochondral bone ossification	Mammalian_phenotype	5
MP:0003418	MP:0003418	premature intramembranous bone ossification	Mammalian_phenotype	5
MP:0003419	MP:0003419	delayed endochondral bone ossification	Mammalian_phenotype	5
MP:0003420	MP:0003420	delayed intramembranous bone ossification	Mammalian_phenotype	5
MP:0003424	MP:0003424	premature neuronal precursor differentiation	Mammalian_phenotype	5
MP:0003426	MP:0003426	pulmonary interstitial fibrosis	Mammalian_phenotype	5
MP:0003439	MP:0003439	abnormal glycerol level	Mammalian_phenotype	5
MP:0003444	MP:0003444	abnormal neurotransmitter uptake	Mammalian_phenotype	5
MP:0003450	MP:0003450	enlarged pancreas	Mammalian_phenotype	5
MP:0003452	MP:0003452	abnormal parotid gland morphology	Mammalian_phenotype	5
MP:0003458	MP:0003458	decreased circulating ketone body level	Mammalian_phenotype	5
MP:0003461	MP:0003461	abnormal response to novel object	Mammalian_phenotype	5
MP:0003462	MP:0003462	abnormal response to novel odor	Mammalian_phenotype	5
MP:0003464	MP:0003464	abnormal single cell response threshold	Mammalian_phenotype	5
MP:0003467	MP:0003467	abnormal single cell response intensity	Mammalian_phenotype	5
MP:0003471	MP:0003471	abnormal summary potential threshold	Mammalian_phenotype	5
MP:0003474	MP:0003474	abnormal summary potential intensity	Mammalian_phenotype	5
MP:0003478	MP:0003478	abnormal nerve fiber response threshold	Mammalian_phenotype	5
MP:0003479	MP:0003479	abnormal nerve fiber response intensity	Mammalian_phenotype	5
MP:0003485	MP:0003485	abnormal channel response threshold	Mammalian_phenotype	5
MP:0003486	MP:0003486	abnormal channel response intensity	Mammalian_phenotype	5
MP:0003493	MP:0003493	parathyroid gland hyperplasia	Mammalian_phenotype	5
MP:0003494	MP:0003494	parathyroid hypoplasia	Mammalian_phenotype	5
MP:0003498	MP:0003498	thyroid gland hyperplasia	Mammalian_phenotype	5
MP:0003499	MP:0003499	thyroid hypoplasia	Mammalian_phenotype	5
MP:0003506	MP:0003506	acromegaly	Mammalian_phenotype	5
MP:0003542	MP:0003542	abnormal vascular endothelial cell development	Mammalian_phenotype	5
MP:0003548	MP:0003548	pulmonary hypertension	Mammalian_phenotype	5
MP:0003549	MP:0003549	pulmonary hypotension	Mammalian_phenotype	5
MP:0003550	MP:0003550	short perineum	Mammalian_phenotype	5
MP:0003562	MP:0003562	abnormal pancreatic beta cell physiology	Mammalian_phenotype	5
MP:0003563	MP:0003563	abnormal pancreatic alpha cell physiology	Mammalian_phenotype	5
MP:0003598	MP:0003598	epispadia	Mammalian_phenotype	5
MP:0003608	MP:0003608	prostate gland inflammation	Mammalian_phenotype	5
MP:0003613	MP:0003613	abnormal kidney medulla development	Mammalian_phenotype	5
MP:0003625	MP:0003625	kidney medulla hyperplasia	Mammalian_phenotype	5
MP:0003626	MP:0003626	kidney medulla hypoplasia	Mammalian_phenotype	5
MP:0003641	MP:0003641	small lung	Mammalian_phenotype	5
MP:0003648	MP:0003648	abnormal radial glial cell morphology	Mammalian_phenotype	5
MP:0003651	MP:0003651	abnormal axon extension	Mammalian_phenotype	5
MP:0003653	MP:0003653	decreased skin turgor	Mammalian_phenotype	5
MP:0003660	MP:0003660	chylothorax	Mammalian_phenotype	5
MP:0003662	MP:0003662	abnormal long bone epiphyseal plate proliferative zone	Mammalian_phenotype	5
MP:0003664	MP:0003664	ocular pterygium	Mammalian_phenotype	5
MP:0003666	MP:0003666	impaired sperm capacitation	Mammalian_phenotype	5
MP:0003677	MP:0003677	abnormal ear lobe morphology	Mammalian_phenotype	5
MP:0003694	MP:0003694	failure of blastocyst to hatch from the zona pellucida	Mammalian_phenotype	5
MP:0003695	MP:0003695	delayed blastocyst hatching from the zona pellucida	Mammalian_phenotype	5
MP:0003700	MP:0003700	abnormal oviduct transport	Mammalian_phenotype	5
MP:0003701	MP:0003701	elevated level of mitotic sister chromatid exchange	Mammalian_phenotype	5
MP:0003707	MP:0003707	increased cell nucleus count	Mammalian_phenotype	5
MP:0003709	MP:0003709	anucleate	Mammalian_phenotype	5
MP:0003720	MP:0003720	abnormal neural tube closure	Mammalian_phenotype	5
MP:0003737	MP:0003737	ossification of pinnae	Mammalian_phenotype	5
MP:0003742	MP:0003742	narrow head	Mammalian_phenotype	5
MP:0003744	MP:0003744	abnormal orofacial morphology	Mammalian_phenotype	5
MP:0003777	MP:0003777	lip inflammation	Mammalian_phenotype	5
MP:0003793	MP:0003793	abnormal submandibular gland morphology	Mammalian_phenotype	5
MP:0003794	MP:0003794	delayed somite formation	Mammalian_phenotype	5
MP:0003800	MP:0003800	monodactyly	Mammalian_phenotype	5
MP:0003807	MP:0003807	camptodactyly	Mammalian_phenotype	5
MP:0003810	MP:0003810	abnormal hair cuticle	Mammalian_phenotype	5
MP:0003811	MP:0003811	abnormal hair cortex morphology	Mammalian_phenotype	5
MP:0003812	MP:0003812	abnormal hair medulla	Mammalian_phenotype	5
MP:0003813	MP:0003813	abnormal hair follicle dermal papilla morphology	Mammalian_phenotype	5
MP:0003814	MP:0003814	vascular smooth muscle cell hypoplasia	Mammalian_phenotype	5
MP:0003819	MP:0003819	increased left ventricle diastolic pressure	Mammalian_phenotype	5
MP:0003820	MP:0003820	increased left ventricle systolic pressure	Mammalian_phenotype	5
MP:0003821	MP:0003821	decreased left ventricle diastolic pressure	Mammalian_phenotype	5
MP:0003822	MP:0003822	decreased left ventricle systolic pressure	Mammalian_phenotype	5
MP:0003823	MP:0003823	increased left ventricle developed pressure	Mammalian_phenotype	5
MP:0003824	MP:0003824	decreased left ventricle developed pressure	Mammalian_phenotype	5
MP:0003826	MP:0003826	abnormal Mullerian duct morphology	Mammalian_phenotype	5
MP:0003827	MP:0003827	abnormal Wolffian duct morphology	Mammalian_phenotype	5
MP:0003838	MP:0003838	abnormal milk ejection	Mammalian_phenotype	5
MP:0003847	MP:0003847	disorganized lens bow	Mammalian_phenotype	5
MP:0003849	MP:0003849	greasy coat	Mammalian_phenotype	5
MP:0003850	MP:0003850	abnormal thymocyte activation	Mammalian_phenotype	5
MP:0003851	MP:0003851	skeletal muscle interstitial fibrosis	Mammalian_phenotype	5
MP:0003858	MP:0003858	enhanced coordination	Mammalian_phenotype	5
MP:0003864	MP:0003864	abnormal midbrain development	Mammalian_phenotype	5
MP:0003867	MP:0003867	increased defecation amount	Mammalian_phenotype	5
MP:0003870	MP:0003870	decreased urine glucose level	Mammalian_phenotype	5
MP:0003874	MP:0003874	absent branchial arches	Mammalian_phenotype	5
MP:0003886	MP:0003886	abnormal embryonic epiblast morphology	Mammalian_phenotype	5
MP:0003887	MP:0003887	increased hepatocyte apoptosis	Mammalian_phenotype	5
MP:0003891	MP:0003891	increased allantois apoptosis	Mammalian_phenotype	5
MP:0003893	MP:0003893	increased hepatocyte proliferation	Mammalian_phenotype	5
MP:0003897	MP:0003897	abnormal ST segment	Mammalian_phenotype	5
MP:0003898	MP:0003898	abnormal QRS complex	Mammalian_phenotype	5
MP:0003899	MP:0003899	abnormal QT interval	Mammalian_phenotype	5
MP:0003901	MP:0003901	abnormal PR interval	Mammalian_phenotype	5
MP:0003908	MP:0003908	decreased stereotypic behavior	Mammalian_phenotype	5
MP:0003920	MP:0003920	abnormal heart right ventricle morphology	Mammalian_phenotype	5
MP:0003921	MP:0003921	abnormal heart left ventricle morphology	Mammalian_phenotype	5
MP:0003922	MP:0003922	abnormal heart right atrium morphology	Mammalian_phenotype	5
MP:0003923	MP:0003923	abnormal heart left atrium morphology	Mammalian_phenotype	5
MP:0012082	MP:0012082	delayed heart development	Mammalian_phenotype	5
MP:0012083	MP:0012083	absent foregut	Mammalian_phenotype	5
MP:0012084	MP:0012084	truncated foregut	Mammalian_phenotype	5
MP:0012085	MP:0012085	midface hypoplasia	Mammalian_phenotype	5
MP:0012086	MP:0012086	absent hindgut	Mammalian_phenotype	5
MP:0012088	MP:0012088	abnormal midbrain size	Mammalian_phenotype	5
MP:0012093	MP:0012093	absent nodal flow	Mammalian_phenotype	5
MP:0012104	MP:0012104	small amniotic cavity	Mammalian_phenotype	5
MP:0012105	MP:0012105	delayed gastrulation	Mammalian_phenotype	5
MP:0012112	MP:0012112	increased inner cell mass proliferation	Mammalian_phenotype	5
MP:0012113	MP:0012113	decreased inner cell mass proliferation	Mammalian_phenotype	5
MP:0012114	MP:0012114	absent inner cell mass proliferation	Mammalian_phenotype	5
MP:0012116	MP:0012116	increased trophectoderm cell proliferation	Mammalian_phenotype	5
MP:0012117	MP:0012117	decreased trophectoderm cell proliferation	Mammalian_phenotype	5
MP:0012118	MP:0012118	absent trophectoderm cell proliferation	Mammalian_phenotype	5
MP:0012126	MP:0012126	abnormal placenta hemotrichorial membrane morphology	Mammalian_phenotype	5
MP:0012128	MP:0012128	abnormal blastocyst formation	Mammalian_phenotype	5
MP:0012130	MP:0012130	abnormal morula formation	Mammalian_phenotype	5
MP:0012131	MP:0012131	small visceral yolk sac	Mammalian_phenotype	5
MP:0012132	MP:0012132	abnormal midbrain-hindbrain boundary morphology	Mammalian_phenotype	5
MP:0012134	MP:0012134	absent umbilical cord	Mammalian_phenotype	5
MP:0012136	MP:0012136	absent forebrain	Mammalian_phenotype	5
MP:0012137	MP:0012137	abnormal forebrain size	Mammalian_phenotype	5
MP:0012141	MP:0012141	absent hindbrain	Mammalian_phenotype	5
MP:0012142	MP:0012142	absent amniotic cavity	Mammalian_phenotype	5
MP:0012156	MP:0012156	rostral-caudal axis duplication	Mammalian_phenotype	5
MP:0012157	MP:0012157	rostral body truncation	Mammalian_phenotype	5
MP:0012159	MP:0012159	absent anterior visceral endoderm	Mammalian_phenotype	5
MP:0012160	MP:0012160	expanded anterior visceral endoderm	Mammalian_phenotype	5
MP:0012161	MP:0012161	absent distal visceral endoderm	Mammalian_phenotype	5
MP:0012165	MP:0012165	absent neural folds	Mammalian_phenotype	5
MP:0012166	MP:0012166	absent neural plate	Mammalian_phenotype	5
MP:0012173	MP:0012173	short rostral-caudal axis	Mammalian_phenotype	5
MP:0012174	MP:0012174	flat head	Mammalian_phenotype	5
MP:0012175	MP:0012175	flat face	Mammalian_phenotype	5
MP:0012177	MP:0012177	delayed head development	Mammalian_phenotype	5
MP:0012178	MP:0012178	absent frontonasal prominence	Mammalian_phenotype	5
MP:0012181	MP:0012181	increased somite number	Mammalian_phenotype	5
MP:0012185	MP:0012185	abnormal muscle precursor cell morphology	Mammalian_phenotype	5
MP:0012193	MP:0012193	increased keratinocyte migration	Mammalian_phenotype	5
MP:0012194	MP:0012194	decreased keratinocyte migration	Mammalian_phenotype	5
MP:0012197	MP:0012197	impaired myofibroblast differentiation	Mammalian_phenotype	5
MP:0012198	MP:0012198	absent interphalangeal joint	Mammalian_phenotype	5
MP:0012200	MP:0012200	increased endothelial cell proliferation	Mammalian_phenotype	5
MP:0012201	MP:0012201	decreased endothelial cell proliferation	Mammalian_phenotype	5
MP:0012206	MP:0012206	increased neuronal stem cell self-renewal	Mammalian_phenotype	5
MP:0012207	MP:0012207	decreased neuronal stem cell self-renewal	Mammalian_phenotype	5
MP:0012209	MP:0012209	decreased hypoxanthine-guanine phosphoribosyltransferase level	Mammalian_phenotype	5
MP:0012210	MP:0012210	increased hypoxanthine-guanine phosphoribosyltransferase level	Mammalian_phenotype	5
MP:0012222	MP:0012222	decreased prothrombin level	Mammalian_phenotype	5
MP:0012223	MP:0012223	increased prothrombin level	Mammalian_phenotype	5
MP:0012224	MP:0012224	abnormal sterol level	Mammalian_phenotype	5
MP:0012230	MP:0012230	abnormal sphingolipid level	Mammalian_phenotype	5
MP:0012235	MP:0012235	abnormal liver bud morphology	Mammalian_phenotype	5
MP:0012236	MP:0012236	abnormal cholangiocyte morphology	Mammalian_phenotype	5
MP:0012242	MP:0012242	abnormal hepatoblast differentiation	Mammalian_phenotype	5
MP:0012243	MP:0012243	decreased hepatoblast number	Mammalian_phenotype	5
MP:0012247	MP:0012247	absent cornea	Mammalian_phenotype	5
MP:0012248	MP:0012248	absent dermatome	Mammalian_phenotype	5
MP:0012249	MP:0012249	absent myotome	Mammalian_phenotype	5
MP:0012250	MP:0012250	absent heart valves	Mammalian_phenotype	5
MP:0012254	MP:0012254	absent intersomitic vessels	Mammalian_phenotype	5
MP:0012255	MP:0012255	abnormal intersomitic vein morphology	Mammalian_phenotype	5
MP:0012262	MP:0012262	abnormal hindbrain size	Mammalian_phenotype	5
MP:0012270	MP:0012270	cardiac edema	Mammalian_phenotype	5
MP:0012277	MP:0012277	increased tail bud apoptosis	Mammalian_phenotype	5
MP:0012288	MP:0012288	abnormal paradoxical sleep pattern	Mammalian_phenotype	5
MP:0012289	MP:0012289	abnormal non-rapid eye movement sleep pattern	Mammalian_phenotype	5
MP:0012295	MP:0012295	enhanced discrimination learning	Mammalian_phenotype	5
MP:0012296	MP:0012296	impaired discrimination learning	Mammalian_phenotype	5
MP:0012300	MP:0012300	abnormal umbilical cord blood vessel morphology	Mammalian_phenotype	5
MP:0012304	MP:0012304	short umbilical cord	Mammalian_phenotype	5
MP:0012305	MP:0012305	umbilical cord hemorrhage	Mammalian_phenotype	5
MP:0012306	MP:0012306	enhanced spatial learning	Mammalian_phenotype	5
MP:0012307	MP:0012307	impaired spatial learning	Mammalian_phenotype	5
MP:0012311	MP:0012311	decreased defecation amount	Mammalian_phenotype	5
MP:0012312	MP:0012312	impaired avoidance learning behavior	Mammalian_phenotype	5
MP:0012313	MP:0012313	enhanced avoidance learning behavior	Mammalian_phenotype	5
MP:0012324	MP:0012324	abnormal circulating antithrombin level	Mammalian_phenotype	5
MP:0012327	MP:0012327	abnormal circulating factor VIII level	Mammalian_phenotype	5
MP:0012341	MP:0012341	low preference for an addictive substance	Mammalian_phenotype	5
MP:0012342	MP:0012342	high preference for an addictive substance	Mammalian_phenotype	5
MP:0012343	MP:0012343	increased gnawing activity	Mammalian_phenotype	5
MP:0012344	MP:0012344	decreased gnawing activity	Mammalian_phenotype	5
MP:0012348	MP:0012348	decreased susceptibility to induction of seizure by inducing agent	Mammalian_phenotype	5
MP:0012349	MP:0012349	increased susceptibility to induction of seizure by inducing agent	Mammalian_phenotype	5
MP:0012350	MP:0012350	increased aggression towards males in competition for females	Mammalian_phenotype	5
MP:0012351	MP:0012351	cornea degeneration	Mammalian_phenotype	5
MP:0012361	MP:0012361	decreased large unstained cell number	Mammalian_phenotype	5
MP:0012362	MP:0012362	increased large unstained cell number	Mammalian_phenotype	5
MP:0012455	MP:0012455	increased mammillothalamic tract size	Mammalian_phenotype	5
MP:0012456	MP:0012456	dereased mammillothalamic tract size	Mammalian_phenotype	5
MP:0012483	MP:0012483	increased corticospinal tract size	Mammalian_phenotype	5
MP:0012484	MP:0012484	decreased corticospinal tract size	Mammalian_phenotype	5
MP:0012490	MP:0012490	abnormal cochlear VIII nucleus morphology	Mammalian_phenotype	5
MP:0012497	MP:0012497	absent pleuropericardial membrane	Mammalian_phenotype	5
MP:0012499	MP:0012499	absent cardiogenic plate	Mammalian_phenotype	5
MP:0012507	MP:0012507	midbrain atrophy	Mammalian_phenotype	5
MP:0012508	MP:0012508	forebrain atrophy	Mammalian_phenotype	5
MP:0012509	MP:0012509	neural tube degeneration	Mammalian_phenotype	5
MP:0012511	MP:0012511	dilated aortic sac	Mammalian_phenotype	5
MP:0012525	MP:0012525	abnormal rhombic lip morphology	Mammalian_phenotype	5
MP:0012528	MP:0012528	abnormal zone of polarizing activity morphology	Mammalian_phenotype	5
MP:0012536	MP:0012536	delayed optic fissure closure	Mammalian_phenotype	5
MP:0012540	MP:0012540	abnormal lamina terminalis morphology	Mammalian_phenotype	5
MP:0012542	MP:0012542	abnormal neuropore morphology	Mammalian_phenotype	5
MP:0012546	MP:0012546	triangular face	Mammalian_phenotype	5
MP:0012549	MP:0012549	hypoxemia	Mammalian_phenotype	5
MP:0012551	MP:0012551	metabolic acidosis	Mammalian_phenotype	5
MP:0012553	MP:0012553	decreased serum complement activity	Mammalian_phenotype	5
MP:0012554	MP:0012554	increased serum complement activity	Mammalian_phenotype	5
MP:0012561	MP:0012561	decreased foot pad temperature	Mammalian_phenotype	5
MP:0012565	MP:0012565	perivasculitis	Mammalian_phenotype	5
MP:0012574	MP:0012574	decreased noradrenaline level	Mammalian_phenotype	5
MP:0012575	MP:0012575	increased noradrenaline level	Mammalian_phenotype	5
MP:0012580	MP:0012580	decreased peroxidase activity	Mammalian_phenotype	5
MP:0012582	MP:0012582	increased peroxidase activity	Mammalian_phenotype	5
MP:0012585	MP:0012585	decreased catechol O-methyltransferase activity	Mammalian_phenotype	5
MP:0012586	MP:0012586	increased catechol O-methyltransferase activity	Mammalian_phenotype	5
MP:0012590	MP:0012590	decreased choline acetyltransferase activity	Mammalian_phenotype	5
MP:0012591	MP:0012591	increased choline acetyltransferase activity	Mammalian_phenotype	5
MP:0012595	MP:0012595	decreased glutamate decarboxylase activity	Mammalian_phenotype	5
MP:0012596	MP:0012596	increased glutamate decarboxylase activity	Mammalian_phenotype	5
MP:0012598	MP:0012598	decreased nicotinamide N-methyltransferase activity	Mammalian_phenotype	5
MP:0012599	MP:0012599	increased nicotinamide N-methyltransferase activity	Mammalian_phenotype	5
MP:0012601	MP:0012601	decreased alpha-fetoprotein level	Mammalian_phenotype	5
MP:0012602	MP:0012602	increased alpha-fetoprotein level	Mammalian_phenotype	5
MP:0012604	MP:0012604	decreased glutathione level	Mammalian_phenotype	5
MP:0012606	MP:0012606	increased glutathione level	Mammalian_phenotype	5
MP:0012612	MP:0012612	decreased ceruloplasmin level	Mammalian_phenotype	5
MP:0012613	MP:0012613	increased ceruloplasmin level	Mammalian_phenotype	5
MP:0012624	MP:0012624	decreased acetylcholinesterase activity	Mammalian_phenotype	5
MP:0012625	MP:0012625	increased acetylcholinesterase activity	Mammalian_phenotype	5
MP:0012629	MP:0012629	decreased glutathione reductase level	Mammalian_phenotype	5
MP:0012630	MP:0012630	increased glutathione reductase level	Mammalian_phenotype	5
MP:0012633	MP:0012633	increased phospholipase A2 level	Mammalian_phenotype	5
MP:0012634	MP:0012634	decreased phospholipase A2 level	Mammalian_phenotype	5
MP:0012636	MP:0012636	decreased monoamine oxidase activity	Mammalian_phenotype	5
MP:0012637	MP:0012637	increased monoamine oxidase activity	Mammalian_phenotype	5
MP:0012641	MP:0012641	decreased benz (alpha) pyrene hydroxylase activity	Mammalian_phenotype	5
MP:0012642	MP:0012642	increased benz (alpha) pyrene hydroxylase activity	Mammalian_phenotype	5
MP:0012644	MP:0012644	decreased 3 aminolaevulinic acid synthetase activity	Mammalian_phenotype	5
MP:0012645	MP:0012645	increased 3 aminolaevulinic acid synthetase activity	Mammalian_phenotype	5
MP:0012647	MP:0012647	decreased urokinase activity	Mammalian_phenotype	5
MP:0012648	MP:0012648	increased urokinase activity	Mammalian_phenotype	5
MP:0012650	MP:0012650	abnormal erythrocyte catalase level	Mammalian_phenotype	5
MP:0012651	MP:0012651	abnormal kidney catalase level	Mammalian_phenotype	5
MP:0012652	MP:0012652	decreased catalase level	Mammalian_phenotype	5
MP:0012655	MP:0012655	increased catalase level	Mammalian_phenotype	5
MP:0012659	MP:0012659	decreased superoxide dismutase level	Mammalian_phenotype	5
MP:0012660	MP:0012660	increased superoxide dismutase level	Mammalian_phenotype	5
MP:0012661	MP:0012661	decreased circulating ceruloplasmin level	Mammalian_phenotype	5
MP:0012662	MP:0012662	increased circulating ceruloplasmin level	Mammalian_phenotype	5
MP:0012663	MP:0012663	decreased haptoglobin	Mammalian_phenotype	5
MP:0012665	MP:0012665	increased haptoglobin	Mammalian_phenotype	5
MP:0012669	MP:0012669	abnormal somite segmentation clock	Mammalian_phenotype	5
MP:0012687	MP:0012687	abnormal heart atrium weight	Mammalian_phenotype	5
MP:0012688	MP:0012688	abnormal heart ventricles weight	Mammalian_phenotype	5
MP:0012697	MP:0012697	abnormal maternal body weight gain	Mammalian_phenotype	5
MP:0012700	MP:0012700	abnormal endocardial heart tube morphology	Mammalian_phenotype	5
MP:0012713	MP:0012713	abnormal ventral ectodermal ridge morphology	Mammalian_phenotype	5
MP:0012715	MP:0012715	abnormal hemangioblast morphology	Mammalian_phenotype	5
MP:0012724	MP:0012724	failure of head fold formation	Mammalian_phenotype	5
MP:0012728	MP:0012728	abnormal somite border morphology	Mammalian_phenotype	5
MP:0012732	MP:0012732	abnormal perineural vascular plexus morphology	Mammalian_phenotype	5
MP:0012733	MP:0012733	abnormal behavioral response to methamphetamine	Mammalian_phenotype	5
MP:0012746	MP:0012746	abnormal neural crest cell delamination	Mammalian_phenotype	5
MP:0012775	MP:0012775	abnormal brain weight	Mammalian_phenotype	5
MP:0012781	MP:0012781	increased phospholipid transfer protein activity	Mammalian_phenotype	5
MP:0012782	MP:0012782	decreased phospholipid transfer protein activity	Mammalian_phenotype	5
MP:0013127	MP:0013127	epistaxis	Mammalian_phenotype	5
MP:0013128	MP:0013128	nipple hemorrhage	Mammalian_phenotype	5
MP:0013134	MP:0013134	poor circulation in autopods	Mammalian_phenotype	5
MP:0013135	MP:0013135	poor circulation in tail	Mammalian_phenotype	5
MP:0013137	MP:0013137	nipple discharge	Mammalian_phenotype	5
MP:0013138	MP:0013138	thin body	Mammalian_phenotype	5
MP:0013141	MP:0013141	sexually aggressive behaviour	Mammalian_phenotype	5
MP:0013142	MP:0013142	anal soreness	Mammalian_phenotype	5
MP:0013149	MP:0013149	macrodactyly	Mammalian_phenotype	5
MP:0013163	MP:0013163	absent thyroid gland isthmus	Mammalian_phenotype	5
MP:0013164	MP:0013164	abnormal forelimb bud morphology	Mammalian_phenotype	5
MP:0013167	MP:0013167	abnormal hindlimb bud morphology	Mammalian_phenotype	5
MP:0020003	MP:0020003	abnormal sulfolipid level	Mammalian_phenotype	5
MP:0020009	MP:0020009	abnormal mineral bone density of femur	Mammalian_phenotype	5
MP:0020013	MP:0020013	decreased arylsulphatase activity	Mammalian_phenotype	5
MP:0020014	MP:0020014	increased arylsulphatase activity	Mammalian_phenotype	5
MP:0020016	MP:0020016	decreased aldehyde dehydrogenase activity	Mammalian_phenotype	5
MP:0020017	MP:0020017	increased aldehyde dehydrogenase activity	Mammalian_phenotype	5
MP:0020019	MP:0020019	decreased phenylalanine decarboxylase activity	Mammalian_phenotype	5
MP:0020020	MP:0020020	increased phenylalanine decarboxylase activity	Mammalian_phenotype	5
MP:0020022	MP:0020022	decreased delta-aminolaevulinate dehydratase activity	Mammalian_phenotype	5
MP:0020024	MP:0020024	increased delta-aminolaevulinate dehydratase activity	Mammalian_phenotype	5
MP:0020027	MP:0020027	decreased aldehyde oxidase activity	Mammalian_phenotype	5
MP:0020028	MP:0020028	increased aldehyde oxidase activity	Mammalian_phenotype	5
MP:0020030	MP:0020030	abnormal circulating cholinesterase activity	Mammalian_phenotype	5
MP:0020033	MP:0020033	increased cholinesterase activity	Mammalian_phenotype	5
MP:0020034	MP:0020034	decreased cholinesterase activity	Mammalian_phenotype	5
MP:0020036	MP:0020036	decreased coumarin hydroxylase activity	Mammalian_phenotype	5
MP:0020037	MP:0020037	increased coumarin hydroxylase activity	Mammalian_phenotype	5
MP:0020043	MP:0020043	decreased glucose-6-phosphate dehydrogenase activity	Mammalian_phenotype	5
MP:0020044	MP:0020044	increased glucose-6-phosphate dehydrogenase activity	Mammalian_phenotype	5
MP:0020046	MP:0020046	decreased tyrosine aminotransferase activity	Mammalian_phenotype	5
MP:0020047	MP:0020047	increased tyrosine aminotransferase activity	Mammalian_phenotype	5
MP:0020049	MP:0020049	decreased maltase activity	Mammalian_phenotype	5
MP:0020050	MP:0020050	increased maltase activity	Mammalian_phenotype	5
MP:0020052	MP:0020052	decreased procollagen-proline 4-dioxygenase activity	Mammalian_phenotype	5
MP:0020053	MP:0020053	increased procollagen-proline 4-dioxygenase activity	Mammalian_phenotype	5
MP:0020055	MP:0020055	abnormal spermatazoal beta-glucuronidase activity	Mammalian_phenotype	5
MP:0020056	MP:0020056	decreased beta-glucuronidase activity	Mammalian_phenotype	5
MP:0020058	MP:0020058	increased beta-glucuronidase activity	Mammalian_phenotype	5
MP:0020061	MP:0020061	decreased hypoxanthine phosphoribosyltransferase activity	Mammalian_phenotype	5
MP:0020062	MP:0020062	increased hypoxanthine phosphoribosyltransferase activity	Mammalian_phenotype	5
MP:0020064	MP:0020064	decreased thiopurine S-methyltransferase activity	Mammalian_phenotype	5
MP:0020065	MP:0020065	increased thiopurine S-methyltransferase activity	Mammalian_phenotype	5
MP:0020074	MP:0020074	abnormal brain tyrosine hydroxylase activity	Mammalian_phenotype	5
MP:0020075	MP:0020075	increased tyrosine hydroxylase activity	Mammalian_phenotype	5
MP:0020077	MP:0020077	decreased tyrosine hydroxylase activity	Mammalian_phenotype	5
MP:0020084	MP:0020084	short ears	Mammalian_phenotype	5
MP:0020085	MP:0020085	long ears	Mammalian_phenotype	5
MP:0020089	MP:0020089	increased susceptibility to diet-induced non-insulin dependent diabetes	Mammalian_phenotype	5
MP:0020090	MP:0020090	decreased susceptibility to diet-induced non-insulin dependent diabetes	Mammalian_phenotype	5
MP:0020102	MP:0020102	increased hepatic glucose production	Mammalian_phenotype	5
MP:0020103	MP:0020103	decreased hepatic glucose production	Mammalian_phenotype	5
MP:0020105	MP:0020105	increased nitrate level	Mammalian_phenotype	5
MP:0020106	MP:0020106	decreased nitrate level	Mammalian_phenotype	5
MP:0020108	MP:0020108	increased nitrite level	Mammalian_phenotype	5
MP:0020109	MP:0020109	decreased nitrite level	Mammalian_phenotype	5
MP:0020112	MP:0020112	abnormal carcass lipid	Mammalian_phenotype	5
MP:0020115	MP:0020115	abnormal sphingosine level	Mammalian_phenotype	5
MP:0020119	MP:0020119	decreased alcohol dehydrogenase activity	Mammalian_phenotype	5
MP:0020120	MP:0020120	increased alcohol dehydrogenase activity	Mammalian_phenotype	5
MP:0020122	MP:0020122	decreased tyrosine 3-monooxygenase activity	Mammalian_phenotype	5
MP:0020123	MP:0020123	increased tyrosine 3-monooxygenase activity	Mammalian_phenotype	5
MP:0020134	MP:0020134	abnormal gallbladder size	Mammalian_phenotype	5
MP:0020135	MP:0020135	abnormal heart ventricle thickness	Mammalian_phenotype	5
MP:0020153	MP:0020153	abnormal urine albumin level	Mammalian_phenotype	5
MP:0020157	MP:0020157	abnormal behavioral response to alcohol	Mammalian_phenotype	5
MP:0020158	MP:0020158	abnormal behavioral response to cocaine	Mammalian_phenotype	5
MP:0020159	MP:0020159	abnormal behavioral response to morphine	Mammalian_phenotype	5
MP:0020160	MP:0020160	abnormal behavioral response to nicotine	Mammalian_phenotype	5
MP:0020168	MP:0020168	decreased thyroid gland weight	Mammalian_phenotype	5
MP:0020169	MP:0020169	increased thyroid gland weight	Mammalian_phenotype	5
MP:0020182	MP:0020182	abnormal body mass index	Mammalian_phenotype	5
MP:0020183	MP:0020183	altered susceptibility to fungal infection	Mammalian_phenotype	5
MP:0020184	MP:0020184	altered susceptibility to parasitic infection	Mammalian_phenotype	5
MP:0020185	MP:0020185	altered susceptibility to viral infection	Mammalian_phenotype	5
MP:0020186	MP:0020186	altered susceptibility to bacterial infection	Mammalian_phenotype	5
MP:0020187	MP:0020187	altered susceptibility to prion infection	Mammalian_phenotype	5
MP:0020189	MP:0020189	abnormal adenoma incidence	Mammalian_phenotype	5
MP:0020194	MP:0020194	abnormal glycosphingolipid level	Mammalian_phenotype	5
MP:0003945	MP:0003945	abnormal lymphocyte physiology	Mammalian_phenotype	5
MP:0003946	MP:0003946	renal necrosis	Mammalian_phenotype	5
MP:0003947	MP:0003947	abnormal cholesterol level	Mammalian_phenotype	5
MP:0003952	MP:0003952	abnormal copper level	Mammalian_phenotype	5
MP:0003955	MP:0003955	abnormal ultimobranchial body morphology	Mammalian_phenotype	5
MP:0003958	MP:0003958	heart valve hyperplasia	Mammalian_phenotype	5
MP:0003966	MP:0003966	abnormal adrenocorticotropin level	Mammalian_phenotype	5
MP:0003967	MP:0003967	abnormal follicle stimulating hormone level	Mammalian_phenotype	5
MP:0003968	MP:0003968	abnormal growth hormone level	Mammalian_phenotype	5
MP:0003969	MP:0003969	abnormal luteinizing hormone level	Mammalian_phenotype	5
MP:0003970	MP:0003970	abnormal prolactin level	Mammalian_phenotype	5
MP:0003971	MP:0003971	abnormal thyroid-stimulating hormone level	Mammalian_phenotype	5
MP:0003972	MP:0003972	decreased pituitary hormone level	Mammalian_phenotype	5
MP:0003973	MP:0003973	increased pituitary hormone level	Mammalian_phenotype	5
MP:0003974	MP:0003974	abnormal endocardium morphology	Mammalian_phenotype	5
MP:0003977	MP:0003977	abnormal circulating carnitine level	Mammalian_phenotype	5
MP:0003991	MP:0003991	arteriosclerosis	Mammalian_phenotype	5
MP:0003992	MP:0003992	increased mortality induced by ionizing radiation	Mammalian_phenotype	5
MP:0003993	MP:0003993	abnormal ventral spinal root morphology	Mammalian_phenotype	5
MP:0003994	MP:0003994	abnormal dorsal spinal root morphology	Mammalian_phenotype	5
MP:0003996	MP:0003996	clonic seizures	Mammalian_phenotype	5
MP:0003997	MP:0003997	tonic-clonic seizures	Mammalian_phenotype	5
MP:0004001	MP:0004001	decreased hepatocyte proliferation	Mammalian_phenotype	5
MP:0004002	MP:0004002	abnormal jejunum morphology	Mammalian_phenotype	5
MP:0004008	MP:0004008	abnormal GABA-mediated receptor currents	Mammalian_phenotype	5
MP:0004010	MP:0004010	increased diastolic filling velocity	Mammalian_phenotype	5
MP:0004011	MP:0004011	decreased diastolic filling velocity	Mammalian_phenotype	5
MP:0004014	MP:0004014	abnormal uterine environment	Mammalian_phenotype	5
MP:0004015	MP:0004015	abnormal oviduct environment	Mammalian_phenotype	5
MP:0004024	MP:0004024	aneuploidy	Mammalian_phenotype	5
MP:0004025	MP:0004025	polyploidy	Mammalian_phenotype	5
MP:0004028	MP:0004028	chromosome breakage	Mammalian_phenotype	5
MP:0004032	MP:0004032	abnormal interventricular groove morphology	Mammalian_phenotype	5
MP:0004035	MP:0004035	abnormal sublingual gland morphology	Mammalian_phenotype	5
MP:0004038	MP:0004038	lymphangiectasis	Mammalian_phenotype	5
MP:0004041	MP:0004041	increased susceptibility to kidney reperfusion injury	Mammalian_phenotype	5
MP:0004047	MP:0004047	abnormal milk composition	Mammalian_phenotype	5
MP:0004051	MP:0004051	increased renal sympathetic nerve activity	Mammalian_phenotype	5
MP:0004052	MP:0004052	decreased renal sympathetic nerve activity	Mammalian_phenotype	5
MP:0004053	MP:0004053	abnormal synchondrosis	Mammalian_phenotype	5
MP:0004055	MP:0004055	atrium hypoplasia	Mammalian_phenotype	5
MP:0004070	MP:0004070	abnormal P wave	Mammalian_phenotype	5
MP:0004073	MP:0004073	caudal body truncation	Mammalian_phenotype	5
MP:0004076	MP:0004076	abnormal vitelline vascular remodeling	Mammalian_phenotype	5
MP:0004089	MP:0004089	dilated sarcoplasmic reticulum	Mammalian_phenotype	5
MP:0004091	MP:0004091	abnormal Z lines	Mammalian_phenotype	5
MP:0004094	MP:0004094	abnormal M lines	Mammalian_phenotype	5
MP:0004100	MP:0004100	abnormal spinal cord interneuron morphology	Mammalian_phenotype	5
MP:0004105	MP:0004105	corneal abrasion	Mammalian_phenotype	5
MP:0004106	MP:0004106	lymphatic vessel hyperplasia	Mammalian_phenotype	5
MP:0004111	MP:0004111	abnormal coronary artery morphology	Mammalian_phenotype	5
MP:0004112	MP:0004112	abnormal arteriole morphology	Mammalian_phenotype	5
MP:0004114	MP:0004114	abnormal atrioventricular node morphology	Mammalian_phenotype	5
MP:0004115	MP:0004115	abnormal sinoatrial node morphology	Mammalian_phenotype	5
MP:0004117	MP:0004117	abnormal atrioventricular bundle morphology	Mammalian_phenotype	5
MP:0004120	MP:0004120	cardiac ischemia	Mammalian_phenotype	5
MP:0004122	MP:0004122	abnormal sinus arrhythmia	Mammalian_phenotype	5
MP:0004124	MP:0004124	abnormal Purkinje fiber morphology	Mammalian_phenotype	5
MP:0004125	MP:0004125	abnormal venule morphology	Mammalian_phenotype	5
MP:0004135	MP:0004135	abnormal mammary gland embryonic development	Mammalian_phenotype	5
MP:0004166	MP:0004166	abnormal limbic system morphology	Mammalian_phenotype	5
MP:0004174	MP:0004174	abnormal spine curvature	Mammalian_phenotype	5
MP:0004184	MP:0004184	abnormal baroreceptor physiology	Mammalian_phenotype	5
MP:0004192	MP:0004192	abnormal kidney pyramid morphology	Mammalian_phenotype	5
MP:0004193	MP:0004193	abnormal kidney papilla morphology	Mammalian_phenotype	5
MP:0004195	MP:0004195	abnormal kidney calyx morphology	Mammalian_phenotype	5
MP:0004199	MP:0004199	increased fetal size	Mammalian_phenotype	5
MP:0004200	MP:0004200	decreased fetal size	Mammalian_phenotype	5
MP:0004214	MP:0004214	abnormal long bone diaphysis morphology	Mammalian_phenotype	5
MP:0004229	MP:0004229	abnormal embryonic erythropoiesis	Mammalian_phenotype	5
MP:0004235	MP:0004235	abnormal masseter muscle morphology	Mammalian_phenotype	5
MP:0004237	MP:0004237	abnormal pterygoid muscle morphology	Mammalian_phenotype	5
MP:0004239	MP:0004239	abnormal temporalis muscle morphology	Mammalian_phenotype	5
MP:0004241	MP:0004241	acantholysis	Mammalian_phenotype	5
MP:0004243	MP:0004243	abnormal motor nerve collateral sprouting	Mammalian_phenotype	5
MP:0004246	MP:0004246	abnormal extensor digitorum longus morphology	Mammalian_phenotype	5
MP:0004247	MP:0004247	small pancreas	Mammalian_phenotype	5
MP:0004256	MP:0004256	abnormal maternal decidual layer morphology	Mammalian_phenotype	5
MP:0004258	MP:0004258	abnormal placenta size	Mammalian_phenotype	5
MP:0004261	MP:0004261	abnormal embryonic neuroepithelium morphology	Mammalian_phenotype	5
MP:0004263	MP:0004263	abnormal limb posture	Mammalian_phenotype	5
MP:0004265	MP:0004265	abnormal placental transport	Mammalian_phenotype	5
MP:0004266	MP:0004266	pale placenta	Mammalian_phenotype	5
MP:0004270	MP:0004270	analgesia	Mammalian_phenotype	5
MP:0004276	MP:0004276	abnormal medial ganglionic eminence morphology	Mammalian_phenotype	5
MP:0004277	MP:0004277	abnormal lateral ganglionic eminence morphology	Mammalian_phenotype	5
MP:0004278	MP:0004278	abnormal caudal ganglionic eminence morphology	Mammalian_phenotype	5
MP:0004284	MP:0004284	abnormal Descemet membrane	Mammalian_phenotype	5
MP:0004287	MP:0004287	abnormal spiral limbus morphology	Mammalian_phenotype	5
MP:0004305	MP:0004305	abnormal Rosenthal canal morphology	Mammalian_phenotype	5
MP:0004308	MP:0004308	abnormal basilar membrane morphology	Mammalian_phenotype	5
MP:0004309	MP:0004309	absent otic vesicle	Mammalian_phenotype	5
MP:0004310	MP:0004310	small otic vesicle	Mammalian_phenotype	5
MP:0004314	MP:0004314	absent inner ear vestibule	Mammalian_phenotype	5
MP:0004324	MP:0004324	vestibular hair cell degeneration	Mammalian_phenotype	5
MP:0004362	MP:0004362	cochlear hair cell degeneration	Mammalian_phenotype	5
MP:0004388	MP:0004388	absent prechordal plate	Mammalian_phenotype	5
MP:0004415	MP:0004415	abnormal cochlear nerve compound action potential	Mammalian_phenotype	5
MP:0004425	MP:0004425	abnormal otolith organ morphology	Mammalian_phenotype	5
MP:0004426	MP:0004426	abnormal cochlear labyrinth morphology	Mammalian_phenotype	5
MP:0004427	MP:0004427	abnormal vestibular labyrinth morphology	Mammalian_phenotype	5
MP:0004439	MP:0004439	absent Meckel's cartilage	Mammalian_phenotype	5
MP:0004481	MP:0004481	abnormal conjunctival epithelium morphology	Mammalian_phenotype	5
MP:0004493	MP:0004493	dilated cochlea	Mammalian_phenotype	5
MP:0004506	MP:0004506	abnormal pubis morphology	Mammalian_phenotype	5
MP:0004507	MP:0004507	abnormal ischium morphology	Mammalian_phenotype	5
MP:0004541	MP:0004541	absent auditory tube	Mammalian_phenotype	5
MP:0004546	MP:0004546	esophagus hyperplasia	Mammalian_phenotype	5
MP:0004550	MP:0004550	short trachea	Mammalian_phenotype	5
MP:0004551	MP:0004551	decreased tracheal cartilage ring number	Mammalian_phenotype	5
MP:0004552	MP:0004552	fused tracheal cartilage rings	Mammalian_phenotype	5
MP:0004553	MP:0004553	absent tracheal cartilage rings	Mammalian_phenotype	5
MP:0004555	MP:0004555	pharynx hypoplasia	Mammalian_phenotype	5
MP:0004556	MP:0004556	enlarged allantois	Mammalian_phenotype	5
MP:0004557	MP:0004557	dilated allantois	Mammalian_phenotype	5
MP:0004558	MP:0004558	delayed allantois development	Mammalian_phenotype	5
MP:0004559	MP:0004559	small allantois	Mammalian_phenotype	5
MP:0004560	MP:0004560	abnormal chorionic plate morphology	Mammalian_phenotype	5
MP:0004573	MP:0004573	absent limb buds	Mammalian_phenotype	5
MP:0004574	MP:0004574	broad limb buds	Mammalian_phenotype	5
MP:0004575	MP:0004575	small limb buds	Mammalian_phenotype	5
MP:0004597	MP:0004597	increased susceptibility to noise-induced hearing loss	Mammalian_phenotype	5
MP:0004609	MP:0004609	vertebral fusion	Mammalian_phenotype	5
MP:0004625	MP:0004625	abnormal rib attachment	Mammalian_phenotype	5
MP:0004661	MP:0004661	absent thyroid parafollicular C-cells	Mammalian_phenotype	5
MP:0004662	MP:0004662	abnormal thyroid diverticulum morphology	Mammalian_phenotype	5
MP:0004664	MP:0004664	delayed inner ear development	Mammalian_phenotype	5
MP:0004686	MP:0004686	decreased length of long bones	Mammalian_phenotype	5
MP:0004695	MP:0004695	increased length of long bones	Mammalian_phenotype	5
MP:0004697	MP:0004697	abnormal thyroid follicular cell morphology	Mammalian_phenotype	5
MP:0004699	MP:0004699	unilateral deafness	Mammalian_phenotype	5
MP:0004700	MP:0004700	abnormal circulating insulin-like growth factor I level	Mammalian_phenotype	5
MP:0004704	MP:0004704	short vertebral column	Mammalian_phenotype	5
MP:0004710	MP:0004710	small notochord	Mammalian_phenotype	5
MP:0004711	MP:0004711	persistence of notochord tissue	Mammalian_phenotype	5
MP:0004712	MP:0004712	notochord degeneration	Mammalian_phenotype	5
MP:0004713	MP:0004713	split notochord	Mammalian_phenotype	5
MP:0004714	MP:0004714	truncated notochord	Mammalian_phenotype	5
MP:0004723	MP:0004723	abnormal platelet serotonin level	Mammalian_phenotype	5
MP:0004730	MP:0004730	abnormal circulating gastrin level	Mammalian_phenotype	5
MP:0004736	MP:0004736	abnormal distortion product otoacoustic emission	Mammalian_phenotype	5
MP:0004738	MP:0004738	abnormal auditory brainstem response	Mammalian_phenotype	5
MP:0004744	MP:0004744	reduced vestibular evoked myogenic potential	Mammalian_phenotype	5
MP:0004745	MP:0004745	absent vestibular evoked myogenic potential	Mammalian_phenotype	5
MP:0004748	MP:0004748	increased susceptibility to age-related hearing loss	Mammalian_phenotype	5
MP:0004753	MP:0004753	abnormal miniature excitatory postsynaptic currents	Mammalian_phenotype	5
MP:0004759	MP:0004759	decreased mitotic index	Mammalian_phenotype	5
MP:0004760	MP:0004760	increased mitotic index	Mammalian_phenotype	5
MP:0004766	MP:0004766	decreased susceptibility to age-related hearing loss	Mammalian_phenotype	5
MP:0004769	MP:0004769	abnormal synaptic vesicle morphology	Mammalian_phenotype	5
MP:0004774	MP:0004774	abnormal bile salt level	Mammalian_phenotype	5
MP:0004775	MP:0004775	abnormal vestibular dark cell morphology	Mammalian_phenotype	5
MP:0004777	MP:0004777	abnormal phospholipid level	Mammalian_phenotype	5
MP:0004778	MP:0004778	increased macrophage derived foam cell number	Mammalian_phenotype	5
MP:0004813	MP:0004813	absent linear vestibular evoked potential	Mammalian_phenotype	5
MP:0004814	MP:0004814	reduced linear vestibular evoked potential	Mammalian_phenotype	5
MP:0004818	MP:0004818	increased skeletal muscle mass	Mammalian_phenotype	5
MP:0004819	MP:0004819	decreased skeletal muscle mass	Mammalian_phenotype	5
MP:0004834	MP:0004834	ovary hemorrhage	Mammalian_phenotype	5
MP:0004835	MP:0004835	abnormal miniature endplate potential	Mammalian_phenotype	5
MP:0004837	MP:0004837	abnormal neural fold formation	Mammalian_phenotype	5
MP:0004839	MP:0004839	bile duct hyperplasia	Mammalian_phenotype	5
MP:0004841	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology	Mammalian_phenotype	5
MP:0004842	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology	Mammalian_phenotype	5
MP:0004847	MP:0004847	abnormal liver weight	Mammalian_phenotype	5
MP:0004857	MP:0004857	abnormal heart weight	Mammalian_phenotype	5
MP:0004860	MP:0004860	dilated kidney collecting duct	Mammalian_phenotype	5
MP:0004861	MP:0004861	abnormal Raphe nucleus morphology	Mammalian_phenotype	5
MP:0004865	MP:0004865	abnormal platelet calcium level	Mammalian_phenotype	5
MP:0004875	MP:0004875	increased mean systemic arterial blood pressure	Mammalian_phenotype	5
MP:0004876	MP:0004876	decreased mean systemic arterial blood pressure	Mammalian_phenotype	5
MP:0004877	MP:0004877	abnormal systemic vascular resistance	Mammalian_phenotype	5
MP:0004882	MP:0004882	enlarged lung	Mammalian_phenotype	5
MP:0004889	MP:0004889	increased energy expenditure	Mammalian_phenotype	5
MP:0004890	MP:0004890	decreased energy expenditure	Mammalian_phenotype	5
MP:0004892	MP:0004892	increased adiponectin level	Mammalian_phenotype	5
MP:0004893	MP:0004893	decreased adiponectin level	Mammalian_phenotype	5
MP:0004897	MP:0004897	otosclerosis	Mammalian_phenotype	5
MP:0004898	MP:0004898	uterine hemorrhage	Mammalian_phenotype	5
MP:0004916	MP:0004916	absent Reichert cartilage	Mammalian_phenotype	5
MP:0004925	MP:0004925	decreased susceptibility to noise-induced hearing loss	Mammalian_phenotype	5
MP:0004948	MP:0004948	abnormal neuronal precursor proliferation	Mammalian_phenotype	5
MP:0004963	MP:0004963	abnormal blastocoele morphology	Mammalian_phenotype	5
MP:0004968	MP:0004968	kidney epithelium hyperplasia	Mammalian_phenotype	5
MP:0004979	MP:0004979	abnormal neuronal precursor cell number	Mammalian_phenotype	5
MP:0004987	MP:0004987	abnormal osteoblast cell number	Mammalian_phenotype	5
MP:0004992	MP:0004992	increased bone resorption	Mammalian_phenotype	5
MP:0004993	MP:0004993	decreased bone resorption	Mammalian_phenotype	5
MP:0004995	MP:0004995	abnormal B cell clonal deletion	Mammalian_phenotype	5
MP:0004997	MP:0004997	increased CNS synapse formation	Mammalian_phenotype	5
MP:0004998	MP:0004998	decreased CNS synapse formation	Mammalian_phenotype	5
MP:0005002	MP:0005002	abnormal T cell clonal deletion	Mammalian_phenotype	5
MP:0005028	MP:0005028	abnormal trophectoderm morphology	Mammalian_phenotype	5
MP:0005030	MP:0005030	absent amnion	Mammalian_phenotype	5
MP:0005031	MP:0005031	abnormal trophoblast layer morphology	Mammalian_phenotype	5
MP:0005035	MP:0005035	perianal ulceration	Mammalian_phenotype	5
MP:0005037	MP:0005037	mucous diarrhea	Mammalian_phenotype	5
MP:0005039	MP:0005039	hypoxia	Mammalian_phenotype	5
MP:0005061	MP:0005061	abnormal eosinophil morphology	Mammalian_phenotype	5
MP:0005087	MP:0005087	decreased acute inflammation	Mammalian_phenotype	5
MP:0005088	MP:0005088	increased acute inflammation	Mammalian_phenotype	5
MP:0005099	MP:0005099	abnormal ciliary body morphology	Mammalian_phenotype	5
MP:0005101	MP:0005101	abnormal ciliary body pigmentation	Mammalian_phenotype	5
MP:0005108	MP:0005108	abnormal ulna morphology	Mammalian_phenotype	5
MP:0005111	MP:0005111	hyperdipsia	Mammalian_phenotype	5
MP:0005112	MP:0005112	abnormal spinal cord ventral horn morphology	Mammalian_phenotype	5
MP:0005116	MP:0005116	abnormal circulating pituitary hormone level	Mammalian_phenotype	5
MP:0005140	MP:0005140	decreased cardiac muscle contractility	Mammalian_phenotype	5
MP:0005144	MP:0005144	abnormal circulating VLDL cholesterol level	Mammalian_phenotype	5
MP:0005151	MP:0005151	diffuse hepatic necrosis	Mammalian_phenotype	5
MP:0005157	MP:0005157	holoprosencephaly	Mammalian_phenotype	5
MP:0005159	MP:0005159	azoospermia	Mammalian_phenotype	5
MP:0005168	MP:0005168	abnormal female meiosis	Mammalian_phenotype	5
MP:0005169	MP:0005169	abnormal male meiosis	Mammalian_phenotype	5
MP:0005176	MP:0005176	eyelids fail to open	Mammalian_phenotype	5
MP:0005180	MP:0005180	abnormal circulating testosterone level	Mammalian_phenotype	5
MP:0005184	MP:0005184	abnormal circulating progesterone level	Mammalian_phenotype	5
MP:0005198	MP:0005198	abnormal aqueous drainage system morphology	Mammalian_phenotype	5
MP:0005199	MP:0005199	abnormal iris pigment epithelium	Mammalian_phenotype	5
MP:0005201	MP:0005201	abnormal retinal pigment epithelium morphology	Mammalian_phenotype	5
MP:0005206	MP:0005206	abnormal aqueous humor	Mammalian_phenotype	5
MP:0005214	MP:0005214	regional gastric metaplasia	Mammalian_phenotype	5
MP:0005215	MP:0005215	abnormal pancreatic islet morphology	Mammalian_phenotype	5
MP:0005222	MP:0005222	abnormal somite size	Mammalian_phenotype	5
MP:0005223	MP:0005223	abnormal dorsal-ventral polarity of the somites	Mammalian_phenotype	5
MP:0005224	MP:0005224	abnormal left-right axis symmetry of the somites	Mammalian_phenotype	5
MP:0005229	MP:0005229	abnormal intervertebral disk development	Mammalian_phenotype	5
MP:0005230	MP:0005230	ectrodactyly	Mammalian_phenotype	5
MP:0005236	MP:0005236	abnormal olfactory nerve morphology	Mammalian_phenotype	5
MP:0005238	MP:0005238	increased brain size	Mammalian_phenotype	5
MP:0005242	MP:0005242	cryptophthalmos	Mammalian_phenotype	5
MP:0005243	MP:0005243	hemothorax	Mammalian_phenotype	5
MP:0005244	MP:0005244	hemopericardium	Mammalian_phenotype	5
MP:0005279	MP:0005279	narcolepsy	Mammalian_phenotype	5
MP:0005280	MP:0005280	abnormal fatty acid level	Mammalian_phenotype	5
MP:0005287	MP:0005287	narrow eye opening	Mammalian_phenotype	5
MP:0005289	MP:0005289	increased oxygen consumption	Mammalian_phenotype	5
MP:0005290	MP:0005290	decreased oxygen consumption	Mammalian_phenotype	5
MP:0005292	MP:0005292	improved glucose tolerance	Mammalian_phenotype	5
MP:0005293	MP:0005293	impaired glucose tolerance	Mammalian_phenotype	5
MP:0005296	MP:0005296	abnormal humerus morphology	Mammalian_phenotype	5
MP:0005298	MP:0005298	abnormal clavicle morphology	Mammalian_phenotype	5
MP:0005300	MP:0005300	abnormal corneal stroma morphology	Mammalian_phenotype	5
MP:0005301	MP:0005301	abnormal corneal endothelium morphology	Mammalian_phenotype	5
MP:0005306	MP:0005306	abnormal phalanx morphology	Mammalian_phenotype	5
MP:0005307	MP:0005307	head tossing	Mammalian_phenotype	5
MP:0005309	MP:0005309	increased circulating ammonia level	Mammalian_phenotype	5
MP:0005314	MP:0005314	absent thyroid gland	Mammalian_phenotype	5
MP:0005316	MP:0005316	abnormal response to tactile stimuli	Mammalian_phenotype	5
MP:0005321	MP:0005321	abnormal neopterin level	Mammalian_phenotype	5
MP:0005328	MP:0005328	abnormal circulating creatinine level	Mammalian_phenotype	5
MP:0005329	MP:0005329	abnormal myocardium layer morphology	Mammalian_phenotype	5
MP:0005333	MP:0005333	decreased heart rate	Mammalian_phenotype	5
MP:0005335	MP:0005335	abnormal gonadal fat pad morphology	Mammalian_phenotype	5
MP:0005336	MP:0005336	abnormal inguinal fat pad morphology	Mammalian_phenotype	5
MP:0005337	MP:0005337	abnormal retroperitoneal fat pad morphology	Mammalian_phenotype	5
MP:0005344	MP:0005344	increased circulating bilirubin level	Mammalian_phenotype	5
MP:0005346	MP:0005346	abnormal circulating aldosterone level	Mammalian_phenotype	5
MP:0005353	MP:0005353	abnormal patella morphology	Mammalian_phenotype	5
MP:0005354	MP:0005354	abnormal ilium morphology	Mammalian_phenotype	5
MP:0005401	MP:0005401	abnormal fat-soluble vitamin level	Mammalian_phenotype	5
MP:0005404	MP:0005404	abnormal axon morphology	Mammalian_phenotype	5
MP:0005413	MP:0005413	vascular restenosis	Mammalian_phenotype	5
MP:0005414	MP:0005414	extrahepatic cholestasis	Mammalian_phenotype	5
MP:0005424	MP:0005424	jerky movement	Mammalian_phenotype	5
MP:0005437	MP:0005437	abnormal glycogen level	Mammalian_phenotype	5
MP:0005441	MP:0005441	increased urine calcium level	Mammalian_phenotype	5
MP:0005444	MP:0005444	abnormal retinol metabolism	Mammalian_phenotype	5
MP:0005445	MP:0005445	abnormal neurotransmitter secretion	Mammalian_phenotype	5
MP:0005449	MP:0005449	abnormal food intake	Mammalian_phenotype	5
MP:0005458	MP:0005458	increased percent body fat	Mammalian_phenotype	5
MP:0005459	MP:0005459	decreased percent body fat	Mammalian_phenotype	5
MP:0005461	MP:0005461	abnormal dendritic cell morphology	Mammalian_phenotype	5
MP:0005469	MP:0005469	abnormal thyroxine level	Mammalian_phenotype	5
MP:0005472	MP:0005472	abnormal triiodothyronine level	Mammalian_phenotype	5
MP:0005475	MP:0005475	abnormal circulating thyroxine level	Mammalian_phenotype	5
MP:0005476	MP:0005476	abnormal circulating triiodothyronine level	Mammalian_phenotype	5
MP:0005489	MP:0005489	vascular smooth muscle cell hyperplasia	Mammalian_phenotype	5
MP:0005492	MP:0005492	exocrine pancreas hypoplasia	Mammalian_phenotype	5
MP:0005516	MP:0005516	increased liver regeneration	Mammalian_phenotype	5
MP:0005517	MP:0005517	decreased liver regeneration	Mammalian_phenotype	5
MP:0005519	MP:0005519	increased pancreas regeneration	Mammalian_phenotype	5
MP:0005520	MP:0005520	decreased pancreas regeneration	Mammalian_phenotype	5
MP:0005521	MP:0005521	abnormal circulating atrial natriuretic factor level	Mammalian_phenotype	5
MP:0005527	MP:0005527	increased renal glomerular filtration rate	Mammalian_phenotype	5
MP:0005528	MP:0005528	decreased renal glomerular filtration rate	Mammalian_phenotype	5
MP:0005537	MP:0005537	abnormal cerebral aqueduct morphology	Mammalian_phenotype	5
MP:0005542	MP:0005542	corneal vascularization	Mammalian_phenotype	5
MP:0005544	MP:0005544	corneal deposits	Mammalian_phenotype	5
MP:0005547	MP:0005547	abnormal Muller cell morphology	Mammalian_phenotype	5
MP:0005553	MP:0005553	increased circulating creatinine level	Mammalian_phenotype	5
MP:0005557	MP:0005557	increased creatinine clearance	Mammalian_phenotype	5
MP:0005558	MP:0005558	decreased creatinine clearance	Mammalian_phenotype	5
MP:0005559	MP:0005559	increased circulating glucose level	Mammalian_phenotype	5
MP:0005560	MP:0005560	decreased circulating glucose level	Mammalian_phenotype	5
MP:0005565	MP:0005565	increased blood urea nitrogen level	Mammalian_phenotype	5
MP:0005566	MP:0005566	decreased blood urea nitrogen level	Mammalian_phenotype	5
MP:0005571	MP:0005571	decreased lactate dehydrogenase level	Mammalian_phenotype	5
MP:0005578	MP:0005578	teratozoospermia	Mammalian_phenotype	5
MP:0005579	MP:0005579	absent outer ear	Mammalian_phenotype	5
MP:0005582	MP:0005582	increased renin activity	Mammalian_phenotype	5
MP:0005583	MP:0005583	decreased renin activity	Mammalian_phenotype	5
MP:0005599	MP:0005599	increased cardiac muscle contractility	Mammalian_phenotype	5
MP:0005608	MP:0005608	cardiac interstitial fibrosis	Mammalian_phenotype	5
MP:0005609	MP:0005609	abnormal circulating antidiuretic hormone level	Mammalian_phenotype	5
MP:0005625	MP:0005625	increased plasma anion gap	Mammalian_phenotype	5
MP:0005626	MP:0005626	decreased plasma anion gap	Mammalian_phenotype	5
MP:0005629	MP:0005629	abnormal lung weight	Mammalian_phenotype	5
MP:0005635	MP:0005635	decreased circulating bilirubin level	Mammalian_phenotype	5
MP:0005643	MP:0005643	decreased dopamine level	Mammalian_phenotype	5
MP:0005644	MP:0005644	agonadal	Mammalian_phenotype	5
MP:0005654	MP:0005654	porphyria	Mammalian_phenotype	5
MP:0005655	MP:0005655	increased aggression	Mammalian_phenotype	5
MP:0005656	MP:0005656	decreased aggression	Mammalian_phenotype	5
MP:0005660	MP:0005660	abnormal circulating adrenaline level	Mammalian_phenotype	5
MP:0005663	MP:0005663	abnormal circulating noradrenaline level	Mammalian_phenotype	5
MP:0005667	MP:0005667	abnormal circulating leptin level	Mammalian_phenotype	5
MP:0005675	MP:0005675	small gallbladder	Mammalian_phenotype	5
MP:0006000	MP:0006000	abnormal corneal epithelium morphology	Mammalian_phenotype	5
MP:0006002	MP:0006002	abnormal small intestinal transit time	Mammalian_phenotype	5
MP:0006003	MP:0006003	abnormal large intestinal transit time	Mammalian_phenotype	5
MP:0006007	MP:0006007	abnormal basal ganglion morphology	Mammalian_phenotype	5
MP:0006019	MP:0006019	absent tympanic membrane	Mammalian_phenotype	5
MP:0006020	MP:0006020	decreased tympanic ring size	Mammalian_phenotype	5
MP:0006021	MP:0006021	abnormal Reissner membrane morphology	Mammalian_phenotype	5
MP:0006030	MP:0006030	abnormal otic vesicle development	Mammalian_phenotype	5
MP:0006033	MP:0006033	abnormal external auditory canal morphology	Mammalian_phenotype	5
MP:0006038	MP:0006038	increased mitochondrial proliferation	Mammalian_phenotype	5
MP:0006039	MP:0006039	decreased mitochondrial proliferation	Mammalian_phenotype	5
MP:0006042	MP:0006042	increased apoptosis	Mammalian_phenotype	5
MP:0006043	MP:0006043	decreased apoptosis	Mammalian_phenotype	5
MP:0006046	MP:0006046	atrioventricular valve regurgitation	Mammalian_phenotype	5
MP:0006049	MP:0006049	semilunar valve regurgitation	Mammalian_phenotype	5
MP:0006055	MP:0006055	abnormal vascular endothelial cell morphology	Mammalian_phenotype	5
MP:0006058	MP:0006058	decreased cerebral infarction size	Mammalian_phenotype	5
MP:0006060	MP:0006060	increased cerebral infarction size	Mammalian_phenotype	5
MP:0006062	MP:0006062	abnormal vena cava morphology	Mammalian_phenotype	5
MP:0006076	MP:0006076	abnormal circulating homocysteine level	Mammalian_phenotype	5
MP:0006077	MP:0006077	inguinal hernia	Mammalian_phenotype	5
MP:0006107	MP:0006107	abnormal fetal atrioventricular canal morphology	Mammalian_phenotype	5
MP:0006108	MP:0006108	abnormal hindbrain development	Mammalian_phenotype	5
MP:0006109	MP:0006109	fibrillation	Mammalian_phenotype	5
MP:0006112	MP:0006112	angina	Mammalian_phenotype	5
MP:0006133	MP:0006133	calcified artery	Mammalian_phenotype	5
MP:0006134	MP:0006134	artery occlusion	Mammalian_phenotype	5
MP:0006135	MP:0006135	artery stenosis	Mammalian_phenotype	5
MP:0006136	MP:0006136	varicose veins	Mammalian_phenotype	5
MP:0006137	MP:0006137	venoocclusion	Mammalian_phenotype	5
MP:0006143	MP:0006143	increased systemic arterial diastolic blood pressure	Mammalian_phenotype	5
MP:0006144	MP:0006144	increased systemic arterial systolic blood pressure	Mammalian_phenotype	5
MP:0006145	MP:0006145	legal blindness	Mammalian_phenotype	5
MP:0006147	MP:0006147	monocular blindness	Mammalian_phenotype	5
MP:0006148	MP:0006148	binocular blindness	Mammalian_phenotype	5
MP:0006149	MP:0006149	decreased visual acuity	Mammalian_phenotype	5
MP:0006151	MP:0006151	astigmatism	Mammalian_phenotype	5
MP:0006159	MP:0006159	ocular albinism	Mammalian_phenotype	5
MP:0006166	MP:0006166	eyelid retraction	Mammalian_phenotype	5
MP:0006191	MP:0006191	conjunctival deposits	Mammalian_phenotype	5
MP:0006200	MP:0006200	vitreous body deposition	Mammalian_phenotype	5
MP:0006201	MP:0006201	vitreous body inflammation	Mammalian_phenotype	5
MP:0006202	MP:0006202	vitreous body hemorrhage	Mammalian_phenotype	5
MP:0006208	MP:0006208	lethality throughout fetal growth and development	Mammalian_phenotype	5
MP:0006223	MP:0006223	optic nerve swelling	Mammalian_phenotype	5
MP:0006236	MP:0006236	absent meibomian glands	Mammalian_phenotype	5
MP:0006245	MP:0006245	dislocated lens	Mammalian_phenotype	5
MP:0006253	MP:0006253	clinodactyly	Mammalian_phenotype	5
MP:0006263	MP:0006263	decreased systemic arterial diastolic blood pressure	Mammalian_phenotype	5
MP:0006264	MP:0006264	decreased systemic arterial systolic blood pressure	Mammalian_phenotype	5
MP:0006265	MP:0006265	increased pulse pressure	Mammalian_phenotype	5
MP:0006266	MP:0006266	decreased pulse pressure	Mammalian_phenotype	5
MP:0006269	MP:0006269	abnormal mammary gland growth during pregnancy	Mammalian_phenotype	5
MP:0006270	MP:0006270	abnormal mammary gland growth during lactation	Mammalian_phenotype	5
MP:0006271	MP:0006271	abnormal involution of the mammary gland	Mammalian_phenotype	5
MP:0006282	MP:0006282	abnormal spinal cord dorsal horn morphology	Mammalian_phenotype	5
MP:0006284	MP:0006284	absent hypaxial muscle	Mammalian_phenotype	5
MP:0006288	MP:0006288	small otic capsule	Mammalian_phenotype	5
MP:0006290	MP:0006290	proboscis	Mammalian_phenotype	5
MP:0006293	MP:0006293	absent nasal placodes	Mammalian_phenotype	5
MP:0006294	MP:0006294	absent optic vesicle	Mammalian_phenotype	5
MP:0006295	MP:0006295	absent sclerotome	Mammalian_phenotype	5
MP:0006296	MP:0006296	arachnodactyly	Mammalian_phenotype	5
MP:0006299	MP:0006299	abnormal latent inhibition of conditioning behavior	Mammalian_phenotype	5
MP:0006302	MP:0006302	abnormal ectomesenchyme morphology	Mammalian_phenotype	5
MP:0006319	MP:0006319	abnormal epididymal fat pad morphology	Mammalian_phenotype	5
MP:0006324	MP:0006324	abnormal cochlear nerve fiber response	Mammalian_phenotype	5
MP:0006326	MP:0006326	conductive hearing impairment	Mammalian_phenotype	5
MP:0006327	MP:0006327	mixed hearing impairment	Mammalian_phenotype	5
MP:0006328	MP:0006328	nonsyndromic hearing impairment	Mammalian_phenotype	5
MP:0006329	MP:0006329	sensorineural hearing impairment	Mammalian_phenotype	5
MP:0006330	MP:0006330	syndromic hearing impairment	Mammalian_phenotype	5
MP:0006332	MP:0006332	abnormal cochlear potential	Mammalian_phenotype	5
MP:0006337	MP:0006337	abnormal first branchial arch morphology	Mammalian_phenotype	5
MP:0006338	MP:0006338	abnormal second branchial arch morphology	Mammalian_phenotype	5
MP:0006339	MP:0006339	abnormal third branchial arch morphology	Mammalian_phenotype	5
MP:0006340	MP:0006340	abnormal fourth branchial arch morphology	Mammalian_phenotype	5
MP:0006346	MP:0006346	small branchial arch	Mammalian_phenotype	5
MP:0006347	MP:0006347	abnormal sixth branchial arch morphology	Mammalian_phenotype	5
MP:0006351	MP:0006351	abnormal glycosylated hemoglobin level	Mammalian_phenotype	5
MP:0006361	MP:0006361	abnormal female germ cell morphology	Mammalian_phenotype	5
MP:0006362	MP:0006362	abnormal male germ cell morphology	Mammalian_phenotype	5
MP:0006363	MP:0006363	absent auchene hairs	Mammalian_phenotype	5
MP:0006364	MP:0006364	absent awl hair	Mammalian_phenotype	5
MP:0006365	MP:0006365	absent guard hair	Mammalian_phenotype	5
MP:0006366	MP:0006366	absent zigzag hairs	Mammalian_phenotype	5
MP:0006372	MP:0006372	impaired placental function	Mammalian_phenotype	5
MP:0006373	MP:0006373	abnormal circulating angiotensinogen level	Mammalian_phenotype	5
MP:0006379	MP:0006379	abnormal spermatocyte morphology	Mammalian_phenotype	5
MP:0006380	MP:0006380	abnormal spermatid morphology	Mammalian_phenotype	5
MP:0006383	MP:0006383	abnormal cochlear frequency tuning	Mammalian_phenotype	5
MP:0006388	MP:0006388	abnormal auditory summating potential	Mammalian_phenotype	5
MP:0006391	MP:0006391	abnormal vestibular endolymph ionic homeostasis	Mammalian_phenotype	5
MP:0006394	MP:0006394	abnormal vertebral epiphyseal plate morphology	Mammalian_phenotype	5
MP:0006412	MP:0006412	abnormal T cell apoptosis	Mammalian_phenotype	5
MP:0006433	MP:0006433	abnormal articular cartilage morphology	Mammalian_phenotype	5
MP:0008001	MP:0008001	hypochlorhydria	Mammalian_phenotype	5
MP:0008002	MP:0008002	hyperchlorhydria	Mammalian_phenotype	5
MP:0008003	MP:0008003	achlorhydria	Mammalian_phenotype	5
MP:0008012	MP:0008012	duodenum polyps	Mammalian_phenotype	5
MP:0008013	MP:0008013	cecum polyps	Mammalian_phenotype	5
MP:0008022	MP:0008022	dilated heart ventricle	Mammalian_phenotype	5
MP:0008024	MP:0008024	absent lymph nodes	Mammalian_phenotype	5
MP:0008033	MP:0008033	impaired lipolysis	Mammalian_phenotype	5
MP:0008034	MP:0008034	enhanced lipolysis	Mammalian_phenotype	5
MP:0008055	MP:0008055	increased urine osmolality	Mammalian_phenotype	5
MP:0008063	MP:0008063	increased otic epithelium apoptosis	Mammalian_phenotype	5
MP:0008064	MP:0008064	decreased otic epithelium proliferation	Mammalian_phenotype	5
MP:0008067	MP:0008067	retinal ganglion cell degeneration	Mammalian_phenotype	5
MP:0008103	MP:0008103	amacrine cell degeneration	Mammalian_phenotype	5
MP:0008108	MP:0008108	abnormal small intestinal villus morphology	Mammalian_phenotype	5
MP:0008128	MP:0008128	abnormal brain internal capsule morphology	Mammalian_phenotype	5
MP:0008143	MP:0008143	abnormal dendrite morphology	Mammalian_phenotype	5
MP:0008144	MP:0008144	nyctalopia	Mammalian_phenotype	5
MP:0008149	MP:0008149	abnormal rib-vertebral column attachment	Mammalian_phenotype	5
MP:0008150	MP:0008150	decreased diameter of long bones	Mammalian_phenotype	5
MP:0008151	MP:0008151	increased diameter of long bones	Mammalian_phenotype	5
MP:0008171	MP:0008171	abnormal mature B cell morphology	Mammalian_phenotype	5
MP:0008199	MP:0008199	increased follicular dendritic cell number	Mammalian_phenotype	5
MP:0008200	MP:0008200	decreased follicular dendritic cell number	Mammalian_phenotype	5
MP:0008259	MP:0008259	abnormal optic disc morphology	Mammalian_phenotype	5
MP:0008275	MP:0008275	failure of endochondral bone ossification	Mammalian_phenotype	5
MP:0008276	MP:0008276	failure of intramembranous bone ossification	Mammalian_phenotype	5
MP:0008277	MP:0008277	abnormal sternum ossification	Mammalian_phenotype	5
MP:0008290	MP:0008290	absent adrenal cortex	Mammalian_phenotype	5
MP:0008291	MP:0008291	abnormal adrenocortical cell morphology	Mammalian_phenotype	5
MP:0008293	MP:0008293	abnormal zona glomerulosa morphology	Mammalian_phenotype	5
MP:0008294	MP:0008294	abnormal zona fasciculata morphology	Mammalian_phenotype	5
MP:0008295	MP:0008295	abnormal zona reticularis morphology	Mammalian_phenotype	5
MP:0008296	MP:0008296	abnormal x-zone morphology	Mammalian_phenotype	5
MP:0008299	MP:0008299	adrenal cortical hyperplasia	Mammalian_phenotype	5
MP:0008300	MP:0008300	enlarged adrenal medulla	Mammalian_phenotype	5
MP:0008302	MP:0008302	thin adrenal cortex	Mammalian_phenotype	5
MP:0008310	MP:0008310	abnormal sympathetic preganglionic fiber morphology	Mammalian_phenotype	5
MP:0008311	MP:0008311	abnormal parasympathetic preganglionic fiber morphology	Mammalian_phenotype	5
MP:0008312	MP:0008312	abnormal sympathetic postganglionic fiber morphology	Mammalian_phenotype	5
MP:0008313	MP:0008313	abnormal parasympathetic postganglionic fiber morphology	Mammalian_phenotype	5
MP:0008318	MP:0008318	abnormal splanchnic nerve morphology	Mammalian_phenotype	5
MP:0008319	MP:0008319	abnormal sympathetic afferent fiber morphology	Mammalian_phenotype	5
MP:0008391	MP:0008391	abnormal primordial germ cell morphology	Mammalian_phenotype	5
MP:0008431	MP:0008431	abnormal short term spatial reference memory	Mammalian_phenotype	5
MP:0008432	MP:0008432	abnormal long term spatial reference memory	Mammalian_phenotype	5
MP:0008450	MP:0008450	retinal photoreceptor degeneration	Mammalian_phenotype	5
MP:0008459	MP:0008459	abnormal circulating pancreatic peptide level	Mammalian_phenotype	5
MP:0008463	MP:0008463	abnormal peripheral lymph node morphology	Mammalian_phenotype	5
MP:0008489	MP:0008489	slow postnatal weight gain	Mammalian_phenotype	5
MP:0008504	MP:0008504	abnormal adrenal chromaffin cell morphology	Mammalian_phenotype	5
MP:0008521	MP:0008521	abnormal Bowman membrane	Mammalian_phenotype	5
MP:0008528	MP:0008528	polycystic kidney	Mammalian_phenotype	5
MP:0008530	MP:0008530	abnormal rostral-caudal patterning of the somites	Mammalian_phenotype	5
MP:0008538	MP:0008538	decreased zigzag hair amount	Mammalian_phenotype	5
MP:0008541	MP:0008541	leukostasis	Mammalian_phenotype	5
MP:0008555	MP:0008555	abnormal interferon secretion	Mammalian_phenotype	5
MP:0008556	MP:0008556	abnormal tumor necrosis factor secretion	Mammalian_phenotype	5
MP:0008568	MP:0008568	abnormal interleukin secretion	Mammalian_phenotype	5
MP:0008570	MP:0008570	lipidosis	Mammalian_phenotype	5
MP:0008579	MP:0008579	abnormal Purkinje cell differentiation	Mammalian_phenotype	5
MP:0008720	MP:0008720	impaired neutrophil chemotaxis	Mammalian_phenotype	5
MP:0008722	MP:0008722	abnormal chemokine secretion	Mammalian_phenotype	5
MP:0008724	MP:0008724	impaired eosinophil chemotaxis	Mammalian_phenotype	5
MP:0008725	MP:0008725	enlarged heart atrium	Mammalian_phenotype	5
MP:0008739	MP:0008739	abnormal spleen iron level	Mammalian_phenotype	5
MP:0008744	MP:0008744	abnormal B cell anergy	Mammalian_phenotype	5
MP:0008747	MP:0008747	abnormal T cell anergy	Mammalian_phenotype	5
MP:0008753	MP:0008753	abnormal osteocyte morphology	Mammalian_phenotype	5
MP:0008762	MP:0008762	embryonic lethality	Mammalian_phenotype	5
MP:0008771	MP:0008771	elongated vertebral column	Mammalian_phenotype	5
MP:0008772	MP:0008772	increased heart ventricle size	Mammalian_phenotype	5
MP:0008776	MP:0008776	increased right ventricle peak pressure	Mammalian_phenotype	5
MP:0008777	MP:0008777	increased right ventricle diastolic pressure	Mammalian_phenotype	5
MP:0008779	MP:0008779	abnormal maternal behavior	Mammalian_phenotype	5
MP:0008781	MP:0008781	abnormal B cell apoptosis	Mammalian_phenotype	5
MP:0008784	MP:0008784	craniorachischisis	Mammalian_phenotype	5
MP:0008788	MP:0008788	abnormal fetal cardiomyocyte morphology	Mammalian_phenotype	5
MP:0008797	MP:0008797	facial cleft	Mammalian_phenotype	5
MP:0008800	MP:0008800	increased small intestinal crypt cell apoptosis	Mammalian_phenotype	5
MP:0008814	MP:0008814	decreased nerve conduction velocity	Mammalian_phenotype	5
MP:0008817	MP:0008817	hematoma	Mammalian_phenotype	5
MP:0008819	MP:0008819	abnormal mastication	Mammalian_phenotype	5
MP:0008821	MP:0008821	increased blood uric acid level	Mammalian_phenotype	5
MP:0008822	MP:0008822	decreased blood uric acid level	Mammalian_phenotype	5
MP:0008826	MP:0008826	abnormal splenic cell ratio	Mammalian_phenotype	5
MP:0008827	MP:0008827	abnormal thymus cell ratio	Mammalian_phenotype	5
MP:0008828	MP:0008828	abnormal lymph node cell ratio	Mammalian_phenotype	5
MP:0008829	MP:0008829	triphalangia	Mammalian_phenotype	5
MP:0008836	MP:0008836	abnormal transforming growth factor beta level	Mammalian_phenotype	5
MP:0008843	MP:0008843	absent subcutaneous adipose tissue	Mammalian_phenotype	5
MP:0008844	MP:0008844	decreased subcutaneous adipose tissue amount	Mammalian_phenotype	5
MP:0008853	MP:0008853	decreased abdominal adipose tissue amount	Mammalian_phenotype	5
MP:0008864	MP:0008864	abnormal intestinal secretion	Mammalian_phenotype	5
MP:0008867	MP:0008867	uniparental disomy	Mammalian_phenotype	5
MP:0008869	MP:0008869	anovulation	Mammalian_phenotype	5
MP:0008884	MP:0008884	abnormal enterocyte apoptosis	Mammalian_phenotype	5
MP:0008891	MP:0008891	decreased hepatocyte apoptosis	Mammalian_phenotype	5
MP:0008899	MP:0008899	plush coat	Mammalian_phenotype	5
MP:0008900	MP:0008900	abnormal uterine fat pad morphology	Mammalian_phenotype	5
MP:0008903	MP:0008903	abnormal mesenteric fat pad morphology	Mammalian_phenotype	5
MP:0008906	MP:0008906	abnormal parametrial fat pad morphology	Mammalian_phenotype	5
MP:0008907	MP:0008907	decreased total fat pad weight	Mammalian_phenotype	5
MP:0008908	MP:0008908	increased total fat pad weight	Mammalian_phenotype	5
MP:0008918	MP:0008918	microgliosis	Mammalian_phenotype	5
MP:0008943	MP:0008943	increased sensitivity to induced cell death	Mammalian_phenotype	5
MP:0008944	MP:0008944	decreased sensitivity to induced cell death	Mammalian_phenotype	5
MP:0008947	MP:0008947	increased neuron number	Mammalian_phenotype	5
MP:0008948	MP:0008948	decreased neuron number	Mammalian_phenotype	5
MP:0008952	MP:0008952	abnormal pancreatic delta cell physiology	Mammalian_phenotype	5
MP:0008953	MP:0008953	abnormal pancreatic somatostatin secretion	Mammalian_phenotype	5
MP:0008957	MP:0008957	abnormal placenta junctional zone morphology	Mammalian_phenotype	5
MP:0008960	MP:0008960	abnormal axon pruning	Mammalian_phenotype	5
MP:0008963	MP:0008963	increased carbon dioxide production	Mammalian_phenotype	5
MP:0008964	MP:0008964	decreased carbon dioxide production	Mammalian_phenotype	5
MP:0008966	MP:0008966	abnormal chiasmata formation	Mammalian_phenotype	5
MP:0008974	MP:0008974	proportional dwarf	Mammalian_phenotype	5
MP:0008987	MP:0008987	abnormal liver lobule morphology	Mammalian_phenotype	5
MP:0008989	MP:0008989	abnormal liver sinusoid morphology	Mammalian_phenotype	5
MP:0008992	MP:0008992	abnormal portal lobule morphology	Mammalian_phenotype	5
MP:0008997	MP:0008997	increased blood osmolality	Mammalian_phenotype	5
MP:0008998	MP:0008998	decreased blood osmolality	Mammalian_phenotype	5
MP:0008999	MP:0008999	absent anus	Mammalian_phenotype	5
MP:0009005	MP:0009005	abnormal sesamoid bone of gastrocnemius morphology	Mammalian_phenotype	5
MP:0009024	MP:0009024	abnormal brain arachnoid mater morphology	Mammalian_phenotype	5
MP:0009025	MP:0009025	abnormal brain dura mater morphology	Mammalian_phenotype	5
MP:0003954	MP:0003954	abnormal Reichert's membrane morphology	Mammalian_phenotype	6
MP:0003978	MP:0003978	decreased circulating carnitine level	Mammalian_phenotype	6
MP:0003979	MP:0003979	increased circulating carnitine level	Mammalian_phenotype	6
MP:0003987	MP:0003987	small vestibular ganglion	Mammalian_phenotype	6
MP:0003990	MP:0003990	decreased neurotransmitter release	Mammalian_phenotype	6
MP:0003995	MP:0003995	abnormal uterine artery morphology	Mammalian_phenotype	6
MP:0003998	MP:0003998	decreased thermal nociceptive threshold	Mammalian_phenotype	6
MP:0004005	MP:0004005	impaired contractility of intestinal smooth muscle	Mammalian_phenotype	6
MP:0004026	MP:0004026	monosomy	Mammalian_phenotype	6
MP:0004027	MP:0004027	trisomy	Mammalian_phenotype	6
MP:0004029	MP:0004029	spontaneous chromosome breakage	Mammalian_phenotype	6
MP:0004030	MP:0004030	induced chromosome breakage	Mammalian_phenotype	6
MP:0004031	MP:0004031	insulitis	Mammalian_phenotype	6
MP:0004034	MP:0004034	belly blaze	Mammalian_phenotype	6
MP:0004056	MP:0004056	abnormal myocardium compact layer morphology	Mammalian_phenotype	6
MP:0004062	MP:0004062	dilated heart right atrium	Mammalian_phenotype	6
MP:0004063	MP:0004063	dilated heart left atrium	Mammalian_phenotype	6
MP:0004066	MP:0004066	abnormal primitive node morphology	Mammalian_phenotype	6
MP:0004071	MP:0004071	prolonged P wave	Mammalian_phenotype	6
MP:0004074	MP:0004074	abnormal Schwann cell precursor morphology	Mammalian_phenotype	6
MP:0004077	MP:0004077	abnormal striatum morphology	Mammalian_phenotype	6
MP:0004080	MP:0004080	abnormal nucleus accumbens morphology	Mammalian_phenotype	6
MP:0004081	MP:0004081	abnormal globus pallidus morphology	Mammalian_phenotype	6
MP:0004083	MP:0004083	polysyndactyly	Mammalian_phenotype	6
MP:0004092	MP:0004092	absent Z lines	Mammalian_phenotype	6
MP:0004093	MP:0004093	diffuse Z lines	Mammalian_phenotype	6
MP:0004096	MP:0004096	abnormal midbrain-hindbrain boundary development	Mammalian_phenotype	6
MP:0004110	MP:0004110	transposition of great arteries	Mammalian_phenotype	6
MP:0004137	MP:0004137	abnormal gastric surface mucous cell morphology	Mammalian_phenotype	6
MP:0004146	MP:0004146	absent M lines	Mammalian_phenotype	6
MP:0004148	MP:0004148	increased compact bone thickness	Mammalian_phenotype	6
MP:0004152	MP:0004152	abnormal circulating iron level	Mammalian_phenotype	6
MP:0004154	MP:0004154	renal tubular necrosis	Mammalian_phenotype	6
MP:0004156	MP:0004156	abnormal QT variability	Mammalian_phenotype	6
MP:0004162	MP:0004162	abnormal mammillary body morphology	Mammalian_phenotype	6
MP:0004169	MP:0004169	abnormal fornicate gyrus morphology	Mammalian_phenotype	6
MP:0004170	MP:0004170	abnormal orbitofrontal cortex morphology	Mammalian_phenotype	6
MP:0004175	MP:0004175	telangiectases	Mammalian_phenotype	6
MP:0004180	MP:0004180	failure of initiation of embryo turning	Mammalian_phenotype	6
MP:0004181	MP:0004181	abnormal carotid artery morphology	Mammalian_phenotype	6
MP:0004182	MP:0004182	abnormal spermiation	Mammalian_phenotype	6
MP:0004187	MP:0004187	cardia bifida	Mammalian_phenotype	6
MP:0004188	MP:0004188	delayed embryo turning	Mammalian_phenotype	6
MP:0004190	MP:0004190	abnormal direction of embryo turning	Mammalian_phenotype	6
MP:0004202	MP:0004202	pulmonary hyperplasia	Mammalian_phenotype	6
MP:0004203	MP:0004203	abnormal cranial flexure morphology	Mammalian_phenotype	6
MP:0004206	MP:0004206	abnormal dermomyotome development	Mammalian_phenotype	6
MP:0004216	MP:0004216	salt-resistant hypertension	Mammalian_phenotype	6
MP:0004217	MP:0004217	salt-sensitive hypertension	Mammalian_phenotype	6
MP:0004218	MP:0004218	meiotic nondisjunction during M1 phase	Mammalian_phenotype	6
MP:0004219	MP:0004219	meiotic nondisjunction during M2 phase	Mammalian_phenotype	6
MP:0004221	MP:0004221	abnormal iridocorneal angle	Mammalian_phenotype	6
MP:0004222	MP:0004222	iris synechia	Mammalian_phenotype	6
MP:0004225	MP:0004225	patent foramen ovale	Mammalian_phenotype	6
MP:0004227	MP:0004227	increased cellular sensitivity to ionizing radiation	Mammalian_phenotype	6
MP:0004228	MP:0004228	decreased cellular sensitivity to ionizing radiation	Mammalian_phenotype	6
MP:0004230	MP:0004230	abnormal embryonic erythrocyte morphology	Mammalian_phenotype	6
MP:0004236	MP:0004236	absent masseter muscle	Mammalian_phenotype	6
MP:0004238	MP:0004238	absent pterygoid muscle	Mammalian_phenotype	6
MP:0004240	MP:0004240	absent temporalis muscle	Mammalian_phenotype	6
MP:0004251	MP:0004251	failure of heart looping	Mammalian_phenotype	6
MP:0004252	MP:0004252	abnormal direction of heart looping	Mammalian_phenotype	6
MP:0004253	MP:0004253	bifid atrial appendage	Mammalian_phenotype	6
MP:0004255	MP:0004255	abnormal spongiotrophoblast layer morphology	Mammalian_phenotype	6
MP:0004257	MP:0004257	abnormal placenta weight	Mammalian_phenotype	6
MP:0004259	MP:0004259	small placenta	Mammalian_phenotype	6
MP:0004260	MP:0004260	enlarged placenta	Mammalian_phenotype	6
MP:0004280	MP:0004280	abnormal oculomotor nucleus morphology	Mammalian_phenotype	6
MP:0004281	MP:0004281	abnormal hypoglossal nucleus morphology	Mammalian_phenotype	6
MP:0004283	MP:0004283	absent corneal endothelium	Mammalian_phenotype	6
MP:0004285	MP:0004285	absent Descemet membrane	Mammalian_phenotype	6
MP:0004297	MP:0004297	abnormal proprioceptive neuron morphology	Mammalian_phenotype	6
MP:0004298	MP:0004298	vestibular ganglion degeneration	Mammalian_phenotype	6
MP:0004299	MP:0004299	absent vestibular ganglion	Mammalian_phenotype	6
MP:0004304	MP:0004304	absent spiral limbus	Mammalian_phenotype	6
MP:0004306	MP:0004306	small Rosenthal canal	Mammalian_phenotype	6
MP:0004307	MP:0004307	absent Rosenthal canal	Mammalian_phenotype	6
MP:0004311	MP:0004311	otic vesicle hypoplasia	Mammalian_phenotype	6
MP:0004313	MP:0004313	absent vestibulocochlear ganglion	Mammalian_phenotype	6
MP:0004320	MP:0004320	split sternum	Mammalian_phenotype	6
MP:0004321	MP:0004321	short sternum	Mammalian_phenotype	6
MP:0004322	MP:0004322	abnormal sternebra morphology	Mammalian_phenotype	6
MP:0004323	MP:0004323	sternum hypoplasia	Mammalian_phenotype	6
MP:0004338	MP:0004338	small clavicle	Mammalian_phenotype	6
MP:0004339	MP:0004339	absent clavicle	Mammalian_phenotype	6
MP:0004341	MP:0004341	absent scapula	Mammalian_phenotype	6
MP:0004342	MP:0004342	scapular bone foramen	Mammalian_phenotype	6
MP:0004343	MP:0004343	small scapula	Mammalian_phenotype	6
MP:0004345	MP:0004345	abnormal acromion morphology	Mammalian_phenotype	6
MP:0004347	MP:0004347	abnormal scapular spine morphology	Mammalian_phenotype	6
MP:0004348	MP:0004348	long femur	Mammalian_phenotype	6
MP:0004350	MP:0004350	long humerus	Mammalian_phenotype	6
MP:0004351	MP:0004351	short humerus	Mammalian_phenotype	6
MP:0004355	MP:0004355	short radius	Mammalian_phenotype	6
MP:0004357	MP:0004357	long tibia	Mammalian_phenotype	6
MP:0004359	MP:0004359	short ulna	Mammalian_phenotype	6
MP:0004363	MP:0004363	stria vascularis degeneration	Mammalian_phenotype	6
MP:0004370	MP:0004370	long ulna	Mammalian_phenotype	6
MP:0004389	MP:0004389	abnormal respiratory bronchiole morphology	Mammalian_phenotype	6
MP:0004410	MP:0004410	absent endocochlear potential	Mammalian_phenotype	6
MP:0004411	MP:0004411	decreased endocochlear potential	Mammalian_phenotype	6
MP:0004412	MP:0004412	abnormal cochlear microphonics	Mammalian_phenotype	6
MP:0004416	MP:0004416	absent cochlear nerve compound action potential	Mammalian_phenotype	6
MP:0004417	MP:0004417	decreased cochlear nerve compound action potential	Mammalian_phenotype	6
MP:0004431	MP:0004431	abnormal hair cell mechanoelectric transduction	Mammalian_phenotype	6
MP:0004432	MP:0004432	abnormal cochlear hair cell physiology	Mammalian_phenotype	6
MP:0004438	MP:0004438	abnormal vestibular hair cell physiology	Mammalian_phenotype	6
MP:0004482	MP:0004482	abnormal interdental cell morphology	Mammalian_phenotype	6
MP:0004494	MP:0004494	abnormal synaptic glutamate release	Mammalian_phenotype	6
MP:0004500	MP:0004500	increased incidence of tumors by ionizing radiation induction	Mammalian_phenotype	6
MP:0004501	MP:0004501	increased incidence of tumors by UV-induction	Mammalian_phenotype	6
MP:0004503	MP:0004503	decreased incidence of tumors by ionizing radiation induction	Mammalian_phenotype	6
MP:0004504	MP:0004504	decreased incidence of tumors by UV induction	Mammalian_phenotype	6
MP:0004514	MP:0004514	dystocia	Mammalian_phenotype	6
MP:0004561	MP:0004561	absent facial nerve	Mammalian_phenotype	6
MP:0004568	MP:0004568	fusion of glossopharyngeal and vagus nerve	Mammalian_phenotype	6
MP:0004569	MP:0004569	glossopharyngeal nerve hypoplasia	Mammalian_phenotype	6
MP:0004570	MP:0004570	absent glossopharyngeal nerve	Mammalian_phenotype	6
MP:0004571	MP:0004571	absent vagus nerve	Mammalian_phenotype	6
MP:0004599	MP:0004599	abnormal vertebral arch morphology	Mammalian_phenotype	6
MP:0004610	MP:0004610	small vertebrae	Mammalian_phenotype	6
MP:0004626	MP:0004626	vertebral compression	Mammalian_phenotype	6
MP:0004629	MP:0004629	abnormal spiral modiolar artery morphology	Mammalian_phenotype	6
MP:0004630	MP:0004630	spiral modiolar artery stenosis	Mammalian_phenotype	6
MP:0004634	MP:0004634	short metacarpal bones	Mammalian_phenotype	6
MP:0004635	MP:0004635	short metatarsal bones	Mammalian_phenotype	6
MP:0004636	MP:0004636	decreased metacarpal bone number	Mammalian_phenotype	6
MP:0004637	MP:0004637	metacarpal bone hypoplasia	Mammalian_phenotype	6
MP:0004638	MP:0004638	elongated metacarpal bones	Mammalian_phenotype	6
MP:0004639	MP:0004639	fused metacarpal bones	Mammalian_phenotype	6
MP:0004640	MP:0004640	decreased metatarsal bone number	Mammalian_phenotype	6
MP:0004641	MP:0004641	elongated metatarsal bones	Mammalian_phenotype	6
MP:0004642	MP:0004642	fused metatarsal bones	Mammalian_phenotype	6
MP:0004643	MP:0004643	abnormal vertebrae number	Mammalian_phenotype	6
MP:0004660	MP:0004660	absent thyroid follicular cells	Mammalian_phenotype	6
MP:0004665	MP:0004665	abnormal stapedial artery morphology	Mammalian_phenotype	6
MP:0004671	MP:0004671	long ribs	Mammalian_phenotype	6
MP:0004672	MP:0004672	short ribs	Mammalian_phenotype	6
MP:0004673	MP:0004673	splayed ribs	Mammalian_phenotype	6
MP:0004674	MP:0004674	thin ribs	Mammalian_phenotype	6
MP:0004675	MP:0004675	rib fractures	Mammalian_phenotype	6
MP:0004676	MP:0004676	wide ribs	Mammalian_phenotype	6
MP:0004677	MP:0004677	truncated ribs	Mammalian_phenotype	6
MP:0004682	MP:0004682	small intervertebral disk	Mammalian_phenotype	6
MP:0004683	MP:0004683	absent intervertebral disk	Mammalian_phenotype	6
MP:0004684	MP:0004684	intervertebral disk degeneration	Mammalian_phenotype	6
MP:0004685	MP:0004685	calcified intervertebral disk	Mammalian_phenotype	6
MP:0004687	MP:0004687	split vertebrae	Mammalian_phenotype	6
MP:0004688	MP:0004688	absent ilium	Mammalian_phenotype	6
MP:0004689	MP:0004689	small ischium	Mammalian_phenotype	6
MP:0004691	MP:0004691	absent pubis	Mammalian_phenotype	6
MP:0004692	MP:0004692	small pubis	Mammalian_phenotype	6
MP:0004694	MP:0004694	absent patella	Mammalian_phenotype	6
MP:0004701	MP:0004701	decreased circulating insulin-like growth factor I level	Mammalian_phenotype	6
MP:0004702	MP:0004702	increased circulating insulin-like growth factor I level	Mammalian_phenotype	6
MP:0004715	MP:0004715	absent vestibulocochlear nerve	Mammalian_phenotype	6
MP:0004716	MP:0004716	abnormal cochlear nerve morphology	Mammalian_phenotype	6
MP:0004718	MP:0004718	abnormal vestibular nerve morphology	Mammalian_phenotype	6
MP:0004724	MP:0004724	increased platelet serotonin level	Mammalian_phenotype	6
MP:0004725	MP:0004725	decreased platelet serotonin level	Mammalian_phenotype	6
MP:0004731	MP:0004731	increased circulating gastrin level	Mammalian_phenotype	6
MP:0004732	MP:0004732	decreased circulating gastrin level	Mammalian_phenotype	6
MP:0004737	MP:0004737	absent distortion product otoacoustic emissions	Mammalian_phenotype	6
MP:0004739	MP:0004739	conductive hearing loss	Mammalian_phenotype	6
MP:0004740	MP:0004740	sensorineural hearing loss	Mammalian_phenotype	6
MP:0004741	MP:0004741	mixed hearing loss	Mammalian_phenotype	6
MP:0004749	MP:0004749	nonsyndromic hearing loss	Mammalian_phenotype	6
MP:0004750	MP:0004750	syndromic hearing loss	Mammalian_phenotype	6
MP:0004755	MP:0004755	abnormal loop of Henle morphology	Mammalian_phenotype	6
MP:0004756	MP:0004756	abnormal proximal convoluted tubule morphology	Mammalian_phenotype	6
MP:0004757	MP:0004757	abnormal distal convoluted tubule morphology	Mammalian_phenotype	6
MP:0004761	MP:0004761	increased susceptibility to induced pancreatitis	Mammalian_phenotype	6
MP:0004767	MP:0004767	increased cochlear nerve compound action potential	Mammalian_phenotype	6
MP:0004776	MP:0004776	vestibular dark cell degeneration	Mammalian_phenotype	6
MP:0004789	MP:0004789	increased bile salt level	Mammalian_phenotype	6
MP:0004792	MP:0004792	abnormal synaptic vesicle number	Mammalian_phenotype	6
MP:0004806	MP:0004806	absent germ cells	Mammalian_phenotype	6
MP:0004836	MP:0004836	abnormal synaptic acetylcholine release	Mammalian_phenotype	6
MP:0004838	MP:0004838	abnormal neural fold elevation formation	Mammalian_phenotype	6
MP:0004862	MP:0004862	small scala tympani	Mammalian_phenotype	6
MP:0004864	MP:0004864	spiral ligament degeneration	Mammalian_phenotype	6
MP:0004878	MP:0004878	increased systemic vascular resistance	Mammalian_phenotype	6
MP:0004879	MP:0004879	decreased systemic vascular resistance	Mammalian_phenotype	6
MP:0004901	MP:0004901	decreased male germ cell number	Mammalian_phenotype	6
MP:0004914	MP:0004914	absent ultimobranchial body	Mammalian_phenotype	6
MP:0004922	MP:0004922	abnormal common crus morphology	Mammalian_phenotype	6
MP:0004936	MP:0004936	impaired branching involved in ureteric bud morphogenesis	Mammalian_phenotype	6
MP:0004951	MP:0004951	abnormal spleen weight	Mammalian_phenotype	6
MP:0004954	MP:0004954	abnormal thymus weight	Mammalian_phenotype	6
MP:0004964	MP:0004964	absent inner cell mass	Mammalian_phenotype	6
MP:0004965	MP:0004965	inner cell mass degeneration	Mammalian_phenotype	6
MP:0004970	MP:0004970	kidney atrophy	Mammalian_phenotype	6
MP:0004980	MP:0004980	increased neuronal precursor cell number	Mammalian_phenotype	6
MP:0004981	MP:0004981	decreased neuronal precursor cell number	Mammalian_phenotype	6
MP:0004988	MP:0004988	increased osteoblast cell number	Mammalian_phenotype	6
MP:0004989	MP:0004989	decreased osteoblast cell number	Mammalian_phenotype	6
MP:0004990	MP:0004990	abnormal ciliary ganglion morphology	Mammalian_phenotype	6
MP:0005026	MP:0005026	decreased susceptibility to parasitic infection	Mammalian_phenotype	6
MP:0005027	MP:0005027	increased susceptibility to parasitic infection	Mammalian_phenotype	6
MP:0005032	MP:0005032	abnormal ectoplacental cone morphology	Mammalian_phenotype	6
MP:0005033	MP:0005033	abnormal trophoblast giant cells	Mammalian_phenotype	6
MP:0005046	MP:0005046	absent spleen white pulp	Mammalian_phenotype	6
MP:0005048	MP:0005048	thrombosis	Mammalian_phenotype	6
MP:0005074	MP:0005074	impaired granulocyte bactericidal activity	Mammalian_phenotype	6
MP:0005098	MP:0005098	abnormal choroid morphology	Mammalian_phenotype	6
MP:0005106	MP:0005106	abnormal incus morphology	Mammalian_phenotype	6
MP:0005107	MP:0005107	abnormal stapes morphology	Mammalian_phenotype	6
MP:0005109	MP:0005109	abnormal talus morphology	Mammalian_phenotype	6
MP:0005113	MP:0005113	decreased spinal cord ventral horn cell number	Mammalian_phenotype	6
MP:0005114	MP:0005114	premature hair loss	Mammalian_phenotype	6
MP:0005117	MP:0005117	increased circulating pituitary hormone level	Mammalian_phenotype	6
MP:0005118	MP:0005118	decreased circulating pituitary hormone level	Mammalian_phenotype	6
MP:0005128	MP:0005128	decreased adrenocorticotropin level	Mammalian_phenotype	6
MP:0005129	MP:0005129	increased adrenocorticotropin level	Mammalian_phenotype	6
MP:0005130	MP:0005130	decreased follicle stimulating hormone level	Mammalian_phenotype	6
MP:0005131	MP:0005131	increased follicle stimulating hormone level	Mammalian_phenotype	6
MP:0005132	MP:0005132	decreased luteinizing hormone level	Mammalian_phenotype	6
MP:0005133	MP:0005133	increased luteinizing hormone level	Mammalian_phenotype	6
MP:0005134	MP:0005134	decreased thyroid-stimulating hormone level	Mammalian_phenotype	6
MP:0005135	MP:0005135	increased thyroid-stimulating hormone level	Mammalian_phenotype	6
MP:0005136	MP:0005136	decreased growth hormone level	Mammalian_phenotype	6
MP:0005137	MP:0005137	increased growth hormone level	Mammalian_phenotype	6
MP:0005138	MP:0005138	decreased prolactin level	Mammalian_phenotype	6
MP:0005139	MP:0005139	increased prolactin level	Mammalian_phenotype	6
MP:0005141	MP:0005141	liver hyperplasia	Mammalian_phenotype	6
MP:0005156	MP:0005156	bradykinesia	Mammalian_phenotype	6
MP:0005162	MP:0005162	carpoptosis	Mammalian_phenotype	6
MP:0005171	MP:0005171	absent coat pigmentation	Mammalian_phenotype	6
MP:0005175	MP:0005175	non-pigmented tail tip	Mammalian_phenotype	6
MP:0005183	MP:0005183	abnormal circulating estradiol level	Mammalian_phenotype	6
MP:0005185	MP:0005185	decreased circulating progesterone level	Mammalian_phenotype	6
MP:0005186	MP:0005186	increased circulating progesterone level	Mammalian_phenotype	6
MP:0005192	MP:0005192	increased motor neuron number	Mammalian_phenotype	6
MP:0005208	MP:0005208	abnormal iris stroma morphology	Mammalian_phenotype	6
MP:0005210	MP:0005210	disorganized stomach mucosa	Mammalian_phenotype	6
MP:0005216	MP:0005216	abnormal pancreatic alpha cell morphology	Mammalian_phenotype	6
MP:0005217	MP:0005217	abnormal pancreatic beta cell morphology	Mammalian_phenotype	6
MP:0005218	MP:0005218	abnormal pancreatic delta cell morphology	Mammalian_phenotype	6
MP:0005231	MP:0005231	abnormal brachial lymph node morphology	Mammalian_phenotype	6
MP:0005232	MP:0005232	abnormal mesenteric lymph node morphology	Mammalian_phenotype	6
MP:0005240	MP:0005240	abnormal amacrine cell morphology	Mammalian_phenotype	6
MP:0005274	MP:0005274	abnormal viscerocranium morphology	Mammalian_phenotype	6
MP:0005281	MP:0005281	increased fatty acid level	Mammalian_phenotype	6
MP:0005282	MP:0005282	decreased fatty acid level	Mammalian_phenotype	6
MP:0005317	MP:0005317	increased triglyceride level	Mammalian_phenotype	6
MP:0005318	MP:0005318	decreased triglyceride level	Mammalian_phenotype	6
MP:0005325	MP:0005325	abnormal renal glomerulus morphology	Mammalian_phenotype	6
MP:0005338	MP:0005338	atherosclerotic lesions	Mammalian_phenotype	6
MP:0005345	MP:0005345	abnormal circulating corticosterone level	Mammalian_phenotype	6
MP:0005357	MP:0005357	novel environmental response-related retropulsion	Mammalian_phenotype	6
MP:0005362	MP:0005362	abnormal Langerhans cell physiology	Mammalian_phenotype	6
MP:0005363	MP:0005363	decreased susceptibility to prion infection	Mammalian_phenotype	6
MP:0005364	MP:0005364	increased susceptibility to prion infection	Mammalian_phenotype	6
MP:0005398	MP:0005398	decreased susceptibility to fungal infection	Mammalian_phenotype	6
MP:0005399	MP:0005399	increased susceptibility to fungal infection	Mammalian_phenotype	6
MP:0005407	MP:0005407	hyperalgesia	Mammalian_phenotype	6
MP:0005419	MP:0005419	decreased circulating serum albumin level	Mammalian_phenotype	6
MP:0005431	MP:0005431	decreased oocyte number	Mammalian_phenotype	6
MP:0005435	MP:0005435	hemoperitoneum	Mammalian_phenotype	6
MP:0005439	MP:0005439	decreased glycogen level	Mammalian_phenotype	6
MP:0005440	MP:0005440	increased glycogen level	Mammalian_phenotype	6
MP:0005446	MP:0005446	abnormal synaptic epinephrine release	Mammalian_phenotype	6
MP:0005447	MP:0005447	abnormal synaptic norepinephrine release	Mammalian_phenotype	6
MP:0005455	MP:0005455	increased susceptibility to weight gain	Mammalian_phenotype	6
MP:0005470	MP:0005470	increased thyroxine level	Mammalian_phenotype	6
MP:0005471	MP:0005471	decreased thyroxine level	Mammalian_phenotype	6
MP:0005473	MP:0005473	decreased triiodothyronine level	Mammalian_phenotype	6
MP:0005474	MP:0005474	increased triiodothyronine level	Mammalian_phenotype	6
MP:0005477	MP:0005477	increased circulating thyroxine level	Mammalian_phenotype	6
MP:0005478	MP:0005478	decreased circulating thyroxine level	Mammalian_phenotype	6
MP:0005479	MP:0005479	decreased circulating triiodothyronine level	Mammalian_phenotype	6
MP:0005480	MP:0005480	increased circulating triiodothyronine level	Mammalian_phenotype	6
MP:0005497	MP:0005497	optic nerve cupping	Mammalian_phenotype	6
MP:0005522	MP:0005522	increased circulating atrial natriuretic factor	Mammalian_phenotype	6
MP:0005523	MP:0005523	decreased circulating atrial natriuretic factor	Mammalian_phenotype	6
MP:0005525	MP:0005525	increased renal plasma flow rate	Mammalian_phenotype	6
MP:0005526	MP:0005526	decreased renal plasma flow rate	Mammalian_phenotype	6
MP:0005530	MP:0005530	decreased renal vascular resistance	Mammalian_phenotype	6
MP:0005531	MP:0005531	increased renal vascular resistance	Mammalian_phenotype	6
MP:0005540	MP:0005540	decreased urine albumin level	Mammalian_phenotype	6
MP:0005543	MP:0005543	decreased cornea thickness	Mammalian_phenotype	6
MP:0005554	MP:0005554	decreased circulating creatinine level	Mammalian_phenotype	6
MP:0005567	MP:0005567	decreased circulating total protein level	Mammalian_phenotype	6
MP:0005568	MP:0005568	increased circulating total protein level	Mammalian_phenotype	6
MP:0005572	MP:0005572	abnormal pulmonary respiratory rate	Mammalian_phenotype	6
MP:0005575	MP:0005575	increased pulmonary ventilation	Mammalian_phenotype	6
MP:0005576	MP:0005576	decreased pulmonary ventilation	Mammalian_phenotype	6
MP:0005580	MP:0005580	periinsulitis	Mammalian_phenotype	6
MP:0005585	MP:0005585	increased tidal volume	Mammalian_phenotype	6
MP:0005586	MP:0005586	decreased tidal volume	Mammalian_phenotype	6
MP:0005590	MP:0005590	increased vasodilation	Mammalian_phenotype	6
MP:0005591	MP:0005591	decreased vasodilation	Mammalian_phenotype	6
MP:0005596	MP:0005596	increased susceptibility to type I hypersensitivity reaction	Mammalian_phenotype	6
MP:0005597	MP:0005597	decreased susceptibility to type I hypersensitivity reaction	Mammalian_phenotype	6
MP:0005598	MP:0005598	decreased ventricle muscle contractility	Mammalian_phenotype	6
MP:0005600	MP:0005600	increased ventricle muscle contractility	Mammalian_phenotype	6
MP:0005601	MP:0005601	increased angiogenesis	Mammalian_phenotype	6
MP:0005602	MP:0005602	decreased angiogenesis	Mammalian_phenotype	6
MP:0005606	MP:0005606	increased bleeding time	Mammalian_phenotype	6
MP:0005607	MP:0005607	decreased bleeding time	Mammalian_phenotype	6
MP:0005610	MP:0005610	increased circulating antidiuretic hormone level	Mammalian_phenotype	6
MP:0005611	MP:0005611	decreased circulating antidiuretic hormone level	Mammalian_phenotype	6
MP:0005612	MP:0005612	decreased susceptibility to type II hypersensitivity reaction	Mammalian_phenotype	6
MP:0005613	MP:0005613	increased susceptibility to type II hypersensitivity reaction	Mammalian_phenotype	6
MP:0005614	MP:0005614	decreased susceptibility to type III hypersensitivity reaction	Mammalian_phenotype	6
MP:0005615	MP:0005615	increased susceptibility to type III hypersensitivity reaction	Mammalian_phenotype	6
MP:0005616	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction	Mammalian_phenotype	6
MP:0005617	MP:0005617	increased susceptibility to type IV hypersensitivity reaction	Mammalian_phenotype	6
MP:0005618	MP:0005618	decreased urine potassium level	Mammalian_phenotype	6
MP:0005619	MP:0005619	increased urine potassium level	Mammalian_phenotype	6
MP:0005630	MP:0005630	increased lung weight	Mammalian_phenotype	6
MP:0005631	MP:0005631	decreased lung weight	Mammalian_phenotype	6
MP:0005638	MP:0005638	hemochromatosis	Mammalian_phenotype	6
MP:0005639	MP:0005639	hemosiderosis	Mammalian_phenotype	6
MP:0005648	MP:0005648	heart right ventricle degeneration	Mammalian_phenotype	6
MP:0005658	MP:0005658	increased susceptibility to diet-induced obesity	Mammalian_phenotype	6
MP:0005659	MP:0005659	decreased susceptibility to diet-induced obesity	Mammalian_phenotype	6
MP:0005661	MP:0005661	decreased circulating adrenaline level	Mammalian_phenotype	6
MP:0005662	MP:0005662	increased circulating adrenaline level	Mammalian_phenotype	6
MP:0005664	MP:0005664	decreased circulating noradrenaline level	Mammalian_phenotype	6
MP:0005665	MP:0005665	increased circulating noradrenaline level	Mammalian_phenotype	6
MP:0005668	MP:0005668	decreased circulating leptin level	Mammalian_phenotype	6
MP:0005669	MP:0005669	increased circulating leptin level	Mammalian_phenotype	6
MP:0006006	MP:0006006	increased sensory neuron number	Mammalian_phenotype	6
MP:0006011	MP:0006011	abnormal endolymphatic duct morphology	Mammalian_phenotype	6
MP:0006022	MP:0006022	absent Reissner membrane	Mammalian_phenotype	6
MP:0006023	MP:0006023	detached Reissner membrane	Mammalian_phenotype	6
MP:0006024	MP:0006024	collapsed Reissner membrane	Mammalian_phenotype	6
MP:0006025	MP:0006025	distended Reissner membrane	Mammalian_phenotype	6
MP:0006027	MP:0006027	impaired lung alveolus development	Mammalian_phenotype	6
MP:0006034	MP:0006034	myoglobinuria	Mammalian_phenotype	6
MP:0006044	MP:0006044	tricuspid valve regurgitation	Mammalian_phenotype	6
MP:0006045	MP:0006045	mitral valve regurgitation	Mammalian_phenotype	6
MP:0006047	MP:0006047	aortic valve regurgitation	Mammalian_phenotype	6
MP:0006048	MP:0006048	pulmonary valve regurgitation	Mammalian_phenotype	6
MP:0006056	MP:0006056	increased vascular endothelial cell number	Mammalian_phenotype	6
MP:0006057	MP:0006057	decreased vascular endothelial cell number	Mammalian_phenotype	6
MP:0006063	MP:0006063	abnormal inferior vena cava morphology	Mammalian_phenotype	6
MP:0006064	MP:0006064	abnormal superior vena cava morphology	Mammalian_phenotype	6
MP:0006068	MP:0006068	abnormal horizontal cell morphology	Mammalian_phenotype	6
MP:0006073	MP:0006073	abnormal retinal bipolar cell morphology	Mammalian_phenotype	6
MP:0006084	MP:0006084	abnormal circulating phospholipid level	Mammalian_phenotype	6
MP:0006085	MP:0006085	myocardial necrosis	Mammalian_phenotype	6
MP:0006086	MP:0006086	decreased body mass index	Mammalian_phenotype	6
MP:0006087	MP:0006087	increased body mass index	Mammalian_phenotype	6
MP:0006100	MP:0006100	abnormal tegmentum morphology	Mammalian_phenotype	6
MP:0006103	MP:0006103	abnormal midbrain roof plate morphology	Mammalian_phenotype	6
MP:0006110	MP:0006110	ventricular fibrillation	Mammalian_phenotype	6
MP:0006185	MP:0006185	retinal hemorrhage	Mammalian_phenotype	6
MP:0006186	MP:0006186	retinal fibrosis	Mammalian_phenotype	6
MP:0006187	MP:0006187	retinal deposits	Mammalian_phenotype	6
MP:0006193	MP:0006193	conjunctival telangiectasia	Mammalian_phenotype	6
MP:0006203	MP:0006203	eye hemorrhage	Mammalian_phenotype	6
MP:0006204	MP:0006204	embryonic lethality before implantation	Mammalian_phenotype	6
MP:0006207	MP:0006207	embryonic lethality during organogenesis	Mammalian_phenotype	6
MP:0006219	MP:0006219	optic nerve degeneration	Mammalian_phenotype	6
MP:0006220	MP:0006220	optic nerve compression	Mammalian_phenotype	6
MP:0006221	MP:0006221	optic nerve hypoplasia	Mammalian_phenotype	6
MP:0006222	MP:0006222	optic neuropathy	Mammalian_phenotype	6
MP:0006226	MP:0006226	iris hypoplasia	Mammalian_phenotype	6
MP:0006228	MP:0006228	iris atrophy	Mammalian_phenotype	6
MP:0006229	MP:0006229	iris inflammation	Mammalian_phenotype	6
MP:0006234	MP:0006234	iridoschisis	Mammalian_phenotype	6
MP:0006289	MP:0006289	otic capsule hypoplasia	Mammalian_phenotype	6
MP:0006291	MP:0006291	aprosencephaly	Mammalian_phenotype	6
MP:0006316	MP:0006316	increased urine sodium level	Mammalian_phenotype	6
MP:0006317	MP:0006317	decreased urine sodium level	Mammalian_phenotype	6
MP:0006341	MP:0006341	small first branchial arch	Mammalian_phenotype	6
MP:0006342	MP:0006342	absent first branchial arch	Mammalian_phenotype	6
MP:0006343	MP:0006343	enlarged first branchial arch	Mammalian_phenotype	6
MP:0006344	MP:0006344	small second branchial arch	Mammalian_phenotype	6
MP:0006345	MP:0006345	absent second branchial arch	Mammalian_phenotype	6
MP:0006348	MP:0006348	abnormal circulating copper level	Mammalian_phenotype	6
MP:0006354	MP:0006354	abnormal fourth branchial arch artery morphology	Mammalian_phenotype	6
MP:0006355	MP:0006355	abnormal sixth branchial arch artery morphology	Mammalian_phenotype	6
MP:0006356	MP:0006356	abnormal third branchial arch artery morphology	Mammalian_phenotype	6
MP:0006375	MP:0006375	increased circulating angiotensinogen level	Mammalian_phenotype	6
MP:0006376	MP:0006376	decreased circulating angiotensinogen level	Mammalian_phenotype	6
MP:0006378	MP:0006378	abnormal spermatogonia morphology	Mammalian_phenotype	6
MP:0006384	MP:0006384	enhanced cochlear frequency tuning	Mammalian_phenotype	6
MP:0006392	MP:0006392	abnormal nucleus pulposus morphology	Mammalian_phenotype	6
MP:0006396	MP:0006396	decreased long bone epiphyseal plate size	Mammalian_phenotype	6
MP:0006397	MP:0006397	disorganized long bone epiphyseal plate	Mammalian_phenotype	6
MP:0006398	MP:0006398	increased long bone epiphyseal plate size	Mammalian_phenotype	6
MP:0006399	MP:0006399	abnormal long bone epiphyseal ossification zone morphology	Mammalian_phenotype	6
MP:0006403	MP:0006403	abnormal cochlear endolymph ionic homeostasis	Mammalian_phenotype	6
MP:0006411	MP:0006411	upturned snout	Mammalian_phenotype	6
MP:0006413	MP:0006413	increased T cell apoptosis	Mammalian_phenotype	6
MP:0006414	MP:0006414	decreased T cell apoptosis	Mammalian_phenotype	6
MP:0006415	MP:0006415	absent testes	Mammalian_phenotype	6
MP:0006425	MP:0006425	absent Mullerian ducts	Mammalian_phenotype	6
MP:0006426	MP:0006426	Mullerian duct degeneration	Mammalian_phenotype	6
MP:0008031	MP:0008031	decreased Cajal-Retzius cell number	Mammalian_phenotype	6
MP:0008056	MP:0008056	abnormal retinal ganglion cell morphology	Mammalian_phenotype	6
MP:0008125	MP:0008125	abnormal dendritic cell number	Mammalian_phenotype	6
MP:0008129	MP:0008129	absent brain internal capsule	Mammalian_phenotype	6
MP:0008131	MP:0008131	abnormal Peyer's patch number	Mammalian_phenotype	6
MP:0008134	MP:0008134	abnormal Peyer's patch size	Mammalian_phenotype	6
MP:0008148	MP:0008148	abnormal rib-sternum attachment	Mammalian_phenotype	6
MP:0008152	MP:0008152	decreased diameter of femur	Mammalian_phenotype	6
MP:0008153	MP:0008153	decreased diameter of fibula	Mammalian_phenotype	6
MP:0008154	MP:0008154	decreased diameter of humerus	Mammalian_phenotype	6
MP:0008155	MP:0008155	decreased diameter of radius	Mammalian_phenotype	6
MP:0008156	MP:0008156	decreased diameter of tibia	Mammalian_phenotype	6
MP:0008157	MP:0008157	decreased diameter of ulna	Mammalian_phenotype	6
MP:0008158	MP:0008158	increased diameter of femur	Mammalian_phenotype	6
MP:0008159	MP:0008159	increased diameter of fibula	Mammalian_phenotype	6
MP:0008160	MP:0008160	increased diameter of humerus	Mammalian_phenotype	6
MP:0008161	MP:0008161	increased diameter of radius	Mammalian_phenotype	6
MP:0008162	MP:0008162	increased diameter of tibia	Mammalian_phenotype	6
MP:0008163	MP:0008163	increased diameter of ulna	Mammalian_phenotype	6
MP:0008201	MP:0008201	absent follicular dendritic cells	Mammalian_phenotype	6
MP:0008219	MP:0008219	abnormal dorsal telencephalic commissure morphology	Mammalian_phenotype	6
MP:0008220	MP:0008220	abnormal ventral commissure morphology	Mammalian_phenotype	6
MP:0008237	MP:0008237	abnormal ventral coat pigmentation	Mammalian_phenotype	6
MP:0008238	MP:0008238	abnormal dorsoventral coat patterning	Mammalian_phenotype	6
MP:0008241	MP:0008241	abnormal metallophilic macrophage morphology	Mammalian_phenotype	6
MP:0008245	MP:0008245	abnormal alveolar macrophage morphology	Mammalian_phenotype	6
MP:0008247	MP:0008247	abnormal mononuclear cell morphology	Mammalian_phenotype	6
MP:0008250	MP:0008250	abnormal myeloid leukocyte morphology	Mammalian_phenotype	6
MP:0008254	MP:0008254	increased megakaryocyte cell number	Mammalian_phenotype	6
MP:0008255	MP:0008255	decreased megakaryocyte cell number	Mammalian_phenotype	6
MP:0008261	MP:0008261	arrest of male meiosis	Mammalian_phenotype	6
MP:0008279	MP:0008279	arrest of spermiogenesis	Mammalian_phenotype	6
MP:0008297	MP:0008297	retention of the x-zone	Mammalian_phenotype	6
MP:0008301	MP:0008301	adrenal medulla hyperplasia	Mammalian_phenotype	6
MP:0008303	MP:0008303	early degeneration of the x-zone	Mammalian_phenotype	6
MP:0008314	MP:0008314	abnormal pterygopalatine ganglion morphology	Mammalian_phenotype	6
MP:0008315	MP:0008315	abnormal otic ganglion morphology	Mammalian_phenotype	6
MP:0008316	MP:0008316	abnormal prevertebral ganglion morphology	Mammalian_phenotype	6
MP:0008317	MP:0008317	abnormal paravertebral ganglion morphology	Mammalian_phenotype	6
MP:0008380	MP:0008380	abnormal gonial bone morphology	Mammalian_phenotype	6
MP:0008392	MP:0008392	decreased primordial germ cell number	Mammalian_phenotype	6
MP:0008394	MP:0008394	increased primordial germ cell number	Mammalian_phenotype	6
MP:0008402	MP:0008402	increased cellular sensitivity to alkylating agents	Mammalian_phenotype	6
MP:0008403	MP:0008403	decreased cellular sensitivity to alkylating agents	Mammalian_phenotype	6
MP:0008410	MP:0008410	increased cellular sensitivity to ultraviolet irradiation	Mammalian_phenotype	6
MP:0008411	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation	Mammalian_phenotype	6
MP:0008412	MP:0008412	increased cellular sensitivity to oxidative stress	Mammalian_phenotype	6
MP:0008413	MP:0008413	decreased cellular sensitivity to oxidative stress	Mammalian_phenotype	6
MP:0008429	MP:0008429	absent parotid gland	Mammalian_phenotype	6
MP:0008464	MP:0008464	absent peripheral lymph nodes	Mammalian_phenotype	6
MP:0008470	MP:0008470	abnormal spleen B cell follicle morphology	Mammalian_phenotype	6
MP:0008475	MP:0008475	intermingled spleen red and white pulp	Mammalian_phenotype	6
MP:0008476	MP:0008476	increased spleen red pulp amount	Mammalian_phenotype	6
MP:0008477	MP:0008477	decreased spleen red pulp amount	Mammalian_phenotype	6
MP:0008478	MP:0008478	increased spleen white pulp amount	Mammalian_phenotype	6
MP:0008479	MP:0008479	decreased spleen white pulp amount	Mammalian_phenotype	6
MP:0008488	MP:0008488	abnormal semicircular canal ampulla morphology	Mammalian_phenotype	6
MP:0008505	MP:0008505	absent adrenal chromaffin cells	Mammalian_phenotype	6
MP:0008506	MP:0008506	abnormal noradrenergic chromaffin cell morphology	Mammalian_phenotype	6
MP:0008527	MP:0008527	embryonic lethality at implantation	Mammalian_phenotype	6
MP:0008529	MP:0008529	enlarged optic nerve	Mammalian_phenotype	6
MP:0008531	MP:0008531	increased chemical nociceptive threshold	Mammalian_phenotype	6
MP:0008532	MP:0008532	decreased chemical nociceptive threshold	Mammalian_phenotype	6
MP:0008540	MP:0008540	abnormal cerebrum morphology	Mammalian_phenotype	6
MP:0008543	MP:0008543	atrial fibrillation	Mammalian_phenotype	6
MP:0008557	MP:0008557	abnormal interferon-alpha secretion	Mammalian_phenotype	6
MP:0008558	MP:0008558	abnormal interferon-beta secretion	Mammalian_phenotype	6
MP:0008559	MP:0008559	abnormal interferon-gamma secretion	Mammalian_phenotype	6
MP:0008560	MP:0008560	increased tumor necrosis factor secretion	Mammalian_phenotype	6
MP:0008561	MP:0008561	decreased tumor necrosis factor secretion	Mammalian_phenotype	6
MP:0008571	MP:0008571	abnormal synaptic bouton morphology	Mammalian_phenotype	6
MP:0008572	MP:0008572	abnormal Purkinje cell dendrite morphology	Mammalian_phenotype	6
MP:0008650	MP:0008650	abnormal interleukin-1 secretion	Mammalian_phenotype	6
MP:0008659	MP:0008659	abnormal interleukin-10 secretion	Mammalian_phenotype	6
MP:0008662	MP:0008662	abnormal interleukin-12 secretion	Mammalian_phenotype	6
MP:0008668	MP:0008668	abnormal interleukin-12b secretion	Mammalian_phenotype	6
MP:0008671	MP:0008671	abnormal interleukin-13 secretion	Mammalian_phenotype	6
MP:0008674	MP:0008674	abnormal interleukin-15 secretion	Mammalian_phenotype	6
MP:0008677	MP:0008677	abnormal interleukin-16 secretion	Mammalian_phenotype	6
MP:0008680	MP:0008680	abnormal interleukin-17 secretion	Mammalian_phenotype	6
MP:0008683	MP:0008683	abnormal interleukin-18 secretion	Mammalian_phenotype	6
MP:0008686	MP:0008686	abnormal interleukin-2 secretion	Mammalian_phenotype	6
MP:0008689	MP:0008689	abnormal interleukin-23 secretion	Mammalian_phenotype	6
MP:0008695	MP:0008695	abnormal interleukin-3 secretion	Mammalian_phenotype	6
MP:0008698	MP:0008698	abnormal interleukin-4 secretion	Mammalian_phenotype	6
MP:0008701	MP:0008701	abnormal interleukin-5 secretion	Mammalian_phenotype	6
MP:0008704	MP:0008704	abnormal interleukin-6 secretion	Mammalian_phenotype	6
MP:0008707	MP:0008707	abnormal interleukin-7 secretion	Mammalian_phenotype	6
MP:0008710	MP:0008710	abnormal interleukin-9 secretion	Mammalian_phenotype	6
MP:0008721	MP:0008721	abnormal chemokine level	Mammalian_phenotype	6
MP:0008726	MP:0008726	enlarged heart left atrium	Mammalian_phenotype	6
MP:0008727	MP:0008727	enlarged heart right atrium	Mammalian_phenotype	6
MP:0008730	MP:0008730	fused phalanges	Mammalian_phenotype	6
MP:0008734	MP:0008734	decreased susceptibility to endotoxin shock	Mammalian_phenotype	6
MP:0008735	MP:0008735	increased susceptibility to endotoxin shock	Mammalian_phenotype	6
MP:0008745	MP:0008745	abnormal central B cell anergy	Mammalian_phenotype	6
MP:0008746	MP:0008746	abnormal peripheral B cell anergy	Mammalian_phenotype	6
MP:0008748	MP:0008748	abnormal central T cell anergy	Mammalian_phenotype	6
MP:0008749	MP:0008749	abnormal peripheral T cell anergy	Mammalian_phenotype	6
MP:0008750	MP:0008750	abnormal interferon level	Mammalian_phenotype	6
MP:0008751	MP:0008751	abnormal interleukin level	Mammalian_phenotype	6
MP:0008752	MP:0008752	abnormal tumor necrosis factor level	Mammalian_phenotype	6
MP:0008767	MP:0008767	abnormal hair medullary septa cells	Mammalian_phenotype	6
MP:0008768	MP:0008768	abnormal hair medulla air spaces	Mammalian_phenotype	6
MP:0008769	MP:0008769	abnormal plasmacytoid dendritic cell physiology	Mammalian_phenotype	6
MP:0008782	MP:0008782	increased B cell apoptosis	Mammalian_phenotype	6
MP:0008783	MP:0008783	decreased B cell apoptosis	Mammalian_phenotype	6
MP:0008785	MP:0008785	abnormal sternum manubrium morphology	Mammalian_phenotype	6
MP:0008794	MP:0008794	increased lens epithelium apoptosis	Mammalian_phenotype	6
MP:0008796	MP:0008796	increased lens fiber apoptosis	Mammalian_phenotype	6
MP:0008798	MP:0008798	lateral facial cleft	Mammalian_phenotype	6
MP:0008799	MP:0008799	oblique facial cleft	Mammalian_phenotype	6
MP:0008803	MP:0008803	abnormal placental labyrinth vasculature morphology	Mammalian_phenotype	6
MP:0008804	MP:0008804	abnormal circulating amylase level	Mammalian_phenotype	6
MP:0008812	MP:0008812	abnormal rostrocaudal coat patterning	Mammalian_phenotype	6
MP:0008813	MP:0008813	decreased common myeloid progenitor cell number	Mammalian_phenotype	6
MP:0008816	MP:0008816	petechiae	Mammalian_phenotype	6
MP:0008823	MP:0008823	abnormal interventricular septum membranous part morphology	Mammalian_phenotype	6
MP:0008832	MP:0008832	hemivertebra	Mammalian_phenotype	6
MP:0008837	MP:0008837	increased transforming growth factor level	Mammalian_phenotype	6
MP:0008838	MP:0008838	decreased transforming growth factor level	Mammalian_phenotype	6
MP:0008840	MP:0008840	abnormal spike wave discharge	Mammalian_phenotype	6
MP:0008841	MP:0008841	ruptured lens capsule	Mammalian_phenotype	6
MP:0008857	MP:0008857	myelencephalic blebs	Mammalian_phenotype	6
MP:0008862	MP:0008862	asymmetric snout	Mammalian_phenotype	6
MP:0008879	MP:0008879	submandibular gland inflammation	Mammalian_phenotype	6
MP:0008885	MP:0008885	increased enterocyte apoptosis	Mammalian_phenotype	6
MP:0008901	MP:0008901	absent epididymal fat pad	Mammalian_phenotype	6
MP:0008910	MP:0008910	thin long bone epiphysis	Mammalian_phenotype	6
MP:0008915	MP:0008915	fused carpal bones	Mammalian_phenotype	6
MP:0008919	MP:0008919	fused tarsal bones	Mammalian_phenotype	6
MP:0008921	MP:0008921	increased neurotransmitter release	Mammalian_phenotype	6
MP:0008922	MP:0008922	abnormal cervical rib	Mammalian_phenotype	6
MP:0008924	MP:0008924	decreased cerebellar granule cell number	Mammalian_phenotype	6
MP:0008925	MP:0008925	increased cerebellar granule cell number	Mammalian_phenotype	6
MP:0008949	MP:0008949	increased Cajal-Retzius cell number	Mammalian_phenotype	6
MP:0008950	MP:0008950	ventricular tachycardia	Mammalian_phenotype	6
MP:0008951	MP:0008951	long radius	Mammalian_phenotype	6
MP:0008967	MP:0008967	absent chiasmata formation	Mammalian_phenotype	6
MP:0008988	MP:0008988	abnormal liver perisinusoidal space morphology	Mammalian_phenotype	6
MP:0008991	MP:0008991	abnormal bile canaliculus morphology	Mammalian_phenotype	6
MP:0008993	MP:0008993	abnormal portal triad morphology	Mammalian_phenotype	6
MP:0009000	MP:0009000	absent cecum	Mammalian_phenotype	6
MP:0009001	MP:0009001	absent hallux	Mammalian_phenotype	6
MP:0009002	MP:0009002	premature hair regrowth	Mammalian_phenotype	6
MP:0009004	MP:0009004	progressive hair loss	Mammalian_phenotype	6
MP:0009006	MP:0009006	prolonged estrous cycle	Mammalian_phenotype	6
MP:0009007	MP:0009007	short estrous cycle	Mammalian_phenotype	6
MP:0009008	MP:0009008	delayed estrous cycle	Mammalian_phenotype	6
MP:0009009	MP:0009009	absent estrous cycle	Mammalian_phenotype	6
MP:0009010	MP:0009010	abnormal diestrus	Mammalian_phenotype	6
MP:0009013	MP:0009013	abnormal proestrus	Mammalian_phenotype	6
MP:0009016	MP:0009016	abnormal estrus	Mammalian_phenotype	6
MP:0009019	MP:0009019	abnormal metestrus	Mammalian_phenotype	6
MP:0000024	MP:0000024	lowered ear position	Mammalian_phenotype	6
MP:0000025	MP:0000025	otic hypertelorism	Mammalian_phenotype	6
MP:0000029	MP:0000029	abnormal malleus morphology	Mammalian_phenotype	6
MP:0000036	MP:0000036	absent semicircular canals	Mammalian_phenotype	6
MP:0000037	MP:0000037	abnormal lateral semicircular canal morphology	Mammalian_phenotype	6
MP:0000040	MP:0000040	absent middle ear ossicles	Mammalian_phenotype	6
MP:0000043	MP:0000043	organ of Corti degeneration	Mammalian_phenotype	6
MP:0000069	MP:0000069	kyphoscoliosis	Mammalian_phenotype	6
MP:0000074	MP:0000074	abnormal neurocranium morphology	Mammalian_phenotype	6
MP:0000081	MP:0000081	premature suture closure	Mammalian_phenotype	6
MP:0000108	MP:0000108	midline facial cleft	Mammalian_phenotype	6
MP:0000120	MP:0000120	malocclusion	Mammalian_phenotype	6
MP:0000132	MP:0000132	thickened long bone epiphysis	Mammalian_phenotype	6
MP:0000135	MP:0000135	decreased compact bone thickness	Mammalian_phenotype	6
MP:0000138	MP:0000138	absent vertebrae	Mammalian_phenotype	6
MP:0000141	MP:0000141	abnormal vertebral body morphology	Mammalian_phenotype	6
MP:0000153	MP:0000153	rib bifurcation	Mammalian_phenotype	6
MP:0000154	MP:0000154	rib fusion	Mammalian_phenotype	6
MP:0000155	MP:0000155	asymmetric rib attachment	Mammalian_phenotype	6
MP:0000158	MP:0000158	absent sternum	Mammalian_phenotype	6
MP:0000159	MP:0000159	abnormal xiphoid process morphology	Mammalian_phenotype	6
MP:0000160	MP:0000160	kyphosis	Mammalian_phenotype	6
MP:0000161	MP:0000161	scoliosis	Mammalian_phenotype	6
MP:0000162	MP:0000162	lordosis	Mammalian_phenotype	6
MP:0000175	MP:0000175	absent bone marrow cell	Mammalian_phenotype	6
MP:0000180	MP:0000180	abnormal circulating cholesterol level	Mammalian_phenotype	6
MP:0000189	MP:0000189	hypoglycemia	Mammalian_phenotype	6
MP:0000202	MP:0000202	abnormal circulating alkaline phosphatase level	Mammalian_phenotype	6
MP:0000203	MP:0000203	abnormal circulating aspartate transaminase level	Mammalian_phenotype	6
MP:0000217	MP:0000217	abnormal leukocyte cell number	Mammalian_phenotype	6
MP:0000263	MP:0000263	absent organized vascular network	Mammalian_phenotype	6
MP:0000272	MP:0000272	abnormal aorta morphology	Mammalian_phenotype	6
MP:0000273	MP:0000273	overriding aortic valve	Mammalian_phenotype	6
MP:0000275	MP:0000275	heart hyperplasia	Mammalian_phenotype	6
MP:0000280	MP:0000280	thin ventricular wall	Mammalian_phenotype	6
MP:0000284	MP:0000284	double outlet right ventricle	Mammalian_phenotype	6
MP:0000286	MP:0000286	abnormal mitral valve morphology	Mammalian_phenotype	6
MP:0000297	MP:0000297	abnormal atrioventricular cushion morphology	Mammalian_phenotype	6
MP:0000315	MP:0000315	hemoglobinuria	Mammalian_phenotype	6
MP:0000370	MP:0000370	head blaze	Mammalian_phenotype	6
MP:0000371	MP:0000371	diluted coat color	Mammalian_phenotype	6
MP:0000372	MP:0000372	irregular coat pigmentation	Mammalian_phenotype	6
MP:0000390	MP:0000390	disorganized matrix sheath cells	Mammalian_phenotype	6
MP:0000412	MP:0000412	excessive hair	Mammalian_phenotype	6
MP:0000413	MP:0000413	polyphalangy	Mammalian_phenotype	6
MP:0000414	MP:0000414	alopecia	Mammalian_phenotype	6
MP:0000416	MP:0000416	sparse hair	Mammalian_phenotype	6
MP:0000417	MP:0000417	short hair	Mammalian_phenotype	6
MP:0000418	MP:0000418	focal hair loss	Mammalian_phenotype	6
MP:0000422	MP:0000422	delayed hair appearance	Mammalian_phenotype	6
MP:0000424	MP:0000424	retarded hair growth	Mammalian_phenotype	6
MP:0000426	MP:0000426	ectopic hair growth	Mammalian_phenotype	6
MP:0000436	MP:0000436	abnormal head movements	Mammalian_phenotype	6
MP:0000440	MP:0000440	domed cranium	Mammalian_phenotype	6
MP:0000445	MP:0000445	short snout	Mammalian_phenotype	6
MP:0000446	MP:0000446	long snout	Mammalian_phenotype	6
MP:0000447	MP:0000447	flattened snout	Mammalian_phenotype	6
MP:0000448	MP:0000448	pointed snout	Mammalian_phenotype	6
MP:0000449	MP:0000449	broad nasal bridge	Mammalian_phenotype	6
MP:0000450	MP:0000450	absent snout	Mammalian_phenotype	6
MP:0000451	MP:0000451	scaly muzzle	Mammalian_phenotype	6
MP:0000452	MP:0000452	abnormal mouth morphology	Mammalian_phenotype	6
MP:0000459	MP:0000459	abnormal presacral vertebrae morphology	Mammalian_phenotype	6
MP:0000471	MP:0000471	abnormal stomach epithelium morphology	Mammalian_phenotype	6
MP:0000480	MP:0000480	increased rib number	Mammalian_phenotype	6
MP:0000481	MP:0000481	abnormal enterocyte cell number	Mammalian_phenotype	6
MP:0000482	MP:0000482	long fibula	Mammalian_phenotype	6
MP:0000493	MP:0000493	rectal prolapse	Mammalian_phenotype	6
MP:0000498	MP:0000498	absent jejunum	Mammalian_phenotype	6
MP:0000499	MP:0000499	absent ileum	Mammalian_phenotype	6
MP:0000504	MP:0000504	excessive digestive mucosecretion	Mammalian_phenotype	6
MP:0000506	MP:0000506	decreased digestive mucosecretion	Mammalian_phenotype	6
MP:0000509	MP:0000509	absent digestive mucosecretion	Mammalian_phenotype	6
MP:0000510	MP:0000510	remittent intestinal hemorrhage	Mammalian_phenotype	6
MP:0000524	MP:0000524	decreased renal tubule number	Mammalian_phenotype	6
MP:0000526	MP:0000526	small inner medullary pyramid	Mammalian_phenotype	6
MP:0000543	MP:0000543	absent urinary bladder transitional epithelium	Mammalian_phenotype	6
MP:0000544	MP:0000544	thin urinary bladder transitional epithelium	Mammalian_phenotype	6
MP:0000555	MP:0000555	absent carpal bone	Mammalian_phenotype	6
MP:0000571	MP:0000571	interdigital webbing	Mammalian_phenotype	6
MP:0000600	MP:0000600	liver hypoplasia	Mammalian_phenotype	6
MP:0000607	MP:0000607	abnormal hepatocyte morphology	Mammalian_phenotype	6
MP:0000629	MP:0000629	absent mammary gland	Mammalian_phenotype	6
MP:0000646	MP:0000646	enlarged adrenocortical cells	Mammalian_phenotype	6
MP:0000688	MP:0000688	lymphoid hyperplasia	Mammalian_phenotype	6
MP:0000691	MP:0000691	enlarged spleen	Mammalian_phenotype	6
MP:0000692	MP:0000692	small spleen	Mammalian_phenotype	6
MP:0000702	MP:0000702	enlarged lymph nodes	Mammalian_phenotype	6
MP:0000706	MP:0000706	small thymus	Mammalian_phenotype	6
MP:0000709	MP:0000709	enlarged thymus	Mammalian_phenotype	6
MP:0000755	MP:0000755	hindlimb paralysis	Mammalian_phenotype	6
MP:0000756	MP:0000756	forelimb paralysis	Mammalian_phenotype	6
MP:0000761	MP:0000761	thin diaphragm muscle	Mammalian_phenotype	6
MP:0000785	MP:0000785	telencephalon hypoplasia	Mammalian_phenotype	6
MP:0000807	MP:0000807	abnormal hippocampus morphology	Mammalian_phenotype	6
MP:0000808	MP:0000808	abnormal hippocampus development	Mammalian_phenotype	6
MP:0000818	MP:0000818	abnormal amygdala morphology	Mammalian_phenotype	6
MP:0000820	MP:0000820	abnormal choroid plexus morphology	Mammalian_phenotype	6
MP:0000823	MP:0000823	abnormal lateral ventricle morphology	Mammalian_phenotype	6
MP:0000826	MP:0000826	abnormal third ventricle morphology	Mammalian_phenotype	6
MP:0000831	MP:0000831	diencephalon hyperplasia	Mammalian_phenotype	6
MP:0000832	MP:0000832	abnormal thalamus morphology	Mammalian_phenotype	6
MP:0000834	MP:0000834	abnormal subthalamus morphology	Mammalian_phenotype	6
MP:0000835	MP:0000835	abnormal subthalamic nucleus morphology	Mammalian_phenotype	6
MP:0000836	MP:0000836	abnormal substantia nigra morphology	Mammalian_phenotype	6
MP:0000837	MP:0000837	abnormal hypothalamus morphology	Mammalian_phenotype	6
MP:0000840	MP:0000840	abnormal epithalamus morphology	Mammalian_phenotype	6
MP:0000849	MP:0000849	abnormal cerebellum morphology	Mammalian_phenotype	6
MP:0000854	MP:0000854	abnormal cerebellum development	Mammalian_phenotype	6
MP:0000879	MP:0000879	increased Purkinje cell number	Mammalian_phenotype	6
MP:0000880	MP:0000880	decreased Purkinje cell number	Mammalian_phenotype	6
MP:0000906	MP:0000906	abnormal trigeminal V mesencephalic nucleus morphology	Mammalian_phenotype	6
MP:0000917	MP:0000917	obstructive hydrocephaly	Mammalian_phenotype	6
MP:0000919	MP:0000919	cranioschisis	Mammalian_phenotype	6
MP:0000924	MP:0000924	absent roof plate	Mammalian_phenotype	6
MP:0000926	MP:0000926	absent floor plate	Mammalian_phenotype	6
MP:0000927	MP:0000927	small floor plate	Mammalian_phenotype	6
MP:0000928	MP:0000928	incomplete rostral neuropore closure	Mammalian_phenotype	6
MP:0000929	MP:0000929	open neural tube	Mammalian_phenotype	6
MP:0000933	MP:0000933	abnormal rhombomere morphology	Mammalian_phenotype	6
MP:0000934	MP:0000934	abnormal telencephalon development	Mammalian_phenotype	6
MP:0000939	MP:0000939	decreased motor neuron number	Mammalian_phenotype	6
MP:0000961	MP:0000961	abnormal dorsal root ganglion morphology	Mammalian_phenotype	6
MP:0000966	MP:0000966	decreased sensory neuron number	Mammalian_phenotype	6
MP:0000969	MP:0000969	abnormal nociceptor morphology	Mammalian_phenotype	6
MP:0000970	MP:0000970	abnormal polymodal receptor morphology	Mammalian_phenotype	6
MP:0000971	MP:0000971	abnormal thermoreceptor morphology	Mammalian_phenotype	6
MP:0000972	MP:0000972	abnormal mechanoreceptor morphology	Mammalian_phenotype	6
MP:0001001	MP:0001001	abnormal chemoreceptor morphology	Mammalian_phenotype	6
MP:0001004	MP:0001004	abnormal retinal photoreceptor morphology	Mammalian_phenotype	6
MP:0001035	MP:0001035	abnormal submandibular ganglion morphology	Mammalian_phenotype	6
MP:0001048	MP:0001048	absent enteric neurons	Mammalian_phenotype	6
MP:0001054	MP:0001054	failure of neuromuscular synapse presynaptic differentiation	Mammalian_phenotype	6
MP:0001055	MP:0001055	failure of neuromuscular synapse postsynaptic differentiation	Mammalian_phenotype	6
MP:0001059	MP:0001059	optic nerve atrophy	Mammalian_phenotype	6
MP:0001062	MP:0001062	absent oculomotor nerve	Mammalian_phenotype	6
MP:0001064	MP:0001064	absent trochlear nerve	Mammalian_phenotype	6
MP:0001066	MP:0001066	absent trigeminal nerve	Mammalian_phenotype	6
MP:0001069	MP:0001069	absent trigeminal nerve connections to hindbrain	Mammalian_phenotype	6
MP:0001079	MP:0001079	absent phrenic nerve	Mammalian_phenotype	6
MP:0001080	MP:0001080	defasiculated phrenic nerve	Mammalian_phenotype	6
MP:0001084	MP:0001084	abnormal petrosal ganglion morphology	Mammalian_phenotype	6
MP:0001087	MP:0001087	abnormal nodose ganglion morphology	Mammalian_phenotype	6
MP:0001097	MP:0001097	abnormal superior glossopharyngeal ganglion morphology	Mammalian_phenotype	6
MP:0001101	MP:0001101	abnormal superior vagus ganglion morphology	Mammalian_phenotype	6
MP:0001107	MP:0001107	decreased Schwann cell number	Mammalian_phenotype	6
MP:0001117	MP:0001117	absent gametes	Mammalian_phenotype	6
MP:0001120	MP:0001120	abnormal uterus morphology	Mammalian_phenotype	6
MP:0001127	MP:0001127	small ovary	Mammalian_phenotype	6
MP:0001139	MP:0001139	abnormal vagina morphology	Mammalian_phenotype	6
MP:0001147	MP:0001147	small testis	Mammalian_phenotype	6
MP:0001178	MP:0001178	pulmonary hypoplasia	Mammalian_phenotype	6
MP:0001194	MP:0001194	dermatitis	Mammalian_phenotype	6
MP:0001261	MP:0001261	obese	Mammalian_phenotype	6
MP:0001263	MP:0001263	weight loss	Mammalian_phenotype	6
MP:0001288	MP:0001288	abnormal lens induction	Mammalian_phenotype	6
MP:0001309	MP:0001309	hydropic eye lens fibers	Mammalian_phenotype	6
MP:0001317	MP:0001317	abnormal pupil morphology	Mammalian_phenotype	6
MP:0001326	MP:0001326	retinal degeneration	Mammalian_phenotype	6
MP:0001329	MP:0001329	retina hyperplasia	Mammalian_phenotype	6
MP:0001332	MP:0001332	abnormal optic nerve innervation	Mammalian_phenotype	6
MP:0001333	MP:0001333	absent optic nerve	Mammalian_phenotype	6
MP:0001334	MP:0001334	absent optic tract	Mammalian_phenotype	6
MP:0001357	MP:0001357	increased aggression toward humans	Mammalian_phenotype	6
MP:0001358	MP:0001358	aggression toward inanimate objects	Mammalian_phenotype	6
MP:0001363	MP:0001363	increased anxiety-related response	Mammalian_phenotype	6
MP:0001364	MP:0001364	decreased anxiety-related response	Mammalian_phenotype	6
MP:0001380	MP:0001380	reduced male mating frequency	Mammalian_phenotype	6
MP:0001386	MP:0001386	abnormal maternal nurturing	Mammalian_phenotype	6
MP:0001391	MP:0001391	abnormal tail movements	Mammalian_phenotype	6
MP:0001395	MP:0001395	bidirectional circling	Mammalian_phenotype	6
MP:0001396	MP:0001396	unidirectional circling	Mammalian_phenotype	6
MP:0001415	MP:0001415	increased exploration in new environment	Mammalian_phenotype	6
MP:0001417	MP:0001417	decreased exploration in new environment	Mammalian_phenotype	6
MP:0001435	MP:0001435	no suckling reflex	Mammalian_phenotype	6
MP:0001437	MP:0001437	no swallowing reflex	Mammalian_phenotype	6
MP:0001438	MP:0001438	aphagia	Mammalian_phenotype	6
MP:0001473	MP:0001473	reduced long term potentiation	Mammalian_phenotype	6
MP:0001485	MP:0001485	abnormal pinna reflex	Mammalian_phenotype	6
MP:0001486	MP:0001486	abnormal startle reflex	Mammalian_phenotype	6
MP:0001490	MP:0001490	abnormal vibrissae reflex	Mammalian_phenotype	6
MP:0001491	MP:0001491	unresponsive to tactile stimuli	Mammalian_phenotype	6
MP:0001492	MP:0001492	abnormal pilomotor reflex	Mammalian_phenotype	6
MP:0001499	MP:0001499	abnormal kindling response	Mammalian_phenotype	6
MP:0001513	MP:0001513	limb grasping	Mammalian_phenotype	6
MP:0001548	MP:0001548	hyperlipidemia	Mammalian_phenotype	6
MP:0001553	MP:0001553	abnormal circulating free fatty acids level	Mammalian_phenotype	6
MP:0001559	MP:0001559	hyperglycemia	Mammalian_phenotype	6
MP:0001573	MP:0001573	abnormal circulating alanine transaminase level	Mammalian_phenotype	6
MP:0001586	MP:0001586	abnormal erythrocyte cell number	Mammalian_phenotype	6
MP:0001601	MP:0001601	abnormal myelopoiesis	Mammalian_phenotype	6
MP:0001625	MP:0001625	cardiac hypertrophy	Mammalian_phenotype	6
MP:0001652	MP:0001652	colonic necrosis	Mammalian_phenotype	6
MP:0001658	MP:0001658	increased mortality induced by gamma-irradiation	Mammalian_phenotype	6
MP:0001668	MP:0001668	abnormal fructose absorption	Mammalian_phenotype	6
MP:0001669	MP:0001669	abnormal glucose absorption	Mammalian_phenotype	6
MP:0001675	MP:0001675	abnormal ectoderm development	Mammalian_phenotype	6
MP:0001680	MP:0001680	abnormal mesoderm development	Mammalian_phenotype	6
MP:0001685	MP:0001685	abnormal endoderm development	Mammalian_phenotype	6
MP:0001689	MP:0001689	incomplete somite formation	Mammalian_phenotype	6
MP:0001690	MP:0001690	failure of somite differentiation	Mammalian_phenotype	6
MP:0001701	MP:0001701	incomplete embryo turning	Mammalian_phenotype	6
MP:0001719	MP:0001719	absent vitelline blood vessels	Mammalian_phenotype	6
MP:0001721	MP:0001721	absent visceral yolk sac blood islands	Mammalian_phenotype	6
MP:0001728	MP:0001728	failure of embryo implantation	Mammalian_phenotype	6
MP:0001729	MP:0001729	impaired embryo implantation	Mammalian_phenotype	6
MP:0001742	MP:0001742	absent circulating adrenaline	Mammalian_phenotype	6
MP:0001743	MP:0001743	absent circulating noradrenaline	Mammalian_phenotype	6
MP:0001747	MP:0001747	hypersecretion of adrenocorticotropin	Mammalian_phenotype	6
MP:0001798	MP:0001798	impaired macrophage phagocytosis	Mammalian_phenotype	6
MP:0001840	MP:0001840	increased level of surface class I molecules	Mammalian_phenotype	6
MP:0001841	MP:0001841	decreased level of surface class I molecules	Mammalian_phenotype	6
MP:0001847	MP:0001847	brain inflammation	Mammalian_phenotype	6
MP:0001848	MP:0001848	choroid inflammation	Mammalian_phenotype	6
MP:0001850	MP:0001850	increased susceptibility to otitis media	Mammalian_phenotype	6
MP:0001854	MP:0001854	atrial endocarditis	Mammalian_phenotype	6
MP:0001856	MP:0001856	myocarditis	Mammalian_phenotype	6
MP:0001857	MP:0001857	pericarditis	Mammalian_phenotype	6
MP:0001861	MP:0001861	lung inflammation	Mammalian_phenotype	6
MP:0001864	MP:0001864	vasculitis	Mammalian_phenotype	6
MP:0001866	MP:0001866	nasal inflammation	Mammalian_phenotype	6
MP:0001872	MP:0001872	sinus inflammation	Mammalian_phenotype	6
MP:0001874	MP:0001874	acanthosis	Mammalian_phenotype	6
MP:0001884	MP:0001884	mammary gland alveolar hyperplasia	Mammalian_phenotype	6
MP:0001893	MP:0001893	non-obstructive hydrocephaly	Mammalian_phenotype	6
MP:0001898	MP:0001898	abnormal long term depression	Mammalian_phenotype	6
MP:0001938	MP:0001938	delayed sexual maturation	Mammalian_phenotype	6
MP:0001954	MP:0001954	respiratory distress	Mammalian_phenotype	6
MP:0001956	MP:0001956	hypopnea	Mammalian_phenotype	6
MP:0001957	MP:0001957	apnea	Mammalian_phenotype	6
MP:0001973	MP:0001973	increased thermal nociceptive threshold	Mammalian_phenotype	6
MP:0001980	MP:0001980	abnormal chemically-elicited antinociception	Mammalian_phenotype	6
MP:0001993	MP:0001993	abnormal blinking	Mammalian_phenotype	6
MP:0002014	MP:0002014	increased papilloma incidence	Mammalian_phenotype	6
MP:0002018	MP:0002018	increased malignant tumor incidence	Mammalian_phenotype	6
MP:0002026	MP:0002026	increased leukemia incidence	Mammalian_phenotype	6
MP:0002058	MP:0002058	neonatal lethality	Mammalian_phenotype	6
MP:0002079	MP:0002079	increased circulating insulin level	Mammalian_phenotype	6
MP:0002119	MP:0002119	dipsosis	Mammalian_phenotype	6
MP:0002175	MP:0002175	decreased brain weight	Mammalian_phenotype	6
MP:0002176	MP:0002176	increased brain weight	Mammalian_phenotype	6
MP:0002190	MP:0002190	disorganized myocardium	Mammalian_phenotype	6
MP:0002193	MP:0002193	minimal clonic seizures	Mammalian_phenotype	6
MP:0002194	MP:0002194	maximal tonic hindlimb extension seizures	Mammalian_phenotype	6
MP:0002195	MP:0002195	psychomotor seizures	Mammalian_phenotype	6
MP:0002217	MP:0002217	small lymph nodes	Mammalian_phenotype	6
MP:0002218	MP:0002218	increased lymph node number	Mammalian_phenotype	6
MP:0002219	MP:0002219	decreased lymph node number	Mammalian_phenotype	6
MP:0002223	MP:0002223	lymphoid hypoplasia	Mammalian_phenotype	6
MP:0002230	MP:0002230	abnormal primitive streak formation	Mammalian_phenotype	6
MP:0002235	MP:0002235	abnormal external nares morphology	Mammalian_phenotype	6
MP:0002236	MP:0002236	abnormal internal nares morphology	Mammalian_phenotype	6
MP:0002237	MP:0002237	abnormal nasal cavity morphology	Mammalian_phenotype	6
MP:0002239	MP:0002239	abnormal nasal septum morphology	Mammalian_phenotype	6
MP:0002241	MP:0002241	abnormal laryngeal mucosa goblet cell morphology	Mammalian_phenotype	6
MP:0002244	MP:0002244	abnormal turbinate morphology	Mammalian_phenotype	6
MP:0002245	MP:0002245	abnormal ethmoid sinus morphology	Mammalian_phenotype	6
MP:0002246	MP:0002246	abnormal frontal sinus morphology	Mammalian_phenotype	6
MP:0002247	MP:0002247	abnormal maxillary sinus morphology	Mammalian_phenotype	6
MP:0002248	MP:0002248	abnormal sphenoid sinus morphology	Mammalian_phenotype	6
MP:0002265	MP:0002265	abnormal left major bronchus morphology	Mammalian_phenotype	6
MP:0002266	MP:0002266	abnormal right major bronchus morphology	Mammalian_phenotype	6
MP:0002268	MP:0002268	abnormal terminal bronchiole morphology	Mammalian_phenotype	6
MP:0002270	MP:0002270	abnormal pulmonary alveolus morphology	Mammalian_phenotype	6
MP:0002271	MP:0002271	abnormal pulmonary alveolar duct morphology	Mammalian_phenotype	6
MP:0002273	MP:0002273	abnormal pulmonary alveolus epithelial cell morphology	Mammalian_phenotype	6
MP:0002325	MP:0002325	abnormal pulmonary diffusing capacity	Mammalian_phenotype	6
MP:0002334	MP:0002334	abnormal airway responsiveness	Mammalian_phenotype	6
MP:0002340	MP:0002340	abnormal axillary lymph node morphology	Mammalian_phenotype	6
MP:0002344	MP:0002344	abnormal lymph node B cell domain morphology	Mammalian_phenotype	6
MP:0002347	MP:0002347	abnormal lymph node T cell domain morphology	Mammalian_phenotype	6
MP:0002351	MP:0002351	abnormal cervical lymph node morphology	Mammalian_phenotype	6
MP:0002352	MP:0002352	abnormal popliteal lymph node morphology	Mammalian_phenotype	6
MP:0002353	MP:0002353	abnormal inguinal lymph node morphology	Mammalian_phenotype	6
MP:0002358	MP:0002358	abnormal spleen periarteriolar lymphoid sheath morphology	Mammalian_phenotype	6
MP:0002361	MP:0002361	abnormal spleen central arteriole morphology	Mammalian_phenotype	6
MP:0002362	MP:0002362	abnormal spleen marginal zone morphology	Mammalian_phenotype	6
MP:0002363	MP:0002363	abnormal spleen marginal sinus morphology	Mammalian_phenotype	6
MP:0002369	MP:0002369	abnormal thymus subcapsular epithelium morphology	Mammalian_phenotype	6
MP:0002371	MP:0002371	abnormal thymus cortex morphology	Mammalian_phenotype	6
MP:0002375	MP:0002375	abnormal thymus medulla morphology	Mammalian_phenotype	6
MP:0002380	MP:0002380	abnormal palatine tonsil morphology	Mammalian_phenotype	6
MP:0002384	MP:0002384	abnormal nasopharyngeal tonsil morphology	Mammalian_phenotype	6
MP:0002385	MP:0002385	abnormal lingual tonsillar tissue morphology	Mammalian_phenotype	6
MP:0002386	MP:0002386	abnormal tubal tonsil morphology	Mammalian_phenotype	6
MP:0002389	MP:0002389	abnormal Peyer's patch follicle morphology	Mammalian_phenotype	6
MP:0002401	MP:0002401	abnormal lymphopoiesis	Mammalian_phenotype	6
MP:0002410	MP:0002410	decreased susceptibility to viral infection	Mammalian_phenotype	6
MP:0002411	MP:0002411	decreased susceptibility to bacterial infection	Mammalian_phenotype	6
MP:0002412	MP:0002412	increased susceptibility to bacterial infection	Mammalian_phenotype	6
MP:0002418	MP:0002418	increased susceptibility to viral infection	Mammalian_phenotype	6
MP:0002423	MP:0002423	abnormal mast cell physiology	Mammalian_phenotype	6
MP:0002424	MP:0002424	abnormal reticulocyte morphology	Mammalian_phenotype	6
MP:0002425	MP:0002425	altered susceptibility to autoimmune disorder	Mammalian_phenotype	6
MP:0002444	MP:0002444	abnormal T cell physiology	Mammalian_phenotype	6
MP:0002447	MP:0002447	abnormal erythrocyte morphology	Mammalian_phenotype	6
MP:0002464	MP:0002464	abnormal basophil physiology	Mammalian_phenotype	6
MP:0002465	MP:0002465	abnormal eosinophil physiology	Mammalian_phenotype	6
MP:0002543	MP:0002543	brachyphalangia	Mammalian_phenotype	6
MP:0002579	MP:0002579	disorganized secondary lens fibers	Mammalian_phenotype	6
MP:0002580	MP:0002580	duodenal lesions	Mammalian_phenotype	6
MP:0002621	MP:0002621	delayed neural tube closure	Mammalian_phenotype	6
MP:0002622	MP:0002622	abnormal cochlear hair cell morphology	Mammalian_phenotype	6
MP:0002624	MP:0002624	abnormal tricuspid valve morphology	Mammalian_phenotype	6
MP:0002627	MP:0002627	increased teratoma incidence	Mammalian_phenotype	6
MP:0002631	MP:0002631	abnormal epididymis morphology	Mammalian_phenotype	6
MP:0002633	MP:0002633	persistent truncus arteriosis	Mammalian_phenotype	6
MP:0002645	MP:0002645	abnormal intestinal cholesterol absorption	Mammalian_phenotype	6
MP:0002652	MP:0002652	thin myocardium	Mammalian_phenotype	6
MP:0002663	MP:0002663	failure to form blastocele	Mammalian_phenotype	6
MP:0002669	MP:0002669	abnormal scrotum morphology	Mammalian_phenotype	6
MP:0002671	MP:0002671	belted	Mammalian_phenotype	6
MP:0002675	MP:0002675	asthenozoospermia	Mammalian_phenotype	6
MP:0002696	MP:0002696	decreased circulating glucagon level	Mammalian_phenotype	6
MP:0002704	MP:0002704	tubular nephritis	Mammalian_phenotype	6
MP:0002705	MP:0002705	dilated renal tubules	Mammalian_phenotype	6
MP:0002712	MP:0002712	increased circulating glucagon level	Mammalian_phenotype	6
MP:0002714	MP:0002714	increased glycogen catabolism rate	Mammalian_phenotype	6
MP:0002715	MP:0002715	decreased glycogen catabolism rate	Mammalian_phenotype	6
MP:0002727	MP:0002727	decreased circulating insulin level	Mammalian_phenotype	6
MP:0002731	MP:0002731	megacolon	Mammalian_phenotype	6
MP:0002740	MP:0002740	heart hypoplasia	Mammalian_phenotype	6
MP:0002747	MP:0002747	abnormal aortic valve morphology	Mammalian_phenotype	6
MP:0002748	MP:0002748	abnormal pulmonary valve morphology	Mammalian_phenotype	6
MP:0002753	MP:0002753	dilated heart left ventricle	Mammalian_phenotype	6
MP:0002754	MP:0002754	dilated heart right ventricle	Mammalian_phenotype	6
MP:0002764	MP:0002764	short tibia	Mammalian_phenotype	6
MP:0002765	MP:0002765	short fibula	Mammalian_phenotype	6
MP:0002769	MP:0002769	abnormal vas deferens morphology	Mammalian_phenotype	6
MP:0002788	MP:0002788	female pseudohermaphroditism	Mammalian_phenotype	6
MP:0002789	MP:0002789	male pseudohermaphroditism	Mammalian_phenotype	6
MP:0002798	MP:0002798	abnormal active avoidance behavior	Mammalian_phenotype	6
MP:0002799	MP:0002799	abnormal passive avoidance behavior	Mammalian_phenotype	6
MP:0002805	MP:0002805	abnormal conditioned taste aversion behavior	Mammalian_phenotype	6
MP:0002824	MP:0002824	abnormal chorioallantoic fusion	Mammalian_phenotype	6
MP:0002828	MP:0002828	abnormal renal glomerular capsule morphology	Mammalian_phenotype	6
MP:0002831	MP:0002831	absent Peyer's patches	Mammalian_phenotype	6
MP:0002832	MP:0002832	coarse hair	Mammalian_phenotype	6
MP:0002833	MP:0002833	increased heart weight	Mammalian_phenotype	6
MP:0002834	MP:0002834	decreased heart weight	Mammalian_phenotype	6
MP:0002835	MP:0002835	abnormal cranial suture morphology	Mammalian_phenotype	6
MP:0002849	MP:0002849	abnormal saccharin consumption	Mammalian_phenotype	6
MP:0002851	MP:0002851	abnormal circulating sulfate level	Mammalian_phenotype	6
MP:0002858	MP:0002858	abnormal posterior semicircular canal morphology	Mammalian_phenotype	6
MP:0002871	MP:0002871	albuminuria	Mammalian_phenotype	6
MP:0002881	MP:0002881	long hair	Mammalian_phenotype	6
MP:0002885	MP:0002885	abnormal AMPA-mediated synaptic currents	Mammalian_phenotype	6
MP:0002887	MP:0002887	decreased susceptibility to pharmacologically induced seizures	Mammalian_phenotype	6
MP:0002888	MP:0002888	abnormal NMDA-mediated synaptic currents	Mammalian_phenotype	6
MP:0002895	MP:0002895	abnormal otolithic membrane morphology	Mammalian_phenotype	6
MP:0002904	MP:0002904	increased circulating parathyroid hormone level	Mammalian_phenotype	6
MP:0002905	MP:0002905	decreased circulating parathyroid hormone level	Mammalian_phenotype	6
MP:0002906	MP:0002906	increased susceptibility to pharmacologically induced seizures	Mammalian_phenotype	6
MP:0002916	MP:0002916	increased synaptic depression	Mammalian_phenotype	6
MP:0002917	MP:0002917	decreased synaptic depression	Mammalian_phenotype	6
MP:0002922	MP:0002922	decreased post-tetanic potentiation	Mammalian_phenotype	6
MP:0002923	MP:0002923	increased post-tetanic potentiation	Mammalian_phenotype	6
MP:0002931	MP:0002931	glutaricadicuria	Mammalian_phenotype	6
MP:0002934	MP:0002934	acute joint inflammation	Mammalian_phenotype	6
MP:0002935	MP:0002935	chronic joint inflammation	Mammalian_phenotype	6
MP:0002938	MP:0002938	white spotting	Mammalian_phenotype	6
MP:0002946	MP:0002946	delayed axon extension	Mammalian_phenotype	6
MP:0002947	MP:0002947	increased hemangioma incidence	Mammalian_phenotype	6
MP:0002953	MP:0002953	thick ventricular wall	Mammalian_phenotype	6
MP:0002959	MP:0002959	increased urine microalbumin level	Mammalian_phenotype	6
MP:0002960	MP:0002960	decreased urine microalbumin level	Mammalian_phenotype	6
MP:0002965	MP:0002965	increased circulating serum albumin level	Mammalian_phenotype	6
MP:0002969	MP:0002969	impaired social transmission of food preference	Mammalian_phenotype	6
MP:0002980	MP:0002980	abnormal postural reflex	Mammalian_phenotype	6
MP:0002981	MP:0002981	increased liver weight	Mammalian_phenotype	6
MP:0002984	MP:0002984	retina hypoplasia	Mammalian_phenotype	6
MP:0002993	MP:0002993	arthritis	Mammalian_phenotype	6
MP:0003008	MP:0003008	enhanced long term potentiation	Mammalian_phenotype	6
MP:0003019	MP:0003019	increased circulating chloride level	Mammalian_phenotype	6
MP:0003020	MP:0003020	decreased circulating chloride level	Mammalian_phenotype	6
MP:0003022	MP:0003022	increased coronary flow rate	Mammalian_phenotype	6
MP:0003023	MP:0003023	decreased coronary flow rate	Mammalian_phenotype	6
MP:0003024	MP:0003024	coronary artery stenosis	Mammalian_phenotype	6
MP:0003025	MP:0003025	increased vasoconstriction	Mammalian_phenotype	6
MP:0003026	MP:0003026	decreased vasoconstriction	Mammalian_phenotype	6
MP:0003034	MP:0003034	increased pulmonary vascular resistance	Mammalian_phenotype	6
MP:0003035	MP:0003035	decreased pulmonary vascular resistance	Mammalian_phenotype	6
MP:0003036	MP:0003036	vertebral transformation	Mammalian_phenotype	6
MP:0003043	MP:0003043	hypoalgesia	Mammalian_phenotype	6
MP:0003050	MP:0003050	abnormal sacral vertebrae morphology	Mammalian_phenotype	6
MP:0003063	MP:0003063	increased coping response	Mammalian_phenotype	6
MP:0003064	MP:0003064	decreased coping response	Mammalian_phenotype	6
MP:0003069	MP:0003069	abnormal superior semicircular canal morphology	Mammalian_phenotype	6
MP:0003074	MP:0003074	absent metacarpal bones	Mammalian_phenotype	6
MP:0003079	MP:0003079	decreased susceptibility to induced joint inflammation	Mammalian_phenotype	6
MP:0003092	MP:0003092	decreased corneal stroma thickness	Mammalian_phenotype	6
MP:0003093	MP:0003093	abnormal anterior stroma morphology	Mammalian_phenotype	6
MP:0003094	MP:0003094	abnormal posterior stroma morphology	Mammalian_phenotype	6
MP:0003099	MP:0003099	retinal detachment	Mammalian_phenotype	6
MP:0003104	MP:0003104	acrania	Mammalian_phenotype	6
MP:0003109	MP:0003109	short femur	Mammalian_phenotype	6
MP:0003127	MP:0003127	abnormal clitoris morphology	Mammalian_phenotype	6
MP:0003139	MP:0003139	patent ductus arteriosus	Mammalian_phenotype	6
MP:0003142	MP:0003142	anotia	Mammalian_phenotype	6
MP:0003155	MP:0003155	abnormal telomere length	Mammalian_phenotype	6
MP:0003177	MP:0003177	allodynia	Mammalian_phenotype	6
MP:0003194	MP:0003194	abnormal frequency of paradoxical sleep	Mammalian_phenotype	6
MP:0003203	MP:0003203	increased neuron apoptosis	Mammalian_phenotype	6
MP:0003204	MP:0003204	decreased neuron apoptosis	Mammalian_phenotype	6
MP:0003222	MP:0003222	increased cardiomyocyte apoptosis	Mammalian_phenotype	6
MP:0003223	MP:0003223	decreased cardiomyocyte apoptosis	Mammalian_phenotype	6
MP:0003226	MP:0003226	absent modiolus	Mammalian_phenotype	6
MP:0003227	MP:0003227	abnormal vascular branching morphogenesis	Mammalian_phenotype	6
MP:0003230	MP:0003230	abnormal umbilical artery morphology	Mammalian_phenotype	6
MP:0003233	MP:0003233	prolonged QT interval	Mammalian_phenotype	6
MP:0003238	MP:0003238	slow REM	Mammalian_phenotype	6
MP:0003239	MP:0003239	fast REM	Mammalian_phenotype	6
MP:0003242	MP:0003242	loss of basal ganglia neurons	Mammalian_phenotype	6
MP:0003272	MP:0003272	duodenal atresia	Mammalian_phenotype	6
MP:0003293	MP:0003293	rectal hemorrhage	Mammalian_phenotype	6
MP:0003296	MP:0003296	microcolon	Mammalian_phenotype	6
MP:0003302	MP:0003302	perirectal abscess	Mammalian_phenotype	6
MP:0003304	MP:0003304	large intestinal inflammation	Mammalian_phenotype	6
MP:0003306	MP:0003306	small intestinal inflammation	Mammalian_phenotype	6
MP:0003310	MP:0003310	reduced modiolus	Mammalian_phenotype	6
MP:0003312	MP:0003312	abnormal locomotor coordination	Mammalian_phenotype	6
MP:0003313	MP:0003313	abnormal locomotor activation	Mammalian_phenotype	6
MP:0003320	MP:0003320	rectovaginal fistula	Mammalian_phenotype	6
MP:0003340	MP:0003340	acute pancreas inflammation	Mammalian_phenotype	6
MP:0003341	MP:0003341	chronic pancreas inflammation	Mammalian_phenotype	6
MP:0003345	MP:0003345	decreased rib number	Mammalian_phenotype	6
MP:0003349	MP:0003349	abnormal circulating renin level	Mammalian_phenotype	6
MP:0003362	MP:0003362	increased circulating gonadotropin level	Mammalian_phenotype	6
MP:0003363	MP:0003363	decreased circulating gonadotropin level	Mammalian_phenotype	6
MP:0003370	MP:0003370	increased circulating estrogen level	Mammalian_phenotype	6
MP:0003371	MP:0003371	decreased circulating estrogen level	Mammalian_phenotype	6
MP:0003376	MP:0003376	amenorrhea	Mammalian_phenotype	6
MP:0003378	MP:0003378	early sexual maturation	Mammalian_phenotype	6
MP:0003379	MP:0003379	absent sexual maturation	Mammalian_phenotype	6
MP:0003391	MP:0003391	increased myxoma incidence	Mammalian_phenotype	6
MP:0003395	MP:0003395	abnormal subclavian artery morphology	Mammalian_phenotype	6
MP:0003398	MP:0003398	increased skeletal muscle size	Mammalian_phenotype	6
MP:0003402	MP:0003402	decreased liver weight	Mammalian_phenotype	6
MP:0003403	MP:0003403	absent placental labyrinth	Mammalian_phenotype	6
MP:0003422	MP:0003422	abnormal thrombolysis	Mammalian_phenotype	6
MP:0003427	MP:0003427	parakeratosis	Mammalian_phenotype	6
MP:0003440	MP:0003440	decreased glycerol level	Mammalian_phenotype	6
MP:0003441	MP:0003441	increased glycerol level	Mammalian_phenotype	6
MP:0003446	MP:0003446	renal hypoplasia	Mammalian_phenotype	6
MP:0003449	MP:0003449	abnormal intestinal goblet cell morphology	Mammalian_phenotype	6
MP:0003455	MP:0003455	decreased susceptibility to induced retinal damage	Mammalian_phenotype	6
MP:0003459	MP:0003459	increased fear-related response	Mammalian_phenotype	6
MP:0003460	MP:0003460	decreased fear-related response	Mammalian_phenotype	6
MP:0003465	MP:0003465	increased single cell response threshold	Mammalian_phenotype	6
MP:0003466	MP:0003466	decreased single cell response threshold	Mammalian_phenotype	6
MP:0003468	MP:0003468	increased single cell response intensity	Mammalian_phenotype	6
MP:0003469	MP:0003469	decreased single cell response intensity	Mammalian_phenotype	6
MP:0003472	MP:0003472	increased summary potential threshold	Mammalian_phenotype	6
MP:0003473	MP:0003473	decreased summary potential threshold	Mammalian_phenotype	6
MP:0003475	MP:0003475	increased summary potential intensity	Mammalian_phenotype	6
MP:0003476	MP:0003476	decreased summary potential intensity	Mammalian_phenotype	6
MP:0003480	MP:0003480	increased nerve fiber response intensity	Mammalian_phenotype	6
MP:0003481	MP:0003481	decreased nerve fiber response intensity	Mammalian_phenotype	6
MP:0003482	MP:0003482	increased nerve fiber response threshold	Mammalian_phenotype	6
MP:0003483	MP:0003483	decreased nerve fiber response threshold	Mammalian_phenotype	6
MP:0003487	MP:0003487	increased channel response intensity	Mammalian_phenotype	6
MP:0003488	MP:0003488	decreased channel response intensity	Mammalian_phenotype	6
MP:0003489	MP:0003489	increased channel response threshold	Mammalian_phenotype	6
MP:0003490	MP:0003490	decreased channel response threshold	Mammalian_phenotype	6
MP:0003508	MP:0003508	abnormal circulating dihydrotestosterone level	Mammalian_phenotype	6
MP:0003511	MP:0003511	abnormal labium morphology	Mammalian_phenotype	6
MP:0003525	MP:0003525	vulva warts	Mammalian_phenotype	6
MP:0003526	MP:0003526	vulva cysts	Mammalian_phenotype	6
MP:0003527	MP:0003527	small vulva	Mammalian_phenotype	6
MP:0003528	MP:0003528	enlarged vulva	Mammalian_phenotype	6
MP:0003541	MP:0003541	vaginal inflammation	Mammalian_phenotype	6
MP:0003545	MP:0003545	increased alcohol consumption	Mammalian_phenotype	6
MP:0003546	MP:0003546	decreased alcohol consumption	Mammalian_phenotype	6
MP:0003561	MP:0003561	rheumatoid arthritis	Mammalian_phenotype	6
MP:0003569	MP:0003569	increased leiomyoma incidence	Mammalian_phenotype	6
MP:0003574	MP:0003574	abnormal oviduct morphology	Mammalian_phenotype	6
MP:0003578	MP:0003578	absent ovary	Mammalian_phenotype	6
MP:0003580	MP:0003580	increased fibroma incidence	Mammalian_phenotype	6
MP:0003596	MP:0003596	epididymal inflammation	Mammalian_phenotype	6
MP:0003628	MP:0003628	abnormal leukocyte adhesion	Mammalian_phenotype	6
MP:0003657	MP:0003657	abnormal erythrocyte osmotic lysis	Mammalian_phenotype	6
MP:0003678	MP:0003678	absent ear lobes	Mammalian_phenotype	6
MP:0003679	MP:0003679	ear lobe hypoplasia	Mammalian_phenotype	6
MP:0003680	MP:0003680	thick ear lobes	Mammalian_phenotype	6
MP:0003681	MP:0003681	protruding ear lobes	Mammalian_phenotype	6
MP:0003682	MP:0003682	linear crease in ear lobe	Mammalian_phenotype	6
MP:0003684	MP:0003684	abnormal inferior olivary complex morphology	Mammalian_phenotype	6
MP:0003685	MP:0003685	abnormal cardiac ganglion morphology	Mammalian_phenotype	6
MP:0003708	MP:0003708	binucleate	Mammalian_phenotype	6
MP:0003710	MP:0003710	abnormal physiological neovascularization	Mammalian_phenotype	6
MP:0003711	MP:0003711	pathological neovascularization	Mammalian_phenotype	6
MP:0003712	MP:0003712	raised ear position	Mammalian_phenotype	6
MP:0003713	MP:0003713	abnormal ear rotation	Mammalian_phenotype	6
MP:0003725	MP:0003725	increased autoantibody level	Mammalian_phenotype	6
MP:0003726	MP:0003726	decreased autoantibody level	Mammalian_phenotype	6
MP:0003727	MP:0003727	abnormal retinal layer morphology	Mammalian_phenotype	6
MP:0003735	MP:0003735	cup-shaped ears	Mammalian_phenotype	6
MP:0003736	MP:0003736	folded helix	Mammalian_phenotype	6
MP:0003739	MP:0003739	dense middle ear ossicles	Mammalian_phenotype	6
MP:0003740	MP:0003740	fusion of middle ear ossicles	Mammalian_phenotype	6
MP:0003769	MP:0003769	abnormal lip morphology	Mammalian_phenotype	6
MP:0003815	MP:0003815	hairless	Mammalian_phenotype	6
MP:0003834	MP:0003834	abnormal adrenergic chromaffin cell morphology	Mammalian_phenotype	6
MP:0003845	MP:0003845	abnormal decidualization	Mammalian_phenotype	6
MP:0003846	MP:0003846	matted coat	Mammalian_phenotype	6
MP:0003848	MP:0003848	brittle hair	Mammalian_phenotype	6
MP:0003871	MP:0003871	abnormal myelin sheath morphology	Mammalian_phenotype	6
MP:0003872	MP:0003872	absent heart right ventricle	Mammalian_phenotype	6
MP:0003873	MP:0003873	branchial arch hypoplasia	Mammalian_phenotype	6
MP:0003892	MP:0003892	abnormal gastric gland morphology	Mammalian_phenotype	6
MP:0003895	MP:0003895	increased ectoderm apoptosis	Mammalian_phenotype	6
MP:0003896	MP:0003896	prolonged PR interval	Mammalian_phenotype	6
MP:0003900	MP:0003900	shortened QT interval	Mammalian_phenotype	6
MP:0003917	MP:0003917	increased kidney weight	Mammalian_phenotype	6
MP:0003918	MP:0003918	decreased kidney weight	Mammalian_phenotype	6
MP:0003924	MP:0003924	herniated diaphragm	Mammalian_phenotype	6
MP:0003928	MP:0003928	increased heart rate variability	Mammalian_phenotype	6
MP:0003929	MP:0003929	decreased heart rate variability	Mammalian_phenotype	6
MP:0009028	MP:0009028	abnormal chiasmatic cistern morphology	Mammalian_phenotype	6
MP:0009029	MP:0009029	abnormal basal cistern morphology	Mammalian_phenotype	6
MP:0009030	MP:0009030	abnormal pontine cistern morphology	Mammalian_phenotype	6
MP:0009031	MP:0009031	abnormal cerebellomedullary cistern morphology	Mammalian_phenotype	6
MP:0009035	MP:0009035	abnormal quadrigeminal cistern morphology	Mammalian_phenotype	6
MP:0009056	MP:0009056	abnormal interleukin-21 secretion	Mammalian_phenotype	6
MP:0009073	MP:0009073	absent Wolffian ducts	Mammalian_phenotype	6
MP:0009074	MP:0009074	Wolffian duct degeneration	Mammalian_phenotype	6
MP:0009075	MP:0009075	rudimentary Wolffian ducts	Mammalian_phenotype	6
MP:0009076	MP:0009076	rudimentary Mullerian ducts	Mammalian_phenotype	6
MP:0009079	MP:0009079	prolapsed intervertebral disk	Mammalian_phenotype	6
MP:0009080	MP:0009080	uterus inflammation	Mammalian_phenotype	6
MP:0009093	MP:0009093	oocyte degeneration	Mammalian_phenotype	6
MP:0009108	MP:0009108	increased pancreas weight	Mammalian_phenotype	6
MP:0009109	MP:0009109	decreased pancreas weight	Mammalian_phenotype	6
MP:0009110	MP:0009110	pancreas hyperplasia	Mammalian_phenotype	6
MP:0009111	MP:0009111	pancreas hypoplasia	Mammalian_phenotype	6
MP:0009121	MP:0009121	increased white fat cell lipid droplet size	Mammalian_phenotype	6
MP:0009122	MP:0009122	decreased white fat cell lipid droplet size	Mammalian_phenotype	6
MP:0009124	MP:0009124	increased brown fat cell lipid droplet size	Mammalian_phenotype	6
MP:0009125	MP:0009125	decreased brown fat cell lipid droplet size	Mammalian_phenotype	6
MP:0009127	MP:0009127	increased brown fat cell number	Mammalian_phenotype	6
MP:0009128	MP:0009128	decreased brown fat cell number	Mammalian_phenotype	6
MP:0009130	MP:0009130	increased white fat cell number	Mammalian_phenotype	6
MP:0009131	MP:0009131	decreased white fat cell number	Mammalian_phenotype	6
MP:0009137	MP:0009137	decreased brown fat lipid droplet number	Mammalian_phenotype	6
MP:0009138	MP:0009138	increased brown fat lipid droplet number	Mammalian_phenotype	6
MP:0009139	MP:0009139	failure of Mullerian duct regression	Mammalian_phenotype	6
MP:0009141	MP:0009141	increased prepulse inhibition	Mammalian_phenotype	6
MP:0009142	MP:0009142	decreased prepulse inhibition	Mammalian_phenotype	6
MP:0009144	MP:0009144	dilated pancreatic duct	Mammalian_phenotype	6
MP:0009146	MP:0009146	abnormal pancreatic acinar cell morphology	Mammalian_phenotype	6
MP:0009154	MP:0009154	pancreatic acinar hypoplasia	Mammalian_phenotype	6
MP:0009155	MP:0009155	pancreatic acinar hyperplasia	Mammalian_phenotype	6
MP:0009156	MP:0009156	absent pancreatic acini	Mammalian_phenotype	6
MP:0009163	MP:0009163	absent pancreatic duct	Mammalian_phenotype	6
MP:0009166	MP:0009166	abnormal pancreatic islet number	Mammalian_phenotype	6
MP:0009170	MP:0009170	abnormal pancreatic islet size	Mammalian_phenotype	6
MP:0009173	MP:0009173	absent pancreatic islets	Mammalian_phenotype	6
MP:0009184	MP:0009184	abnormal PP cell morphology	Mammalian_phenotype	6
MP:0009189	MP:0009189	abnormal pancreatic epsilon cell morphology	Mammalian_phenotype	6
MP:0009200	MP:0009200	enlarged external male genitalia	Mammalian_phenotype	6
MP:0009202	MP:0009202	small external male genitalia	Mammalian_phenotype	6
MP:0009204	MP:0009204	absent external male genitalia	Mammalian_phenotype	6
MP:0009206	MP:0009206	absent internal male genitalia	Mammalian_phenotype	6
MP:0009207	MP:0009207	internal male genitalia hypoplasia	Mammalian_phenotype	6
MP:0009210	MP:0009210	absent internal female genitalia	Mammalian_phenotype	6
MP:0009211	MP:0009211	absent external female genitalia	Mammalian_phenotype	6
MP:0009218	MP:0009218	absent peritoneal vaginal process	Mammalian_phenotype	6
MP:0009254	MP:0009254	disorganized pancreatic islets	Mammalian_phenotype	6
MP:0009264	MP:0009264	failure of eyelid fusion	Mammalian_phenotype	6
MP:0009265	MP:0009265	delayed eyelid fusion	Mammalian_phenotype	6
MP:0009271	MP:0009271	increased guard hair length	Mammalian_phenotype	6
MP:0009272	MP:0009272	decreased guard hair length	Mammalian_phenotype	6
MP:0009275	MP:0009275	bruising	Mammalian_phenotype	6
MP:0009276	MP:0009276	ecchymosis	Mammalian_phenotype	6
MP:0009279	MP:0009279	abnormal activated sperm motility	Mammalian_phenotype	6
MP:0009281	MP:0009281	abnormal hyperactivated sperm motility	Mammalian_phenotype	6
MP:0009283	MP:0009283	decreased gonadal fat pad weight	Mammalian_phenotype	6
MP:0009285	MP:0009285	increased gonadal fat pad weight	Mammalian_phenotype	6
MP:0009288	MP:0009288	increased epididymal fat pad weight	Mammalian_phenotype	6
MP:0009289	MP:0009289	decreased epididymal fat pad weight	Mammalian_phenotype	6
MP:0009292	MP:0009292	increased inguinal fat pad weight	Mammalian_phenotype	6
MP:0009293	MP:0009293	decreased inguinal fat pad weight	Mammalian_phenotype	6
MP:0009298	MP:0009298	increased mesenteric fat pad weight	Mammalian_phenotype	6
MP:0009299	MP:0009299	decreased mesenteric fat pad weight	Mammalian_phenotype	6
MP:0009300	MP:0009300	increased parametrial fat pad weight	Mammalian_phenotype	6
MP:0009301	MP:0009301	decreased parametrial fat pad weight	Mammalian_phenotype	6
MP:0009304	MP:0009304	increased retroperitoneal fat pad weight	Mammalian_phenotype	6
MP:0009305	MP:0009305	decreased retroperitoneal fat pad weight	Mammalian_phenotype	6
MP:0009306	MP:0009306	increased uterine fat pad weight	Mammalian_phenotype	6
MP:0009307	MP:0009307	decreased uterine fat pad weight	Mammalian_phenotype	6
MP:0009322	MP:0009322	increased splenocyte apoptosis	Mammalian_phenotype	6
MP:0009328	MP:0009328	delayed heart looping	Mammalian_phenotype	6
MP:0009329	MP:0009329	abnormal primitive pit morphology	Mammalian_phenotype	6
MP:0009330	MP:0009330	abnormal primitive groove morphology	Mammalian_phenotype	6
MP:0009337	MP:0009337	abnormal splenocyte number	Mammalian_phenotype	6
MP:0009341	MP:0009341	decreased splenocyte apoptosis	Mammalian_phenotype	6
MP:0009346	MP:0009346	decreased trabecular bone thickness	Mammalian_phenotype	6
MP:0009347	MP:0009347	increased trabecular bone thickness	Mammalian_phenotype	6
MP:0009352	MP:0009352	impaired spacing of implantation sites	Mammalian_phenotype	6
MP:0009353	MP:0009353	twin decidual capsule	Mammalian_phenotype	6
MP:0009392	MP:0009392	retinal gliosis	Mammalian_phenotype	6
MP:0009399	MP:0009399	increased skeletal muscle fiber size	Mammalian_phenotype	6
MP:0009400	MP:0009400	decreased skeletal muscle fiber size	Mammalian_phenotype	6
MP:0009403	MP:0009403	increased variability of skeletal muscle fiber size	Mammalian_phenotype	6
MP:0009421	MP:0009421	increased gastrocnemius weight	Mammalian_phenotype	6
MP:0009422	MP:0009422	decreased gastrocnemius weight	Mammalian_phenotype	6
MP:0009429	MP:0009429	decreased embryo weight	Mammalian_phenotype	6
MP:0009430	MP:0009430	increased embryo weight	Mammalian_phenotype	6
MP:0009431	MP:0009431	decreased fetal weight	Mammalian_phenotype	6
MP:0009432	MP:0009432	increased fetal weight	Mammalian_phenotype	6
MP:0009434	MP:0009434	paraparesis	Mammalian_phenotype	6
MP:0009437	MP:0009437	arytenoid and cricoid cartilage fusion	Mammalian_phenotype	6
MP:0009440	MP:0009440	increased myeloma incidence	Mammalian_phenotype	6
MP:0009443	MP:0009443	parthenogenesis	Mammalian_phenotype	6
MP:0009476	MP:0009476	enlarged cecum	Mammalian_phenotype	6
MP:0009477	MP:0009477	small cecum	Mammalian_phenotype	6
MP:0009478	MP:0009478	coiled cecum	Mammalian_phenotype	6
MP:0009479	MP:0009479	abnormal cecum development	Mammalian_phenotype	6
MP:0009480	MP:0009480	distended cecum	Mammalian_phenotype	6
MP:0009483	MP:0009483	enlarged ileum	Mammalian_phenotype	6
MP:0009485	MP:0009485	distended ileum	Mammalian_phenotype	6
MP:0009486	MP:0009486	rectovaginal fusion	Mammalian_phenotype	6
MP:0009487	MP:0009487	rectourethral fusion	Mammalian_phenotype	6
MP:0009490	MP:0009490	abnormal heart left atrium auricular region morphology	Mammalian_phenotype	6
MP:0009491	MP:0009491	abnormal heart right atrium auricular region morphology	Mammalian_phenotype	6
MP:0009494	MP:0009494	abnormal biliary ductule morphology	Mammalian_phenotype	6
MP:0009495	MP:0009495	abnormal common bile duct morphology	Mammalian_phenotype	6
MP:0009496	MP:0009496	abnormal common hepatic duct morphology	Mammalian_phenotype	6
MP:0009499	MP:0009499	abnormal intralobular bile duct morphology	Mammalian_phenotype	6
MP:0009500	MP:0009500	abnormal interlobular bile duct morphology	Mammalian_phenotype	6
MP:0009509	MP:0009509	absent rectum	Mammalian_phenotype	6
MP:0009510	MP:0009510	cecal atresia	Mammalian_phenotype	6
MP:0009520	MP:0009520	decreased submandibular gland size	Mammalian_phenotype	6
MP:0009521	MP:0009521	increased submandibular gland size	Mammalian_phenotype	6
MP:0009524	MP:0009524	absent submandibular gland	Mammalian_phenotype	6
MP:0009526	MP:0009526	absent sublingual gland	Mammalian_phenotype	6
MP:0009531	MP:0009531	increased parotid gland size	Mammalian_phenotype	6
MP:0009532	MP:0009532	decreased parotid gland size	Mammalian_phenotype	6
MP:0009533	MP:0009533	absent palatine gland	Mammalian_phenotype	6
MP:0009534	MP:0009534	absent anterior lingual gland	Mammalian_phenotype	6
MP:0009539	MP:0009539	abnormal Hassall's corpuscle morphology	Mammalian_phenotype	6
MP:0009543	MP:0009543	abnormal thymus corticomedullary boundary morphology	Mammalian_phenotype	6
MP:0009565	MP:0009565	multivalent meiotic configurations	Mammalian_phenotype	6
MP:0009575	MP:0009575	abnormal pubic symphysis morphology	Mammalian_phenotype	6
MP:0009577	MP:0009577	abnormal developmental vascular remodeling	Mammalian_phenotype	6
MP:0009580	MP:0009580	increased keratinocyte apoptosis	Mammalian_phenotype	6
MP:0009581	MP:0009581	decreased keratinocyte apoptosis	Mammalian_phenotype	6
MP:0009595	MP:0009595	enlarged corneocyte envelope	Mammalian_phenotype	6
MP:0009600	MP:0009600	hypergranulosis	Mammalian_phenotype	6
MP:0009604	MP:0009604	increased keratohyalin granule number	Mammalian_phenotype	6
MP:0009605	MP:0009605	decreased keratohyalin granule number	Mammalian_phenotype	6
MP:0009606	MP:0009606	increased keratohyalin granule size	Mammalian_phenotype	6
MP:0009607	MP:0009607	decreased keratohyalin granule size	Mammalian_phenotype	6
MP:0009617	MP:0009617	decreased brain zinc level	Mammalian_phenotype	6
MP:0009618	MP:0009618	increased brain zinc level	Mammalian_phenotype	6
MP:0009619	MP:0009619	abnormal optokinetic reflex	Mammalian_phenotype	6
MP:0009621	MP:0009621	primary vitreous hyperplasia	Mammalian_phenotype	6
MP:0009626	MP:0009626	abnormal celiac lymph node morphology	Mammalian_phenotype	6
MP:0009627	MP:0009627	abnormal submandibular lymph node morphology	Mammalian_phenotype	6
MP:0009637	MP:0009637	abnormal pretectal region morphology	Mammalian_phenotype	6
MP:0009649	MP:0009649	delayed embryo implantation	Mammalian_phenotype	6
MP:0009650	MP:0009650	dormant blastocysts	Mammalian_phenotype	6
MP:0009662	MP:0009662	abnormal uterine receptivity	Mammalian_phenotype	6
MP:0009663	MP:0009663	abnormal uterine-embryonic axis	Mammalian_phenotype	6
MP:0009664	MP:0009664	abnormal luminal closure	Mammalian_phenotype	6
MP:0009665	MP:0009665	abnormal embryo apposition	Mammalian_phenotype	6
MP:0009666	MP:0009666	abnormal embryo attachment	Mammalian_phenotype	6
MP:0009667	MP:0009667	abnormal embryo invasion	Mammalian_phenotype	6
MP:0009675	MP:0009675	orthokeratosis	Mammalian_phenotype	6
MP:0009680	MP:0009680	abnormal medulla oblongata anterior median fissure morphology	Mammalian_phenotype	6
MP:0009687	MP:0009687	empty decidua capsularis	Mammalian_phenotype	6
MP:0009692	MP:0009692	abnormal spinal cord alar plate morphology	Mammalian_phenotype	6
MP:0009693	MP:0009693	abnormal spinal cord basal plate morphology	Mammalian_phenotype	6
MP:0009698	MP:0009698	heart hemorrhage	Mammalian_phenotype	6
MP:0009707	MP:0009707	absent external auditory canal	Mammalian_phenotype	6
MP:0009721	MP:0009721	supernumerary mammary glands	Mammalian_phenotype	6
MP:0009727	MP:0009727	abnormal navicular morphology	Mammalian_phenotype	6
MP:0009728	MP:0009728	abnormal calcaneum morphology	Mammalian_phenotype	6
MP:0009729	MP:0009729	absent tarsus bones	Mammalian_phenotype	6
MP:0009741	MP:0009741	ectopic mammary gland	Mammalian_phenotype	6
MP:0009742	MP:0009742	increased corneal stroma thickness	Mammalian_phenotype	6
MP:0009743	MP:0009743	preaxial polydactyly	Mammalian_phenotype	6
MP:0009744	MP:0009744	postaxial polydactyly	Mammalian_phenotype	6
MP:0009751	MP:0009751	enhanced behavioral response to alcohol	Mammalian_phenotype	6
MP:0009752	MP:0009752	enhanced behavioral response to nicotine	Mammalian_phenotype	6
MP:0009753	MP:0009753	enhanced behavioral response to morphine	Mammalian_phenotype	6
MP:0009754	MP:0009754	enhanced behavioral response to cocaine	Mammalian_phenotype	6
MP:0009755	MP:0009755	impaired behavioral response to alcohol	Mammalian_phenotype	6
MP:0009756	MP:0009756	impaired behavioral response to nicotine	Mammalian_phenotype	6
MP:0009757	MP:0009757	impaired behavioral response to morphine	Mammalian_phenotype	6
MP:0009758	MP:0009758	impaired behavioral response to cocaine	Mammalian_phenotype	6
MP:0009770	MP:0009770	abnormal optic chiasm morphology	Mammalian_phenotype	6
MP:0009773	MP:0009773	absent retina	Mammalian_phenotype	6
MP:0009775	MP:0009775	increased behavioral withdrawal response	Mammalian_phenotype	6
MP:0009776	MP:0009776	decreased behavioral withdrawal response	Mammalian_phenotype	6
MP:0009784	MP:0009784	abnormal melanoblast migration	Mammalian_phenotype	6
MP:0009786	MP:0009786	decreased susceptibility to infection induced morbidity/mortality	Mammalian_phenotype	6
MP:0009787	MP:0009787	increased susceptibility to infection induced morbidity/mortality	Mammalian_phenotype	6
MP:0009795	MP:0009795	epidermal spongiosis	Mammalian_phenotype	6
MP:0009798	MP:0009798	abnormal ophthalmic nerve morphology	Mammalian_phenotype	6
MP:0009799	MP:0009799	abnormal maxillary nerve morphology	Mammalian_phenotype	6
MP:0009800	MP:0009800	abnormal mandibular nerve morphology	Mammalian_phenotype	6
MP:0009801	MP:0009801	abnormal hair cortex keratinization	Mammalian_phenotype	6
MP:0009805	MP:0009805	absent median aperture	Mammalian_phenotype	6
MP:0009808	MP:0009808	decreased oligodendrocyte number	Mammalian_phenotype	6
MP:0009814	MP:0009814	increased prostaglandin level	Mammalian_phenotype	6
MP:0009815	MP:0009815	decreased prostaglandin level	Mammalian_phenotype	6
MP:0009816	MP:0009816	increased leukotriene level	Mammalian_phenotype	6
MP:0009817	MP:0009817	decreased leukotriene level	Mammalian_phenotype	6
MP:0009823	MP:0009823	abnormal sphingomyelin level	Mammalian_phenotype	6
MP:0009824	MP:0009824	spermatic granuloma	Mammalian_phenotype	6
MP:0009845	MP:0009845	abnormal neural crest cell morphology	Mammalian_phenotype	6
MP:0009848	MP:0009848	increased horizontal stereotypic behavior	Mammalian_phenotype	6
MP:0009849	MP:0009849	increased vertical stereotypic behavior	Mammalian_phenotype	6
MP:0009850	MP:0009850	embryonic lethality between implantation and placentation	Mammalian_phenotype	6
MP:0009851	MP:0009851	abnormal Sertoli cell phagocytosis	Mammalian_phenotype	6
MP:0009858	MP:0009858	abnormal cellular extravasation	Mammalian_phenotype	6
MP:0009863	MP:0009863	abnormal heart elastic tissue morphology	Mammalian_phenotype	6
MP:0009875	MP:0009875	absent interdigital cell death	Mammalian_phenotype	6
MP:0009928	MP:0009928	abnormal pinna hair pigmentation	Mammalian_phenotype	6
MP:0009930	MP:0009930	fuzzy hair	Mammalian_phenotype	6
MP:0009933	MP:0009933	abnormal tail hair pigmentation	Mammalian_phenotype	6
MP:0009934	MP:0009934	abnormal hind foot hair pigmentation	Mammalian_phenotype	6
MP:0009936	MP:0009936	abnormal dendritic spine morphology	Mammalian_phenotype	6
MP:0009941	MP:0009941	abnormal olfactory bulb interneuron morphology	Mammalian_phenotype	6
MP:0009944	MP:0009944	abnormal olfactory lobe morphology	Mammalian_phenotype	6
MP:0009970	MP:0009970	increased hippocampus pyramidal cell number	Mammalian_phenotype	6
MP:0009971	MP:0009971	decreased hippocampus pyramidal cell number	Mammalian_phenotype	6
MP:0009973	MP:0009973	increased cerebral cortex pyramidal cell number	Mammalian_phenotype	6
MP:0009974	MP:0009974	decreased cerebral cortex pyramidal cell number	Mammalian_phenotype	6
MP:0010023	MP:0010023	cerebral vascular congestion	Mammalian_phenotype	6
MP:0010029	MP:0010029	abnormal basicranium morphology	Mammalian_phenotype	6
MP:0010031	MP:0010031	abnormal cranium size	Mammalian_phenotype	6
MP:0010035	MP:0010035	increased erythrocyte clearance	Mammalian_phenotype	6
MP:0010036	MP:0010036	decreased erythrocyte clearance	Mammalian_phenotype	6
MP:0010045	MP:0010045	increased omental fat pad weight	Mammalian_phenotype	6
MP:0010046	MP:0010046	decreased omental fat pad weight	Mammalian_phenotype	6
MP:0010048	MP:0010048	abnormal primitive streak regression	Mammalian_phenotype	6
MP:0010052	MP:0010052	increased grip strength	Mammalian_phenotype	6
MP:0010053	MP:0010053	decreased grip strength	Mammalian_phenotype	6
MP:0010064	MP:0010064	increased circulating creatine level	Mammalian_phenotype	6
MP:0010065	MP:0010065	decreased circulating creatine level	Mammalian_phenotype	6
MP:0010075	MP:0010075	abnormal circulating plant sterol level	Mammalian_phenotype	6
MP:0010076	MP:0010076	abnormal plant sterol level	Mammalian_phenotype	6
MP:0010089	MP:0010089	abnormal circulating creatine kinase level	Mammalian_phenotype	6
MP:0010105	MP:0010105	abnormal sublingual ganglion morphology	Mammalian_phenotype	6
MP:0010106	MP:0010106	abnormal circulating pyruvate kinase level	Mammalian_phenotype	6
MP:0010112	MP:0010112	abnormal coccygeal vertebrae morphology	Mammalian_phenotype	6
MP:0010145	MP:0010145	abnormal spermatic cord morphology	Mammalian_phenotype	6
MP:0010149	MP:0010149	abnormal synaptic dopamine release	Mammalian_phenotype	6
MP:0010160	MP:0010160	increased oligodendrocyte number	Mammalian_phenotype	6
MP:0010171	MP:0010171	abnormal centroacinar cell of Langerhans morphology	Mammalian_phenotype	6
MP:0010179	MP:0010179	rough coat	Mammalian_phenotype	6
MP:0010180	MP:0010180	increased susceptibility to weight loss	Mammalian_phenotype	6
MP:0010181	MP:0010181	decreased susceptibility to weight loss	Mammalian_phenotype	6
MP:0010182	MP:0010182	decreased susceptibility to weight gain	Mammalian_phenotype	6
MP:0010198	MP:0010198	decreased lymphatic vessel endothelial cell number	Mammalian_phenotype	6
MP:0010231	MP:0010231	transverse fur striping	Mammalian_phenotype	6
MP:0010235	MP:0010235	abnormal retina inner limiting membrane morphology	Mammalian_phenotype	6
MP:0010236	MP:0010236	abnormal retina outer limiting membrane morphology	Mammalian_phenotype	6
MP:0010240	MP:0010240	decreased skeletal muscle size	Mammalian_phenotype	6
MP:0010242	MP:0010242	abnormal kidney copper level	Mammalian_phenotype	6
MP:0010246	MP:0010246	abnormal intestine copper level	Mammalian_phenotype	6
MP:0010251	MP:0010251	subcapsular cataracts	Mammalian_phenotype	6
MP:0010254	MP:0010254	nuclear cataracts	Mammalian_phenotype	6
MP:0010255	MP:0010255	cortical cataracts	Mammalian_phenotype	6
MP:0010258	MP:0010258	polar cataracts	Mammalian_phenotype	6
MP:0010261	MP:0010261	sutural cataracts	Mammalian_phenotype	6
MP:0010262	MP:0010262	lamellar cataracts	Mammalian_phenotype	6
MP:0010263	MP:0010263	total cataracts	Mammalian_phenotype	6
MP:0010267	MP:0010267	decreased lung tumor incidence	Mammalian_phenotype	6
MP:0010268	MP:0010268	decreased lymphoma incidence	Mammalian_phenotype	6
MP:0010280	MP:0010280	increased skeletal tumor incidence	Mammalian_phenotype	6
MP:0010281	MP:0010281	increased nervous system tumor incidence	Mammalian_phenotype	6
MP:0010284	MP:0010284	decreased plasmacytoma incidence	Mammalian_phenotype	6
MP:0010286	MP:0010286	increased plasmacytoma incidence	Mammalian_phenotype	6
MP:0010287	MP:0010287	increased reproductive system tumor incidence	Mammalian_phenotype	6
MP:0010288	MP:0010288	increased gland tumor incidence	Mammalian_phenotype	6
MP:0010289	MP:0010289	increased urinary system tumor incidence	Mammalian_phenotype	6
MP:0010290	MP:0010290	increased muscle tumor incidence	Mammalian_phenotype	6
MP:0010291	MP:0010291	increased cardiovascular system tumor incidence	Mammalian_phenotype	6
MP:0010292	MP:0010292	increased alimentary system tumor incidence	Mammalian_phenotype	6
MP:0010293	MP:0010293	increased integument system tumor incidence	Mammalian_phenotype	6
MP:0010295	MP:0010295	increased eye tumor incidence	Mammalian_phenotype	6
MP:0010296	MP:0010296	increased hemolymphoid system tumor incidence	Mammalian_phenotype	6
MP:0010297	MP:0010297	increased hepatobiliary system tumor incidence	Mammalian_phenotype	6
MP:0010298	MP:0010298	increased respiratory system tumor incidence	Mammalian_phenotype	6
MP:0010306	MP:0010306	increased hamartoma incidence	Mammalian_phenotype	6
MP:0010309	MP:0010309	increased mesothelioma incidence	Mammalian_phenotype	6
MP:0010333	MP:0010333	abnormal circulating apolipoprotein E level	Mammalian_phenotype	6
MP:0010335	MP:0010335	fused first branchial arch	Mammalian_phenotype	6
MP:0010343	MP:0010343	increased lipoma incidence	Mammalian_phenotype	6
MP:0010353	MP:0010353	increased odontoma incidence	Mammalian_phenotype	6
MP:0010355	MP:0010355	abnormal first branchial arch artery morphology	Mammalian_phenotype	6
MP:0010356	MP:0010356	abnormal second branchial arch artery morphology	Mammalian_phenotype	6
MP:0010358	MP:0010358	abnormal free fatty acids level	Mammalian_phenotype	6
MP:0010364	MP:0010364	increased fibroadenoma incidence	Mammalian_phenotype	6
MP:0010383	MP:0010383	increased adenoma incidence	Mammalian_phenotype	6
MP:0010391	MP:0010391	increased rhabdomyoma incidence	Mammalian_phenotype	6
MP:0010392	MP:0010392	prolonged QRS complex duration	Mammalian_phenotype	6
MP:0010393	MP:0010393	shortened QRS complex duration	Mammalian_phenotype	6
MP:0010394	MP:0010394	decreased QRS amplitude	Mammalian_phenotype	6
MP:0010402	MP:0010402	ventricular septal defect	Mammalian_phenotype	6
MP:0010403	MP:0010403	atrial septal defect	Mammalian_phenotype	6
MP:0010410	MP:0010410	cor triatriatum sinistrum	Mammalian_phenotype	6
MP:0010411	MP:0010411	cor triatriatum dextrum	Mammalian_phenotype	6
MP:0010412	MP:0010412	atrioventricular septal defect	Mammalian_phenotype	6
MP:0010416	MP:0010416	interventricular septum membranous part aneurysm	Mammalian_phenotype	6
MP:0010423	MP:0010423	heart right ventricle aneurysm	Mammalian_phenotype	6
MP:0010424	MP:0010424	double chambered heart right ventricle	Mammalian_phenotype	6
MP:0010427	MP:0010427	double outlet left ventricle	Mammalian_phenotype	6
MP:0010428	MP:0010428	abnormal heart right ventricle outflow tract morphology	Mammalian_phenotype	6
MP:0010429	MP:0010429	abnormal heart left ventricle outflow tract morphology	Mammalian_phenotype	6
MP:0010432	MP:0010432	common ventricle	Mammalian_phenotype	6
MP:0010437	MP:0010437	absent coronary sinus	Mammalian_phenotype	6
MP:0010441	MP:0010441	total anomalous pulmonary venous connection	Mammalian_phenotype	6
MP:0010442	MP:0010442	partial anomalous pulmonary venous connection	Mammalian_phenotype	6
MP:0010447	MP:0010447	heart left ventricle aneurysm	Mammalian_phenotype	6
MP:0010455	MP:0010455	aortopulmonary window	Mammalian_phenotype	6
MP:0010456	MP:0010456	hemitruncus	Mammalian_phenotype	6
MP:0010457	MP:0010457	pulmonary artery stenosis	Mammalian_phenotype	6
MP:0010458	MP:0010458	pulmonary trunk hypoplasia	Mammalian_phenotype	6
MP:0010459	MP:0010459	supravalvar pulmonary trunk stenosis	Mammalian_phenotype	6
MP:0010460	MP:0010460	pulmonary artery hypoplasia	Mammalian_phenotype	6
MP:0010461	MP:0010461	discontinuous pulmonary artery	Mammalian_phenotype	6
MP:0010463	MP:0010463	aorta stenosis	Mammalian_phenotype	6
MP:0010472	MP:0010472	abnormal ascending aorta and coronary artery attachment	Mammalian_phenotype	6
MP:0010476	MP:0010476	coronary fistula	Mammalian_phenotype	6
MP:0010481	MP:0010481	left ventricle to aorta tunnel	Mammalian_phenotype	6
MP:0010495	MP:0010495	abnormal crista terminalis morphology	Mammalian_phenotype	6
MP:0010497	MP:0010497	abnormal vena cava sinus morphology	Mammalian_phenotype	6
MP:0010498	MP:0010498	abnormal interventricular septum muscular part morphology	Mammalian_phenotype	6
MP:0010500	MP:0010500	myocardium hypoplasia	Mammalian_phenotype	6
MP:0010506	MP:0010506	prolonged RR interval	Mammalian_phenotype	6
MP:0010507	MP:0010507	shortened RR interval	Mammalian_phenotype	6
MP:0010509	MP:0010509	decreased P wave amplitude	Mammalian_phenotype	6
MP:0010510	MP:0010510	absent P wave	Mammalian_phenotype	6
MP:0010511	MP:0010511	shortened PR interval	Mammalian_phenotype	6
MP:0010512	MP:0010512	absent PR interval	Mammalian_phenotype	6
MP:0010513	MP:0010513	abnormal ventricular activation time	Mammalian_phenotype	6
MP:0010514	MP:0010514	fragmented QRS complex	Mammalian_phenotype	6
MP:0010515	MP:0010515	abnormal Q wave	Mammalian_phenotype	6
MP:0010521	MP:0010521	absent pulmonary artery	Mammalian_phenotype	6
MP:0010522	MP:0010522	calcified aorta	Mammalian_phenotype	6
MP:0010528	MP:0010528	pulmonary vein hypoplasia	Mammalian_phenotype	6
MP:0010534	MP:0010534	calcified myocardium	Mammalian_phenotype	6
MP:0010535	MP:0010535	myocardial steatosis	Mammalian_phenotype	6
MP:0010548	MP:0010548	abnormal dorsal mesocardium morphology	Mammalian_phenotype	6
MP:0010553	MP:0010553	prolonged HV interval	Mammalian_phenotype	6
MP:0010554	MP:0010554	shortened HV interval	Mammalian_phenotype	6
MP:0010555	MP:0010555	absent epicardium	Mammalian_phenotype	6
MP:0010557	MP:0010557	dilated pulmonary artery	Mammalian_phenotype	6
MP:0010558	MP:0010558	sinus venosus hypoplasia	Mammalian_phenotype	6
MP:0010562	MP:0010562	absent sinus venosus	Mammalian_phenotype	6
MP:0010563	MP:0010563	increased heart right ventricle size	Mammalian_phenotype	6
MP:0010565	MP:0010565	absent fetal ductus arteriosus	Mammalian_phenotype	6
MP:0010568	MP:0010568	abnormal bulbus cordis morphology	Mammalian_phenotype	6
MP:0010570	MP:0010570	prolonged ST segment	Mammalian_phenotype	6
MP:0010571	MP:0010571	shortened ST segment	Mammalian_phenotype	6
MP:0010576	MP:0010576	premature closure of the ductus arteriosus	Mammalian_phenotype	6
MP:0010577	MP:0010577	abnormal heart right ventricle size	Mammalian_phenotype	6
MP:0010578	MP:0010578	abnormal heart left ventricle size	Mammalian_phenotype	6
MP:0010579	MP:0010579	increased heart left ventricle size	Mammalian_phenotype	6
MP:0010583	MP:0010583	abnormal conotruncus morphology	Mammalian_phenotype	6
MP:0010593	MP:0010593	thick aortic valve cusps	Mammalian_phenotype	6
MP:0010599	MP:0010599	abnormal fetal atrioventricular canal septation	Mammalian_phenotype	6
MP:0010605	MP:0010605	thick pulmonary valve cusps	Mammalian_phenotype	6
MP:0010607	MP:0010607	common atrioventricular valve	Mammalian_phenotype	6
MP:0010608	MP:0010608	abnormal chordae tendineae morphology	Mammalian_phenotype	6
MP:0010617	MP:0010617	thick mitral valve cusps	Mammalian_phenotype	6
MP:0010626	MP:0010626	thick tricuspid valve cusps	Mammalian_phenotype	6
MP:0010633	MP:0010633	myocardial hypertrophy	Mammalian_phenotype	6
MP:0010634	MP:0010634	increased QRS amplitude	Mammalian_phenotype	6
MP:0010636	MP:0010636	bundle branch block	Mammalian_phenotype	6
MP:0010637	MP:0010637	sinus bradycardia	Mammalian_phenotype	6
MP:0010642	MP:0010642	absent third branchial arch	Mammalian_phenotype	6
MP:0010643	MP:0010643	absent fourth branchial arch	Mammalian_phenotype	6
MP:0010644	MP:0010644	absent sixth branchial arch	Mammalian_phenotype	6
MP:0010646	MP:0010646	absent pulmonary vein	Mammalian_phenotype	6
MP:0010647	MP:0010647	left atrium hypoplasia	Mammalian_phenotype	6
MP:0010648	MP:0010648	right atrium hypoplasia	Mammalian_phenotype	6
MP:0010649	MP:0010649	dilated pulmonary trunk	Mammalian_phenotype	6
MP:0010651	MP:0010651	aorticopulmonary septal defect	Mammalian_phenotype	6
MP:0010655	MP:0010655	absent cardiac jelly	Mammalian_phenotype	6
MP:0010656	MP:0010656	thick myocardium	Mammalian_phenotype	6
MP:0010657	MP:0010657	absent pulmonary trunk	Mammalian_phenotype	6
MP:0010663	MP:0010663	abnormal brachiocephalic trunk morphology	Mammalian_phenotype	6
MP:0010664	MP:0010664	abnormal vitelline artery morphology	Mammalian_phenotype	6
MP:0010666	MP:0010666	abnormal vitelline vein morphology	Mammalian_phenotype	6
MP:0010667	MP:0010667	abnormal umbilical vein morphology	Mammalian_phenotype	6
MP:0010674	MP:0010674	increased activation-induced B cell apoptosis	Mammalian_phenotype	6
MP:0010675	MP:0010675	decreased activation-induced B cell apoptosis	Mammalian_phenotype	6
MP:0010676	MP:0010676	increased activation-induced cell death of T cells	Mammalian_phenotype	6
MP:0010677	MP:0010677	decreased activation-induced cell death of T cells	Mammalian_phenotype	6
MP:0010687	MP:0010687	absent hair follicle dermal papilla	Mammalian_phenotype	6
MP:0010706	MP:0010706	ventral rotation of lens	Mammalian_phenotype	6
MP:0010707	MP:0010707	decreased ventral retina size	Mammalian_phenotype	6
MP:0010711	MP:0010711	persistent hyperplastic primary vitreous	Mammalian_phenotype	6
MP:0010714	MP:0010714	iris coloboma	Mammalian_phenotype	6
MP:0010718	MP:0010718	choroid coloboma	Mammalian_phenotype	6
MP:0010719	MP:0010719	ciliary body coloboma	Mammalian_phenotype	6
MP:0010722	MP:0010722	persistent cervical thymus	Mammalian_phenotype	6
MP:0010732	MP:0010732	abnormal node of Ranvier morphology	Mammalian_phenotype	6
MP:0010733	MP:0010733	abnormal axon initial segment morphology	Mammalian_phenotype	6
MP:0010734	MP:0010734	abnormal paranode morphology	Mammalian_phenotype	6
MP:0010737	MP:0010737	abnormal juxtaparanode morphology	Mammalian_phenotype	6
MP:0010738	MP:0010738	abnormal internode morphology	Mammalian_phenotype	6
MP:0010739	MP:0010739	abnormal axolemma morphology	Mammalian_phenotype	6
MP:0010742	MP:0010742	increased Schwann cell number	Mammalian_phenotype	6
MP:0010743	MP:0010743	delayed suture closure	Mammalian_phenotype	6
MP:0010767	MP:0010767	abnormal female meiosis I arrest	Mammalian_phenotype	6
MP:0010775	MP:0010775	abnormal scaphoid morphology	Mammalian_phenotype	6
MP:0010780	MP:0010780	abnormal stomach smooth muscle circular layer morphology	Mammalian_phenotype	6
MP:0010781	MP:0010781	pyloric sphincter hypertrophy	Mammalian_phenotype	6
MP:0010799	MP:0010799	stomach mucosa hyperplasia	Mammalian_phenotype	6
MP:0010804	MP:0010804	abnormal stomach smooth muscle inner oblique layer morphology	Mammalian_phenotype	6
MP:0010805	MP:0010805	abnormal stomach smooth muscle outer longitudinal layer morphology	Mammalian_phenotype	6
MP:0010824	MP:0010824	absent right lung accessory lobe	Mammalian_phenotype	6
MP:0010826	MP:0010826	absent lung saccules	Mammalian_phenotype	6
MP:0010827	MP:0010827	small lung saccule	Mammalian_phenotype	6
MP:0010829	MP:0010829	increased bronchioalveolar stem cell number	Mammalian_phenotype	6
MP:0010830	MP:0010830	decreased bronchioalveolar stem cell number	Mammalian_phenotype	6
MP:0010852	MP:0010852	absent epidermal lamellar bodies	Mammalian_phenotype	6
MP:0010861	MP:0010861	increased respiratory mucosa goblet cell number	Mammalian_phenotype	6
MP:0010862	MP:0010862	decreased respiratory mucosa goblet cell number	Mammalian_phenotype	6
MP:0010868	MP:0010868	increased bone trabecula number	Mammalian_phenotype	6
MP:0010869	MP:0010869	decreased bone trabecula number	Mammalian_phenotype	6
MP:0010870	MP:0010870	absent bone trabeculae	Mammalian_phenotype	6
MP:0010878	MP:0010878	increased trabecular bone volume	Mammalian_phenotype	6
MP:0010879	MP:0010879	decreased trabecular bone volume	Mammalian_phenotype	6
MP:0010893	MP:0010893	abnormal posterior commissure morphology	Mammalian_phenotype	6
MP:0010894	MP:0010894	pulmonary alveolar edema	Mammalian_phenotype	6
MP:0010895	MP:0010895	increased lung compliance	Mammalian_phenotype	6
MP:0010896	MP:0010896	decreased lung compliance	Mammalian_phenotype	6
MP:0010900	MP:0010900	abnormal pulmonary interalveolar septum morphology	Mammalian_phenotype	6
MP:0010902	MP:0010902	abnormal pulmonary alveolar sac morphology	Mammalian_phenotype	6
MP:0010907	MP:0010907	absent lung buds	Mammalian_phenotype	6
MP:0010915	MP:0010915	increased solitary pulmonary neuroendocrine cell number	Mammalian_phenotype	6
MP:0010916	MP:0010916	decreased solitary pulmonary neuroendocrine cell number	Mammalian_phenotype	6
MP:0010917	MP:0010917	absent solitary pulmonary neuroendocrine cells	Mammalian_phenotype	6
MP:0010919	MP:0010919	increased number of pulmonary neuroendocrine bodies	Mammalian_phenotype	6
MP:0010920	MP:0010920	decreased number of pulmonary neuroendocrine bodies	Mammalian_phenotype	6
MP:0010921	MP:0010921	absent pulmonary neuroendocrine bodies	Mammalian_phenotype	6
MP:0010926	MP:0010926	increased osteoid volume	Mammalian_phenotype	6
MP:0010927	MP:0010927	decreased osteoid volume	Mammalian_phenotype	6
MP:0010929	MP:0010929	increased osteoid thickness	Mammalian_phenotype	6
MP:0010930	MP:0010930	decreased osteoid thickness	Mammalian_phenotype	6
MP:0010932	MP:0010932	increased trabecular bone connectivity density	Mammalian_phenotype	6
MP:0010933	MP:0010933	decreased trabecular bone connectivity density	Mammalian_phenotype	6
MP:0010935	MP:0010935	increased airway resistance	Mammalian_phenotype	6
MP:0010936	MP:0010936	decreased airway resistance	Mammalian_phenotype	6
MP:0010937	MP:0010937	increased total lung capacity	Mammalian_phenotype	6
MP:0010938	MP:0010938	decreased total lung capacity	Mammalian_phenotype	6
MP:0010946	MP:0010946	hyperpnea	Mammalian_phenotype	6
MP:0010952	MP:0010952	abnormal fatty acid beta-oxidation	Mammalian_phenotype	6
MP:0010964	MP:0010964	increased compact bone volume	Mammalian_phenotype	6
MP:0010965	MP:0010965	decreased compact bone volume	Mammalian_phenotype	6
MP:0010967	MP:0010967	increased compact bone area	Mammalian_phenotype	6
MP:0010968	MP:0010968	decreased compact bone area	Mammalian_phenotype	6
MP:0010983	MP:0010983	abnormal ureteric bud invasion	Mammalian_phenotype	6
MP:0010984	MP:0010984	abnormal metanephric mesenchyme morphology	Mammalian_phenotype	6
MP:0010986	MP:0010986	abnormal mesonephric mesenchyme morphology	Mammalian_phenotype	6
MP:0010987	MP:0010987	abnormal nephrogenic mesenchyme morphogenesis	Mammalian_phenotype	6
MP:0010988	MP:0010988	abnormal bronchial cartilage morphology	Mammalian_phenotype	6
MP:0011008	MP:0011008	abnormal circulating glutamate dehydrogenase level	Mammalian_phenotype	6
MP:0011025	MP:0011025	abnormal branching involved in trachea morphogenesis	Mammalian_phenotype	6
MP:0011027	MP:0011027	abnormal branching involved in bronchus morphogenesis	Mammalian_phenotype	6
MP:0011029	MP:0011029	abnormal branching involved in preterminal bronchiole morphogenesis	Mammalian_phenotype	6
MP:0011031	MP:0011031	abnormal branching involved in terminal bronchiole morphogenesis	Mammalian_phenotype	6
MP:0011033	MP:0011033	abnormal branching involved in respiratory bronchiole morphogenesis	Mammalian_phenotype	6
MP:0011035	MP:0011035	abnormal branching involved in alveolar duct morphogenesis	Mammalian_phenotype	6
MP:0011037	MP:0011037	abnormal branching involved in alveolar sac morphogenesis	Mammalian_phenotype	6
MP:0011052	MP:0011052	increased respiratory motile cilia number	Mammalian_phenotype	6
MP:0011053	MP:0011053	decreased respiratory motile cilia number	Mammalian_phenotype	6
MP:0011066	MP:0011066	abnormal renal tubule epithelial cell primary cilium morphology	Mammalian_phenotype	6
MP:0011072	MP:0011072	abnormal macrophage cytokine production	Mammalian_phenotype	6
MP:0011075	MP:0011075	abnormal macrophage activation involved in immune response	Mammalian_phenotype	6
MP:0011080	MP:0011080	increased macrophage apoptosis	Mammalian_phenotype	6
MP:0011081	MP:0011081	decreased macrophage apoptosis	Mammalian_phenotype	6
MP:0011085	MP:0011085	complete postnatal lethality	Mammalian_phenotype	6
MP:0011086	MP:0011086	partial postnatal lethality	Mammalian_phenotype	6
MP:0011089	MP:0011089	complete perinatal lethality	Mammalian_phenotype	6
MP:0011090	MP:0011090	partial perinatal lethality	Mammalian_phenotype	6
MP:0011092	MP:0011092	complete embryonic lethality	Mammalian_phenotype	6
MP:0011099	MP:0011099	complete lethality throughout fetal growth and development	Mammalian_phenotype	6
MP:0011102	MP:0011102	partial embryonic lethality	Mammalian_phenotype	6
MP:0011109	MP:0011109	partial lethality throughout fetal growth and development	Mammalian_phenotype	6
MP:0011162	MP:0011162	abnormal wet-to-dry lung weight ratio	Mammalian_phenotype	6
MP:0011181	MP:0011181	increased hematopoietic cell number	Mammalian_phenotype	6
MP:0011182	MP:0011182	decreased hematopoietic cell number	Mammalian_phenotype	6
MP:0011184	MP:0011184	absent embryonic epiblast	Mammalian_phenotype	6
MP:0011185	MP:0011185	absent primitive endoderm	Mammalian_phenotype	6
MP:0011189	MP:0011189	small embryonic epiblast	Mammalian_phenotype	6
MP:0011190	MP:0011190	thick embryonic epiblast	Mammalian_phenotype	6
MP:0011191	MP:0011191	increased embryonic epiblast cell apoptosis	Mammalian_phenotype	6
MP:0011193	MP:0011193	embryonic epiblast cell degeneration	Mammalian_phenotype	6
MP:0011219	MP:0011219	abnormal intestinal calcium absorption	Mammalian_phenotype	6
MP:0011222	MP:0011222	abnormal lymph node medullary sinus morphology	Mammalian_phenotype	6
MP:0011224	MP:0011224	abnormal lymph node medullary cord morphology	Mammalian_phenotype	6
MP:0011228	MP:0011228	abnormal vitamin D level	Mammalian_phenotype	6
MP:0011231	MP:0011231	abnormal vitamin E level	Mammalian_phenotype	6
MP:0011232	MP:0011232	abnormal vitamin A level	Mammalian_phenotype	6
MP:0011251	MP:0011251	bronchial situs inversus	Mammalian_phenotype	6
MP:0011262	MP:0011262	abnormal branchial arch mesenchyme morphology	Mammalian_phenotype	6
MP:0011263	MP:0011263	abnormal spleen mesenchyme morphology	Mammalian_phenotype	6
MP:0011266	MP:0011266	abnormal frontonasal mesenchyme morphology	Mammalian_phenotype	6
MP:0011267	MP:0011267	abnormal excitatory postsynaptic current amplitude	Mammalian_phenotype	6
MP:0011271	MP:0011271	prolonged excitatory postsynaptic current rise time	Mammalian_phenotype	6
MP:0011272	MP:0011272	short excitatory postsynaptic current rise time	Mammalian_phenotype	6
MP:0011273	MP:0011273	prolonged excitatory postsynaptic current decay time	Mammalian_phenotype	6
MP:0011274	MP:0011274	short excitatory postsynaptic current decay time	Mammalian_phenotype	6
MP:0011280	MP:0011280	abnormal flank coat pigmentation	Mammalian_phenotype	6
MP:0011285	MP:0011285	increased circulating erythropoietin level	Mammalian_phenotype	6
MP:0011286	MP:0011286	decreased circulating erythropoietin level	Mammalian_phenotype	6
MP:0011290	MP:0011290	decreased nephron number	Mammalian_phenotype	6
MP:0011299	MP:0011299	abnormal macula densa morphology	Mammalian_phenotype	6
MP:0011300	MP:0011300	abnormal juxtaglomerular cell morphology	Mammalian_phenotype	6
MP:0011302	MP:0011302	abnormal extraglomerular mesangial cell morphology	Mammalian_phenotype	6
MP:0011305	MP:0011305	dilated kidney calyx	Mammalian_phenotype	6
MP:0011312	MP:0011312	abnormal kidney afferent arteriole morphology	Mammalian_phenotype	6
MP:0011313	MP:0011313	abnormal kidney efferent arteriole morphology	Mammalian_phenotype	6
MP:0011320	MP:0011320	abnormal glomerular capillary morphology	Mammalian_phenotype	6
MP:0011321	MP:0011321	abnormal peritubular capillary morphology	Mammalian_phenotype	6
MP:0011323	MP:0011323	abnormal renal vein morphology	Mammalian_phenotype	6
MP:0011329	MP:0011329	abnormal inner renal medulla vasa recta morphology	Mammalian_phenotype	6
MP:0011330	MP:0011330	abnormal kidney outer medulla vasa recta morphology	Mammalian_phenotype	6
MP:0011340	MP:0011340	abnormal extraglomerular mesangium morphology	Mammalian_phenotype	6
MP:0011346	MP:0011346	renal tubule atrophy	Mammalian_phenotype	6
MP:0011348	MP:0011348	abnormal renal glomerulus basement membrane morphology	Mammalian_phenotype	6
MP:0011356	MP:0011356	renal artery stenosis	Mammalian_phenotype	6
MP:0011365	MP:0011365	small metanephros	Mammalian_phenotype	6
MP:0011366	MP:0011366	absent metanephros	Mammalian_phenotype	6
MP:0011368	MP:0011368	increased kidney apoptosis	Mammalian_phenotype	6
MP:0011371	MP:0011371	decreased kidney apoptosis	Mammalian_phenotype	6
MP:0011378	MP:0011378	abnormal kidney outer medulla inner stripe morphology	Mammalian_phenotype	6
MP:0011379	MP:0011379	abnormal kidney outer medulla outer stripe morphology	Mammalian_phenotype	6
MP:0011380	MP:0011380	enlarged brain ventricles	Mammalian_phenotype	6
MP:0011386	MP:0011386	increased metanephric mesenchyme apoptosis	Mammalian_phenotype	6
MP:0011392	MP:0011392	increased fetal cardiomyocyte apoptosis	Mammalian_phenotype	6
MP:0011393	MP:0011393	decreased fetal cardiomyocyte apoptosis	Mammalian_phenotype	6
MP:0011406	MP:0011406	abnormal retrotrapezoid nucleus morphology	Mammalian_phenotype	6
MP:0011407	MP:0011407	absent nephrogenic zone	Mammalian_phenotype	6
MP:0011408	MP:0011408	renal tubule hypertrophy	Mammalian_phenotype	6
MP:0011446	MP:0011446	abnormal renal albumin reabsorption	Mammalian_phenotype	6
MP:0011459	MP:0011459	increased urine chloride ion level	Mammalian_phenotype	6
MP:0011460	MP:0011460	decreased urine chloride ion level	Mammalian_phenotype	6
MP:0011464	MP:0011464	bilirubinuria	Mammalian_phenotype	6
MP:0011470	MP:0011470	increased urine creatinine level	Mammalian_phenotype	6
MP:0011471	MP:0011471	decreased urine creatinine level	Mammalian_phenotype	6
MP:0011503	MP:0011503	distended jejunum	Mammalian_phenotype	6
MP:0011505	MP:0011505	camptomelia	Mammalian_phenotype	6
MP:0011513	MP:0011513	abnormal vertebral artery morphology	Mammalian_phenotype	6
MP:0011515	MP:0011515	purpura	Mammalian_phenotype	6
MP:0011516	MP:0011516	aspartylglucosaminuria	Mammalian_phenotype	6
MP:0011519	MP:0011519	abnormal placenta labyrinth size	Mammalian_phenotype	6
MP:0011522	MP:0011522	abnormal placental labyrinth villi morphology	Mammalian_phenotype	6
MP:0011525	MP:0011525	abnormal placenta intervillous maternal lacunae morphology	Mammalian_phenotype	6
MP:0011526	MP:0011526	abnormal placenta fetal blood space morphology	Mammalian_phenotype	6
MP:0011527	MP:0011527	disorganized placental labyrinth	Mammalian_phenotype	6
MP:0011531	MP:0011531	abnormal syncytiotrophoblast morphology	Mammalian_phenotype	6
MP:0011532	MP:0011532	decreased urine major urinary protein level	Mammalian_phenotype	6
MP:0011533	MP:0011533	increased urine major urinary protein level	Mammalian_phenotype	6
MP:0011537	MP:0011537	uraturia	Mammalian_phenotype	6
MP:0011540	MP:0011540	increased urine aldosterone level	Mammalian_phenotype	6
MP:0011541	MP:0011541	decreased urine aldosterone level	Mammalian_phenotype	6
MP:0011543	MP:0011543	increased urine antidiuretic hormone level	Mammalian_phenotype	6
MP:0011544	MP:0011544	decreased urine antidiuretic hormone level	Mammalian_phenotype	6
MP:0011546	MP:0011546	increased urine progesterone level	Mammalian_phenotype	6
MP:0011547	MP:0011547	decreased urine progesterone level	Mammalian_phenotype	6
MP:0011555	MP:0011555	increased urine microglobulin level	Mammalian_phenotype	6
MP:0011602	MP:0011602	increased glutathione peroxidase activity	Mammalian_phenotype	6
MP:0011603	MP:0011603	decreased glutathione peroxidase activity	Mammalian_phenotype	6
MP:0011612	MP:0011612	increased circulating ghrelin level	Mammalian_phenotype	6
MP:0011613	MP:0011613	decreased circulating ghrelin level	Mammalian_phenotype	6
MP:0011620	MP:0011620	abnormal habituation to a new environment	Mammalian_phenotype	6
MP:0011621	MP:0011621	abnormal habituation to a novel object	Mammalian_phenotype	6
MP:0011622	MP:0011622	abnormal habituation to a novel odor	Mammalian_phenotype	6
MP:0011636	MP:0011636	disorganized mitochondrial cristae	Mammalian_phenotype	6
MP:0011647	MP:0011647	absent sinuatrial valve	Mammalian_phenotype	6
MP:0011650	MP:0011650	abnormal corneal stroma collagen fibril morphology	Mammalian_phenotype	6
MP:0011652	MP:0011652	increased circulating histidine level	Mammalian_phenotype	6
MP:0011653	MP:0011653	decreased circulating histidine level	Mammalian_phenotype	6
MP:0011654	MP:0011654	increased urine histidine level	Mammalian_phenotype	6
MP:0011688	MP:0011688	absent epidermal stem cells	Mammalian_phenotype	6
MP:0011693	MP:0011693	absent chondrocytes	Mammalian_phenotype	6
MP:0011697	MP:0011697	vacuolated lens	Mammalian_phenotype	6
MP:0011705	MP:0011705	absent fibroblast proliferation	Mammalian_phenotype	6
MP:0011707	MP:0011707	impaired fibroblast cell migration	Mammalian_phenotype	6
MP:0011710	MP:0011710	enhanced osteoblast differentiation	Mammalian_phenotype	6
MP:0011711	MP:0011711	impaired osteoblast differentiation	Mammalian_phenotype	6
MP:0011716	MP:0011716	abnormal interleukin-8 secretion	Mammalian_phenotype	6
MP:0011732	MP:0011732	decreased somite size	Mammalian_phenotype	6
MP:0011751	MP:0011751	abnormal X-Y chromosome synapsis during male meiosis	Mammalian_phenotype	6
MP:0011752	MP:0011752	abnormal X-Y chromosome synaptonemal complex assembly during male meiosis	Mammalian_phenotype	6
MP:0011754	MP:0011754	abnormal kidney collecting duct intercalated cell morphology	Mammalian_phenotype	6
MP:0011757	MP:0011757	abnormal kidney collecting duct principal cell morphology	Mammalian_phenotype	6
MP:0011763	MP:0011763	urethritis	Mammalian_phenotype	6
MP:0011764	MP:0011764	ureteritis	Mammalian_phenotype	6
MP:0011775	MP:0011775	rectal atresia	Mammalian_phenotype	6
MP:0011802	MP:0011802	seminal vesiculitis	Mammalian_phenotype	6
MP:0011806	MP:0011806	decreased dermal fibroblast proliferation	Mammalian_phenotype	6
MP:0011807	MP:0011807	decreased lung fibroblast proliferation	Mammalian_phenotype	6
MP:0011810	MP:0011810	increased anoikis	Mammalian_phenotype	6
MP:0011811	MP:0011811	decreased anoikis	Mammalian_phenotype	6
MP:0011826	MP:0011826	increased lymphocyte chemotaxis	Mammalian_phenotype	6
MP:0011838	MP:0011838	abnormal navicular fossa morphology	Mammalian_phenotype	6
MP:0011846	MP:0011846	decreased kidney collecting duct number	Mammalian_phenotype	6
MP:0011847	MP:0011847	increased kidney collecting duct number	Mammalian_phenotype	6
MP:0011848	MP:0011848	abnormal vagina vestibule morphology	Mammalian_phenotype	6
MP:0011852	MP:0011852	patent urachus	Mammalian_phenotype	6
MP:0011869	MP:0011869	detached podocyte	Mammalian_phenotype	6
MP:0011878	MP:0011878	jejunum atresia	Mammalian_phenotype	6
MP:0011879	MP:0011879	ileum atresia	Mammalian_phenotype	6
MP:0011880	MP:0011880	absent duodenum	Mammalian_phenotype	6
MP:0011881	MP:0011881	distended duodenum	Mammalian_phenotype	6
MP:0011882	MP:0011882	enlarged duodenum	Mammalian_phenotype	6
MP:0011883	MP:0011883	absent diaphragm	Mammalian_phenotype	6
MP:0011884	MP:0011884	absent colon	Mammalian_phenotype	6
MP:0011885	MP:0011885	abnormal circulating lipase level	Mammalian_phenotype	6
MP:0011890	MP:0011890	increased circulating ferritin level	Mammalian_phenotype	6
MP:0011891	MP:0011891	decreased circulating ferritin level	Mammalian_phenotype	6
MP:0011893	MP:0011893	increased circulating transferrin level	Mammalian_phenotype	6
MP:0011894	MP:0011894	decreased circulating transferrin level	Mammalian_phenotype	6
MP:0011895	MP:0011895	abnormal circulating unsaturated transferrin level	Mammalian_phenotype	6
MP:0011898	MP:0011898	abnormal platelet cell number	Mammalian_phenotype	6
MP:0011935	MP:0011935	abnormal pancreatic bud formation	Mammalian_phenotype	6
MP:0011937	MP:0011937	shortened PP interval	Mammalian_phenotype	6
MP:0011938	MP:0011938	prolonged PP interval	Mammalian_phenotype	6
MP:0011939	MP:0011939	increased food intake	Mammalian_phenotype	6
MP:0011940	MP:0011940	decreased food intake	Mammalian_phenotype	6
MP:0011941	MP:0011941	increased fluid intake	Mammalian_phenotype	6
MP:0011942	MP:0011942	decreased fluid intake	Mammalian_phenotype	6
MP:0011945	MP:0011945	increased eating frequency	Mammalian_phenotype	6
MP:0011946	MP:0011946	decreased eating frequency	Mammalian_phenotype	6
MP:0011949	MP:0011949	increased drinking frequency	Mammalian_phenotype	6
MP:0011950	MP:0011950	decreased drinking frequency	Mammalian_phenotype	6
MP:0011953	MP:0011953	prolonged PQ interval	Mammalian_phenotype	6
MP:0011954	MP:0011954	shortened PQ interval	Mammalian_phenotype	6
MP:0011957	MP:0011957	decreased compensatory feeding amount	Mammalian_phenotype	6
MP:0011958	MP:0011958	increased compensatory feeding amount	Mammalian_phenotype	6
MP:0011962	MP:0011962	increased cornea thickness	Mammalian_phenotype	6
MP:0011963	MP:0011963	abnormal total retina thickness	Mammalian_phenotype	6
MP:0011966	MP:0011966	abnormal auditory brainstem response waveform shape	Mammalian_phenotype	6
MP:0011967	MP:0011967	increased or absent threshold for auditory brainstem response	Mammalian_phenotype	6
MP:0011968	MP:0011968	decreased threshold for auditory brainstem response	Mammalian_phenotype	6
MP:0011969	MP:0011969	abnormal circulating triglyceride level	Mammalian_phenotype	6
MP:0011971	MP:0011971	increased circulating lactate dehydrogenase level	Mammalian_phenotype	6
MP:0011972	MP:0011972	decreased circulating lactate dehydrogenase level	Mammalian_phenotype	6
MP:0011973	MP:0011973	abnormal circulating glycerol level	Mammalian_phenotype	6
MP:0011976	MP:0011976	sweet preference	Mammalian_phenotype	6
MP:0011988	MP:0011988	increased mating frequency	Mammalian_phenotype	6
MP:0011992	MP:0011992	increased erythrocyte catalase activity	Mammalian_phenotype	6
MP:0011995	MP:0011995	decreased leukemia incidence	Mammalian_phenotype	6
MP:0012003	MP:0012003	abnormal septum of telencephalon morphology	Mammalian_phenotype	6
MP:0012008	MP:0012008	delayed parturition	Mammalian_phenotype	6
MP:0012009	MP:0012009	early parturition	Mammalian_phenotype	6
MP:0012010	MP:0012010	parturition failure	Mammalian_phenotype	6
MP:0012017	MP:0012017	grizzled coat color	Mammalian_phenotype	6
MP:0012025	MP:0012025	abnormal comma shaped body morphology	Mammalian_phenotype	6
MP:0012026	MP:0012026	abnormal S-shaped body morphology	Mammalian_phenotype	6
MP:0012042	MP:0012042	low alcohol preference	Mammalian_phenotype	6
MP:0012043	MP:0012043	increased myoepithelioma incidence	Mammalian_phenotype	6
MP:0012045	MP:0012045	increased susceptibility to hypertension	Mammalian_phenotype	6
MP:0012046	MP:0012046	decreased susceptibility to hypertension	Mammalian_phenotype	6
MP:0012052	MP:0012052	hypertonicity	Mammalian_phenotype	6
MP:0012056	MP:0012056	abnormal polar trophectoderm morphology	Mammalian_phenotype	6
MP:0012057	MP:0012057	abnormal mural trophectoderm morphology	Mammalian_phenotype	6
MP:0012059	MP:0012059	thick diaphragm muscle	Mammalian_phenotype	6
MP:0012060	MP:0012060	diaphragm muscle hyperplasia	Mammalian_phenotype	6
MP:0012064	MP:0012064	abnormal astrocyte number	Mammalian_phenotype	6
MP:0012073	MP:0012073	premature mammary gland growth during pregnancy	Mammalian_phenotype	6
MP:0012075	MP:0012075	impaired mammary gland growth during pregnancy	Mammalian_phenotype	6
MP:0012076	MP:0012076	abnormal agouti pigmentation	Mammalian_phenotype	6
MP:0012079	MP:0012079	abnormal spinal reflex	Mammalian_phenotype	6
MP:0012081	MP:0012081	absent heart tube	Mammalian_phenotype	6
MP:0012087	MP:0012087	absent midbrain	Mammalian_phenotype	6
MP:0012089	MP:0012089	decreased midbrain size	Mammalian_phenotype	6
MP:0012091	MP:0012091	increased midbrain size	Mammalian_phenotype	6
MP:0012092	MP:0012092	diencephalon hypoplasia	Mammalian_phenotype	6
MP:0012102	MP:0012102	absent trophectoderm	Mammalian_phenotype	6
MP:0012121	MP:0012121	sclerocornea	Mammalian_phenotype	6
MP:0012122	MP:0012122	abnormal iris transillumination	Mammalian_phenotype	6
MP:0012127	MP:0012127	absent placenta hemotrichorial membrane	Mammalian_phenotype	6
MP:0012129	MP:0012129	failure of blastocyst formation	Mammalian_phenotype	6
MP:0012133	MP:0012133	absent midbrain-hindbrain boundary	Mammalian_phenotype	6
MP:0012138	MP:0012138	decreased forebrain size	Mammalian_phenotype	6
MP:0012139	MP:0012139	increased forebrain size	Mammalian_phenotype	6
MP:0012143	MP:0012143	decreased a wave amplitude	Mammalian_phenotype	6
MP:0012144	MP:0012144	decreased b wave amplitude	Mammalian_phenotype	6
MP:0012145	MP:0012145	increased a wave amplitude	Mammalian_phenotype	6
MP:0012146	MP:0012146	increased b wave amplitude	Mammalian_phenotype	6
MP:0012147	MP:0012147	increased a wave implicit time	Mammalian_phenotype	6
MP:0012148	MP:0012148	decreased a wave implicit time	Mammalian_phenotype	6
MP:0012149	MP:0012149	decreased b wave implicit time	Mammalian_phenotype	6
MP:0012150	MP:0012150	increased b wave implicit time	Mammalian_phenotype	6
MP:0012151	MP:0012151	increased a wave latency	Mammalian_phenotype	6
MP:0012152	MP:0012152	decreased a wave latency	Mammalian_phenotype	6
MP:0012153	MP:0012153	increased b wave latency	Mammalian_phenotype	6
MP:0012154	MP:0012154	decreased b wave latency	Mammalian_phenotype	6
MP:0012162	MP:0012162	absent parietal endoderm	Mammalian_phenotype	6
MP:0012163	MP:0012163	abnormal dental mesenchyme morphology	Mammalian_phenotype	6
MP:0012164	MP:0012164	abnormal conjunctiva goblet cell morphology	Mammalian_phenotype	6
MP:0012168	MP:0012168	abnormal optic placode morphology	Mammalian_phenotype	6
MP:0012211	MP:0012211	decreased thalamus hypoxanthine-guanine phosphoribosyltransferase level	Mammalian_phenotype	6
MP:0012212	MP:0012212	increased thalamus hypoxanthine-guanine phosphoribosyltransferase level	Mammalian_phenotype	6
MP:0012213	MP:0012213	decreased hypothalamus hypoxanthine-guanine phosphoribosyltransferase level	Mammalian_phenotype	6
MP:0012214	MP:0012214	increased hypothalamus hypoxanthine-guanine phosphoribosyltransferase level	Mammalian_phenotype	6
MP:0012220	MP:0012220	abnormal ether lipid level	Mammalian_phenotype	6
MP:0012225	MP:0012225	decreased sterol level	Mammalian_phenotype	6
MP:0012226	MP:0012226	increased sterol level	Mammalian_phenotype	6
MP:0012232	MP:0012232	abnormal ceramide level	Mammalian_phenotype	6
MP:0012233	MP:0012233	abnormal acidic glycosphingolipid level	Mammalian_phenotype	6
MP:0012238	MP:0012238	abnormal cholangiocyte primary cilium morphology	Mammalian_phenotype	6
MP:0012251	MP:0012251	abnormal diaphragm development	Mammalian_phenotype	6
MP:0012263	MP:0012263	decreased hindbrain size	Mammalian_phenotype	6
MP:0012265	MP:0012265	increased hindbrain size	Mammalian_phenotype	6
MP:0012279	MP:0012279	wide sternum	Mammalian_phenotype	6
MP:0012290	MP:0012290	abnormal slow-wave sleep pattern	Mammalian_phenotype	6
MP:0012301	MP:0012301	absent umbilical cord blood vessels	Mammalian_phenotype	6
MP:0012308	MP:0012308	salt preference	Mammalian_phenotype	6
MP:0012318	MP:0012318	slow extinction of fear memory	Mammalian_phenotype	6
MP:0012319	MP:0012319	fast extinction of fear memory	Mammalian_phenotype	6
MP:0012325	MP:0012325	decreased circulating antithrombin level	Mammalian_phenotype	6
MP:0012326	MP:0012326	increased circulating antithrombin level	Mammalian_phenotype	6
MP:0012328	MP:0012328	decreased circulating factor VIII level	Mammalian_phenotype	6
MP:0012329	MP:0012329	increased circulating factor VIII level	Mammalian_phenotype	6
MP:0012330	MP:0012330	decreased circulating fibrinogen level	Mammalian_phenotype	6
MP:0012331	MP:0012331	increased circulating fibrinogen level	Mammalian_phenotype	6
MP:0012332	MP:0012332	decreased circulating fibronectin level	Mammalian_phenotype	6
MP:0012333	MP:0012333	increased circulating fibronectin level	Mammalian_phenotype	6
MP:0012334	MP:0012334	decreased circulating homocysteine level	Mammalian_phenotype	6
MP:0012335	MP:0012335	increased circulating homocysteine level	Mammalian_phenotype	6
MP:0012338	MP:0012338	decreased bile salt level	Mammalian_phenotype	6
MP:0012352	MP:0012352	progressive cornea degeneration	Mammalian_phenotype	6
MP:0012353	MP:0012353	bilateral cornea degeneration	Mammalian_phenotype	6
MP:0012354	MP:0012354	abnormal prothrombin time	Mammalian_phenotype	6
MP:0012357	MP:0012357	abnormal partial thromboplastin time	Mammalian_phenotype	6
MP:0012385	MP:0012385	abnormal erythrocyte potassium:chloride symporter activity	Mammalian_phenotype	6
MP:0012388	MP:0012388	abnormal erythrocyte sodium:hydrogen antiporter activity	Mammalian_phenotype	6
MP:0012391	MP:0012391	abnormal erythrocyte sodium:potassium-exchanging ATPase activity	Mammalian_phenotype	6
MP:0012394	MP:0012394	abnormal erythrocyte calcium-activated potassium channel activity	Mammalian_phenotype	6
MP:0012413	MP:0012413	decreased muscle tumor incidence	Mammalian_phenotype	6
MP:0012415	MP:0012415	decreased sarcoma incidence	Mammalian_phenotype	6
MP:0012416	MP:0012416	decreased gland tumor incidence	Mammalian_phenotype	6
MP:0012417	MP:0012417	decreased reproductive system tumor incidence	Mammalian_phenotype	6
MP:0012418	MP:0012418	decreased eye tumor incidence	Mammalian_phenotype	6
MP:0012419	MP:0012419	decreased cardiovascular system tumor incidence	Mammalian_phenotype	6
MP:0012420	MP:0012420	decreased hemolymphoid system tumor incidence	Mammalian_phenotype	6
MP:0012421	MP:0012421	decreased hepatobiliary system tumor incidence	Mammalian_phenotype	6
MP:0012422	MP:0012422	decreased integument system tumor incidence	Mammalian_phenotype	6
MP:0012423	MP:0012423	decreased nervous system tumor incidence	Mammalian_phenotype	6
MP:0012424	MP:0012424	decreased alimentary system tumor incidence	Mammalian_phenotype	6
MP:0012425	MP:0012425	decreased respiratory system tumor incidence	Mammalian_phenotype	6
MP:0012426	MP:0012426	decreased skeletal tumor incidence	Mammalian_phenotype	6
MP:0012427	MP:0012427	decreased urinary system tumor incidence	Mammalian_phenotype	6
MP:0012429	MP:0012429	decreased myoepithelioma incidence	Mammalian_phenotype	6
MP:0012431	MP:0012431	increased lymphoma incidence	Mammalian_phenotype	6
MP:0012461	MP:0012461	increased brain internal capsule size	Mammalian_phenotype	6
MP:0012462	MP:0012462	decreased brain internal capsule size	Mammalian_phenotype	6
MP:0012463	MP:0012463	increased optic tract size	Mammalian_phenotype	6
MP:0012464	MP:0012464	decreased optic tract size	Mammalian_phenotype	6
MP:0012469	MP:0012469	increased genu of the facial nerve size	Mammalian_phenotype	6
MP:0012470	MP:0012470	decreased genu of the facial nerve size	Mammalian_phenotype	6
MP:0012512	MP:0012512	abnormal sternum body morphology	Mammalian_phenotype	6
MP:0012516	MP:0012516	absent metencephalon	Mammalian_phenotype	6
MP:0012517	MP:0012517	absent diencephalon	Mammalian_phenotype	6
MP:0012526	MP:0012526	abnormal upper rhombic lip morphology	Mammalian_phenotype	6
MP:0012527	MP:0012527	abnormal lower rhombic lip morphology	Mammalian_phenotype	6
MP:0012539	MP:0012539	Bergmeister's papilla	Mammalian_phenotype	6
MP:0012541	MP:0012541	absent lamina terminalis	Mammalian_phenotype	6
MP:0012543	MP:0012543	abnormal rostral neuropore morphology	Mammalian_phenotype	6
MP:0012544	MP:0012544	abnormal caudal neuropore morphology	Mammalian_phenotype	6
MP:0012552	MP:0012552	lactic acidosis	Mammalian_phenotype	6
MP:0012563	MP:0012563	increased tumor incidence following infection	Mammalian_phenotype	6
MP:0012564	MP:0012564	decreased tumor incidence following infection	Mammalian_phenotype	6
MP:0012572	MP:0012572	increased susceptility to chemically induced skin inflammation	Mammalian_phenotype	6
MP:0012573	MP:0012573	decreased susceptility to chemically induced skin inflammation	Mammalian_phenotype	6
MP:0012581	MP:0012581	decreased eosinophil peroxidase activity	Mammalian_phenotype	6
MP:0012583	MP:0012583	increased eosinophil peroxidase activity	Mammalian_phenotype	6
MP:0012587	MP:0012587	decreased brain catechol O-methyltransferase activity	Mammalian_phenotype	6
MP:0012588	MP:0012588	increased brain catechol O-methyltransferase activity	Mammalian_phenotype	6
MP:0012592	MP:0012592	decreased brain choline acetyltransferase activity	Mammalian_phenotype	6
MP:0012593	MP:0012593	increased brain choline acetyltransferase activity	Mammalian_phenotype	6
MP:0012605	MP:0012605	decreased kidney glutathione level	Mammalian_phenotype	6
MP:0012607	MP:0012607	increased kidney glutathione level	Mammalian_phenotype	6
MP:0012608	MP:0012608	abnormal complement C5 level	Mammalian_phenotype	6
MP:0012614	MP:0012614	abnormal circulating factor IX level	Mammalian_phenotype	6
MP:0012617	MP:0012617	abnormal circulating factor X level	Mammalian_phenotype	6
MP:0012620	MP:0012620	abnormal circulating factor XIII level	Mammalian_phenotype	6
MP:0012626	MP:0012626	decreased brain acetylcholinesterase activity	Mammalian_phenotype	6
MP:0012627	MP:0012627	increased brain acetylcholinesterase activity	Mammalian_phenotype	6
MP:0012631	MP:0012631	decreased kidney glutathione reductase level	Mammalian_phenotype	6
MP:0012632	MP:0012632	increased kidney glutathione reductase level	Mammalian_phenotype	6
MP:0012638	MP:0012638	decreased brain monoamine oxidase activity	Mammalian_phenotype	6
MP:0012639	MP:0012639	increased brain monoamine oxidase activity	Mammalian_phenotype	6
MP:0012653	MP:0012653	decreased erythrocyte catalase level	Mammalian_phenotype	6
MP:0012654	MP:0012654	decreased kidney catalase level	Mammalian_phenotype	6
MP:0012656	MP:0012656	increased erythrocyte catalase level	Mammalian_phenotype	6
MP:0012657	MP:0012657	increased kidney catalase level	Mammalian_phenotype	6
MP:0012664	MP:0012664	decreased circulating haptoglobin level	Mammalian_phenotype	6
MP:0012666	MP:0012666	increased circulating haptoglobin level	Mammalian_phenotype	6
MP:0012670	MP:0012670	prolonged somite segmentation clock period	Mammalian_phenotype	6
MP:0012671	MP:0012671	retinal spots	Mammalian_phenotype	6
MP:0012675	MP:0012675	enlarged floor plate	Mammalian_phenotype	6
MP:0012676	MP:0012676	dilated brain ventricles	Mammalian_phenotype	6
MP:0012677	MP:0012677	absent brain ventricles	Mammalian_phenotype	6
MP:0012681	MP:0012681	collapsed brain ventricles	Mammalian_phenotype	6
MP:0012683	MP:0012683	absent telencephalon	Mammalian_phenotype	6
MP:0012685	MP:0012685	abnormal primitive streak elongation	Mammalian_phenotype	6
MP:0012686	MP:0012686	everted embryonic neuroepithelium	Mammalian_phenotype	6
MP:0012698	MP:0012698	increased maternal body weight gain	Mammalian_phenotype	6
MP:0012699	MP:0012699	decreased maternal body weight gain	Mammalian_phenotype	6
MP:0012702	MP:0012702	increased embryonic neuroepithelium thickness	Mammalian_phenotype	6
MP:0012703	MP:0012703	decreased embryonic neuroepithelium thickness	Mammalian_phenotype	6
MP:0012707	MP:0012707	incomplete caudal neuropore closure	Mammalian_phenotype	6
MP:0012714	MP:0012714	decreased ventral ectodermal ridge size	Mammalian_phenotype	6
MP:0012716	MP:0012716	abnormal hemangioblast number	Mammalian_phenotype	6
MP:0012736	MP:0012736	abnormal polar body morphology	Mammalian_phenotype	6
MP:0012739	MP:0012739	abnormal anterior primitive streak morphology	Mammalian_phenotype	6
MP:0012740	MP:0012740	abnormal posterior primitive streak morphology	Mammalian_phenotype	6
MP:0012741	MP:0012741	decreased neural crest cell proliferation	Mammalian_phenotype	6
MP:0012742	MP:0012742	increased neural crest cell proliferation	Mammalian_phenotype	6
MP:0012743	MP:0012743	increased inner cell mass apoptosis	Mammalian_phenotype	6
MP:0012744	MP:0012744	increased neural crest cell apoptosis	Mammalian_phenotype	6
MP:0012752	MP:0012752	abnormal cardiac neural crest cell migration	Mammalian_phenotype	6
MP:0012757	MP:0012757	abnormal cranial neural crest cell migration	Mammalian_phenotype	6
MP:0012758	MP:0012758	abnormal cranial neural crest cell proliferation	Mammalian_phenotype	6
MP:0012783	MP:0012783	abnormal extensor digitorum longus weight	Mammalian_phenotype	6
MP:0013004	MP:0013004	abnormal enteric neural crest cell proliferation	Mammalian_phenotype	6
MP:0013006	MP:0013006	abnormal enteric neural crest cell migration	Mammalian_phenotype	6
MP:0013007	MP:0013007	abnormal vagal neural crest cell migration	Mammalian_phenotype	6
MP:0013008	MP:0013008	abnormal sacral neural crest cell migration	Mammalian_phenotype	6
MP:0013012	MP:0013012	abnormal trunk neural crest cell migration	Mammalian_phenotype	6
MP:0013111	MP:0013111	greasy abdomen coat	Mammalian_phenotype	6
MP:0013112	MP:0013112	greasy thorax coat	Mammalian_phenotype	6
MP:0013147	MP:0013147	limb paralysis	Mammalian_phenotype	6
MP:0013159	MP:0013159	Purkinje cell axonal dystrophy	Mammalian_phenotype	6
MP:0013165	MP:0013165	absent forelimb buds	Mammalian_phenotype	6
MP:0013166	MP:0013166	small forelimb buds	Mammalian_phenotype	6
MP:0013168	MP:0013168	absent hindlimb buds	Mammalian_phenotype	6
MP:0013169	MP:0013169	small hindlimb buds	Mammalian_phenotype	6
MP:0020004	MP:0020004	abnormal sulfatide level	Mammalian_phenotype	6
MP:0020010	MP:0020010	decreased bone mineral density of femur	Mammalian_phenotype	6
MP:0020011	MP:0020011	increased bone mineral density of femur	Mammalian_phenotype	6
MP:0020023	MP:0020023	decreased hepatic delta-aminolaevulinate dehydratase activity	Mammalian_phenotype	6
MP:0020025	MP:0020025	increased hepatic delta-aminolaevulinate dehydratase activity	Mammalian_phenotype	6
MP:0020031	MP:0020031	decreased plasma cholinesterase activity	Mammalian_phenotype	6
MP:0020032	MP:0020032	increased plasma cholinesterase activity	Mammalian_phenotype	6
MP:0020057	MP:0020057	decreased spermatazoal beta-glucuronidase activity	Mammalian_phenotype	6
MP:0020059	MP:0020059	increased spermatazoal beta-glucuronidase activity	Mammalian_phenotype	6
MP:0020071	MP:0020071	decreased blood catalase activity	Mammalian_phenotype	6
MP:0020072	MP:0020072	increased blood catalase activity	Mammalian_phenotype	6
MP:0020076	MP:0020076	increased brain tyrosine hydroxylase activity	Mammalian_phenotype	6
MP:0020078	MP:0020078	decreased brain tyrosine hydroxylase activity	Mammalian_phenotype	6
MP:0020079	MP:0020079	increased incidence of epicardial mineralization	Mammalian_phenotype	6
MP:0020110	MP:0020110	increased thromboxane level	Mammalian_phenotype	6
MP:0020111	MP:0020111	decreased thromboxane level	Mammalian_phenotype	6
MP:0020113	MP:0020113	high carcass lipid	Mammalian_phenotype	6
MP:0020114	MP:0020114	low carcass lipid	Mammalian_phenotype	6
MP:0020116	MP:0020116	increased sphingosine level	Mammalian_phenotype	6
MP:0020117	MP:0020117	decreased sphingosine level	Mammalian_phenotype	6
MP:0020131	MP:0020131	abnormal gallbladder volume	Mammalian_phenotype	6
MP:0020132	MP:0020132	increased gallbladder volume	Mammalian_phenotype	6
MP:0020133	MP:0020133	decreased gallbladder volume	Mammalian_phenotype	6
MP:0020136	MP:0020136	abnormal interventricular septum thickness	Mammalian_phenotype	6
MP:0020143	MP:0020143	abnormal adrenal gland x-zone size	Mammalian_phenotype	6
MP:0020150	MP:0020150	abnormal timing of vaginal opening	Mammalian_phenotype	6
MP:0020164	MP:0020164	abnormal quadriceps weight	Mammalian_phenotype	6
MP:0020165	MP:0020165	abnormal soleus weight	Mammalian_phenotype	6
MP:0020166	MP:0020166	abnormal tibialis anterior weight	Mammalian_phenotype	6
MP:0020170	MP:0020170	vacuolated thymus epithelium	Mammalian_phenotype	6
MP:0020190	MP:0020190	abnormal lung adenoma incidence	Mammalian_phenotype	6
MP:0020191	MP:0020191	abnormal lymphocyte activation involved in immune response	Mammalian_phenotype	6
MP:0020197	MP:0020197	decreased reticular tumor incidence	Mammalian_phenotype	6
MP:0020199	MP:0020199	increased reticular tumor incidence	Mammalian_phenotype	6
MP:0020201	MP:0020201	abnormal granulocyte number	Mammalian_phenotype	6
MP:0020202	MP:0020202	abnormal macrophage cell number	Mammalian_phenotype	6
MP:0020204	MP:0020204	abnormal heart left ventricle weight	Mammalian_phenotype	6
MP:0020205	MP:0020205	abnormal heart right ventricle weight	Mammalian_phenotype	6
MP:0020206	MP:0020206	abnormal heart left atrium weight	Mammalian_phenotype	6
MP:0020207	MP:0020207	abnormal heart right atrium weight	Mammalian_phenotype	6
MP:0012094	MP:0012094	abnormal Reichert's membrane thickness	Mammalian_phenotype	7
MP:0012097	MP:0012097	abnormal spongiotrophoblast size	Mammalian_phenotype	7
MP:0012100	MP:0012100	absent spongiotrophoblast	Mammalian_phenotype	7
MP:0012101	MP:0012101	acoria	Mammalian_phenotype	7
MP:0012140	MP:0012140	forebrain hyperplasia	Mammalian_phenotype	7
MP:0012169	MP:0012169	optic placode degeneration	Mammalian_phenotype	7
MP:0012170	MP:0012170	absent optic placodes	Mammalian_phenotype	7
MP:0012215	MP:0012215	abnormal plasmalogen level	Mammalian_phenotype	7
MP:0012227	MP:0012227	decreased brain sterol level	Mammalian_phenotype	7
MP:0012228	MP:0012228	increased brain sterol level	Mammalian_phenotype	7
MP:0012229	MP:0012229	abnormal sulfoglycosphingolipid level	Mammalian_phenotype	7
MP:0012231	MP:0012231	abnormal ganglioside level	Mammalian_phenotype	7
MP:0012264	MP:0012264	hindbrain hypoplasia	Mammalian_phenotype	7
MP:0012266	MP:0012266	hindbrain hyperplasia	Mammalian_phenotype	7
MP:0012267	MP:0012267	abnormal red nucleus morphology	Mammalian_phenotype	7
MP:0012280	MP:0012280	abnormal sternebra size	Mammalian_phenotype	7
MP:0012282	MP:0012282	abnormal sternebra number	Mammalian_phenotype	7
MP:0012285	MP:0012285	misaligned sternebrae	Mammalian_phenotype	7
MP:0012286	MP:0012286	decreased frequency of paradoxical sleep	Mammalian_phenotype	7
MP:0012287	MP:0012287	increased frequency of paradoxical sleep	Mammalian_phenotype	7
MP:0012291	MP:0012291	increased slow-wave sleep duration	Mammalian_phenotype	7
MP:0012292	MP:0012292	decreased slow-wave sleep duration	Mammalian_phenotype	7
MP:0012293	MP:0012293	impaired active avoidance behavior	Mammalian_phenotype	7
MP:0012294	MP:0012294	enhanced active avoidance behavior	Mammalian_phenotype	7
MP:0012336	MP:0012336	decreased vitamin D level	Mammalian_phenotype	7
MP:0012337	MP:0012337	increased vitamin D level	Mammalian_phenotype	7
MP:0012340	MP:0012340	decreased testicular teratoma incidence	Mammalian_phenotype	7
MP:0012345	MP:0012345	increased tail rattling	Mammalian_phenotype	7
MP:0012346	MP:0012346	decreased tail rattling	Mammalian_phenotype	7
MP:0012347	MP:0012347	low sweet preference	Mammalian_phenotype	7
MP:0012355	MP:0012355	decreased prothrombin time	Mammalian_phenotype	7
MP:0012356	MP:0012356	increased prothrombin time	Mammalian_phenotype	7
MP:0012358	MP:0012358	decreased partial thromboplastin time	Mammalian_phenotype	7
MP:0012359	MP:0012359	increased partial thromboplastin time	Mammalian_phenotype	7
MP:0012363	MP:0012363	abnormal erythrocyte sodium level	Mammalian_phenotype	7
MP:0012366	MP:0012366	abnormal erythrocyte magnesium level	Mammalian_phenotype	7
MP:0012369	MP:0012369	abnormal erythrocyte potassium level	Mammalian_phenotype	7
MP:0012372	MP:0012372	abnormal erythrocyte ion content	Mammalian_phenotype	7
MP:0012386	MP:0012386	decreased erythrocyte potassium:chloride symporter activity	Mammalian_phenotype	7
MP:0012387	MP:0012387	increased erythrocyte potassium:chloride symporter activity	Mammalian_phenotype	7
MP:0012389	MP:0012389	decreased erythrocyte sodium:hydrogen antiporter activity	Mammalian_phenotype	7
MP:0012390	MP:0012390	increased erythrocyte sodium:hydrogen antiporter activity	Mammalian_phenotype	7
MP:0012392	MP:0012392	decreased erythrocyte sodium:potassium-exchanging ATPase activity	Mammalian_phenotype	7
MP:0012393	MP:0012393	increased erythrocyte sodium:potassium-exchanging ATPase activity	Mammalian_phenotype	7
MP:0012395	MP:0012395	decreased erythrocyte calcium-activated potassium channel activity	Mammalian_phenotype	7
MP:0012396	MP:0012396	increased erythrocyte calcium-activated potassium channel activity	Mammalian_phenotype	7
MP:0012397	MP:0012397	abnormal nucleated erythrocyte cell number	Mammalian_phenotype	7
MP:0012412	MP:0012412	increased Type B reticulum cell tumor incidence	Mammalian_phenotype	7
MP:0012414	MP:0012414	decreased rhabdomyosarcoma incidence	Mammalian_phenotype	7
MP:0012430	MP:0012430	decreased Type B reticulum cell tumor incidence	Mammalian_phenotype	7
MP:0012432	MP:0012432	decreased prostate gland tumor incidence	Mammalian_phenotype	7
MP:0012433	MP:0012433	decreased ovarian tumor incidence	Mammalian_phenotype	7
MP:0012434	MP:0012434	decreased intestinal adenoma incidence	Mammalian_phenotype	7
MP:0012435	MP:0012435	decreased colon tumor incidence	Mammalian_phenotype	7
MP:0012437	MP:0012437	increased Harderian gland tumor incidence	Mammalian_phenotype	7
MP:0012438	MP:0012438	decreased Harderian gland tumor incidence	Mammalian_phenotype	7
MP:0012439	MP:0012439	decreased pituitary gland tumor incidence	Mammalian_phenotype	7
MP:0012441	MP:0012441	abnormal monocyte cell number	Mammalian_phenotype	7
MP:0012467	MP:0012467	increased striatum area	Mammalian_phenotype	7
MP:0012468	MP:0012468	decreased striatum area	Mammalian_phenotype	7
MP:0012479	MP:0012479	increased amygdala size	Mammalian_phenotype	7
MP:0012480	MP:0012480	decreased amygdala size	Mammalian_phenotype	7
MP:0012513	MP:0012513	absent sternum body	Mammalian_phenotype	7
MP:0012519	MP:0012519	dilated Brunner's glands	Mammalian_phenotype	7
MP:0012520	MP:0012520	absent Brunner's glands	Mammalian_phenotype	7
MP:0012523	MP:0012523	abnormal upper lip morphology	Mammalian_phenotype	7
MP:0012524	MP:0012524	abnormal lower lip morphology	Mammalian_phenotype	7
MP:0012532	MP:0012532	abnorrmal surface ectoderm morphology	Mammalian_phenotype	7
MP:0012559	MP:0012559	decreased forebrain volume	Mammalian_phenotype	7
MP:0012560	MP:0012560	increased forebrain volume	Mammalian_phenotype	7
MP:0012577	MP:0012577	decreased kidney glutathione peroxidase activity	Mammalian_phenotype	7
MP:0012578	MP:0012578	increased kidney glutathione peroxidase activity	Mammalian_phenotype	7
MP:0012609	MP:0012609	decreased complement C5 level	Mammalian_phenotype	7
MP:0012610	MP:0012610	increased complement C5 level	Mammalian_phenotype	7
MP:0012615	MP:0012615	decreased circulating factor IX level	Mammalian_phenotype	7
MP:0012616	MP:0012616	increased circulating factor IX level	Mammalian_phenotype	7
MP:0012618	MP:0012618	decreased circulating factor X level	Mammalian_phenotype	7
MP:0012619	MP:0012619	increased circulating factor X level	Mammalian_phenotype	7
MP:0012621	MP:0012621	decreased circulating factor XIII level	Mammalian_phenotype	7
MP:0012622	MP:0012622	increased circulating factor XIII level	Mammalian_phenotype	7
MP:0012667	MP:0012667	split sternal manubrium	Mammalian_phenotype	7
MP:0012668	MP:0012668	absent sternal manubrium	Mammalian_phenotype	7
MP:0012674	MP:0012674	tomacula	Mammalian_phenotype	7
MP:0012678	MP:0012678	absent fourth ventricle	Mammalian_phenotype	7
MP:0012679	MP:0012679	absent third ventricle	Mammalian_phenotype	7
MP:0012680	MP:0012680	absent lateral ventricles	Mammalian_phenotype	7
MP:0012682	MP:0012682	abnormal septal nucleus morphology	Mammalian_phenotype	7
MP:0012708	MP:0012708	delayed rostral neuropore closure	Mammalian_phenotype	7
MP:0012709	MP:0012709	delayed caudal neuropore closure	Mammalian_phenotype	7
MP:0012717	MP:0012717	increased hemangioblast number	Mammalian_phenotype	7
MP:0012718	MP:0012718	decreased hemangioblast number	Mammalian_phenotype	7
MP:0012729	MP:0012729	abnormal common carotid artery morphology	Mammalian_phenotype	7
MP:0012730	MP:0012730	abnormal internal carotid artery morphology	Mammalian_phenotype	7
MP:0012731	MP:0012731	abnormal external carotid artery morphology	Mammalian_phenotype	7
MP:0012737	MP:0012737	abnormal primary polar body morphology	Mammalian_phenotype	7
MP:0012738	MP:0012738	abnormal secondary polar body morphology	Mammalian_phenotype	7
MP:0012753	MP:0012753	increased cardiac neural crest cell apoptosis	Mammalian_phenotype	7
MP:0012754	MP:0012754	abnormal cranial neural crest cell morphology	Mammalian_phenotype	7
MP:0012759	MP:0012759	increased cranial neural crest cell proliferation	Mammalian_phenotype	7
MP:0012760	MP:0012760	decreased cranial neural crest cell proliferation	Mammalian_phenotype	7
MP:0012761	MP:0012761	increased cranial neural crest cell apoptosis	Mammalian_phenotype	7
MP:0012784	MP:0012784	abnormal rhombomere 1 morphology	Mammalian_phenotype	7
MP:0012788	MP:0012788	abnormal rhombomere 2 morphology	Mammalian_phenotype	7
MP:0012792	MP:0012792	abnormal rhombomere 3 morphology	Mammalian_phenotype	7
MP:0012796	MP:0012796	abnormal rhombomere 4 morphology	Mammalian_phenotype	7
MP:0012800	MP:0012800	abnormal rhombomere 5 morphology	Mammalian_phenotype	7
MP:0012804	MP:0012804	abnormal rhombomere 6 morphology	Mammalian_phenotype	7
MP:0012808	MP:0012808	abnormal rhombomere 7 morphology	Mammalian_phenotype	7
MP:0012812	MP:0012812	abnormal rhombomere 8 morphology	Mammalian_phenotype	7
MP:0012816	MP:0012816	abnormal rhombomere boundary morphology	Mammalian_phenotype	7
MP:0012817	MP:0012817	rhombomere fusion	Mammalian_phenotype	7
MP:0012818	MP:0012818	rhombomere transformation	Mammalian_phenotype	7
MP:0013000	MP:0013000	absent cerebral aqueduct	Mammalian_phenotype	7
MP:0013001	MP:0013001	abnormal enteric neural crest cell morphology	Mammalian_phenotype	7
MP:0013005	MP:0013005	decreased enteric neural crest cell proliferation	Mammalian_phenotype	7
MP:0013009	MP:0013009	increased vagal neural crest cell apoptosis	Mammalian_phenotype	7
MP:0013010	MP:0013010	abnormal vagal neural crest cell morphology	Mammalian_phenotype	7
MP:0013013	MP:0013013	abnormal trunk neural crest cell morphology	Mammalian_phenotype	7
MP:0013014	MP:0013014	increased trunk neural crest cell apoptosis	Mammalian_phenotype	7
MP:0013115	MP:0013115	focal hair loss in abdominal region	Mammalian_phenotype	7
MP:0013116	MP:0013116	focal hair loss in head/neck region	Mammalian_phenotype	7
MP:0013117	MP:0013117	focal hair loss in thorax region	Mammalian_phenotype	7
MP:0013130	MP:0013130	abnormal gum color	Mammalian_phenotype	7
MP:0013131	MP:0013131	pale lips	Mammalian_phenotype	7
MP:0013150	MP:0013150	head/neck piloerection	Mammalian_phenotype	7
MP:0020005	MP:0020005	decreased sulfatide level	Mammalian_phenotype	7
MP:0020006	MP:0020006	increased sulfatide level	Mammalian_phenotype	7
MP:0020124	MP:0020124	abnormal circulating HDL phospholipid level	Mammalian_phenotype	7
MP:0020127	MP:0020127	abnormal circulating non-HDL phospholipid level	Mammalian_phenotype	7
MP:0020144	MP:0020144	small adrenal gland x-zone	Mammalian_phenotype	7
MP:0020145	MP:0020145	enlarged adrenal gland x-zone	Mammalian_phenotype	7
MP:0020152	MP:0020152	abnormal oocyte number	Mammalian_phenotype	7
MP:0020156	MP:0020156	multinucleated pancreatic acinar cells	Mammalian_phenotype	7
MP:0020162	MP:0020162	decreased susceptibility to virus induced diabetes	Mammalian_phenotype	7
MP:0020163	MP:0020163	increased susceptibility to virus induced diabetes	Mammalian_phenotype	7
MP:0020167	MP:0020167	abnormal vertical activity	Mammalian_phenotype	7
MP:0020192	MP:0020192	decreased lymphocyte activation involved in immune response	Mammalian_phenotype	7
MP:0020193	MP:0020193	increased lymphocyte activation involved in immune response	Mammalian_phenotype	7
MP:0020198	MP:0020198	decreased mononuclear phagocyte tumor incidence	Mammalian_phenotype	7
MP:0020200	MP:0020200	increased mononuclear phagocyte tumor incidence	Mammalian_phenotype	7
MP:0000033	MP:0000033	absent scala media	Mammalian_phenotype	7
MP:0000041	MP:0000041	absent endolymphatic duct	Mammalian_phenotype	7
MP:0000042	MP:0000042	abnormal organ of Corti morphology	Mammalian_phenotype	7
MP:0000048	MP:0000048	abnormal stria vascularis morphology	Mammalian_phenotype	7
MP:0000075	MP:0000075	absent neurocranium	Mammalian_phenotype	7
MP:0000077	MP:0000077	abnormal interparietal bone morphology	Mammalian_phenotype	7
MP:0000079	MP:0000079	abnormal basioccipital bone morphology	Mammalian_phenotype	7
MP:0000082	MP:0000082	overlapping parietal bones	Mammalian_phenotype	7
MP:0000098	MP:0000098	abnormal vomer bone morphology	Mammalian_phenotype	7
MP:0000100	MP:0000100	abnormal ethmoidal bone morphology	Mammalian_phenotype	7
MP:0000102	MP:0000102	abnormal nasal bone morphology	Mammalian_phenotype	7
MP:0000104	MP:0000104	abnormal sphenoid bone morphology	Mammalian_phenotype	7
MP:0000106	MP:0000106	abnormal basisphenoid bone morphology	Mammalian_phenotype	7
MP:0000107	MP:0000107	abnormal frontal bone morphology	Mammalian_phenotype	7
MP:0000109	MP:0000109	abnormal parietal bone morphology	Mammalian_phenotype	7
MP:0000151	MP:0000151	absent ribs	Mammalian_phenotype	7
MP:0000194	MP:0000194	increased circulating calcium level	Mammalian_phenotype	7
MP:0000195	MP:0000195	decreased circulating calcium level	Mammalian_phenotype	7
MP:0000198	MP:0000198	decreased circulating phosphate level	Mammalian_phenotype	7
MP:0000218	MP:0000218	increased leukocyte cell number	Mammalian_phenotype	7
MP:0000221	MP:0000221	decreased leukocyte cell number	Mammalian_phenotype	7
MP:0000226	MP:0000226	abnormal mean corpuscular volume	Mammalian_phenotype	7
MP:0000239	MP:0000239	absent common myeloid progenitor cells	Mammalian_phenotype	7
MP:0000248	MP:0000248	macrocytosis	Mammalian_phenotype	7
MP:0000256	MP:0000256	echinocytosis	Mammalian_phenotype	7
MP:0000262	MP:0000262	poor arterial differentiation	Mammalian_phenotype	7
MP:0000264	MP:0000264	failure of vascular branching	Mammalian_phenotype	7
MP:0000276	MP:0000276	heart right ventricle hypertrophy	Mammalian_phenotype	7
MP:0000293	MP:0000293	absent myocardial trabeculae	Mammalian_phenotype	7
MP:0000298	MP:0000298	absent atrioventricular cushions	Mammalian_phenotype	7
MP:0000299	MP:0000299	failure of atrioventricular cushion closure	Mammalian_phenotype	7
MP:0000301	MP:0000301	decreased atrioventricular cushion size	Mammalian_phenotype	7
MP:0000328	MP:0000328	increased enterocyte cell number	Mammalian_phenotype	7
MP:0000339	MP:0000339	decreased enterocyte cell number	Mammalian_phenotype	7
MP:0000364	MP:0000364	abnormal vascular regression	Mammalian_phenotype	7
MP:0000373	MP:0000373	belly spot	Mammalian_phenotype	7
MP:0000439	MP:0000439	enlarged cranium	Mammalian_phenotype	7
MP:0000441	MP:0000441	increased cranium width	Mammalian_phenotype	7
MP:0000453	MP:0000453	absent mouth	Mammalian_phenotype	7
MP:0000454	MP:0000454	abnormal jaw morphology	Mammalian_phenotype	7
MP:0000461	MP:0000461	decreased presacral vertebrae number	Mammalian_phenotype	7
MP:0000464	MP:0000464	increased presacral vertebrae number	Mammalian_phenotype	7
MP:0000472	MP:0000472	abnormal stomach squamous epithelium morphology	Mammalian_phenotype	7
MP:0000473	MP:0000473	abnormal stomach glandular epithelium morphology	Mammalian_phenotype	7
MP:0000491	MP:0000491	crypts of Lieberkuhn abscesses	Mammalian_phenotype	7
MP:0000523	MP:0000523	cortical renal glomerulopathies	Mammalian_phenotype	7
MP:0000553	MP:0000553	absent radius	Mammalian_phenotype	7
MP:0000602	MP:0000602	enlarged liver sinusoidal spaces	Mammalian_phenotype	7
MP:0000606	MP:0000606	decreased hepatocyte number	Mammalian_phenotype	7
MP:0000608	MP:0000608	dissociated hepatocytes	Mammalian_phenotype	7
MP:0000645	MP:0000645	absent adrenergic chromaffin cells	Mammalian_phenotype	7
MP:0000671	MP:0000671	bulbourethral gland hypoplasia	Mammalian_phenotype	7
MP:0000693	MP:0000693	spleen hyperplasia	Mammalian_phenotype	7
MP:0000694	MP:0000694	spleen hypoplasia	Mammalian_phenotype	7
MP:0000708	MP:0000708	thymus hyperplasia	Mammalian_phenotype	7
MP:0000711	MP:0000711	thymus cortex hypoplasia	Mammalian_phenotype	7
MP:0000717	MP:0000717	abnormal lymphocyte cell number	Mammalian_phenotype	7
MP:0000742	MP:0000742	impaired contractility of ileal smooth muscle	Mammalian_phenotype	7
MP:0000780	MP:0000780	abnormal corpus callosum morphology	Mammalian_phenotype	7
MP:0000784	MP:0000784	forebrain hypoplasia	Mammalian_phenotype	7
MP:0000788	MP:0000788	abnormal cerebral cortex morphology	Mammalian_phenotype	7
MP:0000792	MP:0000792	abnormal cortical marginal zone morphology	Mammalian_phenotype	7
MP:0000794	MP:0000794	abnormal parietal lobe morphology	Mammalian_phenotype	7
MP:0000798	MP:0000798	abnormal frontal lobe morphology	Mammalian_phenotype	7
MP:0000801	MP:0000801	abnormal temporal lobe morphology	Mammalian_phenotype	7
MP:0000804	MP:0000804	abnormal occipital lobe morphology	Mammalian_phenotype	7
MP:0000819	MP:0000819	abnormal olfactory bulb morphology	Mammalian_phenotype	7
MP:0000821	MP:0000821	choroid plexus hyperplasia	Mammalian_phenotype	7
MP:0000825	MP:0000825	dilated lateral ventricles	Mammalian_phenotype	7
MP:0000827	MP:0000827	dilated third ventricle	Mammalian_phenotype	7
MP:0000829	MP:0000829	dilated fourth ventricle	Mammalian_phenotype	7
MP:0000833	MP:0000833	thalamus hyperplasia	Mammalian_phenotype	7
MP:0000839	MP:0000839	hypothalamus hyperplasia	Mammalian_phenotype	7
MP:0000842	MP:0000842	absent superior olivary complex	Mammalian_phenotype	7
MP:0000850	MP:0000850	absent cerebellum	Mammalian_phenotype	7
MP:0000852	MP:0000852	small cerebellum	Mammalian_phenotype	7
MP:0000907	MP:0000907	small mesencephalic trigeminal nucleus	Mammalian_phenotype	7
MP:0000908	MP:0000908	absent mesencephalic trigeminal nucleus	Mammalian_phenotype	7
MP:0000909	MP:0000909	abnormal facial motor nucleus morphology	Mammalian_phenotype	7
MP:0000911	MP:0000911	abnormal trigeminal motor nucleus morphology	Mammalian_phenotype	7
MP:0000935	MP:0000935	abnormal folding of telencephalic vesicles	Mammalian_phenotype	7
MP:0000936	MP:0000936	small embryonic telencephalon	Mammalian_phenotype	7
MP:0000962	MP:0000962	disorganized dorsal root ganglion	Mammalian_phenotype	7
MP:0000963	MP:0000963	fused dorsal root ganglion	Mammalian_phenotype	7
MP:0000964	MP:0000964	small dorsal root ganglion	Mammalian_phenotype	7
MP:0000973	MP:0000973	abnormal cutaneous/subcutaneous mechanoreceptor morphology	Mammalian_phenotype	7
MP:0000986	MP:0000986	increased Merkel's receptor number	Mammalian_phenotype	7
MP:0001009	MP:0001009	paravertebral ganglia hyperplasia	Mammalian_phenotype	7
MP:0001010	MP:0001010	prevertebral ganglia hyperplasia	Mammalian_phenotype	7
MP:0001011	MP:0001011	abnormal superior cervical ganglion morphology	Mammalian_phenotype	7
MP:0001016	MP:0001016	abnormal middle cervical ganglion morphology	Mammalian_phenotype	7
MP:0001017	MP:0001017	abnormal stellate ganglion morphology	Mammalian_phenotype	7
MP:0001036	MP:0001036	small submandibular ganglion	Mammalian_phenotype	7
MP:0001049	MP:0001049	abnormal enteric cholinergic innervation	Mammalian_phenotype	7
MP:0001067	MP:0001067	absent mandibular nerve	Mammalian_phenotype	7
MP:0001068	MP:0001068	abnormal mandibular nerve branching	Mammalian_phenotype	7
MP:0001083	MP:0001083	small geniculate ganglion	Mammalian_phenotype	7
MP:0001085	MP:0001085	small petrosal ganglion	Mammalian_phenotype	7
MP:0001086	MP:0001086	absent petrosal ganglion	Mammalian_phenotype	7
MP:0001088	MP:0001088	small nodose ganglion	Mammalian_phenotype	7
MP:0001089	MP:0001089	absent nodose ganglion	Mammalian_phenotype	7
MP:0001093	MP:0001093	small trigeminal ganglion	Mammalian_phenotype	7
MP:0001095	MP:0001095	enlarged trigeminal ganglion	Mammalian_phenotype	7
MP:0001098	MP:0001098	small superior glossopharyngeal ganglion	Mammalian_phenotype	7
MP:0001102	MP:0001102	small superior vagus ganglion	Mammalian_phenotype	7
MP:0001108	MP:0001108	absent Schwann cells	Mammalian_phenotype	7
MP:0001123	MP:0001123	dilated uterus	Mammalian_phenotype	7
MP:0001131	MP:0001131	abnormal ovarian follicle morphology	Mammalian_phenotype	7
MP:0001135	MP:0001135	abnormal uterine cervix morphology	Mammalian_phenotype	7
MP:0001140	MP:0001140	abnormal vagina epithelium morphology	Mammalian_phenotype	7
MP:0001142	MP:0001142	abnormal vagina orifice morphology	Mammalian_phenotype	7
MP:0001150	MP:0001150	enlarged scrotum	Mammalian_phenotype	7
MP:0001159	MP:0001159	absent prostate gland	Mammalian_phenotype	7
MP:0001163	MP:0001163	abnormal prostate gland anterior lobe morphology	Mammalian_phenotype	7
MP:0001168	MP:0001168	abnormal prostate gland epithelium morphology	Mammalian_phenotype	7
MP:0001170	MP:0001170	bulbourethral gland hyperplasia	Mammalian_phenotype	7
MP:0001179	MP:0001179	thick pulmonary interalveolar septum	Mammalian_phenotype	7
MP:0001183	MP:0001183	overexpanded pulmonary alveoli	Mammalian_phenotype	7
MP:0001184	MP:0001184	absent pulmonary alveoli	Mammalian_phenotype	7
MP:0001292	MP:0001292	abnormal lens vesicle development	Mammalian_phenotype	7
MP:0001318	MP:0001318	pupil opacity	Mammalian_phenotype	7
MP:0001319	MP:0001319	irregularly shaped pupil	Mammalian_phenotype	7
MP:0001320	MP:0001320	small pupils	Mammalian_phenotype	7
MP:0001327	MP:0001327	decreased retinal photoreceptor cell number	Mammalian_phenotype	7
MP:0001328	MP:0001328	disorganized retinal layers	Mammalian_phenotype	7
MP:0001354	MP:0001354	increased aggression towards males	Mammalian_phenotype	7
MP:0001356	MP:0001356	increased aggression towards females	Mammalian_phenotype	7
MP:0001382	MP:0001382	abnormal nursing	Mammalian_phenotype	7
MP:0001385	MP:0001385	pup cannibalization	Mammalian_phenotype	7
MP:0001399	MP:0001399	hyperactivity	Mammalian_phenotype	7
MP:0001402	MP:0001402	hypoactivity	Mammalian_phenotype	7
MP:0001404	MP:0001404	no spontaneous movement	Mammalian_phenotype	7
MP:0001406	MP:0001406	abnormal gait	Mammalian_phenotype	7
MP:0001426	MP:0001426	polydipsia	Mammalian_phenotype	7
MP:0001433	MP:0001433	polyphagia	Mammalian_phenotype	7
MP:0001475	MP:0001475	reduced long term depression	Mammalian_phenotype	7
MP:0001488	MP:0001488	increased startle reflex	Mammalian_phenotype	7
MP:0001489	MP:0001489	decreased startle reflex	Mammalian_phenotype	7
MP:0001500	MP:0001500	reduced kindling response	Mammalian_phenotype	7
MP:0001539	MP:0001539	decreased caudal vertebrae number	Mammalian_phenotype	7
MP:0001552	MP:0001552	increased circulating triglyceride level	Mammalian_phenotype	7
MP:0001554	MP:0001554	increased circulating free fatty acid level	Mammalian_phenotype	7
MP:0001566	MP:0001566	increased circulating phosphate level	Mammalian_phenotype	7
MP:0001577	MP:0001577	anemia	Mammalian_phenotype	7
MP:0001588	MP:0001588	abnormal hemoglobin	Mammalian_phenotype	7
MP:0001602	MP:0001602	impaired myelopoiesis	Mammalian_phenotype	7
MP:0001603	MP:0001603	failure of myelopoiesis	Mammalian_phenotype	7
MP:0001683	MP:0001683	absent mesoderm	Mammalian_phenotype	7
MP:0001684	MP:0001684	abnormal axial mesoderm	Mammalian_phenotype	7
MP:0001687	MP:0001687	thin endoderm	Mammalian_phenotype	7
MP:0001693	MP:0001693	failure of primitive streak formation	Mammalian_phenotype	7
MP:0001748	MP:0001748	increased circulating adrenocorticotropin level	Mammalian_phenotype	7
MP:0001750	MP:0001750	increased circulating follicle stimulating hormone level	Mammalian_phenotype	7
MP:0001751	MP:0001751	increased circulating luteinizing hormone level	Mammalian_phenotype	7
MP:0001823	MP:0001823	thymus hypoplasia	Mammalian_phenotype	7
MP:0001828	MP:0001828	abnormal T cell activation	Mammalian_phenotype	7
MP:0001855	MP:0001855	atrial thrombosis	Mammalian_phenotype	7
MP:0001862	MP:0001862	interstitial pneumonia	Mammalian_phenotype	7
MP:0001867	MP:0001867	rhinitis	Mammalian_phenotype	7
MP:0001899	MP:0001899	absent long term depression	Mammalian_phenotype	7
MP:0001901	MP:0001901	absence of NMDA-mediated synaptic currents	Mammalian_phenotype	7
MP:0001902	MP:0001902	reduced NMDA-mediated synaptic currents	Mammalian_phenotype	7
MP:0001916	MP:0001916	intracerebral hemorrhage	Mammalian_phenotype	7
MP:0001952	MP:0001952	increased airway responsiveness	Mammalian_phenotype	7
MP:0001981	MP:0001981	increased chemically-elicited antinociception	Mammalian_phenotype	7
MP:0001982	MP:0001982	decreased chemically-elicited antinociception	Mammalian_phenotype	7
MP:0001994	MP:0001994	increased blinking frequency	Mammalian_phenotype	7
MP:0001995	MP:0001995	decreased blinking frequency	Mammalian_phenotype	7
MP:0002003	MP:0002003	miotic pupils	Mammalian_phenotype	7
MP:0002007	MP:0002007	increased cellular sensitivity to gamma-irradiation	Mammalian_phenotype	7
MP:0002016	MP:0002016	ovary cysts	Mammalian_phenotype	7
MP:0002030	MP:0002030	increased neurofibrosarcoma incidence	Mammalian_phenotype	7
MP:0002031	MP:0002031	increased adrenal gland tumor incidence	Mammalian_phenotype	7
MP:0002032	MP:0002032	increased sarcoma incidence	Mammalian_phenotype	7
MP:0002033	MP:0002033	increased malignant triton tumor incidence	Mammalian_phenotype	7
MP:0002035	MP:0002035	increased leiomyosarcoma incidence	Mammalian_phenotype	7
MP:0002036	MP:0002036	increased rhabdomyosarcoma incidence	Mammalian_phenotype	7
MP:0002037	MP:0002037	increased fibrohistocytoma incidence	Mammalian_phenotype	7
MP:0002038	MP:0002038	increased carcinoma incidence	Mammalian_phenotype	7
MP:0002039	MP:0002039	increased neuroblastoma incidence	Mammalian_phenotype	7
MP:0002041	MP:0002041	increased pituitary adenoma incidence	Mammalian_phenotype	7
MP:0002043	MP:0002043	increased colon hamartoma incidence	Mammalian_phenotype	7
MP:0002044	MP:0002044	increased colonic adenoma incidence	Mammalian_phenotype	7
MP:0002045	MP:0002045	increased renal cystadenoma incidence	Mammalian_phenotype	7
MP:0002048	MP:0002048	increased lung adenoma incidence	Mammalian_phenotype	7
MP:0002051	MP:0002051	increased skin papilloma incidence	Mammalian_phenotype	7
MP:0002100	MP:0002100	abnormal tooth morphology	Mammalian_phenotype	7
MP:0002216	MP:0002216	abnormal seminiferous tubule morphology	Mammalian_phenotype	7
MP:0002242	MP:0002242	abnormal olfactory mucosa morphology	Mammalian_phenotype	7
MP:0002262	MP:0002262	abnormal nasal mucosa goblet cell morphology	Mammalian_phenotype	7
MP:0002286	MP:0002286	cryptorchism	Mammalian_phenotype	7
MP:0002320	MP:0002320	hyperventilation	Mammalian_phenotype	7
MP:0002321	MP:0002321	hypoventilation	Mammalian_phenotype	7
MP:0002324	MP:0002324	abnormal alveolocapillary membrane morphology	Mammalian_phenotype	7
MP:0002335	MP:0002335	decreased airway responsiveness	Mammalian_phenotype	7
MP:0002345	MP:0002345	abnormal lymph node primary follicle morphology	Mammalian_phenotype	7
MP:0002346	MP:0002346	abnormal lymph node secondary follicle morphology	Mammalian_phenotype	7
MP:0002391	MP:0002391	abnormal Peyer's patch germinal center morphology	Mammalian_phenotype	7
MP:0002392	MP:0002392	abnormal Peyer's patch T cell area morphology	Mammalian_phenotype	7
MP:0002404	MP:0002404	increased intestinal adenoma incidence	Mammalian_phenotype	7
MP:0002441	MP:0002441	abnormal granulocyte morphology	Mammalian_phenotype	7
MP:0002456	MP:0002456	abnormal Langerhans cell antigen presentation	Mammalian_phenotype	7
MP:0002467	MP:0002467	impaired neutrophil phagocytosis	Mammalian_phenotype	7
MP:0002546	MP:0002546	mydriasis	Mammalian_phenotype	7
MP:0002596	MP:0002596	abnormal hematocrit	Mammalian_phenotype	7
MP:0002619	MP:0002619	abnormal lymphocyte morphology	Mammalian_phenotype	7
MP:0002625	MP:0002625	heart left ventricle hypertrophy	Mammalian_phenotype	7
MP:0002629	MP:0002629	hyperactivity elicited by ethanol administration	Mammalian_phenotype	7
MP:0002636	MP:0002636	delayed vaginal opening	Mammalian_phenotype	7
MP:0002640	MP:0002640	reticulocytosis	Mammalian_phenotype	7
MP:0002641	MP:0002641	anisopoikilocytosis	Mammalian_phenotype	7
MP:0002643	MP:0002643	poikilocytosis	Mammalian_phenotype	7
MP:0002644	MP:0002644	decreased circulating triglyceride level	Mammalian_phenotype	7
MP:0002646	MP:0002646	increased intestinal cholesterol absorption	Mammalian_phenotype	7
MP:0002647	MP:0002647	decreased intestinal cholesterol absorption	Mammalian_phenotype	7
MP:0002660	MP:0002660	abnormal caput epididymis morphology	Mammalian_phenotype	7
MP:0002661	MP:0002661	abnormal corpus epididymis morphology	Mammalian_phenotype	7
MP:0002662	MP:0002662	abnormal cauda epididymis morphology	Mammalian_phenotype	7
MP:0002664	MP:0002664	decreased circulating adrenocorticotropin level	Mammalian_phenotype	7
MP:0002670	MP:0002670	absent scrotum	Mammalian_phenotype	7
MP:0002679	MP:0002679	abnormal corpus luteum morphology	Mammalian_phenotype	7
MP:0002690	MP:0002690	akinesia	Mammalian_phenotype	7
MP:0002702	MP:0002702	decreased circulating free fatty acid level	Mammalian_phenotype	7
MP:0002710	MP:0002710	increased glucagon secretion	Mammalian_phenotype	7
MP:0002711	MP:0002711	decreased glucagon secretion	Mammalian_phenotype	7
MP:0002728	MP:0002728	absent tibia	Mammalian_phenotype	7
MP:0002738	MP:0002738	hyperresponsive to tactile stimuli	Mammalian_phenotype	7
MP:0002742	MP:0002742	enlarged submandibular lymph nodes	Mammalian_phenotype	7
MP:0002743	MP:0002743	glomerulonephritis	Mammalian_phenotype	7
MP:0002770	MP:0002770	absent bulbourethral gland	Mammalian_phenotype	7
MP:0002773	MP:0002773	decreased circulating luteinizing hormone level	Mammalian_phenotype	7
MP:0002780	MP:0002780	decreased circulating testosterone level	Mammalian_phenotype	7
MP:0002781	MP:0002781	increased circulating testosterone level	Mammalian_phenotype	7
MP:0002790	MP:0002790	decreased circulating follicle stimulating hormone level	Mammalian_phenotype	7
MP:0002797	MP:0002797	increased thigmotaxis	Mammalian_phenotype	7
MP:0002812	MP:0002812	spherocytosis	Mammalian_phenotype	7
MP:0002813	MP:0002813	microcytosis	Mammalian_phenotype	7
MP:0002814	MP:0002814	hyperchromasia	Mammalian_phenotype	7
MP:0002816	MP:0002816	colitis	Mammalian_phenotype	7
MP:0002844	MP:0002844	aortic hypertrophy	Mammalian_phenotype	7
MP:0002845	MP:0002845	abnormal aortic weight	Mammalian_phenotype	7
MP:0002846	MP:0002846	abnormal aortic mass	Mammalian_phenotype	7
MP:0002850	MP:0002850	saccharin preference	Mammalian_phenotype	7
MP:0002852	MP:0002852	hypersulfatemia	Mammalian_phenotype	7
MP:0002853	MP:0002853	hyposulfatemia	Mammalian_phenotype	7
MP:0002857	MP:0002857	cochlear ganglion degeneration	Mammalian_phenotype	7
MP:0002869	MP:0002869	increased anti-insulin autoantibody level	Mammalian_phenotype	7
MP:0002870	MP:0002870	decreased anti-insulin autoantibody level	Mammalian_phenotype	7
MP:0002875	MP:0002875	decreased erythrocyte cell number	Mammalian_phenotype	7
MP:0002879	MP:0002879	increased cellular sensitivity to X-ray irradiation	Mammalian_phenotype	7
MP:0002894	MP:0002894	abnormal otolith morphology	Mammalian_phenotype	7
MP:0002926	MP:0002926	aganglionic megacolon	Mammalian_phenotype	7
MP:0002927	MP:0002927	toxic megacolon	Mammalian_phenotype	7
MP:0002939	MP:0002939	head spot	Mammalian_phenotype	7
MP:0002940	MP:0002940	variable body spotting	Mammalian_phenotype	7
MP:0002941	MP:0002941	increased circulating alanine transaminase level	Mammalian_phenotype	7
MP:0002942	MP:0002942	decreased circulating alanine transaminase level	Mammalian_phenotype	7
MP:0002958	MP:0002958	cerebral aqueductal stenosis	Mammalian_phenotype	7
MP:0002966	MP:0002966	decreased circulating alkaline phosphatase level	Mammalian_phenotype	7
MP:0002968	MP:0002968	increased circulating alkaline phosphatase level	Mammalian_phenotype	7
MP:0002983	MP:0002983	increased retinal ganglion cell number	Mammalian_phenotype	7
MP:0003048	MP:0003048	abnormal cervical vertebrae morphology	Mammalian_phenotype	7
MP:0003049	MP:0003049	abnormal lumbar vertebrae morphology	Mammalian_phenotype	7
MP:0003054	MP:0003054	spina bifida	Mammalian_phenotype	7
MP:0003056	MP:0003056	abnormal hyoid bone morphology	Mammalian_phenotype	7
MP:0003058	MP:0003058	increased insulin secretion	Mammalian_phenotype	7
MP:0003059	MP:0003059	decreased insulin secretion	Mammalian_phenotype	7
MP:0003066	MP:0003066	increased liver copper level	Mammalian_phenotype	7
MP:0003067	MP:0003067	decreased liver copper level	Mammalian_phenotype	7
MP:0003128	MP:0003128	splayed clitoris	Mammalian_phenotype	7
MP:0003131	MP:0003131	increased erythrocyte cell number	Mammalian_phenotype	7
MP:0003135	MP:0003135	increased erythroid progenitor cell number	Mammalian_phenotype	7
MP:0003136	MP:0003136	yellow coat color	Mammalian_phenotype	7
MP:0003145	MP:0003145	detached otolithic membrane	Mammalian_phenotype	7
MP:0003146	MP:0003146	absent cochlear ganglion	Mammalian_phenotype	7
MP:0003149	MP:0003149	abnormal tectorial membrane morphology	Mammalian_phenotype	7
MP:0003161	MP:0003161	absent lateral semicircular canal	Mammalian_phenotype	7
MP:0003162	MP:0003162	decreased lateral semicircular canal size	Mammalian_phenotype	7
MP:0003163	MP:0003163	absent posterior semicircular canal	Mammalian_phenotype	7
MP:0003164	MP:0003164	decreased posterior semicircular canal size	Mammalian_phenotype	7
MP:0003165	MP:0003165	absent superior semicircular canal	Mammalian_phenotype	7
MP:0003166	MP:0003166	decreased superior semicircular canal size	Mammalian_phenotype	7
MP:0003179	MP:0003179	decreased platelet cell number	Mammalian_phenotype	7
MP:0003181	MP:0003181	increased pulmonary endothelial cell surface	Mammalian_phenotype	7
MP:0003182	MP:0003182	decreased pulmonary endothelial cell surface	Mammalian_phenotype	7
MP:0003207	MP:0003207	decreased cellular sensitivity to gamma-irradiation	Mammalian_phenotype	7
MP:0003210	MP:0003210	abnormal heart elastic fiber morphology	Mammalian_phenotype	7
MP:0003212	MP:0003212	increased susceptibility to age related obesity	Mammalian_phenotype	7
MP:0003213	MP:0003213	decreased susceptibility to age related obesity	Mammalian_phenotype	7
MP:0003217	MP:0003217	increased spike-wave discharge type I	Mammalian_phenotype	7
MP:0003218	MP:0003218	decreased spike-wave discharge type I	Mammalian_phenotype	7
MP:0003219	MP:0003219	increased spike-wave discharge type II	Mammalian_phenotype	7
MP:0003220	MP:0003220	decreased spike-wave discharge type II	Mammalian_phenotype	7
MP:0003234	MP:0003234	enhanced NMDA-mediated synaptic currents	Mammalian_phenotype	7
MP:0003277	MP:0003277	increased esophageal papilloma incidence	Mammalian_phenotype	7
MP:0003305	MP:0003305	proctitis	Mammalian_phenotype	7
MP:0003324	MP:0003324	increased liver adenoma incidence	Mammalian_phenotype	7
MP:0003339	MP:0003339	decreased pancreatic beta cell number	Mammalian_phenotype	7
MP:0003352	MP:0003352	increased circulating renin level	Mammalian_phenotype	7
MP:0003353	MP:0003353	decreased circulating renin level	Mammalian_phenotype	7
MP:0003367	MP:0003367	increased circulating glucocorticoid level	Mammalian_phenotype	7
MP:0003368	MP:0003368	decreased circulating glucocorticoid level	Mammalian_phenotype	7
MP:0003373	MP:0003373	increased circulating mineralocorticoid level	Mammalian_phenotype	7
MP:0003374	MP:0003374	decreased circulating mineralocorticoid level	Mammalian_phenotype	7
MP:0003377	MP:0003377	late onset of menarche	Mammalian_phenotype	7
MP:0003382	MP:0003382	straub tail	Mammalian_phenotype	7
MP:0003387	MP:0003387	aorta coarctation	Mammalian_phenotype	7
MP:0003392	MP:0003392	increased atrial myxoma incidence	Mammalian_phenotype	7
MP:0003408	MP:0003408	increased width of hypertrophic chondrocyte zone	Mammalian_phenotype	7
MP:0003409	MP:0003409	decreased width of hypertrophic chondrocyte zone	Mammalian_phenotype	7
MP:0003423	MP:0003423	reduced thrombolysis	Mammalian_phenotype	7
MP:0003435	MP:0003435	herniated seminal vesicle	Mammalian_phenotype	7
MP:0003436	MP:0003436	decreased susceptibility to induced arthritis	Mammalian_phenotype	7
MP:0003437	MP:0003437	abnormal carotid body morphology	Mammalian_phenotype	7
MP:0003442	MP:0003442	decreased circulating glycerol level	Mammalian_phenotype	7
MP:0003443	MP:0003443	increased circulating glycerol level	Mammalian_phenotype	7
MP:0003454	MP:0003454	erythroderma	Mammalian_phenotype	7
MP:0003495	MP:0003495	increased parathyroid adenoma incidence	Mammalian_phenotype	7
MP:0003496	MP:0003496	increased thyroid adenoma incidence	Mammalian_phenotype	7
MP:0003509	MP:0003509	increased circulating dihydrotestosterone level	Mammalian_phenotype	7
MP:0003510	MP:0003510	decreased circulating dihydrotestosterone level	Mammalian_phenotype	7
MP:0003512	MP:0003512	enlarged labia	Mammalian_phenotype	7
MP:0003513	MP:0003513	small labia	Mammalian_phenotype	7
MP:0003514	MP:0003514	interlabial sulcus	Mammalian_phenotype	7
MP:0003515	MP:0003515	abnormal labia majora morphology	Mammalian_phenotype	7
MP:0003520	MP:0003520	abnormal labia minora morphology	Mammalian_phenotype	7
MP:0003533	MP:0003533	bifid vagina	Mammalian_phenotype	7
MP:0003534	MP:0003534	blind vagina	Mammalian_phenotype	7
MP:0003535	MP:0003535	absent vagina	Mammalian_phenotype	7
MP:0003536	MP:0003536	vagina dryness	Mammalian_phenotype	7
MP:0003537	MP:0003537	hydrometrocolpos	Mammalian_phenotype	7
MP:0003552	MP:0003552	vagina cysts	Mammalian_phenotype	7
MP:0003553	MP:0003553	abnormal foreskin morphology	Mammalian_phenotype	7
MP:0003554	MP:0003554	phimosis	Mammalian_phenotype	7
MP:0003557	MP:0003557	absent vas deferens	Mammalian_phenotype	7
MP:0003558	MP:0003558	absent uterus	Mammalian_phenotype	7
MP:0003559	MP:0003559	bifid uterus	Mammalian_phenotype	7
MP:0003560	MP:0003560	osteoarthritis	Mammalian_phenotype	7
MP:0003568	MP:0003568	uterus atresia	Mammalian_phenotype	7
MP:0003571	MP:0003571	uterus rupture	Mammalian_phenotype	7
MP:0003575	MP:0003575	absent oviduct	Mammalian_phenotype	7
MP:0003581	MP:0003581	increased ovarian fibroma incidence	Mammalian_phenotype	7
MP:0003595	MP:0003595	epididymal cyst	Mammalian_phenotype	7
MP:0003597	MP:0003597	increased epididymal cystadenoma incidence	Mammalian_phenotype	7
MP:0003599	MP:0003599	large penis	Mammalian_phenotype	7
MP:0003602	MP:0003602	increased renal hamartoma incidence	Mammalian_phenotype	7
MP:0003609	MP:0003609	small scrotum	Mammalian_phenotype	7
MP:0003612	MP:0003612	bifid scrotum	Mammalian_phenotype	7
MP:0003623	MP:0003623	hydrocele	Mammalian_phenotype	7
MP:0003627	MP:0003627	abnormal leukocyte tethering or rolling	Mammalian_phenotype	7
MP:0003642	MP:0003642	absent seminal vesicle	Mammalian_phenotype	7
MP:0003643	MP:0003643	spleen atrophy	Mammalian_phenotype	7
MP:0003644	MP:0003644	thymus atrophy	Mammalian_phenotype	7
MP:0003645	MP:0003645	increased pancreatic beta cell number	Mammalian_phenotype	7
MP:0003647	MP:0003647	absent oligodendrocytes	Mammalian_phenotype	7
MP:0003649	MP:0003649	decreased heart right ventricle size	Mammalian_phenotype	7
MP:0003661	MP:0003661	abnormal locus ceruleus morphology	Mammalian_phenotype	7
MP:0003667	MP:0003667	increased hemangiosarcoma incidence	Mammalian_phenotype	7
MP:0003670	MP:0003670	dilated renal glomerular capsule	Mammalian_phenotype	7
MP:0003683	MP:0003683	prominent ear lobes	Mammalian_phenotype	7
MP:0003696	MP:0003696	abnormal zona pellucida morphology	Mammalian_phenotype	7
MP:0003715	MP:0003715	posteriorly rotated ears	Mammalian_phenotype	7
MP:0003716	MP:0003716	anteriorly rotated ears	Mammalian_phenotype	7
MP:0003724	MP:0003724	increased susceptibility to induced arthritis	Mammalian_phenotype	7
MP:0003749	MP:0003749	down-turned corners of mouth	Mammalian_phenotype	7
MP:0003750	MP:0003750	increased mouth tumor incidence	Mammalian_phenotype	7
MP:0003752	MP:0003752	increased oral papilloma incidence	Mammalian_phenotype	7
MP:0003768	MP:0003768	palatal telangiectases	Mammalian_phenotype	7
MP:0003770	MP:0003770	lip ulceration	Mammalian_phenotype	7
MP:0003771	MP:0003771	abnormal lip shape	Mammalian_phenotype	7
MP:0003772	MP:0003772	lip pits	Mammalian_phenotype	7
MP:0003773	MP:0003773	everted lip	Mammalian_phenotype	7
MP:0003774	MP:0003774	fleshy lip	Mammalian_phenotype	7
MP:0003775	MP:0003775	thin lip	Mammalian_phenotype	7
MP:0003776	MP:0003776	lip atrophy	Mammalian_phenotype	7
MP:0003778	MP:0003778	lip telangiectases	Mammalian_phenotype	7
MP:0003779	MP:0003779	lip cysts	Mammalian_phenotype	7
MP:0003781	MP:0003781	increased lip neuroma incidence	Mammalian_phenotype	7
MP:0003782	MP:0003782	short lip	Mammalian_phenotype	7
MP:0003784	MP:0003784	thin lip vermillion border	Mammalian_phenotype	7
MP:0003785	MP:0003785	lip mucosal nodules	Mammalian_phenotype	7
MP:0003789	MP:0003789	increased osteosarcoma incidence	Mammalian_phenotype	7
MP:0003799	MP:0003799	impaired macrophage chemotaxis	Mammalian_phenotype	7
MP:0003808	MP:0003808	increased atrioventricular cushion size	Mammalian_phenotype	7
MP:0003816	MP:0003816	abnormal pituitary gland development	Mammalian_phenotype	7
MP:0003840	MP:0003840	abnormal coronal suture morphology	Mammalian_phenotype	7
MP:0003841	MP:0003841	abnormal lambdoidal suture morphology	Mammalian_phenotype	7
MP:0003842	MP:0003842	abnormal metopic suture morphology	Mammalian_phenotype	7
MP:0003843	MP:0003843	abnormal sagittal suture morphology	Mammalian_phenotype	7
MP:0003844	MP:0003844	abnormal squamo-parietal suture morphology	Mammalian_phenotype	7
MP:0003862	MP:0003862	decreased aggression towards males	Mammalian_phenotype	7
MP:0003913	MP:0003913	increased heart right ventricle weight	Mammalian_phenotype	7
MP:0003914	MP:0003914	decreased heart right ventricle weight	Mammalian_phenotype	7
MP:0003915	MP:0003915	increased left ventricle weight	Mammalian_phenotype	7
MP:0003916	MP:0003916	decreased heart left ventricle weight	Mammalian_phenotype	7
MP:0003980	MP:0003980	increased circulating phospholipid level	Mammalian_phenotype	7
MP:0003981	MP:0003981	decreased circulating phospholipid level	Mammalian_phenotype	7
MP:0003982	MP:0003982	increased cholesterol level	Mammalian_phenotype	7
MP:0003983	MP:0003983	decreased cholesterol level	Mammalian_phenotype	7
MP:0003986	MP:0003986	small cochlear ganglion	Mammalian_phenotype	7
MP:0003999	MP:0003999	enhanced passive avoidance behavior	Mammalian_phenotype	7
MP:0004000	MP:0004000	impaired passive avoidance behavior	Mammalian_phenotype	7
MP:0004006	MP:0004006	impaired contractility of jejunal smooth muscle	Mammalian_phenotype	7
MP:0004044	MP:0004044	aortic dissection	Mammalian_phenotype	7
MP:0004057	MP:0004057	thin myocardium compact layer	Mammalian_phenotype	7
MP:0004058	MP:0004058	abnormal ventricle papillary muscle morphology	Mammalian_phenotype	7
MP:0004067	MP:0004067	abnormal trabecula carnea morphology	Mammalian_phenotype	7
MP:0004075	MP:0004075	decreased Schwann cell precursor number	Mammalian_phenotype	7
MP:0004082	MP:0004082	abnormal habenula morphology	Mammalian_phenotype	7
MP:0004097	MP:0004097	abnormal cerebellar cortex morphology	Mammalian_phenotype	7
MP:0004102	MP:0004102	abnormal dorsal striatum morphology	Mammalian_phenotype	7
MP:0004103	MP:0004103	abnormal ventral striatum morphology	Mammalian_phenotype	7
MP:0004118	MP:0004118	abnormal baroreceptor morphology	Mammalian_phenotype	7
MP:0004131	MP:0004131	abnormal embryonic cilium morphology	Mammalian_phenotype	7
MP:0004138	MP:0004138	abnormal mucous neck cell morphology	Mammalian_phenotype	7
MP:0004139	MP:0004139	abnormal gastric parietal cell morphology	Mammalian_phenotype	7
MP:0004140	MP:0004140	abnormal chief cell morphology	Mammalian_phenotype	7
MP:0004151	MP:0004151	decreased circulating iron level	Mammalian_phenotype	7
MP:0004153	MP:0004153	increased renal tubule apoptosis	Mammalian_phenotype	7
MP:0004163	MP:0004163	abnormal adenohypophysis morphology	Mammalian_phenotype	7
MP:0004164	MP:0004164	abnormal neurohypophysis morphology	Mammalian_phenotype	7
MP:0004165	MP:0004165	abnormal lateral geniculate nucleus morphology	Mammalian_phenotype	7
MP:0004167	MP:0004167	abnormal cingulate gyrus morphology	Mammalian_phenotype	7
MP:0004168	MP:0004168	abnormal parahippocampal gyrus morphology	Mammalian_phenotype	7
MP:0004171	MP:0004171	abnormal pallium development	Mammalian_phenotype	7
MP:0004172	MP:0004172	abnormal subpallium development	Mammalian_phenotype	7
MP:0004176	MP:0004176	ear telangiectases	Mammalian_phenotype	7
MP:0004177	MP:0004177	tail telangiectases	Mammalian_phenotype	7
MP:0004178	MP:0004178	neck telangiectases	Mammalian_phenotype	7
MP:0004186	MP:0004186	abnormal area postrema morphology	Mammalian_phenotype	7
MP:0004204	MP:0004204	absent stapes	Mammalian_phenotype	7
MP:0004242	MP:0004242	abnormal plasmacytoid dendritic cell morphology	Mammalian_phenotype	7
MP:0004249	MP:0004249	abnormal crista ampullaris morphology	Mammalian_phenotype	7
MP:0004290	MP:0004290	abnormal stapes footplate morphology	Mammalian_phenotype	7
MP:0004318	MP:0004318	absent incus	Mammalian_phenotype	7
MP:0004319	MP:0004319	absent malleus	Mammalian_phenotype	7
MP:0004327	MP:0004327	increased vestibular hair cell number	Mammalian_phenotype	7
MP:0004328	MP:0004328	decreased vestibular hair cell number	Mammalian_phenotype	7
MP:0004337	MP:0004337	clavicle hypoplasia	Mammalian_phenotype	7
MP:0004340	MP:0004340	short scapula	Mammalian_phenotype	7
MP:0004344	MP:0004344	scapular bone hypoplasia	Mammalian_phenotype	7
MP:0004346	MP:0004346	absent acromion	Mammalian_phenotype	7
MP:0004349	MP:0004349	absent femur	Mammalian_phenotype	7
MP:0004352	MP:0004352	absent humerus	Mammalian_phenotype	7
MP:0004353	MP:0004353	abnormal deltoid tuberosity morphology	Mammalian_phenotype	7
MP:0004356	MP:0004356	radius hypoplasia	Mammalian_phenotype	7
MP:0004358	MP:0004358	bowed tibia	Mammalian_phenotype	7
MP:0004360	MP:0004360	absent ulna	Mammalian_phenotype	7
MP:0004361	MP:0004361	bowed ulna	Mammalian_phenotype	7
MP:0004371	MP:0004371	bowed femur	Mammalian_phenotype	7
MP:0004372	MP:0004372	bowed fibula	Mammalian_phenotype	7
MP:0004373	MP:0004373	bowed humerus	Mammalian_phenotype	7
MP:0004374	MP:0004374	bowed radius	Mammalian_phenotype	7
MP:0004390	MP:0004390	abnormal bronchoalveolar duct junction morphology	Mammalian_phenotype	7
MP:0004392	MP:0004392	abnormal CD8-positive T cell physiology	Mammalian_phenotype	7
MP:0004407	MP:0004407	increased cochlear hair cell number	Mammalian_phenotype	7
MP:0004408	MP:0004408	decreased cochlear hair cell number	Mammalian_phenotype	7
MP:0004430	MP:0004430	abnormal Claudius cell morphology	Mammalian_phenotype	7
MP:0004433	MP:0004433	abnormal cochlear inner hair cell physiology	Mammalian_phenotype	7
MP:0004434	MP:0004434	abnormal cochlear outer hair cell physiology	Mammalian_phenotype	7
MP:0004457	MP:0004457	abnormal orbitosphenoid bone morphology	Mammalian_phenotype	7
MP:0004469	MP:0004469	abnormal zygomatic arch morphology	Mammalian_phenotype	7
MP:0004478	MP:0004478	increased testicular teratoma incidence	Mammalian_phenotype	7
MP:0004483	MP:0004483	absent interdental cells	Mammalian_phenotype	7
MP:0004495	MP:0004495	decreased synaptic glutamate release	Mammalian_phenotype	7
MP:0004505	MP:0004505	decreased renal glomerulus number	Mammalian_phenotype	7
MP:0004564	MP:0004564	enlarged myocardial fiber	Mammalian_phenotype	7
MP:0004565	MP:0004565	small myocardial fiber	Mammalian_phenotype	7
MP:0004566	MP:0004566	myocardial fiber degeneration	Mammalian_phenotype	7
MP:0004567	MP:0004567	decreased myocardial fiber number	Mammalian_phenotype	7
MP:0004587	MP:0004587	decreased cellular sensitivity to X-ray irradiation	Mammalian_phenotype	7
MP:0004600	MP:0004600	abnormal vertebral transverse process morphology	Mammalian_phenotype	7
MP:0004601	MP:0004601	abnormal vertebral spinous process morphology	Mammalian_phenotype	7
MP:0004602	MP:0004602	abnormal vertebral articular process morphology	Mammalian_phenotype	7
MP:0004603	MP:0004603	absent vertebral arch	Mammalian_phenotype	7
MP:0004604	MP:0004604	abnormal vertebral pedicle morphology	Mammalian_phenotype	7
MP:0004605	MP:0004605	abnormal vertebral lamina morphology	Mammalian_phenotype	7
MP:0004612	MP:0004612	fusion of vertebral bodies	Mammalian_phenotype	7
MP:0004613	MP:0004613	fusion of vertebral arches	Mammalian_phenotype	7
MP:0004614	MP:0004614	caudal vertebral transformation	Mammalian_phenotype	7
MP:0004615	MP:0004615	cervical vertebral transformation	Mammalian_phenotype	7
MP:0004616	MP:0004616	lumbar vertebral transformation	Mammalian_phenotype	7
MP:0004617	MP:0004617	sacral vertebral transformation	Mammalian_phenotype	7
MP:0004618	MP:0004618	thoracic vertebral transformation	Mammalian_phenotype	7
MP:0004619	MP:0004619	caudal vertebral fusion	Mammalian_phenotype	7
MP:0004620	MP:0004620	cervical vertebral fusion	Mammalian_phenotype	7
MP:0004621	MP:0004621	lumbar vertebral fusion	Mammalian_phenotype	7
MP:0004622	MP:0004622	sacral vertebral fusion	Mammalian_phenotype	7
MP:0004623	MP:0004623	thoracic vertebral fusion	Mammalian_phenotype	7
MP:0004627	MP:0004627	abnormal trochanter morphology	Mammalian_phenotype	7
MP:0004632	MP:0004632	abnormal cochlear OHC efferent innervation pattern	Mammalian_phenotype	7
MP:0004633	MP:0004633	abnormal cochlear IHC efferent innervation pattern	Mammalian_phenotype	7
MP:0004644	MP:0004644	increased vertebrae number	Mammalian_phenotype	7
MP:0004645	MP:0004645	decreased vertebrae number	Mammalian_phenotype	7
MP:0004649	MP:0004649	decreased sacral vertebrae number	Mammalian_phenotype	7
MP:0004652	MP:0004652	small caudal vertebrae	Mammalian_phenotype	7
MP:0004653	MP:0004653	absent caudal vertebrae	Mammalian_phenotype	7
MP:0004656	MP:0004656	absent sacral vertebrae	Mammalian_phenotype	7
MP:0004657	MP:0004657	small sacral vertebrae	Mammalian_phenotype	7
MP:0004668	MP:0004668	absent vertebral body	Mammalian_phenotype	7
MP:0004669	MP:0004669	enlarged vertebral body	Mammalian_phenotype	7
MP:0004670	MP:0004670	small vertebral body	Mammalian_phenotype	7
MP:0004678	MP:0004678	split xiphoid process	Mammalian_phenotype	7
MP:0004679	MP:0004679	xiphoid process foramen	Mammalian_phenotype	7
MP:0004680	MP:0004680	small xiphoid process	Mammalian_phenotype	7
MP:0004681	MP:0004681	intervertebral disk hypoplasia	Mammalian_phenotype	7
MP:0004690	MP:0004690	ischium hypoplasia	Mammalian_phenotype	7
MP:0004693	MP:0004693	pubis hypoplasia	Mammalian_phenotype	7
MP:0004705	MP:0004705	elongated vertebral body	Mammalian_phenotype	7
MP:0004717	MP:0004717	absent cochlear nerve	Mammalian_phenotype	7
MP:0004719	MP:0004719	absent vestibular nerve	Mammalian_phenotype	7
MP:0004720	MP:0004720	abnormal platelet morphology	Mammalian_phenotype	7
MP:0004727	MP:0004727	absent epididymis	Mammalian_phenotype	7
MP:0004728	MP:0004728	abnormal efferent ductules of testis morphology	Mammalian_phenotype	7
MP:0004746	MP:0004746	abnormal cochlear IHC afferent innervation pattern	Mammalian_phenotype	7
MP:0004747	MP:0004747	abnormal cochlear OHC afferent innervation pattern	Mammalian_phenotype	7
MP:0004783	MP:0004783	abnormal cardinal vein morphology	Mammalian_phenotype	7
MP:0004787	MP:0004787	abnormal dorsal aorta morphology	Mammalian_phenotype	7
MP:0004794	MP:0004794	increased anti-nuclear antigen antibody level	Mammalian_phenotype	7
MP:0004795	MP:0004795	decreased anti-nuclear antigen antibody level	Mammalian_phenotype	7
MP:0004797	MP:0004797	increased anti-erythrocyte antigen antibody level	Mammalian_phenotype	7
MP:0004845	MP:0004845	absent vestibuloocular reflex	Mammalian_phenotype	7
MP:0004849	MP:0004849	abnormal testis size	Mammalian_phenotype	7
MP:0004853	MP:0004853	abnormal ovary size	Mammalian_phenotype	7
MP:0004872	MP:0004872	absent nasal septum	Mammalian_phenotype	7
MP:0004896	MP:0004896	abnormal endometrium morphology	Mammalian_phenotype	7
MP:0004902	MP:0004902	abnormal uterus size	Mammalian_phenotype	7
MP:0004907	MP:0004907	abnormal seminal vesicle size	Mammalian_phenotype	7
MP:0004920	MP:0004920	increased placenta weight	Mammalian_phenotype	7
MP:0004921	MP:0004921	decreased placenta weight	Mammalian_phenotype	7
MP:0004923	MP:0004923	absent common crus	Mammalian_phenotype	7
MP:0004926	MP:0004926	abnormal epididymis size	Mammalian_phenotype	7
MP:0004933	MP:0004933	abnormal epididymis epithelium morphology	Mammalian_phenotype	7
MP:0004935	MP:0004935	epididymis degeneration	Mammalian_phenotype	7
MP:0004946	MP:0004946	abnormal regulatory T cell physiology	Mammalian_phenotype	7
MP:0004949	MP:0004949	absent neuronal precursor cells	Mammalian_phenotype	7
MP:0004952	MP:0004952	increased spleen weight	Mammalian_phenotype	7
MP:0004953	MP:0004953	decreased spleen weight	Mammalian_phenotype	7
MP:0004955	MP:0004955	increased thymus weight	Mammalian_phenotype	7
MP:0004956	MP:0004956	decreased thymus weight	Mammalian_phenotype	7
MP:0004959	MP:0004959	abnormal prostate gland size	Mammalian_phenotype	7
MP:0005040	MP:0005040	abnormal MHC II cell surface expression on macrophages	Mammalian_phenotype	7
MP:0005047	MP:0005047	enlarged celiac lymph nodes	Mammalian_phenotype	7
MP:0005097	MP:0005097	polychromatophilia	Mammalian_phenotype	7
MP:0005110	MP:0005110	absent talus	Mammalian_phenotype	7
MP:0005119	MP:0005119	decreased circulating thyroid-stimulating hormone level	Mammalian_phenotype	7
MP:0005120	MP:0005120	decreased circulating growth hormone level	Mammalian_phenotype	7
MP:0005121	MP:0005121	decreased circulating prolactin level	Mammalian_phenotype	7
MP:0005122	MP:0005122	increased circulating thyroid-stimulating hormone level	Mammalian_phenotype	7
MP:0005123	MP:0005123	increased circulating growth hormone level	Mammalian_phenotype	7
MP:0005124	MP:0005124	increased circulating prolactin level	Mammalian_phenotype	7
MP:0005150	MP:0005150	cachexia	Mammalian_phenotype	7
MP:0005152	MP:0005152	pancytopenia	Mammalian_phenotype	7
MP:0005181	MP:0005181	decreased circulating estradiol level	Mammalian_phenotype	7
MP:0005182	MP:0005182	increased circulating estradiol level	Mammalian_phenotype	7
MP:0005188	MP:0005188	small penis	Mammalian_phenotype	7
MP:0005191	MP:0005191	head tilt	Mammalian_phenotype	7
MP:0005202	MP:0005202	lethargy	Mammalian_phenotype	7
MP:0005203	MP:0005203	abnormal trabecular meshwork morphology	Mammalian_phenotype	7
MP:0005204	MP:0005204	abnormal canal of Schlemm morphology	Mammalian_phenotype	7
MP:0005207	MP:0005207	abnormal aqueous vein morphology	Mammalian_phenotype	7
MP:0005211	MP:0005211	increased stomach mucosa thickness	Mammalian_phenotype	7
MP:0005226	MP:0005226	abnormal vertebral arch development	Mammalian_phenotype	7
MP:0005227	MP:0005227	abnormal vertebral body development	Mammalian_phenotype	7
MP:0005239	MP:0005239	abnormal Bruch membrane morphology	Mammalian_phenotype	7
MP:0005249	MP:0005249	abnormal palatine bone morphology	Mammalian_phenotype	7
MP:0005267	MP:0005267	abnormal olfactory cortex morphology	Mammalian_phenotype	7
MP:0005269	MP:0005269	abnormal occipital bone morphology	Mammalian_phenotype	7
MP:0005270	MP:0005270	abnormal zygomatic bone morphology	Mammalian_phenotype	7
MP:0005271	MP:0005271	abnormal lacrimal bone morphology	Mammalian_phenotype	7
MP:0005272	MP:0005272	abnormal temporal bone morphology	Mammalian_phenotype	7
MP:0005283	MP:0005283	increased unsaturated fatty acid level	Mammalian_phenotype	7
MP:0005284	MP:0005284	increased saturated fatty acid level	Mammalian_phenotype	7
MP:0005285	MP:0005285	decreased unsaturated fatty acid level	Mammalian_phenotype	7
MP:0005286	MP:0005286	decreased saturated fatty acid level	Mammalian_phenotype	7
MP:0005304	MP:0005304	cystic bulbourethral gland	Mammalian_phenotype	7
MP:0005315	MP:0005315	absent pituitary gland	Mammalian_phenotype	7
MP:0005340	MP:0005340	altered susceptibility to atherosclerosis	Mammalian_phenotype	7
MP:0005343	MP:0005343	increased circulating aspartate transaminase level	Mammalian_phenotype	7
MP:0005350	MP:0005350	increased susceptibility to autoimmune disorder	Mammalian_phenotype	7
MP:0005351	MP:0005351	decreased susceptibility to autoimmune disorder	Mammalian_phenotype	7
MP:0005352	MP:0005352	small cranium	Mammalian_phenotype	7
MP:0005356	MP:0005356	positive geotaxis	Mammalian_phenotype	7
MP:0005366	MP:0005366	variegated coat color	Mammalian_phenotype	7
MP:0005409	MP:0005409	darkened coat color	Mammalian_phenotype	7
MP:0005430	MP:0005430	absent fibula	Mammalian_phenotype	7
MP:0005462	MP:0005462	abnormal mast cell differentiation	Mammalian_phenotype	7
MP:0005463	MP:0005463	abnormal CD4-positive T cell physiology	Mammalian_phenotype	7
MP:0005488	MP:0005488	bronchial epithelial hyperplasia	Mammalian_phenotype	7
MP:0005493	MP:0005493	stomach epithelial hyperplasia	Mammalian_phenotype	7
MP:0005498	MP:0005498	hyporesponsive to tactile stimuli	Mammalian_phenotype	7
MP:0005505	MP:0005505	increased platelet cell number	Mammalian_phenotype	7
MP:0005507	MP:0005507	tail dragging	Mammalian_phenotype	7
MP:0005541	MP:0005541	abnormal iris stromal pigmentation	Mammalian_phenotype	7
MP:0005546	MP:0005546	choroidal neovascularization	Mammalian_phenotype	7
MP:0005573	MP:0005573	increased pulmonary respiratory rate	Mammalian_phenotype	7
MP:0005574	MP:0005574	decreased pulmonary respiratory rate	Mammalian_phenotype	7
MP:0005577	MP:0005577	uterus prolapse	Mammalian_phenotype	7
MP:0005604	MP:0005604	hyperekplexia	Mammalian_phenotype	7
MP:0005627	MP:0005627	increased circulating potassium level	Mammalian_phenotype	7
MP:0005628	MP:0005628	decreased circulating potassium level	Mammalian_phenotype	7
MP:0005632	MP:0005632	decreased circulating aspartate transaminase level	Mammalian_phenotype	7
MP:0005633	MP:0005633	increased circulating sodium level	Mammalian_phenotype	7
MP:0005634	MP:0005634	decreased circulating sodium level	Mammalian_phenotype	7
MP:0005649	MP:0005649	increased spleen neoplasm incidence	Mammalian_phenotype	7
MP:0006012	MP:0006012	dilated endolymphatic duct	Mammalian_phenotype	7
MP:0006013	MP:0006013	absent endolymphatic sac	Mammalian_phenotype	7
MP:0006014	MP:0006014	dilated endolymphatic sac	Mammalian_phenotype	7
MP:0006015	MP:0006015	dilated lateral semicircular canal	Mammalian_phenotype	7
MP:0006016	MP:0006016	dilated posterior semicircular canal	Mammalian_phenotype	7
MP:0006017	MP:0006017	dilated superior semicircular canal	Mammalian_phenotype	7
MP:0006026	MP:0006026	dilated terminal bronchiole tubes	Mammalian_phenotype	7
MP:0006051	MP:0006051	brainstem hemorrhage	Mammalian_phenotype	7
MP:0006052	MP:0006052	cerebellum hemorrhage	Mammalian_phenotype	7
MP:0006053	MP:0006053	hypothalamus hemorrhage	Mammalian_phenotype	7
MP:0006069	MP:0006069	abnormal retinal neuronal layer morphology	Mammalian_phenotype	7
MP:0006070	MP:0006070	increased retinal photoreceptor cell number	Mammalian_phenotype	7
MP:0006071	MP:0006071	abnormal retinal progenitor cell morphology	Mammalian_phenotype	7
MP:0006074	MP:0006074	abnormal retinal rod bipolar cell morphology	Mammalian_phenotype	7
MP:0006075	MP:0006075	abnormal retinal cone bipolar cell morphology	Mammalian_phenotype	7
MP:0006089	MP:0006089	abnormal vestibular saccule morphology	Mammalian_phenotype	7
MP:0006090	MP:0006090	abnormal utricle morphology	Mammalian_phenotype	7
MP:0006092	MP:0006092	abnormal olfactory sensory neuron morphology	Mammalian_phenotype	7
MP:0006096	MP:0006096	absent retinal bipolar cells	Mammalian_phenotype	7
MP:0006101	MP:0006101	absent tegmentum	Mammalian_phenotype	7
MP:0006102	MP:0006102	decreased tegmentum size	Mammalian_phenotype	7
MP:0006104	MP:0006104	abnormal tectum morphology	Mammalian_phenotype	7
MP:0006119	MP:0006119	mitral valve atresia	Mammalian_phenotype	7
MP:0006120	MP:0006120	mitral valve prolapse	Mammalian_phenotype	7
MP:0006121	MP:0006121	calcified mitral valve	Mammalian_phenotype	7
MP:0006122	MP:0006122	mitral valve stenosis	Mammalian_phenotype	7
MP:0006123	MP:0006123	tricuspid valve atresia	Mammalian_phenotype	7
MP:0006124	MP:0006124	tricuspid valve stenosis	Mammalian_phenotype	7
MP:0006125	MP:0006125	tricuspid valve prolapse	Mammalian_phenotype	7
MP:0006132	MP:0006132	calcified tricuspid valve	Mammalian_phenotype	7
MP:0006140	MP:0006140	increased cardiac rhabdomyoma incidence	Mammalian_phenotype	7
MP:0006154	MP:0006154	eye abduction	Mammalian_phenotype	7
MP:0006155	MP:0006155	eye adduction	Mammalian_phenotype	7
MP:0006156	MP:0006156	abnormal visual pursuit	Mammalian_phenotype	7
MP:0006157	MP:0006157	palsy of the eye	Mammalian_phenotype	7
MP:0006160	MP:0006160	heterochromatic iridis	Mammalian_phenotype	7
MP:0006170	MP:0006170	increased eyelid myxoma incidence	Mammalian_phenotype	7
MP:0006171	MP:0006171	increased eyelid neuroma incidence	Mammalian_phenotype	7
MP:0006173	MP:0006173	abnormal myeloid dendritic cell morphology	Mammalian_phenotype	7
MP:0006175	MP:0006175	choroid atrophy	Mammalian_phenotype	7
MP:0006176	MP:0006176	choroid degeneration	Mammalian_phenotype	7
MP:0006177	MP:0006177	choroid sclerosis	Mammalian_phenotype	7
MP:0006183	MP:0006183	increased retina hamartoma incidence	Mammalian_phenotype	7
MP:0006194	MP:0006194	keratoconjunctivitis	Mammalian_phenotype	7
MP:0006205	MP:0006205	embryonic lethality between implantation and somite formation	Mammalian_phenotype	7
MP:0006206	MP:0006206	embryonic lethality between somite formation and embryo turning	Mammalian_phenotype	7
MP:0006210	MP:0006210	abnormal orbit size	Mammalian_phenotype	7
MP:0006214	MP:0006214	asymmetrical orbits	Mammalian_phenotype	7
MP:0006216	MP:0006216	abnormal optic disc size	Mammalian_phenotype	7
MP:0006224	MP:0006224	oculomotor apraxia	Mammalian_phenotype	7
MP:0006230	MP:0006230	iris stroma hypoplasia	Mammalian_phenotype	7
MP:0006232	MP:0006232	increased Lisch nodule incidence	Mammalian_phenotype	7
MP:0006235	MP:0006235	polycoria	Mammalian_phenotype	7
MP:0006240	MP:0006240	anisocoria	Mammalian_phenotype	7
MP:0006241	MP:0006241	abnormal placement of pupils	Mammalian_phenotype	7
MP:0006242	MP:0006242	white pupil	Mammalian_phenotype	7
MP:0006243	MP:0006243	impaired pupillary reflex	Mammalian_phenotype	7
MP:0006262	MP:0006262	increased testis tumor incidence	Mammalian_phenotype	7
MP:0006267	MP:0006267	abnormal intercalated disc morphology	Mammalian_phenotype	7
MP:0006268	MP:0006268	absent cardiac desmosomes	Mammalian_phenotype	7
MP:0006298	MP:0006298	abnormal platelet activation	Mammalian_phenotype	7
MP:0006309	MP:0006309	decreased retinal ganglion cell number	Mammalian_phenotype	7
MP:0006321	MP:0006321	increased myocardial fiber number	Mammalian_phenotype	7
MP:0006349	MP:0006349	decreased circulating copper level	Mammalian_phenotype	7
MP:0006350	MP:0006350	increased circulating copper level	Mammalian_phenotype	7
MP:0006358	MP:0006358	absent pinna reflex	Mammalian_phenotype	7
MP:0006359	MP:0006359	absent startle reflex	Mammalian_phenotype	7
MP:0006370	MP:0006370	abnormal phaeomelanin content	Mammalian_phenotype	7
MP:0006386	MP:0006386	absent somites	Mammalian_phenotype	7
MP:0006393	MP:0006393	absent nucleus pulposus	Mammalian_phenotype	7
MP:0006404	MP:0006404	abnormal lumbar dorsal root ganglion morphology	Mammalian_phenotype	7
MP:0006409	MP:0006409	vestibular ganglion hypoplasia	Mammalian_phenotype	7
MP:0006416	MP:0006416	abnormal rete testis morphology	Mammalian_phenotype	7
MP:0008000	MP:0008000	increased ovary tumor incidence	Mammalian_phenotype	7
MP:0008014	MP:0008014	increased lung tumor incidence	Mammalian_phenotype	7
MP:0008018	MP:0008018	increased facial tumor incidence	Mammalian_phenotype	7
MP:0008019	MP:0008019	increased liver tumor incidence	Mammalian_phenotype	7
MP:0008021	MP:0008021	increased blastoma incidence	Mammalian_phenotype	7
MP:0008029	MP:0008029	abnormal paraxial mesoderm morphology	Mammalian_phenotype	7
MP:0008035	MP:0008035	behavioral arrest	Mammalian_phenotype	7
MP:0008042	MP:0008042	abnormal NK T cell physiology	Mammalian_phenotype	7
MP:0008051	MP:0008051	abnormal memory T cell physiology	Mammalian_phenotype	7
MP:0008066	MP:0008066	small endolymphatic duct	Mammalian_phenotype	7
MP:0008101	MP:0008101	lymph node hypoplasia	Mammalian_phenotype	7
MP:0008102	MP:0008102	lymph node hyperplasia	Mammalian_phenotype	7
MP:0008104	MP:0008104	abnormal amacrine cell number	Mammalian_phenotype	7
MP:0008105	MP:0008105	increased amacrine cell number	Mammalian_phenotype	7
MP:0008106	MP:0008106	decreased amacrine cell number	Mammalian_phenotype	7
MP:0008107	MP:0008107	absent horizontal cells	Mammalian_phenotype	7
MP:0008109	MP:0008109	abnormal small intestinal microvillus morphology	Mammalian_phenotype	7
MP:0008112	MP:0008112	abnormal monocyte differentiation	Mammalian_phenotype	7
MP:0008113	MP:0008113	abnormal macrophage differentiation	Mammalian_phenotype	7
MP:0008114	MP:0008114	abnormal Kupffer cell morphology	Mammalian_phenotype	7
MP:0008123	MP:0008123	abnormal plasmacytoid dendritic cell number	Mammalian_phenotype	7
MP:0008126	MP:0008126	increased dendritic cell number	Mammalian_phenotype	7
MP:0008127	MP:0008127	decreased dendritic cell number	Mammalian_phenotype	7
MP:0008130	MP:0008130	abnormal pituitary intermediate lobe morphology	Mammalian_phenotype	7
MP:0008132	MP:0008132	increased Peyer's patch number	Mammalian_phenotype	7
MP:0008133	MP:0008133	decreased Peyer's patch number	Mammalian_phenotype	7
MP:0008135	MP:0008135	small Peyer's patches	Mammalian_phenotype	7
MP:0008136	MP:0008136	enlarged Peyer's patches	Mammalian_phenotype	7
MP:0008142	MP:0008142	decreased small intestinal villus size	Mammalian_phenotype	7
MP:0008146	MP:0008146	asymmetric rib-sternum attachment	Mammalian_phenotype	7
MP:0008147	MP:0008147	asymmetric rib-vertebral column attachment	Mammalian_phenotype	7
MP:0008180	MP:0008180	abnormal marginal zone B cell morphology	Mammalian_phenotype	7
MP:0008191	MP:0008191	abnormal follicular B cell physiology	Mammalian_phenotype	7
MP:0008192	MP:0008192	abnormal germinal center B cell physiology	Mammalian_phenotype	7
MP:0008193	MP:0008193	abnormal marginal zone B cell physiology	Mammalian_phenotype	7
MP:0008194	MP:0008194	abnormal memory B cell physiology	Mammalian_phenotype	7
MP:0008217	MP:0008217	abnormal B cell activation	Mammalian_phenotype	7
MP:0008221	MP:0008221	abnormal hippocampal commissure morphology	Mammalian_phenotype	7
MP:0008225	MP:0008225	abnormal anterior commissure morphology	Mammalian_phenotype	7
MP:0008231	MP:0008231	abnormal habenular commissure morphology	Mammalian_phenotype	7
MP:0008234	MP:0008234	absent spleen marginal zone	Mammalian_phenotype	7
MP:0008240	MP:0008240	abnormal spleen marginal zone macrophage morphology	Mammalian_phenotype	7
MP:0008248	MP:0008248	abnormal mononuclear phagocyte morphology	Mammalian_phenotype	7
MP:0008251	MP:0008251	abnormal phagocyte morphology	Mammalian_phenotype	7
MP:0008253	MP:0008253	absent megakaryocytes	Mammalian_phenotype	7
MP:0008256	MP:0008256	abnormal myometrium morphology	Mammalian_phenotype	7
MP:0008278	MP:0008278	failure of sternum ossification	Mammalian_phenotype	7
MP:0008292	MP:0008292	enlarged adrenocortical cell nuclei	Mammalian_phenotype	7
MP:0008298	MP:0008298	adrenergic chromaffin cell hyperplasia	Mammalian_phenotype	7
MP:0008308	MP:0008308	small scala media	Mammalian_phenotype	7
MP:0008309	MP:0008309	dilated scala media	Mammalian_phenotype	7
MP:0008372	MP:0008372	small malleus	Mammalian_phenotype	7
MP:0008374	MP:0008374	abnormal malleus manubrium morphology	Mammalian_phenotype	7
MP:0008381	MP:0008381	absent gonial bone	Mammalian_phenotype	7
MP:0008382	MP:0008382	gonial bone hypoplasia	Mammalian_phenotype	7
MP:0008383	MP:0008383	enlarged gonial bone	Mammalian_phenotype	7
MP:0008384	MP:0008384	absent nasal capsule	Mammalian_phenotype	7
MP:0008393	MP:0008393	absent primordial germ cells	Mammalian_phenotype	7
MP:0008404	MP:0008404	increased cellular sensitivity to methylmethanesulfonate	Mammalian_phenotype	7
MP:0008405	MP:0008405	decreased cellular sensitivity to methylmethanesulfonate	Mammalian_phenotype	7
MP:0008406	MP:0008406	increased cellular sensitivity to hydrogen peroxide	Mammalian_phenotype	7
MP:0008407	MP:0008407	decreased cellular sensitivity to hydrogen peroxide	Mammalian_phenotype	7
MP:0008408	MP:0008408	decreased cellular sensitivity to hydroxyurea	Mammalian_phenotype	7
MP:0008409	MP:0008409	increased cellular sensitivity to hydroxyurea	Mammalian_phenotype	7
MP:0008439	MP:0008439	abnormal cortical plate morphology	Mammalian_phenotype	7
MP:0008440	MP:0008440	abnormal subplate morphology	Mammalian_phenotype	7
MP:0008457	MP:0008457	abnormal cortical intermediate zone morphology	Mammalian_phenotype	7
MP:0008458	MP:0008458	abnormal cortical ventricular zone morphology	Mammalian_phenotype	7
MP:0008460	MP:0008460	absent dorsal root ganglion	Mammalian_phenotype	7
MP:0008465	MP:0008465	absent mesenteric lymph nodes	Mammalian_phenotype	7
MP:0008466	MP:0008466	enlarged mesenteric lymph nodes	Mammalian_phenotype	7
MP:0008471	MP:0008471	abnormal spleen primary B follicle morphology	Mammalian_phenotype	7
MP:0008472	MP:0008472	abnormal spleen secondary B follicle morphology	Mammalian_phenotype	7
MP:0008473	MP:0008473	abnormal spleen follicular dendritic cell network	Mammalian_phenotype	7
MP:0008490	MP:0008490	enlarged dorsal root ganglion	Mammalian_phenotype	7
MP:0008492	MP:0008492	dorsal root ganglion degeneration	Mammalian_phenotype	7
MP:0008525	MP:0008525	decreased cranium height	Mammalian_phenotype	7
MP:0008526	MP:0008526	decreased cranium width	Mammalian_phenotype	7
MP:0008534	MP:0008534	enlarged fourth ventricle	Mammalian_phenotype	7
MP:0008535	MP:0008535	enlarged lateral ventricles	Mammalian_phenotype	7
MP:0008536	MP:0008536	enlarged third ventricle	Mammalian_phenotype	7
MP:0008542	MP:0008542	enlarged cervical lymph nodes	Mammalian_phenotype	7
MP:0008548	MP:0008548	abnormal circulating interferon level	Mammalian_phenotype	7
MP:0008552	MP:0008552	abnormal circulating tumor necrosis factor level	Mammalian_phenotype	7
MP:0008562	MP:0008562	increased interferon-alpha secretion	Mammalian_phenotype	7
MP:0008563	MP:0008563	decreased interferon-alpha secretion	Mammalian_phenotype	7
MP:0008564	MP:0008564	increased interferon-beta secretion	Mammalian_phenotype	7
MP:0008565	MP:0008565	decreased interferon-beta secretion	Mammalian_phenotype	7
MP:0008566	MP:0008566	increased interferon-gamma secretion	Mammalian_phenotype	7
MP:0008567	MP:0008567	decreased interferon-gamma secretion	Mammalian_phenotype	7
MP:0008588	MP:0008588	abnormal circulating interleukin level	Mammalian_phenotype	7
MP:0008651	MP:0008651	increased interleukin-1 secretion	Mammalian_phenotype	7
MP:0008652	MP:0008652	decreased interleukin-1 secretion	Mammalian_phenotype	7
MP:0008653	MP:0008653	abnormal interleukin-1 alpha secretion	Mammalian_phenotype	7
MP:0008656	MP:0008656	abnormal interleukin-1 beta secretion	Mammalian_phenotype	7
MP:0008660	MP:0008660	increased interleukin-10 secretion	Mammalian_phenotype	7
MP:0008661	MP:0008661	decreased interleukin-10 secretion	Mammalian_phenotype	7
MP:0008663	MP:0008663	increased interleukin-12 secretion	Mammalian_phenotype	7
MP:0008664	MP:0008664	decreased interleukin-12 secretion	Mammalian_phenotype	7
MP:0008665	MP:0008665	abnormal interleukin-12a secretion	Mammalian_phenotype	7
MP:0008669	MP:0008669	increased interleukin-12b secretion	Mammalian_phenotype	7
MP:0008670	MP:0008670	decreased interleukin-12b secretion	Mammalian_phenotype	7
MP:0008672	MP:0008672	increased interleukin-13 secretion	Mammalian_phenotype	7
MP:0008673	MP:0008673	decreased interleukin-13 secretion	Mammalian_phenotype	7
MP:0008675	MP:0008675	increased interleukin-15 secretion	Mammalian_phenotype	7
MP:0008676	MP:0008676	decreased interleukin-15 secretion	Mammalian_phenotype	7
MP:0008678	MP:0008678	increased interleukin-16 secretion	Mammalian_phenotype	7
MP:0008679	MP:0008679	decreased interleukin-16 secretion	Mammalian_phenotype	7
MP:0008681	MP:0008681	increased interleukin-17 secretion	Mammalian_phenotype	7
MP:0008682	MP:0008682	decreased interleukin-17 secretion	Mammalian_phenotype	7
MP:0008684	MP:0008684	increased interleukin-18 secretion	Mammalian_phenotype	7
MP:0008685	MP:0008685	decreased interleukin-18 secretion	Mammalian_phenotype	7
MP:0008687	MP:0008687	increased interleukin-2 secretion	Mammalian_phenotype	7
MP:0008688	MP:0008688	decreased interleukin-2 secretion	Mammalian_phenotype	7
MP:0008690	MP:0008690	increased interleukin-23 secretion	Mammalian_phenotype	7
MP:0008691	MP:0008691	decreased interleukin-23 secretion	Mammalian_phenotype	7
MP:0008692	MP:0008692	abnormal interleukin-23a secretion	Mammalian_phenotype	7
MP:0008696	MP:0008696	increased interleukin-3 secretion	Mammalian_phenotype	7
MP:0008697	MP:0008697	decreased interleukin-3 secretion	Mammalian_phenotype	7
MP:0008699	MP:0008699	increased interleukin-4 secretion	Mammalian_phenotype	7
MP:0008700	MP:0008700	decreased interleukin-4 secretion	Mammalian_phenotype	7
MP:0008702	MP:0008702	increased interleukin-5 secretion	Mammalian_phenotype	7
MP:0008703	MP:0008703	decreased interleukin-5 secretion	Mammalian_phenotype	7
MP:0008705	MP:0008705	increased interleukin-6 secretion	Mammalian_phenotype	7
MP:0008706	MP:0008706	decreased interleukin-6 secretion	Mammalian_phenotype	7
MP:0008708	MP:0008708	increased interleukin-7 secretion	Mammalian_phenotype	7
MP:0008709	MP:0008709	decreased interleukin-7 secretion	Mammalian_phenotype	7
MP:0008711	MP:0008711	increased interleukin-9 secretion	Mammalian_phenotype	7
MP:0008712	MP:0008712	decreased interleukin-9 secretion	Mammalian_phenotype	7
MP:0008719	MP:0008719	impaired neutrophil recruitment	Mammalian_phenotype	7
MP:0008723	MP:0008723	impaired eosinophil recruitment	Mammalian_phenotype	7
MP:0008732	MP:0008732	reduced hair shaft melanin granule number	Mammalian_phenotype	7
MP:0008733	MP:0008733	abnormal hair shaft melanin granule distribution	Mammalian_phenotype	7
MP:0008743	MP:0008743	decreased liver iron level	Mammalian_phenotype	7
MP:0008763	MP:0008763	abnormal mast cell degranulation	Mammalian_phenotype	7
MP:0008805	MP:0008805	decreased circulating amylase level	Mammalian_phenotype	7
MP:0008806	MP:0008806	increased circulating amylase level	Mammalian_phenotype	7
MP:0008807	MP:0008807	increased liver iron level	Mammalian_phenotype	7
MP:0008808	MP:0008808	decreased spleen iron level	Mammalian_phenotype	7
MP:0008809	MP:0008809	increased spleen iron level	Mammalian_phenotype	7
MP:0008810	MP:0008810	increased circulating iron level	Mammalian_phenotype	7
MP:0008818	MP:0008818	abnormal interfrontal bone morphology	Mammalian_phenotype	7
MP:0008824	MP:0008824	absent interventricular septum membranous part	Mammalian_phenotype	7
MP:0008833	MP:0008833	caudal hemivertebra	Mammalian_phenotype	7
MP:0008845	MP:0008845	abnormal paraventricular hypothalamic nucleus morphology	Mammalian_phenotype	7
MP:0008846	MP:0008846	abnormal supraoptic nucleus morphology	Mammalian_phenotype	7
MP:0008847	MP:0008847	abnormal suprachiasmatic nucleus morphology	Mammalian_phenotype	7
MP:0008848	MP:0008848	abnormal anterior hypothalamic nucleus morphology	Mammalian_phenotype	7
MP:0008852	MP:0008852	retinal neovascularization	Mammalian_phenotype	7
MP:0008892	MP:0008892	abnormal sperm flagellum morphology	Mammalian_phenotype	7
MP:0008913	MP:0008913	weaving	Mammalian_phenotype	7
MP:0008914	MP:0008914	enlarged cerebellum	Mammalian_phenotype	7
MP:0008927	MP:0008927	abnormal parafascicular nucleus morphology	Mammalian_phenotype	7
MP:0008928	MP:0008928	abnormal paracentral nucleus morphology	Mammalian_phenotype	7
MP:0008929	MP:0008929	abnormal central medial nucleus morphology	Mammalian_phenotype	7
MP:0008930	MP:0008930	abnormal medial geniculate nucleus morphology	Mammalian_phenotype	7
MP:0008931	MP:0008931	abnormal paraventricular thalamic nucleus morphology	Mammalian_phenotype	7
MP:0008934	MP:0008934	absent choroid plexus	Mammalian_phenotype	7
MP:0008936	MP:0008936	abnormal pituitary gland size	Mammalian_phenotype	7
MP:0008940	MP:0008940	delayed balanopreputial separation	Mammalian_phenotype	7
MP:0008941	MP:0008941	reticulocytopenia	Mammalian_phenotype	7
MP:0008958	MP:0008958	abnormal trophoblast glycogen cell morphology	Mammalian_phenotype	7
MP:0008959	MP:0008959	abnormal spongiotrophoblast cell morphology	Mammalian_phenotype	7
MP:0008970	MP:0008970	choanal atresia	Mammalian_phenotype	7
MP:0008973	MP:0008973	decreased erythroid progenitor cell number	Mammalian_phenotype	7
MP:0008975	MP:0008975	delayed male fertility	Mammalian_phenotype	7
MP:0008976	MP:0008976	delayed female fertility	Mammalian_phenotype	7
MP:0008977	MP:0008977	abnormal vagina size	Mammalian_phenotype	7
MP:0008990	MP:0008990	abnormal Ito cell morphology	Mammalian_phenotype	7
MP:0008994	MP:0008994	early vaginal opening	Mammalian_phenotype	7
MP:0009011	MP:0009011	prolonged diestrus	Mammalian_phenotype	7
MP:0009012	MP:0009012	short diestrus	Mammalian_phenotype	7
MP:0009014	MP:0009014	prolonged proestrus	Mammalian_phenotype	7
MP:0009015	MP:0009015	short proestrus	Mammalian_phenotype	7
MP:0009017	MP:0009017	prolonged estrus	Mammalian_phenotype	7
MP:0009018	MP:0009018	short estrus	Mammalian_phenotype	7
MP:0009020	MP:0009020	prolonged metestrus	Mammalian_phenotype	7
MP:0009021	MP:0009021	absent estrus	Mammalian_phenotype	7
MP:0009033	MP:0009033	abnormal posterior cerebellomedullary cistern	Mammalian_phenotype	7
MP:0009034	MP:0009034	abnormal lateral cerebellomedullary cistern morphology	Mammalian_phenotype	7
MP:0009043	MP:0009043	increased pancreas adenoma incidence	Mammalian_phenotype	7
MP:0009044	MP:0009044	increased adrenal gland adenoma incidence	Mammalian_phenotype	7
MP:0009047	MP:0009047	short metestrus	Mammalian_phenotype	7
MP:0009050	MP:0009050	dilated proximal convoluted tubules	Mammalian_phenotype	7
MP:0009051	MP:0009051	dilated distal convoluted tubules	Mammalian_phenotype	7
MP:0009057	MP:0009057	increased interleukin-21 secretion	Mammalian_phenotype	7
MP:0009058	MP:0009058	decreased interleukin-21 secretion	Mammalian_phenotype	7
MP:0009063	MP:0009063	abnormal oviduct size	Mammalian_phenotype	7
MP:0009077	MP:0009077	abnormal cranial vagina morphology	Mammalian_phenotype	7
MP:0009082	MP:0009082	uterus cysts	Mammalian_phenotype	7
MP:0009084	MP:0009084	blind uterus	Mammalian_phenotype	7
MP:0009085	MP:0009085	abnormal uterine horn morphology	Mammalian_phenotype	7
MP:0009098	MP:0009098	anovaginal fistula	Mammalian_phenotype	7
MP:0009100	MP:0009100	abnormal clitoris size	Mammalian_phenotype	7
MP:0009102	MP:0009102	abnormal glans penis morphology	Mammalian_phenotype	7
MP:0009105	MP:0009105	penis prolapse	Mammalian_phenotype	7
MP:0009112	MP:0009112	abnormal pancreatic beta cell mass	Mammalian_phenotype	7
MP:0009149	MP:0009149	decreased pancreatic acinar cell number	Mammalian_phenotype	7
MP:0009150	MP:0009150	pancreatic acinar cell atrophy	Mammalian_phenotype	7
MP:0009153	MP:0009153	increased pancreas tumor incidence	Mammalian_phenotype	7
MP:0009157	MP:0009157	ectopic pancreatic acinar cells	Mammalian_phenotype	7
MP:0009158	MP:0009158	absent pancreatic acinar cells	Mammalian_phenotype	7
MP:0009159	MP:0009159	increased pancreatic acinar cell number	Mammalian_phenotype	7
MP:0009160	MP:0009160	abnormal pancreatic acinar cell zymogen granule morphology	Mammalian_phenotype	7
MP:0009167	MP:0009167	increased pancreatic islet number	Mammalian_phenotype	7
MP:0009168	MP:0009168	decreased pancreatic islet number	Mammalian_phenotype	7
MP:0009171	MP:0009171	enlarged pancreatic islets	Mammalian_phenotype	7
MP:0009172	MP:0009172	small pancreatic islets	Mammalian_phenotype	7
MP:0009176	MP:0009176	increased pancreatic alpha cell number	Mammalian_phenotype	7
MP:0009177	MP:0009177	decreased pancreatic alpha cell number	Mammalian_phenotype	7
MP:0009180	MP:0009180	increased pancreatic delta cell number	Mammalian_phenotype	7
MP:0009181	MP:0009181	decreased pancreatic delta cell number	Mammalian_phenotype	7
MP:0009185	MP:0009185	increased PP cell number	Mammalian_phenotype	7
MP:0009186	MP:0009186	decreased PP cell number	Mammalian_phenotype	7
MP:0009190	MP:0009190	increased pancreatic epsilon cell number	Mammalian_phenotype	7
MP:0009191	MP:0009191	decreased pancreatic epsilon cell number	Mammalian_phenotype	7
MP:0009201	MP:0009201	external male genitalia atrophy	Mammalian_phenotype	7
MP:0009203	MP:0009203	external male genitalia hypoplasia	Mammalian_phenotype	7
MP:0009212	MP:0009212	vulva atrophy	Mammalian_phenotype	7
MP:0009214	MP:0009214	vas deferens hypoplasia	Mammalian_phenotype	7
MP:0009221	MP:0009221	uterus adenomyosis	Mammalian_phenotype	7
MP:0009222	MP:0009222	increased uterus tumor incidence	Mammalian_phenotype	7
MP:0009229	MP:0009229	abnormal median eminence morphology	Mammalian_phenotype	7
MP:0009230	MP:0009230	abnormal sperm head morphology	Mammalian_phenotype	7
MP:0009255	MP:0009255	degranulated pancreatic beta cells	Mammalian_phenotype	7
MP:0009262	MP:0009262	absent semicircular canal ampulla	Mammalian_phenotype	7
MP:0009266	MP:0009266	abnormal mesendoderm development	Mammalian_phenotype	7
MP:0009273	MP:0009273	abnormal hair shaft melanin granule shape	Mammalian_phenotype	7
MP:0009277	MP:0009277	increased brain tumor incidence	Mammalian_phenotype	7
MP:0009280	MP:0009280	reduced activated sperm motility	Mammalian_phenotype	7
MP:0009282	MP:0009282	reduced hyperactivated sperm motility	Mammalian_phenotype	7
MP:0009327	MP:0009327	abnormal maternal grooming	Mammalian_phenotype	7
MP:0009331	MP:0009331	absent primitive node	Mammalian_phenotype	7
MP:0009338	MP:0009338	increased splenocyte number	Mammalian_phenotype	7
MP:0009339	MP:0009339	decreased splenocyte number	Mammalian_phenotype	7
MP:0009355	MP:0009355	increased liver triglyceride level	Mammalian_phenotype	7
MP:0009356	MP:0009356	decreased liver triglyceride level	Mammalian_phenotype	7
MP:0009376	MP:0009376	abnormal manchette morphology	Mammalian_phenotype	7
MP:0009380	MP:0009380	abnormal prostate gland ventral lobe morphology	Mammalian_phenotype	7
MP:0009381	MP:0009381	abnormal prostate gland dorsolateral lobe morphology	Mammalian_phenotype	7
MP:0009401	MP:0009401	increased skeletal muscle fiber diameter	Mammalian_phenotype	7
MP:0009402	MP:0009402	decreased skeletal muscle fiber diameter	Mammalian_phenotype	7
MP:0009413	MP:0009413	skeletal muscle fiber atrophy	Mammalian_phenotype	7
MP:0009423	MP:0009423	increased extensor digitorum longus weight	Mammalian_phenotype	7
MP:0009424	MP:0009424	decreased extensor digitorum longus weight	Mammalian_phenotype	7
MP:0009425	MP:0009425	increased soleus weight	Mammalian_phenotype	7
MP:0009426	MP:0009426	decreased soleus weight	Mammalian_phenotype	7
MP:0009427	MP:0009427	increased tibialis anterior weight	Mammalian_phenotype	7
MP:0009428	MP:0009428	decreased tibialis anterior weight	Mammalian_phenotype	7
MP:0009439	MP:0009439	increased myeloid sarcoma incidence	Mammalian_phenotype	7
MP:0009442	MP:0009442	increased ovarian teratoma incidence	Mammalian_phenotype	7
MP:0009446	MP:0009446	abnormal platelet dense granule physiology	Mammalian_phenotype	7
MP:0009459	MP:0009459	skeletal muscle hyperplasia	Mammalian_phenotype	7
MP:0009460	MP:0009460	skeletal muscle hypoplasia	Mammalian_phenotype	7
MP:0009461	MP:0009461	skeletal muscle hypertrophy	Mammalian_phenotype	7
MP:0009462	MP:0009462	skeletal muscle hypotrophy	Mammalian_phenotype	7
MP:0009466	MP:0009466	abnormal uterine tube infundibulum morphology	Mammalian_phenotype	7
MP:0009469	MP:0009469	increased skin hamartoma incidence	Mammalian_phenotype	7
MP:0009481	MP:0009481	cecum inflammation	Mammalian_phenotype	7
MP:0009482	MP:0009482	ileum inflammation	Mammalian_phenotype	7
MP:0009484	MP:0009484	ileum hypertrophy	Mammalian_phenotype	7
MP:0009522	MP:0009522	submandibular gland hypoplasia	Mammalian_phenotype	7
MP:0009523	MP:0009523	submandibular gland hyperplasia	Mammalian_phenotype	7
MP:0009528	MP:0009528	abnormal major sublingual duct morphology	Mammalian_phenotype	7
MP:0009529	MP:0009529	abnormal minor sublingual duct morphology	Mammalian_phenotype	7
MP:0009546	MP:0009546	absent gastric milk in neonates	Mammalian_phenotype	7
MP:0009547	MP:0009547	elliptocytosis	Mammalian_phenotype	7
MP:0009550	MP:0009550	increased urinary bladder carcinoma incidence	Mammalian_phenotype	7
MP:0009553	MP:0009553	fused lips	Mammalian_phenotype	7
MP:0009559	MP:0009559	thymus cortex hyperplasia	Mammalian_phenotype	7
MP:0009568	MP:0009568	abnormal red blood cell deformability	Mammalian_phenotype	7
MP:0009576	MP:0009576	oral atresia	Mammalian_phenotype	7
MP:0009590	MP:0009590	increased gonad tumor incidence	Mammalian_phenotype	7
MP:0009603	MP:0009603	absent keratohyalin granules	Mammalian_phenotype	7
MP:0009622	MP:0009622	absent inguinal lymph nodes	Mammalian_phenotype	7
MP:0009623	MP:0009623	enlarged inguinal lymph nodes	Mammalian_phenotype	7
MP:0009624	MP:0009624	small inguinal lymph nodes	Mammalian_phenotype	7
MP:0009628	MP:0009628	absent brachial lymph nodes	Mammalian_phenotype	7
MP:0009629	MP:0009629	small brachial lymph nodes	Mammalian_phenotype	7
MP:0009630	MP:0009630	absent axillary lymph nodes	Mammalian_phenotype	7
MP:0009631	MP:0009631	enlarged axillary lymph nodes	Mammalian_phenotype	7
MP:0009632	MP:0009632	small axillary lymph nodes	Mammalian_phenotype	7
MP:0009633	MP:0009633	absent cervical lymph nodes	Mammalian_phenotype	7
MP:0009634	MP:0009634	absent popliteal lymph nodes	Mammalian_phenotype	7
MP:0009635	MP:0009635	enlarged popliteal lymph nodes	Mammalian_phenotype	7
MP:0009636	MP:0009636	small popliteal lymph nodes	Mammalian_phenotype	7
MP:0009638	MP:0009638	abnormal pretectal nuclei morphology	Mammalian_phenotype	7
MP:0009656	MP:0009656	delayed chorioallantoic fusion	Mammalian_phenotype	7
MP:0009657	MP:0009657	failure of chorioallantoic fusion	Mammalian_phenotype	7
MP:0009670	MP:0009670	abnormal uterine angiogenesis	Mammalian_phenotype	7
MP:0009681	MP:0009681	abnormal pyramidal decussation morphology	Mammalian_phenotype	7
MP:0009709	MP:0009709	hydrometra	Mammalian_phenotype	7
MP:0009731	MP:0009731	abnormal offspring retrieval	Mammalian_phenotype	7
MP:0009734	MP:0009734	abnormal prostate gland duct morphology	Mammalian_phenotype	7
MP:0009735	MP:0009735	abnormal prostate gland development	Mammalian_phenotype	7
MP:0009737	MP:0009737	prostate gland cysts	Mammalian_phenotype	7
MP:0009771	MP:0009771	absent optic chiasm	Mammalian_phenotype	7
MP:0009782	MP:0009782	abnormal basicranium angle	Mammalian_phenotype	7
MP:0009783	MP:0009783	abnormal melanoblast morphology	Mammalian_phenotype	7
MP:0009788	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality	Mammalian_phenotype	7
MP:0009789	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality	Mammalian_phenotype	7
MP:0009790	MP:0009790	decreased susceptibility to viral infection induced morbidity/mortality	Mammalian_phenotype	7
MP:0009791	MP:0009791	increased susceptibility to viral infection induced morbidity/mortality	Mammalian_phenotype	7
MP:0009792	MP:0009792	seborrheic dermatitis	Mammalian_phenotype	7
MP:0009843	MP:0009843	decreased neural crest cell number	Mammalian_phenotype	7
MP:0009852	MP:0009852	increased Sertoli cell phagocytosis	Mammalian_phenotype	7
MP:0009853	MP:0009853	decreased Sertoli cell phagocytosis	Mammalian_phenotype	7
MP:0009866	MP:0009866	abnormal aorta wall morphology	Mammalian_phenotype	7
MP:0009869	MP:0009869	abnormal descending aorta morphology	Mammalian_phenotype	7
MP:0009876	MP:0009876	increased cellular sensitivity to thiophosphamide	Mammalian_phenotype	7
MP:0009880	MP:0009880	microstomia	Mammalian_phenotype	7
MP:0009881	MP:0009881	macrostomia	Mammalian_phenotype	7
MP:0009945	MP:0009945	abnormal accessory olfactory bulb morphology	Mammalian_phenotype	7
MP:0009979	MP:0009979	abnormal cerebellum deep nucleus morphology	Mammalian_phenotype	7
MP:0010033	MP:0010033	paraphimosis	Mammalian_phenotype	7
MP:0010043	MP:0010043	abnormal frontonasal suture morphology	Mammalian_phenotype	7
MP:0010066	MP:0010066	abnormal red blood cell distribution width	Mammalian_phenotype	7
MP:0010074	MP:0010074	stomatocytosis	Mammalian_phenotype	7
MP:0010077	MP:0010077	increased plant sterol level	Mammalian_phenotype	7
MP:0010079	MP:0010079	increased osteochondroma incidence	Mammalian_phenotype	7
MP:0010082	MP:0010082	sternebra fusion	Mammalian_phenotype	7
MP:0010090	MP:0010090	increased circulating creatine kinase level	Mammalian_phenotype	7
MP:0010091	MP:0010091	decreased circulating creatine kinase level	Mammalian_phenotype	7
MP:0010092	MP:0010092	increased circulating magnesium level	Mammalian_phenotype	7
MP:0010093	MP:0010093	decreased circulating magnesium level	Mammalian_phenotype	7
MP:0010097	MP:0010097	abnormal retinal blood vessel morphology	Mammalian_phenotype	7
MP:0010098	MP:0010098	abnormal retinal blood vessel pattern	Mammalian_phenotype	7
MP:0010101	MP:0010101	increased sacral vertebrae number	Mammalian_phenotype	7
MP:0010102	MP:0010102	increased caudal vertebrae number	Mammalian_phenotype	7
MP:0010117	MP:0010117	abnormal lateral plate mesoderm morphology	Mammalian_phenotype	7
MP:0010118	MP:0010118	abnormal intermediate mesoderm	Mammalian_phenotype	7
MP:0010138	MP:0010138	arteritis	Mammalian_phenotype	7
MP:0010140	MP:0010140	phlebitis	Mammalian_phenotype	7
MP:0010141	MP:0010141	lymphangitis	Mammalian_phenotype	7
MP:0010175	MP:0010175	leptocytosis	Mammalian_phenotype	7
MP:0010176	MP:0010176	dacryocytosis	Mammalian_phenotype	7
MP:0010177	MP:0010177	acanthocytosis	Mammalian_phenotype	7
MP:0010178	MP:0010178	increased number of Howell-Jolly bodies	Mammalian_phenotype	7
MP:0010199	MP:0010199	absent lymphatic vessel endothelial cells	Mammalian_phenotype	7
MP:0010202	MP:0010202	focal dorsal hair loss	Mammalian_phenotype	7
MP:0010203	MP:0010203	focal ventral hair loss	Mammalian_phenotype	7
MP:0010209	MP:0010209	abnormal circulating chemokine level	Mammalian_phenotype	7
MP:0010226	MP:0010226	increased quadriceps weight	Mammalian_phenotype	7
MP:0010227	MP:0010227	decreased quadriceps weight	Mammalian_phenotype	7
MP:0010243	MP:0010243	increased kidney copper level	Mammalian_phenotype	7
MP:0010244	MP:0010244	decreased kidney copper level	Mammalian_phenotype	7
MP:0010247	MP:0010247	increased intestine copper level	Mammalian_phenotype	7
MP:0010248	MP:0010248	decreased intestine copper level	Mammalian_phenotype	7
MP:0010250	MP:0010250	absent thymus cortex	Mammalian_phenotype	7
MP:0010252	MP:0010252	anterior subcapsular cataracts	Mammalian_phenotype	7
MP:0010253	MP:0010253	posterior subcapsular cataracts	Mammalian_phenotype	7
MP:0010256	MP:0010256	anterior cortical cataracts	Mammalian_phenotype	7
MP:0010257	MP:0010257	posterior cortical cataracts	Mammalian_phenotype	7
MP:0010259	MP:0010259	anterior polar cataracts	Mammalian_phenotype	7
MP:0010260	MP:0010260	posterior polar cataracts	Mammalian_phenotype	7
MP:0010266	MP:0010266	decreased liver tumor incidence	Mammalian_phenotype	7
MP:0010269	MP:0010269	decreased mammary gland tumor incidence	Mammalian_phenotype	7
MP:0010270	MP:0010270	decreased stomach tumor incidence	Mammalian_phenotype	7
MP:0010271	MP:0010271	decreased tongue tumor incidence	Mammalian_phenotype	7
MP:0010275	MP:0010275	increased melanoma incidence	Mammalian_phenotype	7
MP:0010278	MP:0010278	increased glioma incidence	Mammalian_phenotype	7
MP:0010279	MP:0010279	increased gastrointestinal tumor incidence	Mammalian_phenotype	7
MP:0010285	MP:0010285	decreased skin tumor incidence	Mammalian_phenotype	7
MP:0010294	MP:0010294	increased kidney tumor incidence	Mammalian_phenotype	7
MP:0010299	MP:0010299	increased mammary gland tumor incidence	Mammalian_phenotype	7
MP:0010302	MP:0010302	increased uvea tumor incidence	Mammalian_phenotype	7
MP:0010303	MP:0010303	increased retina tumor incidence	Mammalian_phenotype	7
MP:0010310	MP:0010310	increased Schwannoma incidence	Mammalian_phenotype	7
MP:0010311	MP:0010311	increased meningioma incidence	Mammalian_phenotype	7
MP:0010313	MP:0010313	increased osteoma incidence	Mammalian_phenotype	7
MP:0010314	MP:0010314	increased neurofibroma incidence	Mammalian_phenotype	7
MP:0010315	MP:0010315	increased cholangiocarcinoma incidence	Mammalian_phenotype	7
MP:0010316	MP:0010316	increased thyroid tumor incidence	Mammalian_phenotype	7
MP:0010318	MP:0010318	increased salivary gland tumor incidence	Mammalian_phenotype	7
MP:0010320	MP:0010320	increased pituitary gland tumor incidence	Mammalian_phenotype	7
MP:0010321	MP:0010321	increased parathyroid gland tumor incidence	Mammalian_phenotype	7
MP:0010323	MP:0010323	retropulsion	Mammalian_phenotype	7
MP:0010324	MP:0010324	abnormal malleus processus brevis morphology	Mammalian_phenotype	7
MP:0010325	MP:0010325	abnormal malleus head morphology	Mammalian_phenotype	7
MP:0010327	MP:0010327	abnormal malleus neck morphology	Mammalian_phenotype	7
MP:0010338	MP:0010338	increased desmoid tumor incidence	Mammalian_phenotype	7
MP:0010339	MP:0010339	increased cardiac fibroma incidence	Mammalian_phenotype	7
MP:0010340	MP:0010340	increased lung fibroma incidence	Mammalian_phenotype	7
MP:0010341	MP:0010341	increased mammary gland fibroma incidence	Mammalian_phenotype	7
MP:0010342	MP:0010342	increased facial angiofibroma incidence	Mammalian_phenotype	7
MP:0010344	MP:0010344	increased hibernoma incidence	Mammalian_phenotype	7
MP:0010349	MP:0010349	increased teratocarcinoma incidence	Mammalian_phenotype	7
MP:0010354	MP:0010354	increased odontosarcoma incidence	Mammalian_phenotype	7
MP:0010357	MP:0010357	increased prostate gland tumor incidence	Mammalian_phenotype	7
MP:0010361	MP:0010361	increased gangliosarcoma incidence	Mammalian_phenotype	7
MP:0010362	MP:0010362	increased ganglioneuroma incidence	Mammalian_phenotype	7
MP:0010365	MP:0010365	increased thymus tumor incidence	Mammalian_phenotype	7
MP:0010373	MP:0010373	myeloid hyperplasia	Mammalian_phenotype	7
MP:0010375	MP:0010375	increased kidney iron level	Mammalian_phenotype	7
MP:0010376	MP:0010376	decreased kidney iron level	Mammalian_phenotype	7
MP:0010398	MP:0010398	decreased liver glycogen level	Mammalian_phenotype	7
MP:0010400	MP:0010400	increased liver glycogen level	Mammalian_phenotype	7
MP:0010404	MP:0010404	ostium primum atrial septal defect	Mammalian_phenotype	7
MP:0010405	MP:0010405	ostium secundum atrial septal defect	Mammalian_phenotype	7
MP:0010406	MP:0010406	common atrium	Mammalian_phenotype	7
MP:0010407	MP:0010407	coronary sinus atrial septal defect	Mammalian_phenotype	7
MP:0010408	MP:0010408	sinus venosus atrial septal defect	Mammalian_phenotype	7
MP:0010413	MP:0010413	complete atrioventricular septal defect	Mammalian_phenotype	7
MP:0010414	MP:0010414	partial atrioventricular septal defect	Mammalian_phenotype	7
MP:0010415	MP:0010415	intermediate atrioventricular septal defect	Mammalian_phenotype	7
MP:0010417	MP:0010417	subarterial ventricular septal defect	Mammalian_phenotype	7
MP:0010418	MP:0010418	perimembraneous ventricular septal defect	Mammalian_phenotype	7
MP:0010419	MP:0010419	inlet ventricular septal defect	Mammalian_phenotype	7
MP:0010420	MP:0010420	muscular ventricular septal defect	Mammalian_phenotype	7
MP:0010430	MP:0010430	total anomalous pulmonary venous connection, supracardiac	Mammalian_phenotype	7
MP:0010443	MP:0010443	total anomalous pulmonary venous connection, intracardiac	Mammalian_phenotype	7
MP:0010444	MP:0010444	total anomalous pulmonary venous connection, infracardiac	Mammalian_phenotype	7
MP:0010445	MP:0010445	total anomalous pulmonary venous connection, mixed	Mammalian_phenotype	7
MP:0010448	MP:0010448	heart left ventricle outflow tract stenosis	Mammalian_phenotype	7
MP:0010449	MP:0010449	heart right ventricle outflow tract stenosis	Mammalian_phenotype	7
MP:0010468	MP:0010468	abnormal thoracic aorta morphology	Mammalian_phenotype	7
MP:0010487	MP:0010487	abnormal right subclavian artery morphology	Mammalian_phenotype	7
MP:0010488	MP:0010488	abnormal left subclavian artery morphology	Mammalian_phenotype	7
MP:0010496	MP:0010496	abnormal pectinate muscle morphology	Mammalian_phenotype	7
MP:0010501	MP:0010501	atrium myocardium hypoplasia	Mammalian_phenotype	7
MP:0010502	MP:0010502	ventricle myocardium hypoplasia	Mammalian_phenotype	7
MP:0010503	MP:0010503	myocardial trabeculae hypoplasia	Mammalian_phenotype	7
MP:0010516	MP:0010516	absent Q wave	Mammalian_phenotype	7
MP:0010532	MP:0010532	absent atrioventricular node	Mammalian_phenotype	7
MP:0010533	MP:0010533	atrioventricular node hypoplasia	Mammalian_phenotype	7
MP:0010536	MP:0010536	Ebstein's malformation of tricuspid valve	Mammalian_phenotype	7
MP:0010541	MP:0010541	aorta hypoplasia	Mammalian_phenotype	7
MP:0010544	MP:0010544	interrupted aorta	Mammalian_phenotype	7
MP:0010549	MP:0010549	absent dorsal mesocardium	Mammalian_phenotype	7
MP:0010566	MP:0010566	abnormal left posterior bundle morphology	Mammalian_phenotype	7
MP:0010567	MP:0010567	abnormal right bundle morphology	Mammalian_phenotype	7
MP:0010574	MP:0010574	aorta dilation	Mammalian_phenotype	7
MP:0010580	MP:0010580	decreased heart left ventricle size	Mammalian_phenotype	7
MP:0010581	MP:0010581	abnormal atrium myocardial trabeculae morphology	Mammalian_phenotype	7
MP:0010582	MP:0010582	abnormal bulbus cordis septation	Mammalian_phenotype	7
MP:0010584	MP:0010584	abnormal conotruncus septation	Mammalian_phenotype	7
MP:0010590	MP:0010590	common truncal valve stenosis	Mammalian_phenotype	7
MP:0010609	MP:0010609	absent chordae tendineae	Mammalian_phenotype	7
MP:0010613	MP:0010613	abnormal mitral valve anulus morphology	Mammalian_phenotype	7
MP:0010614	MP:0010614	abnormal mitral valve cusp morphology	Mammalian_phenotype	7
MP:0010618	MP:0010618	enlarged mitral valve	Mammalian_phenotype	7
MP:0010619	MP:0010619	patent mitral valve	Mammalian_phenotype	7
MP:0010620	MP:0010620	thick mitral valve	Mammalian_phenotype	7
MP:0010621	MP:0010621	abnormal tricuspid valve anulus morphology	Mammalian_phenotype	7
MP:0010622	MP:0010622	abnormal tricuspid valve cusp morphology	Mammalian_phenotype	7
MP:0010627	MP:0010627	enlarged tricuspid valve	Mammalian_phenotype	7
MP:0010628	MP:0010628	patent tricuspid valve	Mammalian_phenotype	7
MP:0010629	MP:0010629	thick tricuspid valve	Mammalian_phenotype	7
MP:0010631	MP:0010631	increased Q wave amplitude	Mammalian_phenotype	7
MP:0010640	MP:0010640	ventricular myocardium compact layer hypoplasia	Mammalian_phenotype	7
MP:0010652	MP:0010652	absent aorticopulmonary septum	Mammalian_phenotype	7
MP:0010696	MP:0010696	increased siderocyte number	Mammalian_phenotype	7
MP:0010708	MP:0010708	absent iris stroma	Mammalian_phenotype	7
MP:0010720	MP:0010720	absent sublingual duct	Mammalian_phenotype	7
MP:0010721	MP:0010721	short sublingual duct	Mammalian_phenotype	7
MP:0010724	MP:0010724	thick interventricular septum	Mammalian_phenotype	7
MP:0010725	MP:0010725	thin interventricular septum	Mammalian_phenotype	7
MP:0010735	MP:0010735	abnormal paranodal axoglial junction morphology	Mammalian_phenotype	7
MP:0010750	MP:0010750	increased susceptibility to parasitic infection induced morbidity/mortality	Mammalian_phenotype	7
MP:0010751	MP:0010751	decreased susceptibility to parasitic infection induced morbidity/mortality	Mammalian_phenotype	7
MP:0010761	MP:0010761	abnormal microglial cell chemotaxis	Mammalian_phenotype	7
MP:0010762	MP:0010762	abnormal microglial cell activation	Mammalian_phenotype	7
MP:0010765	MP:0010765	impaired granulocyte chemotaxis	Mammalian_phenotype	7
MP:0010782	MP:0010782	stomach smooth muscle circular layer hypertrophy	Mammalian_phenotype	7
MP:0010796	MP:0010796	abnormal intermediate gastric gland morphology	Mammalian_phenotype	7
MP:0010809	MP:0010809	abnormal Clara cell morphology	Mammalian_phenotype	7
MP:0010863	MP:0010863	absent respiratory mucosa goblet cells	Mammalian_phenotype	7
MP:0010903	MP:0010903	abnormal pulmonary alveolus wall morphology	Mammalian_phenotype	7
MP:0010904	MP:0010904	abnormal alveolar pore morphology	Mammalian_phenotype	7
MP:0010908	MP:0010908	dilated pulmonary alveolar ducts	Mammalian_phenotype	7
MP:0010909	MP:0010909	pulmonary alveolar hemorrhage	Mammalian_phenotype	7
MP:0010910	MP:0010910	bronchiolar epithelial hyperplasia	Mammalian_phenotype	7
MP:0010922	MP:0010922	alveolitis	Mammalian_phenotype	7
MP:0010923	MP:0010923	calcified pulmonary alveolus	Mammalian_phenotype	7
MP:0010989	MP:0010989	fused bronchial cartilage rings	Mammalian_phenotype	7
MP:0011001	MP:0011001	absence of AMPA-mediated synaptic currents	Mammalian_phenotype	7
MP:0011002	MP:0011002	enhanced AMPA-mediated synaptic currents	Mammalian_phenotype	7
MP:0011003	MP:0011003	reduced AMPA-mediated synaptic currents	Mammalian_phenotype	7
MP:0011009	MP:0011009	increased circulating glutamate dehydrogenase level	Mammalian_phenotype	7
MP:0011010	MP:0011010	decreased circulating glutamate dehydrogenase level	Mammalian_phenotype	7
MP:0011012	MP:0011012	bronchiectasis	Mammalian_phenotype	7
MP:0011026	MP:0011026	impaired branching involved in trachea morphogenesis	Mammalian_phenotype	7
MP:0011028	MP:0011028	impaired branching involved in bronchus morphogenesis	Mammalian_phenotype	7
MP:0011030	MP:0011030	impaired branching involved in preterminal bronchiole morphogenesis	Mammalian_phenotype	7
MP:0011039	MP:0011039	abnormal vestibuloocular dark reflex	Mammalian_phenotype	7
MP:0011040	MP:0011040	abnormal vestibuloocular light reflex	Mammalian_phenotype	7
MP:0011041	MP:0011041	abnormal vertical vestibuloocular reflex	Mammalian_phenotype	7
MP:0011042	MP:0011042	abnormal horizontal vestibuloocular reflex	Mammalian_phenotype	7
MP:0011054	MP:0011054	absent respiratory motile cilia	Mammalian_phenotype	7
MP:0011076	MP:0011076	increased macrophage nitric oxide production	Mammalian_phenotype	7
MP:0011077	MP:0011077	decreased macrophage nitric oxide production	Mammalian_phenotype	7
MP:0011078	MP:0011078	increased macrophage cytokine production	Mammalian_phenotype	7
MP:0011079	MP:0011079	decreased macrophage cytokine production	Mammalian_phenotype	7
MP:0011087	MP:0011087	complete neonatal lethality	Mammalian_phenotype	7
MP:0011088	MP:0011088	partial neonatal lethality	Mammalian_phenotype	7
MP:0011093	MP:0011093	complete embryonic lethality at implantation	Mammalian_phenotype	7
MP:0011094	MP:0011094	complete embryonic lethality before implantation	Mammalian_phenotype	7
MP:0011095	MP:0011095	complete embryonic lethality between implantation and placentation	Mammalian_phenotype	7
MP:0011098	MP:0011098	complete embryonic lethality during organogenesis	Mammalian_phenotype	7
MP:0011103	MP:0011103	partial embryonic lethality at implantation	Mammalian_phenotype	7
MP:0011104	MP:0011104	partial embryonic lethality before implantation	Mammalian_phenotype	7
MP:0011105	MP:0011105	partial embryonic lethality between implantation and placentation	Mammalian_phenotype	7
MP:0011108	MP:0011108	partial embryonic lethality during organogenesis	Mammalian_phenotype	7
MP:0011116	MP:0011116	absent Reichert's membrane	Mammalian_phenotype	7
MP:0011163	MP:0011163	increased wet-to-dry lung weight ratio	Mammalian_phenotype	7
MP:0011171	MP:0011171	increased number of Heinz bodies	Mammalian_phenotype	7
MP:0011175	MP:0011175	platyspondylia	Mammalian_phenotype	7
MP:0011176	MP:0011176	abnormal erythroblast morphology	Mammalian_phenotype	7
MP:0011214	MP:0011214	increased brain copper level	Mammalian_phenotype	7
MP:0011215	MP:0011215	decreased brain copper level	Mammalian_phenotype	7
MP:0011220	MP:0011220	increased intestinal calcium absorption	Mammalian_phenotype	7
MP:0011221	MP:0011221	decreased intestinal calcium absorption	Mammalian_phenotype	7
MP:0011223	MP:0011223	dilated lymph node medullary sinus	Mammalian_phenotype	7
MP:0011225	MP:0011225	lymph node medullary cord hyperplasia	Mammalian_phenotype	7
MP:0011234	MP:0011234	abnormal retinol level	Mammalian_phenotype	7
MP:0011240	MP:0011240	abnormal fetal derived definitive erythrocyte morphology	Mammalian_phenotype	7
MP:0011268	MP:0011268	biphasic excitatory postsynaptic current amplitude	Mammalian_phenotype	7
MP:0011269	MP:0011269	increased excitatory postsynaptic current amplitude	Mammalian_phenotype	7
MP:0011270	MP:0011270	decreased excitatory postsynaptic current amplitude	Mammalian_phenotype	7
MP:0011281	MP:0011281	abnormal olfactory epithelium cilium morphology	Mammalian_phenotype	7
MP:0011282	MP:0011282	increased podocyte apoptosis	Mammalian_phenotype	7
MP:0011294	MP:0011294	renal glomerulus hypertrophy	Mammalian_phenotype	7
MP:0011301	MP:0011301	juxtaglomerular cell hyperplasia	Mammalian_phenotype	7
MP:0011303	MP:0011303	absent kidney papilla	Mammalian_phenotype	7
MP:0011304	MP:0011304	kidney papillary atrophy	Mammalian_phenotype	7
MP:0011317	MP:0011317	abnormal renal artery morphology	Mammalian_phenotype	7
MP:0011325	MP:0011325	abnormal kidney arcuate vein morphology	Mammalian_phenotype	7
MP:0011326	MP:0011326	abnormal interlobular vein morphology	Mammalian_phenotype	7
MP:0011327	MP:0011327	abnormal left renal vein morphology	Mammalian_phenotype	7
MP:0011328	MP:0011328	abnormal right renal vein morphology	Mammalian_phenotype	7
MP:0011339	MP:0011339	abnormal glomerular mesangium morphology	Mammalian_phenotype	7
MP:0011341	MP:0011341	abnormal loop of Henle descending limb morphology	Mammalian_phenotype	7
MP:0011342	MP:0011342	abnormal loop of Henle ascending limb morphology	Mammalian_phenotype	7
MP:0011345	MP:0011345	truncated loop of Henle	Mammalian_phenotype	7
MP:0011349	MP:0011349	abnormal renal glomerulus basement membrane thickness	Mammalian_phenotype	7
MP:0011350	MP:0011350	abnormal proximal convoluted tubule brush border morphology	Mammalian_phenotype	7
MP:0011354	MP:0011354	absent renal glomerulus	Mammalian_phenotype	7
MP:0011355	MP:0011355	abnormal kidney interlobar artery morphology	Mammalian_phenotype	7
MP:0011363	MP:0011363	renal glomerulus atrophy	Mammalian_phenotype	7
MP:0011369	MP:0011369	increased renal glomerulus apoptosis	Mammalian_phenotype	7
MP:0011370	MP:0011370	increased mesangial cell apoptosis	Mammalian_phenotype	7
MP:0011372	MP:0011372	decreased renal tubule apoptosis	Mammalian_phenotype	7
MP:0011373	MP:0011373	decreased mesangial cell apoptosis	Mammalian_phenotype	7
MP:0011374	MP:0011374	decreased podocyte apoptosis	Mammalian_phenotype	7
MP:0011375	MP:0011375	decreased renal glomerulus apoptosis	Mammalian_phenotype	7
MP:0011387	MP:0011387	absent metanephric mesenchyme	Mammalian_phenotype	7
MP:0011389	MP:0011389	absent optic disc	Mammalian_phenotype	7
MP:0011403	MP:0011403	pyelonephritis	Mammalian_phenotype	7
MP:0011404	MP:0011404	pyelitis	Mammalian_phenotype	7
MP:0011405	MP:0011405	tubulointerstitial nephritis	Mammalian_phenotype	7
MP:0011410	MP:0011410	ectopic testis	Mammalian_phenotype	7
MP:0011416	MP:0011416	abnormal testis interstitial tissue morphology	Mammalian_phenotype	7
MP:0011433	MP:0011433	glomerular capillary congestion	Mammalian_phenotype	7
MP:0011437	MP:0011437	glomerulus hemorrhage	Mammalian_phenotype	7
MP:0011482	MP:0011482	posterior iris synechia	Mammalian_phenotype	7
MP:0011483	MP:0011483	renal glomerular synechia	Mammalian_phenotype	7
MP:0011497	MP:0011497	abnormal glomerular capsule visceral layer morphology	Mammalian_phenotype	7
MP:0011498	MP:0011498	abnormal glomerular capsule parietal layer morphology	Mammalian_phenotype	7
MP:0011499	MP:0011499	abnormal glomerular capsule space morphology	Mammalian_phenotype	7
MP:0011506	MP:0011506	glomerular crescent	Mammalian_phenotype	7
MP:0011520	MP:0011520	increased placental labyrinth size	Mammalian_phenotype	7
MP:0011521	MP:0011521	decreased placental labyrinth size	Mammalian_phenotype	7
MP:0011528	MP:0011528	abnormal placental labyrinth villi branching morphogenesis	Mammalian_phenotype	7
MP:0011529	MP:0011529	increased placenta intervillous maternal lacunae size	Mammalian_phenotype	7
MP:0011530	MP:0011530	fused radius and ulna	Mammalian_phenotype	7
MP:0011549	MP:0011549	increased urine corticosterone level	Mammalian_phenotype	7
MP:0011550	MP:0011550	decreased urine corticosterone level	Mammalian_phenotype	7
MP:0011556	MP:0011556	increased urine beta2-microglobulin level	Mammalian_phenotype	7
MP:0011561	MP:0011561	renal glomerulus lipidosis	Mammalian_phenotype	7
MP:0011565	MP:0011565	kidney papillary hypoplasia	Mammalian_phenotype	7
MP:0011567	MP:0011567	increased renal glomerulus lobularity	Mammalian_phenotype	7
MP:0011571	MP:0011571	enlarged inferior vena cava valve	Mammalian_phenotype	7
MP:0011644	MP:0011644	abnormal oviduct epithelium motile cilium morphology	Mammalian_phenotype	7
MP:0011656	MP:0011656	coronary arterio-venous fistula	Mammalian_phenotype	7
MP:0011657	MP:0011657	coronary-cameral fistula	Mammalian_phenotype	7
MP:0011665	MP:0011665	d-loop transposition of the great arteries	Mammalian_phenotype	7
MP:0011666	MP:0011666	double outlet right ventricle, ventricular defect committed to aorta	Mammalian_phenotype	7
MP:0011667	MP:0011667	double outlet right ventricle with atrioventricular septal defect	Mammalian_phenotype	7
MP:0011668	MP:0011668	double outlet right ventricle, Taussig bing type	Mammalian_phenotype	7
MP:0011669	MP:0011669	double outlet right ventricle, doubly committed ventricular septal defect	Mammalian_phenotype	7
MP:0011670	MP:0011670	double outlet right ventricle, noncommitted ventricular septal defect	Mammalian_phenotype	7
MP:0011679	MP:0011679	abnormal vomeronasal sensory neuron morphology	Mammalian_phenotype	7
MP:0011680	MP:0011680	tricuspid valve hypoplasia	Mammalian_phenotype	7
MP:0011683	MP:0011683	dual inferior vena cava	Mammalian_phenotype	7
MP:0011691	MP:0011691	absent bronchioalveolar stem cells	Mammalian_phenotype	7
MP:0011712	MP:0011712	arrested osteoblast differentiation	Mammalian_phenotype	7
MP:0011717	MP:0011717	increased interleukin-8 secretion	Mammalian_phenotype	7
MP:0011718	MP:0011718	decreased interleukin-8 secretion	Mammalian_phenotype	7
MP:0011719	MP:0011719	abnormal natural killer cell mediated cytotoxicity	Mammalian_phenotype	7
MP:0011727	MP:0011727	ectopic ovary	Mammalian_phenotype	7
MP:0011730	MP:0011730	increased myelin sheath thickness	Mammalian_phenotype	7
MP:0011731	MP:0011731	decreased myelin sheath thickness	Mammalian_phenotype	7
MP:0011755	MP:0011755	abnormal kidney collecting duct alpha-intercalated cell morphology	Mammalian_phenotype	7
MP:0011756	MP:0011756	abnormal kidney collecting duct beta-intercalated cell morphology	Mammalian_phenotype	7
MP:0011789	MP:0011789	increased urethra carcinoma incidence	Mammalian_phenotype	7
MP:0011790	MP:0011790	increased urethral gland adenocarcinoma incidence	Mammalian_phenotype	7
MP:0011791	MP:0011791	increased bulbourethral gland adenocarcinoma incidence	Mammalian_phenotype	7
MP:0011812	MP:0011812	increased cranium length	Mammalian_phenotype	7
MP:0011819	MP:0011819	increased pancreatic beta cell proliferation	Mammalian_phenotype	7
MP:0011820	MP:0011820	decreased pancreatic beta cell proliferation	Mammalian_phenotype	7
MP:0011839	MP:0011839	abnormal Guérin's valve morphology	Mammalian_phenotype	7
MP:0011855	MP:0011855	abnormal glomerular filtration barrier morphology	Mammalian_phenotype	7
MP:0011857	MP:0011857	short kidney papilla	Mammalian_phenotype	7
MP:0011858	MP:0011858	elongated kidney papilla	Mammalian_phenotype	7
MP:0011860	MP:0011860	abnormal peritubular capillary endothelium morphology	Mammalian_phenotype	7
MP:0011861	MP:0011861	increased cranium height	Mammalian_phenotype	7
MP:0011862	MP:0011862	decreased cranium length	Mammalian_phenotype	7
MP:0011872	MP:0011872	absent xiphoid process	Mammalian_phenotype	7
MP:0011876	MP:0011876	absent penis	Mammalian_phenotype	7
MP:0011886	MP:0011886	increased circulating lipase level	Mammalian_phenotype	7
MP:0011887	MP:0011887	decreased circulating lipase level	Mammalian_phenotype	7
MP:0011896	MP:0011896	increased circulating unsaturated transferrin level	Mammalian_phenotype	7
MP:0011897	MP:0011897	decreased circulating unsaturated transferrin level	Mammalian_phenotype	7
MP:0011913	MP:0011913	abnormal reticulocyte cell number	Mammalian_phenotype	7
MP:0011914	MP:0011914	decreased heart left atrium weight	Mammalian_phenotype	7
MP:0011915	MP:0011915	increased heart left atrium weight	Mammalian_phenotype	7
MP:0011916	MP:0011916	decreased heart right atrium weight	Mammalian_phenotype	7
MP:0011917	MP:0011917	increased heart right atrium weight	Mammalian_phenotype	7
MP:0011964	MP:0011964	increased total retina thickness	Mammalian_phenotype	7
MP:0011965	MP:0011965	decreased total retina thickness	Mammalian_phenotype	7
MP:0011991	MP:0011991	aortic cartilaginous metaplasia	Mammalian_phenotype	7
MP:0012004	MP:0012004	abnormal septum pellucidum morphology	Mammalian_phenotype	7
MP:0012014	MP:0012014	abnormal olfactory neuron innervation pattern	Mammalian_phenotype	7
MP:0012053	MP:0012053	limb hypertonicity	Mammalian_phenotype	7
MP:0012065	MP:0012065	increased astrocyte number	Mammalian_phenotype	7
MP:0012066	MP:0012066	decreased astrocyte number	Mammalian_phenotype	7
MP:0012068	MP:0012068	abnormal globose cell of olfactory epithelium morphology	Mammalian_phenotype	7
MP:0012069	MP:0012069	abnormal horizontal basal cell morphology	Mammalian_phenotype	7
MP:0012074	MP:0012074	failure of mammary gland growth during pregnancy	Mammalian_phenotype	7
MP:0009036	MP:0009036	absent posterior cerebellomedullary cistern	Mammalian_phenotype	8
MP:0009048	MP:0009048	enlarged tectum	Mammalian_phenotype	8
MP:0009059	MP:0009059	abnormal circulating interleukin-21 level	Mammalian_phenotype	8
MP:0009065	MP:0009065	abnormal oviduct weight	Mammalian_phenotype	8
MP:0009068	MP:0009068	enlarged oviduct	Mammalian_phenotype	8
MP:0009069	MP:0009069	dilated oviduct	Mammalian_phenotype	8
MP:0009070	MP:0009070	small oviduct	Mammalian_phenotype	8
MP:0009072	MP:0009072	absent cranial vagina	Mammalian_phenotype	8
MP:0009086	MP:0009086	blind uterine horn	Mammalian_phenotype	8
MP:0009087	MP:0009087	dilated uterine horn	Mammalian_phenotype	8
MP:0009088	MP:0009088	thin uterine horn	Mammalian_phenotype	8
MP:0009089	MP:0009089	short uterine horn	Mammalian_phenotype	8
MP:0009090	MP:0009090	myometrium hypoplasia	Mammalian_phenotype	8
MP:0009091	MP:0009091	endometrium hypoplasia	Mammalian_phenotype	8
MP:0009092	MP:0009092	endometrium hyperplasia	Mammalian_phenotype	8
MP:0009094	MP:0009094	abnormal endometrial gland morphology	Mammalian_phenotype	8
MP:0009103	MP:0009103	abnormal penile bone morphology	Mammalian_phenotype	8
MP:0009113	MP:0009113	increased pancreatic beta cell mass	Mammalian_phenotype	8
MP:0009114	MP:0009114	decreased pancreatic beta cell mass	Mammalian_phenotype	8
MP:0009140	MP:0009140	dilated efferent ductules of testis	Mammalian_phenotype	8
MP:0009151	MP:0009151	increased pancreatic ductal adenocarcinoma incidence	Mammalian_phenotype	8
MP:0009152	MP:0009152	increased pancreatic intraepithelial neoplasia incidence	Mammalian_phenotype	8
MP:0009161	MP:0009161	pancreatic acinar cell zymogen granule accumulation	Mammalian_phenotype	8
MP:0009162	MP:0009162	absent pancreatic acinar cell zymogen granule	Mammalian_phenotype	8
MP:0009169	MP:0009169	pancreatic islet hypoplasia	Mammalian_phenotype	8
MP:0009174	MP:0009174	absent pancreatic beta cells	Mammalian_phenotype	8
MP:0009178	MP:0009178	absent pancreatic alpha cells	Mammalian_phenotype	8
MP:0009182	MP:0009182	absent pancreatic delta cells	Mammalian_phenotype	8
MP:0009187	MP:0009187	absent PP cells	Mammalian_phenotype	8
MP:0009192	MP:0009192	absent pancreatic epsilon cells	Mammalian_phenotype	8
MP:0009215	MP:0009215	absent uterine horn	Mammalian_phenotype	8
MP:0009219	MP:0009219	increased prostate intraepithelial neoplasia incidence	Mammalian_phenotype	8
MP:0009220	MP:0009220	increased prostate gland adenocarcinoma incidence	Mammalian_phenotype	8
MP:0009223	MP:0009223	increased uterus carcinoma incidence	Mammalian_phenotype	8
MP:0009224	MP:0009224	absent endometrium	Mammalian_phenotype	8
MP:0009225	MP:0009225	abnormal uterine cervix size	Mammalian_phenotype	8
MP:0009232	MP:0009232	abnormal sperm nucleus morphology	Mammalian_phenotype	8
MP:0009233	MP:0009233	enlarged sperm head	Mammalian_phenotype	8
MP:0009234	MP:0009234	absent sperm head	Mammalian_phenotype	8
MP:0009235	MP:0009235	small sperm head	Mammalian_phenotype	8
MP:0009236	MP:0009236	pinhead sperm	Mammalian_phenotype	8
MP:0009237	MP:0009237	kinked sperm flagellum	Mammalian_phenotype	8
MP:0009238	MP:0009238	coiled sperm flagellum	Mammalian_phenotype	8
MP:0009239	MP:0009239	short sperm flagellum	Mammalian_phenotype	8
MP:0009240	MP:0009240	elongated sperm flagellum	Mammalian_phenotype	8
MP:0009241	MP:0009241	thick sperm flagellum	Mammalian_phenotype	8
MP:0009242	MP:0009242	thin sperm flagellum	Mammalian_phenotype	8
MP:0009243	MP:0009243	hairpin sperm flagellum	Mammalian_phenotype	8
MP:0009248	MP:0009248	small caput epididymis	Mammalian_phenotype	8
MP:0009249	MP:0009249	enlarged caput epididymis	Mammalian_phenotype	8
MP:0009256	MP:0009256	enlarged corpus epididymis	Mammalian_phenotype	8
MP:0009257	MP:0009257	dilated seminiferous tubules	Mammalian_phenotype	8
MP:0009259	MP:0009259	abnormal vestibular saccule duct morphology	Mammalian_phenotype	8
MP:0009260	MP:0009260	abnormal utricle duct morphology	Mammalian_phenotype	8
MP:0009261	MP:0009261	abnormal utricle valve morphology	Mammalian_phenotype	8
MP:0009267	MP:0009267	abnormal cerebellum fissure morphology	Mammalian_phenotype	8
MP:0009308	MP:0009308	increased adenocarcinoma incidence	Mammalian_phenotype	8
MP:0009321	MP:0009321	increased histiocytic sarcoma incidence	Mammalian_phenotype	8
MP:0009326	MP:0009326	absent maternal crouching	Mammalian_phenotype	8
MP:0009359	MP:0009359	endometrium atrophy	Mammalian_phenotype	8
MP:0009361	MP:0009361	abnormal primordial ovarian follicle morphology	Mammalian_phenotype	8
MP:0009362	MP:0009362	abnormal primary ovarian follicle morphology	Mammalian_phenotype	8
MP:0009363	MP:0009363	abnormal secondary ovarian follicle morphology	Mammalian_phenotype	8
MP:0009364	MP:0009364	abnormal mature ovarian follicle morphology	Mammalian_phenotype	8
MP:0009375	MP:0009375	thin zona pellucida	Mammalian_phenotype	8
MP:0009377	MP:0009377	ectopic manchette	Mammalian_phenotype	8
MP:0009395	MP:0009395	increased nucleated erythrocyte cell number	Mammalian_phenotype	8
MP:0009397	MP:0009397	increased trophoblast giant cell number	Mammalian_phenotype	8
MP:0009433	MP:0009433	polyovular ovarian follicle	Mammalian_phenotype	8
MP:0009444	MP:0009444	ovarian follicular cyst	Mammalian_phenotype	8
MP:0009463	MP:0009463	abnormal pituitary infundibular stalk morphology	Mammalian_phenotype	8
MP:0009468	MP:0009468	absent magnocellular neurosecretory cells	Mammalian_phenotype	8
MP:0009508	MP:0009508	increased mammary gland ductal carcinoma incidence	Mammalian_phenotype	8
MP:0009515	MP:0009515	increased gastrointestinal stromal tumor incidence	Mammalian_phenotype	8
MP:0009540	MP:0009540	absent Hassall's corpuscle	Mammalian_phenotype	8
MP:0009548	MP:0009548	abnormal platelet aggregation	Mammalian_phenotype	8
MP:0009554	MP:0009554	abnormal hair follicle melanin granule shape	Mammalian_phenotype	8
MP:0009555	MP:0009555	abnormal hair follicle melanin granule distribution	Mammalian_phenotype	8
MP:0009561	MP:0009561	superior cervical ganglion degeneration	Mammalian_phenotype	8
MP:0009591	MP:0009591	increased liver adenocarcinoma incidence	Mammalian_phenotype	8
MP:0009639	MP:0009639	abnormal olivary pretectal nucleus morphology	Mammalian_phenotype	8
MP:0009660	MP:0009660	abnormal induced retinal neovascularization	Mammalian_phenotype	8
MP:0009704	MP:0009704	increased skin squamous cell carcinoma incidence	Mammalian_phenotype	8
MP:0009725	MP:0009725	absent lens vesicle	Mammalian_phenotype	8
MP:0009736	MP:0009736	abnormal prostate gland branching morphogenesis	Mammalian_phenotype	8
MP:0009738	MP:0009738	enlarged prostate gland anterior lobe	Mammalian_phenotype	8
MP:0009739	MP:0009739	enlarged prostate gland dorsolateral lobe	Mammalian_phenotype	8
MP:0009740	MP:0009740	small prostate gland dorsolateral lobe	Mammalian_phenotype	8
MP:0009822	MP:0009822	abnormal subarcuate fossa morphology	Mammalian_phenotype	8
MP:0009830	MP:0009830	abnormal sperm connecting piece morphology	Mammalian_phenotype	8
MP:0009831	MP:0009831	abnormal sperm midpiece morphology	Mammalian_phenotype	8
MP:0009836	MP:0009836	abnormal sperm principal piece morphology	Mammalian_phenotype	8
MP:0009837	MP:0009837	abnormal sperm end piece morphology	Mammalian_phenotype	8
MP:0009838	MP:0009838	abnormal sperm axoneme morphology	Mammalian_phenotype	8
MP:0009839	MP:0009839	multiflagellated sperm	Mammalian_phenotype	8
MP:0009867	MP:0009867	abnormal ascending aorta morphology	Mammalian_phenotype	8
MP:0009868	MP:0009868	abnormal descending thoracic aorta morphology	Mammalian_phenotype	8
MP:0009870	MP:0009870	abnormal abdominal aorta morphology	Mammalian_phenotype	8
MP:0009871	MP:0009871	abnormal aorta tunica adventitia morphology	Mammalian_phenotype	8
MP:0009872	MP:0009872	abnormal aorta tunica intima morphology	Mammalian_phenotype	8
MP:0009873	MP:0009873	abnormal aorta tunica media morphology	Mammalian_phenotype	8
MP:0009900	MP:0009900	vomer bone hypoplasia	Mammalian_phenotype	8
MP:0009905	MP:0009905	absent tongue	Mammalian_phenotype	8
MP:0009906	MP:0009906	increased tongue size	Mammalian_phenotype	8
MP:0009907	MP:0009907	decreased tongue size	Mammalian_phenotype	8
MP:0009908	MP:0009908	protruding tongue	Mammalian_phenotype	8
MP:0009909	MP:0009909	bifid tongue	Mammalian_phenotype	8
MP:0009911	MP:0009911	increased hyoid bone size	Mammalian_phenotype	8
MP:0009912	MP:0009912	decreased hyoid bone size	Mammalian_phenotype	8
MP:0009913	MP:0009913	abnormal hyoid bone greater horn morphology	Mammalian_phenotype	8
MP:0009914	MP:0009914	abnormal hyoid bone lesser horn morphology	Mammalian_phenotype	8
MP:0009917	MP:0009917	abnormal hyoid bone body morphology	Mammalian_phenotype	8
MP:0009946	MP:0009946	abnormal olfactory bulb layer morphology	Mammalian_phenotype	8
MP:0009953	MP:0009953	abnormal olfactory tubercle morphology	Mammalian_phenotype	8
MP:0009956	MP:0009956	abnormal cerebellar layer morphology	Mammalian_phenotype	8
MP:0009959	MP:0009959	abnormal cerebellar hemisphere morphology	Mammalian_phenotype	8
MP:0009960	MP:0009960	abnormal cerebellum anterior lobe morphology	Mammalian_phenotype	8
MP:0009961	MP:0009961	abnormal flocculonodular lobe morphology	Mammalian_phenotype	8
MP:0009962	MP:0009962	abnormal cerebellum posterior lobe morphology	Mammalian_phenotype	8
MP:0009964	MP:0009964	abnormal cerebellum lobule morphology	Mammalian_phenotype	8
MP:0009976	MP:0009976	abnormal cerebellar peduncle morphology	Mammalian_phenotype	8
MP:0009980	MP:0009980	abnormal cerebellum dentate nucleus morphology	Mammalian_phenotype	8
MP:0009983	MP:0009983	abnormal cerebellum fastigial nucleus morphology	Mammalian_phenotype	8
MP:0009984	MP:0009984	abnormal cerebellum interpositus nucleus morphology	Mammalian_phenotype	8
MP:0010009	MP:0010009	abnormal piriform cortex morphology	Mammalian_phenotype	8
MP:0010015	MP:0010015	abnormal cuticular plate morphology	Mammalian_phenotype	8
MP:0010026	MP:0010026	decreased liver cholesterol level	Mammalian_phenotype	8
MP:0010027	MP:0010027	increased liver cholesterol level	Mammalian_phenotype	8
MP:0010054	MP:0010054	increased hepatoblastoma incidence	Mammalian_phenotype	8
MP:0010058	MP:0010058	enlarged olfactory bulb	Mammalian_phenotype	8
MP:0010067	MP:0010067	increased red blood cell distribution width	Mammalian_phenotype	8
MP:0010068	MP:0010068	decreased red blood cell distribution width	Mammalian_phenotype	8
MP:0010078	MP:0010078	increased circulating plant sterol level	Mammalian_phenotype	8
MP:0010100	MP:0010100	increased cervical vertebrae number	Mammalian_phenotype	8
MP:0010139	MP:0010139	aortitis	Mammalian_phenotype	8
MP:0010161	MP:0010161	decreased brain cholesterol level	Mammalian_phenotype	8
MP:0010162	MP:0010162	increased brain cholesterol level	Mammalian_phenotype	8
MP:0010189	MP:0010189	abnormal T follicular helper cell physiology	Mammalian_phenotype	8
MP:0010208	MP:0010208	prognathia	Mammalian_phenotype	8
MP:0010222	MP:0010222	abnormal T-helper 17 cell physiology	Mammalian_phenotype	8
MP:0010264	MP:0010264	increased hepatoma incidence	Mammalian_phenotype	8
MP:0010265	MP:0010265	decreased hepatoma incidence	Mammalian_phenotype	8
MP:0010272	MP:0010272	increased tongue tumor incidence	Mammalian_phenotype	8
MP:0010276	MP:0010276	increased intraocular melanoma incidence	Mammalian_phenotype	8
MP:0010277	MP:0010277	increased astrocytoma incidence	Mammalian_phenotype	8
MP:0010301	MP:0010301	increased stomach tumor incidence	Mammalian_phenotype	8
MP:0010304	MP:0010304	increased choroid tumor incidence	Mammalian_phenotype	8
MP:0010305	MP:0010305	increased iris tumor incidence	Mammalian_phenotype	8
MP:0010312	MP:0010312	increased oligodendroglioma incidence	Mammalian_phenotype	8
MP:0010322	MP:0010322	increased cutaneous melanoma incidence	Mammalian_phenotype	8
MP:0010326	MP:0010326	malleus hypoplasia	Mammalian_phenotype	8
MP:0010328	MP:0010328	thin malleus neck	Mammalian_phenotype	8
MP:0010336	MP:0010336	increased acute lymphoblastic leukemia incidence	Mammalian_phenotype	8
MP:0010337	MP:0010337	increased chronic lymphocytic leukemia incidence	Mammalian_phenotype	8
MP:0010346	MP:0010346	increased thyroid carcinoma incidence	Mammalian_phenotype	8
MP:0010348	MP:0010348	increased pancreatic islet cell carcinoma incidence	Mammalian_phenotype	8
MP:0010350	MP:0010350	increased pituitary adenohypophysis tumor incidence	Mammalian_phenotype	8
MP:0010351	MP:0010351	increased pituitary melanotroph tumor incidence	Mammalian_phenotype	8
MP:0010363	MP:0010363	increased fibrosarcoma incidence	Mammalian_phenotype	8
MP:0010366	MP:0010366	increased adrenal cortical tumor incidence	Mammalian_phenotype	8
MP:0010367	MP:0010367	increased spindle cell carcinoma incidence	Mammalian_phenotype	8
MP:0010384	MP:0010384	increased renal carcinoma incidence	Mammalian_phenotype	8
MP:0010389	MP:0010389	mosaic coat color	Mammalian_phenotype	8
MP:0010422	MP:0010422	heart right ventricle hypoplasia	Mammalian_phenotype	8
MP:0010446	MP:0010446	heart left ventricle hypoplasia	Mammalian_phenotype	8
MP:0010465	MP:0010465	aberrant origin of the right subclavian artery	Mammalian_phenotype	8
MP:0010471	MP:0010471	supravalvar aortic stenosis	Mammalian_phenotype	8
MP:0010473	MP:0010473	descending aorta dilation	Mammalian_phenotype	8
MP:0010474	MP:0010474	descending aorta hypoplasia	Mammalian_phenotype	8
MP:0010486	MP:0010486	absent right subclavian artery	Mammalian_phenotype	8
MP:0010523	MP:0010523	calcified thoracic aorta	Mammalian_phenotype	8
MP:0010525	MP:0010525	abdominal aorta coarctation	Mammalian_phenotype	8
MP:0010526	MP:0010526	aortic arch coarctation	Mammalian_phenotype	8
MP:0010540	MP:0010540	long stride length	Mammalian_phenotype	8
MP:0010542	MP:0010542	right ventricular myocardium hypoplasia	Mammalian_phenotype	8
MP:0010543	MP:0010543	aorta tubular hypoplasia	Mammalian_phenotype	8
MP:0010556	MP:0010556	thin ventricle myocardium compact layer	Mammalian_phenotype	8
MP:0010569	MP:0010569	papillary muscle hypertrophy	Mammalian_phenotype	8
MP:0010572	MP:0010572	persistent right dorsal aorta	Mammalian_phenotype	8
MP:0010573	MP:0010573	left dorsal aorta regression	Mammalian_phenotype	8
MP:0010586	MP:0010586	absent conotruncal ridges	Mammalian_phenotype	8
MP:0010587	MP:0010587	conotruncal ridge hypoplasia	Mammalian_phenotype	8
MP:0010588	MP:0010588	conotruncal ridge hyperplasia	Mammalian_phenotype	8
MP:0010591	MP:0010591	enlarged aortic valve	Mammalian_phenotype	8
MP:0010594	MP:0010594	thick aortic valve	Mammalian_phenotype	8
MP:0010595	MP:0010595	abnormal aortic valve cusp morphology	Mammalian_phenotype	8
MP:0010598	MP:0010598	abnormal aortic valve anulus morphology	Mammalian_phenotype	8
MP:0010600	MP:0010600	enlarged pulmonary valve	Mammalian_phenotype	8
MP:0010601	MP:0010601	thick pulmonary valve	Mammalian_phenotype	8
MP:0010602	MP:0010602	abnormal pulmonary valve cusp morphology	Mammalian_phenotype	8
MP:0010606	MP:0010606	abnormal pulmonary valve anulus morphology	Mammalian_phenotype	8
MP:0010610	MP:0010610	patent aortic valve	Mammalian_phenotype	8
MP:0010611	MP:0010611	patent pulmonary valve	Mammalian_phenotype	8
MP:0010612	MP:0010612	muscular subaortic stenosis	Mammalian_phenotype	8
MP:0010615	MP:0010615	unicuspid mitral valve	Mammalian_phenotype	8
MP:0010616	MP:0010616	absent mitral valve cusps	Mammalian_phenotype	8
MP:0010623	MP:0010623	bicuspid tricuspid valve	Mammalian_phenotype	8
MP:0010624	MP:0010624	unicuspid tricuspid valve	Mammalian_phenotype	8
MP:0010625	MP:0010625	absent tricuspid valve cusps	Mammalian_phenotype	8
MP:0010638	MP:0010638	absent intercalated discs	Mammalian_phenotype	8
MP:0010641	MP:0010641	descending aorta stenosis	Mammalian_phenotype	8
MP:0010645	MP:0010645	failure of conotruncal ridge closure	Mammalian_phenotype	8
MP:0010658	MP:0010658	thoracic aorta aneurysm	Mammalian_phenotype	8
MP:0010659	MP:0010659	abdominal aorta aneurysm	Mammalian_phenotype	8
MP:0010665	MP:0010665	persistent vitelline artery	Mammalian_phenotype	8
MP:0010669	MP:0010669	abnormal activation-induced B cell apoptosis	Mammalian_phenotype	8
MP:0010670	MP:0010670	abnormal activation-induced cell death of T cells	Mammalian_phenotype	8
MP:0010727	MP:0010727	increased glioblastoma incidence	Mammalian_phenotype	8
MP:0010728	MP:0010728	fusion of atlas and occipital bones	Mammalian_phenotype	8
MP:0010774	MP:0010774	abnormal lymph node follicular mantle morphology	Mammalian_phenotype	8
MP:0010776	MP:0010776	abnormal placenta metrial gland morphology	Mammalian_phenotype	8
MP:0010859	MP:0010859	abnormal anterior commissure pars anterior morphology	Mammalian_phenotype	8
MP:0010860	MP:0010860	abnormal anterior commissure pars posterior morphology	Mammalian_phenotype	8
MP:0010905	MP:0010905	absent alveolar pores	Mammalian_phenotype	8
MP:0010941	MP:0010941	abnormal foramen magnum morphology	Mammalian_phenotype	8
MP:0010949	MP:0010949	decreased Clara cell number	Mammalian_phenotype	8
MP:0010996	MP:0010996	increased aorta wall thickness	Mammalian_phenotype	8
MP:0010997	MP:0010997	decreased aorta wall thickness	Mammalian_phenotype	8
MP:0011013	MP:0011013	bronchiolectasis	Mammalian_phenotype	8
MP:0011032	MP:0011032	impaired branching involved in terminal bronchiole morphogenesis	Mammalian_phenotype	8
MP:0011034	MP:0011034	impaired branching involved in respiratory bronchiole morphogenesis	Mammalian_phenotype	8
MP:0011036	MP:0011036	impaired branching involved in alveolar duct morphogenesis	Mammalian_phenotype	8
MP:0011038	MP:0011038	impaired branching involved in alveolar sac morphogenesis	Mammalian_phenotype	8
MP:0011057	MP:0011057	absent brain ependyma motile cilia	Mammalian_phenotype	8
MP:0011060	MP:0011060	abnormal kinocilium morphology	Mammalian_phenotype	8
MP:0011096	MP:0011096	complete embryonic lethality between implantation and somite formation	Mammalian_phenotype	8
MP:0011097	MP:0011097	complete embryonic lethality between somite formation and embryo turning	Mammalian_phenotype	8
MP:0011106	MP:0011106	partial embryonic lethality between implantation and somite formation	Mammalian_phenotype	8
MP:0011107	MP:0011107	partial embryonic lethality between somite formation and embryo turning	Mammalian_phenotype	8
MP:0011177	MP:0011177	abnormal erythroblast number	Mammalian_phenotype	8
MP:0011217	MP:0011217	increased brainstem copper level	Mammalian_phenotype	8
MP:0011218	MP:0011218	decreased brainstem copper level	Mammalian_phenotype	8
MP:0011241	MP:0011241	abnormal fetal derived definitive erythrocyte cell number	Mammalian_phenotype	8
MP:0011315	MP:0011315	abnormal kidney arcuate artery morphology	Mammalian_phenotype	8
MP:0011316	MP:0011316	abnormal kidney interlobular artery morphology	Mammalian_phenotype	8
MP:0011318	MP:0011318	abnormal right renal artery morphology	Mammalian_phenotype	8
MP:0011319	MP:0011319	abnormal left renal artery morphology	Mammalian_phenotype	8
MP:0011338	MP:0011338	abnormal mesangial matrix morphology	Mammalian_phenotype	8
MP:0011343	MP:0011343	abnormal loop of Henle ascending limb thin segment morphology	Mammalian_phenotype	8
MP:0011344	MP:0011344	abnormal loop of Henle ascending limb thick segment morphology	Mammalian_phenotype	8
MP:0011351	MP:0011351	absent proximal convoluted tubule brush border	Mammalian_phenotype	8
MP:0011352	MP:0011352	proximal convoluted tubule brush border loss	Mammalian_phenotype	8
MP:0011357	MP:0011357	supernumerary renal arteries	Mammalian_phenotype	8
MP:0011359	MP:0011359	decreased glomerular capillary number	Mammalian_phenotype	8
MP:0011409	MP:0011409	increased renal glomerulus basement membrane thickness	Mammalian_phenotype	8
MP:0011430	MP:0011430	mesangiolysis	Mammalian_phenotype	8
MP:0011451	MP:0011451	increased susceptibility to dopaminergic neuron neurotoxicity	Mammalian_phenotype	8
MP:0011452	MP:0011452	decreased susceptibility to dopaminergic neuron neurotoxicity	Mammalian_phenotype	8
MP:0011453	MP:0011453	abnormal glomerular capillary endothelium morphology	Mammalian_phenotype	8
MP:0011500	MP:0011500	decreased glomerular capsule space	Mammalian_phenotype	8
MP:0011501	MP:0011501	increased glomerular capsule space	Mammalian_phenotype	8
MP:0011502	MP:0011502	parietal capsular epithelium metaplasia	Mammalian_phenotype	8
MP:0011508	MP:0011508	glomerular capillary thrombosis	Mammalian_phenotype	8
MP:0011509	MP:0011509	dilated glomerular capillary	Mammalian_phenotype	8
MP:0011523	MP:0011523	thin placenta labyrinth	Mammalian_phenotype	8
MP:0011524	MP:0011524	thick placenta labyrinth	Mammalian_phenotype	8
MP:0011645	MP:0011645	absent oviduct epithelium motile cilium	Mammalian_phenotype	8
MP:0011661	MP:0011661	persistent truncus arteriosus type i	Mammalian_phenotype	8
MP:0011662	MP:0011662	persistent truncus arteriosus type ii	Mammalian_phenotype	8
MP:0011663	MP:0011663	persistent truncus arteriosus type iii	Mammalian_phenotype	8
MP:0011664	MP:0011664	persistent truncus arteriosus type iv	Mammalian_phenotype	8
MP:0011671	MP:0011671	balanced complete atrioventricular canal	Mammalian_phenotype	8
MP:0011673	MP:0011673	unbalanced complete common atrioventricular canal	Mammalian_phenotype	8
MP:0011674	MP:0011674	multiple major aortopulmonary collateral arteries	Mammalian_phenotype	8
MP:0011684	MP:0011684	coronary-cameral fistula to right ventricle	Mammalian_phenotype	8
MP:0011713	MP:0011713	abnormal circulating interleukin-8 level	Mammalian_phenotype	8
MP:0011745	MP:0011745	isolation of the left subclavian artery	Mammalian_phenotype	8
MP:0011750	MP:0011750	abnormal seminiferous tubule epithelium morphology	Mammalian_phenotype	8
MP:0011830	MP:0011830	ectopic hair follicle melanin granules	Mammalian_phenotype	8
MP:0011850	MP:0011850	absent clitoral bone	Mammalian_phenotype	8
MP:0011859	MP:0011859	decreased renal glomerulus basement membrane thickness	Mammalian_phenotype	8
MP:0011873	MP:0011873	enlarged uterine horn	Mammalian_phenotype	8
MP:0011980	MP:0011980	absent Langerhans cell precursors	Mammalian_phenotype	8
MP:0011983	MP:0011983	abnormal Ito cell differentiation	Mammalian_phenotype	8
MP:0011998	MP:0011998	decreased embryonic cilium length	Mammalian_phenotype	8
MP:0012005	MP:0012005	abnormal septum pellucidum size	Mammalian_phenotype	8
MP:0012027	MP:0012027	abnormal embryonic cilium location or orientation	Mammalian_phenotype	8
MP:0000044	MP:0000044	absent organ of Corti	Mammalian_phenotype	8
MP:0000078	MP:0000078	abnormal supraoccipital bone morphology	Mammalian_phenotype	8
MP:0000080	MP:0000080	abnormal exoccipital bone morphology	Mammalian_phenotype	8
MP:0000085	MP:0000085	large anterior fontanelle	Mammalian_phenotype	8
MP:0000099	MP:0000099	absent vomer bone	Mammalian_phenotype	8
MP:0000101	MP:0000101	absent ethmoidal bone	Mammalian_phenotype	8
MP:0000111	MP:0000111	cleft palate	Mammalian_phenotype	8
MP:0000119	MP:0000119	abnormal tooth eruption	Mammalian_phenotype	8
MP:0000124	MP:0000124	absent teeth	Mammalian_phenotype	8
MP:0000126	MP:0000126	brittle teeth	Mammalian_phenotype	8
MP:0000139	MP:0000139	absent vertebral transverse processes	Mammalian_phenotype	8
MP:0000140	MP:0000140	absent vertebral pedicles	Mammalian_phenotype	8
MP:0000152	MP:0000152	absent proximal rib	Mammalian_phenotype	8
MP:0000208	MP:0000208	decreased hematocrit	Mammalian_phenotype	8
MP:0000216	MP:0000216	absent erythroid progenitor cell	Mammalian_phenotype	8
MP:0000220	MP:0000220	increased monocyte cell number	Mammalian_phenotype	8
MP:0000223	MP:0000223	decreased monocyte cell number	Mammalian_phenotype	8
MP:0000295	MP:0000295	trabecula carnea hypoplasia	Mammalian_phenotype	8
MP:0000296	MP:0000296	absent trabeculae carneae	Mammalian_phenotype	8
MP:0000300	MP:0000300	thin atrioventricular cushion	Mammalian_phenotype	8
MP:0000314	MP:0000314	schistocytosis	Mammalian_phenotype	8
MP:0000322	MP:0000322	increased granulocyte number	Mammalian_phenotype	8
MP:0000334	MP:0000334	decreased granulocyte number	Mammalian_phenotype	8
MP:0000359	MP:0000359	abnormal mast cell morphology	Mammalian_phenotype	8
MP:0000394	MP:0000394	absent hair follicle melanin granules	Mammalian_phenotype	8
MP:0000421	MP:0000421	mottled coat	Mammalian_phenotype	8
MP:0000455	MP:0000455	abnormal maxilla morphology	Mammalian_phenotype	8
MP:0000458	MP:0000458	abnormal mandible morphology	Mammalian_phenotype	8
MP:0000487	MP:0000487	absent enterocytes	Mammalian_phenotype	8
MP:0000636	MP:0000636	enlarged pituitary gland	Mammalian_phenotype	8
MP:0000661	MP:0000661	small prostate gland ventral lobe	Mammalian_phenotype	8
MP:0000664	MP:0000664	small prostate gland anterior lobe	Mammalian_phenotype	8
MP:0000666	MP:0000666	decreased prostate gland duct number	Mammalian_phenotype	8
MP:0000764	MP:0000764	abnormal tongue epithelium morphology	Mammalian_phenotype	8
MP:0000781	MP:0000781	decreased corpus callosum size	Mammalian_phenotype	8
MP:0000789	MP:0000789	thickened cerebral cortex	Mammalian_phenotype	8
MP:0000790	MP:0000790	abnormal stratification in cerebral cortex	Mammalian_phenotype	8
MP:0000791	MP:0000791	delaminated cerebral cortex	Mammalian_phenotype	8
MP:0000795	MP:0000795	abnormal postcentral gyrus morphology	Mammalian_phenotype	8
MP:0000796	MP:0000796	abnormal sensory dissociation area morphology	Mammalian_phenotype	8
MP:0000797	MP:0000797	abnormal supramarginal gyrus morphology	Mammalian_phenotype	8
MP:0000799	MP:0000799	abnormal precentral gyrus morphology	Mammalian_phenotype	8
MP:0000800	MP:0000800	abnormal prefrontal gyrus morphology	Mammalian_phenotype	8
MP:0000802	MP:0000802	abnormal superior temporal gyrus morphology	Mammalian_phenotype	8
MP:0000805	MP:0000805	abnormal visual cortex morphology	Mammalian_phenotype	8
MP:0000843	MP:0000843	absent facial nuclei	Mammalian_phenotype	8
MP:0000851	MP:0000851	cerebellum hypoplasia	Mammalian_phenotype	8
MP:0000855	MP:0000855	accelerated formation of intralobular fissures	Mammalian_phenotype	8
MP:0000856	MP:0000856	abnormal cerebellar plate morphology	Mammalian_phenotype	8
MP:0000857	MP:0000857	abnormal cerebellar foliation	Mammalian_phenotype	8
MP:0000859	MP:0000859	abnormal somatosensory cortex morphology	Mammalian_phenotype	8
MP:0000864	MP:0000864	abnormal cerebellum vermis morphology	Mammalian_phenotype	8
MP:0000872	MP:0000872	abnormal cerebellum external granule cell layer morphology	Mammalian_phenotype	8
MP:0000898	MP:0000898	midbrain hyperplasia	Mammalian_phenotype	8
MP:0000899	MP:0000899	abnormal corpora quadrigemina morphology	Mammalian_phenotype	8
MP:0000910	MP:0000910	small facial motor nucleus	Mammalian_phenotype	8
MP:0000912	MP:0000912	small trigeminal motor nucleus	Mammalian_phenotype	8
MP:0000974	MP:0000974	abnormal hair guard neuron morphology	Mammalian_phenotype	8
MP:0000977	MP:0000977	abnormal hair-tylotrich neuron morphology	Mammalian_phenotype	8
MP:0000979	MP:0000979	abnormal hair-down neuron morphology	Mammalian_phenotype	8
MP:0000982	MP:0000982	abnormal Meissner's corpuscle morphology	Mammalian_phenotype	8
MP:0000985	MP:0000985	abnormal Merkel's receptor morphology	Mammalian_phenotype	8
MP:0000988	MP:0000988	abnormal pacinian corpuscle morphology	Mammalian_phenotype	8
MP:0000989	MP:0000989	abnormal Ruffini's corpuscle morphology	Mammalian_phenotype	8
MP:0000999	MP:0000999	abnormal golgi tendon organ morphology	Mammalian_phenotype	8
MP:0001003	MP:0001003	abnormal olfactory receptor morphology	Mammalian_phenotype	8
MP:0001013	MP:0001013	enlarged superior cervical ganglion	Mammalian_phenotype	8
MP:0001014	MP:0001014	absent superior cervical ganglion	Mammalian_phenotype	8
MP:0001015	MP:0001015	small superior cervical ganglion	Mammalian_phenotype	8
MP:0001019	MP:0001019	abnormal L4 dorsal root ganglion morphology	Mammalian_phenotype	8
MP:0001022	MP:0001022	abnormal L5 dorsal root ganglion morphology	Mammalian_phenotype	8
MP:0001040	MP:0001040	deficient enteric cholinergic innervation	Mammalian_phenotype	8
MP:0001094	MP:0001094	trigeminal ganglion hypertrophy	Mammalian_phenotype	8
MP:0001109	MP:0001109	absent Schwann cell precursors	Mammalian_phenotype	8
MP:0001130	MP:0001130	abnormal ovarian folliculogenesis	Mammalian_phenotype	8
MP:0001134	MP:0001134	absent corpus luteum	Mammalian_phenotype	8
MP:0001136	MP:0001136	dilated uterine cervix	Mammalian_phenotype	8
MP:0001137	MP:0001137	abnormal uterine cervix epithelium morphology	Mammalian_phenotype	8
MP:0001141	MP:0001141	thickened vaginal epithelium	Mammalian_phenotype	8
MP:0001143	MP:0001143	constricted vagina orifice	Mammalian_phenotype	8
MP:0001144	MP:0001144	vagina atresia	Mammalian_phenotype	8
MP:0001148	MP:0001148	enlarged testis	Mammalian_phenotype	8
MP:0001151	MP:0001151	enlarged foreskin	Mammalian_phenotype	8
MP:0001154	MP:0001154	seminiferous tubule degeneration	Mammalian_phenotype	8
MP:0001157	MP:0001157	small seminal vesicle	Mammalian_phenotype	8
MP:0001167	MP:0001167	prostate gland epithelial hyperplasia	Mammalian_phenotype	8
MP:0001384	MP:0001384	abnormal pup retrieval	Mammalian_phenotype	8
MP:0001407	MP:0001407	short stride length	Mammalian_phenotype	8
MP:0001523	MP:0001523	impaired righting response	Mammalian_phenotype	8
MP:0001585	MP:0001585	hemolytic anemia	Mammalian_phenotype	8
MP:0001589	MP:0001589	abnormal mean corpuscular hemoglobin	Mammalian_phenotype	8
MP:0001677	MP:0001677	absent apical ectodermal ridge	Mammalian_phenotype	8
MP:0001678	MP:0001678	thick apical ectodermal ridge	Mammalian_phenotype	8
MP:0001679	MP:0001679	thin apical ectodermal ridge	Mammalian_phenotype	8
MP:0001713	MP:0001713	decreased trophoblast giant cell number	Mammalian_phenotype	8
MP:0001715	MP:0001715	placental labyrinth hypoplasia	Mammalian_phenotype	8
MP:0001717	MP:0001717	absent ectoplacental cone	Mammalian_phenotype	8
MP:0001745	MP:0001745	increased circulating corticosterone level	Mammalian_phenotype	8
MP:0001749	MP:0001749	suppressed circulating follicle stimulating hormone level	Mammalian_phenotype	8
MP:0001883	MP:0001883	increased mammary adenocarcinoma incidence	Mammalian_phenotype	8
MP:0001917	MP:0001917	intraventricular hemorrhage	Mammalian_phenotype	8
MP:0002013	MP:0002013	increased pilomatricoma incidence	Mammalian_phenotype	8
MP:0002023	MP:0002023	increased B cell derived lymphoma incidence	Mammalian_phenotype	8
MP:0002024	MP:0002024	increased T cell derived lymphoma incidence	Mammalian_phenotype	8
MP:0002047	MP:0002047	increased hepatic hemangioma incidence	Mammalian_phenotype	8
MP:0002050	MP:0002050	increased pheochromocytoma incidence	Mammalian_phenotype	8
MP:0002196	MP:0002196	absent corpus callosum	Mammalian_phenotype	8
MP:0002359	MP:0002359	abnormal spleen germinal center morphology	Mammalian_phenotype	8
MP:0002360	MP:0002360	abnormal spleen B cell corona morphology	Mammalian_phenotype	8
MP:0002460	MP:0002460	decreased immunoglobulin level	Mammalian_phenotype	8
MP:0002461	MP:0002461	increased immunoglobulin level	Mammalian_phenotype	8
MP:0002574	MP:0002574	increased vertical activity	Mammalian_phenotype	8
MP:0002584	MP:0002584	small ectoplacental cone	Mammalian_phenotype	8
MP:0002586	MP:0002586	abnormal platelet volume	Mammalian_phenotype	8
MP:0002590	MP:0002590	increased mean corpuscular volume	Mammalian_phenotype	8
MP:0002591	MP:0002591	decreased mean corpuscular volume	Mammalian_phenotype	8
MP:0002608	MP:0002608	increased hematocrit	Mammalian_phenotype	8
MP:0002637	MP:0002637	small uterus	Mammalian_phenotype	8
MP:0002639	MP:0002639	micrognathia	Mammalian_phenotype	8
MP:0002665	MP:0002665	decreased circulating corticosterone level	Mammalian_phenotype	8
MP:0002666	MP:0002666	increased circulating aldosterone level	Mammalian_phenotype	8
MP:0002667	MP:0002667	decreased circulating aldosterone level	Mammalian_phenotype	8
MP:0002680	MP:0002680	decreased corpora lutea number	Mammalian_phenotype	8
MP:0002681	MP:0002681	increased corpora lutea number	Mammalian_phenotype	8
MP:0002689	MP:0002689	abnormal molar morphology	Mammalian_phenotype	8
MP:0002732	MP:0002732	increased trichoepithelioma incidence	Mammalian_phenotype	8
MP:0002741	MP:0002741	small olfactory bulb	Mammalian_phenotype	8
MP:0002757	MP:0002757	decreased vertical activity	Mammalian_phenotype	8
MP:0002771	MP:0002771	absent prostate gland anterior lobe	Mammalian_phenotype	8
MP:0002774	MP:0002774	small prostate gland	Mammalian_phenotype	8
MP:0002786	MP:0002786	abnormal Leydig cell morphology	Mammalian_phenotype	8
MP:0002810	MP:0002810	microcytic anemia	Mammalian_phenotype	8
MP:0002811	MP:0002811	macrocytic anemia	Mammalian_phenotype	8
MP:0002819	MP:0002819	abnormal pulp cavity morphology	Mammalian_phenotype	8
MP:0002863	MP:0002863	improved righting response	Mammalian_phenotype	8
MP:0002957	MP:0002957	increased intestinal adenocarcinoma incidence	Mammalian_phenotype	8
MP:0002978	MP:0002978	absent otoliths	Mammalian_phenotype	8
MP:0002997	MP:0002997	enlarged seminal vesicle	Mammalian_phenotype	8
MP:0003080	MP:0003080	increased natural killer cell mediated cytotoxicity	Mammalian_phenotype	8
MP:0003110	MP:0003110	absent malleus processus brevis	Mammalian_phenotype	8
MP:0003143	MP:0003143	enlarged otoliths	Mammalian_phenotype	8
MP:0003144	MP:0003144	decreased otolith number	Mammalian_phenotype	8
MP:0003150	MP:0003150	detached tectorial membrane	Mammalian_phenotype	8
MP:0003151	MP:0003151	absent tunnel of Corti	Mammalian_phenotype	8
MP:0003154	MP:0003154	abnormal soft palate morphology	Mammalian_phenotype	8
MP:0003235	MP:0003235	abnormal alisphenoid bone morphology	Mammalian_phenotype	8
MP:0003241	MP:0003241	loss of cortex neurons	Mammalian_phenotype	8
MP:0003287	MP:0003287	increased intestinal hemangioma incidence	Mammalian_phenotype	8
MP:0003331	MP:0003331	increased hepatocellular carcinoma incidence	Mammalian_phenotype	8
MP:0003405	MP:0003405	abnormal platelet shape	Mammalian_phenotype	8
MP:0003451	MP:0003451	absent olfactory bulb	Mammalian_phenotype	8
MP:0003516	MP:0003516	absent labia majora	Mammalian_phenotype	8
MP:0003517	MP:0003517	enlarged labia majora	Mammalian_phenotype	8
MP:0003518	MP:0003518	small labia majora	Mammalian_phenotype	8
MP:0003519	MP:0003519	splayed labia majora	Mammalian_phenotype	8
MP:0003521	MP:0003521	absent labia minora	Mammalian_phenotype	8
MP:0003522	MP:0003522	enlarged labia minora	Mammalian_phenotype	8
MP:0003523	MP:0003523	small labia minora	Mammalian_phenotype	8
MP:0003524	MP:0003524	splayed labia minora	Mammalian_phenotype	8
MP:0003529	MP:0003529	enlarged clitoris	Mammalian_phenotype	8
MP:0003530	MP:0003530	small clitoris	Mammalian_phenotype	8
MP:0003538	MP:0003538	abnormal hymen development	Mammalian_phenotype	8
MP:0003570	MP:0003570	increased uterus leiomyoma incidence	Mammalian_phenotype	8
MP:0003579	MP:0003579	increased ovarian carcinoma incidence	Mammalian_phenotype	8
MP:0003603	MP:0003603	increased renal hemangioblastoma incidence	Mammalian_phenotype	8
MP:0003610	MP:0003610	scrotum hyperplasia	Mammalian_phenotype	8
MP:0003611	MP:0003611	scrotum hypoplasia	Mammalian_phenotype	8
MP:0003618	MP:0003618	uterine cervical atresia	Mammalian_phenotype	8
MP:0003637	MP:0003637	cochlear ganglion hypoplasia	Mammalian_phenotype	8
MP:0003697	MP:0003697	absent zona pellucida	Mammalian_phenotype	8
MP:0003728	MP:0003728	abnormal retinal photoreceptor layer morphology	Mammalian_phenotype	8
MP:0003731	MP:0003731	abnormal retinal outer nuclear layer morphology	Mammalian_phenotype	8
MP:0003732	MP:0003732	abnormal retinal outer plexiform layer morphology	Mammalian_phenotype	8
MP:0003733	MP:0003733	abnormal retinal inner nuclear layer morphology	Mammalian_phenotype	8
MP:0003734	MP:0003734	abnormal retinal inner plexiform layer morphology	Mammalian_phenotype	8
MP:0003747	MP:0003747	mouth mucosal ulceration	Mammalian_phenotype	8
MP:0003748	MP:0003748	increased oral mucosa hemangioma incidence	Mammalian_phenotype	8
MP:0003751	MP:0003751	oral leukoplakia	Mammalian_phenotype	8
MP:0003756	MP:0003756	abnormal hard palate morphology	Mammalian_phenotype	8
MP:0003757	MP:0003757	high palate	Mammalian_phenotype	8
MP:0003758	MP:0003758	narrow palate	Mammalian_phenotype	8
MP:0003759	MP:0003759	broad palate	Mammalian_phenotype	8
MP:0003760	MP:0003760	short palate	Mammalian_phenotype	8
MP:0003761	MP:0003761	arched palate	Mammalian_phenotype	8
MP:0003764	MP:0003764	abnormal palatal depth	Mammalian_phenotype	8
MP:0003780	MP:0003780	increased lip tumor incidence	Mammalian_phenotype	8
MP:0003783	MP:0003783	tented upper lip	Mammalian_phenotype	8
MP:0003817	MP:0003817	abnormal pituitary diverticulum morphology	Mammalian_phenotype	8
MP:0003884	MP:0003884	decreased macrophage cell number	Mammalian_phenotype	8
MP:0003930	MP:0003930	abnormal tooth hard tissue morphology	Mammalian_phenotype	8
MP:0012090	MP:0012090	midbrain hypoplasia	Mammalian_phenotype	8
MP:0012095	MP:0012095	increased Reichert's membrane thickness	Mammalian_phenotype	8
MP:0012096	MP:0012096	decreased Reichert's membrane thickness	Mammalian_phenotype	8
MP:0012098	MP:0012098	increased spongiotrophoblast size	Mammalian_phenotype	8
MP:0012099	MP:0012099	decreased spongiotrophoblast size	Mammalian_phenotype	8
MP:0012108	MP:0012108	increased trophoblast glycogen cell number	Mammalian_phenotype	8
MP:0012109	MP:0012109	decreased trophoblast glycogen cell number	Mammalian_phenotype	8
MP:0012179	MP:0012179	abnormal splanchnic mesoderm morphology	Mammalian_phenotype	8
MP:0012180	MP:0012180	abnormal somatic mesoderm morphology	Mammalian_phenotype	8
MP:0012182	MP:0012182	abnormal presomitic mesoderm morphology	Mammalian_phenotype	8
MP:0012183	MP:0012183	decreased paraxial mesoderm size	Mammalian_phenotype	8
MP:0012184	MP:0012184	absent paraxial mesoderm	Mammalian_phenotype	8
MP:0012188	MP:0012188	increased regulatory T cell apoptosis	Mammalian_phenotype	8
MP:0012189	MP:0012189	decreased regulatory T cell apoptosis	Mammalian_phenotype	8
MP:0012216	MP:0012216	decreased plasmalogen level	Mammalian_phenotype	8
MP:0012217	MP:0012217	increased plasmalogen level	Mammalian_phenotype	8
MP:0012256	MP:0012256	abnormal philtrum morphology	Mammalian_phenotype	8
MP:0012268	MP:0012268	absent red nucleus	Mammalian_phenotype	8
MP:0012271	MP:0012271	abnormal chordamesoderm morphology	Mammalian_phenotype	8
MP:0012272	MP:0012272	decreased axial mesoderm size	Mammalian_phenotype	8
MP:0012274	MP:0012274	increased axial mesoderm size	Mammalian_phenotype	8
MP:0012275	MP:0012275	abnormal prechordal mesoderm morphology	Mammalian_phenotype	8
MP:0012281	MP:0012281	decreased sternebra size	Mammalian_phenotype	8
MP:0012283	MP:0012283	decreased sternebra number	Mammalian_phenotype	8
MP:0012284	MP:0012284	increased sternebra number	Mammalian_phenotype	8
MP:0012298	MP:0012298	hypoactivity in response to feed restriction	Mammalian_phenotype	8
MP:0012302	MP:0012302	umbilical artery stenosis	Mammalian_phenotype	8
MP:0012303	MP:0012303	umbilical vein stenosis	Mammalian_phenotype	8
MP:0012309	MP:0012309	abnormal ductus caroticus morphology	Mammalian_phenotype	8
MP:0012339	MP:0012339	hyperkalemia	Mammalian_phenotype	8
MP:0012364	MP:0012364	decreased erythrocyte sodium level	Mammalian_phenotype	8
MP:0012365	MP:0012365	increased erythrocyte sodium level	Mammalian_phenotype	8
MP:0012367	MP:0012367	decreased erythrocyte magnesium level	Mammalian_phenotype	8
MP:0012368	MP:0012368	increased erythrocyte magnesium level	Mammalian_phenotype	8
MP:0012370	MP:0012370	decreased erythrocyte potassium level	Mammalian_phenotype	8
MP:0012371	MP:0012371	increased erythrocyte potassium level	Mammalian_phenotype	8
MP:0012373	MP:0012373	abnormal erythrocyte magnesium ion content	Mammalian_phenotype	8
MP:0012376	MP:0012376	abnormal erythrocyte potassium ion content	Mammalian_phenotype	8
MP:0012379	MP:0012379	abnormal erythrocyte sodium ion content	Mammalian_phenotype	8
MP:0012398	MP:0012398	decreased nucleated erythrocyte cell number	Mammalian_phenotype	8
MP:0012408	MP:0012408	increased duodenum glandular epithelium tumor incidence	Mammalian_phenotype	8
MP:0012410	MP:0012410	increased pancreatic gastrinoma incidence	Mammalian_phenotype	8
MP:0012428	MP:0012428	decreased granulosa cell tumor incidence	Mammalian_phenotype	8
MP:0012436	MP:0012436	increased colon tumor incidence	Mammalian_phenotype	8
MP:0012443	MP:0012443	increased corpus callosum size	Mammalian_phenotype	8
MP:0012448	MP:0012448	abnormal primary motor cortex morphology	Mammalian_phenotype	8
MP:0012481	MP:0012481	increased habenula size	Mammalian_phenotype	8
MP:0012482	MP:0012482	decreased habenula size	Mammalian_phenotype	8
MP:0012485	MP:0012485	increased cochlear VIII nucleus size	Mammalian_phenotype	8
MP:0012486	MP:0012486	decreased cochlear VIII nucleus size	Mammalian_phenotype	8
MP:0012492	MP:0012492	branchial arch artery hypoplasia	Mammalian_phenotype	8
MP:0012493	MP:0012493	absent branchial arch arteries	Mammalian_phenotype	8
MP:0012494	MP:0012494	dilated branchial arch arteries	Mammalian_phenotype	8
MP:0012495	MP:0012495	branchial arch artery stenosis	Mammalian_phenotype	8
MP:0012529	MP:0012529	abnormal decidua basalis morphology	Mammalian_phenotype	8
MP:0012530	MP:0012530	abnormal decidua capsularis morphology	Mammalian_phenotype	8
MP:0012547	MP:0012547	spina bifida cystica	Mammalian_phenotype	8
MP:0012566	MP:0012566	decreased susceptibility to experimental autoimmune orchitis	Mammalian_phenotype	8
MP:0012567	MP:0012567	increased susceptibility to experimental autoimmune orchitis	Mammalian_phenotype	8
MP:0012568	MP:0012568	decreased mammary gland tumor incidence in breeding females	Mammalian_phenotype	8
MP:0012569	MP:0012569	decreased mammary gland tumor incidence in virgin females	Mammalian_phenotype	8
MP:0012570	MP:0012570	increased mammary gland tumor incidence in breeding females	Mammalian_phenotype	8
MP:0012571	MP:0012571	increased mammary gland tumor incidence in virgin females	Mammalian_phenotype	8
MP:0012673	MP:0012673	aberrant crypt foci	Mammalian_phenotype	8
MP:0012690	MP:0012690	abnormal stride length	Mammalian_phenotype	8
MP:0012726	MP:0012726	abnormal uterine spiral artery morphology	Mammalian_phenotype	8
MP:0012727	MP:0012727	abnormal uterine spiral artery remodeling	Mammalian_phenotype	8
MP:0012748	MP:0012748	increased cardiac neural crest cell number	Mammalian_phenotype	8
MP:0012749	MP:0012749	decreased cardiac neural crest cell number	Mammalian_phenotype	8
MP:0012751	MP:0012751	impaired cardiac neural crest cell differentiation	Mammalian_phenotype	8
MP:0012755	MP:0012755	decreased cranial neural crest cell number	Mammalian_phenotype	8
MP:0012756	MP:0012756	impaired cranial neural crest cell differentiation	Mammalian_phenotype	8
MP:0012785	MP:0012785	decreased rhombomere 1 size	Mammalian_phenotype	8
MP:0012786	MP:0012786	increased rhombomere 1 size	Mammalian_phenotype	8
MP:0012787	MP:0012787	absent rhombomere 1	Mammalian_phenotype	8
MP:0012789	MP:0012789	decreased rhombomere 2 size	Mammalian_phenotype	8
MP:0012790	MP:0012790	increased rhombomere 2 size	Mammalian_phenotype	8
MP:0012791	MP:0012791	absent rhombomere 2	Mammalian_phenotype	8
MP:0012793	MP:0012793	decreased rhombomere 3 size	Mammalian_phenotype	8
MP:0012794	MP:0012794	increased rhombomere 3 size	Mammalian_phenotype	8
MP:0012795	MP:0012795	absent rhombomere 3	Mammalian_phenotype	8
MP:0012797	MP:0012797	decreased rhombomere 4 size	Mammalian_phenotype	8
MP:0012798	MP:0012798	increased rhombomere 4 size	Mammalian_phenotype	8
MP:0012799	MP:0012799	absent rhombomere 4	Mammalian_phenotype	8
MP:0012801	MP:0012801	decreased rhombomere 5 size	Mammalian_phenotype	8
MP:0012802	MP:0012802	increased rhombomere 5 size	Mammalian_phenotype	8
MP:0012803	MP:0012803	absent rhombomere 5	Mammalian_phenotype	8
MP:0012805	MP:0012805	decreased rhombomere 6 size	Mammalian_phenotype	8
MP:0012806	MP:0012806	increased rhombomere 6 size	Mammalian_phenotype	8
MP:0012807	MP:0012807	absent rhombomere 6	Mammalian_phenotype	8
MP:0012809	MP:0012809	decreased rhombomere 7 size	Mammalian_phenotype	8
MP:0012810	MP:0012810	increased rhombomere 7 size	Mammalian_phenotype	8
MP:0012811	MP:0012811	absent rhombomere 7	Mammalian_phenotype	8
MP:0012813	MP:0012813	decreased rhombomere 8 size	Mammalian_phenotype	8
MP:0012814	MP:0012814	increased rhombomere 8 size	Mammalian_phenotype	8
MP:0012815	MP:0012815	absent rhombomere 8	Mammalian_phenotype	8
MP:0013002	MP:0013002	decreased enteric neural crest cell number	Mammalian_phenotype	8
MP:0013011	MP:0013011	absent vagal neural crest cells	Mammalian_phenotype	8
MP:0013129	MP:0013129	abnormal tooth color	Mammalian_phenotype	8
MP:0013132	MP:0013132	pale gums	Mammalian_phenotype	8
MP:0020007	MP:0020007	decreased brain sulfatide level	Mammalian_phenotype	8
MP:0020008	MP:0020008	increased brain sulfatide level	Mammalian_phenotype	8
MP:0020125	MP:0020125	increased circulating HDL phospholipid level	Mammalian_phenotype	8
MP:0020126	MP:0020126	decreased circulating HDL phospholipid level	Mammalian_phenotype	8
MP:0020128	MP:0020128	increased circulating non-HDL phospholipid level	Mammalian_phenotype	8
MP:0020129	MP:0020129	decreased circulating non-HDL phospholipid level	Mammalian_phenotype	8
MP:0020151	MP:0020151	abnormal circulating non-HDL cholesterol level	Mammalian_phenotype	8
MP:0020171	MP:0020171	abnormal IgA level	Mammalian_phenotype	8
MP:0020172	MP:0020172	abnormal IgD level	Mammalian_phenotype	8
MP:0020173	MP:0020173	abnormal IgE level	Mammalian_phenotype	8
MP:0020174	MP:0020174	abnormal IgG level	Mammalian_phenotype	8
MP:0020180	MP:0020180	abnormal IgM level	Mammalian_phenotype	8
MP:0003975	MP:0003975	increased circulating VLDL triglyceride level	Mammalian_phenotype	8
MP:0003976	MP:0003976	decreased circulating VLDL triglyceride level	Mammalian_phenotype	8
MP:0004004	MP:0004004	patent ductus venosus	Mammalian_phenotype	8
MP:0004033	MP:0004033	supernumerary teeth	Mammalian_phenotype	8
MP:0004049	MP:0004049	increased acute promyelocytic leukemia incidence	Mammalian_phenotype	8
MP:0004060	MP:0004060	absent papillary muscle	Mammalian_phenotype	8
MP:0004061	MP:0004061	papillary muscle hypoplasia	Mammalian_phenotype	8
MP:0004068	MP:0004068	dilated dorsal aorta	Mammalian_phenotype	8
MP:0004069	MP:0004069	abnormal muscle spindle morphology	Mammalian_phenotype	8
MP:0004078	MP:0004078	abnormal caudate nucleus morphology	Mammalian_phenotype	8
MP:0004079	MP:0004079	abnormal putamen morphology	Mammalian_phenotype	8
MP:0004109	MP:0004109	abnormal Sertoli cell development	Mammalian_phenotype	8
MP:0004113	MP:0004113	abnormal aortic arch morphology	Mammalian_phenotype	8
MP:0004119	MP:0004119	hypokalemia	Mammalian_phenotype	8
MP:0004132	MP:0004132	absent embryonic cilia	Mammalian_phenotype	8
MP:0004157	MP:0004157	interrupted aortic arch	Mammalian_phenotype	8
MP:0004189	MP:0004189	abnormal alveolar process morphology	Mammalian_phenotype	8
MP:0004205	MP:0004205	absent hyoid bone	Mammalian_phenotype	8
MP:0004207	MP:0004207	increased squamous cell carcinoma incidence	Mammalian_phenotype	8
MP:0004208	MP:0004208	increased basal cell carcinoma incidence	Mammalian_phenotype	8
MP:0004223	MP:0004223	hypoplastic trabecular meshwork	Mammalian_phenotype	8
MP:0004224	MP:0004224	absent trabecular meshwork	Mammalian_phenotype	8
MP:0004226	MP:0004226	absent Schlemm's canal	Mammalian_phenotype	8
MP:0004282	MP:0004282	retrognathia	Mammalian_phenotype	8
MP:0004292	MP:0004292	abnormal spiral ligament fibrocyte morphology	Mammalian_phenotype	8
MP:0004300	MP:0004300	abnormal organ of Corti supporting cell morphology	Mammalian_phenotype	8
MP:0004315	MP:0004315	absent vestibular saccule	Mammalian_phenotype	8
MP:0004316	MP:0004316	enlarged vestibular saccule	Mammalian_phenotype	8
MP:0004317	MP:0004317	small vestibular saccule	Mammalian_phenotype	8
MP:0004329	MP:0004329	vestibular saccular degeneration	Mammalian_phenotype	8
MP:0004330	MP:0004330	abnormal vestibular saccular macula morphology	Mammalian_phenotype	8
MP:0004332	MP:0004332	utricular degeneration	Mammalian_phenotype	8
MP:0004333	MP:0004333	abnormal utricular macula morphology	Mammalian_phenotype	8
MP:0004335	MP:0004335	enlarged utricle	Mammalian_phenotype	8
MP:0004336	MP:0004336	small utricle	Mammalian_phenotype	8
MP:0004354	MP:0004354	absent deltoid tuberosity	Mammalian_phenotype	8
MP:0004364	MP:0004364	thin stria vascularis	Mammalian_phenotype	8
MP:0004365	MP:0004365	abnormal strial basal cell morphology	Mammalian_phenotype	8
MP:0004366	MP:0004366	abnormal strial marginal cell morphology	Mammalian_phenotype	8
MP:0004369	MP:0004369	absent utricle	Mammalian_phenotype	8
MP:0004375	MP:0004375	enlarged frontal bone	Mammalian_phenotype	8
MP:0004376	MP:0004376	absent frontal bone	Mammalian_phenotype	8
MP:0004377	MP:0004377	small frontal bone	Mammalian_phenotype	8
MP:0004378	MP:0004378	frontal bone foramen	Mammalian_phenotype	8
MP:0004379	MP:0004379	wide frontal bone	Mammalian_phenotype	8
MP:0004380	MP:0004380	short frontal bone	Mammalian_phenotype	8
MP:0004383	MP:0004383	absent interparietal bone	Mammalian_phenotype	8
MP:0004384	MP:0004384	small interparietal bone	Mammalian_phenotype	8
MP:0004386	MP:0004386	enlarged interparietal bone	Mammalian_phenotype	8
MP:0004409	MP:0004409	abnormal crista ampullaris neuroepithelium morphology	Mammalian_phenotype	8
MP:0004418	MP:0004418	small parietal bone	Mammalian_phenotype	8
MP:0004419	MP:0004419	absent parietal bone	Mammalian_phenotype	8
MP:0004421	MP:0004421	enlarged parietal bone	Mammalian_phenotype	8
MP:0004422	MP:0004422	small temporal bone	Mammalian_phenotype	8
MP:0004423	MP:0004423	abnormal squamosal bone morphology	Mammalian_phenotype	8
MP:0004435	MP:0004435	abnormal cochlear outer hair cell electromotility	Mammalian_phenotype	8
MP:0004440	MP:0004440	absent occipital bone	Mammalian_phenotype	8
MP:0004441	MP:0004441	small occipital bone	Mammalian_phenotype	8
MP:0004442	MP:0004442	occipital bone foramen	Mammalian_phenotype	8
MP:0004448	MP:0004448	abnormal presphenoid bone morphology	Mammalian_phenotype	8
MP:0004452	MP:0004452	abnormal pterygoid process morphology	Mammalian_phenotype	8
MP:0004467	MP:0004467	absent zygomatic bone	Mammalian_phenotype	8
MP:0004468	MP:0004468	small zygomatic bone	Mammalian_phenotype	8
MP:0004470	MP:0004470	small nasal bone	Mammalian_phenotype	8
MP:0004472	MP:0004472	broad nasal bone	Mammalian_phenotype	8
MP:0004473	MP:0004473	absent nasal bone	Mammalian_phenotype	8
MP:0004474	MP:0004474	enlarged nasal bone	Mammalian_phenotype	8
MP:0004475	MP:0004475	palatine bone hypoplasia	Mammalian_phenotype	8
MP:0004476	MP:0004476	absent palatine bone	Mammalian_phenotype	8
MP:0004477	MP:0004477	turbinate hypoplasia	Mammalian_phenotype	8
MP:0004537	MP:0004537	abnormal palatine shelf morphology	Mammalian_phenotype	8
MP:0004591	MP:0004591	enlarged tectorial membrane	Mammalian_phenotype	8
MP:0004606	MP:0004606	absent vertebral spinous process	Mammalian_phenotype	8
MP:0004607	MP:0004607	abnormal cervical atlas morphology	Mammalian_phenotype	8
MP:0004608	MP:0004608	abnormal cervical axis morphology	Mammalian_phenotype	8
MP:0004631	MP:0004631	abnormal auditory cortex morphology	Mammalian_phenotype	8
MP:0004646	MP:0004646	decreased cervical vertebrae number	Mammalian_phenotype	8
MP:0004647	MP:0004647	decreased lumbar vertebrae number	Mammalian_phenotype	8
MP:0004648	MP:0004648	decreased thoracic vertebrae number	Mammalian_phenotype	8
MP:0004650	MP:0004650	increased lumbar vertebrae number	Mammalian_phenotype	8
MP:0004651	MP:0004651	increased thoracic vertebrae number	Mammalian_phenotype	8
MP:0004654	MP:0004654	absent lumbar vertebrae	Mammalian_phenotype	8
MP:0004655	MP:0004655	absent thoracic vertebrae	Mammalian_phenotype	8
MP:0004666	MP:0004666	absent stapedial artery	Mammalian_phenotype	8
MP:0004667	MP:0004667	vertebral body hypoplasia	Mammalian_phenotype	8
MP:0004706	MP:0004706	short vertebral body	Mammalian_phenotype	8
MP:0004707	MP:0004707	enlarged lumbar vertebrae	Mammalian_phenotype	8
MP:0004708	MP:0004708	short lumbar vertebrae	Mammalian_phenotype	8
MP:0004709	MP:0004709	cervical vertebrae degeneration	Mammalian_phenotype	8
MP:0004721	MP:0004721	abnormal platelet dense granule morphology	Mammalian_phenotype	8
MP:0004729	MP:0004729	absent efferent ductules of testis	Mammalian_phenotype	8
MP:0004762	MP:0004762	increased anti-double stranded DNA antibody level	Mammalian_phenotype	8
MP:0004771	MP:0004771	increased anti-single stranded DNA antibody level	Mammalian_phenotype	8
MP:0004784	MP:0004784	abnormal anterior cardinal vein morphology	Mammalian_phenotype	8
MP:0004785	MP:0004785	abnormal posterior cardinal vein morphology	Mammalian_phenotype	8
MP:0004786	MP:0004786	abnormal common cardinal vein morphology	Mammalian_phenotype	8
MP:0004796	MP:0004796	increased anti-histone antibody level	Mammalian_phenotype	8
MP:0004798	MP:0004798	decreased anti-double stranded DNA antibody level	Mammalian_phenotype	8
MP:0004799	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis	Mammalian_phenotype	8
MP:0004800	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis	Mammalian_phenotype	8
MP:0004801	MP:0004801	increased susceptibility to systemic lupus erythematosus	Mammalian_phenotype	8
MP:0004802	MP:0004802	decreased susceptibility to systemic lupus erythematosus	Mammalian_phenotype	8
MP:0004803	MP:0004803	increased susceptibility to autoimmune diabetes	Mammalian_phenotype	8
MP:0004804	MP:0004804	decreased susceptibility to autoimmune diabetes	Mammalian_phenotype	8
MP:0004805	MP:0004805	absent oocytes	Mammalian_phenotype	8
MP:0004821	MP:0004821	increased susceptibility to experimental autoimmune uveoretinitis	Mammalian_phenotype	8
MP:0004822	MP:0004822	decreased susceptibility to experimental autoimmune uveoretinitis	Mammalian_phenotype	8
MP:0004823	MP:0004823	increased susceptibility to experimental autoimmune myasthenia gravis	Mammalian_phenotype	8
MP:0004824	MP:0004824	decreased susceptibility to experimental autoimmune myasthenia gravis	Mammalian_phenotype	8
MP:0004825	MP:0004825	increased susceptibility to experimental autoimmune thyroiditis	Mammalian_phenotype	8
MP:0004826	MP:0004826	decreased susceptibility to experimental autoimmune thyroiditis	Mammalian_phenotype	8
MP:0004827	MP:0004827	increased susceptibility to autoimmune hemolytic anemia	Mammalian_phenotype	8
MP:0004828	MP:0004828	decreased susceptibility to autoimmune hemolytic anemia	Mammalian_phenotype	8
MP:0004829	MP:0004829	increased anti-chromatin antibody level	Mammalian_phenotype	8
MP:0004832	MP:0004832	enlarged ovary	Mammalian_phenotype	8
MP:0004843	MP:0004843	abnormal Paneth cell morphology	Mammalian_phenotype	8
MP:0004850	MP:0004850	abnormal testis weight	Mammalian_phenotype	8
MP:0004854	MP:0004854	abnormal ovary weight	Mammalian_phenotype	8
MP:0004863	MP:0004863	thin spiral ligament	Mammalian_phenotype	8
MP:0004868	MP:0004868	increased endometrial carcinoma incidence	Mammalian_phenotype	8
MP:0004873	MP:0004873	absent turbinates	Mammalian_phenotype	8
MP:0004900	MP:0004900	absent zygomatic arch	Mammalian_phenotype	8
MP:0004903	MP:0004903	abnormal uterus weight	Mammalian_phenotype	8
MP:0004906	MP:0004906	enlarged uterus	Mammalian_phenotype	8
MP:0004908	MP:0004908	abnormal seminal vesicle weight	Mammalian_phenotype	8
MP:0004927	MP:0004927	abnormal epididymis weight	Mammalian_phenotype	8
MP:0004930	MP:0004930	small epididymis	Mammalian_phenotype	8
MP:0004931	MP:0004931	enlarged epididymis	Mammalian_phenotype	8
MP:0004934	MP:0004934	epididymis epithelium degeneration	Mammalian_phenotype	8
MP:0004939	MP:0004939	abnormal B cell morphology	Mammalian_phenotype	8
MP:0004958	MP:0004958	enlarged prostate gland	Mammalian_phenotype	8
MP:0004960	MP:0004960	abnormal prostate gland weight	Mammalian_phenotype	8
MP:0005013	MP:0005013	increased lymphocyte cell number	Mammalian_phenotype	8
MP:0005016	MP:0005016	decreased lymphocyte cell number	Mammalian_phenotype	8
MP:0005065	MP:0005065	abnormal neutrophil morphology	Mammalian_phenotype	8
MP:0005068	MP:0005068	abnormal NK cell morphology	Mammalian_phenotype	8
MP:0005070	MP:0005070	impaired natural killer cell mediated cytotoxicity	Mammalian_phenotype	8
MP:0005071	MP:0005071	enlarged hair follicle melanin granules	Mammalian_phenotype	8
MP:0005078	MP:0005078	abnormal cytotoxic T cell physiology	Mammalian_phenotype	8
MP:0005103	MP:0005103	abnormal retinal pigmentation	Mammalian_phenotype	8
MP:0005170	MP:0005170	cleft lip	Mammalian_phenotype	8
MP:0005178	MP:0005178	increased circulating cholesterol level	Mammalian_phenotype	8
MP:0005179	MP:0005179	decreased circulating cholesterol level	Mammalian_phenotype	8
MP:0005237	MP:0005237	abnormal olfactory tract morphology	Mammalian_phenotype	8
MP:0005241	MP:0005241	abnormal retinal ganglion layer morphology	Mammalian_phenotype	8
MP:0005264	MP:0005264	glomerulosclerosis	Mammalian_phenotype	8
MP:0005297	MP:0005297	spina bifida occulta	Mammalian_phenotype	8
MP:0005305	MP:0005305	prostate gland anterior lobe hyperplasia	Mammalian_phenotype	8
MP:0005326	MP:0005326	abnormal podocyte morphology	Mammalian_phenotype	8
MP:0005327	MP:0005327	abnormal mesangial cell morphology	Mammalian_phenotype	8
MP:0005339	MP:0005339	increased susceptibility to atherosclerosis	Mammalian_phenotype	8
MP:0005341	MP:0005341	decreased susceptibility to atherosclerosis	Mammalian_phenotype	8
MP:0005358	MP:0005358	abnormal incisor morphology	Mammalian_phenotype	8
MP:0005361	MP:0005361	small pituitary gland	Mammalian_phenotype	8
MP:0005425	MP:0005425	increased macrophage cell number	Mammalian_phenotype	8
MP:0005426	MP:0005426	tachypnea	Mammalian_phenotype	8
MP:0005465	MP:0005465	abnormal T-helper 1 physiology	Mammalian_phenotype	8
MP:0005466	MP:0005466	abnormal T-helper 2 physiology	Mammalian_phenotype	8
MP:0005481	MP:0005481	increased chronic myelocytic leukemia incidence	Mammalian_phenotype	8
MP:0005490	MP:0005490	increased Clara cell number	Mammalian_phenotype	8
MP:0005491	MP:0005491	pancreatic islet hyperplasia	Mammalian_phenotype	8
MP:0005548	MP:0005548	retinal pigment epithelium atrophy	Mammalian_phenotype	8
MP:0005549	MP:0005549	retinal pigment epithelium hyperplasia	Mammalian_phenotype	8
MP:0005563	MP:0005563	abnormal hemoglobin content	Mammalian_phenotype	8
MP:0005640	MP:0005640	abnormal mean corpuscular hemoglobin concentration	Mammalian_phenotype	8
MP:0006066	MP:0006066	decreased clearance of atrial thrombosis	Mammalian_phenotype	8
MP:0006067	MP:0006067	increased clearance of atrial thrombosis	Mammalian_phenotype	8
MP:0006105	MP:0006105	small tectum	Mammalian_phenotype	8
MP:0006106	MP:0006106	absent tectum	Mammalian_phenotype	8
MP:0006115	MP:0006115	aortic valve atresia	Mammalian_phenotype	8
MP:0006116	MP:0006116	calcified aortic valve	Mammalian_phenotype	8
MP:0006117	MP:0006117	aortic valve stenosis	Mammalian_phenotype	8
MP:0006118	MP:0006118	aortic valve prolapse	Mammalian_phenotype	8
MP:0006128	MP:0006128	pulmonary valve stenosis	Mammalian_phenotype	8
MP:0006129	MP:0006129	pulmonary valve prolapse	Mammalian_phenotype	8
MP:0006130	MP:0006130	pulmonary valve atresia	Mammalian_phenotype	8
MP:0006131	MP:0006131	calcified pulmonary valve	Mammalian_phenotype	8
MP:0006158	MP:0006158	vertical supranuclear palsy	Mammalian_phenotype	8
MP:0006169	MP:0006169	increased eyelid tumor incidence	Mammalian_phenotype	8
MP:0006180	MP:0006180	increased choroid hemangioma incidence	Mammalian_phenotype	8
MP:0006182	MP:0006182	increased retinal hemangioma incidence	Mammalian_phenotype	8
MP:0006184	MP:0006184	increased retinal astrocytoma incidence	Mammalian_phenotype	8
MP:0006211	MP:0006211	small orbits	Mammalian_phenotype	8
MP:0006212	MP:0006212	large orbits	Mammalian_phenotype	8
MP:0006213	MP:0006213	shallow orbits	Mammalian_phenotype	8
MP:0006217	MP:0006217	small optic disc	Mammalian_phenotype	8
MP:0006218	MP:0006218	large optic disc	Mammalian_phenotype	8
MP:0006238	MP:0006238	abnormal choriocapillaris morphology	Mammalian_phenotype	8
MP:0006250	MP:0006250	abnormal line of Schwalbe morphology	Mammalian_phenotype	8
MP:0006252	MP:0006252	lateral rectus palsy	Mammalian_phenotype	8
MP:0006254	MP:0006254	thin cerebral cortex	Mammalian_phenotype	8
MP:0006283	MP:0006283	increased medulloblastoma incidence	Mammalian_phenotype	8
MP:0006303	MP:0006303	abnormal retinal nerve fiber layer morphology	Mammalian_phenotype	8
MP:0006307	MP:0006307	abnormal seminiferous tubule size	Mammalian_phenotype	8
MP:0006310	MP:0006310	increased retinoblastoma incidence	Mammalian_phenotype	8
MP:0006331	MP:0006331	abnormal patterning of the organ of Corti	Mammalian_phenotype	8
MP:0006371	MP:0006371	absent phaeomelanin	Mammalian_phenotype	8
MP:0006405	MP:0006405	abnormal L3 dorsal root ganglion morphology	Mammalian_phenotype	8
MP:0006408	MP:0006408	dorsal root ganglion hypoplasia	Mammalian_phenotype	8
MP:0006417	MP:0006417	rete testis obstruction	Mammalian_phenotype	8
MP:0006418	MP:0006418	abnormal testis cord formation	Mammalian_phenotype	8
MP:0006420	MP:0006420	abnormal peritubular myoid cell morphology	Mammalian_phenotype	8
MP:0006423	MP:0006423	dilated rete testis	Mammalian_phenotype	8
MP:0008023	MP:0008023	abnormal styloid process morphology	Mammalian_phenotype	8
MP:0008037	MP:0008037	abnormal T cell morphology	Mammalian_phenotype	8
MP:0008065	MP:0008065	short endolymphatic duct	Mammalian_phenotype	8
MP:0008120	MP:0008120	abnormal myeloid dendritic cell number	Mammalian_phenotype	8
MP:0008124	MP:0008124	decreased plasmacytoid dendritic cell number	Mammalian_phenotype	8
MP:0008141	MP:0008141	decreased small intestinal microvillus size	Mammalian_phenotype	8
MP:0008222	MP:0008222	decreased hippocampal commissure size	Mammalian_phenotype	8
MP:0008223	MP:0008223	absent hippocampal commissure	Mammalian_phenotype	8
MP:0008224	MP:0008224	increased hippocampal commissure size	Mammalian_phenotype	8
MP:0008226	MP:0008226	decreased anterior commissure size	Mammalian_phenotype	8
MP:0008227	MP:0008227	absent anterior commissure	Mammalian_phenotype	8
MP:0008228	MP:0008228	increased anterior commissure size	Mammalian_phenotype	8
MP:0008252	MP:0008252	abnormal multinucleated phagocyte morphology	Mammalian_phenotype	8
MP:0008257	MP:0008257	thin myometrium	Mammalian_phenotype	8
MP:0008258	MP:0008258	thin endometrium	Mammalian_phenotype	8
MP:0008307	MP:0008307	short scala media	Mammalian_phenotype	8
MP:0008320	MP:0008320	absent adenohypophysis	Mammalian_phenotype	8
MP:0008321	MP:0008321	small adenohypophysis	Mammalian_phenotype	8
MP:0008322	MP:0008322	abnormal somatotroph morphology	Mammalian_phenotype	8
MP:0008323	MP:0008323	abnormal lactotroph morphology	Mammalian_phenotype	8
MP:0008324	MP:0008324	abnormal melanotroph morphology	Mammalian_phenotype	8
MP:0008325	MP:0008325	abnormal gonadotroph morphology	Mammalian_phenotype	8
MP:0008326	MP:0008326	abnormal thyrotroph morphology	Mammalian_phenotype	8
MP:0008327	MP:0008327	abnormal corticotroph morphology	Mammalian_phenotype	8
MP:0008366	MP:0008366	enlarged adenohypophysis	Mammalian_phenotype	8
MP:0008367	MP:0008367	absent pituitary intermediate lobe	Mammalian_phenotype	8
MP:0008368	MP:0008368	small pituitary intermediate lobe	Mammalian_phenotype	8
MP:0008370	MP:0008370	enlarged pituitary intermediate lobe	Mammalian_phenotype	8
MP:0008373	MP:0008373	short malleus	Mammalian_phenotype	8
MP:0008376	MP:0008376	small malleus manubrium	Mammalian_phenotype	8
MP:0008377	MP:0008377	absent malleus manubrium	Mammalian_phenotype	8
MP:0008378	MP:0008378	small malleus processus brevis	Mammalian_phenotype	8
MP:0008379	MP:0008379	absent malleus head	Mammalian_phenotype	8
MP:0008387	MP:0008387	hypochromic anemia	Mammalian_phenotype	8
MP:0008441	MP:0008441	thin cortical plate	Mammalian_phenotype	8
MP:0008442	MP:0008442	disorganized cortical plate	Mammalian_phenotype	8
MP:0008443	MP:0008443	absent subplate	Mammalian_phenotype	8
MP:0008467	MP:0008467	absent proprioceptive neurons	Mammalian_phenotype	8
MP:0008491	MP:0008491	dorsal root ganglion hyperplasia	Mammalian_phenotype	8
MP:0008522	MP:0008522	abnormal lymph node germinal center morphology	Mammalian_phenotype	8
MP:0008524	MP:0008524	increased plasmacytoid dendritic cell number	Mammalian_phenotype	8
MP:0008537	MP:0008537	increased susceptibility to induced colitis	Mammalian_phenotype	8
MP:0008539	MP:0008539	decreased susceptibility to induced colitis	Mammalian_phenotype	8
MP:0008545	MP:0008545	absent sperm flagellum	Mammalian_phenotype	8
MP:0008547	MP:0008547	abnormal neocortex morphology	Mammalian_phenotype	8
MP:0008549	MP:0008549	abnormal circulating interferon-alpha level	Mammalian_phenotype	8
MP:0008550	MP:0008550	abnormal circulating interferon-beta level	Mammalian_phenotype	8
MP:0008551	MP:0008551	abnormal circulating interferon-gamma level	Mammalian_phenotype	8
MP:0008553	MP:0008553	increased circulating tumor necrosis factor level	Mammalian_phenotype	8
MP:0008554	MP:0008554	decreased circulating tumor necrosis factor level	Mammalian_phenotype	8
MP:0008589	MP:0008589	abnormal circulating interleukin-1 level	Mammalian_phenotype	8
MP:0008590	MP:0008590	abnormal circulating interleukin-10 level	Mammalian_phenotype	8
MP:0008595	MP:0008595	abnormal circulating interleukin-6 level	Mammalian_phenotype	8
MP:0008598	MP:0008598	abnormal circulating interleukin-2 level	Mammalian_phenotype	8
MP:0008601	MP:0008601	abnormal circulating interleukin-4 level	Mammalian_phenotype	8
MP:0008604	MP:0008604	abnormal circulating interleukin-7 level	Mammalian_phenotype	8
MP:0008607	MP:0008607	abnormal circulating interleukin-13 level	Mammalian_phenotype	8
MP:0008610	MP:0008610	abnormal circulating interleukin-15 level	Mammalian_phenotype	8
MP:0008613	MP:0008613	abnormal circulating interleukin-17 level	Mammalian_phenotype	8
MP:0008616	MP:0008616	abnormal circulating interleukin-12 level	Mammalian_phenotype	8
MP:0008619	MP:0008619	abnormal circulating interleukin-23 level	Mammalian_phenotype	8
MP:0008622	MP:0008622	abnormal circulating interleukin-3 level	Mammalian_phenotype	8
MP:0008625	MP:0008625	abnormal circulating interleukin-5 level	Mammalian_phenotype	8
MP:0008628	MP:0008628	abnormal circulating interleukin-9 level	Mammalian_phenotype	8
MP:0008631	MP:0008631	abnormal circulating interleukin-16 level	Mammalian_phenotype	8
MP:0008634	MP:0008634	abnormal circulating interleukin-18 level	Mammalian_phenotype	8
MP:0008646	MP:0008646	abnormal circulating interleukin-12b level	Mammalian_phenotype	8
MP:0008654	MP:0008654	increased interleukin-1 alpha secretion	Mammalian_phenotype	8
MP:0008655	MP:0008655	decreased interleukin-1 alpha secretion	Mammalian_phenotype	8
MP:0008657	MP:0008657	increased interleukin-1 beta secretion	Mammalian_phenotype	8
MP:0008658	MP:0008658	decreased interleukin-1 beta secretion	Mammalian_phenotype	8
MP:0008666	MP:0008666	increased interleukin-12a secretion	Mammalian_phenotype	8
MP:0008667	MP:0008667	decreased interleukin-12a secretion	Mammalian_phenotype	8
MP:0008693	MP:0008693	increased interleukin-23a secretion	Mammalian_phenotype	8
MP:0008694	MP:0008694	decreased interleukin-23a secretion	Mammalian_phenotype	8
MP:0008714	MP:0008714	increased lung carcinoma incidence	Mammalian_phenotype	8
MP:0008764	MP:0008764	increased mast cell degranulation	Mammalian_phenotype	8
MP:0008765	MP:0008765	decreased mast cell degranulation	Mammalian_phenotype	8
MP:0008780	MP:0008780	increased pancreatic acinar cell carcinoma incidence	Mammalian_phenotype	8
MP:0008790	MP:0008790	abnormal NK cell degranulation	Mammalian_phenotype	8
MP:0008868	MP:0008868	abnormal granulosa cell morphology	Mammalian_phenotype	8
MP:0008871	MP:0008871	abnormal ovarian follicle number	Mammalian_phenotype	8
MP:0008893	MP:0008893	detached sperm flagellum	Mammalian_phenotype	8
MP:0008898	MP:0008898	abnormal acrosome morphology	Mammalian_phenotype	8
MP:0008911	MP:0008911	induced hyperactivity	Mammalian_phenotype	8
MP:0008937	MP:0008937	abnormal pituitary gland weight	Mammalian_phenotype	8
MP:0008971	MP:0008971	abnormal ethmoturbinate morphology	Mammalian_phenotype	8
MP:0008978	MP:0008978	abnormal vagina weight	Mammalian_phenotype	8
MP:0008981	MP:0008981	enlarged vagina	Mammalian_phenotype	8
MP:0008983	MP:0008983	small vagina	Mammalian_phenotype	8
MP:0004158	MP:0004158	right aortic arch	Mammalian_phenotype	9
MP:0004161	MP:0004161	cervical aortic arch	Mammalian_phenotype	9
MP:0004279	MP:0004279	abnormal rostral migratory stream morphology	Mammalian_phenotype	9
MP:0004293	MP:0004293	abnormal type I spiral ligament fibrocytes	Mammalian_phenotype	9
MP:0004294	MP:0004294	abnormal type II spiral ligament fibrocytes	Mammalian_phenotype	9
MP:0004295	MP:0004295	abnormal type III spiral ligament fibrocytes	Mammalian_phenotype	9
MP:0004296	MP:0004296	abnormal type IV spiral ligament fibrocytes	Mammalian_phenotype	9
MP:0004302	MP:0004302	abnormal Deiters cell morphology	Mammalian_phenotype	9
MP:0004303	MP:0004303	abnormal Hensen cell morphology	Mammalian_phenotype	9
MP:0004326	MP:0004326	abnormal vestibular hair cell number	Mammalian_phenotype	9
MP:0004331	MP:0004331	vestibular saccular macula degeneration	Mammalian_phenotype	9
MP:0004334	MP:0004334	utricular macular degeneration	Mammalian_phenotype	9
MP:0004385	MP:0004385	interparietal bone hypoplasia	Mammalian_phenotype	9
MP:0004393	MP:0004393	abnormal cochlear inner hair cell morphology	Mammalian_phenotype	9
MP:0004399	MP:0004399	abnormal cochlear outer hair cell morphology	Mammalian_phenotype	9
MP:0004406	MP:0004406	abnormal cochlear hair cell number	Mammalian_phenotype	9
MP:0004413	MP:0004413	absent cochlear microphonics	Mammalian_phenotype	9
MP:0004414	MP:0004414	decreased cochlear microphonics	Mammalian_phenotype	9
MP:0004420	MP:0004420	parietal bone hypoplasia	Mammalian_phenotype	9
MP:0004424	MP:0004424	temporal bone hypoplasia	Mammalian_phenotype	9
MP:0004428	MP:0004428	abnormal type I vestibular cell	Mammalian_phenotype	9
MP:0004429	MP:0004429	abnormal type II vestibular cells	Mammalian_phenotype	9
MP:0004436	MP:0004436	absent cochlear outer hair cell electromotility	Mammalian_phenotype	9
MP:0004437	MP:0004437	decreased cochlear outer hair cell electromotility	Mammalian_phenotype	9
MP:0004443	MP:0004443	absent supraoccipital bone	Mammalian_phenotype	9
MP:0004444	MP:0004444	small supraoccipital bone	Mammalian_phenotype	9
MP:0004445	MP:0004445	small exoccipital bone	Mammalian_phenotype	9
MP:0004446	MP:0004446	split exoccipital bone	Mammalian_phenotype	9
MP:0004447	MP:0004447	small basioccipital bone	Mammalian_phenotype	9
MP:0004449	MP:0004449	absent presphenoid bone	Mammalian_phenotype	9
MP:0004450	MP:0004450	presphenoid bone hypoplasia	Mammalian_phenotype	9
MP:0004451	MP:0004451	short presphenoid bone	Mammalian_phenotype	9
MP:0004453	MP:0004453	abnormal pterygoid bone morphology	Mammalian_phenotype	9
MP:0004454	MP:0004454	absent pterygoid process	Mammalian_phenotype	9
MP:0004458	MP:0004458	absent alisphenoid bone	Mammalian_phenotype	9
MP:0004459	MP:0004459	small alisphenoid bone	Mammalian_phenotype	9
MP:0004462	MP:0004462	small basisphenoid bone	Mammalian_phenotype	9
MP:0004463	MP:0004463	basisphenoid bone foramen	Mammalian_phenotype	9
MP:0004464	MP:0004464	absent strial basal cell tight junctions	Mammalian_phenotype	9
MP:0004465	MP:0004465	degeneration of organ of Corti supporting cells	Mammalian_phenotype	9
MP:0004471	MP:0004471	short nasal bone	Mammalian_phenotype	9
MP:0004496	MP:0004496	abnormal organ of Corti supporting cell number	Mammalian_phenotype	9
MP:0004515	MP:0004515	abnormal vestibular hair cell stereociliary bundle morphology	Mammalian_phenotype	9
MP:0004521	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology	Mammalian_phenotype	9
MP:0004538	MP:0004538	abnormal maxillary shelf morphology	Mammalian_phenotype	9
MP:0004539	MP:0004539	absent maxilla	Mammalian_phenotype	9
MP:0004540	MP:0004540	small maxilla	Mammalian_phenotype	9
MP:0004572	MP:0004572	fusion of basioccipital and basisphenoid bone	Mammalian_phenotype	9
MP:0004592	MP:0004592	small mandible	Mammalian_phenotype	9
MP:0004593	MP:0004593	long mandible	Mammalian_phenotype	9
MP:0004596	MP:0004596	abnormal mandibular angle morphology	Mammalian_phenotype	9
MP:0004658	MP:0004658	abnormal ventral tubercle of atlas morphology	Mammalian_phenotype	9
MP:0004659	MP:0004659	abnormal odontoid process morphology	Mammalian_phenotype	9
MP:0004722	MP:0004722	abnormal platelet dense granule number	Mammalian_phenotype	9
MP:0004758	MP:0004758	absent strial marginal cells	Mammalian_phenotype	9
MP:0004788	MP:0004788	abnormal auditory cortex tonotopy	Mammalian_phenotype	9
MP:0004830	MP:0004830	short incisors	Mammalian_phenotype	9
MP:0004831	MP:0004831	long incisors	Mammalian_phenotype	9
MP:0004833	MP:0004833	ovary atrophy	Mammalian_phenotype	9
MP:0004851	MP:0004851	increased testis weight	Mammalian_phenotype	9
MP:0004852	MP:0004852	decreased testis weight	Mammalian_phenotype	9
MP:0004855	MP:0004855	increased ovary weight	Mammalian_phenotype	9
MP:0004856	MP:0004856	decreased ovary weight	Mammalian_phenotype	9
MP:0004869	MP:0004869	frontal bone hypoplasia	Mammalian_phenotype	9
MP:0004894	MP:0004894	uterus atrophy	Mammalian_phenotype	9
MP:0004895	MP:0004895	vagina atrophy	Mammalian_phenotype	9
MP:0004899	MP:0004899	absent squamosal bone	Mammalian_phenotype	9
MP:0004904	MP:0004904	increased uterus weight	Mammalian_phenotype	9
MP:0004905	MP:0004905	decreased uterus weight	Mammalian_phenotype	9
MP:0004909	MP:0004909	increased seminal vesicle weight	Mammalian_phenotype	9
MP:0004910	MP:0004910	decreased seminal vesicle weight	Mammalian_phenotype	9
MP:0004928	MP:0004928	increased epididymis weight	Mammalian_phenotype	9
MP:0004929	MP:0004929	decreased epididymis weight	Mammalian_phenotype	9
MP:0004932	MP:0004932	epididymis hypoplasia	Mammalian_phenotype	9
MP:0004941	MP:0004941	abnormal regulatory T cell morphology	Mammalian_phenotype	9
MP:0004961	MP:0004961	increased prostate gland weight	Mammalian_phenotype	9
MP:0004962	MP:0004962	decreased prostate gland weight	Mammalian_phenotype	9
MP:0005022	MP:0005022	abnormal immature B cell morphology	Mammalian_phenotype	9
MP:0005042	MP:0005042	abnormal level of surface class II molecules	Mammalian_phenotype	9
MP:0005043	MP:0005043	defective assembly of class II molecules	Mammalian_phenotype	9
MP:0005079	MP:0005079	defective cytotoxic T cell cytolysis	Mammalian_phenotype	9
MP:0005145	MP:0005145	increased circulating VLDL cholesterol level	Mammalian_phenotype	9
MP:0005146	MP:0005146	decreased circulating VLDL cholesterol level	Mammalian_phenotype	9
MP:0005147	MP:0005147	prostate gland hypoplasia	Mammalian_phenotype	9
MP:0005148	MP:0005148	seminal vesicle hypoplasia	Mammalian_phenotype	9
MP:0005158	MP:0005158	ovary hypoplasia	Mammalian_phenotype	9
MP:0005250	MP:0005250	Sertoli cell hypoplasia	Mammalian_phenotype	9
MP:0005359	MP:0005359	growth retardation of incisors	Mammalian_phenotype	9
MP:0005536	MP:0005536	Leydig cell hypoplasia	Mammalian_phenotype	9
MP:0005561	MP:0005561	increased mean corpuscular hemoglobin	Mammalian_phenotype	9
MP:0005562	MP:0005562	decreased mean corpuscular hemoglobin	Mammalian_phenotype	9
MP:0005564	MP:0005564	increased hemoglobin content	Mammalian_phenotype	9
MP:0005641	MP:0005641	increased mean corpuscular hemoglobin concentration	Mammalian_phenotype	9
MP:0005642	MP:0005642	decreased mean corpuscular hemoglobin concentration	Mammalian_phenotype	9
MP:0006010	MP:0006010	absent strial intermediate cells	Mammalian_phenotype	9
MP:0006095	MP:0006095	absent amacrine cells	Mammalian_phenotype	9
MP:0006098	MP:0006098	absent cerebellar lobules	Mammalian_phenotype	9
MP:0006172	MP:0006172	increased eyelid lipodermoid incidence	Mammalian_phenotype	9
MP:0006239	MP:0006239	absent choriocapillaris	Mammalian_phenotype	9
MP:0006256	MP:0006256	abnormal gustatory papillae morphology	Mammalian_phenotype	9
MP:0006300	MP:0006300	abnormal entorhinal cortex morphology	Mammalian_phenotype	9
MP:0006308	MP:0006308	enlarged seminiferous tubules	Mammalian_phenotype	9
MP:0006369	MP:0006369	supernumerary incisors	Mammalian_phenotype	9
MP:0006387	MP:0006387	abnormal T cell number	Mammalian_phenotype	9
MP:0006400	MP:0006400	decreased molar number	Mammalian_phenotype	9
MP:0006401	MP:0006401	absent male preputial gland	Mammalian_phenotype	9
MP:0006402	MP:0006402	small molars	Mammalian_phenotype	9
MP:0006419	MP:0006419	disorganized testis cords	Mammalian_phenotype	9
MP:0006421	MP:0006421	decreased number of peritubular myoid cells	Mammalian_phenotype	9
MP:0006424	MP:0006424	absent testis cords	Mammalian_phenotype	9
MP:0006427	MP:0006427	ectopic Leydig cells	Mammalian_phenotype	9
MP:0008010	MP:0008010	increased gastric adenocarcinoma incidence	Mammalian_phenotype	9
MP:0008036	MP:0008036	abnormal NK T cell morphology	Mammalian_phenotype	9
MP:0008043	MP:0008043	abnormal NK cell number	Mammalian_phenotype	9
MP:0008053	MP:0008053	abnormal NK cell differentiation	Mammalian_phenotype	9
MP:0008054	MP:0008054	abnormal uterine NK cell morphology	Mammalian_phenotype	9
MP:0008059	MP:0008059	abnormal podocyte foot process morphology	Mammalian_phenotype	9
MP:0008062	MP:0008062	abnormal podocyte slit junction morphology	Mammalian_phenotype	9
MP:0008121	MP:0008121	increased myeloid dendritic cell number	Mammalian_phenotype	9
MP:0008122	MP:0008122	decreased myeloid dendritic cell number	Mammalian_phenotype	9
MP:0008137	MP:0008137	absent podocytes	Mammalian_phenotype	9
MP:0008262	MP:0008262	abnormal hippocampus region morphology	Mammalian_phenotype	9
MP:0008281	MP:0008281	abnormal hippocampus size	Mammalian_phenotype	9
MP:0008287	MP:0008287	abnormal subiculum morphology	Mammalian_phenotype	9
MP:0008328	MP:0008328	increased somatotroph cell number	Mammalian_phenotype	9
MP:0008329	MP:0008329	decreased somatotroph cell number	Mammalian_phenotype	9
MP:0008331	MP:0008331	increased lactotroph cell number	Mammalian_phenotype	9
MP:0008332	MP:0008332	decreased lactotroph cell number	Mammalian_phenotype	9
MP:0008334	MP:0008334	increased gonadotroph cell number	Mammalian_phenotype	9
MP:0008335	MP:0008335	decreased gonadotroph cell number	Mammalian_phenotype	9
MP:0008337	MP:0008337	increased thyrotroph cell number	Mammalian_phenotype	9
MP:0008338	MP:0008338	decreased thyrotroph cell number	Mammalian_phenotype	9
MP:0008340	MP:0008340	increased corticotroph cell number	Mammalian_phenotype	9
MP:0008341	MP:0008341	decreased corticotroph cell number	Mammalian_phenotype	9
MP:0008343	MP:0008343	abnormal gamma-delta T cell morphology	Mammalian_phenotype	9
MP:0008365	MP:0008365	adenohypophysis hypoplasia	Mammalian_phenotype	9
MP:0008369	MP:0008369	pituitary intermediate lobe hypoplasia	Mammalian_phenotype	9
MP:0008371	MP:0008371	pituitary intermediate lobe hyperplasia	Mammalian_phenotype	9
MP:0008375	MP:0008375	short malleus manubrium	Mammalian_phenotype	9
MP:0008385	MP:0008385	absent basisphenoid bone	Mammalian_phenotype	9
MP:0008386	MP:0008386	absent styloid process	Mammalian_phenotype	9
MP:0008388	MP:0008388	hypochromic microcytic anemia	Mammalian_phenotype	9
MP:0008389	MP:0008389	hypochromic macrocytic anemia	Mammalian_phenotype	9
MP:0008416	MP:0008416	increased somatotroph cell size	Mammalian_phenotype	9
MP:0008417	MP:0008417	decreased somatotroph cell size	Mammalian_phenotype	9
MP:0008420	MP:0008420	increased thyrotroph cell size	Mammalian_phenotype	9
MP:0008421	MP:0008421	decreased thyrotroph cell size	Mammalian_phenotype	9
MP:0008422	MP:0008422	increased lactotroph cell size	Mammalian_phenotype	9
MP:0008423	MP:0008423	decreased lactotroph cell size	Mammalian_phenotype	9
MP:0008424	MP:0008424	increased gonadotroph cell size	Mammalian_phenotype	9
MP:0008425	MP:0008425	decreased gonadotroph cell size	Mammalian_phenotype	9
MP:0008426	MP:0008426	increased corticotroph cell size	Mammalian_phenotype	9
MP:0008427	MP:0008427	decreased corticotroph cell size	Mammalian_phenotype	9
MP:0008430	MP:0008430	short squamosal bone	Mammalian_phenotype	9
MP:0008433	MP:0008433	abnormal somatotroph cell nucleus	Mammalian_phenotype	9
MP:0008436	MP:0008436	decreased somatotroph secretory granule number	Mammalian_phenotype	9
MP:0008474	MP:0008474	absent spleen germinal center	Mammalian_phenotype	9
MP:0008481	MP:0008481	increased spleen germinal center number	Mammalian_phenotype	9
MP:0008482	MP:0008482	decreased spleen germinal center number	Mammalian_phenotype	9
MP:0008483	MP:0008483	increased spleen germinal center size	Mammalian_phenotype	9
MP:0008484	MP:0008484	decreased spleen germinal center size	Mammalian_phenotype	9
MP:0008485	MP:0008485	increased muscle spindle number	Mammalian_phenotype	9
MP:0008486	MP:0008486	decreased muscle spindle number	Mammalian_phenotype	9
MP:0008507	MP:0008507	thin retinal ganglion layer	Mammalian_phenotype	9
MP:0008508	MP:0008508	thick retinal ganglion layer	Mammalian_phenotype	9
MP:0008509	MP:0008509	disorganized retinal ganglion layer	Mammalian_phenotype	9
MP:0008510	MP:0008510	absent retinal ganglion layer	Mammalian_phenotype	9
MP:0008512	MP:0008512	disorganized retinal inner nuclear layer	Mammalian_phenotype	9
MP:0008513	MP:0008513	thin retinal inner plexiform layer	Mammalian_phenotype	9
MP:0008514	MP:0008514	absent retinal inner plexiform layer	Mammalian_phenotype	9
MP:0008516	MP:0008516	disorganized retinal outer nuclear layer	Mammalian_phenotype	9
MP:0008518	MP:0008518	retinal outer nuclear layer degeneration	Mammalian_phenotype	9
MP:0008519	MP:0008519	thin retinal outer plexiform layer	Mammalian_phenotype	9
MP:0008520	MP:0008520	disorganized retinal outer plexiform layer	Mammalian_phenotype	9
MP:0008523	MP:0008523	absent lymph node germinal center	Mammalian_phenotype	9
MP:0008573	MP:0008573	increased circulating interferon-alpha level	Mammalian_phenotype	9
MP:0008574	MP:0008574	decreased circulating interferon-alpha level	Mammalian_phenotype	9
MP:0008575	MP:0008575	increased circulating interferon-beta level	Mammalian_phenotype	9
MP:0008576	MP:0008576	decreased circulating interferon-beta level	Mammalian_phenotype	9
MP:0008577	MP:0008577	increased circulating interferon-gamma level	Mammalian_phenotype	9
MP:0008578	MP:0008578	decreased circulating interferon-gamma level	Mammalian_phenotype	9
MP:0008591	MP:0008591	increased circulating interleukin-1 level	Mammalian_phenotype	9
MP:0008592	MP:0008592	decreased circulating interleukin-1 level	Mammalian_phenotype	9
MP:0008593	MP:0008593	increased circulating interleukin-10 level	Mammalian_phenotype	9
MP:0008594	MP:0008594	decreased circulating interleukin-10 level	Mammalian_phenotype	9
MP:0008596	MP:0008596	increased circulating interleukin-6 level	Mammalian_phenotype	9
MP:0008597	MP:0008597	decreased circulating interleukin-6 level	Mammalian_phenotype	9
MP:0008599	MP:0008599	increased circulating interleukin-2 level	Mammalian_phenotype	9
MP:0008600	MP:0008600	decreased circulating interleukin-2 level	Mammalian_phenotype	9
MP:0008602	MP:0008602	increased circulating interleukin-4 level	Mammalian_phenotype	9
MP:0008603	MP:0008603	decreased circulating interleukin-4 level	Mammalian_phenotype	9
MP:0008605	MP:0008605	increased circulating interleukin-7 level	Mammalian_phenotype	9
MP:0008606	MP:0008606	decreased circulating interleukin-7 level	Mammalian_phenotype	9
MP:0008608	MP:0008608	increased circulating interleukin-13 level	Mammalian_phenotype	9
MP:0008609	MP:0008609	decreased circulating interleukin-13 level	Mammalian_phenotype	9
MP:0008611	MP:0008611	increased circulating interleukin-15 level	Mammalian_phenotype	9
MP:0008612	MP:0008612	decreased circulating interleukin-15 level	Mammalian_phenotype	9
MP:0008614	MP:0008614	increased circulating interleukin-17 level	Mammalian_phenotype	9
MP:0008615	MP:0008615	decreased circulating interleukin-17 level	Mammalian_phenotype	9
MP:0008617	MP:0008617	increased circulating interleukin-12 level	Mammalian_phenotype	9
MP:0008618	MP:0008618	decreased circulating interleukin-12 level	Mammalian_phenotype	9
MP:0008620	MP:0008620	increased circulating interleukin-23 level	Mammalian_phenotype	9
MP:0008621	MP:0008621	decreased circulating interleukin-23 level	Mammalian_phenotype	9
MP:0008623	MP:0008623	increased circulating interleukin-3 level	Mammalian_phenotype	9
MP:0008624	MP:0008624	decreased circulating interleukin-3 level	Mammalian_phenotype	9
MP:0008626	MP:0008626	increased circulating interleukin-5 level	Mammalian_phenotype	9
MP:0008627	MP:0008627	decreased circulating interleukin-5 level	Mammalian_phenotype	9
MP:0008629	MP:0008629	increased circulating interleukin-9 level	Mammalian_phenotype	9
MP:0008630	MP:0008630	decreased circulating interleukin-9 level	Mammalian_phenotype	9
MP:0008632	MP:0008632	increased circulating interleukin-16 level	Mammalian_phenotype	9
MP:0008633	MP:0008633	decreased circulating interleukin-16 level	Mammalian_phenotype	9
MP:0008635	MP:0008635	increased circulating interleukin-18 level	Mammalian_phenotype	9
MP:0008636	MP:0008636	decreased circulating interleukin-18 level	Mammalian_phenotype	9
MP:0008637	MP:0008637	abnormal circulating interleukin-1 alpha level	Mammalian_phenotype	9
MP:0008640	MP:0008640	abnormal circulating interleukin-1 beta level	Mammalian_phenotype	9
MP:0008643	MP:0008643	abnormal circulating interleukin-12a level	Mammalian_phenotype	9
MP:0008647	MP:0008647	increased circulating interleukin-12b level	Mammalian_phenotype	9
MP:0008648	MP:0008648	decreased circulating interleukin-12b level	Mammalian_phenotype	9
MP:0008649	MP:0008649	abnormal circulating interleukin-23a level	Mammalian_phenotype	9
MP:0008715	MP:0008715	increased lung small cell carcinoma incidence	Mammalian_phenotype	9
MP:0008716	MP:0008716	increased lung non-small cell carcinoma incidence	Mammalian_phenotype	9
MP:0008717	MP:0008717	increased lung squamous cell carcinoma incidence	Mammalian_phenotype	9
MP:0008791	MP:0008791	decreased NK cell degranulation	Mammalian_phenotype	9
MP:0008792	MP:0008792	increased NK cell degranulation	Mammalian_phenotype	9
MP:0008839	MP:0008839	absent acrosome	Mammalian_phenotype	9
MP:0008849	MP:0008849	abnormal hemoglobin concentration distribution width	Mammalian_phenotype	9
MP:0008870	MP:0008870	increased mature ovarian follicle number	Mammalian_phenotype	9
MP:0008894	MP:0008894	abnormal intraepithelial T cell morphology	Mammalian_phenotype	9
MP:0008912	MP:0008912	nervous	Mammalian_phenotype	9
MP:0008920	MP:0008920	absent cervical axis	Mammalian_phenotype	9
MP:0008935	MP:0008935	decreased mean platelet volume	Mammalian_phenotype	9
MP:0008938	MP:0008938	decreased pituitary gland weight	Mammalian_phenotype	9
MP:0008939	MP:0008939	increased pituitary gland weight	Mammalian_phenotype	9
MP:0008945	MP:0008945	hyperchromic macrocytic anemia	Mammalian_phenotype	9
MP:0008954	MP:0008954	abnormal cellular hemoglobin content	Mammalian_phenotype	9
MP:0008972	MP:0008972	ethmoturbinate hypoplasia	Mammalian_phenotype	9
MP:0008979	MP:0008979	increased vagina weight	Mammalian_phenotype	9
MP:0008980	MP:0008980	decreased vagina weight	Mammalian_phenotype	9
MP:0008982	MP:0008982	vagina hyperplasia	Mammalian_phenotype	9
MP:0008984	MP:0008984	vagina hypoplasia	Mammalian_phenotype	9
MP:0000087	MP:0000087	absent mandible	Mammalian_phenotype	9
MP:0000094	MP:0000094	absent alveolar process	Mammalian_phenotype	9
MP:0000103	MP:0000103	nasal bone hypoplasia	Mammalian_phenotype	9
MP:0000114	MP:0000114	cleft chin	Mammalian_phenotype	9
MP:0000117	MP:0000117	absent tooth primordium	Mammalian_phenotype	9
MP:0000118	MP:0000118	arrest of tooth development	Mammalian_phenotype	9
MP:0000121	MP:0000121	failure of tooth eruption	Mammalian_phenotype	9
MP:0000122	MP:0000122	accelerated tooth eruption	Mammalian_phenotype	9
MP:0000125	MP:0000125	absent incisors	Mammalian_phenotype	9
MP:0000127	MP:0000127	degenerate molars	Mammalian_phenotype	9
MP:0000128	MP:0000128	growth retardation of molars	Mammalian_phenotype	9
MP:0000182	MP:0000182	increased circulating LDL cholesterol level	Mammalian_phenotype	9
MP:0000183	MP:0000183	decreased circulating LDL cholesterol level	Mammalian_phenotype	9
MP:0000186	MP:0000186	decreased circulating HDL cholesterol level	Mammalian_phenotype	9
MP:0000215	MP:0000215	absent erythrocytes	Mammalian_phenotype	9
MP:0000361	MP:0000361	decreased mast cell protease storage	Mammalian_phenotype	9
MP:0000362	MP:0000362	decreased mast cell histamine storage	Mammalian_phenotype	9
MP:0000621	MP:0000621	increased salivary adenocarcinoma incidence	Mammalian_phenotype	9
MP:0000635	MP:0000635	pituitary gland hyperplasia	Mammalian_phenotype	9
MP:0000659	MP:0000659	prostate gland hyperplasia	Mammalian_phenotype	9
MP:0000665	MP:0000665	decreased ductal branching in the coagulating gland	Mammalian_phenotype	9
MP:0000763	MP:0000763	abnormal filiform papillae morphology	Mammalian_phenotype	9
MP:0000765	MP:0000765	abnormal tongue squamous epithelium morphology	Mammalian_phenotype	9
MP:0000776	MP:0000776	abnormal inferior colliculus morphology	Mammalian_phenotype	9
MP:0000803	MP:0000803	abnormal transverse gyrus of Heschl morphology	Mammalian_phenotype	9
MP:0000809	MP:0000809	absent hippocampus	Mammalian_phenotype	9
MP:0000812	MP:0000812	abnormal dentate gyrus morphology	Mammalian_phenotype	9
MP:0000813	MP:0000813	abnormal hippocampus layer morphology	Mammalian_phenotype	9
MP:0000815	MP:0000815	abnormal Ammon gyrus morphology	Mammalian_phenotype	9
MP:0000860	MP:0000860	abnormal primary somatosensory cortex morphology	Mammalian_phenotype	9
MP:0000863	MP:0000863	abnormal secondary somatosensory cortex morphology	Mammalian_phenotype	9
MP:0000865	MP:0000865	absent cerebellum vermis	Mammalian_phenotype	9
MP:0000866	MP:0000866	cerebellum vermis hypoplasia	Mammalian_phenotype	9
MP:0000867	MP:0000867	abnormal cerebellum anterior vermis morphology	Mammalian_phenotype	9
MP:0000869	MP:0000869	abnormal cerebellum posterior vermis morphology	Mammalian_phenotype	9
MP:0000873	MP:0000873	thin external granule cell layer	Mammalian_phenotype	9
MP:0000874	MP:0000874	irregular external granule cell layer	Mammalian_phenotype	9
MP:0000875	MP:0000875	abnormal cerebellar Purkinje cell layer	Mammalian_phenotype	9
MP:0000886	MP:0000886	abnormal cerebellar granule layer morphology	Mammalian_phenotype	9
MP:0000889	MP:0000889	abnormal cerebellar molecular layer	Mammalian_phenotype	9
MP:0000900	MP:0000900	decreased colliculi size	Mammalian_phenotype	9
MP:0000901	MP:0000901	altered position of colliculi	Mammalian_phenotype	9
MP:0000904	MP:0000904	abnormal superior colliculus morphology	Mammalian_phenotype	9
MP:0000975	MP:0000975	absent hair guard neurons	Mammalian_phenotype	9
MP:0000976	MP:0000976	hyperinnervation of hair guard cells	Mammalian_phenotype	9
MP:0000978	MP:0000978	hyperinnervation of hair-tylotrich cells	Mammalian_phenotype	9
MP:0000980	MP:0000980	absent hair-down neurons	Mammalian_phenotype	9
MP:0000981	MP:0000981	hyperinnervation of hair-down cells	Mammalian_phenotype	9
MP:0000983	MP:0000983	enlarged Meissner's corpuscles	Mammalian_phenotype	9
MP:0000984	MP:0000984	hyperinnervation of Meissner's corpuscle	Mammalian_phenotype	9
MP:0000987	MP:0000987	hyperinnervation of Merkel's receptor	Mammalian_phenotype	9
MP:0000991	MP:0000991	abnormal primary muscle spindle morphology	Mammalian_phenotype	9
MP:0000994	MP:0000994	abnormal secondary muscle spindle morphology	Mammalian_phenotype	9
MP:0001000	MP:0001000	absent golgi tendon organ	Mammalian_phenotype	9
MP:0001012	MP:0001012	superior cervical ganglion hypertrophy	Mammalian_phenotype	9
MP:0001020	MP:0001020	L4 dorsal root ganglion hypertrophy	Mammalian_phenotype	9
MP:0001021	MP:0001021	small L4 dorsal root ganglion	Mammalian_phenotype	9
MP:0001023	MP:0001023	L5 dorsal root ganglion hypertrophy	Mammalian_phenotype	9
MP:0001024	MP:0001024	small L5 dorsal root ganglion	Mammalian_phenotype	9
MP:0001121	MP:0001121	uterus hypoplasia	Mammalian_phenotype	9
MP:0001128	MP:0001128	ovary hyperplasia	Mammalian_phenotype	9
MP:0001129	MP:0001129	impaired ovarian folliculogenesis	Mammalian_phenotype	9
MP:0001132	MP:0001132	absent mature ovarian follicles	Mammalian_phenotype	9
MP:0001138	MP:0001138	abnormal uterine cervix squamous epithelium morphology	Mammalian_phenotype	9
MP:0001149	MP:0001149	testicular hyperplasia	Mammalian_phenotype	9
MP:0001152	MP:0001152	Leydig cell hyperplasia	Mammalian_phenotype	9
MP:0001153	MP:0001153	small seminiferous tubules	Mammalian_phenotype	9
MP:0001556	MP:0001556	increased circulating HDL cholesterol level	Mammalian_phenotype	9
MP:0001649	MP:0001649	abnormal symphysis menti morphology	Mammalian_phenotype	9
MP:0001714	MP:0001714	absent trophoblast giant cells	Mammalian_phenotype	9
MP:0001805	MP:0001805	decreased IgG level	Mammalian_phenotype	9
MP:0001806	MP:0001806	decreased IgM level	Mammalian_phenotype	9
MP:0001807	MP:0001807	decreased IgA level	Mammalian_phenotype	9
MP:0001940	MP:0001940	testis hypoplasia	Mammalian_phenotype	9
MP:0002012	MP:0002012	increased trichofolliculoma incidence	Mammalian_phenotype	9
MP:0002027	MP:0002027	increased lung adenocarcinoma incidence	Mammalian_phenotype	9
MP:0002049	MP:0002049	increased extremity angiosarcoma incidence	Mammalian_phenotype	9
MP:0002144	MP:0002144	abnormal B cell differentiation	Mammalian_phenotype	9
MP:0002145	MP:0002145	abnormal T cell differentiation	Mammalian_phenotype	9
MP:0002274	MP:0002274	abnormal type I pneumocyte morphology	Mammalian_phenotype	9
MP:0002275	MP:0002275	abnormal type II pneumocyte morphology	Mammalian_phenotype	9
MP:0002435	MP:0002435	abnormal effector T cell morphology	Mammalian_phenotype	9
MP:0002439	MP:0002439	abnormal plasma cell morphology	Mammalian_phenotype	9
MP:0002443	MP:0002443	abnormal eosinophil differentiation	Mammalian_phenotype	9
MP:0002458	MP:0002458	abnormal B cell number	Mammalian_phenotype	9
MP:0002491	MP:0002491	decreased IgD level	Mammalian_phenotype	9
MP:0002492	MP:0002492	decreased IgE level	Mammalian_phenotype	9
MP:0002493	MP:0002493	increased IgG level	Mammalian_phenotype	9
MP:0002494	MP:0002494	increased IgM level	Mammalian_phenotype	9
MP:0002495	MP:0002495	increased IgA level	Mammalian_phenotype	9
MP:0002496	MP:0002496	increased IgD level	Mammalian_phenotype	9
MP:0002497	MP:0002497	increased IgE level	Mammalian_phenotype	9
MP:0002576	MP:0002576	abnormal enamel morphology	Mammalian_phenotype	9
MP:0002593	MP:0002593	high mean erythrocyte cell number	Mammalian_phenotype	9
MP:0002594	MP:0002594	low mean erythrocyte cell number	Mammalian_phenotype	9
MP:0002599	MP:0002599	increased mean platelet volume	Mammalian_phenotype	9
MP:0002602	MP:0002602	abnormal eosinophil cell number	Mammalian_phenotype	9
MP:0002620	MP:0002620	abnormal monocyte morphology	Mammalian_phenotype	9
MP:0002642	MP:0002642	anisocytosis	Mammalian_phenotype	9
MP:0002650	MP:0002650	abnormal ameloblast morphology	Mammalian_phenotype	9
MP:0002659	MP:0002659	pituitary gland hypoplasia	Mammalian_phenotype	9
MP:0002676	MP:0002676	uterus hyperplasia	Mammalian_phenotype	9
MP:0002678	MP:0002678	increased follicle recruitment	Mammalian_phenotype	9
MP:0002682	MP:0002682	decreased mature ovarian follicle number	Mammalian_phenotype	9
MP:0002686	MP:0002686	globozoospermia	Mammalian_phenotype	9
MP:0002716	MP:0002716	small male preputial glands	Mammalian_phenotype	9
MP:0002761	MP:0002761	abnormal hippocampal mossy fiber morphology	Mammalian_phenotype	9
MP:0002776	MP:0002776	Sertoli cell hyperplasia	Mammalian_phenotype	9
MP:0002777	MP:0002777	absent ovarian follicles	Mammalian_phenotype	9
MP:0002784	MP:0002784	abnormal Sertoli cell morphology	Mammalian_phenotype	9
MP:0002785	MP:0002785	absent Leydig cells	Mammalian_phenotype	9
MP:0002817	MP:0002817	abnormal tooth mineralization	Mammalian_phenotype	9
MP:0002818	MP:0002818	abnormal dentin morphology	Mammalian_phenotype	9
MP:0002820	MP:0002820	abnormal premaxilla morphology	Mammalian_phenotype	9
MP:0002872	MP:0002872	polycythemia	Mammalian_phenotype	9
MP:0002874	MP:0002874	decreased hemoglobin content	Mammalian_phenotype	9
MP:0003005	MP:0003005	abnormal hippocampal fimbria morphology	Mammalian_phenotype	9
MP:0003006	MP:0003006	abnormal hippocampal fornix morphology	Mammalian_phenotype	9
MP:0003053	MP:0003053	delayed tooth eruption	Mammalian_phenotype	9
MP:0003108	MP:0003108	short zygomatic bone	Mammalian_phenotype	9
MP:0003205	MP:0003205	testicular atrophy	Mammalian_phenotype	9
MP:0003430	MP:0003430	increased pancreatic islet cell adenoma incidence	Mammalian_phenotype	9
MP:0003434	MP:0003434	decreased susceptibility to induced choroidal neovascularization	Mammalian_phenotype	9
MP:0003505	MP:0003505	increased prolactinoma incidence	Mammalian_phenotype	9
MP:0003539	MP:0003539	absent hymen	Mammalian_phenotype	9
MP:0003540	MP:0003540	imperforate hymen	Mammalian_phenotype	9
MP:0003576	MP:0003576	oviduct hypoplasia	Mammalian_phenotype	9
MP:0003654	MP:0003654	nasal bone hyperplasia	Mammalian_phenotype	9
MP:0003669	MP:0003669	periodontal ligament hypercellularity	Mammalian_phenotype	9
MP:0003753	MP:0003753	increased lip papilloma incidence	Mammalian_phenotype	9
MP:0003754	MP:0003754	increased gingival papilloma incidence	Mammalian_phenotype	9
MP:0003765	MP:0003765	increased palatal depth	Mammalian_phenotype	9
MP:0003766	MP:0003766	decreased palatal depth	Mammalian_phenotype	9
MP:0003825	MP:0003825	abnormal pillar cell morphology	Mammalian_phenotype	9
MP:0003931	MP:0003931	absent molars	Mammalian_phenotype	9
MP:0003932	MP:0003932	abnormal molar crown morphology	Mammalian_phenotype	9
MP:0003933	MP:0003933	abnormal cementum morphology	Mammalian_phenotype	9
MP:0009041	MP:0009041	absent colliculi	Mammalian_phenotype	9
MP:0009060	MP:0009060	increased circulating interleukin-21 level	Mammalian_phenotype	9
MP:0009061	MP:0009061	decreased circulating interleukin-21 level	Mammalian_phenotype	9
MP:0009064	MP:0009064	oviduct atrophy	Mammalian_phenotype	9
MP:0009066	MP:0009066	decreased oviduct weight	Mammalian_phenotype	9
MP:0009067	MP:0009067	increased oviduct weight	Mammalian_phenotype	9
MP:0009071	MP:0009071	short oviduct	Mammalian_phenotype	9
MP:0009081	MP:0009081	thin uterus	Mammalian_phenotype	9
MP:0009083	MP:0009083	uterus hypertrophy	Mammalian_phenotype	9
MP:0009095	MP:0009095	abnormal endometrial gland number	Mammalian_phenotype	9
MP:0009101	MP:0009101	clitoris hypoplasia	Mammalian_phenotype	9
MP:0009104	MP:0009104	small penile bone	Mammalian_phenotype	9
MP:0009226	MP:0009226	small uterine cervix	Mammalian_phenotype	9
MP:0009231	MP:0009231	detached acrosome	Mammalian_phenotype	9
MP:0009251	MP:0009251	enlarged endometrial glands	Mammalian_phenotype	9
MP:0009268	MP:0009268	absent cerebellum fissure	Mammalian_phenotype	9
MP:0009317	MP:0009317	increased follicular lymphoma incidence	Mammalian_phenotype	9
MP:0009318	MP:0009318	increased splenic marginal zone lymphoma incidence	Mammalian_phenotype	9
MP:0009319	MP:0009319	increased small lymphocytic lymphoma incidence	Mammalian_phenotype	9
MP:0009320	MP:0009320	increased lymphoblastic lymphoma incidence	Mammalian_phenotype	9
MP:0009365	MP:0009365	abnormal theca folliculi	Mammalian_phenotype	9
MP:0009369	MP:0009369	abnormal thecal cell number	Mammalian_phenotype	9
MP:0009373	MP:0009373	abnormal cumulus expansion	Mammalian_phenotype	9
MP:0009396	MP:0009396	small endometrial glands	Mammalian_phenotype	9
MP:0009447	MP:0009447	abnormal platelet ATP level	Mammalian_phenotype	9
MP:0009541	MP:0009541	increased thymocyte apoptosis	Mammalian_phenotype	9
MP:0009542	MP:0009542	decreased thymocyte apoptosis	Mammalian_phenotype	9
MP:0009549	MP:0009549	decreased platelet aggregation	Mammalian_phenotype	9
MP:0009551	MP:0009551	increased urinary bladder transitional cell carcinoma incidence	Mammalian_phenotype	9
MP:0009556	MP:0009556	abnormal platelet ADP level	Mammalian_phenotype	9
MP:0009586	MP:0009586	increased platelet aggregation	Mammalian_phenotype	9
MP:0009592	MP:0009592	increased Leydig cell tumor incidence	Mammalian_phenotype	9
MP:0009609	MP:0009609	absent basioccipital bone	Mammalian_phenotype	9
MP:0009652	MP:0009652	abnormal palatal rugae morphology	Mammalian_phenotype	9
MP:0009654	MP:0009654	abnormal primary palate development	Mammalian_phenotype	9
MP:0009655	MP:0009655	abnormal secondary palate development	Mammalian_phenotype	9
MP:0009708	MP:0009708	vaginal septum	Mammalian_phenotype	9
MP:0009832	MP:0009832	abnormal sperm mitochondrial sheath morphology	Mammalian_phenotype	9
MP:0009834	MP:0009834	abnormal sperm annulus morphology	Mammalian_phenotype	9
MP:0009879	MP:0009879	abnormal arcus anterior morphology	Mammalian_phenotype	9
MP:0009890	MP:0009890	cleft secondary palate	Mammalian_phenotype	9
MP:0009891	MP:0009891	abnormal palate bone morphology	Mammalian_phenotype	9
MP:0009893	MP:0009893	cleft primary palate	Mammalian_phenotype	9
MP:0009894	MP:0009894	absent hard palate	Mammalian_phenotype	9
MP:0009899	MP:0009899	hyoid bone hypoplasia	Mammalian_phenotype	9
MP:0009904	MP:0009904	tongue hypoplasia	Mammalian_phenotype	9
MP:0009910	MP:0009910	bifurcated tongue	Mammalian_phenotype	9
MP:0009915	MP:0009915	absent hyoid bone lesser horns	Mammalian_phenotype	9
MP:0009916	MP:0009916	absent hyoid bone greater horns	Mammalian_phenotype	9
MP:0009942	MP:0009942	abnormal olfactory bulb granule cell morphology	Mammalian_phenotype	9
MP:0009943	MP:0009943	abnormal olfactory bulb periglomerular cell morphology	Mammalian_phenotype	9
MP:0009947	MP:0009947	abnormal olfactory bulb external plexiform layer morphology	Mammalian_phenotype	9
MP:0009948	MP:0009948	abnormal olfactory bulb glomerular layer morphology	Mammalian_phenotype	9
MP:0009949	MP:0009949	abnormal olfactory bulb granule cell layer morphology	Mammalian_phenotype	9
MP:0009950	MP:0009950	abnormal olfactory bulb internal plexiform layer morphology	Mammalian_phenotype	9
MP:0009951	MP:0009951	abnormal olfactory bulb mitral cell layer morphology	Mammalian_phenotype	9
MP:0009957	MP:0009957	abnormal cerebellum vermis lobule morphology	Mammalian_phenotype	9
MP:0009963	MP:0009963	abnormal cerebellum hemisphere lobule morphology	Mammalian_phenotype	9
MP:0009965	MP:0009965	abnormal cerebellum lateral hemisphere morphology	Mammalian_phenotype	9
MP:0009966	MP:0009966	abnormal cerebellum intermediate hemisphere morphology	Mammalian_phenotype	9
MP:0009981	MP:0009981	abnormal cerebellum emboliform nucleus morphology	Mammalian_phenotype	9
MP:0009982	MP:0009982	abnormal cerebellum globose nucleus morphology	Mammalian_phenotype	9
MP:0009985	MP:0009985	abnormal inferior cerebellar peduncle morphology	Mammalian_phenotype	9
MP:0009986	MP:0009986	abnormal middle cerebellar peduncle morphology	Mammalian_phenotype	9
MP:0009987	MP:0009987	abnormal superior cerebellar peduncle morphology	Mammalian_phenotype	9
MP:0009997	MP:0009997	abnormal cerebellum vermis lobule X morphology	Mammalian_phenotype	9
MP:0010006	MP:0010006	abnormal flocculus morphology	Mammalian_phenotype	9
MP:0010007	MP:0010007	abnormal paraflocculus morphology	Mammalian_phenotype	9
MP:0010010	MP:0010010	abnormal islands of Calleja morphology	Mammalian_phenotype	9
MP:0010013	MP:0010013	cerebral cortex pyramidal cell degeneration	Mammalian_phenotype	9
MP:0010057	MP:0010057	abnormal olfactory bulb outer nerve layer morphology	Mammalian_phenotype	9
MP:0010059	MP:0010059	olfactory bulb hypoplasia	Mammalian_phenotype	9
MP:0010096	MP:0010096	abnormal incisor color	Mammalian_phenotype	9
MP:0010150	MP:0010150	abnormal mandibule ramus morphology	Mammalian_phenotype	9
MP:0010241	MP:0010241	abnormal aortic arch development	Mammalian_phenotype	9
MP:0010317	MP:0010317	increased parotid gland tumor incidence	Mammalian_phenotype	9
MP:0010319	MP:0010319	increased submandibular gland tumor incidence	Mammalian_phenotype	9
MP:0010345	MP:0010345	increased thyroid C-cell carcinoma incidence	Mammalian_phenotype	9
MP:0010390	MP:0010390	increased adrenocortical adenoma incidence	Mammalian_phenotype	9
MP:0010464	MP:0010464	abnormal aortic arch and aortic arch branch attachment	Mammalian_phenotype	9
MP:0010466	MP:0010466	vascular ring	Mammalian_phenotype	9
MP:0010469	MP:0010469	ascending aorta hypoplasia	Mammalian_phenotype	9
MP:0010470	MP:0010470	ascending aorta dilation	Mammalian_phenotype	9
MP:0010484	MP:0010484	bicuspid aortic valve	Mammalian_phenotype	9
MP:0010485	MP:0010485	aortic arch hypoplasia	Mammalian_phenotype	9
MP:0010524	MP:0010524	calcified aortic arch	Mammalian_phenotype	9
MP:0010527	MP:0010527	bicuspid pulmonary valve	Mammalian_phenotype	9
MP:0010575	MP:0010575	aortic arch dilation	Mammalian_phenotype	9
MP:0010596	MP:0010596	unicuspid aortic valve	Mammalian_phenotype	9
MP:0010597	MP:0010597	absent aortic valve cusps	Mammalian_phenotype	9
MP:0010603	MP:0010603	unicuspid pulmonary valve	Mammalian_phenotype	9
MP:0010604	MP:0010604	absent pulmonary valve cusps	Mammalian_phenotype	9
MP:0010660	MP:0010660	descending thoracic aorta aneurysm	Mammalian_phenotype	9
MP:0010661	MP:0010661	ascending aorta aneurysm	Mammalian_phenotype	9
MP:0010701	MP:0010701	fusion of atlas and odontoid process	Mammalian_phenotype	9
MP:0010702	MP:0010702	split cervical atlas	Mammalian_phenotype	9
MP:0010703	MP:0010703	split cervical axis	Mammalian_phenotype	9
MP:0010704	MP:0010704	abnormal optic canal morphology	Mammalian_phenotype	9
MP:0010747	MP:0010747	abnormal enamel organ morphology	Mammalian_phenotype	9
MP:0010773	MP:0010773	supernumerary molars	Mammalian_phenotype	9
MP:0010777	MP:0010777	absent placenta metrial gland	Mammalian_phenotype	9
MP:0010833	MP:0010833	abnormal memory T cell morphology	Mammalian_phenotype	9
MP:0011061	MP:0011061	abnormal inner hair cell kinocilium morphology	Mammalian_phenotype	9
MP:0011062	MP:0011062	abnormal outer hair cell kinocilium morphology	Mammalian_phenotype	9
MP:0011064	MP:0011064	abnormal vestibular hair cell kinocilium morphology	Mammalian_phenotype	9
MP:0011071	MP:0011071	absent Clara cells	Mammalian_phenotype	9
MP:0011119	MP:0011119	abnormal primordial ovarian follicle number	Mammalian_phenotype	9
MP:0011123	MP:0011123	abnormal primary ovarian follicle number	Mammalian_phenotype	9
MP:0011127	MP:0011127	abnormal secondary ovarian follicle number	Mammalian_phenotype	9
MP:0011165	MP:0011165	abnormal tooth root development	Mammalian_phenotype	9
MP:0011178	MP:0011178	increased erythroblast number	Mammalian_phenotype	9
MP:0011179	MP:0011179	decreased erythroblast number	Mammalian_phenotype	9
MP:0011242	MP:0011242	increased fetal derived definitive erythrocyte cell number	Mammalian_phenotype	9
MP:0011243	MP:0011243	decreased fetal derived definitive erythrocyte cell number	Mammalian_phenotype	9
MP:0011353	MP:0011353	expanded mesangial matrix	Mammalian_phenotype	9
MP:0011427	MP:0011427	mesangial cell hyperplasia	Mammalian_phenotype	9
MP:0011428	MP:0011428	mesangial cell hypoplasia	Mammalian_phenotype	9
MP:0011429	MP:0011429	absent mesangial cell	Mammalian_phenotype	9
MP:0011454	MP:0011454	abnormal glomerular endothelium fenestra morphology	Mammalian_phenotype	9
MP:0011512	MP:0011512	mesangial cell interposition	Mammalian_phenotype	9
MP:0011557	MP:0011557	increased susceptibility to induced choroid neovascularization	Mammalian_phenotype	9
MP:0011572	MP:0011572	abnormal aorta bulb morphology	Mammalian_phenotype	9
MP:0011573	MP:0011573	abnormal sinotubular junction morphology	Mammalian_phenotype	9
MP:0011576	MP:0011576	absent cervical atlas	Mammalian_phenotype	9
MP:0011615	MP:0011615	submucous cleft palate	Mammalian_phenotype	9
MP:0011640	MP:0011640	abnormal aorta collagen fibril morphology	Mammalian_phenotype	9
MP:0011672	MP:0011672	unbalanced complete atrioventricular canal, left dominant	Mammalian_phenotype	9
MP:0011676	MP:0011676	aortic arch obstruction	Mammalian_phenotype	9
MP:0011714	MP:0011714	increased circulating interleukin-8 level	Mammalian_phenotype	9
MP:0011715	MP:0011715	decreased circulating interleukin-8 level	Mammalian_phenotype	9
MP:0011753	MP:0011753	decreased podocyte number	Mammalian_phenotype	9
MP:0011759	MP:0011759	absent Rathke's pouch	Mammalian_phenotype	9
MP:0011813	MP:0011813	long maxilla	Mammalian_phenotype	9
MP:0011868	MP:0011868	podocyte microvillus transformation	Mammalian_phenotype	9
MP:0011870	MP:0011870	abnormal podocyte polarity	Mammalian_phenotype	9
MP:0011871	MP:0011871	podocyte hypertrophy	Mammalian_phenotype	9
MP:0011899	MP:0011899	podocyte vacuolization	Mammalian_phenotype	9
MP:0011996	MP:0011996	abnormal retinal inner nuclear layer thickness	Mammalian_phenotype	9
MP:0011997	MP:0011997	abnormal retinal outer nuclear layer thickness	Mammalian_phenotype	9
MP:0012190	MP:0012190	increased cytotoxic T cell apoptosis	Mammalian_phenotype	9
MP:0012191	MP:0012191	decreased cytotoxic T cell apoptosis	Mammalian_phenotype	9
MP:0012257	MP:0012257	absent philtrum	Mammalian_phenotype	9
MP:0012258	MP:0012258	philtrum hypoplasia	Mammalian_phenotype	9
MP:0012259	MP:0012259	meningocele	Mammalian_phenotype	9
MP:0012273	MP:0012273	axial mesoderm hypoplasia	Mammalian_phenotype	9
MP:0012276	MP:0012276	absent prechordal mesoderm	Mammalian_phenotype	9
MP:0012297	MP:0012297	hyperactivity elicited by feed restriction	Mammalian_phenotype	9
MP:0012374	MP:0012374	decreased erythrocyte magnesium ion content	Mammalian_phenotype	9
MP:0012375	MP:0012375	increased erythrocyte magnesium ion content	Mammalian_phenotype	9
MP:0012377	MP:0012377	decreased erythrocyte potassium ion content	Mammalian_phenotype	9
MP:0012378	MP:0012378	increased erythrocyte potassium ion content	Mammalian_phenotype	9
MP:0012380	MP:0012380	decreased erythrocyte sodium ion content	Mammalian_phenotype	9
MP:0012381	MP:0012381	increased erythrocyte sodium ion content	Mammalian_phenotype	9
MP:0012406	MP:0012406	increased stomach glandular epithelium tumor incidence	Mammalian_phenotype	9
MP:0012409	MP:0012409	increased duodenal gastrinoma incidence	Mammalian_phenotype	9
MP:0012411	MP:0012411	increased granulosa cell tumor incidence	Mammalian_phenotype	9
MP:0012440	MP:0012440	abnormal neutrophil cell number	Mammalian_phenotype	9
MP:0012442	MP:0012442	abnormal basophil cell number	Mammalian_phenotype	9
MP:0012449	MP:0012449	increased primary motor cortex size	Mammalian_phenotype	9
MP:0012450	MP:0012450	decreased primary motor cortex size	Mammalian_phenotype	9
MP:0012471	MP:0012471	increased cerebellum interpositus nucleus size	Mammalian_phenotype	9
MP:0012472	MP:0012472	decreased cerebellum interpositus nucleus size	Mammalian_phenotype	9
MP:0012473	MP:0012473	increased cingulate cortex size	Mammalian_phenotype	9
MP:0012474	MP:0012474	decreased cingulate cortex size	Mammalian_phenotype	9
MP:0012475	MP:0012475	increased piriform cortex size	Mammalian_phenotype	9
MP:0012476	MP:0012476	decreased piriform cortex size	Mammalian_phenotype	9
MP:0012487	MP:0012487	increased cerebellum dentate nucleus size	Mammalian_phenotype	9
MP:0012488	MP:0012488	decreased cerebellum dentate nucleus size	Mammalian_phenotype	9
MP:0012489	MP:0012489	abnormal retrosplenial region morphology	Mammalian_phenotype	9
MP:0012548	MP:0012548	myelocele	Mammalian_phenotype	9
MP:0012750	MP:0012750	absent cardiac neural crest cells	Mammalian_phenotype	9
MP:0012762	MP:0012762	abnormal alpha-beta T cell morphology	Mammalian_phenotype	9
MP:0013003	MP:0013003	absent enteric neural crest cell	Mammalian_phenotype	9
MP:0020066	MP:0020066	abnormal neocortex size	Mammalian_phenotype	9
MP:0020175	MP:0020175	abnormal IgG1 level	Mammalian_phenotype	9
MP:0020176	MP:0020176	abnormal IgG2a level	Mammalian_phenotype	9
MP:0020177	MP:0020177	abnormal IgG2b level	Mammalian_phenotype	9
MP:0020178	MP:0020178	abnormal IgG2c level	Mammalian_phenotype	9
MP:0020179	MP:0020179	abnormal IgG3 level	Mammalian_phenotype	9
MP:0020203	MP:0020203	abnormal mast cell number	Mammalian_phenotype	9
MP:0012310	MP:0012310	persistent ductus caroticus	Mammalian_phenotype	10
MP:0012407	MP:0012407	increased gastric gastrinoma incidence	Mammalian_phenotype	10
MP:0012447	MP:0012447	thick cerebellar granule layer	Mammalian_phenotype	10
MP:0012451	MP:0012451	abnormal retrosplenial granular cortex morphology	Mammalian_phenotype	10
MP:0012459	MP:0012459	increased dentate gyrus size	Mammalian_phenotype	10
MP:0012460	MP:0012460	decreased dentate gyrus size	Mammalian_phenotype	10
MP:0012465	MP:0012465	increased hippocampal fimbria size	Mammalian_phenotype	10
MP:0012466	MP:0012466	decreased hippocampal fimbria size	Mammalian_phenotype	10
MP:0012477	MP:0012477	increased secondary somatosensory cortex size	Mammalian_phenotype	10
MP:0012478	MP:0012478	decreased secondary somatosensory cortex size	Mammalian_phenotype	10
MP:0012763	MP:0012763	abnormal alpha-beta T cell number	Mammalian_phenotype	10
MP:0012766	MP:0012766	abnormal KLRG1-positive NK cell number	Mammalian_phenotype	10
MP:0020067	MP:0020067	increased neocortex size	Mammalian_phenotype	10
MP:0020069	MP:0020069	decreased neocortex size	Mammalian_phenotype	10
MP:0000088	MP:0000088	short mandible	Mammalian_phenotype	10
MP:0000090	MP:0000090	absent premaxilla	Mammalian_phenotype	10
MP:0000097	MP:0000097	short maxilla	Mammalian_phenotype	10
MP:0000129	MP:0000129	ameloblast degeneration	Mammalian_phenotype	10
MP:0000219	MP:0000219	increased neutrophil cell number	Mammalian_phenotype	10
MP:0000222	MP:0000222	decreased neutrophil cell number	Mammalian_phenotype	10
MP:0000324	MP:0000324	increased mast cell number	Mammalian_phenotype	10
MP:0000336	MP:0000336	decreased mast cell number	Mammalian_phenotype	10
MP:0000344	MP:0000344	absent Cajal-Retzius cell	Mammalian_phenotype	10
MP:0000457	MP:0000457	maxilla hypoplasia	Mammalian_phenotype	10
MP:0000460	MP:0000460	mandible hypoplasia	Mammalian_phenotype	10
MP:0000660	MP:0000660	lateral prostate gland hypoplasia	Mammalian_phenotype	10
MP:0000726	MP:0000726	absent lymphocyte	Mammalian_phenotype	10
MP:0000766	MP:0000766	absent tongue squamous epithelium	Mammalian_phenotype	10
MP:0000777	MP:0000777	increased inferior colliculus size	Mammalian_phenotype	10
MP:0000814	MP:0000814	absent dentate gyrus	Mammalian_phenotype	10
MP:0000853	MP:0000853	absent cerebellar foliation	Mammalian_phenotype	10
MP:0000868	MP:0000868	decreased anterior vermis size	Mammalian_phenotype	10
MP:0000884	MP:0000884	delaminated Purkinje cell layer	Mammalian_phenotype	10
MP:0000887	MP:0000887	delaminated cerebellar granule layer	Mammalian_phenotype	10
MP:0000888	MP:0000888	absent cerebellar granule layer	Mammalian_phenotype	10
MP:0000890	MP:0000890	thin cerebellar molecular layer	Mammalian_phenotype	10
MP:0000905	MP:0000905	increased superior colliculus size	Mammalian_phenotype	10
MP:0000992	MP:0000992	absent primary muscle spindle	Mammalian_phenotype	10
MP:0000993	MP:0000993	partial loss of primary muscle spindle	Mammalian_phenotype	10
MP:0000995	MP:0000995	absent secondary muscle spindle	Mammalian_phenotype	10
MP:0000996	MP:0000996	partial loss of secondary muscle spindle	Mammalian_phenotype	10
MP:0001005	MP:0001005	abnormal retinal rod cell morphology	Mammalian_phenotype	10
MP:0001006	MP:0001006	abnormal retinal cone cell morphology	Mammalian_phenotype	10
MP:0001802	MP:0001802	arrested B cell differentiation	Mammalian_phenotype	10
MP:0001825	MP:0001825	arrested T cell differentiation	Mammalian_phenotype	10
MP:0002407	MP:0002407	abnormal double-negative T cell morphology	Mammalian_phenotype	10
MP:0002408	MP:0002408	abnormal double-positive T cell morphology	Mammalian_phenotype	10
MP:0002432	MP:0002432	abnormal CD4-positive T cell morphology	Mammalian_phenotype	10
MP:0002436	MP:0002436	abnormal CD8-positive, alpha-beta cytotoxic T cell morphology	Mammalian_phenotype	10
MP:0002440	MP:0002440	abnormal memory B cell morphology	Mammalian_phenotype	10
MP:0002577	MP:0002577	reduced enamel thickness	Mammalian_phenotype	10
MP:0002606	MP:0002606	increased basophil cell number	Mammalian_phenotype	10
MP:0002607	MP:0002607	decreased basophil cell number	Mammalian_phenotype	10
MP:0002648	MP:0002648	delaminated enamel	Mammalian_phenotype	10
MP:0002649	MP:0002649	abnormal enamel rod pattern	Mammalian_phenotype	10
MP:0002892	MP:0002892	decreased superior colliculus size	Mammalian_phenotype	10
MP:0002964	MP:0002964	aortic elastic tissue lesions	Mammalian_phenotype	10
MP:0003152	MP:0003152	abnormal pillar cell differentiation	Mammalian_phenotype	10
MP:0003211	MP:0003211	abnormal aorta elastic fiber morphology	Mammalian_phenotype	10
MP:0003240	MP:0003240	loss of hippocampal neurons	Mammalian_phenotype	10
MP:0003364	MP:0003364	increased insulinoma incidence	Mammalian_phenotype	10
MP:0003365	MP:0003365	increased glucagonoma incidence	Mammalian_phenotype	10
MP:0003404	MP:0003404	absent enamel	Mammalian_phenotype	10
MP:0003714	MP:0003714	absent platelets	Mammalian_phenotype	10
MP:0003729	MP:0003729	abnormal photoreceptor outer segment morphology	Mammalian_phenotype	10
MP:0003730	MP:0003730	abnormal photoreceptor inner segment morphology	Mammalian_phenotype	10
MP:0003944	MP:0003944	abnormal T cell subpopulation ratio	Mammalian_phenotype	10
MP:0003989	MP:0003989	abnormal barrel cortex morphology	Mammalian_phenotype	10
MP:0004098	MP:0004098	abnormal cerebellar granule cell morphology	Mammalian_phenotype	10
MP:0004099	MP:0004099	abnormal cerebellar glomerulus morphology	Mammalian_phenotype	10
MP:0004159	MP:0004159	double aortic arch	Mammalian_phenotype	10
MP:0004312	MP:0004312	absent pillar cells	Mammalian_phenotype	10
MP:0004394	MP:0004394	abnormal cochlear inner hair cell number	Mammalian_phenotype	10
MP:0004398	MP:0004398	cochlear inner hair cell degeneration	Mammalian_phenotype	10
MP:0004400	MP:0004400	abnormal cochlear outer hair cell number	Mammalian_phenotype	10
MP:0004404	MP:0004404	cochlear outer hair cell degeneration	Mammalian_phenotype	10
MP:0004456	MP:0004456	small pterygoid bone	Mammalian_phenotype	10
MP:0004460	MP:0004460	alisphenoid bone hypoplasia	Mammalian_phenotype	10
MP:0004461	MP:0004461	basisphenoid bone hypoplasia	Mammalian_phenotype	10
MP:0004466	MP:0004466	short cochlear outer hair cells	Mammalian_phenotype	10
MP:0004487	MP:0004487	type I spiral ligament fibrocyte degeneration	Mammalian_phenotype	10
MP:0004488	MP:0004488	type II spiral ligament fibrocyte degeneration	Mammalian_phenotype	10
MP:0004489	MP:0004489	type III spiral ligament fibrocyte degeneration	Mammalian_phenotype	10
MP:0004490	MP:0004490	type IV spiral ligament fibrocyte degeneration	Mammalian_phenotype	10
MP:0004497	MP:0004497	decreased organ of Corti supporting cell number	Mammalian_phenotype	10
MP:0004498	MP:0004498	increased organ of Corti supporting cell number	Mammalian_phenotype	10
MP:0004516	MP:0004516	fused vestibular hair cell stereocilia	Mammalian_phenotype	10
MP:0004517	MP:0004517	decreased vestibular hair cell stereocilia number	Mammalian_phenotype	10
MP:0004518	MP:0004518	absent vestibular hair cell stereocilia	Mammalian_phenotype	10
MP:0004519	MP:0004519	thin vestibular hair cell stereocilia	Mammalian_phenotype	10
MP:0004520	MP:0004520	short vestibular hair cell stereocilia	Mammalian_phenotype	10
MP:0004522	MP:0004522	abnormal orientation of cochlear hair cell stereociliary bundles	Mammalian_phenotype	10
MP:0004523	MP:0004523	decreased cochlear hair cell stereocilia number	Mammalian_phenotype	10
MP:0004524	MP:0004524	short cochlear hair cell stereocilia	Mammalian_phenotype	10
MP:0004525	MP:0004525	thin cochlear hair cell stereocilia	Mammalian_phenotype	10
MP:0004526	MP:0004526	absent cochlear hair cell stereocilia	Mammalian_phenotype	10
MP:0004527	MP:0004527	abnormal outer hair cell stereociliary bundle morphology	Mammalian_phenotype	10
MP:0004532	MP:0004532	abnormal inner hair cell stereociliary bundle morphology	Mammalian_phenotype	10
MP:0004562	MP:0004562	abnormal inner hair cell synaptic ribbon morphology	Mammalian_phenotype	10
MP:0004577	MP:0004577	abnormal cochlear hair cell inter-stereocilial links morphology	Mammalian_phenotype	10
MP:0004583	MP:0004583	abnormal vestibular hair bundle inter-stereocilial links	Mammalian_phenotype	10
MP:0004586	MP:0004586	pillar cell degeneration	Mammalian_phenotype	10
MP:0004590	MP:0004590	absent Deiters cells	Mammalian_phenotype	10
MP:0004594	MP:0004594	abnormal mandibular coronoid process morphology	Mammalian_phenotype	10
MP:0004595	MP:0004595	abnormal mandibular condyloid process morphology	Mammalian_phenotype	10
MP:0004628	MP:0004628	Deiters cell degeneration	Mammalian_phenotype	10
MP:0004790	MP:0004790	absent upper incisors	Mammalian_phenotype	10
MP:0004791	MP:0004791	absent lower incisors	Mammalian_phenotype	10
MP:0004840	MP:0004840	increased Deiters cell number	Mammalian_phenotype	10
MP:0004866	MP:0004866	increased platelet calcium level	Mammalian_phenotype	10
MP:0004867	MP:0004867	decreased platelet calcium level	Mammalian_phenotype	10
MP:0004870	MP:0004870	small premaxilla	Mammalian_phenotype	10
MP:0004913	MP:0004913	absent mandibular angle	Mammalian_phenotype	10
MP:0004917	MP:0004917	abnormal T cell selection	Mammalian_phenotype	10
MP:0004940	MP:0004940	abnormal B-1 B cell morphology	Mammalian_phenotype	10
MP:0004942	MP:0004942	abnormal B cell selection	Mammalian_phenotype	10
MP:0004972	MP:0004972	abnormal regulatory T cell number	Mammalian_phenotype	10
MP:0005010	MP:0005010	abnormal CD8-positive T cell morphology	Mammalian_phenotype	10
MP:0005011	MP:0005011	increased eosinophil cell number	Mammalian_phenotype	10
MP:0005012	MP:0005012	decreased eosinophil cell number	Mammalian_phenotype	10
MP:0005014	MP:0005014	increased B cell number	Mammalian_phenotype	10
MP:0005015	MP:0005015	increased T cell number	Mammalian_phenotype	10
MP:0005017	MP:0005017	decreased B cell number	Mammalian_phenotype	10
MP:0005018	MP:0005018	decreased T cell number	Mammalian_phenotype	10
MP:0005096	MP:0005096	erythroblastosis	Mammalian_phenotype	10
MP:0005432	MP:0005432	abnormal pro-B cell morphology	Mammalian_phenotype	10
MP:0006097	MP:0006097	abnormal cerebellar lobule formation	Mammalian_phenotype	10
MP:0006099	MP:0006099	thin cerebellar granule layer	Mammalian_phenotype	10
MP:0006257	MP:0006257	abnormal fungiform papillae morphology	Mammalian_phenotype	10
MP:0006258	MP:0006258	abnormal circumvallate papillae morphology	Mammalian_phenotype	10
MP:0006259	MP:0006259	abnormal foliate papillae morphology	Mammalian_phenotype	10
MP:0006352	MP:0006352	decreased glycosylated hemoglobin level	Mammalian_phenotype	10
MP:0006353	MP:0006353	increased glycosylated hemoglobin level	Mammalian_phenotype	10
MP:0006422	MP:0006422	increased mammary adenoacanthoma incidence	Mammalian_phenotype	10
MP:0006428	MP:0006428	ectopic Sertoli cells	Mammalian_phenotype	10
MP:0008038	MP:0008038	abnormal NK T cell number	Mammalian_phenotype	10
MP:0008044	MP:0008044	increased NK cell number	Mammalian_phenotype	10
MP:0008045	MP:0008045	decreased NK cell number	Mammalian_phenotype	10
MP:0008048	MP:0008048	abnormal memory T cell number	Mammalian_phenotype	10
MP:0008060	MP:0008060	abnormal podocyte slit diaphragm morphology	Mammalian_phenotype	10
MP:0008073	MP:0008073	abnormal CD4-positive T cell number	Mammalian_phenotype	10
MP:0008076	MP:0008076	abnormal CD4-positive T cell differentiation	Mammalian_phenotype	10
MP:0008077	MP:0008077	abnormal CD8-positive T cell number	Mammalian_phenotype	10
MP:0008080	MP:0008080	abnormal CD8-positive T cell differentiation	Mammalian_phenotype	10
MP:0008081	MP:0008081	abnormal single-positive T cell number	Mammalian_phenotype	10
MP:0008093	MP:0008093	abnormal memory B cell number	Mammalian_phenotype	10
MP:0008095	MP:0008095	abnormal memory B cell differentiation	Mammalian_phenotype	10
MP:0008096	MP:0008096	abnormal plasma cell number	Mammalian_phenotype	10
MP:0008099	MP:0008099	abnormal plasma cell differentiation	Mammalian_phenotype	10
MP:0008117	MP:0008117	abnormal Langerhans cell morphology	Mammalian_phenotype	10
MP:0008138	MP:0008138	absent podocyte foot process	Mammalian_phenotype	10
MP:0008139	MP:0008139	fused podocyte foot processes	Mammalian_phenotype	10
MP:0008140	MP:0008140	podocyte foot process effacement	Mammalian_phenotype	10
MP:0008166	MP:0008166	abnormal B-2 B cell morphology	Mammalian_phenotype	10
MP:0008172	MP:0008172	abnormal follicular B cell morphology	Mammalian_phenotype	10
MP:0008176	MP:0008176	abnormal germinal center B cell morphology	Mammalian_phenotype	10
MP:0008184	MP:0008184	abnormal naive B cell morphology	Mammalian_phenotype	10
MP:0008210	MP:0008210	increased mature B cell number	Mammalian_phenotype	10
MP:0008211	MP:0008211	decreased mature B cell number	Mammalian_phenotype	10
MP:0008244	MP:0008244	abnormal peritoneal macrophage morphology	Mammalian_phenotype	10
MP:0008263	MP:0008263	abnormal hippocampus CA1 region morphology	Mammalian_phenotype	10
MP:0008265	MP:0008265	abnormal hippocampus CA2 region morphology	Mammalian_phenotype	10
MP:0008267	MP:0008267	abnormal hippocampus CA3 region morphology	Mammalian_phenotype	10
MP:0008269	MP:0008269	abnormal hippocampus CA4 region morphology	Mammalian_phenotype	10
MP:0008282	MP:0008282	enlarged hippocampus	Mammalian_phenotype	10
MP:0008283	MP:0008283	small hippocampus	Mammalian_phenotype	10
MP:0008284	MP:0008284	abnormal hippocampus pyramidal cell layer	Mammalian_phenotype	10
MP:0008285	MP:0008285	abnormal hippocampus granule cell layer	Mammalian_phenotype	10
MP:0008286	MP:0008286	abnormal hippocampus molecular cell layer	Mammalian_phenotype	10
MP:0008330	MP:0008330	absent somatotrophs	Mammalian_phenotype	10
MP:0008333	MP:0008333	absent lactotrophs	Mammalian_phenotype	10
MP:0008336	MP:0008336	absent gonadotrophs	Mammalian_phenotype	10
MP:0008339	MP:0008339	absent thyrotrophs	Mammalian_phenotype	10
MP:0008342	MP:0008342	absent corticotrophs	Mammalian_phenotype	10
MP:0008344	MP:0008344	abnormal mature gamma-delta T cell morphology	Mammalian_phenotype	10
MP:0008345	MP:0008345	abnormal gamma-delta T cell number	Mammalian_phenotype	10
MP:0008349	MP:0008349	abnormal gamma-delta intraepithelial T cell morphology	Mammalian_phenotype	10
MP:0008356	MP:0008356	abnormal gamma-delta T cell differentiation	Mammalian_phenotype	10
MP:0008397	MP:0008397	abnormal CD4-positive, CD25-positive, alpha-beta regulatory T cell morphology	Mammalian_phenotype	10
MP:0008398	MP:0008398	abnormal CD8-positive, alpha-beta regulatory T cell morphology	Mammalian_phenotype	10
MP:0008399	MP:0008399	abnormal alpha-beta intraepithelial T cell morphology	Mammalian_phenotype	10
MP:0008400	MP:0008400	abnormal CD4-positive, alpha-beta intraepithelial T cell morphology	Mammalian_phenotype	10
MP:0008401	MP:0008401	abnormal CD8 positive, alpha-beta intraepithelial T cell morphology	Mammalian_phenotype	10
MP:0008434	MP:0008434	small somatotroph cell nucleus	Mammalian_phenotype	10
MP:0008435	MP:0008435	large somatotroph cell nucleus	Mammalian_phenotype	10
MP:0008437	MP:0008437	absent somatotroph secretory granules	Mammalian_phenotype	10
MP:0008468	MP:0008468	absent muscle spindles	Mammalian_phenotype	10
MP:0008495	MP:0008495	decreased IgG1 level	Mammalian_phenotype	10
MP:0008496	MP:0008496	decreased IgG2a level	Mammalian_phenotype	10
MP:0008497	MP:0008497	decreased IgG2b level	Mammalian_phenotype	10
MP:0008498	MP:0008498	decreased IgG3 level	Mammalian_phenotype	10
MP:0008499	MP:0008499	increased IgG1 level	Mammalian_phenotype	10
MP:0008500	MP:0008500	increased IgG2a level	Mammalian_phenotype	10
MP:0008501	MP:0008501	increased IgG2b level	Mammalian_phenotype	10
MP:0008502	MP:0008502	increased IgG3 level	Mammalian_phenotype	10
MP:0008511	MP:0008511	thin retinal inner nuclear layer	Mammalian_phenotype	10
MP:0008515	MP:0008515	thin retinal outer nuclear layer	Mammalian_phenotype	10
MP:0008517	MP:0008517	thick retinal outer nuclear layer	Mammalian_phenotype	10
MP:0008638	MP:0008638	increased circulating interleukin-1 alpha level	Mammalian_phenotype	10
MP:0008639	MP:0008639	decreased circulating interleukin-1 alpha level	Mammalian_phenotype	10
MP:0008641	MP:0008641	increased circulating interleukin-1 beta level	Mammalian_phenotype	10
MP:0008642	MP:0008642	decreased circulating interleukin-1 beta level	Mammalian_phenotype	10
MP:0008644	MP:0008644	increased circulating interleukin-12a level	Mammalian_phenotype	10
MP:0008645	MP:0008645	decreased circulating interleukin-12a level	Mammalian_phenotype	10
MP:0008718	MP:0008718	increased lung large cell carcinoma incidence	Mammalian_phenotype	10
MP:0008754	MP:0008754	abnormal T cell receptor V(D)J recombination	Mammalian_phenotype	10
MP:0008755	MP:0008755	abnormal immunoglobulin V(D)J recombination	Mammalian_phenotype	10
MP:0008766	MP:0008766	abnormal B cell receptor editing	Mammalian_phenotype	10
MP:0008850	MP:0008850	increased hemoglobin concentration distribution width	Mammalian_phenotype	10
MP:0008851	MP:0008851	decreased hemoglobin concentration distribution width	Mammalian_phenotype	10
MP:0008876	MP:0008876	decreased uterine NK cell number	Mammalian_phenotype	10
MP:0008895	MP:0008895	abnormal intraepithelial T cell number	Mammalian_phenotype	10
MP:0008896	MP:0008896	increased IgG2c level	Mammalian_phenotype	10
MP:0008897	MP:0008897	decreased IgG2c level	Mammalian_phenotype	10
MP:0008955	MP:0008955	increased cellular hemoglobin content	Mammalian_phenotype	10
MP:0008956	MP:0008956	decreased cellular hemoglobin content	Mammalian_phenotype	10
MP:0009038	MP:0009038	decreased inferior colliculus size	Mammalian_phenotype	10
MP:0009039	MP:0009039	absent inferior colliculus	Mammalian_phenotype	10
MP:0009040	MP:0009040	absent superior colliculus	Mammalian_phenotype	10
MP:0009096	MP:0009096	decreased endometrial gland number	Mammalian_phenotype	10
MP:0009097	MP:0009097	absent endometrial glands	Mammalian_phenotype	10
MP:0009227	MP:0009227	uterine cervix hypoplasia	Mammalian_phenotype	10
MP:0009309	MP:0009309	increased small intestine adenocarcinoma incidence	Mammalian_phenotype	10
MP:0009310	MP:0009310	increased large intestine adenocarcinoma incidence	Mammalian_phenotype	10
MP:0009324	MP:0009324	absent hippocampal fimbria	Mammalian_phenotype	10
MP:0009366	MP:0009366	abnormal theca interna	Mammalian_phenotype	10
MP:0009367	MP:0009367	abnormal theca externa	Mammalian_phenotype	10
MP:0009368	MP:0009368	absent theca folliculi	Mammalian_phenotype	10
MP:0009370	MP:0009370	decreased thecal cell number	Mammalian_phenotype	10
MP:0009371	MP:0009371	increased thecal cell number	Mammalian_phenotype	10
MP:0009372	MP:0009372	abnormal cumulus oophorus	Mammalian_phenotype	10
MP:0009374	MP:0009374	absent cumulus expansion	Mammalian_phenotype	10
MP:0009394	MP:0009394	increased uterine NK cell number	Mammalian_phenotype	10
MP:0009448	MP:0009448	decreased platelet ATP level	Mammalian_phenotype	10
MP:0009449	MP:0009449	increased platelet ATP level	Mammalian_phenotype	10
MP:0009512	MP:0009512	abnormal cerebellar Golgi cell morphology	Mammalian_phenotype	10
MP:0009557	MP:0009557	decreased platelet ADP level	Mammalian_phenotype	10
MP:0009558	MP:0009558	increased platelet ADP level	Mammalian_phenotype	10
MP:0009718	MP:0009718	absent Purkinje cell layer	Mammalian_phenotype	10
MP:0009719	MP:0009719	reduced cerebellar foliation	Mammalian_phenotype	10
MP:0009833	MP:0009833	absent sperm mitochondrial sheath	Mammalian_phenotype	10
MP:0009835	MP:0009835	absent sperm annulus	Mammalian_phenotype	10
MP:0009882	MP:0009882	absent palatal shelf	Mammalian_phenotype	10
MP:0009883	MP:0009883	palatal shelf hypoplasia	Mammalian_phenotype	10
MP:0009884	MP:0009884	palatal shelf fusion with tongue or mandible	Mammalian_phenotype	10
MP:0009885	MP:0009885	abnormal palatal shelf elevation	Mammalian_phenotype	10
MP:0009887	MP:0009887	abnormal palatal shelf fusion at midline	Mammalian_phenotype	10
MP:0009892	MP:0009892	palate bone hypoplasia	Mammalian_phenotype	10
MP:0009938	MP:0009938	abnormal hippocampus granule cell morphology	Mammalian_phenotype	10
MP:0009940	MP:0009940	abnormal hippocampus pyramidal cell morphology	Mammalian_phenotype	10
MP:0009954	MP:0009954	abnormal mitral cell morphology	Mammalian_phenotype	10
MP:0009955	MP:0009955	abnormal olfactory bulb tufted cell morphology	Mammalian_phenotype	10
MP:0009975	MP:0009975	absent cerebral cortex pyramidal cells	Mammalian_phenotype	10
MP:0009988	MP:0009988	abnormal cerebellum vermis lobule I morphology	Mammalian_phenotype	10
MP:0009989	MP:0009989	abnormal cerebellum vermis lobule II morphology	Mammalian_phenotype	10
MP:0009990	MP:0009990	abnormal cerebellum vermis lobule III morphology	Mammalian_phenotype	10
MP:0009991	MP:0009991	abnormal cerebellum vermis lobule IV morphology	Mammalian_phenotype	10
MP:0009992	MP:0009992	abnormal cerebellum vermis lobule IX morphology	Mammalian_phenotype	10
MP:0009993	MP:0009993	abnormal cerebellum vermis lobule V morphology	Mammalian_phenotype	10
MP:0009994	MP:0009994	abnormal cerebellum vermis lobule VI morphology	Mammalian_phenotype	10
MP:0009995	MP:0009995	abnormal cerebellum vermis lobule VII morphology	Mammalian_phenotype	10
MP:0009996	MP:0009996	abnormal cerebellum vermis lobule VIII morphology	Mammalian_phenotype	10
MP:0010000	MP:0010000	abnormal copula pyramidis morphology	Mammalian_phenotype	10
MP:0010001	MP:0010001	abnormal ansiform lobule morphology	Mammalian_phenotype	10
MP:0010004	MP:0010004	abnormal paramedian lobule morphology	Mammalian_phenotype	10
MP:0010005	MP:0010005	abnormal lobule simplex morphology	Mammalian_phenotype	10
MP:0010084	MP:0010084	abnormal long lived plasma cell morphology	Mammalian_phenotype	10
MP:0010085	MP:0010085	abnormal short lived plasma cell morphology	Mammalian_phenotype	10
MP:0010221	MP:0010221	abnormal T-helper 17 cell differentiation	Mammalian_phenotype	10
MP:0010387	MP:0010387	abnormal Bergmann glial cell morphology	Mammalian_phenotype	10
MP:0010467	MP:0010467	pulmonary artery sling	Mammalian_phenotype	10
MP:0010475	MP:0010475	anomalous pulmonary origin of left coronary artery	Mammalian_phenotype	10
MP:0010482	MP:0010482	abnormal aortic sinus morphology	Mammalian_phenotype	10
MP:0010483	MP:0010483	aortic sinus aneurysm	Mammalian_phenotype	10
MP:0010538	MP:0010538	increased level of surface class II molecules	Mammalian_phenotype	10
MP:0010539	MP:0010539	decreased level of surface class II molecules	Mammalian_phenotype	10
MP:0010705	MP:0010705	absent metoptic pilar	Mammalian_phenotype	10
MP:0010729	MP:0010729	absent arcus anterior	Mammalian_phenotype	10
MP:0010730	MP:0010730	absent odontoid process	Mammalian_phenotype	10
MP:0010731	MP:0010731	absent ventral tubercle of atlas	Mammalian_phenotype	10
MP:0010810	MP:0010810	increased type II pneumocyte number	Mammalian_phenotype	10
MP:0010811	MP:0010811	decreased type II pneumocyte number	Mammalian_phenotype	10
MP:0010813	MP:0010813	abnormal alveolar lamellar body morphology	Mammalian_phenotype	10
MP:0010816	MP:0010816	decreased type I pneumocyte number	Mammalian_phenotype	10
MP:0010834	MP:0010834	abnormal CD4-positive, alpha-beta memory T cell morphology	Mammalian_phenotype	10
MP:0010837	MP:0010837	abnormal CD8-positive, alpha-beta memory T cell morphology	Mammalian_phenotype	10
MP:0010864	MP:0010864	abnormal enamel knot morphology	Mammalian_phenotype	10
MP:0011120	MP:0011120	increased primordial ovarian follicle number	Mammalian_phenotype	10
MP:0011121	MP:0011121	decreased primordial ovarian follicle number	Mammalian_phenotype	10
MP:0011124	MP:0011124	increased primary ovarian follicle number	Mammalian_phenotype	10
MP:0011125	MP:0011125	decreased primary ovarian follicle number	Mammalian_phenotype	10
MP:0011128	MP:0011128	increased secondary ovarian follicle number	Mammalian_phenotype	10
MP:0011129	MP:0011129	decreased secondary ovarian follicle number	Mammalian_phenotype	10
MP:0011149	MP:0011149	abnormal hippocampus stratum lacunosum morphology	Mammalian_phenotype	10
MP:0011150	MP:0011150	abnormal hippocampus stratum oriens morphology	Mammalian_phenotype	10
MP:0011151	MP:0011151	abnormal hippocampus stratum radiatum morphology	Mammalian_phenotype	10
MP:0011166	MP:0011166	absent molar root	Mammalian_phenotype	10
MP:0011244	MP:0011244	absent fetal derived definitive erythrocytes	Mammalian_phenotype	10
MP:0011455	MP:0011455	absent glomerular endothelium fenestra	Mammalian_phenotype	10
MP:0011574	MP:0011574	dilated sinotubular junction	Mammalian_phenotype	10
MP:0011575	MP:0011575	dilated aorta bulb	Mammalian_phenotype	10
MP:0011658	MP:0011658	interrupted aortic arch, type a	Mammalian_phenotype	10
MP:0011659	MP:0011659	interrupted aortic arch, type b	Mammalian_phenotype	10
MP:0011700	MP:0011700	increased cumulus expansion	Mammalian_phenotype	10
MP:0011701	MP:0011701	decreased cumulus expansion	Mammalian_phenotype	10
MP:0009311	MP:0009311	increased duodenum adenocarcinoma incidence	Mammalian_phenotype	11
MP:0009312	MP:0009312	increased jejunum adenocarcinoma incidence	Mammalian_phenotype	11
MP:0009313	MP:0009313	increased cecum adenocarcinoma incidence	Mammalian_phenotype	11
MP:0009314	MP:0009314	increased colon adenocarcinoma incidence	Mammalian_phenotype	11
MP:0009315	MP:0009315	increased rectum adenocarcinoma incidence	Mammalian_phenotype	11
MP:0009316	MP:0009316	increased anal adenocarcinoma incidence	Mammalian_phenotype	11
MP:0009886	MP:0009886	failure of palatal shelf elevation	Mammalian_phenotype	11
MP:0009888	MP:0009888	palatal shelves fail to meet at midline	Mammalian_phenotype	11
MP:0009889	MP:0009889	persistence of medial edge epithelium during palatal shelf fusion	Mammalian_phenotype	11
MP:0009895	MP:0009895	decreased palatine shelf size	Mammalian_phenotype	11
MP:0009897	MP:0009897	decreased maxillary shelf size	Mammalian_phenotype	11
MP:0009998	MP:0009998	abnormal cerebellum vermis lobule VIIa morphology	Mammalian_phenotype	11
MP:0009999	MP:0009999	abnormal cerebellum vermis lobule VIIb morphology	Mammalian_phenotype	11
MP:0010002	MP:0010002	abnormal ansiform lobule crus I morphology	Mammalian_phenotype	11
MP:0010003	MP:0010003	abnormal ansiform lobule crus II morphology	Mammalian_phenotype	11
MP:0010183	MP:0010183	abnormal CD4-positive helper T cell morphology	Mammalian_phenotype	11
MP:0010671	MP:0010671	abnormal Tc17 cell morphology	Mammalian_phenotype	11
MP:0010812	MP:0010812	absent type II pneumocytes	Mammalian_phenotype	11
MP:0010814	MP:0010814	absent alveolar lamellar bodies	Mammalian_phenotype	11
MP:0010815	MP:0010815	enlarged alveolar lamellar bodies	Mammalian_phenotype	11
MP:0010817	MP:0010817	absent type I pneumocytes	Mammalian_phenotype	11
MP:0010849	MP:0010849	abnormal effector memory CD8-positive, alpha-beta T cell number	Mammalian_phenotype	11
MP:0010889	MP:0010889	small alveolar lamellar bodies	Mammalian_phenotype	11
MP:0010890	MP:0010890	decreased alveolar lamellar body number	Mammalian_phenotype	11
MP:0010891	MP:0010891	increased alveolar lamellar body number	Mammalian_phenotype	11
MP:0011122	MP:0011122	absent primordial ovarian follicles	Mammalian_phenotype	11
MP:0011126	MP:0011126	absent primary ovarian follicles	Mammalian_phenotype	11
MP:0011130	MP:0011130	absent secondary ovarian follicles	Mammalian_phenotype	11
MP:0011152	MP:0011152	thick hippocampus molecular cell layer	Mammalian_phenotype	11
MP:0011153	MP:0011153	thick hippocampus stratum oriens	Mammalian_phenotype	11
MP:0011154	MP:0011154	thick hippocampus stratum radiatum	Mammalian_phenotype	11
MP:0011155	MP:0011155	absent hippocampus stratum oriens	Mammalian_phenotype	11
MP:0011675	MP:0011675	double aortic arch, balanced arches	Mammalian_phenotype	11
MP:0011689	MP:0011689	absent neutrophils	Mammalian_phenotype	11
MP:0011690	MP:0011690	absent basophils	Mammalian_phenotype	11
MP:0011694	MP:0011694	absent eosinophils	Mammalian_phenotype	11
MP:0011696	MP:0011696	absent mast cells	Mammalian_phenotype	11
MP:0011814	MP:0011814	abnormal pre-pro B cell morphology	Mammalian_phenotype	11
MP:0011981	MP:0011981	abnormal microglial cell differentiation	Mammalian_phenotype	11
MP:0011982	MP:0011982	decreased microglial cell number	Mammalian_phenotype	11
MP:0000091	MP:0000091	short premaxilla	Mammalian_phenotype	11
MP:0000430	MP:0000430	absent maxillary shelf	Mammalian_phenotype	11
MP:0000431	MP:0000431	absent palatine shelf	Mammalian_phenotype	11
MP:0000861	MP:0000861	disorganized barrel cortex	Mammalian_phenotype	11
MP:0000862	MP:0000862	absent barrels in primary somatosensory cortex	Mammalian_phenotype	11
MP:0000870	MP:0000870	absent cerebellum vermis lobule VIII	Mammalian_phenotype	11
MP:0000871	MP:0000871	absent cerebellum vermis lobule IX	Mammalian_phenotype	11
MP:0000878	MP:0000878	abnormal Purkinje cell number	Mammalian_phenotype	11
MP:0001829	MP:0001829	increased activated T cell number	Mammalian_phenotype	11
MP:0001830	MP:0001830	decreased activated T cell number	Mammalian_phenotype	11
MP:0002403	MP:0002403	abnormal pre-B cell morphology	Mammalian_phenotype	11
MP:0003905	MP:0003905	abnormal aorta elastin content	Mammalian_phenotype	11
MP:0012444	MP:0012444	thin hippocampus molecular cell layer	Mammalian_phenotype	11
MP:0012445	MP:0012445	thin hippocampus stratum radiatum	Mammalian_phenotype	11
MP:0012446	MP:0012446	thin hippocampus stratum oriens	Mammalian_phenotype	11
MP:0012452	MP:0012452	increased retrosplenial granular cortex size	Mammalian_phenotype	11
MP:0012453	MP:0012453	decreased retrosplenial granular cortex size	Mammalian_phenotype	11
MP:0012764	MP:0012764	increased alpha-beta T cell number	Mammalian_phenotype	11
MP:0012765	MP:0012765	decreased alpha-beta T cell number	Mammalian_phenotype	11
MP:0012767	MP:0012767	increased KLRG1-positive NK cell number	Mammalian_phenotype	11
MP:0012768	MP:0012768	decreased KLRG1-positive NK cell number	Mammalian_phenotype	11
MP:0012769	MP:0012769	abnormal CD4-positive, alpha-beta memory T cell number	Mammalian_phenotype	11
MP:0012772	MP:0012772	abnormal central memory CD8-positive, alpha-beta T cell number	Mammalian_phenotype	11
MP:0012773	MP:0012773	abnormal CD4-positive, CD25-positive, alpha-beta regulatory T cell number	Mammalian_phenotype	11
MP:0012774	MP:0012774	abnormal CD8-positive, alpha-beta memory T cell number	Mammalian_phenotype	11
MP:0013015	MP:0013015	abnormal CD4-positive, alpha beta T cell number	Mammalian_phenotype	11
MP:0013021	MP:0013021	abnormal Ly6C high monocyte number	Mammalian_phenotype	11
MP:0013024	MP:0013024	abnormal Ly6C low monocyte number	Mammalian_phenotype	11
MP:0020068	MP:0020068	increased neocortex volume	Mammalian_phenotype	11
MP:0020070	MP:0020070	decreased neocortex volume	Mammalian_phenotype	11
MP:0020082	MP:0020082	increased hippocampus volume	Mammalian_phenotype	11
MP:0020083	MP:0020083	decreased hippocampus volume	Mammalian_phenotype	11
MP:0004160	MP:0004160	retroesophageal right subclavian artery	Mammalian_phenotype	11
MP:0004301	MP:0004301	absent organ of Corti supporting cells	Mammalian_phenotype	11
MP:0004325	MP:0004325	absent vestibular hair cells	Mammalian_phenotype	11
MP:0004395	MP:0004395	increased cochlear inner hair cell number	Mammalian_phenotype	11
MP:0004396	MP:0004396	decreased cochlear inner hair cell number	Mammalian_phenotype	11
MP:0004401	MP:0004401	increased cochlear outer hair cell number	Mammalian_phenotype	11
MP:0004402	MP:0004402	decreased cochlear outer hair cell number	Mammalian_phenotype	11
MP:0004405	MP:0004405	absent cochlear hair cells	Mammalian_phenotype	11
MP:0004455	MP:0004455	pterygoid bone hypoplasia	Mammalian_phenotype	11
MP:0004491	MP:0004491	abnormal orientation of outer hair cell stereociliary bundles	Mammalian_phenotype	11
MP:0004492	MP:0004492	abnormal orientation of inner hair cell stereociliary bundles	Mammalian_phenotype	11
MP:0004528	MP:0004528	fused outer hair cell stereocilia	Mammalian_phenotype	11
MP:0004529	MP:0004529	decreased outer hair cell stereocilia number	Mammalian_phenotype	11
MP:0004530	MP:0004530	absent outer hair cell stereocilia	Mammalian_phenotype	11
MP:0004531	MP:0004531	short outer hair cell stereocilia	Mammalian_phenotype	11
MP:0004533	MP:0004533	fused inner hair cell stereocilia	Mammalian_phenotype	11
MP:0004534	MP:0004534	decreased inner hair cell stereocilia number	Mammalian_phenotype	11
MP:0004535	MP:0004535	absent inner hair cell stereocilia	Mammalian_phenotype	11
MP:0004536	MP:0004536	short inner hair cell stereocilia	Mammalian_phenotype	11
MP:0004563	MP:0004563	absent active-zone-anchored inner hair cell synaptic ribbon	Mammalian_phenotype	11
MP:0004578	MP:0004578	abnormal cochlear hair bundle tip links morphology	Mammalian_phenotype	11
MP:0004579	MP:0004579	abnormal cochlear hair bundle horizontal top connectors morphology	Mammalian_phenotype	11
MP:0004580	MP:0004580	abnormal cochlear hair bundle transient lateral links morphology	Mammalian_phenotype	11
MP:0004581	MP:0004581	abnormal cochlear hair bundle ankle links morphology	Mammalian_phenotype	11
MP:0004584	MP:0004584	abnormal vestibular hair bundle shaft connectors	Mammalian_phenotype	11
MP:0004871	MP:0004871	premaxilla hypoplasia	Mammalian_phenotype	11
MP:0004911	MP:0004911	absent mandibular condyloid process	Mammalian_phenotype	11
MP:0004912	MP:0004912	absent mandibular coronoid process	Mammalian_phenotype	11
MP:0004918	MP:0004918	abnormal negative T cell selection	Mammalian_phenotype	11
MP:0004919	MP:0004919	abnormal positive T cell selection	Mammalian_phenotype	11
MP:0004943	MP:0004943	abnormal B cell positive selection	Mammalian_phenotype	11
MP:0004944	MP:0004944	abnormal B cell negative selection	Mammalian_phenotype	11
MP:0004973	MP:0004973	increased regulatory T cell number	Mammalian_phenotype	11
MP:0004974	MP:0004974	decreased regulatory T cell number	Mammalian_phenotype	11
MP:0004976	MP:0004976	abnormal B-1 B cell number	Mammalian_phenotype	11
MP:0004983	MP:0004983	abnormal osteoclast cell number	Mammalian_phenotype	11
MP:0005019	MP:0005019	abnormal early pro-B cell	Mammalian_phenotype	11
MP:0005020	MP:0005020	abnormal late pro-B cell	Mammalian_phenotype	11
MP:0005089	MP:0005089	decreased double-negative T cell number	Mammalian_phenotype	11
MP:0005090	MP:0005090	increased double-negative T cell number	Mammalian_phenotype	11
MP:0005091	MP:0005091	increased double-positive T cell number	Mammalian_phenotype	11
MP:0005092	MP:0005092	decreased double-positive T cell number	Mammalian_phenotype	11
MP:0005094	MP:0005094	abnormal T cell proliferation	Mammalian_phenotype	11
MP:0005153	MP:0005153	abnormal B cell proliferation	Mammalian_phenotype	11
MP:0008039	MP:0008039	increased NK T cell number	Mammalian_phenotype	11
MP:0008040	MP:0008040	decreased NK T cell number	Mammalian_phenotype	11
MP:0008046	MP:0008046	absent NK cells	Mammalian_phenotype	11
MP:0008047	MP:0008047	absent uterine NK cells	Mammalian_phenotype	11
MP:0008049	MP:0008049	increased memory T cell number	Mammalian_phenotype	11
MP:0008050	MP:0008050	decreased memory T cell number	Mammalian_phenotype	11
MP:0008061	MP:0008061	absent podocyte slit diaphragm	Mammalian_phenotype	11
MP:0008068	MP:0008068	absent retinal ganglion cell	Mammalian_phenotype	11
MP:0008070	MP:0008070	absent T cells	Mammalian_phenotype	11
MP:0008071	MP:0008071	absent B cells	Mammalian_phenotype	11
MP:0008082	MP:0008082	increased single-positive T cell number	Mammalian_phenotype	11
MP:0008083	MP:0008083	decreased single-positive T cell number	Mammalian_phenotype	11
MP:0008097	MP:0008097	increased plasma cell number	Mammalian_phenotype	11
MP:0008098	MP:0008098	decreased plasma cell number	Mammalian_phenotype	11
MP:0008119	MP:0008119	decreased Langerhans cell number	Mammalian_phenotype	11
MP:0008164	MP:0008164	abnormal B-1a B cell morphology	Mammalian_phenotype	11
MP:0008165	MP:0008165	abnormal B-1b B cell morphology	Mammalian_phenotype	11
MP:0008173	MP:0008173	increased follicular B cell number	Mammalian_phenotype	11
MP:0008174	MP:0008174	decreased follicular B cell number	Mammalian_phenotype	11
MP:0008177	MP:0008177	increased germinal center B cell number	Mammalian_phenotype	11
MP:0008178	MP:0008178	decreased germinal center B cell number	Mammalian_phenotype	11
MP:0008181	MP:0008181	increased marginal zone B cell number	Mammalian_phenotype	11
MP:0008182	MP:0008182	decreased marginal zone B cell number	Mammalian_phenotype	11
MP:0008185	MP:0008185	decreased naive B cell number	Mammalian_phenotype	11
MP:0008186	MP:0008186	increased pro-B cell number	Mammalian_phenotype	11
MP:0008188	MP:0008188	abnormal transitional stage B cell morphology	Mammalian_phenotype	11
MP:0008206	MP:0008206	increased B-2 B cell number	Mammalian_phenotype	11
MP:0008207	MP:0008207	decreased B-2 B cell number	Mammalian_phenotype	11
MP:0008208	MP:0008208	decreased pro-B cell number	Mammalian_phenotype	11
MP:0008214	MP:0008214	increased immature B cell number	Mammalian_phenotype	11
MP:0008215	MP:0008215	decreased immature B cell number	Mammalian_phenotype	11
MP:0008233	MP:0008233	abnormal pro-B cell differentiation	Mammalian_phenotype	11
MP:0008264	MP:0008264	absent hippocampus CA1 region	Mammalian_phenotype	11
MP:0008266	MP:0008266	absent hippocampus CA2 region	Mammalian_phenotype	11
MP:0008268	MP:0008268	absent hippocampus CA3 region	Mammalian_phenotype	11
MP:0008270	MP:0008270	absent hippocampus CA4 region	Mammalian_phenotype	11
MP:0008346	MP:0008346	increased gamma-delta T cell number	Mammalian_phenotype	11
MP:0008347	MP:0008347	decreased gamma-delta T cell number	Mammalian_phenotype	11
MP:0008350	MP:0008350	increased gamma-delta intraepithelial T cell number	Mammalian_phenotype	11
MP:0008351	MP:0008351	decreased gamma-delta intraepithelial T cell number	Mammalian_phenotype	11
MP:0008353	MP:0008353	increased mature gamma-delta T cell number	Mammalian_phenotype	11
MP:0008354	MP:0008354	decreased mature gamma-delta T cell number	Mammalian_phenotype	11
MP:0008444	MP:0008444	retinal cone cell degeneration	Mammalian_phenotype	11
MP:0008445	MP:0008445	increased retinal cone cell number	Mammalian_phenotype	11
MP:0008446	MP:0008446	decreased retinal cone cell number	Mammalian_phenotype	11
MP:0008448	MP:0008448	abnormal retinal cone cell inner segment morphology	Mammalian_phenotype	11
MP:0008449	MP:0008449	abnormal retinal cone cell outer segment morphology	Mammalian_phenotype	11
MP:0008451	MP:0008451	retinal rod cell degeneration	Mammalian_phenotype	11
MP:0008452	MP:0008452	increased retinal rod cell number	Mammalian_phenotype	11
MP:0008453	MP:0008453	decreased retinal rod cell number	Mammalian_phenotype	11
MP:0008455	MP:0008455	abnormal retinal rod cell inner segment morphology	Mammalian_phenotype	11
MP:0008456	MP:0008456	abnormal retinal rod cell outer segment morphology	Mammalian_phenotype	11
MP:0008580	MP:0008580	photoreceptor inner segment degeneration	Mammalian_phenotype	11
MP:0008581	MP:0008581	disorganized photoreceptor inner segment	Mammalian_phenotype	11
MP:0008582	MP:0008582	short photoreceptor inner segment	Mammalian_phenotype	11
MP:0008583	MP:0008583	absent photoreceptor inner segment	Mammalian_phenotype	11
MP:0008584	MP:0008584	photoreceptor outer segment degeneration	Mammalian_phenotype	11
MP:0008585	MP:0008585	absent photoreceptor outer segment	Mammalian_phenotype	11
MP:0008586	MP:0008586	disorganized photoreceptor outer segment	Mammalian_phenotype	11
MP:0008587	MP:0008587	short photoreceptor outer segment	Mammalian_phenotype	11
MP:0008756	MP:0008756	abnormal T cell receptor alpha chain V-J recombination	Mammalian_phenotype	11
MP:0008757	MP:0008757	abnormal T cell receptor gamma chain V-J recombination	Mammalian_phenotype	11
MP:0008758	MP:0008758	abnormal T cell receptor beta chain V(D)J recombination	Mammalian_phenotype	11
MP:0008759	MP:0008759	abnormal T cell receptor delta chain V(D)J recombination	Mammalian_phenotype	11
MP:0008760	MP:0008760	abnormal immunoglobulin heavy chain V(D)J recombination	Mammalian_phenotype	11
MP:0008761	MP:0008761	abnormal immunoglobulin light chain V-J recombination	Mammalian_phenotype	11
MP:0004397	MP:0004397	absent cochlear inner hair cells	Mammalian_phenotype	12
MP:0004403	MP:0004403	absent cochlear outer hair cells	Mammalian_phenotype	12
MP:0004582	MP:0004582	absent cochlear hair bundle ankle links	Mammalian_phenotype	12
MP:0004585	MP:0004585	absent vestibular hair bundle shaft connectors	Mammalian_phenotype	12
MP:0004975	MP:0004975	absent regulatory T cells	Mammalian_phenotype	12
MP:0004977	MP:0004977	increased B-1 B cell number	Mammalian_phenotype	12
MP:0004978	MP:0004978	decreased B-1 B cell number	Mammalian_phenotype	12
MP:0004984	MP:0004984	increased osteoclast cell number	Mammalian_phenotype	12
MP:0004985	MP:0004985	decreased osteoclast cell number	Mammalian_phenotype	12
MP:0005093	MP:0005093	decreased B cell proliferation	Mammalian_phenotype	12
MP:0005095	MP:0005095	decreased T cell proliferation	Mammalian_phenotype	12
MP:0005154	MP:0005154	increased B cell proliferation	Mammalian_phenotype	12
MP:0005348	MP:0005348	increased T cell proliferation	Mammalian_phenotype	12
MP:0005433	MP:0005433	absent early pro-B cells	Mammalian_phenotype	12
MP:0005434	MP:0005434	absent late pro-B cells	Mammalian_phenotype	12
MP:0008041	MP:0008041	absent NK T cells	Mammalian_phenotype	12
MP:0008072	MP:0008072	absent double-negative T cells	Mammalian_phenotype	12
MP:0008074	MP:0008074	increased CD4-positive T cell number	Mammalian_phenotype	12
MP:0008075	MP:0008075	decreased CD4-positive T cell number	Mammalian_phenotype	12
MP:0008078	MP:0008078	increased CD8-positive T cell number	Mammalian_phenotype	12
MP:0008079	MP:0008079	decreased CD8-positive T cell number	Mammalian_phenotype	12
MP:0008084	MP:0008084	absent single-positive T cells	Mammalian_phenotype	12
MP:0008085	MP:0008085	abnormal T-helper 1 cell number	Mammalian_phenotype	12
MP:0008088	MP:0008088	abnormal T-helper 1 cell differentiation	Mammalian_phenotype	12
MP:0008089	MP:0008089	abnormal T-helper 2 cell number	Mammalian_phenotype	12
MP:0008092	MP:0008092	abnormal T-helper 2 cell differentiation	Mammalian_phenotype	12
MP:0008167	MP:0008167	increased B-1a cell number	Mammalian_phenotype	12
MP:0008168	MP:0008168	decreased B-1a cell number	Mammalian_phenotype	12
MP:0008169	MP:0008169	increased B-1b cell number	Mammalian_phenotype	12
MP:0008170	MP:0008170	decreased B-1b cell number	Mammalian_phenotype	12
MP:0008187	MP:0008187	absent pro-B cells	Mammalian_phenotype	12
MP:0008189	MP:0008189	increased transitional stage B cell number	Mammalian_phenotype	12
MP:0008190	MP:0008190	decreased transitional stage B cell number	Mammalian_phenotype	12
MP:0008209	MP:0008209	decreased pre-B cell number	Mammalian_phenotype	12
MP:0008212	MP:0008212	absent mature B cells	Mammalian_phenotype	12
MP:0008213	MP:0008213	absent immature B cells	Mammalian_phenotype	12
MP:0008348	MP:0008348	absent gamma-delta T cells	Mammalian_phenotype	12
MP:0008357	MP:0008357	abnormal CD4-positive, gamma-delta intraepithelial T cell morphology	Mammalian_phenotype	12
MP:0008361	MP:0008361	abnormal CD8-positive, gamma-delta intraepithelial T cell morphology	Mammalian_phenotype	12
MP:0008447	MP:0008447	absent retinal cone cells	Mammalian_phenotype	12
MP:0008454	MP:0008454	absent retinal rod cells	Mammalian_phenotype	12
MP:0008728	MP:0008728	increased memory B cell number	Mammalian_phenotype	12
MP:0008729	MP:0008729	decreased memory B cell number	Mammalian_phenotype	12
MP:0002433	MP:0002433	abnormal T-helper 1 cell morphology	Mammalian_phenotype	12
MP:0002434	MP:0002434	abnormal T-helper 2 cell morphology	Mammalian_phenotype	12
MP:0003132	MP:0003132	increased pre-B cell number	Mammalian_phenotype	12
MP:0003133	MP:0003133	increased early pro-B cell number	Mammalian_phenotype	12
MP:0003134	MP:0003134	increased late pro-B cell number	Mammalian_phenotype	12
MP:0003906	MP:0003906	increased aorta elastin content	Mammalian_phenotype	12
MP:0003907	MP:0003907	decreased aorta elastin content	Mammalian_phenotype	12
MP:0009896	MP:0009896	palatine shelf hypoplasia	Mammalian_phenotype	12
MP:0009898	MP:0009898	maxillary shelf hypoplasia	Mammalian_phenotype	12
MP:0009919	MP:0009919	abnormal transitional stage T1 B cell morphology	Mammalian_phenotype	12
MP:0009920	MP:0009920	abnormal transitional stage T2 B cell morphology	Mammalian_phenotype	12
MP:0009921	MP:0009921	abnormal transitional stage T3 B cell morphology	Mammalian_phenotype	12
MP:0009958	MP:0009958	absent cerebellar granule cells	Mammalian_phenotype	12
MP:0010014	MP:0010014	hippocampus pyramidal cell degeneration	Mammalian_phenotype	12
MP:0010129	MP:0010129	increased DN1 thymic pro-T cell number	Mammalian_phenotype	12
MP:0010130	MP:0010130	decreased DN1 thymic pro-T cell number	Mammalian_phenotype	12
MP:0010131	MP:0010131	increased DN2 thymocyte number	Mammalian_phenotype	12
MP:0010132	MP:0010132	decreased DN2 thymocyte number	Mammalian_phenotype	12
MP:0010133	MP:0010133	increased DN3 thymocyte number	Mammalian_phenotype	12
MP:0010134	MP:0010134	decreased DN3 thymocyte number	Mammalian_phenotype	12
MP:0010135	MP:0010135	increased DN4 thymocyte number	Mammalian_phenotype	12
MP:0010136	MP:0010136	decreased DN4 thymocyte number	Mammalian_phenotype	12
MP:0010168	MP:0010168	increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number	Mammalian_phenotype	12
MP:0010169	MP:0010169	decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number	Mammalian_phenotype	12
MP:0010184	MP:0010184	abnormal T follicular helper cell morphology	Mammalian_phenotype	12
MP:0010185	MP:0010185	abnormal T follicular helper cell number	Mammalian_phenotype	12
MP:0010188	MP:0010188	abnormal T follicular helper cell differentiation	Mammalian_phenotype	12
MP:0010217	MP:0010217	abnormal T-helper 17 cell morphology	Mammalian_phenotype	12
MP:0010218	MP:0010218	abnormal T-helper 17 cell number	Mammalian_phenotype	12
MP:0010672	MP:0010672	increased Tc17 cell number	Mammalian_phenotype	12
MP:0010673	MP:0010673	decreased Tc17 cell number	Mammalian_phenotype	12
MP:0010835	MP:0010835	increased CD4-positive, alpha-beta memory T cell number	Mammalian_phenotype	12
MP:0010836	MP:0010836	decreased CD4-positive, alpha-beta memory T cell number	Mammalian_phenotype	12
MP:0010838	MP:0010838	increased CD8-positive, alpha-beta memory T cell number	Mammalian_phenotype	12
MP:0010839	MP:0010839	decreased CD8-positive, alpha-beta memory T cell number	Mammalian_phenotype	12
MP:0010840	MP:0010840	abnormal central memory CD4-positive, alpha-beta T cell morphology	Mammalian_phenotype	12
MP:0010843	MP:0010843	abnormal effector memory CD4-positive, alpha-beta T cell morphology	Mammalian_phenotype	12
MP:0010846	MP:0010846	abnormal central memory CD8 positive, alpha-beta T cell morphology	Mammalian_phenotype	12
MP:0011063	MP:0011063	absent inner hair cell kinocilia	Mammalian_phenotype	12
MP:0011815	MP:0011815	increased pre-pro B cell number	Mammalian_phenotype	12
MP:0011816	MP:0011816	decreased pre-pro B cell number	Mammalian_phenotype	12
MP:0012457	MP:0012457	increased hippocampus pyramidal cell length	Mammalian_phenotype	12
MP:0012458	MP:0012458	decreased hippocampus pyramidal cell length	Mammalian_phenotype	12
MP:0013016	MP:0013016	increased CD4-positive, alpha beta T cell number	Mammalian_phenotype	12
MP:0013017	MP:0013017	decreased CD4-positive, alpha beta T cell number	Mammalian_phenotype	12
MP:0013018	MP:0013018	abnormal CD8-positive alpha beta T cell number	Mammalian_phenotype	12
MP:0013019	MP:0013019	increased CD8-positive, alpha beta T cell number	Mammalian_phenotype	12
MP:0013020	MP:0013020	decreased CD8-positive, alpha beta T cell number	Mammalian_phenotype	12
MP:0013022	MP:0013022	increased Ly6C high monocyte number	Mammalian_phenotype	12
MP:0013023	MP:0013023	decreased Ly6C high monocyte number	Mammalian_phenotype	12
MP:0013025	MP:0013025	increased Ly6C low monocyte number	Mammalian_phenotype	12
MP:0013026	MP:0013026	decreased Ly6C low monocyte number	Mammalian_phenotype	12
MP:0013153	MP:0013153	abnormal KLRG1+ CD8 alpha beta T cell number	Mammalian_phenotype	13
MP:0013156	MP:0013156	abnormal KLRG1+ CD4 alpha beta T cell number	Mammalian_phenotype	13
MP:0000238	MP:0000238	absent pre-B cells	Mammalian_phenotype	13
MP:0000727	MP:0000727	absent CD8-positive T cells	Mammalian_phenotype	13
MP:0003790	MP:0003790	absent CD4-positive T cells	Mammalian_phenotype	13
MP:0008086	MP:0008086	increased T-helper 1 cell number	Mammalian_phenotype	13
MP:0008087	MP:0008087	decreased T helper 1 cell number	Mammalian_phenotype	13
MP:0008090	MP:0008090	increased T-helper 2 cell number	Mammalian_phenotype	13
MP:0008091	MP:0008091	decreased T-helper 2 cell number	Mammalian_phenotype	13
MP:0008094	MP:0008094	absent memory B cells	Mammalian_phenotype	13
MP:0008100	MP:0008100	absent plasma cells	Mammalian_phenotype	13
MP:0008118	MP:0008118	absent Langerhans cell	Mammalian_phenotype	13
MP:0008175	MP:0008175	absent follicular B cells	Mammalian_phenotype	13
MP:0008179	MP:0008179	absent germinal center B cells	Mammalian_phenotype	13
MP:0008183	MP:0008183	absent marginal zone B cells	Mammalian_phenotype	13
MP:0008202	MP:0008202	absent B-1 B cells	Mammalian_phenotype	13
MP:0008205	MP:0008205	absent B-2 B cells	Mammalian_phenotype	13
MP:0008216	MP:0008216	absent transitional stage B cells	Mammalian_phenotype	13
MP:0008355	MP:0008355	absent mature gamma-delta T cells	Mammalian_phenotype	13
MP:0008358	MP:0008358	increased CD4-positive, gamma-delta intraepithelial T cell number	Mammalian_phenotype	13
MP:0008359	MP:0008359	decreased CD4-positive, gamma-delta intraepithelial T cell number	Mammalian_phenotype	13
MP:0008362	MP:0008362	increased CD8-positive, gamma-delta intraepithelial T cell number	Mammalian_phenotype	13
MP:0008363	MP:0008363	decreased CD8-positive, gamma-delta intraepithelial T cell number	Mammalian_phenotype	13
MP:0009922	MP:0009922	increased transitional stage T1 B cell number	Mammalian_phenotype	13
MP:0009923	MP:0009923	decreased transitional stage T1 B cell number	Mammalian_phenotype	13
MP:0009925	MP:0009925	increased transitional stage T2 B cell number	Mammalian_phenotype	13
MP:0009926	MP:0009926	decreased transitional stage T2 B cell number	Mammalian_phenotype	13
MP:0009972	MP:0009972	absent hippocampus pyramidal cells	Mammalian_phenotype	13
MP:0010186	MP:0010186	increased T follicular helper cell number	Mammalian_phenotype	13
MP:0010187	MP:0010187	decreased T follicular helper cell number	Mammalian_phenotype	13
MP:0010219	MP:0010219	increased T-helper 17 cell number	Mammalian_phenotype	13
MP:0010220	MP:0010220	decreased T-helper 17 cell number	Mammalian_phenotype	13
MP:0010228	MP:0010228	decreased transitional stage T3 B cell number	Mammalian_phenotype	13
MP:0010229	MP:0010229	increased transitional stage T3 B cell number	Mammalian_phenotype	13
MP:0010841	MP:0010841	increased central memory CD4-positive, alpha-beta T cell number	Mammalian_phenotype	13
MP:0010842	MP:0010842	decreased central memory CD4-positive, alpha-beta T cell number	Mammalian_phenotype	13
MP:0010844	MP:0010844	increased effector memory CD4-positive, alpha-beta T cell number	Mammalian_phenotype	13
MP:0010845	MP:0010845	decreased effector memory CD4-positive, alpha-beta T cell number	Mammalian_phenotype	13
MP:0011817	MP:0011817	absent pre-pro B cells	Mammalian_phenotype	13
MP:0009924	MP:0009924	absent transitional stage T1 B cells	Mammalian_phenotype	14
MP:0009927	MP:0009927	absent transitional stage T2 B cells	Mammalian_phenotype	14
MP:0010230	MP:0010230	absent transitional stage T3 B cells	Mammalian_phenotype	14
MP:0010847	MP:0010847	increased central memory CD8 positive, alpha-beta T cell number	Mammalian_phenotype	14
MP:0010848	MP:0010848	decreased central memory CD8 positive, alpha-beta T cell number	Mammalian_phenotype	14
MP:0010850	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number	Mammalian_phenotype	14
MP:0010851	MP:0010851	decreased effector memory CD8-positive, alpha-beta T cell number	Mammalian_phenotype	14
MP:0008203	MP:0008203	absent B-1a cells	Mammalian_phenotype	14
MP:0008204	MP:0008204	absent B-1b cells	Mammalian_phenotype	14
MP:0008352	MP:0008352	absent gamma-delta intraepithelial T cell	Mammalian_phenotype	14
MP:0012770	MP:0012770	abnormal effector memory CD4-positive, alpha-beta T cell number	Mammalian_phenotype	14
MP:0012771	MP:0012771	abnormal central memory CD4-positive, alpha-beta T cell number	Mammalian_phenotype	14
MP:0013154	MP:0013154	increased KLRG1+ CD8 alpha beta T cell number	Mammalian_phenotype	14
MP:0013155	MP:0013155	decreased KLRG1+ CD8 alpha beta T cell number	Mammalian_phenotype	14
MP:0013157	MP:0013157	increased KLRG1+ CD4 alpha beta T cell number	Mammalian_phenotype	14
MP:0013158	MP:0013158	decreased KLRG1+ CD4 alpha beta T cell number	Mammalian_phenotype	14
MP:0008360	MP:0008360	absent CD4-positive, gamma-delta intraepithelial T cells	Mammalian_phenotype	15
MP:0008364	MP:0008364	absent CD8-positive, gamma-delta intraepithelial T cells	Mammalian_phenotype	15