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Top SNP Information Show Table

Associated Phenotypes ^ⓘ Shared SNP phenotypes No shared SNP phenotypes

ID	Name	Top Correlation
HP: 0002664	Neoplasm	1/20
HP: 0010614	Fibroma	1/20
HP: 0011623	Muscular ventricular septal defect	1/20
HP: 0011624	Apical muscular ventricular septal defect	1/20
HP: 0011793	Neoplasm by anatomical site	1/20
HP: 0012316	Fibrous tissue neoplasm	1/20

ID	Name	Top Correlation
HP: 0000002	Abnormality of body height	0/20
HP: 0000003	Multicystic kidney dysplasia	0/20
HP: 0000005	Mode of inheritance	0/20
HP: 0000006	Autosomal dominant inheritance	0/20
HP: 0000008	Abnormal morphology of female internal genitalia	0/20
HP: 0000009	Functional abnormality of the bladder	0/20
HP: 0000010	Recurrent urinary tract infections	0/20
HP: 0000013	Hypoplasia of the uterus	0/20
HP: 0000014	Abnormality of the bladder	0/20
HP: 0000015	Bladder diverticulum	0/20
HP: 0000016	Urinary retention	0/20
HP: 0000020	Urinary incontinence	0/20
HP: 0000022	Abnormality of male internal genitalia	0/20
HP: 0000023	Inguinal hernia	0/20
HP: 0000025	Functional abnormality of male internal genitalia	0/20
HP: 0000027	Azoospermia	0/20
HP: 0000028	Cryptorchidism	0/20
HP: 0000032	Abnormality of male external genitalia	0/20
HP: 0000034	Hydrocele testis	0/20
HP: 0000035	Abnormal testis morphology	0/20
HP: 0000036	Abnormality of the penis	0/20
HP: 0000037	Male pseudohermaphroditism	0/20
HP: 0000039	Epispadias	0/20
HP: 0000041	Chordee	0/20
HP: 0000045	Abnormality of the scrotum	0/20
HP: 0000047	Hypospadias	0/20
HP: 0000050	Hypoplastic male external genitalia	0/20
HP: 0000051	Perineal hypospadias	0/20
HP: 0000053	Macroorchidism	0/20
HP: 0000054	Micropenis	0/20
HP: 0000055	Abnormality of female external genitalia	0/20
HP: 0000056	Abnormality of the clitoris	0/20
HP: 0000058	Abnormality of the labia	0/20
HP: 0000059	Hypoplastic labia majora	0/20
HP: 0000063	Fused labia minora	0/20
HP: 0000066	Labial hypoplasia	0/20
HP: 0000068	Urethral atresia	0/20
HP: 0000069	Abnormality of the ureter	0/20
HP: 0000070	Ureterocele	0/20
HP: 0000071	Ureteral stenosis	0/20
HP: 0000072	Hydroureter	0/20
HP: 0000073	Ureteral duplication	0/20
HP: 0000074	Ureteropelvic junction obstruction	0/20
HP: 0000075	Renal duplication	0/20
HP: 0000076	Vesicoureteral reflux	0/20
HP: 0000077	Abnormality of the kidney	0/20
HP: 0000078	Abnormality of the genital system	0/20
HP: 0000079	Abnormality of the urinary system	0/20
HP: 0000080	Abnormality of reproductive system physiology	0/20
HP: 0000083	Renal insufficiency	0/20
HP: 0000085	Horseshoe kidney	0/20
HP: 0000086	Ectopic kidney	0/20
HP: 0000089	Renal hypoplasia	0/20
HP: 0000091	Abnormal renal tubule morphology	0/20
HP: 0000095	Abnormality of renal glomerulus morphology	0/20
HP: 0000098	Tall stature	0/20
HP: 0000100	Nephrotic syndrome	0/20
HP: 0000104	Renal agenesis	0/20
HP: 0000105	Enlarged kidney	0/20
HP: 0000107	Renal cyst	0/20
HP: 0000113	Polycystic kidney dysplasia	0/20
HP: 0000118	Phenotypic abnormality	0/20
HP: 0000119	Abnormality of the genitourinary system	0/20
HP: 0000122	Unilateral renal agenesis	0/20
HP: 0000123	Nephritis	0/20
HP: 0000125	Pelvic kidney	0/20
HP: 0000126	Hydronephrosis	0/20
HP: 0000127	Renal salt wasting	0/20
HP: 0000130	Abnormality of the uterus	0/20
HP: 0000133	Gonadal dysgenesis	0/20
HP: 0000135	Hypogonadism	0/20
HP: 0000137	Abnormality of the ovary	0/20
HP: 0000138	Ovarian cyst	0/20
HP: 0000140	Abnormality of the menstrual cycle	0/20
HP: 0000141	Amenorrhea	0/20
HP: 0000142	Abnormal vagina morphology	0/20
HP: 0000143	Rectovaginal fistula	0/20
HP: 0000148	Vaginal atresia	0/20
HP: 0000150	Gonadoblastoma	0/20
HP: 0000151	Aplasia of the uterus	0/20
HP: 0000152	Abnormality of head or neck	0/20
HP: 0000153	Abnormality of the mouth	0/20
HP: 0000157	Abnormality of the tongue	0/20
HP: 0000158	Macroglossia	0/20
HP: 0000159	Abnormal lip morphology	0/20
HP: 0000160	Narrow mouth	0/20
HP: 0000163	Abnormal oral cavity morphology	0/20
HP: 0000164	Abnormality of the dentition	0/20
HP: 0000168	Abnormality of the gingiva	0/20
HP: 0000172	Abnormality of the uvula	0/20
HP: 0000174	Abnormal palate morphology	0/20
HP: 0000175	Cleft palate	0/20
HP: 0000177	Abnormality of upper lip	0/20
HP: 0000185	Cleft soft palate	0/20
HP: 0000190	Abnormal oral frenulum morphology	0/20
HP: 0000193	Bifid uvula	0/20
HP: 0000202	Oral cleft	0/20
HP: 0000204	Cleft upper lip	0/20
HP: 0000205	Pursed lips	0/20
HP: 0000206	Glossitis	0/20
HP: 0000212	Gingival overgrowth	0/20
HP: 0000215	Thick upper lip vermilion	0/20
HP: 0000221	Furrowed tongue	0/20
HP: 0000234	Abnormality of the head	0/20
HP: 0000235	Abnormality of the fontanelles or cranial sutures	0/20
HP: 0000238	Hydrocephalus	0/20
HP: 0000240	Abnormality of skull size	0/20
HP: 0000252	Microcephaly	0/20
HP: 0000253	Progressive microcephaly	0/20
HP: 0000271	Abnormality of the face	0/20
HP: 0000276	Long face	0/20
HP: 0000277	Abnormality of the mandible	0/20
HP: 0000278	Retrognathia	0/20
HP: 0000282	Facial edema	0/20
HP: 0000286	Epicanthus	0/20
HP: 0000288	Abnormality of the philtrum	0/20
HP: 0000290	Abnormality of the forehead	0/20
HP: 0000309	Abnormality of the midface	0/20
HP: 0000315	Abnormality of the orbital region	0/20
HP: 0000324	Facial asymmetry	0/20
HP: 0000325	Triangular face	0/20
HP: 0000326	Abnormality of the maxilla	0/20
HP: 0000329	Facial hemangioma	0/20
HP: 0000336	Prominent supraorbital ridges	0/20
HP: 0000347	Micrognathia	0/20
HP: 0000356	Abnormality of the outer ear	0/20
HP: 0000357	Abnormal location of ears	0/20
HP: 0000358	Posteriorly rotated ears	0/20
HP: 0000359	Abnormality of the inner ear	0/20
HP: 0000363	Abnormality of earlobe	0/20
HP: 0000364	Hearing abnormality	0/20
HP: 0000365	Hearing impairment	0/20
HP: 0000366	Abnormality of the nose	0/20
HP: 0000369	Low-set ears	0/20
HP: 0000370	Abnormality of the middle ear	0/20
HP: 0000372	Abnormality of the auditory canal	0/20
HP: 0000375	Abnormal cochlea morphology	0/20
HP: 0000377	Abnormality of the pinna	0/20
HP: 0000383	Abnormality of periauricular region	0/20
HP: 0000384	Preauricular skin tag	0/20
HP: 0000387	Absent earlobe	0/20
HP: 0000388	Otitis media	0/20
HP: 0000405	Conductive hearing impairment	0/20
HP: 0000407	Sensorineural hearing impairment	0/20
HP: 0000410	Mixed hearing impairment	0/20
HP: 0000411	Protruding ear	0/20
HP: 0000415	Abnormality of the choanae	0/20
HP: 0000418	Narrow nasal ridge	0/20
HP: 0000422	Abnormality of the nasal bridge	0/20
HP: 0000429	Abnormality of the nasal alae	0/20
HP: 0000436	Abnormality of the nasal tip	0/20
HP: 0000452	Choanal stenosis	0/20
HP: 0000453	Choanal atresia	0/20
HP: 0000458	Anosmia	0/20
HP: 0000464	Abnormality of the neck	0/20
HP: 0000465	Webbed neck	0/20
HP: 0000476	Cystic hygroma	0/20
HP: 0000478	Abnormality of the eye	0/20
HP: 0000479	Abnormal retinal morphology	0/20
HP: 0000481	Abnormal cornea morphology	0/20
HP: 0000482	Microcornea	0/20
HP: 0000485	Megalocornea	0/20
HP: 0000486	Strabismus	0/20
HP: 0000492	Abnormal eyelid morphology	0/20
HP: 0000493	Abnormal foveal morphology	0/20
HP: 0000494	Downslanted palpebral fissures	0/20
HP: 0000496	Abnormality of eye movement	0/20
HP: 0000499	Abnormal eyelash morphology	0/20
HP: 0000501	Glaucoma	0/20
HP: 0000502	Abnormal conjunctiva morphology	0/20
HP: 0000504	Abnormality of vision	0/20
HP: 0000508	Ptosis	0/20
HP: 0000517	Abnormality of the lens	0/20
HP: 0000518	Cataract	0/20
HP: 0000519	Developmental cataract	0/20
HP: 0000520	Proptosis	0/20
HP: 0000525	Abnormality iris morphology	0/20
HP: 0000526	Aniridia	0/20
HP: 0000528	Anophthalmia	0/20
HP: 0000532	Abnormal chorioretinal morphology	0/20
HP: 0000534	Abnormal eyebrow morphology	0/20
HP: 0000541	Retinal detachment	0/20
HP: 0000546	Retinal degeneration	0/20
HP: 0000549	Abnormal conjugate eye movement	0/20
HP: 0000553	Abnormal uvea morphology	0/20
HP: 0000556	Retinal dystrophy	0/20
HP: 0000573	Retinal hemorrhage	0/20
HP: 0000581	Blepharophimosis	0/20
HP: 0000587	Abnormality of the optic nerve	0/20
HP: 0000589	Coloboma	0/20
HP: 0000591	Abnormal sclera morphology	0/20
HP: 0000592	Blue sclerae	0/20
HP: 0000593	Abnormal anterior chamber morphology	0/20
HP: 0000598	Abnormality of the ear	0/20
HP: 0000599	Abnormality of the frontal hairline	0/20
HP: 0000600	Abnormality of the pharynx	0/20
HP: 0000606	Abnormality of the periorbital region	0/20
HP: 0000609	Optic nerve hypoplasia	0/20
HP: 0000610	Abnormal choroid morphology	0/20
HP: 0000612	Iris coloboma	0/20
HP: 0000614	Abnormal nasolacrimal system morphology	0/20
HP: 0000615	Abnormal pupil morphology	0/20
HP: 0000616	Miosis	0/20
HP: 0000620	Dacryocystitis	0/20
HP: 0000622	Blurred vision	0/20
HP: 0000625	Eyelid coloboma	0/20
HP: 0000632	Lacrimation abnormality	0/20
HP: 0000639	Nystagmus	0/20
HP: 0000652	Lower eyelid coloboma	0/20
HP: 0000664	Synophrys	0/20
HP: 0000668	Hypodontia	0/20
HP: 0000676	Abnormality of the incisor	0/20
HP: 0000689	Dental malocclusion	0/20
HP: 0000691	Microdontia	0/20
HP: 0000692	Misalignment of teeth	0/20
HP: 0000707	Abnormality of the nervous system	0/20
HP: 0000708	Behavioral abnormality	0/20
HP: 0000717	Autism	0/20
HP: 0000719	Inappropriate behavior	0/20
HP: 0000729	Autistic behavior	0/20
HP: 0000735	Impaired social interactions	0/20
HP: 0000736	Short attention span	0/20
HP: 0000748	Inappropriate laughter	0/20
HP: 0000749	Paroxysmal bursts of laughter	0/20
HP: 0000750	Delayed speech and language development	0/20
HP: 0000752	Hyperactivity	0/20
HP: 0000759	Abnormal peripheral nervous system morphology	0/20
HP: 0000764	Peripheral axonal degeneration	0/20
HP: 0000765	Abnormality of the thorax	0/20
HP: 0000766	Abnormality of the sternum	0/20
HP: 0000768	Pectus carinatum	0/20
HP: 0000769	Abnormality of the breast	0/20
HP: 0000772	Abnormality of the ribs	0/20
HP: 0000773	Short ribs	0/20
HP: 0000774	Narrow chest	0/20
HP: 0000775	Abnormality of the diaphragm	0/20
HP: 0000776	Congenital diaphragmatic hernia	0/20
HP: 0000777	Abnormality of the thymus	0/20
HP: 0000778	Hypoplasia of the thymus	0/20
HP: 0000782	Abnormality of the scapula	0/20
HP: 0000786	Primary amenorrhea	0/20
HP: 0000787	Nephrolithiasis	0/20
HP: 0000795	Abnormality of the urethra	0/20
HP: 0000796	Urethral obstruction	0/20
HP: 0000803	Renal cortical cysts	0/20
HP: 0000808	Penoscrotal hypospadias	0/20
HP: 0000809	Urinary tract atresia	0/20
HP: 0000811	Abnormal external genitalia	0/20
HP: 0000812	Abnormal internal genitalia	0/20
HP: 0000813	Bicornuate uterus	0/20
HP: 0000826	Precocious puberty	0/20
HP: 0000828	Abnormality of the parathyroid gland	0/20
HP: 0000834	Abnormality of the adrenal glands	0/20
HP: 0000835	Adrenal hypoplasia	0/20
HP: 0000858	Irregular menstruation	0/20
HP: 0000860	Parathyroid hypoplasia	0/20
HP: 0000864	Abnormality of the hypothalamus-pituitary axis	0/20
HP: 0000886	Deformed rib cage	0/20
HP: 0000889	Abnormality of the clavicle	0/20
HP: 0000891	Cervical ribs	0/20
HP: 0000892	Bifid ribs	0/20
HP: 0000896	Rib exostoses	0/20
HP: 0000911	Flat glenoid fossa	0/20
HP: 0000912	Sprengel anomaly	0/20
HP: 0000917	Superior pectus carinatum	0/20
HP: 0000924	Abnormality of the skeletal system	0/20
HP: 0000925	Abnormality of the vertebral column	0/20
HP: 0000926	Platyspondyly	0/20
HP: 0000929	Abnormal skull morphology	0/20
HP: 0000932	Abnormality of the posterior cranial fossa	0/20
HP: 0000940	Abnormal diaphysis morphology	0/20
HP: 0000944	Abnormality of the metaphysis	0/20
HP: 0000951	Abnormality of the skin	0/20
HP: 0000953	Hyperpigmentation of the skin	0/20
HP: 0000954	Single transverse palmar crease	0/20
HP: 0000962	Hyperkeratosis	0/20
HP: 0000968	Ectodermal dysplasia	0/20
HP: 0000969	Edema	0/20
HP: 0000971	Abnormal sweat gland morphology	0/20
HP: 0000974	Hyperextensible skin	0/20
HP: 0000978	Bruising susceptibility	0/20
HP: 0000987	Atypical scarring of skin	0/20
HP: 0000992	Cutaneous photosensitivity	0/20
HP: 0000993	Molluscoid pseudotumors	0/20
HP: 0000995	Melanocytic nevus	0/20
HP: 0000996	Facial capillary hemangioma	0/20
HP: 0000997	Axillary freckling	0/20
HP: 0000998	Hypertrichosis	0/20
HP: 0001000	Abnormality of skin pigmentation	0/20
HP: 0001001	Abnormality of subcutaneous fat tissue	0/20
HP: 0001004	Lymphedema	0/20
HP: 0001007	Hirsutism	0/20
HP: 0001009	Telangiectasia	0/20
HP: 0001010	Hypopigmentation of the skin	0/20
HP: 0001012	Multiple lipomas	0/20
HP: 0001018	Abnormal palmar dermatoglyphics	0/20
HP: 0001019	Erythroderma	0/20
HP: 0001025	Urticaria	0/20
HP: 0001028	Hemangioma	0/20
HP: 0001030	Fragile skin	0/20
HP: 0001031	Subcutaneous lipoma	0/20
HP: 0001032	Absent distal interphalangeal creases	0/20
HP: 0001052	Nevus flammeus	0/20
HP: 0001056	Milia	0/20
HP: 0001057	Aplasia cutis congenita	0/20
HP: 0001059	Pterygium	0/20
HP: 0001060	Axillary pterygium	0/20
HP: 0001067	Neurofibromas	0/20
HP: 0001072	Thickened skin	0/20
HP: 0001073	Cigarette-paper scars	0/20
HP: 0001075	Atrophic scars	0/20
HP: 0001080	Biliary tract abnormality	0/20
HP: 0001083	Ectopia lentis	0/20
HP: 0001087	Developmental glaucoma	0/20
HP: 0001095	Hypertensive retinopathy	0/20
HP: 0001098	Abnormal fundus morphology	0/20
HP: 0001103	Abnormal macular morphology	0/20
HP: 0001120	Abnormality of corneal size	0/20
HP: 0001131	Corneal dystrophy	0/20
HP: 0001132	Lens subluxation	0/20
HP: 0001142	Lenticonus	0/20
HP: 0001144	Orbital cyst	0/20
HP: 0001153	Septate vagina	0/20
HP: 0001155	Abnormality of the hand	0/20
HP: 0001159	Syndactyly	0/20
HP: 0001163	Abnormality of the metacarpal bones	0/20
HP: 0001166	Arachnodactyly	0/20
HP: 0001167	Abnormality of finger	0/20
HP: 0001171	Split hand	0/20
HP: 0001172	Abnormal thumb morphology	0/20
HP: 0001176	Large hands	0/20
HP: 0001194	Abnormalities of placenta or umbilical cord	0/20
HP: 0001197	Abnormality of prenatal development or birth	0/20
HP: 0001211	Abnormal fingertip morphology	0/20
HP: 0001220	Interphalangeal joint contracture of finger	0/20
HP: 0001231	Abnormal fingernail morphology	0/20
HP: 0001238	Slender finger	0/20
HP: 0001249	Intellectual disability	0/20
HP: 0001250	Seizure	0/20
HP: 0001251	Ataxia	0/20
HP: 0001257	Spasticity	0/20
HP: 0001264	Spastic diplegia	0/20
HP: 0001270	Motor delay	0/20
HP: 0001273	Abnormal corpus callosum morphology	0/20
HP: 0001276	Hypertonia	0/20
HP: 0001284	Areflexia	0/20
HP: 0001288	Gait disturbance	0/20
HP: 0001298	Encephalopathy	0/20
HP: 0001302	Pachygyria	0/20
HP: 0001315	Reduced tendon reflexes	0/20
HP: 0001317	Abnormal cerebellum morphology	0/20
HP: 0001324	Muscle weakness	0/20
HP: 0001339	Lissencephaly	0/20
HP: 0001360	Holoprosencephaly	0/20
HP: 0001363	Craniosynostosis	0/20
HP: 0001367	Abnormal joint morphology	0/20
HP: 0001371	Flexion contracture	0/20
HP: 0001373	Joint dislocation	0/20
HP: 0001374	Congenital hip dislocation	0/20
HP: 0001376	Limitation of joint mobility	0/20
HP: 0001382	Joint hypermobility	0/20
HP: 0001384	Abnormality of the hip joint	0/20
HP: 0001385	Hip dysplasia	0/20
HP: 0001387	Joint stiffness	0/20
HP: 0001392	Abnormality of the liver	0/20
HP: 0001395	Hepatic fibrosis	0/20
HP: 0001396	Cholestasis	0/20
HP: 0001401	Intrahepatic biliary dysgenesis	0/20
HP: 0001407	Hepatic cysts	0/20
HP: 0001421	Abnormality of the musculature of the hand	0/20
HP: 0001430	Abnormality of the calf musculature	0/20
HP: 0001435	Abnormality of the shoulder girdle musculature	0/20
HP: 0001437	Abnormality of the musculature of the lower limbs	0/20
HP: 0001438	Abnormality of abdomen morphology	0/20
HP: 0001446	Abnormality of the musculature of the upper limbs	0/20
HP: 0001454	Abnormality of the upper arm	0/20
HP: 0001460	Aplasia/Hypoplasia involving the skeletal musculature	0/20
HP: 0001480	Freckling	0/20
HP: 0001482	Subcutaneous nodule	0/20
HP: 0001488	Bilateral ptosis	0/20
HP: 0001507	Growth abnormality	0/20
HP: 0001510	Growth delay	0/20
HP: 0001511	Intrauterine growth retardation	0/20
HP: 0001518	Small for gestational age	0/20
HP: 0001545	Anteriorly placed anus	0/20
HP: 0001547	Abnormality of the rib cage	0/20
HP: 0001549	Abnormal ileum morphology	0/20
HP: 0001551	Abnormal umbilicus morphology	0/20
HP: 0001557	Prenatal movement abnormality	0/20
HP: 0001558	Decreased fetal movement	0/20
HP: 0001560	Abnormality of the amniotic fluid	0/20
HP: 0001561	Polyhydramnios	0/20
HP: 0001562	Oligohydramnios	0/20
HP: 0001574	Abnormality of the integument	0/20
HP: 0001593	Maxillary lateral incisor microdontia	0/20
HP: 0001595	Abnormal hair morphology	0/20
HP: 0001597	Abnormality of the nail	0/20
HP: 0001600	Abnormality of the larynx	0/20
HP: 0001601	Laryngomalacia	0/20
HP: 0001602	Laryngeal stenosis	0/20
HP: 0001607	Subglottic stenosis	0/20
HP: 0001608	Abnormality of the voice	0/20
HP: 0001609	Hoarse voice	0/20
HP: 0001615	Hoarse cry	0/20
HP: 0001626	Abnormality of the cardiovascular system	0/20
HP: 0001627	Abnormal heart morphology	0/20
HP: 0001629	Ventricular septal defect	0/20
HP: 0001631	Atrial septal defect	0/20
HP: 0001633	Abnormal mitral valve morphology	0/20
HP: 0001635	Congestive heart failure	0/20
HP: 0001636	Tetralogy of Fallot	0/20
HP: 0001637	Abnormal myocardium morphology	0/20
HP: 0001638	Cardiomyopathy	0/20
HP: 0001639	Hypertrophic cardiomyopathy	0/20
HP: 0001640	Cardiomegaly	0/20
HP: 0001641	Abnormal pulmonary valve morphology	0/20
HP: 0001642	Pulmonic stenosis	0/20
HP: 0001643	Patent ductus arteriosus	0/20
HP: 0001646	Abnormal aortic valve morphology	0/20
HP: 0001650	Aortic valve stenosis	0/20
HP: 0001651	Dextrocardia	0/20
HP: 0001653	Mitral regurgitation	0/20
HP: 0001654	Abnormal heart valve morphology	0/20
HP: 0001659	Aortic regurgitation	0/20
HP: 0001667	Right ventricular hypertrophy	0/20
HP: 0001670	Asymmetric septal hypertrophy	0/20
HP: 0001671	Abnormal cardiac septum morphology	0/20
HP: 0001678	Atrioventricular block	0/20
HP: 0001679	Abnormal aortic morphology	0/20
HP: 0001680	Coarctation of aorta	0/20
HP: 0001682	Subvalvular aortic stenosis	0/20
HP: 0001684	Secundum atrial septal defect	0/20
HP: 0001686	Loss of voice	0/20
HP: 0001693	Cardiac shunt	0/20
HP: 0001696	Situs inversus totalis	0/20
HP: 0001702	Abnormal tricuspid valve morphology	0/20
HP: 0001707	Abnormal right ventricle morphology	0/20
HP: 0001708	Right ventricular failure	0/20
HP: 0001709	Third degree atrioventricular block	0/20
HP: 0001710	Conotruncal defect	0/20
HP: 0001711	Abnormal left ventricle morphology	0/20
HP: 0001713	Abnormal cardiac ventricle morphology	0/20
HP: 0001714	Ventricular hypertrophy	0/20
HP: 0001718	Mitral stenosis	0/20
HP: 0001719	Double outlet right ventricle	0/20
HP: 0001732	Abnormality of the pancreas	0/20
HP: 0001734	Annular pancreas	0/20
HP: 0001737	Pancreatic cysts	0/20
HP: 0001743	Abnormality of the spleen	0/20
HP: 0001747	Accessory spleen	0/20
HP: 0001748	Polysplenia	0/20
HP: 0001750	Single ventricle	0/20
HP: 0001751	Vestibular dysfunction	0/20
HP: 0001760	Abnormality of the foot	0/20
HP: 0001761	Pes cavus	0/20
HP: 0001762	Talipes equinovarus	0/20
HP: 0001763	Pes planus	0/20
HP: 0001765	Hammertoe	0/20
HP: 0001770	Toe syndactyly	0/20
HP: 0001771	Achilles tendon contracture	0/20
HP: 0001776	Bilateral talipes equinovarus	0/20
HP: 0001780	Abnormality of toe	0/20
HP: 0001789	Hydrops fetalis	0/20
HP: 0001822	Hallux valgus	0/20
HP: 0001827	Genital tract atresia	0/20
HP: 0001832	Abnormal metatarsal morphology	0/20
HP: 0001840	Metatarsus adductus	0/20
HP: 0001844	Abnormality of the hallux	0/20
HP: 0001848	Calcaneovalgus deformity	0/20
HP: 0001850	Abnormality of the tarsal bones	0/20
HP: 0001869	Deep plantar creases	0/20
HP: 0001871	Abnormality of blood and blood-forming tissues	0/20
HP: 0001877	Abnormal erythrocyte morphology	0/20
HP: 0001881	Abnormal leukocyte morphology	0/20
HP: 0001882	Leukopenia	0/20
HP: 0001883	Talipes	0/20
HP: 0001884	Talipes calcaneovalgus	0/20
HP: 0001888	Lymphopenia	0/20
HP: 0001892	Abnormal bleeding	0/20
HP: 0001903	Anemia	0/20
HP: 0001909	Leukemia	0/20
HP: 0001911	Abnormal granulocyte morphology	0/20
HP: 0001920	Renal artery stenosis	0/20
HP: 0001924	Sideroblastic anemia	0/20
HP: 0001928	Abnormality of coagulation	0/20
HP: 0001933	Subcutaneous hemorrhage	0/20
HP: 0001939	Abnormality of metabolism/homeostasis	0/20
HP: 0001943	Hypoglycemia	0/20
HP: 0001952	Glucose intolerance	0/20
HP: 0001961	Hypoplastic heart	0/20
HP: 0001964	Aplasia/Hypoplasia of metatarsal bones	0/20
HP: 0001965	Abnormality of the scalp	0/20
HP: 0001978	Extramedullary hematopoiesis	0/20
HP: 0001988	Recurrent hypoglycemia	0/20
HP: 0001992	Organic aciduria	0/20
HP: 0001999	Abnormal facial shape	0/20
HP: 0002006	Facial cleft	0/20
HP: 0002009	Potter facies	0/20
HP: 0002011	Morphological central nervous system abnormality	0/20
HP: 0002012	Abnormality of the abdominal organs	0/20
HP: 0002013	Vomiting	0/20
HP: 0002015	Dysphagia	0/20
HP: 0002017	Nausea and vomiting	0/20
HP: 0002020	Gastroesophageal reflux	0/20
HP: 0002021	Pyloric stenosis	0/20
HP: 0002023	Anal atresia	0/20
HP: 0002024	Malabsorption	0/20
HP: 0002031	Abnormal esophagus morphology	0/20
HP: 0002032	Esophageal atresia	0/20
HP: 0002034	Abnormality of the rectum	0/20
HP: 0002036	Hiatus hernia	0/20
HP: 0002037	Inflammation of the large intestine	0/20
HP: 0002043	Esophageal stricture	0/20
HP: 0002060	Abnormal cerebral morphology	0/20
HP: 0002062	Morphological abnormality of the pyramidal tract	0/20
HP: 0002064	Spastic gait	0/20
HP: 0002078	Truncal ataxia	0/20
HP: 0002079	Hypoplasia of the corpus callosum	0/20
HP: 0002084	Encephalocele	0/20
HP: 0002085	Occipital encephalocele	0/20
HP: 0002086	Abnormality of the respiratory system	0/20
HP: 0002087	Abnormality of the upper respiratory tract	0/20
HP: 0002088	Abnormal lung morphology	0/20
HP: 0002089	Pulmonary hypoplasia	0/20
HP: 0002093	Respiratory insufficiency	0/20
HP: 0002094	Dyspnea	0/20
HP: 0002098	Respiratory distress	0/20
HP: 0002103	Abnormality of the pleura	0/20
HP: 0002110	Bronchiectasis	0/20
HP: 0002118	Abnormality of the cerebral ventricles	0/20
HP: 0002119	Ventriculomegaly	0/20
HP: 0002126	Polymicrogyria	0/20
HP: 0002134	Abnormality of the basal ganglia	0/20
HP: 0002138	Subarachnoid hemorrhage	0/20
HP: 0002143	Abnormality of the spinal cord	0/20
HP: 0002144	Tethered cord	0/20
HP: 0002149	Hyperuricemia	0/20
HP: 0002157	Azotemia	0/20
HP: 0002170	Intracranial hemorrhage	0/20
HP: 0002176	Spinal cord compression	0/20
HP: 0002180	Neurodegeneration	0/20
HP: 0002181	Cerebral edema	0/20
HP: 0002187	Intellectual disability, profound	0/20
HP: 0002190	Choroid plexus cyst	0/20
HP: 0002194	Delayed gross motor development	0/20
HP: 0002196	Myelopathy	0/20
HP: 0002199	Hypocalcemic seizures	0/20
HP: 0002204	Pulmonary embolism	0/20
HP: 0002205	Recurrent respiratory infections	0/20
HP: 0002209	Sparse scalp hair	0/20
HP: 0002215	Sparse axillary hair	0/20
HP: 0002219	Facial hypertrichosis	0/20
HP: 0002230	Generalized hirsutism	0/20
HP: 0002239	Gastrointestinal hemorrhage	0/20
HP: 0002242	Abnormal intestine morphology	0/20
HP: 0002244	Abnormality of the small intestine	0/20
HP: 0002245	Meckel diverticulum	0/20
HP: 0002246	Abnormality of the duodenum	0/20
HP: 0002247	Duodenal atresia	0/20
HP: 0002248	Hematemesis	0/20
HP: 0002250	Abnormal large intestine morphology	0/20
HP: 0002251	Aganglionic megacolon	0/20
HP: 0002269	Abnormality of neuronal migration	0/20
HP: 0002270	Abnormality of the autonomic nervous system	0/20
HP: 0002277	Horner syndrome	0/20
HP: 0002282	Gray matter heterotopia	0/20
HP: 0002298	Absent hair	0/20
HP: 0002299	Brittle hair	0/20
HP: 0002308	Arnold-Chiari malformation	0/20
HP: 0002352	Leukoencephalopathy	0/20
HP: 0002363	Abnormality of brainstem morphology	0/20
HP: 0002385	Paraparesis	0/20
HP: 0002408	Cerebral arteriovenous malformation	0/20
HP: 0002410	Aqueductal stenosis	0/20
HP: 0002414	Spina bifida	0/20
HP: 0002415	Leukodystrophy	0/20
HP: 0002418	Abnormality of midbrain morphology	0/20
HP: 0002435	Meningocele	0/20
HP: 0002438	Cerebellar malformation	0/20
HP: 0002445	Tetraplegia	0/20
HP: 0002450	Abnormal motor neuron morphology	0/20
HP: 0002460	Distal muscle weakness	0/20
HP: 0002474	Expressive language delay	0/20
HP: 0002475	Myelomeningocele	0/20
HP: 0002488	Acute leukemia	0/20
HP: 0002492	Morphological abnormality of the corticospinal tract	0/20
HP: 0002493	Upper motor neuron dysfunction	0/20
HP: 0002500	Abnormality of the cerebral white matter	0/20
HP: 0002514	Cerebral calcification	0/20
HP: 0002518	Abnormality of the periventricular white matter	0/20
HP: 0002536	Abnormal cortical gyration	0/20
HP: 0002538	Abnormality of the cerebral cortex	0/20
HP: 0002558	Supernumerary nipple	0/20
HP: 0002566	Intestinal malrotation	0/20
HP: 0002571	Achalasia	0/20
HP: 0002575	Tracheoesophageal fistula	0/20
HP: 0002576	Intussusception	0/20
HP: 0002577	Abnormality of the stomach	0/20
HP: 0002579	Gastrointestinal dysmotility	0/20
HP: 0002583	Colitis	0/20
HP: 0002584	Intestinal bleeding	0/20
HP: 0002587	Projectile vomiting	0/20
HP: 0002589	Gastrointestinal atresia	0/20
HP: 0002595	Ileus	0/20
HP: 0002597	Abnormality of the vasculature	0/20
HP: 0002604	Gastrointestinal telangiectasia	0/20
HP: 0002612	Congenital hepatic fibrosis	0/20
HP: 0002616	Aortic root aneurysm	0/20
HP: 0002617	Dilatation	0/20
HP: 0002623	Overriding aorta	0/20
HP: 0002624	Abnormal venous morphology	0/20
HP: 0002643	Neonatal respiratory distress	0/20
HP: 0002644	Abnormality of pelvic girdle bone morphology	0/20
HP: 0002645	Wormian bones	0/20
HP: 0002647	Aortic dissection	0/20
HP: 0002648	Abnormality of calvarial morphology	0/20
HP: 0002650	Scoliosis	0/20
HP: 0002652	Skeletal dysplasia	0/20
HP: 0002655	Spondyloepiphyseal dysplasia	0/20
HP: 0002659	Increased susceptibility to fractures	0/20
HP: 0002672	Gastrointestinal carcinoma	0/20
HP: 0002673	Coxa valga	0/20
HP: 0002677	Small foramen magnum	0/20
HP: 0002683	Abnormality of the calvaria	0/20
HP: 0002686	Prenatal maternal abnormality	0/20
HP: 0002692	Hypoplastic facial bones	0/20
HP: 0002693	Abnormality of the skull base	0/20
HP: 0002699	Abnormality of the foramen magnum	0/20
HP: 0002715	Abnormality of the immune system	0/20
HP: 0002719	Recurrent infections	0/20
HP: 0002744	Bilateral cleft lip and palate	0/20
HP: 0002751	Kyphoscoliosis	0/20
HP: 0002763	Abnormal cartilage morphology	0/20
HP: 0002777	Tracheal stenosis	0/20
HP: 0002778	Abnormal trachea morphology	0/20
HP: 0002779	Tracheomalacia	0/20
HP: 0002780	Bronchomalacia	0/20
HP: 0002783	Recurrent lower respiratory tract infections	0/20
HP: 0002786	Tracheobronchomalacia	0/20
HP: 0002787	Tracheal calcification	0/20
HP: 0002789	Tachypnea	0/20
HP: 0002793	Abnormal pattern of respiration	0/20
HP: 0002795	Functional respiratory abnormality	0/20
HP: 0002803	Congenital contracture	0/20
HP: 0002804	Arthrogryposis multiplex congenita	0/20
HP: 0002808	Kyphosis	0/20
HP: 0002813	Abnormality of limb bone morphology	0/20
HP: 0002814	Abnormality of the lower limb	0/20
HP: 0002815	Abnormality of the knee	0/20
HP: 0002817	Abnormality of the upper limb	0/20
HP: 0002818	Abnormality of the radius	0/20
HP: 0002823	Abnormality of femur morphology	0/20
HP: 0002827	Hip dislocation	0/20
HP: 0002828	Multiple joint contractures	0/20
HP: 0002835	Aspiration	0/20
HP: 0002836	Bladder exstrophy	0/20
HP: 0002843	Abnormal T cell morphology	0/20
HP: 0002846	Abnormal B cell morphology	0/20
HP: 0002857	Genu valgum	0/20
HP: 0002863	Myelodysplasia	0/20
HP: 0002867	Abnormality of the ilium	0/20
HP: 0002883	Hyperventilation	0/20
HP: 0002896	Neoplasm of the liver	0/20
HP: 0002901	Hypocalcemia	0/20
HP: 0002904	Hyperbilirubinemia	0/20
HP: 0002908	Conjugated hyperbilirubinemia	0/20
HP: 0002916	Abnormality of chromosome segregation	0/20
HP: 0002921	Abnormality of the cerebrospinal fluid	0/20
HP: 0002937	Hemivertebrae	0/20
HP: 0002938	Lumbar hyperlordosis	0/20
HP: 0002942	Thoracic kyphosis	0/20
HP: 0002943	Thoracic scoliosis	0/20
HP: 0002944	Thoracolumbar scoliosis	0/20
HP: 0002947	Cervical kyphosis	0/20
HP: 0002948	Vertebral fusion	0/20
HP: 0002953	Vertebral compression fractures	0/20
HP: 0002967	Cubitus valgus	0/20
HP: 0002970	Genu varum	0/20
HP: 0002973	Abnormality of the forearm	0/20
HP: 0002977	Aplasia/Hypoplasia involving the central nervous system	0/20
HP: 0002979	Bowing of the legs	0/20
HP: 0002981	Abnormality of the calf	0/20
HP: 0002983	Micromelia	0/20
HP: 0002991	Abnormality of fibula morphology	0/20
HP: 0002992	Abnormality of tibia morphology	0/20
HP: 0002997	Abnormality of the ulna	0/20
HP: 0003002	Breast carcinoma	0/20
HP: 0003005	Ganglioneuroma	0/20
HP: 0003011	Abnormality of the musculature	0/20
HP: 0003019	Abnormality of the wrist	0/20
HP: 0003026	Short long bone	0/20
HP: 0003028	Abnormality of the ankles	0/20
HP: 0003042	Elbow dislocation	0/20
HP: 0003043	Abnormality of the shoulder	0/20
HP: 0003045	Abnormal patella morphology	0/20
HP: 0003063	Abnormality of the humerus	0/20
HP: 0003067	Madelung deformity	0/20
HP: 0003077	Hyperlipidemia	0/20
HP: 0003083	Dislocated radial head	0/20
HP: 0003110	Abnormality of urine homeostasis	0/20
HP: 0003111	Abnormal blood ion concentration	0/20
HP: 0003112	Abnormality of serum amino acid level	0/20
HP: 0003113	Hypochloremia	0/20
HP: 0003115	Abnormal EKG	0/20
HP: 0003119	Abnormal circulating lipid concentration	0/20
HP: 0003121	Limb joint contracture	0/20
HP: 0003127	Hypocalciuria	0/20
HP: 0003170	Abnormality of the acetabulum	0/20
HP: 0003187	Breast hypoplasia	0/20
HP: 0003202	Skeletal muscle atrophy	0/20
HP: 0003241	External genital hypoplasia	0/20
HP: 0003244	Penile hypospadias	0/20
HP: 0003250	Aplasia of the vagina	0/20
HP: 0003256	Abnormality of the coagulation cascade	0/20
HP: 0003272	Abnormality of the hip bone	0/20
HP: 0003273	Hip contracture	0/20
HP: 0003298	Spina bifida occulta	0/20
HP: 0003302	Spondylolisthesis	0/20
HP: 0003304	Spondylolysis	0/20
HP: 0003307	Hyperlordosis	0/20
HP: 0003310	Abnormality of the odontoid process	0/20
HP: 0003312	Abnormal form of the vertebral bodies	0/20
HP: 0003319	Abnormality of the cervical spine	0/20
HP: 0003328	Abnormal hair laboratory examination	0/20
HP: 0003330	Abnormal bone structure	0/20
HP: 0003336	Abnormal enchondral ossification	0/20
HP: 0003355	Aminoaciduria	0/20
HP: 0003366	Abnormality of the femoral neck or head region	0/20
HP: 0003367	Abnormality of the femoral neck	0/20
HP: 0003368	Abnormality of the femoral head	0/20
HP: 0003396	Syringomyelia	0/20
HP: 0003398	Abnormal synaptic transmission at the neuromuscular junction	0/20
HP: 0003416	Spinal canal stenosis	0/20
HP: 0003422	Vertebral segmentation defect	0/20
HP: 0003450	Axonal regeneration	0/20
HP: 0003468	Abnormal vertebral morphology	0/20
HP: 0003474	Sensory impairment	0/20
HP: 0003498	Disproportionate short stature	0/20
HP: 0003532	Ornithinuria	0/20
HP: 0003549	Abnormality of connective tissue	0/20
HP: 0003560	Muscular dystrophy	0/20
HP: 0003616	Premature separation of centromeric heterochromatin	0/20
HP: 0003634	Amyoplasia	0/20
HP: 0003693	Distal amyotrophy	0/20
HP: 0003712	Skeletal muscle hypertrophy	0/20
HP: 0003717	Minimal subcutaneous fat	0/20
HP: 0003758	Reduced subcutaneous adipose tissue	0/20
HP: 0003762	Uterus didelphys	0/20
HP: 0003764	Nevus	0/20
HP: 0003774	Stage 5 chronic kidney disease	0/20
HP: 0003797	Limb-girdle muscle atrophy	0/20
HP: 0003808	Abnormal muscle tone	0/20
HP: 0003839	Abnormality of upper limb epiphysis morphology	0/20
HP: 0003995	Abnormality of the radial head	0/20
HP: 0003999	Abnormality of radial epiphyses	0/20
HP: 0004050	Absent hand	0/20
HP: 0004054	Sclerosis of hand bone	0/20
HP: 0004097	Deviation of finger	0/20
HP: 0004099	Macrodactyly	0/20
HP: 0004150	Abnormal 3rd finger morphology	0/20
HP: 0004207	Abnormal 5th finger morphology	0/20
HP: 0004275	Duplication of hand bones	0/20
HP: 0004288	Pseudoepiphyses of hand bones	0/20
HP: 0004296	Abnormality of gastrointestinal vasculature	0/20
HP: 0004297	Abnormality of the biliary system	0/20
HP: 0004298	Abnormality of the abdominal wall	0/20
HP: 0004299	Hernia of the abdominal wall	0/20
HP: 0004305	Involuntary movements	0/20
HP: 0004307	Abnormal anatomic location of the heart	0/20
HP: 0004311	Abnormal macrophage morphology	0/20
HP: 0004320	Vaginal fistula	0/20
HP: 0004322	Short stature	0/20
HP: 0004323	Abnormality of body weight	0/20
HP: 0004325	Decreased body weight	0/20
HP: 0004328	Abnormal anterior eye segment morphology	0/20
HP: 0004329	Abnormal posterior eye segment morphology	0/20
HP: 0004332	Abnormal lymphocyte morphology	0/20
HP: 0004334	Dermal atrophy	0/20
HP: 0004340	Abnormality of vitamin B metabolism	0/20
HP: 0004341	Abnormality of vitamin B12 metabolism	0/20
HP: 0004348	Abnormality of bone mineral density	0/20
HP: 0004352	Abnormal circulating purine concentration	0/20
HP: 0004354	Abnormal circulating carboxylic acid concentration	0/20
HP: 0004362	Abnormality of enteric ganglion morphology	0/20
HP: 0004363	Abnormal circulating calcium concentration	0/20
HP: 0004364	Abnormal circulating nitrogen compound concentration	0/20
HP: 0004368	Increased purine level	0/20
HP: 0004375	Neoplasm of the nervous system	0/20
HP: 0004377	Hematological neoplasm	0/20
HP: 0004378	Abnormality of the anus	0/20
HP: 0004381	Supravalvular aortic stenosis	0/20
HP: 0004383	Hypoplastic left heart	0/20
HP: 0004386	Gastrointestinal inflammation	0/20
HP: 0004387	Enterocolitis	0/20
HP: 0004395	Malnutrition	0/20
HP: 0004397	Ectopic anus	0/20
HP: 0004400	Abnormality of the pylorus	0/20
HP: 0004404	Abnormal nipple morphology	0/20
HP: 0004408	Abnormality of the sense of smell	0/20
HP: 0004409	Hyposmia	0/20
HP: 0004414	Abnormality of the pulmonary artery	0/20
HP: 0004426	Abnormality of the cheek	0/20
HP: 0004428	Elfin facies	0/20
HP: 0004443	Lambdoidal craniosynostosis	0/20
HP: 0004565	Severe platyspondyly	0/20
HP: 0004614	Spina bifida occulta at S1	0/20
HP: 0004626	Lumbar scoliosis	0/20
HP: 0004692	4-5 toe syndactyly	0/20
HP: 0004712	Renal malrotation	0/20
HP: 0004719	Hyperechogenic kidneys	0/20
HP: 0004734	Renal cortical microcysts	0/20
HP: 0004736	Crossed fused renal ectopia	0/20
HP: 0004742	Abnormal renal collecting system morphology	0/20
HP: 0004790	Hypoplasia of the small intestine	0/20
HP: 0004792	Rectoperineal fistula	0/20
HP: 0004794	Malrotation of small bowel	0/20
HP: 0004796	Gastrointestinal obstruction	0/20
HP: 0004828	Refractory anemia with ringed sideroblasts	0/20
HP: 0004871	Perineal fistula	0/20
HP: 0004879	Intermittent hyperventilation	0/20
HP: 0004886	Congenital laryngeal stridor	0/20
HP: 0004894	Laryngotracheal stenosis	0/20
HP: 0004905	Low levels of vitamin A	0/20
HP: 0004914	Recurrent infantile hypoglycemia	0/20
HP: 0004930	Abnormality of the pulmonary vasculature	0/20
HP: 0004942	Aortic aneurysm	0/20
HP: 0004947	Arteriovenous fistula	0/20
HP: 0005105	Abnormal nasal morphology	0/20
HP: 0005107	Abnormal sacrum morphology	0/20
HP: 0005109	Abnormality of the Achilles tendon	0/20
HP: 0005112	Abdominal aortic aneurysm	0/20
HP: 0005120	Abnormal cardiac atrium morphology	0/20
HP: 0005134	Absence of the pulmonary valve	0/20
HP: 0005150	Abnormal atrioventricular conduction	0/20
HP: 0005160	Total anomalous pulmonary venous return	0/20
HP: 0005176	Dysplastic aortic valve	0/20
HP: 0005180	Tricuspid regurgitation	0/20
HP: 0005209	Intrahepatic bile duct cysts	0/20
HP: 0005214	Intestinal obstruction	0/20
HP: 0005240	Esophageal obstruction	0/20
HP: 0005241	Total intestinal aganglionosis	0/20
HP: 0005245	Intestinal hypoplasia	0/20
HP: 0005257	Thoracic hypoplasia	0/20
HP: 0005262	Abnormality of the synovia	0/20
HP: 0005264	Abnormality of the gallbladder	0/20
HP: 0005288	Abnormality of the nares	0/20
HP: 0005306	Capillary hemangioma	0/20
HP: 0005344	Abnormal carotid artery morphology	0/20
HP: 0005348	Inspiratory stridor	0/20
HP: 0005359	Aplasia of the thymus	0/20
HP: 0005365	Severe B lymphocytopenia	0/20
HP: 0005403	Decrease in T cell count	0/20
HP: 0005407	Decreased proportion of CD4-positive T cells	0/20
HP: 0005484	Postnatal microcephaly	0/20
HP: 0005505	Refractory anemia	0/20
HP: 0005547	Myeloproliferative disorder	0/20
HP: 0005557	Abnormality of the zygomatic arch	0/20
HP: 0005561	Abnormality of bone marrow cell morphology	0/20
HP: 0005562	Multiple renal cysts	0/20
HP: 0005563	Decreased numbers of nephrons	0/20
HP: 0005564	Absence of renal corticomedullary differentiation	0/20
HP: 0005580	Duplication of renal pelvis	0/20
HP: 0005595	Generalized hyperkeratosis	0/20
HP: 0005607	Abnormal tracheobronchial morphology	0/20
HP: 0005613	Aplasia/hypoplasia of the femur	0/20
HP: 0005619	Thoracolumbar kyphosis	0/20
HP: 0005622	Broad long bones	0/20
HP: 0005650	Cutaneous syndactyly between fingers 2 and 5	0/20
HP: 0005656	Positional foot deformity	0/20
HP: 0005684	Distal arthrogryposis	0/20
HP: 0005701	Multiple enchondromatosis	0/20
HP: 0005716	Lethal skeletal dysplasia	0/20
HP: 0005750	Contractures of the joints of the lower limbs	0/20
HP: 0005758	Basilar impression	0/20
HP: 0005775	Multiple skeletal anomalies	0/20
HP: 0005815	Supernumerary ribs	0/20
HP: 0005830	Flexion contracture of toe	0/20
HP: 0005850	Congenital talipes calcaneovalgus	0/20
HP: 0005864	Pseudoarthrosis	0/20
HP: 0005871	Metaphyseal chondrodysplasia	0/20
HP: 0005905	Abnormal cervical curvature	0/20
HP: 0005912	Biliary atresia	0/20
HP: 0005913	Abnormality of metacarpal epiphyses	0/20
HP: 0005914	Aplasia/Hypoplasia involving the metacarpal bones	0/20
HP: 0005916	Abnormal metacarpal morphology	0/20
HP: 0005918	Abnormal finger phalanx morphology	0/20
HP: 0005922	Abnormal hand morphology	0/20
HP: 0005924	Abnormality of the epiphyses of the hand	0/20
HP: 0005927	Aplasia/hypoplasia involving bones of the hand	0/20
HP: 0005930	Abnormality of epiphysis morphology	0/20
HP: 0005932	Abnormal renal corticomedullary differentiation	0/20
HP: 0005943	Respiratory arrest	0/20
HP: 0005948	Multiple pulmonary cysts	0/20
HP: 0005950	Laryngeal web	0/20
HP: 0005988	Congenital muscular torticollis	0/20
HP: 0006000	Ureteral obstruction	0/20
HP: 0006009	Broad phalanx	0/20
HP: 0006101	Finger syndactyly	0/20
HP: 0006109	Absent phalangeal crease	0/20
HP: 0006143	Abnormal finger flexion creases	0/20
HP: 0006237	Prominent interphalangeal joints	0/20
HP: 0006261	Abnormal phalangeal joint morphology of the hand	0/20
HP: 0006262	Aplasia/Hypoplasia of the 5th finger	0/20
HP: 0006265	Aplasia/Hypoplasia of fingers	0/20
HP: 0006311	Generalized microdontia	0/20
HP: 0006329	Alveolar process hypoplasia	0/20
HP: 0006380	Knee flexion contracture	0/20
HP: 0006477	Abnormality of the alveolar ridges	0/20
HP: 0006482	Abnormality of dental morphology	0/20
HP: 0006483	Abnormal number of teeth	0/20
HP: 0006486	Abnormality of the dental root	0/20
HP: 0006487	Bowing of the long bones	0/20
HP: 0006489	Abnormality of the femoral metaphysis	0/20
HP: 0006490	Abnormality of lower-limb metaphyses	0/20
HP: 0006493	Aplasia/hypoplasia involving bones of the lower limbs	0/20
HP: 0006494	Aplasia/Hypoplasia involving bones of the feet	0/20
HP: 0006495	Aplasia/Hypoplasia of the ulna	0/20
HP: 0006496	Aplasia/hypoplasia involving bones of the upper limbs	0/20
HP: 0006499	Abnormality of femoral epiphysis	0/20
HP: 0006500	Abnormality of lower limb epiphysis morphology	0/20
HP: 0006503	Aplasia/hypoplasia involving forearm bones	0/20
HP: 0006504	obsolete Anomaly of the limb diaphyses morphology	0/20
HP: 0006505	Abnormality of limb epiphysis morphology	0/20
HP: 0006511	Laryngeal stridor	0/20
HP: 0006539	Bronchial cartilage hypoplasia	0/20
HP: 0006543	Cardiorespiratory arrest	0/20
HP: 0006548	Pulmonary arteriovenous malformation	0/20
HP: 0006557	Polycystic liver disease	0/20
HP: 0006625	Multifocal breast carcinoma	0/20
HP: 0006644	Thoracic dysplasia	0/20
HP: 0006657	Hypoplasia of first ribs	0/20
HP: 0006695	Atrioventricular canal defect	0/20
HP: 0006703	Aplasia/Hypoplasia of the lungs	0/20
HP: 0006705	Abnormal atrioventricular valve morphology	0/20
HP: 0006706	Cystic liver disease	0/20
HP: 0006707	Abnormality of the hepatic vasculature	0/20
HP: 0006711	Aplasia/Hypoplasia involving bones of the thorax	0/20
HP: 0006712	Aplasia/Hypoplasia of the ribs	0/20
HP: 0006722	Small intestine carcinoid	0/20
HP: 0006749	Malignant gastrointestinal tract tumors	0/20
HP: 0006762	Renal pelvic carcinoma	0/20
HP: 0006772	Renal angiomyolipoma	0/20
HP: 0006827	Atrophy of the spinal cord	0/20
HP: 0006919	Abnormal aggressive, impulsive or violent behavior	0/20
HP: 0006946	Recurrent meningitis	0/20
HP: 0007018	Attention deficit hyperactivity disorder	0/20
HP: 0007048	Large basal ganglia	0/20
HP: 0007081	Late-onset muscular dystrophy	0/20
HP: 0007099	Arnold-Chiari type I malformation	0/20
HP: 0007109	Periventricular cysts	0/20
HP: 0007149	Distal upper limb amyotrophy	0/20
HP: 0007221	Progressive truncal ataxia	0/20
HP: 0007229	Intracerebral periventricular calcifications	0/20
HP: 0007260	Type II lissencephaly	0/20
HP: 0007344	Atrophy/Degeneration involving the spinal cord	0/20
HP: 0007359	Focal-onset seizure	0/20
HP: 0007361	Abnormality of the pons	0/20
HP: 0007364	Aplasia/Hypoplasia of the cerebrum	0/20
HP: 0007367	Atrophy/Degeneration affecting the central nervous system	0/20
HP: 0007370	Aplasia/Hypoplasia of the corpus callosum	0/20
HP: 0007376	Abnormality of the choroid plexus	0/20
HP: 0007378	Neoplasm of the gastrointestinal tract	0/20
HP: 0007379	Neoplasm of the genitourinary tract	0/20
HP: 0007477	Abnormal dermatoglyphics	0/20
HP: 0007556	Plantar hyperkeratosis	0/20
HP: 0007559	Localized epidermolytic hyperkeratosis	0/20
HP: 0007583	Telangiectasia macularis eruptiva perstans	0/20
HP: 0007587	Numerous pigmented freckles	0/20
HP: 0007648	Punctate cataract	0/20
HP: 0007670	Abnormal vestibulo-ocular reflex	0/20
HP: 0007686	Abnormal pupillary function	0/20
HP: 0007687	Unilateral ptosis	0/20
HP: 0007700	Ocular anterior segment dysgenesis	0/20
HP: 0007707	Congenital aphakia	0/20
HP: 0007759	Opacification of the corneal stroma	0/20
HP: 0007858	Chorioretinal lacunae	0/20
HP: 0007925	Lacrimal duct aplasia	0/20
HP: 0007957	Corneal opacity	0/20
HP: 0007963	Pattern dystrophy of the retina	0/20
HP: 0007970	Congenital ptosis	0/20
HP: 0007973	Retinal dysplasia	0/20
HP: 0008007	Primary congenital glaucoma	0/20
HP: 0008046	Abnormal retinal vascular morphology	0/20
HP: 0008047	Abnormality of the vasculature of the eye	0/20
HP: 0008050	Abnormality of the palpebral fissures	0/20
HP: 0008053	Aplasia/Hypoplasia of the iris	0/20
HP: 0008055	Aplasia/Hypoplasia affecting the uvea	0/20
HP: 0008056	Aplasia/Hypoplasia affecting the eye	0/20
HP: 0008057	Aplasia/Hypoplasia affecting the fundus	0/20
HP: 0008058	Aplasia/Hypoplasia of the optic nerve	0/20
HP: 0008061	Aplasia/Hypoplasia of the retina	0/20
HP: 0008062	Aplasia/Hypoplasia affecting the anterior segment of the eye	0/20
HP: 0008063	Aplasia/Hypoplasia of the lens	0/20
HP: 0008064	Ichthyosis	0/20
HP: 0008065	Aplasia/Hypoplasia of the skin	0/20
HP: 0008066	Abnormal blistering of the skin	0/20
HP: 0008067	Abnormally lax or hyperextensible skin	0/20
HP: 0008069	Neoplasm of the skin	0/20
HP: 0008070	Sparse hair	0/20
HP: 0008081	Pes valgus	0/20
HP: 0008110	Equinovarus deformity	0/20
HP: 0008119	Deformed tarsal bones	0/20
HP: 0008138	Equinus calcaneus	0/20
HP: 0008165	Decreased proportion circulating T-helper cells	0/20
HP: 0008364	Abnormality of the calcaneus	0/20
HP: 0008366	Contractures involving the joints of the feet	0/20
HP: 0008372	Abnormality of vitamin A metabolism	0/20
HP: 0008373	Puberty and gonadal disorders	0/20
HP: 0008386	Aplasia/Hypoplasia of the nails	0/20
HP: 0008388	Abnormal toenail morphology	0/20
HP: 0008391	Dystrophic fingernails	0/20
HP: 0008404	Nail dystrophy	0/20
HP: 0008438	Vertebral arch anomaly	0/20
HP: 0008455	Dysplastic sacrum	0/20
HP: 0008490	Sacral segmentation defect	0/20
HP: 0008496	Multiple rows of eyelashes	0/20
HP: 0008515	Aplasia/Hypoplasia of the vertebrae	0/20
HP: 0008517	Aplasia/Hypoplasia of the sacrum	0/20
HP: 0008518	Aplasia/Hypoplasia involving the vertebral column	0/20
HP: 0008554	Cochlear malformation	0/20
HP: 0008591	Congenital conductive hearing impairment	0/20
HP: 0008619	Bilateral sensorineural hearing impairment	0/20
HP: 0008625	Severe sensorineural hearing impairment	0/20
HP: 0008660	Renotubular dysgenesis	0/20
HP: 0008661	Urethral stenosis	0/20
HP: 0008669	Abnormal spermatogenesis	0/20
HP: 0008670	Partial vaginal septum	0/20
HP: 0008676	Congenital megaureter	0/20
HP: 0008678	Renal hypoplasia/aplasia	0/20
HP: 0008684	Aplasia/hypoplasia of the uterus	0/20
HP: 0008689	Bilateral cryptorchidism	0/20
HP: 0008696	Renal hamartoma	0/20
HP: 0008702	Absent internal genitalia	0/20
HP: 0008705	Ureteral triplication	0/20
HP: 0008715	Testicular dysgenesis	0/20
HP: 0008716	Urethrovaginal fistula	0/20
HP: 0008720	Primary testicular failure	0/20
HP: 0008722	Urethral diverticulum	0/20
HP: 0008726	Hypoplasia of the vagina	0/20
HP: 0008736	Hypoplasia of penis	0/20
HP: 0008740	Longitudinal vaginal septum	0/20
HP: 0008771	Aplasia/Hypoplasia of the ear	0/20
HP: 0008774	Aplasia/Hypoplasia of the inner ear	0/20
HP: 0008776	Abnormal renal artery morphology	0/20
HP: 0008800	Limited hip movement	0/20
HP: 0008873	Disproportionate short-limb short stature	0/20
HP: 0009004	Hypoplasia of the musculature	0/20
HP: 0009025	Increased connective tissue	0/20
HP: 0009103	Aplasia/Hypoplasia involving the pelvis	0/20
HP: 0009108	Aplasia/Hypoplasia involving the femoral head and neck	0/20
HP: 0009112	Aplasia of the left hemidiaphragm	0/20
HP: 0009115	Aplasia/hypoplasia involving the skeleton	0/20
HP: 0009116	Aplasia/Hypoplasia involving bones of the skull	0/20
HP: 0009118	Aplasia/Hypoplasia of the mandible	0/20
HP: 0009121	Abnormal axial skeleton morphology	0/20
HP: 0009122	Aplasia/hypoplasia affecting bones of the axial skeleton	0/20
HP: 0009124	Abnormal adipose tissue morphology	0/20
HP: 0009126	Increased adipose tissue	0/20
HP: 0009127	Abnormality of the musculature of the limbs	0/20
HP: 0009129	Upper limb amyotrophy	0/20
HP: 0009130	Hand muscle atrophy	0/20
HP: 0009131	Abnormality of the musculature of the thorax	0/20
HP: 0009142	Duplication of bones involving the upper extremities	0/20
HP: 0009144	Supernumerary bones of the axial skeleton	0/20
HP: 0009193	Pseudoepiphyses of the metacarpals	0/20
HP: 0009238	Aplasia of the 5th finger	0/20
HP: 0009380	Aplasia of the fingers	0/20
HP: 0009381	Short finger	0/20
HP: 0009473	Joint contracture of the hand	0/20
HP: 0009484	Deviation of the hand or of fingers of the hand	0/20
HP: 0009553	Abnormality of the hairline	0/20
HP: 0009592	Astrocytoma	0/20
HP: 0009594	Retinal hamartoma	0/20
HP: 0009601	Aplasia/Hypoplasia of the thumb	0/20
HP: 0009602	Abnormality of thumb phalanx	0/20
HP: 0009617	Abnormality of the distal phalanx of the thumb	0/20
HP: 0009641	Aplasia/Hypoplasia of the distal phalanx of the thumb	0/20
HP: 0009650	Short distal phalanx of the thumb	0/20
HP: 0009658	Aplasia/Hypoplasia of the phalanges of the thumb	0/20
HP: 0009660	Short phalanx of the thumb	0/20
HP: 0009719	Hypomelanotic macule	0/20
HP: 0009720	Adenoma sebaceum	0/20
HP: 0009726	Renal neoplasm	0/20
HP: 0009728	Neoplasm of striated muscle	0/20
HP: 0009730	Rhabdomyoma	0/20
HP: 0009732	Plexiform neurofibroma	0/20
HP: 0009733	Glioma	0/20
HP: 0009737	Lisch nodules	0/20
HP: 0009743	Distichiasis	0/20
HP: 0009748	Large earlobe	0/20
HP: 0009756	Popliteal pterygium	0/20
HP: 0009759	Neck pterygia	0/20
HP: 0009767	Aplasia/Hypoplasia of the phalanges of the hand	0/20
HP: 0009774	Triangular shaped phalanges of the hand	0/20
HP: 0009778	Short thumb	0/20
HP: 0009790	Hemisacrum	0/20
HP: 0009794	Branchial anomaly	0/20
HP: 0009795	Branchial fistula	0/20
HP: 0009796	Branchial cyst	0/20
HP: 0009799	Supernumerary spleens	0/20
HP: 0009803	Short phalanx of finger	0/20
HP: 0009804	Reduced number of teeth	0/20
HP: 0009810	Abnormality of upper limb joint	0/20
HP: 0009811	Abnormality of the elbow	0/20
HP: 0009813	Upper limb phocomelia	0/20
HP: 0009814	Upper limb peromelia	0/20
HP: 0009815	Aplasia/hypoplasia of the extremities	0/20
HP: 0009816	Lower limb undergrowth	0/20
HP: 0009817	Aplasia involving bones of the lower limbs	0/20
HP: 0009824	Upper limb undergrowth	0/20
HP: 0009825	Aplasia involving bones of the extremities	0/20
HP: 0009826	Limb undergrowth	0/20
HP: 0009828	Peromelia	0/20
HP: 0009829	Phocomelia	0/20
HP: 0009830	Peripheral neuropathy	0/20
HP: 0009832	Abnormal distal phalanx morphology of finger	0/20
HP: 0009835	Aplasia/Hypoplasia of the distal phalanges of the hand	0/20
HP: 0009879	Simplified gyral pattern	0/20
HP: 0009882	Short distal phalanx of finger	0/20
HP: 0009888	Abnormality of secondary sexual hair	0/20
HP: 0009901	Crumpled ear	0/20
HP: 0009906	Aplasia/Hypoplasia of the earlobes	0/20
HP: 0009911	Abnormal temporal bone morphology	0/20
HP: 0009920	Nevus of Ota	0/20
HP: 0009924	Aplasia/Hypoplasia involving the nose	0/20
HP: 0009934	Supernumerary naris	0/20
HP: 0009942	Duplication of thumb phalanx	0/20
HP: 0009944	Partial duplication of thumb phalanx	0/20
HP: 0009997	Duplication of phalanx of hand	0/20
HP: 0009999	Partial duplication of the phalanx of hand	0/20
HP: 0010049	Short metacarpal	0/20
HP: 0010051	Deviation of the hallux	0/20
HP: 0010052	Abnormal morphology of the proximal phalanx of the hallux	0/20
HP: 0010057	Abnormality of the phalanges of the hallux	0/20
HP: 0010059	Broad hallux phalanx	0/20
HP: 0010086	Broad proximal phalanx of the hallux	0/20
HP: 0010160	Abnormality of the epiphyses of the toes	0/20
HP: 0010161	Abnormality of the phalanges of the toes	0/20
HP: 0010164	Cone-shaped epiphyses of the toes	0/20
HP: 0010173	Aplasia/Hypoplasia of the phalanges of the toes	0/20
HP: 0010174	Broad phalanx of the toes	0/20
HP: 0010183	Abnormality of the middle phalanges of the toes	0/20
HP: 0010184	Abnormality of toe proximal phalanx	0/20
HP: 0010204	Broad proximal phalanx of toe	0/20
HP: 0010296	Ankyloglossia	0/20
HP: 0010301	Spinal dysraphism	0/20
HP: 0010302	Spinal cord tumor	0/20
HP: 0010303	Abnormal spinal meningeal morphology	0/20
HP: 0010305	Absence of the sacrum	0/20
HP: 0010307	Stridor	0/20
HP: 0010311	Aplasia/Hypoplasia of the breasts	0/20
HP: 0010316	Ebstein anomaly of the tricuspid valve	0/20
HP: 0010319	Abnormality of the 2nd toe	0/20
HP: 0010321	Abnormality of the 4th toe	0/20
HP: 0010438	Abnormal ventricular septum morphology	0/20
HP: 0010446	Tricuspid stenosis	0/20
HP: 0010450	Esophageal stenosis	0/20
HP: 0010458	Female pseudohermaphroditism	0/20
HP: 0010460	Abnormality of the female genitalia	0/20
HP: 0010461	Abnormality of the male genitalia	0/20
HP: 0010468	Aplasia/Hypoplasia of the testes	0/20
HP: 0010469	Absent testis	0/20
HP: 0010475	Cloacal exstrophy	0/20
HP: 0010476	Aplasia/Hypoplasia of the bladder	0/20
HP: 0010477	Aplasia of the bladder	0/20
HP: 0010478	Abnormality of the urachus	0/20
HP: 0010480	Urethral fistula	0/20
HP: 0010481	Urethral valve	0/20
HP: 0010490	Abnormality of the palmar creases	0/20
HP: 0010497	Sirenomelia	0/20
HP: 0010511	Long toe	0/20
HP: 0010515	Aplasia/Hypoplasia of the thymus	0/20
HP: 0010516	Thymus hyperplasia	0/20
HP: 0010517	Ectopic thymus tissue	0/20
HP: 0010518	Thyroglossal cyst	0/20
HP: 0010549	Weakness due to upper motor neuron dysfunction	0/20
HP: 0010550	Paraplegia	0/20
HP: 0010551	Paraplegia/paraparesis	0/20
HP: 0010554	Cutaneous finger syndactyly	0/20
HP: 0010566	Hamartoma	0/20
HP: 0010568	Hamartoma of the eye	0/20
HP: 0010576	Intracranial cystic lesion	0/20
HP: 0010579	Cone-shaped epiphysis	0/20
HP: 0010584	Pseudoepiphyses	0/20
HP: 0010609	Skin tags	0/20
HP: 0010610	Palmar pits	0/20
HP: 0010615	Angiofibromas	0/20
HP: 0010619	Fibroadenoma of the breast	0/20
HP: 0010621	Cutaneous syndactyly of toes	0/20
HP: 0010622	Neoplasm of the skeletal system	0/20
HP: 0010631	Abnormality of the epiphyses of the feet	0/20
HP: 0010647	Abnormal elasticity of skin	0/20
HP: 0010648	Dermal translucency	0/20
HP: 0010651	Abnormal meningeal morphology	0/20
HP: 0010662	Abnormality of the diencephalon	0/20
HP: 0010663	Abnormality of thalamus morphology	0/20
HP: 0010668	Abnormality of the zygomatic bone	0/20
HP: 0010674	Abnormality of the curvature of the vertebral column	0/20
HP: 0010693	Pulverulent cataract	0/20
HP: 0010704	1-2 finger syndactyly	0/20
HP: 0010719	Abnormality of hair texture	0/20
HP: 0010720	Abnormal hair pattern	0/20
HP: 0010722	Asymmetry of the ears	0/20
HP: 0010734	Fibrous dysplasia of the bones	0/20
HP: 0010735	Polyostotic fibrous dysplasia	0/20
HP: 0010736	Monostotic fibrous dysplasia	0/20
HP: 0010740	Osteopathia striata	0/20
HP: 0010742	Edema of the upper limbs	0/20
HP: 0010743	Short metatarsal	0/20
HP: 0010745	Aplasia of the phalanges of the toes	0/20
HP: 0010753	Midline defect of mandible	0/20
HP: 0010758	Abnormality of the premaxilla	0/20
HP: 0010766	Ectopic calcification	0/20
HP: 0010772	Anomalous pulmonary venous return	0/20
HP: 0010773	Partial anomalous pulmonary venous return	0/20
HP: 0010775	Vascular ring	0/20
HP: 0010777	Bronchomegaly	0/20
HP: 0010785	Gonadal neoplasm	0/20
HP: 0010786	Urinary tract neoplasm	0/20
HP: 0010787	Genital neoplasm	0/20
HP: 0010815	Nevus sebaceous	0/20
HP: 0010816	Epidermal nevus	0/20
HP: 0010864	Intellectual disability, severe	0/20
HP: 0010865	Oppositional defiant disorder	0/20
HP: 0010866	Abdominal wall defect	0/20
HP: 0010873	Cervical spinal cord atrophy	0/20
HP: 0010880	Increased nuchal translucency	0/20
HP: 0010881	Abnormality of the umbilical cord	0/20
HP: 0010883	Aortic valve atresia	0/20
HP: 0010894	Abnormal circulating serine family amino acid concentration	0/20
HP: 0010895	Abnormal circulating glycine concentration	0/20
HP: 0010899	Abnormal circulating aspartate family amino acid concentration	0/20
HP: 0010908	Abnormal circulating lysine concentration	0/20
HP: 0010920	Zonular cataract	0/20
HP: 0010927	Abnormal blood inorganic cation concentration	0/20
HP: 0010929	Abnormal blood cation concentration	0/20
HP: 0010932	Abnormal circulating nucleobase concentration	0/20
HP: 0010935	Abnormality of the upper urinary tract	0/20
HP: 0010936	Abnormality of the lower urinary tract	0/20
HP: 0010937	Abnormality of the nasal skeleton	0/20
HP: 0010938	Abnormality of the external nose	0/20
HP: 0010939	Abnormality of the nasal bone	0/20
HP: 0010944	Abnormal renal pelvis morphology	0/20
HP: 0010945	Fetal pyelectasis	0/20
HP: 0010946	Dilatation of the renal pelvis	0/20
HP: 0010955	Dilatation of the bladder	0/20
HP: 0010956	Fetal megacystis	0/20
HP: 0010957	Congenital posterior urethral valve	0/20
HP: 0010958	Bilateral renal agenesis	0/20
HP: 0010959	Congenital cystic adenomatoid malformation of the lung	0/20
HP: 0010972	Anemia of inadequate production	0/20
HP: 0010974	Abnormal myeloid leukocyte morphology	0/20
HP: 0010975	Abnormal B cell count	0/20
HP: 0010976	B lymphocytopenia	0/20
HP: 0010978	Abnormality of immune system physiology	0/20
HP: 0010987	Abnormal cellular immune system morphology	0/20
HP: 0010990	Abnormality of the common coagulation pathway	0/20
HP: 0010991	Abnormal morphology of the abdominal musculature	0/20
HP: 0010992	Stress urinary incontinence	0/20
HP: 0010993	Abnormality of the cerebral subcortex	0/20
HP: 0011001	Increased bone mineral density	0/20
HP: 0011004	Abnormal systemic arterial morphology	0/20
HP: 0011006	Abnormal morphology of the musculature of the neck	0/20
HP: 0011014	Abnormal glucose homeostasis	0/20
HP: 0011015	Abnormal blood glucose concentration	0/20
HP: 0011017	Abnormal cellular physiology	0/20
HP: 0011024	Abnormality of the gastrointestinal tract	0/20
HP: 0011025	Abnormal cardiovascular system physiology	0/20
HP: 0011026	Aplasia/Hypoplasia of the vagina	0/20
HP: 0011027	Abnormal fallopian tube morphology	0/20
HP: 0011028	Abnormality of blood circulation	0/20
HP: 0011029	Internal hemorrhage	0/20
HP: 0011032	Abnormality of fluid regulation	0/20
HP: 0011035	Abnormal renal cortex morphology	0/20
HP: 0011040	Abnormality of the intrahepatic bile duct	0/20
HP: 0011061	Abnormality of dental structure	0/20
HP: 0011063	Abnormality of incisor morphology	0/20
HP: 0011072	Rootless teeth	0/20
HP: 0011073	Abnormality of dental color	0/20
HP: 0011094	Overbite	0/20
HP: 0011099	Spastic hemiparesis	0/20
HP: 0011100	Intestinal atresia	0/20
HP: 0011103	Abnormal left ventricular outflow tract morphology	0/20
HP: 0011119	Abnormality of the nasal dorsum	0/20
HP: 0011120	Concave nasal ridge	0/20
HP: 0011121	Abnormality of skin morphology	0/20
HP: 0011122	Abnormality of skin physiology	0/20
HP: 0011123	Inflammatory abnormality of the skin	0/20
HP: 0011124	Abnormality of epidermal morphology	0/20
HP: 0011129	Bilateral fetal pyelectasis	0/20
HP: 0011130	Abnormal renal calyx morphology	0/20
HP: 0011135	Aplasia/Hypoplasia of the sweat glands	0/20
HP: 0011136	Aplasia of the sweat glands	0/20
HP: 0011138	Abnormality of skin adnexa morphology	0/20
HP: 0011139	Gastric duplication	0/20
HP: 0011140	Gastrointestinal duplication	0/20
HP: 0011145	Symptomatic seizures	0/20
HP: 0011153	Focal motor seizure	0/20
HP: 0011174	Focal hyperkinetic seizure	0/20
HP: 0011217	Abnormal shape of the occiput	0/20
HP: 0011226	Aplasia/Hypoplasia of the eyelid	0/20
HP: 0011276	Vascular skin abnormality	0/20
HP: 0011277	Abnormality of the urinary system physiology	0/20
HP: 0011280	Abnormality of urine calcium concentration	0/20
HP: 0011282	Abnormality of hindbrain morphology	0/20
HP: 0011283	Abnormality of the metencephalon	0/20
HP: 0011286	Total colonic aganglionosis	0/20
HP: 0011297	Abnormal digit morphology	0/20
HP: 0011301	Absent foot	0/20
HP: 0011314	Abnormality of long bone morphology	0/20
HP: 0011328	Abnormality of fontanelles	0/20
HP: 0011329	Abnormality of cranial sutures	0/20
HP: 0011334	Facial shape deformation	0/20
HP: 0011337	Abnormality of mouth size	0/20
HP: 0011338	Abnormality of mouth shape	0/20
HP: 0011339	Abnormality of upper lip vermillion	0/20
HP: 0011354	Generalized abnormality of skin	0/20
HP: 0011355	Localized skin lesion	0/20
HP: 0011356	Regional abnormality of skin	0/20
HP: 0011357	obsolete Abnormality of hair density	0/20
HP: 0011361	Congenital abnormal hair pattern	0/20
HP: 0011362	Abnormal hair quantity	0/20
HP: 0011367	Yellow nails	0/20
HP: 0011368	Epidermal thickening	0/20
HP: 0011372	Aplasia of the inner ear	0/20
HP: 0011376	Morphological abnormality of the vestibule of the inner ear	0/20
HP: 0011380	Morphological abnormality of the semicircular canal	0/20
HP: 0011384	Abnormality of the internal auditory canal	0/20
HP: 0011385	Absent internal auditory canal	0/20
HP: 0011388	Enlarged cochlear aqueduct	0/20
HP: 0011389	Functional abnormality of the inner ear	0/20
HP: 0011390	Morphological abnormality of the inner ear	0/20
HP: 0011400	Abnormal CNS myelination	0/20
HP: 0011418	Abnormal insertion of umbilical cord	0/20
HP: 0011422	Abnormal blood chloride concentration	0/20
HP: 0011425	Fetal ultrasound soft marker	0/20
HP: 0011426	Fetal choroid plexus cysts	0/20
HP: 0011436	Abnormal maternal serum screening	0/20
HP: 0011442	Abnormal central motor function	0/20
HP: 0011443	Abnormality of coordination	0/20
HP: 0011446	Abnormality of higher mental function	0/20
HP: 0011450	Unusual CNS infection	0/20
HP: 0011452	Functional abnormality of the middle ear	0/20
HP: 0011458	Abdominal symptom	0/20
HP: 0011464	Aganglionosis of the small intestine	0/20
HP: 0011466	Aplasia/Hypoplasia of the gallbladder	0/20
HP: 0011481	Abnormal lacrimal duct morphology	0/20
HP: 0011492	Abnormality of corneal stroma	0/20
HP: 0011526	Abnormality of lens shape	0/20
HP: 0011534	Abnormal spatial orientation of the cardiac segments	0/20
HP: 0011535	Abnormal atrial arrangement	0/20
HP: 0011537	Left atrial isomerism	0/20
HP: 0011540	Congenitally corrected transposition of the great arteries	0/20
HP: 0011545	Abnormal connection of the cardiac segments	0/20
HP: 0011546	Abnormal atrioventricular connection	0/20
HP: 0011553	Discordant atrioventricular connection	0/20
HP: 0011563	Abnormal ventriculoarterial connection	0/20
HP: 0011565	Common atrium	0/20
HP: 0011567	Sinus venosus atrial septal defect	0/20
HP: 0011570	Congenital mitral stenosis	0/20
HP: 0011571	Parachute mitral valve	0/20
HP: 0011572	Supramitral ring	0/20
HP: 0011581	Double outlet left ventricle	0/20
HP: 0011587	Abnormal branching pattern of the aortic arch	0/20
HP: 0011603	Congenital malformation of the great arteries	0/20
HP: 0011605	Congenitally corrected transposition of the great arteries with ventricular septal defect	0/20
HP: 0011620	Abnormality of abdominal situs	0/20
HP: 0011626	Scimitar anomaly	0/20
HP: 0011627	Aorto-ventricular tunnel	0/20
HP: 0011642	Abnormal coronary sinus morphology	0/20
HP: 0011677	Tetralogy of Fallot with atrioventricular canal defect	0/20
HP: 0011682	Perimembranous ventricular septal defect	0/20
HP: 0011718	Abnormality of the pulmonary veins	0/20
HP: 0011723	Congenital malformation of the right heart	0/20
HP: 0011729	Abnormality of joint mobility	0/20
HP: 0011732	Abnormality of adrenal morphology	0/20
HP: 0011766	Abnormality of the parathyroid morphology	0/20
HP: 0011768	Parathyroid dysgenesis	0/20
HP: 0011772	Abnormality of thyroid morphology	0/20
HP: 0011792	Neoplasm by histology	0/20
HP: 0011799	Abnormality of facial soft tissue	0/20
HP: 0011804	Abnormal muscle physiology	0/20
HP: 0011805	Abnormal skeletal muscle morphology	0/20
HP: 0011815	Cephalocele	0/20
HP: 0011820	Membranous choanal atresia	0/20
HP: 0011821	Abnormality of facial skeleton	0/20
HP: 0011830	Abnormal oral mucosa morphology	0/20
HP: 0011839	Abnormal T cell count	0/20
HP: 0011842	Abnormality of skeletal morphology	0/20
HP: 0011843	Abnormality of skeletal physiology	0/20
HP: 0011844	Abnormal appendicular skeleton morphology	0/20
HP: 0011849	Abnormal bone ossification	0/20
HP: 0011885	Hemorrhage of the eye	0/20
HP: 0011893	Abnormal leukocyte count	0/20
HP: 0011912	Abnormality of the glenoid fossa	0/20
HP: 0011927	Short digit	0/20
HP: 0011947	Respiratory tract infection	0/20
HP: 0011957	Abnormal pectoral muscle morphology	0/20
HP: 0011974	Myelofibrosis	0/20
HP: 0011984	Atretic gallbladder	0/20
HP: 0011985	Acholic stools	0/20
HP: 0011994	Abnormal atrial septum morphology	0/20
HP: 0012025	Abnormal circulating ornithine concentration	0/20
HP: 0012026	Hyperornithinemia	0/20
HP: 0012028	Hepatocellular adenoma	0/20
HP: 0012031	Lipomatous tumor	0/20
HP: 0012032	Lipoma	0/20
HP: 0012033	Sacral lipoma	0/20
HP: 0012072	Aciduria	0/20
HP: 0012090	Abnormal pancreas morphology	0/20
HP: 0012110	Hypoplasia of the pons	0/20
HP: 0012118	Laryngeal carcinoma	0/20
HP: 0012130	Abnormal erythroid lineage cell morphology	0/20
HP: 0012145	Abnormality of multiple cell lineages in the bone marrow	0/20
HP: 0012150	Single lineage myelodysplasia	0/20
HP: 0012165	Oligodactyly	0/20
HP: 0012180	Cystic medial necrosis	0/20
HP: 0012210	Abnormal renal morphology	0/20
HP: 0012211	Abnormal renal physiology	0/20
HP: 0012227	Urethral stricture	0/20
HP: 0012243	Abnormal reproductive system morphology	0/20
HP: 0012248	Prolonged PR interval	0/20
HP: 0012252	Abnormal respiratory system morphology	0/20
HP: 0012261	Abnormal respiratory motile cilium physiology	0/20
HP: 0012262	Abnormal ciliary motility	0/20
HP: 0012263	Immotile cilia	0/20
HP: 0012294	Abnormality of the occipital bone	0/20
HP: 0012303	Abnormal aortic arch morphology	0/20
HP: 0012305	Coarctation of the descending aortic arch	0/20
HP: 0012324	Myeloid leukemia	0/20
HP: 0012325	Chronic myelomonocytic leukemia	0/20
HP: 0012330	Pyelonephritis	0/20
HP: 0012331	Abnormal autonomic nervous system morphology	0/20
HP: 0012332	Abnormal autonomic nervous system physiology	0/20
HP: 0012337	Abnormal homeostasis	0/20
HP: 0012366	Basilar invagination	0/20
HP: 0012369	Abnormality of malar bones	0/20
HP: 0012372	Abnormal eye morphology	0/20
HP: 0012373	Abnormal eye physiology	0/20
HP: 0012382	Left-to-right shunt	0/20
HP: 0012385	Camptodactyly	0/20
HP: 0012429	Aplasia/Hypoplasia of the cerebral white matter	0/20
HP: 0012430	Cerebral white matter hypoplasia	0/20
HP: 0012433	Abnormal social behavior	0/20
HP: 0012437	Abnormal gallbladder morphology	0/20
HP: 0012440	Abnormal biliary tract morphology	0/20
HP: 0012443	Abnormality of brain morphology	0/20
HP: 0012447	Abnormal myelination	0/20
HP: 0012471	Thick vermilion border	0/20
HP: 0012472	Eclabion	0/20
HP: 0012503	Abnormality of the pituitary gland	0/20
HP: 0012531	Pain	0/20
HP: 0012535	Abnormal synaptic transmission	0/20
HP: 0012547	Abnormal involuntary eye movements	0/20
HP: 0012571	Ureter fissus	0/20
HP: 0012572	Ureter duplex	0/20
HP: 0012575	Abnormal nephron morphology	0/20
HP: 0012584	Bilateral renal hypoplasia	0/20
HP: 0012591	Abnormal urinary electrolyte concentration	0/20
HP: 0012614	Abnormal urine cytology	0/20
HP: 0012615	Cylindruria	0/20
HP: 0012618	Urachal cyst	0/20
HP: 0012620	Cloacal abnormality	0/20
HP: 0012622	Chronic kidney disease	0/20
HP: 0012638	Abnormal nervous system physiology	0/20
HP: 0012639	Abnormal nervous system morphology	0/20
HP: 0012646	Retractile testis	0/20
HP: 0012647	Abnormal inflammatory response	0/20
HP: 0012649	Increased inflammatory response	0/20
HP: 0012703	Abnormal subarachnoid space morphology	0/20
HP: 0012704	Widened subarachnoid space	0/20
HP: 0012712	Mild hearing impairment	0/20
HP: 0012714	Severe hearing impairment	0/20
HP: 0012717	Severe conductive hearing impairment	0/20
HP: 0012718	Morphological abnormality of the gastrointestinal tract	0/20
HP: 0012719	Functional abnormality of the gastrointestinal tract	0/20
HP: 0012721	Venous malformation	0/20
HP: 0012722	Heart block	0/20
HP: 0012725	Cutaneous syndactyly	0/20
HP: 0012727	Thoracic aortic aneurysm	0/20
HP: 0012732	Anorectal anomaly	0/20
HP: 0012733	Macule	0/20
HP: 0012739	Agenesis of the small intestine	0/20
HP: 0012741	Unilateral cryptorchidism	0/20
HP: 0012745	Short palpebral fissure	0/20
HP: 0012757	Abnormal neuron morphology	0/20
HP: 0012758	Neurodevelopmental delay	0/20
HP: 0012759	Neurodevelopmental abnormality	0/20
HP: 0012769	Abnormal arm span	0/20
HP: 0012771	Increased arm span	0/20
HP: 0012785	Flexion contracture of finger	0/20
HP: 0012787	Recurrent pyelonephritis	0/20
HP: 0012815	Hypoplastic female external genitalia	0/20
HP: 0012816	Right ventricular noncompaction cardiomyopathy	0/20
HP: 0012817	Noncompaction cardiomyopathy	0/20
HP: 0012848	Small intestinal stenosis	0/20
HP: 0012849	Small intestinal bleeding	0/20
HP: 0012870	Vanishing testis	0/20
HP: 0012874	Abnormal male reproductive system physiology	0/20
HP: 0012880	Abnormality of the labia minora	0/20
HP: 0012881	Abnormality of the labia majora	0/20
HP: 0012883	Fallopian tube cyst	0/20
HP: 0012886	Hemorrhagic ovarian cyst	0/20
HP: 0012888	Abnormality of the uterine cervix	0/20
HP: 0020047	Abnormal myeloid cell morphology	0/20
HP: 0020073	Hypopigmented macule	0/20
HP: 0025011	Pyriform aperture stenosis	0/20
HP: 0025015	Abnormal vascular morphology	0/20
HP: 0025019	Arterial rupture	0/20
HP: 0025025	Rectovestibular fistula	0/20
HP: 0025028	Abnormality of enteric nervous system morphology	0/20
HP: 0025031	Abnormality of the digestive system	0/20
HP: 0025032	Abnormality of digestive system physiology	0/20
HP: 0025033	Abnormality of digestive system morphology	0/20
HP: 0025068	Incomitant strabismus	0/20
HP: 0025104	Capillary malformation	0/20
HP: 0025105	Nevus anemicus	0/20
HP: 0025142	Constitutional symptom	0/20
HP: 0025150	Hypoganglionosis	0/20
HP: 0025193	Posterolateral diaphragmatic hernia	0/20
HP: 0025252	Geographic tongue	0/20
HP: 0025263	Stiff knee	0/20
HP: 0025270	Abnormality of esophagus physiology	0/20
HP: 0025314	Choroidal nevus	0/20
HP: 0025323	Abnormal arterial physiology	0/20
HP: 0025335	Delayed ability to stand	0/20
HP: 0025354	Abnormal cellular phenotype	0/20
HP: 0025360	Polycalycosis	0/20
HP: 0025407	Rectourethral fistula	0/20
HP: 0025408	Abnormal spleen morphology	0/20
HP: 0025422	Pleural cyst	0/20
HP: 0025423	Abnormal larynx morphology	0/20
HP: 0025424	Abnormal larynx physiology	0/20
HP: 0025426	Abnormal bronchus morphology	0/20
HP: 0025429	Abnormal cry	0/20
HP: 0025430	High-pitched cry	0/20
HP: 0025456	Abnormal CSF protein level	0/20
HP: 0025458	Decreased CSF albumin concentration	0/20
HP: 0025461	Abnormal cell morphology	0/20
HP: 0025480	Lipomyelomeningocele	0/20
HP: 0025487	Abnormality of bladder morphology	0/20
HP: 0025491	Venous stenosis	0/20
HP: 0025510	Nevus spilus	0/20
HP: 0025511	Nevus sebaceus	0/20
HP: 0025523	Abnormal morphology of the chordae tendinae of the mitral valve	0/20
HP: 0025590	Abnormal extraocular muscle physiology	0/20
HP: 0025605	Lid lag on downgaze	0/20
HP: 0025633	Abnormal ureter morphology	0/20
HP: 0025634	Abnormal ureter physiology	0/20
HP: 0025639	Increased urinary zinc level	0/20
HP: 0025640	Abnormal urinary mineral level	0/20
HP: 0030008	Cervical agenesis	0/20
HP: 0030012	Abnormal female reproductive system physiology	0/20
HP: 0030021	Auricular tag	0/20
HP: 0030025	Auricular pit	0/20
HP: 0030029	Splayed fingers	0/20
HP: 0030038	Enchondroma	0/20
HP: 0030039	Fused thoracic vertebrae	0/20
HP: 0030044	Flexion contracture of digit	0/20
HP: 0030045	Serpentine fibula	0/20
HP: 0030060	Nervous tissue neoplasm	0/20
HP: 0030061	Neuroectodermal neoplasm	0/20
HP: 0030063	Neuroepithelial neoplasm	0/20
HP: 0030084	Clinodactyly	0/20
HP: 0030151	Cholangitis	0/20
HP: 0030163	Abnormal vascular physiology	0/20
HP: 0030182	Tetraplegia/tetraparesis	0/20
HP: 0030191	Abnormal peripheral nervous system synaptic transmission	0/20
HP: 0030236	Abnormality of muscle size	0/20
HP: 0030261	Absent penis	0/20
HP: 0030264	Webbed penis	0/20
HP: 0030268	Hyperplastic callus formation	0/20
HP: 0030310	Upper extremity joint dislocation	0/20
HP: 0030311	Lower extremity joint dislocation	0/20
HP: 0030448	Soft tissue sarcoma	0/20
HP: 0030450	Neuroplasm of the autonomic nervous system	0/20
HP: 0030451	Mesenteric cyst	0/20
HP: 0030510	Combined hamartoma of the retinal pigment epithelium and retina	0/20
HP: 0030669	Abnormal ocular adnexa morphology	0/20
HP: 0030670	Hamartoma of the orbital region	0/20
HP: 0030676	Satyr ear	0/20
HP: 0030680	Abnormality of cardiovascular system morphology	0/20
HP: 0030711	Hydrocolpos	0/20
HP: 0030724	Central nervous system cyst	0/20
HP: 0030732	Dysplastic tricuspid valve	0/20
HP: 0030791	Abnormal jaw morphology	0/20
HP: 0030809	Abnormal tongue morphology	0/20
HP: 0030829	Abnormal breath sound	0/20
HP: 0030853	Heterotaxy	0/20
HP: 0030854	Scleral staphyloma	0/20
HP: 0030872	Abnormal cardiac ventricular function	0/20
HP: 0030875	Abnormality of pulmonary circulation	0/20
HP: 0030895	Abnormal gastrointestinal motility	0/20
HP: 0030911	Bifid clitoris	0/20
HP: 0030912	Duplicated clitoris	0/20
HP: 0030914	Abnormal peristalsis	0/20
HP: 0030956	Abnormality of cardiovascular system electrophysiology	0/20
HP: 0030961	Microspherophakia	0/20
HP: 0030962	Abnormal morphology of the great vessels	0/20
HP: 0030966	Abnormal pulmonary artery morphology	0/20
HP: 0030968	Abnormal pulmonary vein morphology	0/20
HP: 0030972	Abnormal systemic blood pressure	0/20
HP: 0030994	Pancreas divisum	0/20
HP: 0031045	Acral blistering	0/20
HP: 0031058	Impairment of activities of daily living	0/20
HP: 0031064	Impaired continence	0/20
HP: 0031065	Abnormal ovarian morphology	0/20
HP: 0031066	Abnormal ovarian physiology	0/20
HP: 0031071	Abnormal endocrine morphology	0/20
HP: 0031086	Ectopic ovary	0/20
HP: 0031093	Abnormal breast morphology	0/20
HP: 0031095	Abnormal humerus morphology	0/20
HP: 0031105	Abnormal uterus morphology	0/20
HP: 0031157	Carotid cavernous fistula	0/20
HP: 0031254	Thalamic arteriovenous malformation	0/20
HP: 0031263	Abnormal renal corpuscle morphology	0/20
HP: 0031298	Coronary sinus enlargement	0/20
HP: 0031347	Uterine arteriovenous malformation	0/20
HP: 0031353	Otitis media with effusion	0/20
HP: 0031357	Glomeruloid hemangioma	0/20
HP: 0031367	Metaphyseal striations	0/20
HP: 0031449	Perineal hemangioma	0/20
HP: 0031457	Pulmonary opacity	0/20
HP: 0031459	Soft tissue neoplasm	0/20
HP: 0031460	Benign muscle neoplasm	0/20
HP: 0031461	Intramuscular Myxoma	0/20
HP: 0031466	Impairment in personality functioning	0/20
HP: 0031481	Abnormal mitral valve physiology	0/20
HP: 0031546	Cardiac conduction abnormality	0/20
HP: 0031565	Abdominal situs ambiguus	0/20
HP: 0031593	Abnormal PR interval	0/20
HP: 0031607	Pelvic organ prolapse	0/20
HP: 0031635	Anomalous origin of the left common carotid artery from the brachiocephalic artery	0/20
HP: 0031650	Abnormal atrioventricular valve physiology	0/20
HP: 0031651	Abnormal tricuspid valve physiology	0/20
HP: 0031652	Abnormal aortic valve physiology	0/20
HP: 0031653	Abnormal heart valve physiology	0/20
HP: 0031654	Abnormal pulmonary valve physiology	0/20
HP: 0031684	Renal artery atherosclerosis	0/20
HP: 0031703	Abnormal ear morphology	0/20
HP: 0031704	Abnormal ear physiology	0/20
HP: 0031748	Abnormal vertical rectus muscle physiology	0/20
HP: 0031755	Abnormal rectus muscle physiology	0/20
HP: 0031783	Absent coronary sinus	0/20
HP: 0031785	Abnormal eyelid movement	0/20
HP: 0031803	Fundus hemorrhage	0/20
HP: 0031816	Abnormal oral morphology	0/20
HP: 0031826	Abnormal reflex	0/20
HP: 0031846	Femur fracture	0/20
HP: 0031853	Isomerism	0/20
HP: 0031854	Left Isomerism	0/20
HP: 0031857	Ineffective esophageal peristalsis	0/20
HP: 0031879	Abnormal eyelid physiology	0/20
HP: 0031909	Unicornuate uterus	0/20
HP: 0031910	Abnormal cranial nerve physiology	0/20
HP: 0031911	Abnormal fifth cranial nerve physiology	0/20
HP: 0031912	Trigeminal anesthesia	0/20
HP: 0031918	Ovarian sex cord-stromal tumor	0/20
HP: 0031923	Hematocolpos	0/20
HP: 0031932	Aorto-left ventricular tunnel	0/20
HP: 0031938	Abnormal conus terminalis morphology	0/20
HP: 0031941	Abnormal portal venous system morphology	0/20
HP: 0031957	Spastic hemiparetic gait	0/20
HP: 0031979	Abnormal urine carbohydrate level	0/20
HP: 0031980	Abnormal urine carboxylic acid level	0/20
HP: 0032039	Abnormality of the ocular adnexa	0/20
HP: 0032040	Abnormal ocular adnexa physiology	0/20
HP: 0032043	Odynophagia	0/20
HP: 0032075	Splenopancreatic fusion	0/20
HP: 0032076	Abnormal male urethral meatus morphology	0/20
HP: 0032077	Male urethral meatus stenosis	0/20
HP: 0032092	Left ventricular outflow tract obstruction	0/20
HP: 0032101	Unusual infection	0/20
HP: 0032158	Unusual infection by anatomical site	0/20
HP: 0032180	Abnormal circulating metabolite concentration	0/20
HP: 0032192	Hydatidiform mole	0/20
HP: 0032245	Abnormal metabolism	0/20
HP: 0032251	Abnormal immune system morphology	0/20
HP: 0032263	Increased blood pressure	0/20
HP: 0032327	Interhemispheric cyst	0/20
HP: 0032417	Periglomerular fibrosis	0/20
HP: 0032445	Pulmonary cyst	0/20
HP: 0032527	Inferiorly positioned umbilicus	0/20
HP: 0032537	Delayed fracture healing	0/20
HP: 0040004	Abnormality of corneal shape	0/20
HP: 0040045	Abnormal hemidiaphragm morphology	0/20
HP: 0040046	Abnormal left hemidiaphragm morphology	0/20
HP: 0040047	Abnormal right hemidiaphragm morphology	0/20
HP: 0040048	obsolete Aplasia of the left hemidiaphragm	0/20
HP: 0040063	Decreased adipose tissue	0/20
HP: 0040064	Abnormality of limbs	0/20
HP: 0040068	Abnormality of limb bone	0/20
HP: 0040069	Abnormal lower limb bone morphology	0/20
HP: 0040070	Abnormal upper limb bone morphology	0/20
HP: 0040071	Abnormal morphology of ulna	0/20
HP: 0040072	Abnormality of forearm bone	0/20
HP: 0040073	Abnormal forearm bone morphology	0/20
HP: 0040088	Abnormal lymphocyte count	0/20
HP: 0040093	Asymmetry of the position of the ears	0/20
HP: 0040126	Abnormal vitamin B12 level	0/20
HP: 0040156	Elevated urinary carboxylic acid	0/20
HP: 0040163	Abnormal pelvis bone morphology	0/20
HP: 0040192	APUdoma	0/20
HP: 0040195	Decreased head circumference	0/20
HP: 0040211	Abnormality of the skin of the palm	0/20
HP: 0040223	Pulmonary hemorrhage	0/20
HP: 0040273	Adenocarcinoma of the intestines	0/20
HP: 0040274	Adenocarcinoma of the small intestine	0/20
HP: 0040294	Duplicated tongue	0/20
HP: 0040314	Blind vagina	0/20
HP: 0041047	Bladder outlet obstruction	0/20
HP: 0045005	Neural tube defect	0/20
HP: 0045009	Abnormal morphology of the radius	0/20
HP: 0045017	Congenital malformation of the left heart	0/20
HP: 0045025	Narrow palpebral fissure	0/20
HP: 0045058	Abnormality of the testis size	0/20
HP: 0045060	Aplasia/hypoplasia involving bones of the extremities	0/20
HP: 0100000	Early onset of sexual maturation	0/20
HP: 0100006	Neoplasm of the central nervous system	0/20
HP: 0100007	Neoplasm of the peripheral nervous system	0/20
HP: 0100012	Neoplasm of the eye	0/20
HP: 0100013	Neoplasm of the breast	0/20
HP: 0100016	Abnormality of mesentery morphology	0/20
HP: 0100022	Abnormality of movement	0/20
HP: 0100026	Arteriovenous malformation	0/20
HP: 0100033	Tics	0/20
HP: 0100035	Phonic tics	0/20
HP: 0100037	Abnormality of the scalp hair	0/20
HP: 0100134	Abnormality of the axillary hair	0/20
HP: 0100240	Synostosis of joints	0/20
HP: 0100242	Sarcoma	0/20
HP: 0100255	Metaphyseal dysplasia	0/20
HP: 0100257	Ectrodactyly	0/20
HP: 0100261	Abnormal tendon morphology	0/20
HP: 0100272	Branchial sinus	0/20
HP: 0100274	Gustatory lacrimation	0/20
HP: 0100276	Skin pit	0/20
HP: 0100277	Periauricular skin pits	0/20
HP: 0100279	Ulcerative colitis	0/20
HP: 0100280	Crohn's disease	0/20
HP: 0100281	Chronic colitis	0/20
HP: 0100282	Acute colitis	0/20
HP: 0100326	Immunologic hypersensitivity	0/20
HP: 0100333	Unilateral cleft lip	0/20
HP: 0100335	Non-midline cleft lip	0/20
HP: 0100336	Bilateral cleft lip	0/20
HP: 0100337	Bilateral cleft palate	0/20
HP: 0100338	Non-midline cleft palate	0/20
HP: 0100360	Contractures of the joints of the upper limbs	0/20
HP: 0100490	Camptodactyly of finger	0/20
HP: 0100491	Abnormality of lower limb joint	0/20
HP: 0100492	Joint contractures involving the joints of the feet	0/20
HP: 0100498	Deviation of toes	0/20
HP: 0100500	Fibular deviation of toes	0/20
HP: 0100502	Vitamin B12 deficiency	0/20
HP: 0100508	Abnormality of vitamin metabolism	0/20
HP: 0100526	Neoplasm of the lung	0/20
HP: 0100527	Neoplasia of the pleura	0/20
HP: 0100528	Pleuropulmonary blastoma	0/20
HP: 0100538	Abnormality of the supraorbital ridges	0/20
HP: 0100539	Periorbital edema	0/20
HP: 0100540	Palpebral edema	0/20
HP: 0100542	Abnormal localization of kidney	0/20
HP: 0100543	Cognitive impairment	0/20
HP: 0100544	Neoplasm of the heart	0/20
HP: 0100545	Arterial stenosis	0/20
HP: 0100547	Abnormality of forebrain morphology	0/20
HP: 0100548	Exstrophy	0/20
HP: 0100552	Neoplasm of the tracheobronchial system	0/20
HP: 0100561	Spinal cord lesion	0/20
HP: 0100568	Neoplasm of the endocrine system	0/20
HP: 0100570	Carcinoid tumor	0/20
HP: 0100579	Mucosal telangiectasiae	0/20
HP: 0100589	Urogenital fistula	0/20
HP: 0100590	Rectal fistula	0/20
HP: 0100594	Esophageal web	0/20
HP: 0100605	Neoplasm of the larynx	0/20
HP: 0100606	Neoplasm of the respiratory system	0/20
HP: 0100615	Ovarian neoplasm	0/20
HP: 0100622	Maternal seizures	0/20
HP: 0100627	Displacement of the urethral meatus	0/20
HP: 0100628	Esophageal diverticulum	0/20
HP: 0100634	Neuroendocrine neoplasm	0/20
HP: 0100640	Laryngeal cyst	0/20
HP: 0100643	Abnormality of nail color	0/20
HP: 0100648	Neoplasm of the tongue	0/20
HP: 0100649	Neoplasm of the oral cavity	0/20
HP: 0100659	Abnormality of the cerebral vasculature	0/20
HP: 0100668	Intestinal duplication	0/20
HP: 0100681	Esophageal duplication	0/20
HP: 0100691	Abnormality of the curvature of the cornea	0/20
HP: 0100694	Tibial torsion	0/20
HP: 0100695	Lipedema	0/20
HP: 0100697	Neurofibrosarcoma	0/20
HP: 0100699	Scarring	0/20
HP: 0100705	Abnormality of the glial cells	0/20
HP: 0100707	Abnormality of the astrocytes	0/20
HP: 0100711	Abnormality of the thoracic spine	0/20
HP: 0100712	Abnormality of the lumbar spine	0/20
HP: 0100716	Self-injurious behavior	0/20
HP: 0100728	Germ cell neoplasia	0/20
HP: 0100729	Large face	0/20
HP: 0100730	Bronchogenic cyst	0/20
HP: 0100736	Abnormal soft palate morphology	0/20
HP: 0100737	Abnormal hard palate morphology	0/20
HP: 0100742	Vascular neoplasm	0/20
HP: 0100744	Abnormality of the humeroradial joint	0/20
HP: 0100763	Abnormality of the lymphatic system	0/20
HP: 0100764	Lymphangioma	0/20
HP: 0100771	Hypoperistalsis	0/20
HP: 0100775	Dural ectasia	0/20
HP: 0100777	Exostoses	0/20
HP: 0100779