FANDOM


Haas-Robinson syndrome [↗]
H-ABC [↗]
Haberland syndrome [↗]
Haddad syndrome [↗]
Hadziselimovic syndrome [↗]
HAE [↗]
HAE-I [↗]
HAE-II [↗]
HAE-III [↗]
Hagberg-Santavuori disease [↗]
Hailey-Hailey disease [↗]
Haim-Munk syndrome [↗]
Hair defect - photosensitivity - intellectual deficit [↗]
Hairy cell leukemia [↗]
Hairy elbows [↗]
Hairy throat syndrome [↗]
Hajdu-Cheney syndrome [↗]
Halal-Setton-Wang syndrome [↗]
Halal syndrome [↗]
Halasz syndrome [↗]
Hal-Berg-Rudolph syndrome [↗]
Hallermam-Streiff-François syndrome, severe form [↗]
Hallermam-Streiff like syndrome [↗]
Hallermann-Streiff-François syndrome [↗]
Hallervorden-Spatz syndrome [↗]
Hall-Hittner syndrome [↗]
Hall-Riggs syndrome [↗]
Hallux varus - preaxial polysyndactyly [↗]
Hamanishi-Ueba-Tsuji syndrome [↗]
Hamano-Tsukamoto syndrome [↗]
Hamartomatous intestinal polyposis [↗]
Hamel cerebro-palato-cardiac syndrome [↗]
Hamman-Rich syndrome [↗]
HAM syndrome [↗]
HANAC syndrome [↗]
Hand and foot deformity - flat facies [↗]
Hand-foot-genital syndrome [↗]
Hand-foot-uterus syndrome [↗]
Hand-Schüller-Christian disease [↗]
Hanhart syndrome [↗]
Hanot syndrome [↗]
Hantavirosis [↗]
Hantavirus fever [↗]
Hapnes-Boman-Skeie syndrome [↗]
Harboyan syndrome [↗]
Hardcastle syndrome [↗]
Hardikar syndrome [↗]
Harding ataxia [↗]
Hard-skin syndrome, Parana type [↗]
HARD syndrome [↗]
Harlequin ichthyosis [↗]
Harlequin syndrome [↗]
HARP syndrome [↗]
Harrod syndrome [↗]
Hartnup disorder [↗]
Hartnup syndrome [↗]
Hartsfield-Bixler-Demyer syndrome [↗]
Hashimoto encephalitis [↗]
Hashimoto hypothyroidism [↗]
Hashimoto-Pritzker syndrome [↗]
Hashimoto struma [↗]
Hashimoto thyroiditis [↗]
Haspeslagh-Fryns-Muelenaere syndrome [↗]
Hawkinsinuria [↗]
Hay-Wells syndrome [↗]
Hb Bart's Hydrops Foetalis Syndrome [↗]
HbC - beta-thalassemia [↗]
HbE - beta-thalassemia [↗]
HbH disease [↗]
HbS - beta-thalassemia [↗]
HbSC disease [↗]
HbSD disease [↗]
HbSE disease [↗]
HCDD [↗]
HCL [↗]
HCS [↗]
HDR syndrome [↗]
Head and neck squamous cell carcinoma [↗]
Hearing loss - encephaloneuropathy - obesity - valvulopathy [↗]
Hearing loss - familial salivary gland insensitivity to aldosterone [↗]
Heart defect - round face - congenital developmental delay [↗]
Heart defects - limb shortening [↗]
Heart defect - tongue hamartoma - polysyndactyly [↗]
Heart-hand syndrome, Slovenian type [↗]
Heart-hand syndrome, Spanish type [↗]
Heart-hand syndrome type 1 [↗]
Heart-hand syndrome type 2 [↗]
Heart-hand syndrome type 3 [↗]
Heart-limb syndrome type 3 [↗]
Heart tumor of the child [↗]
Heavy chain deposition disease [↗]
Heavy-chain disease [↗]
Hecht-Scott syndrome [↗]
Hecht syndrome [↗]
Heckenlively syndrome [↗]
HEC syndrome [↗]
Heide syndrome [↗]
Heimler syndrome [↗]
Heiner syndrome [↗]
Heinz body anemia [↗]
Helicoid peripapillary chorioretinal degeneration [↗]
Heller syndrome [↗]
Hemangioblastoma [↗]
Hemangioma-thrombocytopenia syndrome [↗]
Hemangiopericytoma [↗]
Hematopoietic cell transplantation [↗]
Hemi 3 syndrome [↗]
Hemiconvulsion-Hemiplegia-Epilepsy syndrome [↗]
Hemicorporal hypertrophy [↗]
Hemifacial hyperplasia - strabismus [↗]
Hemifacial hypertrophy [↗]
Hemifacial microsomia [↗]
Hemifacial microsomia - radial defects [↗]
Hemifacial myohyperplasia [↗]
Hemihyperplasia-multiple lipomatosis syndrome [↗]
Hemihypertrophy [↗]
Hemihypertrophy intestinal web corneal opacity [↗]
Hemimegalencephaly [↗]
Hemimelia [↗]
Hemochromatosis due to defect in ferroportin [↗]
Hemochromatosis type 2 [↗]
Hemochromatosis type 3 [↗]
Hemochromatosis type 4 [↗]
Hemoglobin C - beta-thalassemia [↗]
Hemoglobin C disease [↗]
Hemoglobin D disease [↗]
Hemoglobin E - beta-thalassemia [↗]
Hemoglobin E disease [↗]
Hemoglobin H disease [↗]
Hemoglobinopathy Toms River [↗]
Hemolytic anemia due to adenylate kinase deficiency [↗]
Hemolytic anemia due to diphosphoglycerate mutase deficiency [↗]
Hemolytic anemia due to erythrocyte adenosine deaminase overproduction [↗]
Hemolytic anemia due to erythrocyte enolase deficiency [↗]
Hemolytic anemia due to glucophosphate isomerase deficiency [↗]
Hemolytic anemia due to glutathione reductase deficiency [↗]
Hemolytic anemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency [↗]
Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency [↗]
Hemolytic anemia due to red cell pyruvate kinase deficiency [↗]
Hemolytic disease of the newborn with Kell allo-immunization [↗]
Hemolytic-uremic syndrome with diarrhea [↗]
Hemolytic-uremic syndrome without diarrhea [↗]
Hemophilia [↗]
Hemophilia A [↗]
Hemophilia B [↗]
Hemophilia C [↗]
Hemorrhagic disease due to alpha-1 antitrypsin Pittsburgh mutation [↗]
Hemorrhagic fever - renal syndrome [↗]
Hemorrhagiparous thrombocytic dystrophy [↗]
Hennekam-Beemer syndrome [↗]
Hennekam-Koss-de Geest syndrome [↗]
Hennekam syndrome [↗]
Henoch-Schönlein purpura [↗]
HEP [↗]
Heparan-alpha-glucosaminide N-acetyltransferase deficiency [↗]
Heparan sulfamidase deficiency [↗]
Heparin-induced thrombocytopenia [↗]
Hepatic amyloidosis with intrahepatic cholestasis [↗]
Hepatic carnitine palmitoyl transferase 1 deficiency [↗]
Hepatic carnitine palmitoyl transferase I deficiency [↗]
Hepatic cystic hamartoma [↗]
Hepatic fibrosis - renal cysts - intellectual deficit [↗]
Hepatic glycogen phosphorylase deficiency [↗]
Hepatic glycogen synthase deficiency [↗]
Hepatic phosphorylase deficiency [↗]
Hepatic veno-occlusive disease [↗]
Hepatic veno-occlusive disease - immunodeficiency [↗]
Hepatitis B re-infection following liver transplantation [↗]
Hepatoblastoma [↗]
Hepatocellular adenoma [↗]
Hepatocellular carcinoma [↗]
Hepatocellular carcinoma, childhood-onset [↗]
Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1 [↗]
Hepatoencephalopathy due to COXPD1 [↗]
Hepatoerythropoietic porphyria [↗]
Hepatolenticular degeneration [↗]
Hepatoportal sclerosis [↗]
Hepatorenal glycogenosis [↗]
Hepatorenal tyrosinemia [↗]
Hepatosplenic T-cell lymphoma [↗]
Hereditary acrokeratotic poikiloderma, Weary type [↗]
Hereditary amyloid nephropathy [↗]
Hereditary amyloid nephropathy due to Apolipoprotein AII variant [↗]
Hereditary amyloid nephropathy due to Apolipoprotein AI variant [↗]
Hereditary amyloid nephropathy due to fibrinogen A alpha-chain variant [↗]
Hereditary amyloid nephropathy due to lysozyme variant [↗]
Hereditary amyloidosis, Finnish type [↗]
Hereditary amyloid precursor protein angiopathy [↗]
Hereditary anetoderma [↗]
Hereditary angioedema [↗]
Hereditary angioedema type 1 [↗]
Hereditary angioedema type 2 [↗]
Hereditary angioedema type 3 [↗]
Hereditary angioneurotic edema [↗]
Hereditary angioneurotic edema type 1 [↗]
Hereditary angioneurotic edema type 2 [↗]
Hereditary angioneurotic edema type 3 [↗]
Hereditary APP amyloid angiopathy [↗]
Hereditary benign chorea [↗]
Hereditary brachial plexus neuropathy [↗]
Hereditary bradykinine-induced angioedema [↗]
Hereditary brain cavernous angioma [↗]
Hereditary breast and ovarian cancer syndrome [↗]
Hereditary breast cancer [↗]
Hereditary breast carcinoma [↗]
Hereditary cerebral cavernoma [↗]
Hereditary cerebral cavernous malformation [↗]
Hereditary cerebral hemorrhage with amyloidosis [↗]
Hereditary cerebral hemorrhage with amyloidosis, Dutch type [↗]
Hereditary cerebral hemorrhage with amyloidosis, Icelandic type [↗]
Hereditary ceruloplasmin deficiency [↗]
Hereditary chin myoclonus [↗]
Hereditary chin-trembling [↗]
Hereditary chronic pancreatitis [↗]
Hereditary combined deficiency of factors II, VII, IX and X [↗]
Hereditary combined deficiency of vitamin K-dependent clotting factors [↗]
Hereditary congenital controlateral synkinesia [↗]
Hereditary congenital mirror movements [↗]
Hereditary continuous muscle fiber activity [↗]
Hereditary coproporphyria [↗]
Hereditary cranium bifidum [↗]
Hereditary cryohydrocytosis with reduced stomatin [↗]
Hereditary cystatin C amyloid angiopathy [↗]
Hereditary dysphasic dementia [↗]
Hereditary elliptocytosis [↗]
Hereditary endotheliopathy - retinopathy - nephropathy - stroke [↗]
Hereditary erythroblastic multinuclearity with a positive acidified-serum test (hempas) [↗]
Hereditary expansile polyostotic osteolytic dysplasia [↗]
Hereditary ferritinopathy [↗]
Hereditary folate malabsorption [↗]
Hereditary fructose-1-phosphate aldolase deficiency [↗]
Hereditary fructosemia [↗]
Hereditary geniospasm [↗]
Hereditary glaucoma [↗]
Hereditary hemorrhagic telangiectasia [↗]
Hereditary hypercarotenemia and vitamin A deficiency [↗]
Hereditary hypercholanemia [↗]
Hereditary hyperekplexia [↗]
Hereditary hyperexplexia [↗]
Hereditary hyperferritinemia with congenital cataracts [↗]
Hereditary hyperphosphatasia [↗]
Hereditary hypotrichosis simplex [↗]
Hereditary hypotrichosis simplex of the scalp [↗]
Hereditary hypotrichosis with recurrent skin vesicles [↗]
Hereditary inclusion body myopathy [↗]
Hereditary inclusion body myopathy - joint contractures - ophthalmoplegia [↗]
Hereditary inclusion body myositis [↗]
Hereditary isolated clubfoot due to 17q23.1-q23.2 microduplication syndrome [↗]
Hereditary juvenile meganoblastic anemia due to intrinsic factor deficiency [↗]
Hereditary keratitis [↗]
Hereditary keratoacanthoma [↗]
Hereditary leiomyomatosis [↗]
Hereditary leiomyomatosis with renal carcinoma [↗]
Hereditary leiomyomatosis with renal cell cancer [↗]
Hereditary lymphedema type I [↗]
Hereditary lymphedema type II [↗]
Hereditary macular atrophy [↗]
Hereditary methemoglobinemia [↗]
Hereditary mixed polyposis syndrome [↗]
Hereditary motor and sensory neuropathy, Lom type [↗]
Hereditary motor and sensory neuropathy, Okinawa type [↗]
Hereditary motor and sensory neuropathy, proximal type [↗]
Hereditary motor and sensory neuropathy, Russe Type [↗]
Hereditary motor and sensory neuropathy type 1 [↗]
Hereditarymotor and sensoryneuropathy type 2 [↗]
Hereditary motor and sensory neuropathy type 3 [↗]
Hereditary motor and sensory neuropathy type 4 [↗]
Hereditary motor and sensory neuropathy type 5 [↗]
Hereditary motor and sensory neuropathy type 6 [↗]
Hereditary motor and sensory neuropathy with deafness, intellectual deficit and absent sensory large myelinated fibers [↗]
Hereditary mucoepithelial dysplasia [↗]
Hereditary mucosal leukokeratosis [↗]
Hereditary multi-infarct dementia [↗]
Hereditary multiple cutaneous leiomyomas [↗]
Hereditary multiple glomangiomas [↗]
Hereditary myoclonus - progressive distal muscular atrophy [↗]
Hereditary myopathy with early respiratory failure [↗]
Hereditary neuralgic amyotrophy [↗]
Hereditary neurocutaneous angioma [↗]
Hereditary neuropathy with liability to pressure palsies [↗]
Hereditary neutrophilia [↗]
Hereditary non histamine-induced angioedema [↗]
Hereditary nonpolyposis colon cancer [↗]
Hereditary nonpolyposis colorectal cancer [↗]
Hereditary North American Indian childhood cirrhosis [↗]
Hereditary ochronosis [↗]
Hereditary orotic aciduria [↗]
Hereditary painful callosities [↗]
Hereditary palmoplantar keratoderma, Gamborg-Nielsen type [↗]
Hereditary parathyroids hyperplasia [↗]
Hereditary Parkinson disease [↗]
Hereditary persistence of alpha-fetoprotein [↗]
Hereditary persistence of fetal hemoglobin - beta-thalassemia [↗]
Hereditary persistence of fetal hemoglobin - sickle cell disease [↗]
Hereditary pheochromocytoma-paraganglioma [↗]
Hereditary prepubertal gynecomastia [↗]
Hereditary progressive arthroophthalmopathy [↗]
Hereditary progressive dystonia with marked diurnal fluctuation [↗]
Hereditary progressive mucinous histiocytosis [↗]
Hereditary pulmonary arterial hypertension [↗]
Hereditary punctate palmoplantar keratoderma [↗]
Hereditary pyropoikilocytosis [↗]
Hereditary renal amyloidosis [↗]
Hereditary renal amyloidosis due to Apolipoprotein AII variant [↗]
Hereditary renal amyloidosis due to Apolipoprotein AI variant [↗]
Hereditary renal amyloidosis due to fibrinogen A alpha-chain variant [↗]
Hereditary renal amyloidosis due to lysozyme variant [↗]
Hereditary renal hypouricemia [↗]
Hereditary resistance to anti-vitamin K [↗]
Hereditary sclerosing poikiloderma Weary type [↗]
Hereditary sclerosing poikiloderma with tendon and pulmonary involvement [↗]
Hereditary sensorimotor neuropathy with hyperelastic skin [↗]
Hereditary sensory and autonomic neuropathy type 1 [↗]
Hereditary sensory and autonomic neuropathy type 1B [↗]
Hereditary sensory and autonomic neuropathy type 1 with cough and gastrooesophageal reflux [↗]
Hereditary sensory and autonomic neuropathy type 2 [↗]
Hereditary sensory and autonomic neuropathy type 3 [↗]
Hereditary sensory and autonomic neuropathy type 4 [↗]
Hereditary sensory and autonomic neuropathy type 5 [↗]
Hereditary sensory and autonomic neuropathy with deafness and global delay [↗]
Hereditary sensory and autonomic neuropathy with spastic paraplegia [↗]
Hereditary site-specific ovarian cancer syndrome [↗]
Hereditary spherocytosis [↗]
Hereditary symmetrical aplastic nevi of temples [↗]
Hereditary thermosensitive neuropathy [↗]
Hereditary thrombocythemia [↗]
Hereditary thrombocytopenia with normal platelets [↗]
Hereditary thrombophilia due to congenital antithrombin 3 deficiency [↗]
Hereditary thrombophilia due to congenital antithrombin deficiency [↗]
Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency [↗]
Hereditary thrombophilia due to congenital HRG deficiency [↗]
Hereditary thrombophilia due to congenital protein C deficiency [↗]
Hereditary thrombophilia due to congenital protein S deficiency [↗]
Hereditary unconjugated hyperbilirubinemia [↗]
Hereditary unconjugated hyperbilirubinemia type 1 [↗]
Hereditary unconjugated hyperbilirubinemia type 2 [↗]
Hereditary vascular retinopathy [↗]
Hereditary vascular retinopathy - Raynaud phenomenon - migraine [↗]
Hereditary whispering dysphonia [↗]
Hereditary Willebrand disease [↗]
Hereditary woolly hair syndrome [↗]
Hereditary wooly hair syndrome [↗]
Hereditary xerocytosis [↗]
Heredopathia atactica polyneuritiformis [↗]
Heritable pulmonary arterial hypertension [↗]
Hermansky-Pudlak syndrome [↗]
Hermansky-Pudlak syndrome type 2 [↗]
Hermansky-Pudlak syndrome type 7 [↗]
Hermansky-Pudlak syndrome type 8 [↗]
Hermansky-Pudlak syndrome type 9 [↗]
Hermansky-Pudlak syndrome with neutropenia [↗]
Hermansky-Pudlak syndrome without pulmonary fibrosis [↗]
Hermansky-Pudlak syndrome with pulmonary fibrosis [↗]
Hernandez-Aguirre Negrete syndrome [↗]
Hernandez-Fragoso syndrome [↗]
HERNS syndrome [↗]
Herpes simplex encephalitis [↗]
Herpes simplex neuroinvasion [↗]
Herpes simplex virus keratitis [↗]
Herpes virus antenatal infection [↗]
Herpetic encephalitis [↗]
Herpetic keratitis [↗]
Herpetiform pemphigus [↗]
Hers disease [↗]
Herva disease [↗]
Heterotaxia [↗]
Heterotaxy syndrome [↗]
Heterozygous OSMED [↗]
Heterozygous otospondylomegaepiphyseal dysplasia [↗]
Hexosaminidase A deficiency [↗]
Hexosaminidases A and B deficiency [↗]
HFGS [↗]
HGPPS [↗]
HGSNAT deficiency [↗]
HHE syndrome [↗]
HHH syndrome [↗]
HHML [↗]
HHT [↗]
HI [↗]
Hidrotic ectodermal dysplasia [↗]
Hidrotic ectodermal dysplasia, Christianson-Fourie type [↗]
Hidrotic ectodermal dysplasia, Halal type [↗]
HIE [↗]
High-grade dysplasia in patients with Barrett esophagus [↗]
High-grade ependymoma [↗]
High scapula [↗]
HIGM1 [↗]
HIGM2 [↗]
HIGM3 [↗]
HIGM4 [↗]
HIGM5 [↗]
HI/HA syndrome [↗]
Hilar CCA [↗]
Hilar cholangiocarcinoma [↗]
Hillig syndrome [↗]
Hinman syndrome [↗]
Hinson-Pepys disease [↗]
Hip dysplasia, Beukes type [↗]
Hip dysplasia - enchondromata - ecchondroma [↗]
Hipo syndrome [↗]
Hippel-Lindau disease [↗]
Hirayama disease [↗]
Hirschsprung disease [↗]
Hirschsprung disease and intellectual deficit due to 2q22 microdeletion [↗]
Hirschsprung disease and intellectual deficit due to a point mutation [↗]
Hirschsprung disease and intellectual deficit due to del(2)(q22) [↗]
Hirschsprung disease and intellectual deficit due to monosomy 2q22 [↗]
Hirschsprung disease - deafness - polydactyly [↗]
Hirschsprung disease - ganglioneuroblastoma [↗]
Hirschsprung disease - intellectual deficit [↗]
Hirschsprung disease - nail hypoplasia - dysmorphism [↗]
Hirschsprung disease - type D brachydactyly [↗]
Hirschsprung disease with pigmentary anomaly [↗]
Hirsutism - congenital gingival hyperplasia [↗]
Hirsutism - skeletal dysplasia - intellectual deficit [↗]
His bundle tachycardia [↗]
Histidase deficiency [↗]
Histidinemia [↗]
Histidinuria - renal tubular defect [↗]
Histiocytic sarcoma [↗]
Histiocytoid cardiomyopathy [↗]
Histiocytosis X [↗]
Histiocytosis X in childhood and adulthood [↗]
Histiocytosis X specific to adulthood [↗]
Histiocytosis X specific to childhood [↗]
Histoplasmosis [↗]
HI syndrome [↗]
HIT [↗]
Hittner-Hirsch-Kreh syndrome [↗]
HLA class 2-negative severe combined immunodeficiency [↗]
HLRCC [↗]
HMC syndrome [↗]
HMG-CoA synthase deficiency [↗]
HMN5B [↗]
HMSN 3 [↗]
HMSN 4 [↗]
HMSN 5 [↗]
HMSNP [↗]
HMSNR [↗]
HNPCC [↗]
HNPP [↗]
HNSCC [↗]
Hodgkin lymphoma, classical [↗]
Hoepffner-Dreyer-Reimers syndrome [↗]
Hoffman's syndrome [↗]
HOGA [↗]
Holmes-Collins syndrome [↗]
Holmes-Gang syndrome [↗]
Holoacardius amorphus [↗]
Holocarboxylase synthetase deficiency [↗]
Holoprosencephaly [↗]
Holoprosencephaly - caudal dysgenesis [↗]
Holoprosencephaly - craniosynostosis [↗]
Holoprosencephaly - ectrodactyly - cleft lip palate [↗]
Holoprosencephaly - postaxial polydactyly [↗]
Holoprosencephaly - radial heart renal anomalies [↗]
Holt-Oram syndrome [↗]
Holzgreve-Wagner-Rehder syndrome [↗]
HOMG1 [↗]
HOMG2 [↗]
HOMG3 [↗]
HOMG4 [↗]
Homocarnosinase deficiency [↗]
Homocarnosinosis [↗]
Homocystinuria due to cystathionine beta-synthase deficiency [↗]
Homocystinuria due to defect in methylation type cbl E [↗]
Homocystinuria due to methionine synthase deficiency, Cbl G type [↗]
Homocystinuria due to methylenetetrahydrofolate reductase deficiency [↗]
Homocystinuria without methylmalonic aciduria [↗]
Homogentisic acid oxidase deficiency [↗]
Homozygous familial hypobetalipoproteinemia [↗]
Homozygous hereditary elliptocytosis [↗]
Honey-droplet corneal dystrophy [↗]
Hookworms infection [↗]
Hoon-Hall syndrome [↗]
Horizontal gaze palsy with progressive scoliosis [↗]
Horton disease [↗]
Houlston-Ironton-Temple syndrome [↗]
House allergic alveolitis [↗]
Hoyeraal-Hreidarsson syndrome [↗]
HP [↗]
HPD with marked diurnal fluctuation [↗]
HPE [↗]
HPMR [↗]
HPP [↗]
HPRT1 partial deficiency [↗]
HPRT complete deficiency [↗]
HPRT deficiency, grade I [↗]
HPRT deficiency grade IV [↗]
HPRT partial deficiency [↗]
HPRT-related gout [↗]
HPRT-related hyperuricemia [↗]
HPS [↗]
HPS2 [↗]
HPS7 [↗]
HPS8 [↗]
HPS9 [↗]
HPS without pulmonary fibrosis [↗]
HPS with pulmonary fibrosis [↗]
HPT-JT [↗]
HSAN 1 [↗]
HSAN1B [↗]
HSAN 2 [↗]
HSAN 3 [↗]
HSAN 4 [↗]
HSAN 5 [↗]
HSAN with cough and gastroesophageal reflux [↗]
HSAN with deafness and global delay [↗]
HSAN with spastic paraplegia [↗]
HSD deficiency [↗]
HSV encephalitis [↗]
HSV keratitis [↗]
H syndrome [↗]
Hughes-Stovin syndrome [↗]
Hughes syndrome [↗]
Humeroradioulnar synostosis [↗]
Humerospinal dysostosis [↗]
Humero-spinal dysostosis [↗]
Humeroulnar synostosis [↗]
Humerus trochlea aplasia [↗]
Hunter-Jurenka-Thompson syndrome [↗]
Hunter-McAlpine craniosynostosis [↗]
Hunter-Rudd-Hoffmann syndrome [↗]
Hunter syndrome [↗]
Hunter syndrome type A [↗]
Hunter syndrome type B [↗]
Hunter-Thompson-Reed syndrome [↗]
Huntington chorea [↗]
Huntington disease [↗]
Huntington disease-like 1 [↗]
Huntington disease-like 2 [↗]
Huntington disease-like 3 [↗]
Huriez syndrome [↗]
Hurler-Scheie syndrome [↗]
Hurler syndrome [↗]
Hutchinson-Gilford progeria syndrome [↗]
HVR [↗]
Hyaline body myopathy [↗]
Hyaline membrane disease [↗]
Hyalinosis cutis et mucosae [↗]
Hyaluronidase deficiency [↗]
Hybrid acute leukemia [↗]
Hydatidiform complete mole [↗]
Hydatidiform mole [↗]
Hydatidiform partial mole [↗]
Hydatidosis [↗]
Hyde Forster-McCarthy-Berry syndrome [↗]
Hydranencephaly [↗]
Hydrocephalus - agyria - retinal dysplasia [↗]
Hydrocephalus-agyria-retinal dysplasia syndrome [↗]
Hydrocephalus - blue sclerae - nephropathy [↗]
Hydrocephalus - cleft palate - joint contractures [↗]
Hydrocephalus - costovertebral dysplasia - Sprengel anomaly [↗]
Hydrocephalus - endocardial fibroelastosis - cataract [↗]
Hydrocephalus - obesity - hypogonadism [↗]
Hydrocephalus with stenosis of aqueduct of Sylvius [↗]
Hydrocephaly/hydranencephaly due to cerebral vasculopathy [↗]
Hydrocephaly - low insertion umbilicus [↗]
Hydrocephaly - tall stature - joint laxity [↗]
Hydrolethalus [↗]
Hydromelia [↗]
Hydrometrocolpos - postaxial polydactyly [↗]
Hydronephrosis - inverted smile [↗]
Hydrops - ectopic calcification - motheaten [↗]
Hydrops fetalis [↗]
Hydrops fetalis of Bart [↗]
Hydroxymethylglutaricaciduria [↗]
Hygroma cysticum [↗]
Hymenolepiasis [↗]
Hyperadrenocorticism [↗]
Hyperammonemia due to N-acetylglutamate synthetase deficiency [↗]
Hyperammonemia - hypoornithinemia - hypocitrullinemia - hypoargininemia - hypoprolinemia [↗]
Hyperandrogenism due to cortisone reductase deficiency [↗]
Hyperargininemia [↗]
Hyperbilirubinemia, Rotor type [↗]
Hyperbilirubinemia type 2 [↗]
Hyperbiliverdinemia [↗]
Hypercalciuria - bilateral macular coloboma [↗]
Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency [↗]
Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency [↗]
Hypercortisolism [↗]
Hyperdibasic aminoaciduria type 1 [↗]
Hyperdibasic aminoaciduria type 2 [↗]
Hyperekplexia [↗]
Hyperekplexia - epilepsy [↗]
Hypereosinophilic syndromes [↗]
Hyperglycerolemia [↗]
Hypergonadotropic hypogonadism - cataract syndrome [↗]
Hypergonadotropic ovarian dysgenesis [↗]
Hyper-IgD syndrome [↗]
Hyper-IgM syndrome due to CD40 deficiency [↗]
Hyper-IgM syndrome due to CD40L deficiency [↗]
Hyper-IgM syndrome due to CD40 ligand deficiency [↗]
Hyper-IgM syndrome due to UNG deficiency [↗]
Hyper-IgM syndrome due to uracil N glycosylase [↗]
Hyper-IgM syndrome type 1 [↗]
Hyper-IgM syndrome type 2 [↗]
Hyper-IgM syndrome type 3 [↗]
Hyper-IgM syndrome type 4 [↗]
Hyper-IgM syndrome type 5 [↗]
Hyperimidodipeptiduria [↗]
Hyperimmunoglobinemia D with recurrent fever [↗]
Hyperimmunoglobulinemia D with periodic fever [↗]
Hyperimmunoglobulin E-recurrent infection syndrome [↗]
Hyperimmunoglobulin E syndrome type 1 [↗]
Hyperimmunoglobulin E syndrome type 2 [↗]
Hyperinsulinemic hypoglycemia due to 3-hydroxylacyl-CoA dehydrogenase deficiency [↗]
Hyperinsulinemic hypoglycemia due to glucokinase deficiency [↗]
Hyperinsulinemic hypoglycemia due to HNF4A deficiency [↗]
Hyperinsulinemic hypoglycemia due to INSR deficiency [↗]
Hyperinsulinemic hypoglycemia due to insulin receptor deficiency [↗]
Hyperinsulinemic hypoglycemia due to Kir6.2 deficiency, diazoxide-resistant focal form [↗]
Hyperinsulinemic hypoglycemia due to SUR1 deficiency, diazoxide-resistant focal form [↗]
Hyperinsulinemic hypoglycemia due to UCP2 deficiency [↗]
Hyperinsulinism due to 3-hydroxylacyl-CoA dehydrogenase deficiency [↗]
Hyperinsulinism due to glucokinase deficiency [↗]
Hyperinsulinism due to glutamodehydrogenase deficiency [↗]
Hyperinsulinism due to glutamodehydrogenase deficiency [↗]
Hyperinsulinism due to HADH deficiency [↗]
Hyperinsulinism due to HNF4A deficiency [↗]
Hyperinsulinism due to INSR deficiency [↗]
Hyperinsulinism due to monocarboxylate transporter 1 deficiency [↗]
Hyperinsulinism due to SCHAD deficiency [↗]
Hyperinsulinism due to short-chain 3-hydroxylacyl-CoA dehydrogenase deficiency [↗]
Hyperinsulinism due to SLC16A1 deficiency [↗]
Hyperinsulinism due to UCP2 deficiency [↗]
Hyperinsulinism-hyperammonemia syndrome [↗]
Hyperkalemic periodic paralysis [↗]
Hyperkalemic PP [↗]
Hyperkalemic renal tubular acidosis [↗]
Hyperkaliemia - hypertension, Gordon type [↗]
Hyperkeratosis - hyperpigmentation syndrome [↗]
Hyperkeratosis lenticularis perstans [↗]
HyperKPP [↗]
Hyperlipidemia due to hepatic triglyceride lipase deficiency [↗]
Hyperlipidemia type 3 [↗]
Hyperlipoproteinemia type 1 [↗]
Hyperlipoproteinemia type 3 [↗]
Hyperlipoproteinemia type 4 [↗]
Hyperlipoproteinemia type 5 [↗]
Hyperlysinemia [↗]
Hypermethioninemia due to S-adenosylhomocysteine hydrolase deficiency [↗]
Hypernychthemeral syndrome [↗]
Hyperornithinemia [↗]
Hyperornithinemia - gyrate atrophy of choroid and retina [↗]
Hyperornithinemia-hyperammonemia-homocitrullinuria [↗]
Hyperostosid corticalis deformans juvenilis [↗]
Hyperostosis corticalis generalisata [↗]
Hyperostosis frontalis interna [↗]
Hyperostosis generalisata with striations [↗]
Hyperoxaluria [↗]
Hyperoxaluria non1-non2 type [↗]
Hyperparathyroidism - jaw tumor syndrome [↗]
Hyperphenylalaninemia [↗]
Hyperphenylalaninemia due to 6-pyruvoyltetrahydropterin synthase deficiency [↗]
Hyperphenylalaninemia due to BH4 deficiency [↗]
Hyperphenylalaninemia due to dehydratase deficiency [↗]
Hyperphenylalaninemia due to dihydropteridine reductase deficiency [↗]
Hyperphenylalaninemia due to GTP cyclohydrolase deficiency [↗]
Hyperphenylalaninemia due to pterin-4-alpha-carbinolamine dehydratase deficiency [↗]
Hyperphenylalaninemia due to tetrahydrobiopterin deficiency [↗]
Hyperphenylalaninemic embryopathy [↗]
Hyperphosphatasia intellectual deficiency syndrome [↗]
Hyperpipecolatemia [↗]
Hyperplastic polyposis syndrome [↗]
HyperPP [↗]
Hyperprolinemia type 1 [↗]
Hyperprolinemia type II [↗]
Hypersensitivity angiitis [↗]
Hypersensitivity pneumonitis [↗]
Hypertelorism - hypospadias - polysyndactyly syndrome [↗]
Hypertelorism-microtia-facial clefting syndrome [↗]
Hypertelorism, Teebi Type [↗]
Hypertension due to gain-of-function mutations in the mineralocorticoid receptor [↗]
Hypertensive hyperkalemia [↗]
Hyperthermia of anesthesia [↗]
Hypertrichosis - atrophic skin - ectropion - macrostomia [↗]
Hypertrichosis cubiti - short stature [↗]
Hypertrichosis lanuginosa congenita [↗]
Hypertrichosis universalis [↗]
Hypertrichosis universalis congenita, Ambras type [↗]
Hypertrichotic osteochondrodysplasia [↗]
Hypertrophic cardiomyopathy due to intensive athletic training [↗]
Hypertrophic neuropathy of infancy [↗]
Hypertrophic or verrucous lupus erythematosus [↗]
Hypertryptophanemia [↗]
Hyperuricemia - anemia - renal failure [↗]
Hyperzincemia and hypercalprotectinemia [↗]
Hypnic headache [↗]
Hypocalcemic rickets [↗]
Hypocalcified amelogenesis imperfecta [↗]
Hypochondrogenesis [↗]
Hypochondroplasia [↗]
Hypocomplementemic leucocytoclasic vasculitis [↗]
Hypodermyiasis [↗]
Hypodontia - dysplasia of nails [↗]
Hypodontia - nail dysgenesis [↗]
Hypogenetic lung syndrome [↗]
Hypoglossia - hypodactyly [↗]
Hypogonadism - gynecomastia - X-linked intellectual deficit [↗]
Hypogonadism - mitral valve prolapse - intellectual deficit [↗]
Hypogonadotropic hypogonadism - frontoparietal alopecia [↗]
Hypogonadotropic hypogonadism - retinitis pigmentosa [↗]
Hypohidrotic ectodermal dysplasia [↗]
Hypohidrotic ectodermal dysplasia - hypothyroidism - ciliary dyskinesia [↗]
Hypohidrotic ectodermal dysplasia with immunodeficiency [↗]
Hypokalemic alkalosis - hypercalciuria [↗]
Hypokalemic periodic paralysis [↗]
Hypomagnesemia caused by selective magnesium malabsorption [↗]
Hypomagnesemia intestinal type 1 [↗]
Hypomagnesemia renal type 3 [↗]
Hypomagnesemia with hypocalciuria [↗]
Hypomagnesemia with normocalciuria [↗]
Hypomandibular faciocranial dysostosis [↗]
Hypomaturation amelogenesis imperfecta [↗]
Hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism [↗]
Hypomelanosis of Ito [↗]
Hypomelanotic and hypermelanotic cutaneous macules - retarded growth - intellectual deficiency [↗]
Hypomyelination - congenital cataract [↗]
Hypomyelination - hypogonadotropic hypogonadism - hypodontia [↗]
Hypomyelination neuropathy - arthrogryposis [↗]
Hypomyelination with atrophy of basal ganglia and cerebellum [↗]
Hypoparathyroidism - Addison's disease - mucocutaneous candidiasis [↗]
Hypoparathyroidism - deafness - renal disease [↗]
Hypoparathyroidism - intellectual deficit - dysmorphism [↗]
Hypoparathyroidism - short stature - intellectual deficit - seizures [↗]
Hypophosphatasia [↗]
Hypophosphatemic rickets [↗]
Hypophosphatemic rickets with hypercalciuria [↗]
Hypopigmentation-deafness syndrome [↗]
Hypopigmentation - immunodeficiency with or without neurologic impairment [↗]
hypopigmentation - neurologic impairment [↗]
Hypopituitarism due to empty sella turcica syndrome [↗]
Hypopituitarism - micropenis - cleft lip/palate [↗]
Hypopituitarism - microphthalmia [↗]
Hypopituitarism - postaxial polydactyly [↗]
Hypopituitarism - short stature - skeletal anomalies [↗]
Hypoplasia of the mitral valve annulus [↗]
Hypoplasminogenemia [↗]
Hypoplastic amelogenesis imperfecta [↗]
Hypoplastic left heart syndrome [↗]
Hypoplastic tibiae - post axial polydactyly [↗]
Hypoprebetalipoproteinemia - acanthocytosis - retinitis pigmentosa - pallidal degeneration [↗]
Hypoproconvertinemia [↗]
Hypoprothrombinemia [↗]
Hyposmia - nasal and ocular hypoplasia - hypogonadotropic hypogonadism [↗]
Hypospadias - dysphaghia [↗]
Hypospadias - hypertelorism [↗]
Hypospadias-hypertelorism-coloboma and deafness [↗]
Hypospadias - intellectual deficit, Goldblatt type [↗]
Hypotelorism - cleft palate - hypospadias [↗]
Hypothalamic hamartoblastoma syndrome [↗]
Hypothalamic hamartomas with gelastic seizures [↗]
Hypothyroidism - cleft palate [↗]
Hypothyroidism due to deficient transcription factors involved in pituitary development or function [↗]
Hypothyroidism due to TSH receptor mutations [↗]
Hypothyroidism - dysmorphism - postaxial polydactyly - intellectual deficit [↗]
Hypotonia and ichthyosis due to dolichol phosphate deficiency [↗]
Hypotonia - cystinuria syndrome [↗]
Hypotonia - failure to thrive - microcephaly [↗]
Hypotonia with lactic acidemia and hyperammonemia [↗]
Hypotrichosis - congenital ichthyosis [↗]
Hypotrichosis-intellectual deficit, Lopes type [↗]
Hypotrichosis - lymphedema - telangiectasia [↗]
Hypotrichosis simplex [↗]
Hypotrichosis simplex of the scalp [↗]
Hypotrichosis with juvenile macular degeneration [↗]
Hypotrichosis with juvenile macular dystrophy [↗]
Hypoxanthine guanine phosphoribosyltransferase 1 partial deficiency [↗]
Hypoxanthine guanine phosphoribosyltransferase complete deficiency [↗]
Hypoxanthine-guanine phosphoribosyltransferase deficiency, grade I [↗]
Hypoxanthine guanine phosphoribosyltransferase deficiency, grade IV [↗]
Hypoxanthine guanine phosphoribosyltransferase partial deficiency [↗]
Hypoxic and ischemic brain injury in the newborn [↗]
Hypoxic-ischemic encephalopathy [↗]
HYPP [↗]
Hystiocytic necrotizing lymphadenitis [↗]

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