List of diseases starting by H           Haas-Robinson syndrome   HAD deficiency   HAE   Haemochromatosis, familial   Haemoglobin D disease   Haemolytic anaemia due to glutathione reductase deficiency   Haemolytic anaemia, lethal - genital anomalies   Haemolytic anaemia, nonspherocytic, due to hexokinase deficiency   Haemolytic uremic syndrome, atypical form   Haemolytic-uremic syndrome, typical   Haemorragic fever - renal syndrome   Haemorrhagiparous thrombocytic dystrophy   Hageman factor deficiency   Hagemoser weinstein bresnick syndrome   Hailey-Hailey disease   Haim-Munk syndrome   HAIRAN syndrome   Hair defect photosensitivity mental retardation   Hairy cell leukaemia   Hairy elbows   Hairy throat syndrome   Hajdu-Cheney syndrome   Halal-Setton-Wang syndrome   Halal syndrome   Hal-Berg-Rudolph syndrome   Hallermam streiff like syndrome   Hallermann-Streiff-Francois syndrome   Hallervorden-Spatz disease   Hall riggs mental retardation syndrome   Hallux varus and preaxial polysyndactyly   Hamanishi ueba tsuji syndrome   Hamano tsukamoto syndrome   Hamman-Rich syndrome   Hanahart syndrome   Hand and foot deformity flat facies   Hand foot uterus syndrome   Hanot syndrome   Hantavirosis   Hantavirus fever   Hapnes boman skeie syndrome   Harboyan syndrome   Hardcastle syndrome   Harding ataxia   Hard skin syndrome, Parana type   HARD syndrome (Hydrocephalus - agyria - retinal dysplasia)   Harrod-Keele syndrome   Harrod syndrome   Hartnup disorder   Hartnup syndrome   Hartsfield bixler demyer syndrome   Hashimoto's encephalitis   Hashimoto struma   Haspeslagh-Fryns-Muelenaere syndrome   Hawkinsinuria   Hay wells syndrome   HCL   Hearing loss - salivary gland insensitivity to aldosterone, familial   Heart block progressive, familial   Heart defect round face congenital retarded development   Heart defects - limb shortening   Heart defect tongue hamartoma polysyndactyly   Heart-hand syndrome   Heart hand syndrome spanish type   Heart hand syndrome type 2   Heart tumor of the adult   Heart tumour of the child   Heavy-chain diseases   Hecht scott syndrome   Hecht syndrome   Heckenlively syndrome   Hec syndrome   Heide syndrome   Heimler syndrome   Helicoid peripapillary chorioretinal degeneration   Helmerhorst heaton crossen syndrome   Hemangiomas cavernous of face supraumbilical midline raphe   Hemangioma-thrombocytopenia syndrome   Hemangiopericytoma   Hematopoietic cell transplantation   Hematopoietic hypoplasia, generalized   Hemeralopia, congenital essential   Hemi 3 syndrome   Hemiconvulsion-Hemiplegia-Epilepsy syndrome   Hemifacial atrophy progressive   Hemifacial hyperplasia strabismus   Hemifacial microsomia   Hemihypertrophy   Hemihypertrophy intestinal web corneal opacity   Hemimelia   Hemiplegic migraine, familial   Hemochromatosis   Hemoglobin C disease   Hemoglobin E disease   Hemolytic anaemia due to adenylate kinase deficiency   Hemolytic anaemia, lethal - genital anomalies   Hemophilia   Hemophilia, acquired   Hemorrhagic disorders due to collagen receptors deficiency   Hemorrhagiparous thrombocytic dystrophy   Hennekam-Beemer syndrome   Hennekam koss de geest syndrome   Hennekam syndrome   Henoch-Schoenlein purpura   Heparane sulfamidase deficiency   Heparin-induced thrombocytopenia   Hepatic amyloidosis with intrahepatic cholestasis   Hepatic cystic hamartoma   Hepatic fibrosis renal cysts mental retardation   Hepatic vein, congenital anomaly of   Hepatic venoocclusive disease   Hepatic veno-occlusive disease - immunodeficiency   Hepatitis B re-infection following liver transplantation   Hepatitis, chronic autoimmune   Hepatoblastoma   Hepatocellular adenoma   Hepatocellular carcinoma   Hepatocellular carcinoma of childhood   Hepatolenticular degeneration   Hepatoportal sclerosis   Hepatorenal glycogenosis   Hepatorenal tyrosinemia   Hepatosplenic T-cell lymphoma   Hereditary endotheliopathy - retinopathy - nephropathy - stroke   Hereditary inclusion body myopathy   Hereditary inclusion body myopathy - joint contractures - ophthalmoplegia   Hereditary keratoacanthoma   Hereditary methemoglobinemia, recessive   Hereditary motor and sensory neuropathy, proximal type   Hereditary motor and sensory neuropathy type 3 (HMSN 3)   Hereditary motor and sensory neuropathy type 4 (HMSN 4)   Hereditary motor and sensory neuropathy, type 5   Hereditary motor and sensory neuropathy, type 6   Hereditary painful callosities   Hereditary persistence of fetal hemoglobin   Hereditary primary fanconi disease   Hereditary progressive dystonia with marked diurnal fluctuation (HPD)   Hereditary renal hypouricemia   Hereditary resistance to anti-vitamin K   Hereditary sensory and autonomic neuropathy, type 1   Hereditary sensory and autonomic neuropathy, type 2   Hereditary sensory and autonomic neuropathy, type 3 (HSAN 3)   Hereditary sensory and autonomic neuropathy, type 4   Hereditary sensory and autonomic neuropathy type 5   Hereditary symmetrical aplastic nevi of temples   Hereditary thrombocythemia   Hereditary vascular retinopathie - Raynaud phenomenon - migraine   Hereditary vascular retinopathy   Heredopathia atactica polyneuritiformis   Hernandez-Aguirre Negrete syndrome   Hernandez fragoso syndrome   HERNS syndrome   Herpes cutaneous, recurrent and disabling, idiopathic   Herpes simplex encephalitis   Herpes simplex neuroinvasion   Herpes virus antenatal infection   Herpes virus infection, congenital   Herpetic encephalopathy   Herrmann opitz arthrogryposis syndrome   Herrmann opitz craniosynostosis   Hersh-Podruch-Weisskopf syndrome   Herva disease   Heterotaxia   Heterozygous OSMED   Heterozygous otospondylomegaepiphyseal dysplasia   Hexosaminidase A deficiency   Hexosaminidases A and B deficiency   HHE syndrome   HHT   Hibernian fever, familial   Hidradenitis suppurativa   Hidrotic ectodermal dysplasia Halal type   Hidrotic ectodermal dysplasia type Christianson-Fourie   HID syndrome   High-molecular-weight kininogen deficiency, congenital   High scapula   Hillig syndrome   Hinman syndrome   Hinson-Pepys disease   Hip dysplasia Beukes type   Hip dysplasia - enchondromata - ecchondromata   Hipopituitarism due to empty sella turcica syndrome   Hipo syndrome   Hirayama disease   Hirschsprung disease   Hirschsprung disease - deafness - polydactyly   Hirschsprung disease ganglioneuroblastoma   Hirschsprung disease - mental retardation   Hirschsprung disease - nail hypoplasia - dysmorphism   Hirschsprung disease - typeD brachydactyly   Hirsutism - congenital gingival hyperplasia   Hirsutism skeletal dysplasia mental retardation   His bundle tachycardia   Histidase deficiency   Histidinemia   Histidinuria renal tubular defect   Histiocytic sarcoma   Histiocytosis X   Histoplasmosis   HIT   Hittner hirsch kreh syndrome   Hmc syndrome   HMSN 5   HMSNP   HNPCC   HNSCC   Hodgkin lymphoma   Hoepffner dreyer reimers syndrome   Hoffman's syndrome   Holmes benacerraf syndrome   Holmes collins syndrome   Holoacardius amorphus   Holoprosencephaly   Holoprosencephaly caudal dysgenesis   Holoprosencephaly craniosynostosis   Holoprosencephaly deletion 2p   Holoprosencephaly ectrodactyly cleft lip palate   Holoprosencephaly postaxial polydactyly   Holoprosencephaly radial heart renal anomalies   Holt-Oram syndrome   Holzgreve wagner rehder syndrome   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   Homogentisic acid oxydase deficiency   Hookworms infection   Hoon hall syndrome   Horner syndrome, congenital   Horseshoe kidney   Horton disease   Houlston ironton temple syndrome de   Howard young syndrome   Howell-Evans syndrome   Hoyeraal syndrome   HPE   HSAN 1   HSAN 2   HSAN 4   HSAN 5   HSD deficiency   HSV encephalitis   Humeroradial synostosis   Humeroradioulnar synostosis   Humerospinal dysostosis   Humeroulnar synostosis   Humerus trochlea aplasia of   Hunter carpenter mc donald syndrome   Hunter jurenka thompson syndrome   Hunter-McAlpine craniosynostosis   Hunter-Rudd-Hoffmann syndrome   Hunter syndrome   Hunter-Thompson-Reed syndrome   Huntington chorea   Huntington disease   Huriez syndrome   HUS   Hutchinson-Gilford syndrome   Hutteroth spranger syndrome   HVR   Hyaline membrane disease   Hyalinosis cutis et mucosae   Hyalinosis, infantile systemic   Hyaluronidase deficiency   Hybrid acute leukaemia   Hydatidosis   Hyde-Forster-Mccarthy-Berry syndrome   Hydranencephaly   Hydrocephalus autosomal recessive   Hydrocephalus - blue sclerae - nephropathy   Hydrocephalus - cleft palate - joint contractures   Hydrocephalus - costovertebral dysplasia - Sprengel anomaly   Hydrocephalus due to stenosis of aqueduct of Sylvius   Hydrocephalus endocardial fibroelastosis cataract   Hydrocephalus - growth delay - skeletal anomalies   Hydrocephalus - obesity - hypogonadism   Hydrocephaly corpus callosum agenesis diaphragmatic hernia   Hydrocephaly low insertion umbilicus   Hydrocephaly tall stature joint laxity   Hydrolethalus   Hydromelia   Hydrometrocolpos, postaxial polydactyly   Hydronephrosis congenital   Hydronephrosis - inverted smile   Hydrops fetalis   Hydrops fetalis - anaemia - immune disorder - absent thumb   Hydroxymethylglutaricaciduria   Hymenolepiasis   Hyperadrenocorticism   Hyperaldosteronism, familial, type 1   Hyperaldosteronism type 2, familial   Hyperalphalipoproteinemia, familial   Hyperammonemia - hypoornithinemia - hypocitrullinemia - hypoargininemia - hypoprolinemia   Hyperandrogenic-insulin resistant-acanthosis nigricans syndrome   Hyperbilirubinemia, Rotor type   Hyperbilirubinemia transient familial neonatal   Hyperbilirubinemia type 1   Hyperbilirubinemia type 2   Hyperbilirubinemia unconjugated, hereditary   Hypercalcemia, familial, benign   Hypercalcemia, familial - nephrocalcinosis - indicanuria   Hypercalciuria idiopathic   Hypercalciuria macular coloboma   Hypercholesterolemia due to arg3500 mutation of Apo B-100   Hypercholesterolemia due to LDL receptor deficiency   Hypercholesterolemia, familial   Hyperchylomicronemia, familial   Hypercoagulability syndrome, due to glycosylphosphatidylinositol deficiency   Hypercortisolism   Hyperdibasic aminoaciduria type 2   Hyperekplexia   Hyperekplexia, hereditary   Hyperexplexia, hereditary   Hyperferritinemia, hereditary, with congenital cataracts   Hyperglycerolemia   Hyperglycinemia, isolated nonketotic   Hyper-IgD syndrome   Hyper IgM syndrome   Hyperimidodipeptiduria   Hyperimmunoglobinemia D with recurrent fever   Hyperimmunoglobulinemia D with periodic fever   Hyperimmunoglobulin e - reccurrent infection syndrome   Hyperimmunoglobulin E syndrome   Hyperinsulinism-hyperammonemia syndrome   Hyperkalemic periodic paralysis   Hyperkaliemia - hypertension, Gordon type   Hyperkeratosis - hyperpigmentation syndrome   Hyperkeratosis lenticularis perstans   Hyperkeratosis palmoplantar, localized, acanthokeratolytic   Hyperkeratosis palmoplantar, localized, epidermolytic   Hyperlipidemia type 3   Hyperlipoproteinemia type 1   Hyperlipoproteinemia type 4   Hyperlipoproteinemia type 5   Hyperlipoproteinemia type I   Hyperlipoproteinemia type IV   Hyperlysinemia   Hypermethioninemia due to S-adenosylhomocysteine hydrolase deficiency   Hypernycthemeral syndrome   Hyperornithinemia   Hyperornithinemia - gyrate atrophy of choroid and retina (HOGA)   Hyperornithinemia-hyperammonemia-homocitrullinuria   Hyperostosid corticalis deformans juvenilis   Hyperostosis corticalis generalisata   Hyperostosis frontalis interna   Hyperostosis generalisata with striations   Hyperoxaluria   Hyperparathyroidism, neonatal severe, primary   Hyperparathyroidism, primary, familial   Hyperphalangism dysmorphy bronchomalacia   Hyperphenilalaninemia due to pterin-4-alpha-carbinolamine dehydratase deficiency   Hyperphenylalalinemia due to dihydropteridine reductase deficiency   Hyperphenylalaninemia due to 6-pyruvoyltetrahydropterin synthase deficiency   Hyperphenylalaninemia due to dehydratase deficiency   Hyperphenylalaninemia due to GTP cyclohydrolase deficiency   Hyperphenylalaninemic embryopathy   Hyperpigmentation, familial progressive   Hyperpipecolatemia   Hyperprolinaemia type I   Hyperprolinaemia type II   Hypersensitivity pneumonitis   Hypertelorism hypospadias polysyndactyly syndrome   Hypertelorism microtia facial clefting syndrome   Hypertension due to gain-of-function mutations in the mineralocorticoid receptor   Hypertensive hyperkalemia   Hypertensive hypokalemia familial   Hypertensive hypokalemia, recessive   Hyperthermia induced defects   Hyperthermia of anesthesia   Hyperthyroidism, familial, due to mutations in TSH receptor   Hypertrichosis, anterior cervical, isolated   Hypertrichosis - atrophic skin - ectropion - macrostomia   Hypertrichosis cubiti - short stature   Hypertrichosis lanuginosa, acquired   Hypertrichosis lanuginosa congenita   Hypertrichosis universalis   Hypertrichosis universalis congenita, Ambras type   Hypertrichotic osteochondrodysplasia   Hypertrophic neuropathy of infancy   Hypertrophic osteoarthropathy, primary or idiopathic   Hypertrophic subaortic stenosis   Hypertryptophanemia   Hypoaldosteronism, familial   Hypoalphalipoproteinemia, familial   Hypobetalipoproteinemia, familial form   Hypobetalipoproteinemia with selective deletion of Apo B-48   Hypocalcemia, autosomal dominant   Hypocalciuric hypercalcemia, familial   Hypochondroplasia   Hypocomplementaemic leucocytoclasic vasculitis   Hypocortisolism, acquired   Hypodermyiasis   Hypodonadotropic hypogonadism alopecia   Hypodontia   Hypodontia dysplasia of nails   Hypodontia - nail dysgenesis   Hypogammaglobulinemia due to CD19 deficiency   Hypogonadism cardiomyopathy   Hypogonadism cataract syndrome   Hypogonadism - gynecomastia - mental retardation, X-linked   Hypogonadism, hypogonadotropic, congenital, normosmic   Hypogonadism male mental retardation skeletal anomalies   Hypogonadism mitral valve prolapse mental retardation   Hypogonadism primary partial alopecia   Hypogonadism - retinitis pigmentosa   Hypogonadotropic hypogonadism, congenital - anosmia   Hypogonadotropic hypogonadism syndactyly   Hypokalemic alkalosis - hypercalciuria   Hypokalemic periodic paralysis   Hypokeratosis, palmo-plantar, circumscribed   Hypomagnesemia caused by selective magnesium malabsorption   Hypomagnesemia-hypokalemia, primary renotubular, with hypocalciuria   Hypomagnesemia, primary, familial (generic term)   Hypomagnesemia with hypocalciuria   Hypomagnesemia with normocalciuria   Hypomandibular faciocranial dysostosis   Hypomelanosis of Ito   Hypomyelination - congenital cataract   Hypomyelination - hypogonadotropic hypogonadism - hypodontia   Hypomyelination neuropathy - arthrogryposis   Hypoparathyroidism, autoimmune   Hypoparathyroidism, deafness and renal disease (HDR)   Hypoparathyroidism familial isolated   Hypoparathyroidism-mental retardation-dysmorphism   Hypoparathyroidism short stature   Hypoparathyroidism short stature mental retardation seizures   Hypoparathyroidism X-linked   Hypophosphatasia   hypopigmentation-deafness syndrome   Hypopigmentation oculocerebral syndrome cross type   Hypopituitarism dwarfism skeletal anomalies   Hypopituitarism - micropenis - cleft lip palate   Hypopituitarism - microphthalmia   Hypopituitarism - postaxial polydactyly   Hypoplastic left heart syndrome   Hypoplastic right heart microcephaly   Hypoplastic thumbs hydranencephaly   Hypoplastic tibiae post axial polydactyly   Hypoproconvertinemia   Hypoprothrombinemia   Hyposmia nasal hypoplasia hypogonadism   Hypospadias - dyspaghia   Hypospadias familial   Hypospadias - hypertelorism   Hypospadias mental retardation goldblatt type   Hypotelorism - cleft palate - hypospadias   Hypothalamic hamartoblastoma syndrome   Hypothalamic hamartoma syndrome, congenital   Hypothyroidism - cleft palate   Hypothyroidism, congenital   Hypothyroidism - dermoid cyst - cleft palate   Hypothyroidism - dysmorphism - postaxial polydactyly - intellectual deficit   Hypotonia and ichthyosis due to dolichol phosphate deficiency   Hypotonia - failure to thrive - microcephaly   Hypotrichosis - ichthyosis, congenital   Hypotrichosis - lymphoedema - telangiectasia   Hypotrichosis-mental retardation lopes type   Hypotrichosis simplex   Hypoxanthine guanine phosphoribosyltransferase (HPRT) complete deficiency   Hystiocytic necrotizing lymphadenitis   Hystrix-like ichthyosis-deafnesss syndrome