List of diseases (H)
A list of diseases in the English wikipedia.
Ha
Hag-Ham
- Hageman factor deficiency
- Hagemoser Weinstein Bresnick syndrome
- Hailey-Hailey disease
- Hair defect with photosensitivity and mental retardation
- Hairy cell leukemia
- Hairy ears, y-linked
- Hairy ears
- Hairy nose tip
- Hairy palms and soles
- Hairy tongue
- Hajdu-Cheney syndrome
- Halal Setton Wang syndrome
- Halal syndrome
- Hall Riggs mental retardation syndrome
- Hallermann Streiff syndrome
- Hallervorden-Spatz disease
- Hallux valgus
- Hamanishi Ueba Tsuji syndrome
- Hamano Tsukamoto syndrome
- Hamartoma sebaceus of Jadassohn
Han-Hay
- Hand and foot deformity flat facies
- Hand foot uterus syndrome
- Hand wringing Rett syndrome
- Hand-foot-mouth disease
- Hand-Schuller-Christian disease
- Hanhart syndrome
- Hantavirosis
- Hantavirus pulmonary syndrome
- Hapnes Boman Skeie syndrome
- Hard skin syndrome Parana type
- HARD syndrome
- Harding ataxia
- Harlequin type ichthyosis
- Harpaxophobia
- Harrod Doman Keele syndrome
- Hartnup disease
- Hartsfield Bixler Demyer syndrome
- Hashimoto struma
- Hashimoto-Pritzker syndrome
- Hashimoto's thyroiditis
- Haspeslagh Fryns Muelenaere syndrome
- Hay Wells syndrome recessive type
- Hay-Wells syndrome
He
Hea-Hei
- Headache, cluster
- Hearing disorder
- Hearing impairment
- Hearing loss
- Heart aneurysm
- Heart block progressive, familial
- Heart block
- Heart defect round face congenital retarded development
- Heart defect tongue hamartoma polysyndactyly
- Heart defects limb shortening
- Heart hand syndrome Spanish type
- Heart hypertrophy, hereditary
- Heart situs anomaly
- Heart tumor of the adult
- Heart tumor of the child
- Heavy metal poisoning
- Hec syndrome
- Hecht Scott syndrome
- Heckenlively syndrome
- Heide syndrome
Hel
Hem
Hema-Hemi
- Hemangioblastoma
- Hemangioendothelioma
- Hemangioma thrombocytopenia syndrome
- Hemangioma, capillary infantile
- Hemangioma
- Hemangiomatosis, familial pulmonary capillary
- Hemangiopericytoma
- Hemeralopia, congenital essential
- Hemeralopia, familial
- Hemi 3 syndrome
- Hemifacial atrophy agenesis of the caudate nucleus
- Hemifacial atrophy progressive
- Hemifacial hyperplasia strabismus
- Hemifacial microsomia
- Hemihypertrophy in context of NF
- Hemihypertrophy intestinal web corneal opacity
- Hemimegalencephaly
- Hemiplegia
- Hemiplegic migraine, familial
Hemo
- Hemoglobin C disease
- Hemoglobin E disease
- Hemoglobin SC disease
- Hemoglobinopathy
- Hemoglobinuria
- Hemolytic anemia lethal genital anomalies
- Hemolytic-uremic syndrome
- Hemophagocytic lymphohistiocytosis
- Hemophagocytic reticulosis
- Hemophilia A
- Hemophilic arthropathy
- Hemophobia
- Hemorragic fever with renal syndrome
- Hemorrhagic fever
- Hemorrhagic proctocolitis
- Hemorrhagic thrombocythemia
- Hemorrhagiparous thrombocytic dystrophy
- Hemosiderosis
- Hemothorax
Hen
- Hennekam Beemer syndrome
- Hennekam Koss de Geest syndrome
- Hennekam syndrome
- Hennekam Van der Horst syndrome
Hep
- Hepadnovirus D
- Heparane sulfamidase deficiency
- Heparin-induced thrombopenia
- Hepatic cystic hamartoma
- Hepatic ductular hypoplasia
- Hepatic encephalopathy
- Hepatic fibrosis renal cysts mental retardation
- Hepatic fibrosis
- Hepatic venoocclusive disease
- Hepatic veno-occlusive disease
- Hepatitis A
- Hepatitis B
- Hepatitis C
- Hepatitis D
- Hepatitis non-A non-B
- Hepatitis non-A
- Hepatitis non-B
- Hepatitis, chronic autoimmune
- Hepatitis
- Hepatoblastoma
- Hepatocellular carcinoma
- Hepatorenal syndrome
- Hepatorenal tyrosinemia
Her
Here
Hered
Heredi
Hereditary a-Hereditary m
- Hereditary amyloidosis
- Hereditary angioedema
- Hereditary ataxia
- Hereditary carnitine deficiency myopathy
- Hereditary carnitine deficiency syndrome
- Hereditary carnitine deficiency
- Hereditary ceroid lipofuscinosis
- Hereditary coproporphyria
- Hereditary deafness
- Hereditary elliptocytosis
- Hereditary fructose intolerance
- Hereditary hearing disorder
- Hereditary hearing loss
- Hereditary hemochromatosis
- Hereditary hemorrhagic telangiectasia
- Hereditary hyperuricemia
- Hereditary macrothrombocytopenia
- Hereditary methemoglobinemia, recessive
- Hereditary myopathy with intranuclear filamentous
Hereditary n-Hereditary t
- Hereditary nodular heterotopia
- Hereditary non-spherocytic hemolytic anemia
- Hereditary pancreatitis
- Hereditary paroxysmal cerebral ataxia
- Hereditary peripheral nervous disorder
- Hereditary primary Fanconi disease
- Hereditary resistance to anti-vitamin K
- Hereditary sensory and autonomic neuropathy 3
- Hereditary sensory and autonomic neuropathy 4
- Hereditary sensory neuropathy type I
- Hereditary sensory neuropathy type II
- Hereditary spastic paraplegia
- Hereditary spherocytic hemolytic anemia
- Hereditary spherocytosis
- Hereditary type 1 neuropathy
- Hereditary type 2 neuropathy
Herm-Hers
- Hermansky-Pudlak syndrome
- Hermaphroditism
- Hernandez Aguire Negrete syndrome
- Herpangina
- Herpes encephalitis
- Herpes simplex disease
- Herpes simplex encephalitis
- Herpes viridae disease
- Herpes virus antenatal infection
- Herpes zoster oticus
- Herpes zoster
- Herpesvirus simiae B virus
- Herpetic embryopathy
- Herpetic keratitis
- Herpetophobia
- Herrmann Opitz arthrogryposis syndrome
- Herrmann Opitz craniosynostosis
- Hers disease
- Hersh Podruch Weisskopk syndrome
Het-Hex
- Heterophobia
- Heterotaxia (generic term)
- Heterotaxia autosomal dominant type
- Heterotaxy with polysplenia or asplenia
- Heterotaxy, visceral, X-linked
- Hexosaminidases A and B deficiency
Hh
Hi
Hib-Hip
- Hibernian fever, familial
- Hiccups
- Hidradenitis suppurativa familial
- Hidradenitis suppurativa
- Hidrotic ectodermal dysplasia type Christianson Fouris
- High scapula
- High-molecular-weight kininogen deficiency, congenital
- Hillig syndrome
- Hing Torack Dowston syndrome
- Hinson-Pepys disease
- Hip dislocation
- Hip dysplasia Beukes type
- Hip dysplasia
- Hip dysplasia (human)
- Hip luxation
- Hip subluxation
- Hipo syndrome
Hir-Hit
- Hirschsprung disease ganglioneuroblastoma
- Hirschsprung disease polydactyly heart disease
- Hirschsprung disease type 2
- Hirschsprung disease type 3
- Hirschsprung disease type d brachydactyly
- Hirschsprung microcephaly cleft palate
- Hirschsprung nail hypoplasia dysmorphism
- Hirschsprung's disease
- Hirsutism congenital gingival hyperplasia
- Hirsutism skeletal dysplasia mental retardation
- His bundle tachycardia
- Histidinemia
- Histidinuria renal tubular defect
- Histiocytosis X
- Histiocytosis, Non-Langerhans-Cell
- Histoplasmosis
- Hittner Hirsch Kreh syndrome
Hm
Ho
Hod-Hol
- Hodgkin lymphoma
- Hodgkin's disease
- Hoepffner Dreyer Reimers syndrome
- Hollow visceral myopathy
- Holmes Benacerraf syndrome
- Holmes Borden syndrome
- Holmes Collins syndrome
- Holmes Gang syndrome
- Holoacardius amorphus
- Holocarboxylase synthetase deficiency
- Holoprosencephaly caudal dysgenesis
- Holoprosencephaly deletion 2p
- Holoprosencephaly ectrodactyly cleft lip palate
- Holoprosencephaly radial heart renal anomalies
- Holoprosencephaly
- Holt-Oram syndrome
- Holzgreve Wagner Rehder syndrome
Hom-Hoy
- Homocarnosinase deficiency
- Homocarnosinosis
- Homocystinuria due to cystathionine beta-synthase
- Homocystinuria due to defect in methylation (cbl g)
- Homocystinuria due to defect in methylation cbl e
- Homocystinuria due to defect in methylation, MTHFR deficiency
- Homocystinuria
- Homologous wasting disease
- Homozygous hypobetalipoproteinemia
- Hoon Hall syndrome
- Hordnes Engebretsen Knudtson syndrome
- Horn Kolb syndrome
- Horner's syndrome
- Hornova Dlurosova syndrome
- Horseshoe kidney
- Horton disease, juvenile
- Horton disease
- Houlston Ironton Temple syndrome
- Howard Young syndrome
- Howell-Evans syndrome
- Hoyeraal Hreidarsson syndrome
- Hoyeraal syndrome
Hs
Hu
- Human granulocytic ehrlichiosis
- Human monocytic ehrlichiosis
- Human parvovirus B19 infection
- Humero spinal dysostosis congenital heart disease
- Humeroradial synostosis
- Humeroradioulnar synostosis
- Humerus trochlea aplasia of
- Hunter Carpenter Mc donald syndrome
- Hunter Jurenka Thompson syndrome
- Hunter Macpherson syndrome
- Hunter Mcalpine syndrome
- Hunter Mcdonald syndrome
- Hunter Rudd Hoffmann syndrome
- Hunter syndrome
- Huntington's disease
- Huriez scleroatrophic syndrome
- Hurler syndrome
- Hurst Hallam Hockey syndrome
- Hutchinson Gilford Progeria Syndrome
- Hutchinson incisors
- Hutchinson-Gilford syndrome
- Hutteroth Spranger syndrome
Hy
Hya
Hyd
Hyda-Hyde
Hydr
- Hydranencephaly
- Hydrocephalus - Arnold Chiari - allied disorders
- Hydrocephalus autosomal recessive
- Hydrocephalus costovertebral dysplasia Sprengel anomaly
- Hydrocephalus craniosynostosis bifid nose
- Hydrocephalus endocardial fibroelastosis cataract
- Hydrocephalus growth retardation skeletal anomalies
- Hydrocephalus obesity hypogonadism
- Hydrocephalus skeletal anomalies
- Hydrocephalus
- Hydrocephaly corpus callosum agenesis diaphragmatic hernia
- Hydrocephaly low insertion umbilicus
- Hydrocephaly tall stature joint laxity
- Hydrolethalus syndrome
- Hydronephrosis
- Hydronephrosis peculiar facial expression
- Hydrophobia
- Hydrops ectrodactyly syndactyly
- Hydrops fetalis anemia immune disorder absent thumb
- Hydrops fetalis
- Hydroxycarboxylic aciduria
- Hydroxymethylglutaricaciduria
Hyg-Hym
Hyp
Hype
Hyper
Hypera-Hyperb
- Hyperadrenalism
- Hyperaldosteronism familial type 2
- Hyperaldosteronism, familial type 1
- Hyperaldosteronism
- Hyperammonemia
- Hyperandrogenism
- Hyperbilirubinemia transient familial neonatal
- Hyperbilirubinemia type 1
- Hyperbilirubinemia type 2
- Hyperbilirubinemia
Hyperc-Hyperg
- Hypercalcemia, familial benign type 1
- Hypercalcemia, familial benign type 2
- Hypercalcemia, familial benign type 3
- Hypercalcemia, familial benign
- Hypercalcemia
- Hypercalcinuria idiopathic
- Hypercalcinuria macular coloboma
- Hypercalcinuria
- Hypercementosis
- Hypercholesterolemia due to arg3500 mutation of Apo B-100
- Hypercholesterolemia due to LDL receptor deficiency
- Hypercholesterolemia
- Hyperchylomicronemia
- Hypereosinophilic syndrome
- Hyperexplexia
- Hyperferritinemia, hereditary, with congenital cataracts
- Hypergeusia
- Hyperglycemia
- Hyperglycerolemia
- Hyperglycinemia, isolated nonketotic type 1
- Hyperglycinemia, isolated nonketotic type 2
- Hyperglycinemia, isolated nonketotic
- Hyperglycinemia
- Hypergonadotropic ovarian failure, familial or sporadic
Hyperh-Hyperk
- Hyperhidrosis
- Hyperhomocysteinemia
- Hyper-IgD syndrome
- Hyperimidodipeptiduria
- Hyperimmunoglobinemia D with recurrent fever
- Hyperimmunoglobulin E - reccurrent infection syndrome
- Hyperimmunoglobulinemia D with periodic fever
- Hyperimmunoglobulinemia E
- Hyperinsulinism due to focal adenomatous hyperplasia
- Hyperinsulinism due to glucokinase deficiency
- Hyperinsulinism due to glutamodehydrogenase deficiency
- Hyperinsulinism in children, congenital
- Hyperinsulinism, diffuse
- Hyperinsulinism, focal
- Hyperkalemia
- Hyperkalemic periodic paralysis
- Hyperkeratosis lenticularis perstans of Flegel
- Hyperkeratosis lenticularis perstans
- Hyperkeratosis palmoplantar localized acanthokeratolytic
- Hyperkeratosis palmoplantar localized epidermolytic
- Hyperkeratosis palmoplantar with palmar crease hyperkeratosis
Hyperl-Hypero
- Hyperlipoproteinemia type I
- Hyperlipoproteinemia type II
- Hyperlipoproteinemia type III
- Hyperlipoproteinemia type IV
- Hyperlipoproteinemia type V
- Hyperlipoproteinemia
- Hyperlysinemia
- Hyperornithinemia
- Hyperornithinemia-hyperammonemia-homocitrullinuria
- Hyperostosid corticalis deformans juvenilis
- Hyperostosis cortical infantile
- Hyperostosis corticalis generalisata
- Hyperostosis frontalis interna
- Hyperoxaluria type 1
- Hyperoxaluria type 2
- Hyperoxaluria
Hyperp-Hypers
- Hyperparathyroidism, familial, primary
- Hyperparathyroidism, neonatal severe primary
- Hyperparathyroidism
- Hyperphalangism dysmorphy bronchomalacia
- Hyperphenilalaninemia due to pterin-4-alpha-carbin
- Hyperphenylalalinemia due to dihydropteridine reductase deficiency
- Hyperphenylalaninemia due to 6-pyruvoyltetrahydrop
- Hyperphenylalaninemia due to dehydratase deficiency
- Hyperphenylalaninemia due to GTP cyclohydrolase deficiency
- Hyperphenylalaninemic embryopathy
- Hyperpipecolatemia
- Hyperprolactinemia
- Hyperprolinemia type II
- Hyperprolinemia
- Hyperreflexia
- Hyper-reninism
- Hypersomnolence
Hypert
Hyperte-Hyperth
- Hypertelorism and tetralogy of Fallot
- Hypertelorism hypospadias syndrome
- Hypertension
- Hypertensive hyperkalemia, familial
- Hypertensive hypokalemia familial
- Hypertensive retinopathy
- Hyperthermia induced defects
- Hyperthermia
- Hyperthyroidism
- Hyperthyroidism due to mutations in TSH receptor
Hypertr
- Hypertrichosis atrophic skin ectropion macrostomia
- Hypertrichosis brachydactyly obesity and mental retardation
- Hypertrichosis congenital generalized X linked
- Hypertrichosis lanuginosa congenita
- Hypertrichosis lanuginosa, acquired
- Hypertrichosis retinopathy dysmorphism
- Hypertrichosis, anterior cervical
- Hypertrichotic osteochondrodysplasia
- Hypertriglycidemia
- Hypertrophic branchial myopathy
- Hypertrophic cardiomyopathy
- Hypertrophic hemangiectasia
- Hypertrophic myocardiopathy
- Hypertrophic osteoarthropathy, primary or idiopathic
- Hypertropia
- Hypertropic neuropathy of Dejerine-Sottas
- Hypertryptophanemia
Hypo
Hypoa-Hypof
- Hypoadrenalism
- Hypoadrenocorticism hypoparathyroidism moniliasis
- Hypoaldosteronism
- Hypo-alphalipoproteinemia primary
- Hypobetalipoproteinaemia ataxia hearing loss
- Hypobetalipoprotéinemia, familial
- Hypocalcemia, autosomal dominant
- Hypocalcemia
- Hypocalcinuric hypercalcemia, familial type 1
- Hypocalcinuric hypercalcemia, familial type 2
- Hypocalcinuric hypercalcemia, familial type 3
- Hypocalcinuric hypercalcemia, familial
- Hypochondrogenesis
- Hypochondroplasia
- Hypocomplementemic urticarial vasculitis
- Hypodermyasis
- Hypodontia dysplasia of nails
- Hypodontia of incisors and premolars
- Hypofibrinogenemia, familial
Hypog-Hypol
- Hypoglycemia with deficiency of glycogen synthetase in the liver
- Hypoglycemia
- Hypogonadism cardiomyopathy
- Hypogonadism hypogonadotropic due to mutations in GR hormone
- Hypogonadism male mental retardation skeletal anomaly
- Hypogonadism mitral valve prolapse mental retardation
- Hypogonadism primary partial alopecia
- Hypogonadism retinitis pigmentosa
- Hypogonadism, isolated, hypogonadotropic
- Hypogonadism
- Hypogonadotropic hypogonadism syndactyly
- Hypogonadotropic hypogonadism without anosmia, X linked
- Hypogonadotropic hypogonadism-anosmia, X linked
- Hypogonadotropic hypogonadism-anosmia
- Hypohidrotic Ectodermal Dysplasia
- Hypokalemia
- Hypokalemic alkalosis with hypercalcinuria
- Hypokalemic periodic paralysis
- Hypokaliemic periodic paralysis type 1
- Hypokalemic sensory overstimulation
- Hypoketonemic hypoglycemia
- Hypolipoproteinemia
Hypom
- Hypomagnesemia primary
- Hypomandibular faciocranial dysostosis
- Hypomelanotic disorder
- Hypomelia mullerian duct anomalies
- Hypomentia
Hypop
- Hypoparathyroidism familial isolated
- Hypoparathyroidism nerve deafness nephrosis
- Hypoparathyroidism short stature mental retardation
- Hypoparathyroidism short stature
- Hypoparathyroidism X linked
- Hypoparathyroidism
- Hypophosphatasia, infantile
- Hypophosphatasia
- Hypophosphatemic rickets
- Hypopigmentation oculocerebral syndrome Cross type
- Hypopituitarism micropenis cleft lip palate
- Hypopituitarism postaxial polydactyly
- Hypopituitarism
- Hypopituitary dwarfism
- Hypoplasia hepatic ductular
- Hypoplasia of the tibia with polydactyly
- Hypoplastic left heart syndrome
- Hypoplastic right heart microcephaly
- Hypoplastic thumb mullerian aplasia
- Hypoplastic thumbs hydranencephaly
- Hypoproconvertinemia
- Hypoprothrombinemia
Hypor-Hypox
- Hyporeninemic hypoaldosteronism
- Hyposmia nasal hypoplasia hypogonadism
- Hypospadias familial
- Hypospadias mental retardation Goldblatt type
- Hyposplenism
- Hypotelorism cleft palate hypospadias
- Hypothalamic dysfunction
- Hypothalamic hamartoblastoma syndrome
- Hypothalamic hamartomas
- Hypothermia
- Hypothyroidism due to iodide transport defect
- Hypothyroidism postaxial polydactyly mental retardation
- Hypothyroidism
- Hypotonic sclerotic muscular dystrophy
- Hypotrichosis mental retardation Lopes type
- Hypotrichosis
- Hypotropia
- Hypoxanthine guanine phosphoribosyltransferase deficiency
- Hypoxia