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List of diseases (H) - Wikipedia, the free encyclopedia

List of diseases (H)

From Wikipedia, the free encyclopedia

A list of diseases in the English wikipedia.

Diseases
Alphabetical list: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
See also: Health  |  Exercise  |  Nutrition



Contents

[edit] Ha

[edit] Hag-Ham

[edit] Han-Hay

[edit] He

[edit] Hea-Hei

[edit] Hel

[edit] Hem

  • HEM dysplasia

[edit] Hema-Hemi

[edit] Hemo

[edit] Hen

  • Hennekam Beemer syndrome
  • Hennekam Koss de Geest syndrome
  • Hennekam syndrome
  • Hennekam Van der Horst syndrome

[edit] Hep

[edit] Her

[edit] Here

[edit] Hered

[edit] Heredi

Hereditary a-Hereditary m

Hereditary n-Hereditary t

[edit] Herm-Hers

[edit] Het-Hex

  • Heterophobia
  • Heterotaxia (generic term)
  • Heterotaxia autosomal dominant type
  • Heterotaxy with polysplenia or asplenia
  • Heterotaxy, visceral, X-linked
  • Hexosaminidases A and B deficiency

[edit] Hh

[edit] Hi

[edit] 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 luxation
  • Hip subluxation
  • Hipo syndrome

[edit] 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

[edit] Hm

  • Hm syndrome
  • HMG CoA lyase deficiency
  • HMG CoA synthetase deficiency

[edit] Ho

[edit] Hod-Hol

[edit] 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

[edit] Hs

[edit] Hu

[edit] Hy

[edit] Hya

  • Hyalinosis systemic short stature
  • Hyaloideoretinal degeneration of wagner

[edit] Hyd

[edit] Hyda-Hyde

[edit] 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

[edit] Hyg-Hym

[edit] Hyp

[edit] Hype

[edit] Hyper

[edit] Hypera-Hyperb

[edit] 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

[edit] 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

[edit] Hyperl-Hypero

[edit] 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

[edit] Hypert

Hyperte-Hyperth

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

[edit] Hypo

[edit] 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

[edit] 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
  • Hypoketonemic hypoglycemia
  • Hypolipoproteinemia

[edit] Hypom
  • Hypomagnesemia primary
  • Hypomandibular faciocranial dysostosis
  • Hypomelanotic disorder
  • Hypomelia mullerian duct anomalies
  • Hypomentia

[edit] 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

[edit] Hypor-Hypox

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