• Source: List of diseases (H)

This is a list of diseases starting with the letter "H".




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 (renamed to Pantothenate kinase-associated neurodegeneration due to Hallervorden's Nazi party associations)
Hallucinogen persisting perception disorder
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 and mouth disease
Hand–Schüller–Christian disease
Hanhart 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 attack
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

=
Heliophobia
HELLP syndrome
Helmerhorst–Heaton–Crossen syndrome
Helminthiasis




= Hem

=
HEM dysplasia



Hema–Hemi

Hemangioblastoma
Hemangioendothelioma
Hemangioma thrombocytopenia syndrome
Hemangioma, capillary infantile
Hemangioma
Hemangiomatosis, familial pulmonary capillary
Hemangiopericytoma
Hematocolpos
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

Hemochromatosis
Hemochromatosis type 1
Hemochromatosis type 2
Hemochromatosis type 3
Hemochromatosis type 4
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
Hemorrhagic fever with renal syndrome
Hemorrhoid
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
Henoch–Schönlein purpura




= 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
Hepatitis A
Hepatitis B
Hepatitis C
Hepatitis D
Hepatitis E
Hepatoblastoma
Hepatocellular carcinoma
Hepatorenal syndrome
Hepatorenal tyrosinemia




= Her

=
Herpes



Here




= Hered
=




Heredi


Hereditary a – Hereditary m

Hereditary amyloidosis
Hereditary angioedema
Hereditary ataxia
Hereditary breast–ovarian cancer syndrome
Hereditary carnitine deficiency myopathy
Hereditary carnitine deficiency syndrome
Hereditary carnitine deficiency
Hereditary ceroid lipofuscinosis
Hereditary coproporphyria
Hereditary deafness
Hereditary elliptocytosis
Hereditary fibrinogen Aα-Chain amyloidosis
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


HHH syndrome




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 (canine)
Hip dysplasia (human)
Hip luxation
Hip subluxation
Hipo syndrome




= Hir–Hiv

=
Hirschsprung disease
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
Hirsutism congenital gingival hyperplasia
Hirsutism skeletal dysplasia mental retardation
His bundle tachycardia
Histadelia
Histapenia
Histidinemia
Histidinuria renal tubular defect syndrome
Histiocytosis X
Histiocytosis, Non-Langerhans-Cell
Histoplasmosis
Histrionic personality disorder
Hittner–Hirsch–Kreh syndrome
HIV




Hm


Hm syndrome
HMG-CoA lyase deficiency
HMG CoA synthetase deficiency




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
Hot tub folliculitis
Houlston–Ironton–Temple syndrome
Howard–Young syndrome
Howel–Evans syndrome
Hoyeraal–Hreidarsson syndrome
Hoyeraal syndrome




Hs


HSV-2 infection




Hu


Human ewingii ehrlichiosis
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–Mcdonald 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
Hutteroth–Spranger syndrome




Hy






= Hya

=
Hyalinosis systemic short stature
Hyaloideoretinal degeneration of wagner




= Hyd

=



Hyda–Hyde

Hydantoin antenatal infection
Hydatidiform mole
Hydatidosis
Hyde–Forster–Mccarthy–Berry syndrome



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
Hydroxymethylglutaric aciduria




= Hyg-Hym

=
Hygroma cervical
Hymenolepiasis




= Hyp

=



Hyper


Hyper IgE
Hyper IgM syndrome



= 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
Hyperekplexia
Hypereosinophilic syndrome
Hyperferritinemia, hereditary, with congenital cataracts
Hypergeusia
Hyperglycemia
Hyperglycerolemia
Hyperglycinemia, isolated nonketotic type 1
Hyperglycinemia, isolated nonketotic type 2
Hyperglycinemia, isolated nonketotic
Hyperglycinemia, ketotic
Hyperglycinemia, non-ketotic
Hypergonadotropic ovarian failure, familial or sporadic



= Hyperh–Hyperk
=
Hyperhidrosis
Hyperhomocysteinemia
Hyper-IgD syndrome
Hyperimidodipeptiduria
Hyperimmunoglobinemia D with recurrent fever
Hyperimmunoglobulin E - recurrent 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
Hyperopia
Hyperornithinemia
Hyperornithinemia, hyperammonemia, homocitrullinuria syndrome
Hyperostosid corticalis deformans juvenilis
Hyperostosis cortical infantile
Hyperostosis corticalis generalisata
Hyperostosis frontalis interna
Hyperoxaluria type 1
Hyperoxaluria type 2
Hyperoxaluria



= Hyperp–Hypers
=
Hyperparathyroidism
Hyperparathyroidism, familial, primary
Hyperparathyroidism, neonatal severe primary
Hyperphalangism dysmorphy bronchomalacia
Hyperphenylalaninemia
Hyperphenylalaninemia due to pterin-4-alpha-carbin
Hyperphenylalaninemia 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
Hypersensitivity
Hypersensitivity type I
Hypersensitivity type II
Hypersensitivity type III
Hypersensitivity type IV
Hypersomnolence



= Hypert–Hyperv
=
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
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
Hypervitaminosis A
Hypervitaminosis D
Hypervitaminosis E



Hypo




= Hypoa–Hypof
=
Hypoactive sexual desire disorder
Hypoadrenalism
Hypoadrenocorticism hypoparathyroidism moniliasis
Hypoaldosteronism
Hypo-alphalipoproteinemia primary
Hypobetalipoproteinaemia ataxia hearing loss
Hypobetalipoprotéinemia, familial
Hypocalcemia, autosomal dominant
Hypocalcemia
Hypocalciuric hypercalcemia, familial
Hypochondriasis
Hypochondrogenesis
Hypochondroplasia
Hypocomplementemic urticarial vasculitis
Hypodermyasis
Hypodontia dysplasia of nails
Hypodontia of incisors and premolars
Hypodysfibrinogenemia
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
Hypokalemic periodic paralysis type 1
Hypokalemic sensory overstimulation
Hypoketonemic hypoglycemia
Hypolipoproteinemia



= Hypom
=
Hypomagnesemia primary
Hypomandibular faciocranial dysostosis
Hypomelanotic disorder
Hypomelia Müllerian 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 Müllerian 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
Hypertonic gingivitus
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

Kata Kunci Pencarian:

• Rifampisin
• Azitromisin
• Antibiotik
• Parasetamol
• Lactococcus lactis
• Radang paru-paru
• Nistatin
• Hama
• Albuminuria
• Propofol
• List of diseases (H)
• List of diseases (Q)
• List of diseases (Z)
• List of diseases (Y)
• Lists of diseases
• List of diseases (V)
• List of diseases (U)
• List of diseases (A)
• List of diseases (X)
• List of diseases (B)