List rare diseases starting with an I

The Council of use of this list

This list contains several hundreds of rare diseases.
  • Liste updated on June 12th, 2005
  • the diseases in italic are not genetic diseases
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Ia

IB

  • IBIDS syndrome

IC

  • ICCA syndrome
  • Ice syndrome
  • ICF syndrome
  • Ichtyose alopecie backwardness ectropion
  • Ichtyose biliary atresy
  • Ichtyose with trichothiodystrophie
  • Ichtyose bulleuse of Siemens
  • Ichtyose congenital, autosomic recessive
  • Ichtyose congenital standard baby collodion
  • Ichtyose congenital standard fetus Harlequin
  • Ichtyose de Curth-Macklin
  • Ichtyose spindle-shaped fingers median labial furrow
  • Ichtyose exfoliative
  • follicular Ichtyose atrichie photophobia syndrome
  • Ichtyose hepatosplenomegalie cerebelleuse degeneration
  • male Ichtyose hypogonadism
  • Ichtyose keratitis deafness
  • lamellate Ichtyose
  • Ichtyose related to X
  • Ichtyose backwardness nanism anomaly renal
  • asymptomatic Ichtyose backwardness spasticite
  • standard Ichtyose backwardness devriendt

Id

  • Iduronate 2-sulfatase, deficit in

IE

Yew

  • Ifap syndrome

IG

  • IGDA syndrome

Ih-Ik

It

  • It syndrome of
  • Ilyina amoashy grygory syndrome

Im

  • Imaizumi kuroki syndrome of
  • Imerslund-Gräsbeck, disease of
  • Iminoglycinurie
  • Immotilité ciliaire, standard Kartagener
  • Immunodéficience primitive in cells T
  • Immunodéficience combined severe
  • bulleux Impétigo
  • Impossible syndrome
  • primitive basilaire Impression

In

  • higher central Incisor single
  • Incisors mandibulaires fusion
  • microvilleuses Inclusions disease of the
  • family Incompetence velopharyngienne
  • Incontinentia pigmenti
  • Incontinentia pigmenti achromians
  • congenital Incurvation of the long bones
  • serpentine Incurvation of the fibula
  • Indometacine, exposure anténatale to the
  • congenital Infection with the cytomegalovirus
  • Infection disseminated by the cytomegalovirus, idiopathic
  • idiopathic Infection by the BCG or atypical mycobacteries
  • cutaneous lymphocytary Infiltration of Inhibiting Jessner-Kanof
  • 1 of the activator of plasminogene, congenital deficit in
  • Insensibility to the pain with anhydrose
  • family fatal Insomnia prion
  • articular Instability syndrome of
  • Instability centromérique-immunodéficience-dysmorphie
  • mitotic Instability not disjunction
  • antéhypophysaire Insufficiency of standard genetic cause
  • Insulino-resistance A-acanthosis nigricans
  • standard Insulino-resistance B
  • Interruption of the aortic stick
  • Internal atrésies multiple
  • Intolerance with dibasic proteins with lysinurie
  • Intoxication to asbestos

Io-Iq

Ir

  • Iridogoniodysgénésie, dominant form

Is

  • Isaacs mertens syndrome of
  • Ischion hypoplasy kidney anomaly immunodéficience supernumerary polydactyly
  • Isochromosome 12p
  • Isochromosome 18p
  • Isotrétinoïne like syndrome
  • Isotrétinoïne syndrome
  • Isovaléryl-CoA déshydrogénase, deficit in

It

  • Itin, syndrome of

Iu

Iv

  • Ivic syndrome D

Sources

  • Site of information on the orphan rare diseases and drugs

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