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
To facilitate research we advise you to serve to you as the
function of search for your navigator :
- Finely: Edition > To seek in the page
- Shortened keyboard: Ctrl + F
Ia
IB
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
IG
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
Iu
Iv
Sources
- Site of information on the orphan rare diseases and drugs