A rare inflammatory eye disease of unknown aetiology characterised by generalised inflammation of the uvea (iris, ciliary body, choroid), retina and vitreous with consequent ciliary spasm and posterior synechiae formation, leading to acute or chronic

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panuvéite idiopathique

SNOMEDCT-BE (iris, ciliary body, choroid), retina and vitreous with consequent ciliary spasm and posterior synechiae formation, leading to acute or chronic / 766933000

SNOMEDCT-BE (disorder) / 766933000

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A rare syndromic microphthalmia disorder with characteristics of microphthalmia with coloboma (which may involve the iris, ciliary body, choroid, retina and/or optic nerve), microcephaly, short stature and intellectual disability. Other eye abnormali

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syndrome de micropthalmie colobomateuse-microcéphalie-déficience intellectuelle-petite taille liée à l'X

SNOMEDCT-BE (which may involve the iris, ciliary body, choroid, retina and/or optic nerve), microcephaly, short stature and intellectual disability. Other eye abnormali / 771148008

SNOMEDCT-BE (disorder) / 771148008

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Choroideremia Dystrophy, choroidal (central areolar)(generalized)(peripapillary) Gyrate atrophy, choroid

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Atrophia gyrata chorioideae Choroïdérémie Dystrophie choroïdienne (aréolaire centrale) (généralisée) (péripapillaire)

WORLD HEALTH ORGANIZATION ICD-10: H31.2

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A rare potentially sight-threatening ocular disease not attributed to any specific ocular or systemic cause. The disease has characteristics of focal, multifocal or diffuse non-infectious inflammation in the posterior uvea (such as choroiditis, chori

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uvéite postérieure idiopathique

SNOMEDCT-BE (such as choroiditis, chori / 773991005

SNOMEDCT-BE (disorder) / 773991005

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Choroid

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Choroïde

WORLD HEALTH ORGANIZATION ICD-10: C69.3

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https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]