Autosomal dominant vitreoretinochoroidopathy

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A rare, genetic, vitreous-retinal disease characterized by ocular developmental anomalies such as microcornea, a shallow anterior chamber, glaucoma and cataract. Abnormal chorioretinal pigmentation is present, usually lying between the vortex veins and the ora serrata for 360 degrees.

Synonyms: ADVIRC

This is just here as a test because I lose it

Term information

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ICD-10:H35.5

UMLS:C3888099

OMIM:193220

MeSH:C536352

notation

ORPHA:3086