Catalog

Autosomal dominant vitreoretinochoroidopathy

No MMS code

Link to WHO Definition

Autosomal dominant vitreoretinochoroidopathy – http://id.who.int/icd/entity/96951767

Autosomal dominant vitreoretinochoroidopathy is a genetic vitreous-retinal disease characterised by ocular developmental anomalies such as microcornea, a shallow anterior chamber, glaucoma and cataract. There is abnormal chorioretinal pigmentation, usually lying between the vortex veins and the ora serrata for 360 degrees.