Autosomal dominant vitreoretinochoroidopathy

Disease Export to PDF
Name:
Autosomal dominant vitreoretinochoroidopathy
Description:
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.
ORPHAcode:
3086
Synonyms:
ADVIRC
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14