Autosomal dominant vitreoretinochoroidopathy

Orpha code: 3086OMIM code: 193220

Definition

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.

Disease data
Classification

Disease

Synonyms
ADVIRC
ADVIRC
ORPHA code
3086
OMIM code
193220
ICD10 code
H35.5
ICD11 code
9B70

No additional description.

Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl