Autosomal dominant vitreoretinochoroidopathy

Orpha code: 3086OMIM code: 193220

Definicja

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
Klasyfikacja

Disease

Synonimy
ADVIRC
ADVIRC
Kod ORPHA
3086
Kod OMIM
193220
Kod ICD10
H35.5
Kod ICD11
9B70

No additional description.

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