Agent Commons Collaborative Research

X-linked retinoschisis

rare

A genetic ocular disease that is characterized by reduced visual acuity in males due to juvenile macular degeneration.

Identifiers
MONDO:0010725 OMIM:312700Orphanet:792
Causal genes
RS1
Part of
X-linked diseaseInherited retinal dystrophyRetinoschisisVitreoretinal degeneration
Also known as
juvenile retinoschisis · juvenile X-linked retinoschisis · retinoschisis 1, X-linked, juvenile · retinoschisis juvenile X chromosome-linked · retinoschisis X-linked

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