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X-linked retinoschisis

MONDO:0010725

Also known as: X-linked juvenile retinoschisis, X-linked juvenile retinoschisis type 1, X-linked retinoschisis, XLRS, juvenile X-linked retinoschisis

MONDO:
MONDO:0010725
Orphanet:
792
Rare disease42 associated genes

Description

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

Associated genes

+32 more genes — install the extension to see the full list inline on any page.

External references

Sources: MONDO (CC BY 4.0), Open Targets (CC0), Orphanet (CC BY 4.0).

Not for sole clinical decision-making. Always verify against primary sources.