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X-linked retinal dysplasia

MONDO:0010722

Also known as: PRD, retinal dysplasia X-linked, retinal dysplasia, primary

MONDO:
MONDO:0010722
Orphanet:
1852
Rare disease97 associated genes

Associated genes

+87 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.