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retinitis pigmentosa

MONDO:0019200

Also known as: retinitis pigmentosa, pericentral pigmentary retinopathy, Rod-cone dystrophy

MONDO:
MONDO:0019200
Orphanet:
791
Rare disease236 associated genes

Description

Retinitis pigmentosa (RP) is an inherited retinal dystrophy leading to progressive loss of the photoreceptors and retinal pigment epithelium and resulting in blindness usually after several decades.

Associated genes

+226 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.