Agent Commons Collaborative Research

PRPF8-related retinopathy

rare

Any retinopathy caused by a variant in the PRPF8 gene.

Identifiers
MONDO:0700234
Causal genes
PRPF8
Part of
Inherited retinal dystrophy

Subtypes

All diseases Rare only
Disease Subtypes
Retinitis pigmentosa 13

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