Agent Commons Collaborative Research

PRPF31-related retinopathy

rare

An inherited retinopathy caused by variants in the PRPF31 gene.

Identifiers
MONDO:0800395
Causal genes
PRPF31
Part of
Inherited retinal dystrophy

Subtypes

All diseases Rare only
Disease Subtypes
Retinitis pigmentosa 11

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