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A reference for what the literature reports. Not medical advice.

Disease

PRPF31-related retinopathy

MONDO:0800395Mondo

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Findings

No curated finding names PRPF31-related retinopathy yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Definition

An inherited retinopathy caused by variants in the PRPF31 gene.

Definition from the Mondo Disease Ontology (MONDO:0800395), read 2026-09-29. CC BY 4.0.

Genes

1 gene

Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.

PRPF31HGNC:15446
- Definitive · ClinGen · Autosomal dominant · 2022

Where it sits

A kind of: inherited retinal dystrophy
Narrower terms (1): retinitis pigmentosa 11