RHO-related retinopathy
MONDO:0700380Mondo
Findings
No curated finding names RHO-related retinopathy yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any retinopathy caused by a variant in the RHO gene, including cases diagnosed as congenital stationary night blindness autosomal dominant 1 or retinitis pigmentosa 4.
Definition from the Mondo Disease Ontology (MONDO:0700380), 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.
- RHOHGNC:10012
- Definitive · ClinGen · Semidominant · 2025
Where it sits
- A kind of