retinitis pigmentosa 9
MONDO:0008378Mondo
Findings
No curated finding names retinitis pigmentosa 9 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any retinitis pigmentosa in which the cause of the disease is a mutation in the RP9 gene.
Definition from the Mondo Disease Ontology (MONDO:0008378), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal dominant inheritance
HPO, annotations 2026-09-02
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.
- RP9HGNC:10288
- Strong · G2P · Autosomal dominant · 2017
- Limited · ClinGen · Autosomal dominant · 2025
- Limited · Labcorp Genetics (formerly Invitae) · Unknown · 2020
- Limited · PanelApp Australia · Autosomal dominant · 2025
Where it sits
- A kind of
Other names
4 names
Resolves to: retinitis pigmentosa 9
- Also called
- retinitis pigmentosa caused by mutation in RP9retinitis pigmentosa type 9RP9RP9 retinitis pigmentosa