retinitis pigmentosa 55
MONDO:0013312Mondo
Findings
No curated finding names retinitis pigmentosa 55 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 ARL6 gene.
Definition from the Mondo Disease Ontology (MONDO:0013312), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal recessive inheritance
HPO, annotations 2026-09-02
Features
1 feature
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Rod-cone dystrophyHPOHP:0000510
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.
- ARL6HGNC:13210
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2019
- Strong · G2P · Autosomal recessive · 2024
Where it sits
Other names
4 names
Resolves to: retinitis pigmentosa 55
- Also called
- ARL6 retinitis pigmentosaretinitis pigmentosa caused by mutation in ARL6retinitis pigmentosa type 55RP55