retinitis pigmentosa 7
MONDO:0011974Mondo
Findings
No curated finding names retinitis pigmentosa 7 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
HPO, annotations 2026-09-02
Features
3 features
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.
- Attenuation of retinal blood vesselsHPOHP:0007843
- NyctalopiaHPOHP:0000662
- Adult onset
- Pigmentary retinopathyHPOHP:0000580
Genes
2 genes
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.
- PRPH2HGNC:9942
- Definitive · Ambry Genetics · Semidominant · 2018
- Definitive · G2P · Autosomal recessive · 2017
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2023
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2023
- ROM1HGNC:10254
- Strong · PanelApp Australia · Autosomal dominant · 2025
- Limited · Labcorp Genetics (formerly Invitae) · Unknown · 2021
Where it sits
Other names
3 names
Resolves to: retinitis pigmentosa 7
- Also called
- retinitis pigmentosa type 7RP 7RP7