retinitis pigmentosa 32
MONDO:0012363Mondo
Findings
No curated finding names retinitis pigmentosa 32 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A retinitis pigmentosa that has material basis in variation in the chromosome region 1p21.3-p13.3.
Definition from the Mondo Disease Ontology (MONDO:0012363), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal recessive inheritance
HPO, annotations 2026-09-02
Features
10 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
- Juvenile onset
- Optic disc pallorHPOHP:0000543
- PhotophobiaHPOHP:0000613
- Photoreceptor layer loss on macular OCTHPOHP:0030609
- Pigmentary retinopathyHPOHP:0000580
- Reduced visual acuityHPOHP:0007663
- Retinal degenerationHPOHP:0000546
- Spicular pigmentation of the retina
Where it sits
- A kind of
Other names
2 names
Resolves to: retinitis pigmentosa 32
- Also called
- retinitis pigmentosa type 32RP32