X-linked cone-rod dystrophy 1
MONDO:0010566Mondo
Findings
No curated finding names X-linked cone-rod dystrophy 1 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- X-linked inheritance
- Onset and course
- Young adult onset
HPO, annotations 2026-09-02
Features
9 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.
- Color vision defectHPOHP:0000551
- Hypoautofluorescent macular lesionHPOHP:0030632
- MyopiaHPOHP:0000545
- NyctalopiaHPOHP:0000662
- PhotophobiaHPOHP:0000613
- Reduced visual acuityHPOHP:0007663
- Male
- Retinal pigment epithelial atrophyHPOHP:0007722
- Retinal pigment epithelial mottlingHPOHP:0007814
- Visual impairmentHPOHP:0000505
- Male
Where it sits
Other names
4 names
Resolves to: X-linked cone-rod dystrophy 1
- Also called
- cone-rod dystrophy, X-linked, 1, X-linked recessivecone-rod dystrophy, X-linked, type 1CORDX1X-linked cone-rod dystrophy type 1