X-linked cone-rod dystrophy 2
MeSH: C564717ORPHA: 1871
Overview
cone-rod dystrophy that has material basis in variation in the chromosome region Xq27
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with X-linked cone-rod dystrophy 2, sourced from HPO and Orphanet clinical annotations.
Visual impairmentAbnormal electroretinogramColor vision defectPhotophobiaAbnormal retinal pigmentation
Classification & Codes
MeSH Code
C564717Orphanet Code
ORPHA:1871X-linked cone-rod dystrophy 2
| MeSH | C564717 |
| Orphanet | ORPHA:1871 |
| Treatments | 0 drug(s) |
| Symptoms on record | 5 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO