xeroderma pigmentosum group B
ORPHA: 276252
Overview
xeroderma pigmentosum characterized by that has material basis in mutation in the ERCC3 gene on chromosome 2q14
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
Orphanet Code
ORPHA:276252xeroderma pigmentosum group B
| Orphanet | ORPHA:276252 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO