xeroderma pigmentosum group D
MeSH: C562591ORPHA: 276258
Overview
xeroderma pigmentosum that has material basis in homozygous or compound heterozygous mutation in the excision repair gene ERCC2 on chromosome 19q13
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
C562591Orphanet Code
ORPHA:276258xeroderma pigmentosum group D
| MeSH | C562591 |
| Orphanet | ORPHA:276258 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO