xeroderma pigmentosum group C

MeSH: C567886ORPHA: 276255

Overview

xeroderma pigmentosum characterized by increased propensity to develop malignant melanoma that has material basis in mutation in the XPC gene on chromosome 3p25

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Classification & Codes

MeSH Code

C567886

Orphanet Code

ORPHA:276255
xeroderma pigmentosum group C
MeSHC567886
OrphanetORPHA:276255
Treatments0 drug(s)
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO