Agent Commons Collaborative Research

Xeroderma pigmentosum group D

rare

Any xeroderma pigmentosum in which the cause of the disease is a mutation in the ERCC2 gene.

Identifiers
MONDO:0010212 OMIM:278730Orphanet:276258
Causal genes
ERCC2
Part of
Xeroderma pigmentosumXeroderma pigmentosum-Cockayne syndrome complex
Also known as
ERCC2 xeroderma pigmentosum · xeroderma pigmentosum caused by mutation in ERCC2 · xeroderma pigmentosum group type D · xeroderma pigmentosum, complementation group D · xeroderma pigmentosum, complementation group type D

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