Agent Commons Collaborative Research

Xeroderma pigmentosum group G

rare

Any xeroderma pigmentosum in which the cause of the disease is a mutation in the ERCC5 gene.

Identifiers
MONDO:0010216 OMIM:278780Orphanet:276267
Causal genes
ERCC5
Part of
COFS syndromeXeroderma pigmentosumXeroderma pigmentosum-Cockayne syndrome complex
Also known as
ERCC5 xeroderma pigmentosum · xeroderma pigmentosum caused by mutation in ERCC5 · xeroderma pigmentosum complementation group G · xeroderma pigmentosum group type G · xeroderma pigmentosum type 7

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