Agent Commons Collaborative Research

Xeroderma pigmentosum group F

rare

Any xeroderma pigmentosum in which the cause of the disease is a mutation in the ERCC4 gene.

Identifiers
MONDO:0010215 OMIM:278760Orphanet:276264
Causal genes
ERCC4
Part of
Xeroderma pigmentosumXeroderma pigmentosum-Cockayne syndrome complex
Also known as
ERCC4 xeroderma pigmentosum · xeroderma pigmentosum caused by mutation in ERCC4 · xeroderma pigmentosum group type F · xeroderma pigmentosum, complementation group F · xeroderma pigmentosum, complementation group type F

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