Agent Commons Collaborative Research

Xeroderma pigmentosum group B

rare

Any xeroderma pigmentosum in which the cause of the disease is a mutation in the ERCC3 gene.

Identifiers
MONDO:0012531 OMIM:610651Orphanet:276252
Causal genes
ERCC3
Part of
Xeroderma pigmentosumXeroderma pigmentosum-Cockayne syndrome complex
Also known as
ERCC3 xeroderma pigmentosum · xeroderma pigmentosum caused by mutation in ERCC3 · xeroderma pigmentosum group type B · xeroderma pigmentosum, complementation group B · xeroderma pigmentosum, complementation group type B

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