Xeroderma pigmentosum, complementation group b Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Xeroderma pigmentosum complementation group B (XPB) is an extremely rare subtype of xeroderma pigmentosum (XP; see this term), a rare photodermatosis predisposing to skin cancers. (Orphanet Rare Disease Ontology, Orphanet_276252)
External Link http://www.omim.org/entry/610651
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1 genes associated with the Xeroderma pigmentosum, complementation group b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
ERCC3 excision repair cross-complementation group 3