Xeroderma Pigmentosum, Complementation Group G Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Xeroderma pigmentosum complementation group G (XPG) is an extremely rare subtype of xeroderma pigmentosum (XP; see this term), a rare photodermatosis predisposing to skin cancers. (Orphanet Rare Disease Ontology, Orphanet_276267)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C562593
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Genes

1 genes/proteins associated with the disease Xeroderma Pigmentosum, Complementation Group G from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
ERCC5 excision repair cross-complementation group 5 2.88009