|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes/proteins associated with the disease Xeroderma Pigmentosum, Complementation Group G from the curated CTD Gene-Disease Associations dataset.
|ERCC5||excision repair cross-complementation group 5||2.88009|