| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| 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://ctdbase.org/detail.go?type=disease&acc=MESH:C562590 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Xeroderma Pigmentosum, Complementation Group B from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| ERCC3 | excision repair cross-complementation group 3 | 2.88009 |
