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Echinobase
Summary Literature (0)
DOID:0110850 - xeroderma pigmentosum group B

Disease Ontology Definition:A xeroderma pigmentosum characterized by that has_material_basis_in mutation in the ERCC3 gene on chromosome 2q14.

Synonyms: XPB, XPBC, XP group B

Echinobase Genes :


MIM:
MIM:610651 - xeroderma pigmentosum, complementation group b; xpb

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): xeroderma pigmentosum (is_a)