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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: XP group B, XPB, XPBC,
Echinobase Genes :
MIM:610651 - xeroderma pigmentosum, complementation group b; xpb |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
xeroderma pigmentosum (is_a)