xeroderma pigmentosum group B

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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

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: ercc3

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012531 - xeroderma pigmentosum group B

MONDO:0012531 - xeroderma pigmentosum group B

MIM:

MIM:610651 - XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B; XPB

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)