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Disease Ontology Browser
xeroderma pigmentosum group B (DOID:0110850)
Alliance: disease page
Synonyms: XP group B; XPB; XPBC
Alt IDs: OMIM:610651, ICD10CM:Q82.1
Definition: A xeroderma pigmentosum characterized by that has_material_basis_in mutation in the ERCC3 gene on chromosome 2q14.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
12/05/2017
MGI 6.11
The Jackson Laboratory