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Disease Ontology Browser
xeroderma pigmentosum group G (DOID:0110849)
Alliance: disease page
Synonyms: xeroderma pigmentosum VII; XP7; XP group G; XPG
Alt IDs: OMIM:278780, ICD10CM:Q82.1
Definition: A xeroderma pigmentosum that has_material_basis_in homozygous or compound heterozygous mutation in the ERCC5 gene on chromosome 13q33.

Disease References using Mouse Models (2)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory