About   Help   FAQ
Disease Ontology Browser
xeroderma pigmentosum group E (DOID:0110846)
Alliance: disease page
Synonyms: xeroderma pigmentosum V; XP5; XP group E; XPE
Alt IDs: OMIM:278740, ICD10CM:Q82.1
Definition: A xeroderma pigmentosum characterized by a mild phenotype that has_material_basis_in homozygous mutation in the DDB2 gene on chromosome 11p11.

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory