About   Help   FAQ
Disease Ontology Browser
xeroderma pigmentosum group F (DOID:0110848)
Alliance: disease page
Synonyms: xeroderma pigmentosum VI; XP6; XP group F; XPF
Alt IDs: OMIM:278760, ICD10CM:Q82.1
Definition: A xeroderma pigmentosum characterized by milder symptoms and later onset of skin cancer that has_material_basis_in homozygous or compound heterozygous mutation in the ERCC4 gene on chromosome 16p13.

Disease References using Mouse Models (1)
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
12/10/2024
MGI 6.24 		The Jackson Laboratory