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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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
10/10/2017
MGI 6.10
The Jackson Laboratory