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Disease Ontology Browser
xeroderma pigmentosum group D (DOID:0110845)
Alliance: disease page
Synonyms: xeroderma pigmentosum IV; xeroderma pigmentosum VIII; XP4; XP8; XP group D; XP group H; XPD; XPDC; XPH
Alt IDs: OMIM:278730, ICD10CM:Q82.1
Definition: A xeroderma pigmentosum that has_material_basis_in homozygous or compound heterozygous mutation in the excision repair gene ERCC2 on chromosome 19q13.

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)
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11/12/2024
MGI 6.24 		The Jackson Laboratory