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Disease Ontology Browser
xeroderma pigmentosum group A (DOID:0110843)
Alliance: disease page
Synonyms: xeroderma pigmentosum 1; xeroderma pigmentosum complementation group A; XP1; XP group A; XPA
Alt IDs: OMIM:278700, ICD10CM:Q82.1
Definition: A xeroderma pigmentosum characterized by involvement of the central and peripheral nervous systems in addition to cutaneous lesions that has_material_basis_in caused by homozygous or compound heterozygous mutation in the XPA gene on chromosome 9q22.

Disease References using Mouse Models (3)
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
04/09/2024
MGI 6.23 		The Jackson Laboratory