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Disease Ontology Browser
xeroderma pigmentosum group A (DOID:0110843)
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 (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
09/19/2017
MGI 6.10
The Jackson Laboratory