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Disease Ontology Browser
xeroderma pigmentosum (DOID:0050427)
Alliance: disease page
Alt IDs: ICD10CM:Q82.1, MESH:D014983, NCI:C3452, ORDO:910, UMLS_CUI:C0043346
Definition: An autosomal recessive disease that is characterized by a deficiency in the ability to repair ultraviolet damage that has_material_basis_in autosomal recessive inheritance of DNA repair.

Disease References using Mouse Models (15)

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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last database update
02/18/2020
MGI 6.14
The Jackson Laboratory