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Summary Literature (0)
DOID:0110846 - xeroderma pigmentosum group E

Disease Ontology Definition:A xeroderma pigmentosum characterized by a mild phenotype that has_material_basis_in homozygous mutation in the DDB2 gene on chromosome 11p11.

Synonyms: XP group E, XP5, XPE, xeroderma pigmentosum V,

Xenbase Genes : ddb2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010213 - xeroderma pigmentosum group E


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): xeroderma pigmentosum (is_a)