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

Echinobase Genes :


MIM:
MIM:278740 - xeroderma pigmentosum, complementation 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)