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Summary Literature (0)
DOID:0111084 - Fanconi anemia complementation group E

Disease Ontology Definition:A Fanconi anemia that has_material_basis_in homozygous mutation in the FANCE gene on chromosome 6p22-p21.

Synonyms: FACE, FANCE

Xenbase Genes : fance

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010953 - Fanconi anemia complementation group E

MIM:
MIM:600901 - FANCONI ANEMIA, COMPLEMENTATION GROUP E; FANCE

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), Fanconi anemia (is_a)