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Summary Literature (0)
DOID:0111081 - Fanconi anemia complementation group T

Disease Ontology Definition:A Fanconi anemia that has_material_basis_in compound heterozygous mutation in the UBE2T gene on chromosome 1q32.

Synonyms: FANCT

Xenbase Genes : ube2t

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014638 - Fanconi anemia complementation group T


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)