Fanconi anemia complementation group T
MONDO:0014638Any Fanconi anemia in which the cause of the disease is a mutation in the UBE2T gene.
Also known as: FANCT, Fanconi Anemia, complementation group type T, Fanconi anaemia caused by mutation in UBE2T, Fanconi anaemia complementation group type T, Fanconi anemia caused by mutation in UBE2T, Fanconi anemia complementation group type T, UBE2T Fanconi anaemia, UBE2T Fanconi anemia
12 clinical trials for this condition and its sub-types, 0 tagged with Fanconi anemia complementation group T itself.
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