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Fanconi anemia complementation group O
MONDO:0013248Any Fanconi anemia in which the cause of the disease is a mutation in the RAD51C gene.
Also known as: FANCO, Fanconi Anemia, complementation group type O, Fanconi anaemia caused by mutation in RAD51C, Fanconi anaemia caused by mutation in Rad51C, Fanconi anaemia complementation group type O, Fanconi anemia caused by mutation in RAD51C, Fanconi anemia caused by mutation in Rad51C, Fanconi anemia complementation group type O
12 clinical trials for this condition and its sub-types, 0 tagged with Fanconi anemia complementation group O itself.
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