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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
110 clinical trials for this condition and its sub-types.
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Can extra care after transplant help older patients live better?
Disease control TerminatedThis study tested two extra care programs—supportive palliative care and clinical management of other health issues—for older or frail patients who had a donor stem cell transplant. The goal was to see if these programs could improve quality of life and survival compared to stand…
Phase: PHASE2, PHASE3 • Sponsor: Fred Hutchinson Cancer Center • Aim: Disease control
Last updated Jun 27, 2026 08:10 UTC
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Scientists gather leftover surgical tissue to unlock secrets of bone disease
Knowledge-focused TerminatedThis study collected bone, cartilage, skin, and fat tissue from 50 patients undergoing surgery at Children's National Medical Center. The goal was to grow cells from these tissues in the lab and analyze them to better understand bone and connective tissue diseases. The study was …
Sponsor: National Institute of Dental and Craniofacial Research (NIDCR) • Aim: Knowledge-focused
Last updated Jun 27, 2026 07:52 UTC