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.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Part of
-
Smartwatch signals may flag anemia, no needle needed
Diagnosis Not yet recruitingAnemia often goes unnoticed because diagnosis requires a blood draw. This study tests whether a wrist-worn smartwatch can identify people likely to have anemia by tracking blood flow, heart rate, oxygen, and movement. About 400 adults, with and without anemia, will wear the watch…
Sponsor: Peking Union Medical College Hospital • Aim: Diagnosis
Last updated Sep 03, 2026 00:00 UTC
-
Could a painless light sensor replace the needle for anemia screening?
Diagnosis Not yet recruitingThis study tests whether a non-invasive device that uses light to measure hemoglobin through the skin can accurately detect anemia. Researchers will compare its readings with standard blood tests in 150 adults in Jakarta. If the device proves reliable, it could offer a quick, pai…
Sponsor: Tarumanagara University • Aim: Diagnosis
Last updated Jul 17, 2026 00:00 UTC