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Fanconi anemia complementation group V
MONDO:0014985Any Fanconi anemia in which the cause of the disease is a mutation in the MAD2L2 gene.
Also known as: FANCV, Fanconi Anemia, complementation group V, Fanconi Anemia, complementation group type V, Fanconi anaemia caused by mutation in MAD2L2, Fanconi anaemia complementation group type V, Fanconi anemia caused by mutation in MAD2L2, Fanconi anemia complementation group type V, MAD2L2 Fanconi anaemia
12 clinical trials for this condition and its sub-types, 0 tagged with Fanconi anemia complementation group V itself.
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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
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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