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Fanconi anemia complementation group J

MONDO:0012187

Fanconi anemia caused by mutations in the BRIP1 gene, encoding Fanconi anemia group J protein.

Also known as: FANCJ, Fanconi Anemia, complementation group type J, Fanconi anaemia complementation group type J, Fanconi anemia complementation group J, Fanconi anemia complementation group type J, Fanconi anemia, complementation group J

10 clinical trials for this condition and its sub-types.

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Broader categories

Disease (680) Anemia (233) Metabolic disease (233) Musculoskeletal system disorder (207) Hereditary disease (176) Hematologic disorder (170) Immune system disorder (148) Aplastic anemia (106) Inborn errors of metabolism (45) Fanconi anemia (28)

Trials to join now! 4 Not yet recruiting 1 Not yet finished but already full! 2 Completed 3

Could a painless light sensor replace the needle for anemia screening?

Diagnosis Not yet recruiting

This 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