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Fanconi anemia complementation group B
MONDO:0010351Fanconi anemia caused by mutations of the FANCB gene. This gene encodes the protein for complementation group B.
Also known as: FA2, FACB, FANCB, Fanconi Anemia, complementation group type B, Fanconi anaemia complementation group type B, Fanconi anemia complementation group B, Fanconi anemia complementation group type B, Fanconi anemia, complementation group B, X-linked recessive
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