Fanconi anemia complementation group F
MONDO:0011325Fanconi anemia caused by mutations of the FANCF gene. This gene encodes a polypeptide with homology to the prokaryotic RNA-binding protein ROM.
Also known as: FANCF, Fanconi Anemia, complementation group type F, Fanconi anaemia complementation group type F, Fanconi anemia complementation group F, Fanconi anemia complementation group type F, Fanconi anemia, complementation group F
12 clinical trials for this condition and its sub-types, 0 tagged with Fanconi anemia complementation group F itself.
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