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Fanconi anemia complementation group F

MONDO:0011325

Fanconi 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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↑ Fanconi anemia (42)

Including sub-types (12) Tagged with Fanconi anemia complementation group F (0)

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