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Fanconi anemia complementation group C

MONDO:0009213

Fanconi anemia caused by mutations of the FANCC gene. This gene provides instructions for making a protein that delays the onset of apoptosis and promotes homologous recombination repair of damaged DNA.

Also known as: FA3, FACC, FANCC, Fanconi Anemia, complementation group type C, Fanconi anaemia complementation group type C, Fanconi anemia complementation group C, Fanconi anemia complementation group type C, Fanconi anemia, complementation group C

12 clinical trials for this condition and its sub-types, 0 tagged with Fanconi anemia complementation group C itself.

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