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. The disease is Monarch Disease Ontology identifier MONDO_0009213 (Fanconi anemia complementation group C). Also known as: FA3, FACC, FANCC, Fanconi Anemia, complementation group type C, Fanconi anaemia complementation group type C, Fanconi anemia complementation group type C, Fanconi pancytopenia type 3.