Human genes for Fanconi anemia complementation group C
Fanconi anemia complementation group C [DOID:0111087]
A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the FANCC gene on chromosome 9q22.
Synonyms: Fanconi anemia complementation group C, DOID:0111087, Fanconi anemia complementation group Cs, FA3, FACC ...