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Summary Literature (0)
DOID:0111087 - Fanconi anemia complementation group C

Disease Ontology Definition:A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the FANCC gene on chromosome 9q22.

Synonyms: FA3, FACC, FANCC, Fanconi pancytopenia type 3

Xenbase Genes : fancc

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009213 - Fanconi anemia complementation group C


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), Fanconi anemia (is_a)