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Echinobase
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,

Echinobase Genes : fancc


OMIM:
MIM:227645 - fanconi anemia, complementation group c; fancc

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

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