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Echinobase
Summary Literature (0)
DOID:0111096 - Fanconi anemia complementation group O


Disease Ontology Definition:A Fanconi anemia that has_material_basis_in homozygous mutation in the RAD51C gene on chromosome 17q21-q24.

Synonyms: FANCO,

Echinobase Genes : rad51c


OMIM:
MIM:613390 - fanconi anemia, complementation group o; fanco

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)