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Summary Literature (0)
DOID:0111086 - Fanconi anemia complementation group G

Disease Ontology Definition:A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the XRCC9 gene on chromosome 9p13.

Synonyms: FANCG

Xenbase Genes : fancg

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013565 - Fanconi anemia complementation group G

MIM:
MIM:614082 - FANCONI ANEMIA, COMPLEMENTATION GROUP G; FANCG

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

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