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Summary Literature (0)
DOID:0111088 - Fanconi anemia complementation group F

Disease Ontology Definition:A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the FANCF gene on chromosome 11p15.

Synonyms: FANCF

Xenbase Genes : fancf

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011325 - Fanconi anemia complementation group F

MIM:
MIM:603467 - FANCONI ANEMIA, COMPLEMENTATION GROUP F; FANCF

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)