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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
Echinobase Genes

OMIM:603467 - fanconi anemia, complementation group f; fancf |
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)