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Summary Literature (1)
DOID:0111095 - Fanconi anemia complementation group A


Disease Ontology Definition:A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the FANCA gene on chromosome 16q24.

Synonyms: FANCA

Referenced OMIM:
OMIM:227650 - FANCONI ANEMIA, COMPLEMENTATION GROUP A; FANCA

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : fancm, fanca

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): Fanconi anemia (is_a)


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