Fanconi anemia complementation group O

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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

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: rad51c

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013248 - Fanconi anemia complementation group O

MONDO:0013248 - Fanconi anemia complementation group O

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive disease (is_a), Fanconi anemia (is_a)