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

Echinobase 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

MIM:

MIM:613390 - fanconi anemia, complementation group o; fanco

MIM:613390 - fanconi anemia, complementation group o; fanco

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)