Fanconi anemia complementation group O Disease Ontology Browser

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Disease Ontology Browser

Fanconi anemia complementation group O (DOID:0111096)
Alliance: disease page
Synonyms: FANCO
Alt IDs: OMIM:613390
Definition: A Fanconi anemia that has_material_basis_in homozygous mutation in the RAD51C gene on chromosome 17q21-q24.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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