Fanconi anemia complementation group G Disease Ontology Browser

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Disease Ontology Browser

Fanconi anemia complementation group G (DOID:0111086)
Alliance: disease page
Synonyms: FANCG
Alt IDs: OMIM:614082
Definition: A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the XRCC9 gene on chromosome 9p13.

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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