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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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
07/31/2018
MGI 6.12
The Jackson Laboratory