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Disease Ontology Browser
Fanconi anemia complementation group N (DOID:0111094)
Alliance: disease page
Synonyms: FANCN
Alt IDs: OMIM:610832
Definition: A Fanconi anemia that has_material_basis_in compound heterozygous mutation in the PALB2 gene on chromosome 16p12.


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
05/15/2018
MGI 6.12
The Jackson Laboratory