Fanconi anemia complementation group N Disease Ontology Browser

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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 Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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