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Summary Literature (0)
DOID:0111094 - Fanconi anemia complementation group N


Disease Ontology Definition:A Fanconi anemia that has_material_basis_in compound heterozygous mutation in the PALB2 gene on chromosome 16p12.

Synonyms: FANCN

Xenbase Genes : palb2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012565 - Fanconi anemia complementation group N

OMIM:
OMIM:610832 - FANCONI ANEMIA, COMPLEMENTATION GROUP N; FANCN

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): Fanconi anemia (is_a)