Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
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

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)