Any Fanconi anemia in which the cause of the disease is a mutation in the PALB2 gene. The disease is Fanconi anemia complementation group N (Monarch Disease Ontology term MONDO_0012565). Also known as: FANCN, Fanconi Anemia, complementation group type N, Fanconi anaemia caused by mutation in PALB2, Fanconi anaemia complementation group type N, Fanconi anemia caused by mutation in PALB2, Fanconi anemia complementation group type N, PALB2 Fanconi anaemia, PALB2 Fanconi anemia.