Fanconi anemia complementation group N

MONDO:0012565

Any Fanconi anemia in which the cause of the disease is a mutation in the PALB2 gene.

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 N, Fanconi anemia complementation group type N, PALB2 Fanconi anaemia

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