Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

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

14 clinical trials for this condition and its sub-types, 2 tagged with Fanconi anemia complementation group N itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →
Sort by