Fanconi anemia complementation group P (MONDO_0013499, a Monarch Disease Ontology entry) is any Fanconi anemia in which the cause of the disease is a mutation in the SLX4 gene. Also known as: FANCP, Fanconi Anemia, complementation group type P, Fanconi anaemia caused by mutation in SLX4, Fanconi anaemia caused by mutation in Slx4, Fanconi anaemia complementation group type P, Fanconi anemia caused by mutation in SLX4, Fanconi anemia caused by mutation in Slx4, Fanconi anemia complementation group type P.