Any Fanconi anemia in which the cause of the disease is a mutation in the MAD2L2 gene. The disease is Fanconi anemia complementation group V (MONDO_0014985, a Monarch Disease Ontology id). Also known as: FANCV, Fanconi Anemia, complementation group V, Fanconi Anemia, complementation group type V, Fanconi anaemia caused by mutation in MAD2L2, Fanconi anaemia complementation group type V, Fanconi anemia caused by mutation in MAD2L2, Fanconi anemia complementation group type V, MAD2L2 Fanconi anaemia.