Fanconi anemia complementation group V

Any Fanconi anemia in which the cause of the disease is a mutation in the MAD2L2 gene.

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

12 clinical trials for this condition and its sub-types, 0 tagged with Fanconi anemia complementation group V itself.