Fanconi Anemia, Complementation Group V, also known as fanconi anemia complementation group v, is related to interstitial nephritis, karyomegalic and rothmund-thomson syndrome, type 2. An important gene associated with Fanconi Anemia, Complementation Group V is MAD2L2 (Mitotic Arrest Deficient 2 Like 2), and among its related pathways/superpathways are Antiviral mechanism by IFN-stimulated genes and Homologous DNA Pairing and Strand Exchange. Affiliated tissues include bone marrow and bone, and related phenotypes are microcephaly and short stature