disease has basis in dysfunction of FANCL Fanconi anemia complementation group L Any Fanconi anemia in which the cause of the disease is a mutation in the FANCL gene. DOID:0111082 FANCL FANCL Fanconi anemia Fanconi Anemia, complementation Group 50 Fanconi Anemia, complementation group type 50 Fanconi anemia caused by mutation in FANCL Fanconi anemia complementation group type L Fanconi anemia, complementation group L MONDO:0013566 OMIM:614083 Fanconi anemia