FANCM, FA complementation group M, 57697

N. diseases: 147; N. variants: 11
Disease: Burkitt Lymphoma ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0006413
Disease: Burkitt Lymphoma
Burkitt Lymphoma 		0.010 GeneticVariation disease BEFREE Finally, we also identified an inherited heterozygous truncating c.5791CT FANCM mutation that may contribute to the unusual recurrence of BL. 30779244 2019