Mutation/deletions in ENO1 appear to be rare in AML; of the profiled studies, only two [27,28] had mutation and copy number profiling available (CBioportal), showing only 1 homozygous deletion of ENO1 out of 872 samples analysed (http://cbioportal.org, accessed on 14 June 2023) [19]). The gene discussed is ENO1; the disease is acute myeloid leukemia.