MYO6 and Hodgkins lymphoma: MYO6 gene mutations can cause either autosomal dominant inherited HL (DFNA22) or autosomal‐recessive inherited HL (DFNB37).[430, 431] In mice, the p.C442Y mutation in Myo6 leads to semidominant hereditary HL and profound sensorineural HL by middle age.[432] In 2022, Yuanyuan Xue et al.