Among these genes, DFNA6 (DFN = deafness, A = dominant), DFNA14, and DFNA38 are associated with low-frequency non-syndromic hearing loss (LF-NSHL), which is caused by variants of the Wolfram syndrome 1 (WFS1) gene [5,6]. Here, WFS1 is linked to nodular sclerosis classical Hodgkin lymphoma.