Variants in the MYO7A gene might be responsible for autosomal dominant (OMIM #601317, DFNA11) and autosomal recessive deafness (OMIM #600060, DFNB2), as well as Usher syndrome (OMIM #276900, USH1), characterized by HL and retinopathy. This evidence concerns the gene MYO7A and Hodgkins lymphoma.