Mutations in MYO7A, USH1C, CDH23, PCDH15, DFNB31, and CIB2 can also cause nonsyndromic hearing loss (NSHL) and mutations in USH2A and CLRN1 give rise to isolated autosomal recessive RP (see retinal and hearing impairment genetic mutation database, which includes USHbases and other NSHL genes: https://grenada.lumc.nl/LOVD2/Usher_montpellier/). The gene discussed is WHRN; the disease is nodular sclerosis classical Hodgkin lymphoma.