MYO7A and autosomal dominant nonsyndromic hearing loss: Thus, MYO7A pathogenic variants can cause both syndromic and NSHL, including autosomal dominant nonsyndromic hearing loss (ADNSHL, DFNA11), autosomal recessive nonsyndromic hearing loss (ARNSHL, DFNB2), and syndromic deaf‐blindness (Usher Type 1B, USH1B).11, 12, 13