has material basis in germline mutation in MIR96 autosomal dominant nonsyndromic hearing loss 50 https://github.com/monarch-initiative/mondo/issues/551 https://www.malacards.org/card/deafness_autosomal_dominant_50 autosomal dominant deafness 50 DOID:0110576 deafness, autosomal dominant type 50 deafness, autosomal dominant 50 autosomal dominant nonsyndromic deafness type 50 GARD:0018132 MONDO:0013114 MEDGEN:854780 OMIM:613074 An autosomal dominant nonsyndromic deafness that is characterized postlingual onset in the second decade of life with flat progressive hearing loss and has material basis in mutation in the MIRN96 gene on chromosome 7q32. UMLS:C3888123 DFNA50 autosomal dominant nonsyndromic deafness 50 autosomal dominant nonsyndromic hearing loss