autosomal dominant nonsyndromic hearing loss 49 https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/551 https://www.malacards.org/card/deafness_autosomal_dominant_49 MEDGEN:331222 An autosomal dominant nonsyndromic deafness that is characterized by moderate loss for low and mid frequencies and mild loss for high frequencies and has material basis in variation in the chromosome region 1q21-q23. OMIM:608372 autosomal dominant nonsyndromic deafness type 49 UMLS:C1842136 DOID:0110572 autosomal dominant nonsyndromic deafness 49 MONDO:0012023 autosomal dominant deafness 49 GARD:0018122 deafness, autosomal dominant 49 MESH:C564250 DFNA49 autosomal dominant nonsyndromic hearing loss