has characteristic has characteristic Autosomal dominant inheritance autosomal dominant disease congenital structural myopathy autosomal dominant centronuclear myopathy https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/5906 https://github.com/monarch-initiative/mondo/issues/6239 https://rarediseases.info.nih.gov/diseases/12719/autosomal-dominant-centronuclear-myopathy https://www.malacards.org/card/myopathy_centronuclear_1 CNM3 myopathy, centronuclear, type 3 GARD:0012719 myotubular myopathy, autosomal dominant SCTID:716696006 centronuclear myopathy 1 centronuclear myopathy, autosomal dominant autosomal dominant centronuclear myopathy MEDGEN:1645741 CNM1 myopathy, centronuclear, type 1 An inherited neuromuscular disorder defined by numerous centrally placed nuclei on muscle biopsy and clinical features of a congenital myopathy. DOID:0111223 myopathy, centronuclear, autosomal dominant NCIT:C126689 autosomal dominant centronuclear myopathy caused by mutation in MYF6 centronuclear myopathy, autosomal, modifier of OMIM:160150 DOID:0111217 myopathy, centronuclear, 3 MONDO:0008048 myopathy, centronuclear, 1 DNM2-related centronuclear myopathy AD-CNM UMLS:C4551952 OMIM:614408 Orphanet:169189 centronuclear myopathy