CUI Disease Vocabulary Name in Vocabulary Code
C2875316 Myotubular (centronuclear) myopathy DO muscular dystrophy-dystroglycanopathy 0050588
C2875316 Myotubular (centronuclear) myopathy DO megaconial type congenital muscular dystrophy 0110632
C2875316 Myotubular (centronuclear) myopathy DO rigid spine muscular dystrophy 1 0110633
C2875316 Myotubular (centronuclear) myopathy DO congenital muscular dystrophy 1B 0110634
C2875316 Myotubular (centronuclear) myopathy DO muscular dystrophy-dystroglycanopathy type B5 0110635
C2875316 Myotubular (centronuclear) myopathy DO muscular dystrophy-dystroglycanopathy type B6 0110637
C2875316 Myotubular (centronuclear) myopathy DO congenital muscular dystrophy due to integrin alpha-7 deficiency 0110639
C2875316 Myotubular (centronuclear) myopathy DO congenital muscular dystrophy due to LMNA mutation 0110640
C2875316 Myotubular (centronuclear) myopathy DO nemaline myopathy 3191
C2875316 Myotubular (centronuclear) myopathy DO central core myopathy 3529
C2875316 Myotubular (centronuclear) myopathy ICD10CM Nemaline myopathy G71.2
C2875316 Myotubular (centronuclear) myopathy ICD10CM Congenital myopathies G71.2
C2875316 Myotubular (centronuclear) myopathy ICD10CM Multicore disease G71.2
C2875316 Myotubular (centronuclear) myopathy ICD10CM Minicore disease G71.2
C2875316 Myotubular (centronuclear) myopathy ICD10CM Fiber-type disproportion G71.2
C2875316 Myotubular (centronuclear) myopathy ICD10CM Central core disease G71.2
C2875316 Myotubular (centronuclear) myopathy ICD10CM Myotubular (centronuclear) myopathy G71.2
C2875316 Myotubular (centronuclear) myopathy MONDO megaconial type congenital muscular dystrophy 0011246
C2875316 Myotubular (centronuclear) myopathy MONDO congenital muscular dystrophy 1B 0011486
C2875316 Myotubular (centronuclear) myopathy MONDO muscular dystrophy-dystroglycanopathy type B5 0011688
C2875316 Myotubular (centronuclear) myopathy MONDO muscular dystrophy-dystroglycanopathy type B6 0012138
C2875316 Myotubular (centronuclear) myopathy MONDO congenital muscular dystrophy due to integrin alpha-7 deficiency 0013177
C2875316 Myotubular (centronuclear) myopathy MONDO congenital muscular dystrophy due to LMNA mutation 0013178
C2875316 Myotubular (centronuclear) myopathy MONDO muscular dystrophy-dystroglycanopathy 0018276