CUI Disease Vocabulary Name in Vocabulary Code
C0206157 Myopathies, Nemaline DO muscular dystrophy-dystroglycanopathy 0050588
C0206157 Myopathies, Nemaline DO megaconial type congenital muscular dystrophy 0110632
C0206157 Myopathies, Nemaline DO rigid spine muscular dystrophy 1 0110633
C0206157 Myopathies, Nemaline DO congenital muscular dystrophy 1B 0110634
C0206157 Myopathies, Nemaline DO muscular dystrophy-dystroglycanopathy type B5 0110635
C0206157 Myopathies, Nemaline DO muscular dystrophy-dystroglycanopathy type B6 0110637
C0206157 Myopathies, Nemaline DO congenital muscular dystrophy due to integrin alpha-7 deficiency 0110639
C0206157 Myopathies, Nemaline DO congenital muscular dystrophy due to LMNA mutation 0110640
C0206157 Myopathies, Nemaline DO nemaline myopathy 3191
C0206157 Myopathies, Nemaline DO central core myopathy 3529
C0206157 Myopathies, Nemaline ICD10CM Nemaline myopathy G71.2
C0206157 Myopathies, Nemaline ICD10CM Congenital myopathies G71.2
C0206157 Myopathies, Nemaline ICD10CM Multicore disease G71.2
C0206157 Myopathies, Nemaline ICD10CM Minicore disease G71.2
C0206157 Myopathies, Nemaline ICD10CM Fiber-type disproportion G71.2
C0206157 Myopathies, Nemaline ICD10CM Central core disease G71.2
C0206157 Myopathies, Nemaline ICD10CM Myotubular (centronuclear) myopathy G71.2
C0206157 Myopathies, Nemaline MONDO megaconial type congenital muscular dystrophy 0011246
C0206157 Myopathies, Nemaline MONDO congenital muscular dystrophy 1B 0011486
C0206157 Myopathies, Nemaline MONDO muscular dystrophy-dystroglycanopathy type B5 0011688
C0206157 Myopathies, Nemaline MONDO muscular dystrophy-dystroglycanopathy type B6 0012138
C0206157 Myopathies, Nemaline MONDO congenital muscular dystrophy due to integrin alpha-7 deficiency 0013177
C0206157 Myopathies, Nemaline MONDO congenital muscular dystrophy due to LMNA mutation 0013178
C0206157 Myopathies, Nemaline MONDO muscular dystrophy-dystroglycanopathy 0018276
C0206157 Myopathies, Nemaline MONDO nemaline myopathy 0018958