Neuromuscular disease caused by qualitative or quantitative defects of tropomyosin

Part of

Sub-types of Neuromuscular disease caused by qualitative or quantitative defects of tropomyosin

• TPM2-related myopathy 1 trial · 3 incl. sub-types
  2 sub-types

  • Central core myopathy 2 trials
  • Congenital myopathy 23 0 trials
• Childhood-onset nemaline myopathy 1 trial · 2 incl. sub-types
  6 sub-types

  • Nemaline myopathy 6 1 trial
  • Congenital myopathy 23 0 trials
  • Congenital myopathy 2a, typical, autosomal dominant 0 trials
  • Congenital myopathy 4B, autosomal recessive 0 trials
  • Nemaline myopathy 2 0 trials
  • Nemaline myopathy 9 0 trials
• TPM3-related myopathy 1 trial
  3 sub-types

  • Cap myopathy 0 trials
  • Congenital myopathy 4A, autosomal dominant 0 trials
  • Congenital myopathy 4B, autosomal recessive 0 trials
• Intermediate nemaline myopathy 0 trials
  4 sub-types

  • Congenital myopathy 2a, typical, autosomal dominant 0 trials
  • Congenital myopathy 4B, autosomal recessive 0 trials
  • Nemaline myopathy 2 0 trials
  • Nemaline myopathy 9 0 trials
• Typical nemaline myopathy 0 trials
  6 sub-types

  • Congenital myopathy 23 0 trials
  • Congenital myopathy 2a, typical, autosomal dominant 0 trials
  • Nemaline myopathy 10 0 trials
  • Nemaline myopathy 2 0 trials
  • Nemaline myopathy 7 0 trials
  • Nemaline myopathy 9 0 trials