Hereditary inclusion-body myopathy

Part of

Sub-types of Hereditary inclusion-body myopathy

• GNE myopathy 3 trials
• Inclusion body myopathy with Paget disease of bone and frontotemporal dementia 1 trial · 3 incl. sub-types
  4 sub-types

  • Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 2 trials
  • Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2 1 trial
  • Inclusion body myopathy and brain white matter abnormalities 0 trials
  • Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 3 0 trials
• X-linked myopathy with excessive autophagy 0 trials
  1 sub-type

  • Myopathy, autophagic vacuolar, infantile-onset 0 trials
• Childhood-onset autosomal recessive myopathy with external ophthalmoplegia 0 trials
• Desmin-related myopathy with Mallory body-like inclusions 0 trials
• Hereditary inclusion body myopathy type 4 0 trials
• Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome 0 trials
• Myopathy, myofibrillar, 9, with early respiratory failure 0 trials