(Q29982088)

English

rigid spine syndrome

human disease

  • severe classic form multicore myopathy
  • severe classic form minicore myopathy
  • Eichsfeld type congenital muscular dystrophy
  • classic multiminicore myopathy
  • desmin-related myopathy with Mallory body-like inclusions
  • RSMD1
  • SEPN1-related myopathy
  • congenital merosin-positive muscular dystrophy with early spine rigidity
  • CMD with spinal rigidity
  • MDRS1
  • desmin-related myopathy with Mallory bodies
  • classic MmD
  • severe classic form multiminicore disease
  • classic multiminicore disease
  • RSS
  • rigid spine muscular dystrophy 1
  • early-onset desmin-related myopathy

Statements

Identifiers

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