nemaline myopathy (Q1507379)

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congenital structural myopathy characterized by generally non-progressive muscle weakness of varying severity
  • nemaline rod myopathy
  • rod myopathy
  • nemaline body disease
  • NEM
  • NM
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Language Label Description Also known as
English
nemaline myopathy
congenital structural myopathy characterized by generally non-progressive muscle weakness of varying severity
  • nemaline rod myopathy
  • rod myopathy
  • nemaline body disease
  • NEM
  • NM

Statements

Identifiers

nemalinová myopatie
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8C72.00
Nemaline myopathy
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