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Hereditary myopathy with early respiratory failure


Classification level: Disorder
  • Synonym(s):
    • Edström Myopathy
    • HIBM-ERF
    • HMERF
    • Hereditary inclusion body myopathy with early respiratory failure
    • MFM-titinopathy
    • Myofibrillar myopathy with early respiratory failure
    • Myofibrillar myopathy-titinopathy
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal dominant 
  • Age of onset: Adult
  • ICD-10: G71.0
  • OMIM: 603689
  • UMLS: C1863599
  • MeSH: -
  • GARD: 12591
  • MedDRA: -

Detailed information


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