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Myotonic dystrophy

ORPHA:206647

Classification level: Group of disorders
  • Synonym(s): -
  • Prevalence: 1-9 / 100 000
  • Inheritance: -
  • Age of onset: -
  • ICD-10: G71.1
  • ICD-11: 8C71.0
  • OMIM: -
  • UMLS: C0027126
  • MeSH: D009223
  • GARD: 10419
  • MedDRA: 10068871

Summary

This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.

Detailed information

General public

Guidelines

Clinical Outcome Assessment (COA)

  • Patient-Centered Outcome Measures (PCOMs)
  • English (2023) - PROQOLIDTM
ERN produced/endorsed by ERN(s)   FSMR produced/endorsed by FSMR(s)

Additional information

Further information on this disease

Patient-centred resources for this disease

Research activities on this disease

Specialised Social Services

Newborn screening

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.