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Juvenile-onset Steinert myotonic dystrophy

ORPHA:589827

Classification level: Subtype of disorder
  • Synonym(s):
    • Juvenile-onset Steinert disease
    • Juvenile-onset myotonic dystrophy type 1
  • Prevalence: Unknown
  • Inheritance: Autosomal dominant 
  • Age of onset: Childhood
  • ICD-10: G71.1
  • ICD-11: 8C71.0
  • OMIM: 160900
  • UMLS: C5680306
  • MeSH: -
  • GARD: -
  • MedDRA: -

Summary

This disease is described under Steinert myotonic dystrophy

Detailed information

General public

Guidelines

Clinical Outcome Assessment (COA)

  • Patient-Centered Outcome Measures (PCOMs)
  • English (2023) - PROQOLIDTM

Genetic Testing

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

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.