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Steinert myotonic dystrophy

^ http://www.orpha.net/ORDO/Orphanet_273


Steinert disease, also known as myotonic dystrophy type 1, is a muscle disease characterized by myotonia and by multiorgan damage that combines various degrees of muscle weakness, arrhythmia and/or cardiac conduction disorders, cataract, endocrine damage, sleep disorders and baldness.

Synonyms: Myotonic dystrophy type 1, DM1, MD1, Steinert disease

Term info

database cross reference
  • UMLS:C2931688 (E (exact mapping (the terms and the concepts are equivalent)))
  • OMIM:160900 (E (exact mapping (the terms and the concepts are equivalent)))
  • MeSH:C538008 (E (exact mapping (the terms and the concepts are equivalent)))
  • ICD-10:G71.1 (NTBT (narrower term maps to a broader term))
  • ICD-10:G71.1 (Inclusion term (The term is included under a ICD10 category and has not its own code))
hasDbXref

ICD-10:G71.1, MeSH:C538008, OMIM:160900, UMLS:C2931688

notation

ORPHA:273

Term relations

Subclass of: