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Facioscapulohumeral dystrophy

^ http://www.orpha.net/ORDO/Orphanet_269


Facioscapulohumeral muscular dystrophy (FSHD) is characterized by progressive muscle weakness with focal involvement of the facial, shoulder and limb muscles.

Synonyms: Landouzy-Dejerine myopathy, Facioscapulohumeral muscular dystrophy, Facioscapulohumeral myopathy, FSH dystrophy, FSHD

Term info

database cross reference
  • OMIM:158901 (BTNT (broader term maps to a narrower term))
  • OMIM:158900 (BTNT (broader term maps to a narrower term))
  • ICD-10:G71.0 (Inclusion term (The term is included under a ICD10 category and has not its own code))
  • OMIM:600416 (BTNT (broader term maps to a narrower term))
  • MedDRA:10064087 (E (exact mapping (the terms and the concepts are equivalent)))
  • UMLS:C0238288 (E (exact mapping (the terms and the concepts are equivalent)))
  • ICD-10:G71.0 (NTBT (narrower term maps to a broader term))
hasDbXref

ICD-10:G71.0, MedDRA:10064087, OMIM:158900, OMIM:600416, UMLS:C0238288, OMIM:158901

notation

ORPHA:269