A rare neuromuscular disease characterized by progressive muscle weakness with focal involvement of the facial, shoulder and limb muscles.

Synonyms:

Facioscapulohumeral myopathy

FSH dystrophy

FSHD

Landouzy-Dejerine myopathy

Landouzy-Dejerine dystrophy

Facioscapulohumeral muscular dystrophy

This is just here as a test because I lose it

Term information

database cross reference
expertlink
  • https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=269
hasDbXref
  • OMIM:600416
  • OMIM:158900
  • OMIM:158901
  • ICD-11:8C70.3
  • ICD-10:G71.0
  • UMLS:C0238288
  • MedDRA:10064087
has age of onset
  • http://www.orpha.net/ORDO/Orphanet_409950
has annual incidence range
  • http://www.orpha.net/ORDO/Orphanet_409976
has inheritance
  • http://www.orpha.net/ORDO/Orphanet_409929
has point prevalence average value
  • 12.0
  • 3.95
  • 2.0
  • 4.5
  • 4.4
has point prevalence range
  • http://www.orpha.net/ORDO/Orphanet_409975
  • http://www.orpha.net/ORDO/Orphanet_409977
notation
  • ORPHA:269
part of
  • http://www.orpha.net/ORDO/Orphanet_206644
present in
  • http://www.orpha.net/ORDO/Orphanet_410100
  • http://www.orpha.net/ORDO/Orphanet_410102
  • http://www.orpha.net/ORDO/Orphanet_409984
  • http://www.orpha.net/ORDO/Orphanet_410147
  • http://www.orpha.net/ORDO/Orphanet_410224