Polymyositis (PM) is a rare idiopathic inflammatory myopathy characterized by symmetric proximal muscle weakness and elevated muscle enzymes. [ Orphanet:732 ]

This is just here as a test because I lose it

Term information

database cross reference
  • SCTID:31384009 (MONDO:equivalentTo)
  • UMLS:C0085655 (Orphanet:732)
  • MedDRA:10036102 (Orphanet:732)
  • ICD10:M33.2 (Orphanet:732)
  • ICD9:710.4 (i2s)
  • EFO:0003063 (MONDO:equivalentTo)
  • Wikipedia:Polymyositis (EFO:0003063)
  • COHD:80800 (MONDO:equivalentTo)
  • GARD:0007425 (shared-umls-xref)
  • Orphanet:732 (MONDO:equivalentTo)
  • MESH:D017285 (Orphanet:732)
  • NCIT:C26925 (MONDO:equivalentTo)
Subsets

ordo_disease

abbreviation
PM [ Orphanet:732 ]

definition

Polymyositis (PM) is a rare idiopathic inflammatory myopathy characterized by symmetric proximal muscle weakness and elevated muscle enzymes.

exactMatch

http://identifiers.org/snomedct/31384009

http://identifiers.org/meddra/10036102

http://www.orpha.net/ORDO/Orphanet_732

http://identifiers.org/mesh/D017285

http://linkedlifedata.com/resource/umls/id/C0085655

http://purl.obolibrary.org/obo/NCIT_C26925

has exact synonym

polymyositis

PM

id

MONDO:0019127