A rare idiopathic inflammatory myopathy characterized by symmetric proximal muscle weakness and elevated muscle enzymes. [ Orphanet:732 https://orcid.org/0000-0001-5208-3432 ]

Synonyms: polymyositis PM

This is just here as a test because I lose it

Term information

database cross reference
  • MESH:D017285 (Orphanet:732/e)
  • UMLS:C0085655 (MONDO:equivalentTo)
  • icd11.foundation:1157134196 (Orphanet:732)
  • MEDGEN:39086 (MONDO:equivalentTo)
  • GARD:7425 (MONDO:GARD)
  • ICD9:710.4 (MONDO:i2s)
  • Wikipedia:Polymyositis (EFO:0003063)
  • DOID:0080745 (MONDO:equivalentTo)
  • EFO:0003063 (MONDO:equivalentTo)
  • MedDRA:10036102 (Orphanet:732/e)
  • NANDO:1200276 (https://orcid.org/0000-0003-0011-764X)
  • NCIT:C26925 (MONDO:equivalentTo)
  • Orphanet:732 (MONDO:equivalentTo)
  • ICD10CM:M33.2 (Orphanet:732/e)
  • SCTID:31384009 (MONDO:equivalentTo)
Subsets

gard_rare, ordo_disorder, otar, rare, nord_rare, orphanet_rare

abbreviation
PM [ Orphanet:732 ]

closeMatch

http://identifiers.org/meddra/10036102

exactMatch

http://identifiers.org/snomedct/31384009

http://purl.bioontology.org/ontology/ICD10CM/M33.2

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

http://purl.obolibrary.org/obo/DOID_0080745

http://identifiers.org/mesh/D017285

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

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

http://identifiers.org/medgen/39086

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0019724

id

MONDO:0019127

Term relations