An idiopathic inflammatory myopathy of childhood resulting in muscle weakness. [ NCIT:C114358 ]

This is just here as a test because I lose it

Term information

database cross reference
  • ICD10:M33.2 (Orphanet:93568)
  • GARD:0012742 (MONDO:equivalentTo)
  • EFO:1001988 (MONDO:equivalentTo)
  • NCIT:C114358 (MONDO:equivalentTo)
  • Orphanet:93568 (MONDO:equivalentTo)
  • SCTID:738526005 (MONDO:equivalentTo)
  • UMLS:C3826988 (NCIT:C114358)
Subsets

gard_rare, ordo_disease

abbreviation
JPM [ NCIT:C114358 ]

definition

An idiopathic inflammatory myopathy of childhood resulting in muscle weakness.

exactMatch

http://www.orpha.net/ORDO/Orphanet_93568

http://linkedlifedata.com/resource/umls/id/C3826988

http://identifiers.org/snomedct/738526005

http://purl.obolibrary.org/obo/NCIT_C114358

has exact synonym

juvenile PM

JPM

id

MONDO:0019734

seeAlso

https://rarediseases.info.nih.gov/diseases/12742/juvenile-polymyositis