Inclusion body myositis (IBM) is a slowly progressive degenerative inflammatory disorder of skeletal muscles characterized by late onset weakness of specific muscles and distinctive histopathological features. [ Orphanet:611 ]

This is just here as a test because I lose it

Term information

database cross reference
  • NCIT:C84786 (MONDO:equivalentTo)
  • GARD:0003896 (Orphanet-shared)
  • MESH:D018979 (MONDO:equivalentTo)
  • EFO:0007323 (MONDO:equivalentTo)
  • SCTID:72315009 (MONDO:equivalentTo)
  • Orphanet:611 (OMIM:147421)
  • ICD9:729.1 (i2s)
  • MedDRA:10066407 (Orphanet:611)
  • DOID:3429 (MONDO:equivalentTo)
  • ICD10:M60.8 (Orphanet:611)
  • UMLS:C0238190 (Orphanet:611)
  • ICD9:359.71 (i2s)
  • ICD10:G72.41 (DOID:3429)
  • OMIM:147421 (Orphanet:611)
  • COHD:4216406 (MONDO:equivalentTo)
Subsets

ordo_disease

abbreviation
IBM2 [ DOID:3429 ]

abbreviation
HIBM [ DOID:3429 ]

abbreviation
IBM [ Orphanet:611 ]

closeMatch

http://linkedlifedata.com/resource/umls/id/C0751713

definition

Inclusion body myositis (IBM) is a slowly progressive degenerative inflammatory disorder of skeletal muscles characterized by late onset weakness of specific muscles and distinctive histopathological features.

exactMatch

http://identifiers.org/mesh/D018979

http://identifiers.org/snomedct/72315009

http://www.orpha.net/ORDO/Orphanet_611

http://linkedlifedata.com/resource/umls/id/C0238190

http://purl.obolibrary.org/obo/NCIT_C84786

http://purl.obolibrary.org/obo/DOID_3429

http://identifiers.org/omim/147421

http://identifiers.org/meddra/10066407

has exact synonym

distal myopathy with rimmed vacuoles

inclusion body myositis

Nonaka myopathy

hereditary inclusion body myopathy

sporadic inclusion body myositis

HIBM

sIBM

IBM

IBM-3

inclusion body myopathy 2

inclusion body myopathy 3

distal myopathy with rimmed vacuoles (DMRV)

IBM2

has related synonym

Ibm

inflammatory myopathy

id

MONDO:0007827

Term relations

Subclass of: