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inclusion body myositis

Go to external page http://purl.obolibrary.org/obo/MONDO_0007827

A slowly progressive degenerative inflammatory disorder of skeletal muscles characterized by late onset weakness of specific muscles and distinctive histopathological features. [ Orphanet:611 https://orcid.org/0000-0001-5208-3432 ]

Synonyms: sIBM inclusion body myositis IBM sporadic inclusion body myositis

This is just here as a test because I lose it

Term information

database cross reference
  • GARD:3896 (Orphanet:611)
  • MESH:D018979 (MONDO:equivalentTo)
  • NORD:1734 (MONDO:NORD)
  • EFO:0007323 (MONDO:equivalentTo)
  • UMLS:C0238190 (Orphanet:611/e)
  • NCIT:C84786 (MONDO:equivalentTo)
  • SCTID:72315009 (MONDO:equivalentTo)
  • DOID:3429 (MONDO:equivalentTo)
  • Orphanet:611 (OMIM:147421)
  • ICD9:359.71 (MONDO:i2s)
  • ICD9:729.1 (MONDO:relatedTo)
  • MedDRA:10066407 (Orphanet:611/e)
  • OMIM:147421 (Orphanet:611/e)
Subsets

gard_rare, ordo_disease, rare, nord_rare, orphanet_rare

closeMatch

http://identifiers.org/meddra/10066407

exactMatch

http://identifiers.org/mesh/D018979

http://identifiers.org/snomedct/72315009

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

https://omim.org/entry/147421

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

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

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

has related synonym

Ibm

inflammatory myopathy

id

MONDO:0007827

Term relations

Subclass of: