Myasthenia gravis (MG) is a rare, clinically heterogeneous, autoimmune disorder of the neuromuscular junction characterized by fatigable weakness of voluntary muscles. [ Orphanet:589 ]

This is just here as a test because I lose it

Term information

database cross reference
  • ICD9:358.00 (i2s)
  • MedDRA:10028417 (Orphanet:589)
  • EFO:0004991 (MONDO:equivalentTo)
  • ICD9:358.0 (i2s)
  • COHD:76685 (MONDO:equivalentTo)
  • NCIT:C60989 (exact-label-match)
  • SCTID:91637004 (MONDO:equivalentTo)
  • UMLS:C0026896 (Orphanet:589)
  • MESH:D009157 (Orphanet:589)
  • OMIM:254200 (Orphanet:589)
  • ICD10:G70.00 (DOID:437)
  • GARD:0007122 (MONDO:equivalentTo)
  • ICD10:G70.0 (Orphanet:589)
  • Orphanet:589 (OMIM:254200)
  • DOID:437 (MONDO:equivalentTo)
Subsets

gard_rare, ordo_disease

closeMatch

http://linkedlifedata.com/resource/umls/id/C1260409

http://identifiers.org/snomedct/155092009

http://identifiers.org/snomedct/193208002

definition

Myasthenia gravis (MG) is a rare, clinically heterogeneous, autoimmune disorder of the neuromuscular junction characterized by fatigable weakness of voluntary muscles.

exactMatch

http://linkedlifedata.com/resource/umls/id/C0026896

http://purl.obolibrary.org/obo/NCIT_C60989

http://identifiers.org/mesh/D009157

http://www.orpha.net/ORDO/Orphanet_589

http://identifiers.org/omim/254200

http://identifiers.org/snomedct/91637004

http://identifiers.org/meddra/10028417

http://purl.obolibrary.org/obo/DOID_437

has exact synonym

acquired myasthenia

myasthenia gravis

autoimmune myasthenia gravis

id

MONDO:0009688

seeAlso

https://rarediseases.info.nih.gov/diseases/7122/myasthenia-gravis