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neuromuscular junction disease

Go to external page http://purl.obolibrary.org/obo/MONDO_0020124

Conditions characterized by impaired transmission of impulses at the neuromuscular junction. This may result from disorders that affect receptor function, pre- or postsynaptic membrane function, or acetylcholinesterase activity. The majority of diseases in this category are associated with autoimmune, toxic, or inherited conditions. [ MESH:D020511 ]

This is just here as a test because I lose it

Term information

database cross reference
  • Orphanet:98495 (MONDO:mondoIsBroaderThanSource)
  • DOID:439 (MONDO:equivalentTo)
  • MESH:D020511 (Orphanet:98491/e)
  • GARD:19473 (Orphanet:98491)
  • UMLS:C0751950 (Orphanet:98491/e)
  • Orphanet:98491 (MONDO:equivalentTo)
  • SCTID:128213006 (MONDO:equivalentTo)
Subsets

gard_rare, disease_grouping, rare, orphanet_rare, ordo_group_of_disorders

exactMatch

http://identifiers.org/snomedct/128213006

http://purl.obolibrary.org/obo/DOID_439

http://www.orpha.net/ORDO/Orphanet_98491

http://identifiers.org/mesh/D020511

http://linkedlifedata.com/resource/umls/id/C0751950

id

MONDO:0020124

narrowMatch

http://www.orpha.net/ORDO/Orphanet_98495

Term relations

Subclass of: