neuromuscular junction disease
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 ]
Term info
- Orphanet:98491 (MONDO:equivalentTo)
- DOID:439 (MONDO:equivalentTo)
- UMLS:C0751950 (Orphanet:98491/e)
- Orphanet:98495 (MONDO:mondoIsBroaderThanSource)
- MESH:D020511 (Orphanet:98491/e)
- SCTID:128213006 (MONDO:equivalentTo)
disease_grouping, ordo_group_of_disorders
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.
http://identifiers.org/snomedct/128213006, http://purl.obolibrary.org/obo/DOID_439, http://identifiers.org/mesh/D020511, http://linkedlifedata.com/resource/umls/id/C0751950, http://purl.obolibrary.org/obo/Orphanet_98491
MONDO:0020124
http://purl.obolibrary.org/obo/Orphanet_98495