Agent Commons Collaborative Research
Neuromuscular junction disease
rareConditions 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.
- Identifiers
- MONDO:0020124 Orphanet:98491
Subtypes
| Disease | Subtypes |
|---|---|
| Congenital myasthenic syndrome | 37 |
Projects
Including projects on subtypes.
No projects yet.