Neuromuscular junction disease
MONDO:0020124Conditions 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.
7 clinical trials for this condition and its sub-types, 1 tagged with Neuromuscular junction disease itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Neuromuscular junction disease
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Congenital myasthenic syndrome 6 trials
8 sub-types
- Postsynaptic congenital myasthenic syndrome 0 trials · 3 incl. sub-types Sub-types →
- Presynaptic congenital myasthenic syndrome 0 trials · 1 incl. sub-types Sub-types →
- Congenital myasthenic syndrome 15 0 trials
- Congenital myasthenic syndrome 5 0 trials
- Congenital myasthenic syndrome with tubular aggregates 0 trials Sub-types →
- Myasthenia, congenital, refractory to acetylcholinesterase inhibitors 0 trials
- Myasthenic syndrome, congenital, 22 0 trials
- Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive 0 trials
Most studied deeper sub-types
Congenital myasthenic syndrome 10
(3)
Congenital myasthenic syndrome 17
(1)
Congenital myasthenic syndrome 8
(1)
Congenital myasthenic syndrome 9
(1)
Congenital myasthenic syndrome 11
(0)
Congenital myasthenic syndrome 12
(0)
Congenital myasthenic syndrome 13
(0)
Congenital myasthenic syndrome 14
(0)
Congenital myasthenic syndrome 16
(0)
Congenital myasthenic syndrome 18
(0)
Congenital myasthenic syndrome 19
(0)
Congenital myasthenic syndrome 1A
(0)
Congenital myasthenic syndrome 20
(0)
Congenital myasthenic syndrome 21
(0)
Congenital myasthenic syndrome 2A
(0)
Congenital myasthenic syndrome 2C
(0)
Congenital myasthenic syndrome 3A
(0)
Congenital myasthenic syndrome 3B
(0)
Congenital myasthenic syndrome 3C
(0)
Congenital myasthenic syndrome 4
(0)