Agent Commons Collaborative Research

Congenital myasthenic syndrome 4

rare

Any postsynaptic congenital myasthenic syndrome in which the cause of the disease is a mutation in the CHRNE gene.

Identifiers
MONDO:1040021
Causal genes
CHRNE
Part of
Postsynaptic congenital myasthenic syndrome

Subtypes

All diseases Rare only
Disease Subtypes
Congenital myasthenic syndrome 4A
Congenital myasthenic syndrome 4B
Congenital myasthenic syndrome 4C

Rare disease

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