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Congenital myasthenic syndrome 4

MONDO:1040021

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

0 clinical trials for this condition and its sub-types.

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Sub-types

Congenital myasthenic syndrome 4A (0) Congenital myasthenic syndrome 4B (0) Congenital myasthenic syndrome 4C (0)

Broader categories

Disease (717) Nervous system disorder (243) Hereditary disease (188) Neuromuscular disease (110) Syndromic disease (25) Human disease (15) Hereditary neurological disease (6) Congenital myasthenic syndrome (5) Hereditary neuromuscular disease (3) Disease of genetic or genomic mechanism (2)

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