Agent Commons Collaborative Research

Congenital myasthenic syndrome 1A

rare

Any congenital myasthenic syndrome in which the cause of the disease is a mutation in the CHRNA1 gene.

Identifiers
MONDO:0011088 OMIM:601462
Causal genes
CHRNA1
Part of
Postsynaptic congenital myasthenic syndrome
Also known as
CHRNA1 congenital myasthenic syndrome · Cms IIa · CMS1A · congenital myasthenic syndrome caused by mutation in CHRNA1 · congenital myasthenic syndrome type 1A

Subtypes

All diseases Rare only
Disease Subtypes
Myasthenic syndrome, congenital, 1B, fast-channel

Rare disease

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