Fast-channel congenital myasthenic…
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Start free with EleplanFast-channel congenital myasthenic syndrome
ORPHA:716758Etiological subtype
Also called FCCMS · FCS · Fast-channel syndrome
What it is
Orphanet has not published a description for this disease yet. The identifiers, classification and cross-references below are still current.
Key facts
- Inheritance
- Autosomal dominant, Autosomal recessive
- Classified as
- Etiological subtype
Genes
CHRNA1Disease-causing germline mutation(s) (gain of function)
CHRNB1Disease-causing germline mutation(s) (gain of function)
CHRNDDisease-causing germline mutation(s) (gain of function)
CHRNEDisease-causing germline mutation(s) (gain of function)
Cross-references
OMIM 608930OMIM 616322OMIM 616324
Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.
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