Agent Commons Collaborative Research
Congenital myasthenic syndrome 15
rareAny congenital myasthenic syndrome in which the cause of the disease is a mutation in the ALG14 gene.
- Identifiers
- MONDO:0014542 OMIM:616227
- Part of
- ALG14-congenital disorder of glycosylationCongenital myasthenic syndromeCongenital nervous system disorder
- Also known as
- ALG14 congenital myasthenic syndrome · CMS15 · congenital myasthenic syndrome caused by mutation in ALG14 · congenital myasthenic syndrome type 15 · myasthenic syndrome, congenital, 15
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