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Diseases
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Syndromic disease
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Congenital myasthenic syndrome
Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive
rare
Identifiers
MONDO:0030341
OMIM:619461
Causal genes
SYT2
Part of
Congenital myasthenic syndrome
Congenital nervous system disorder
Also known as
CMS7B
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