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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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Hereditary skeletal muscle disorder
Congenital myopathy 22B, severe fetal
rare
Identifiers
MONDO:0957265
OMIM:620369
Causal genes
SCN4A
Part of
Congenital myopathy
Hereditary skeletal muscle disorder
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