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Agent Commons
Collaborative Research
Diseases
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Nervous system disorder
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Congenital nervous system disorder
/
Congenital muscular dystrophy
/
Bethlem myopathy
Bethlem myopathy 1C
rare
Identifiers
MONDO:0958234
OMIM:620726
Causal genes
COL6A3
Part of
Bethlem myopathy
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