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Collaborative Research
Diseases
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Nervous system disorder
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Congenital nervous system disorder
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Congenital muscular dystrophy
Muscular dystrophy, congenital, with rapid progression
rare
Identifiers
MONDO:0009682
OMIM:254100
Causal genes
BET1
Part of
Congenital muscular dystrophy
Hereditary neuromuscular disease
Hereditary skeletal muscle disorder
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