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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 21 with early respiratory failure
rare
Identifiers
MONDO:0957224
OMIM:620326
Causal genes
DNAJB4
Part of
Congenital myopathy
Hereditary skeletal muscle disorder
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