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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
Myopathy, congenital, progressive, with scoliosis
rare
Identifiers
MONDO:0032821
OMIM:618578
Causal genes
PAX7
Part of
Congenital myopathy
Hereditary skeletal muscle disorder
Also known as
MYOSCO
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