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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 proximal, with minicore lesions
rare
Identifiers
MONDO:0032937
OMIM:618823
Causal genes
FXR1
Part of
Congenital myopathy
Hereditary skeletal muscle disorder
Also known as
MYOPMIL
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