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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
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FHL1-related myopathy
Myopathy, reducing body, X-linked, childhood-onset
rare
Identifiers
MONDO:0010415
OMIM:300718
Part of
FHL1-related myopathy
Reducing body myopathy
Also known as
RBMX1B
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