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Caveolinopathy
MONDO:0016146A group of muscle diseases with basis in CAV3, which encodes caveolin-3, a muscle-specific membrane protein and the principal component of caveolae membrane in muscle cells in vivo. It is the only gene in which pathogenic variants are known to cause caveolinopathies. Sequence analysis identifies pathogenic variants in more than 99% of affected individuals
Also known as: qualitative or quantitative defects of caveolin-3
33 clinical trials for this condition and its sub-types.
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Disease
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Nervous system disorder
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Musculoskeletal system disorder
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Hereditary disease
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Muscle tissue disorder
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Human disease
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Hereditary neurological disease
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Disease of genetic or genomic mechanism
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Disease by body system or component
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