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ENCap Myopathy
Alias:
Cap Disease
Congenital Myopathy with Caps
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Cap Myopathy, also known as cap disease, is related to congenital myopathy 4a, autosomal dominant and nemaline myopathy. An important gene associated with Cap Myopathy is TPM2 (Tropomyosin 2), and among its related pathways/superpathways are Cardiac conduction and Striated muscle contraction pathway. Affiliated tissues include prostate and skeletal muscle, and related phenotypes are high palate and reduced tendon reflexes
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MALACARDS
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