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ENSevere Congenital Nemaline Myopathy
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Severe Congenital Nemaline Myopathy is related to nemaline myopathy and neuromuscular disease. An important gene associated with Severe Congenital Nemaline Myopathy is ACTA1 (Actin Alpha 1, Skeletal Muscle), and among its related pathways/superpathways is Striated muscle contraction pathway. Affiliated tissues include skeletal muscle, and related phenotypes are dysphagia and facial palsy
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