Intermediate Nemaline Myopathy is related to congenital myopathy 4a, autosomal dominant and nemaline myopathy 10. An important gene associated with Intermediate Nemaline Myopathy is ACTA1 (Actin Alpha 1, Skeletal Muscle), and among its related pathways/superpathways are Cardiac conduction and Striated muscle contraction pathway. Affiliated tissues include skeletal muscle, and related phenotypes are nemaline bodies and severe muscular hypotonia