Miyoshi Muscular Dystrophy 3 (MMD3)

Miyoshi Muscular Dystrophy 3, also known as mmd3, is related to gnathodiaphyseal dysplasia and limb-girdle muscular dystrophy, and has symptoms including calf muscle weakness An important gene associated with Miyoshi Muscular Dystrophy 3 is ANO5 (Anoctamin 5), and among its related pathways/superpathways are Transport of inorganic cations/anions and amino acids/oligopeptides and SARS-CoV-2 Infection. Affiliated tissues include skeletal muscle, and related phenotypes are distal lower limb muscle weakness and progressive muscle weakness