Idiopathic Camptocormia, also known as idiopathic progressive lumbar kyphosis, is related to autosomal dominant progressive external ophthalmoplegia and lactic acidosis. An important gene associated with Idiopathic Camptocormia is MYH7 (Myosin Heavy Chain 7), and among its related pathways/superpathways is Nucleotide metabolism. Affiliated tissues include skeletal muscle and pons, and related phenotypes are emg: myopathic abnormalities and dystonia