Camptocormia

About the Disease
Camptocormism, also known as idiopathic camptocormia, is related to myopathy and mitochondrial myopathy. An important gene associated with Camptocormism is MYH7 (Myosin Heavy Chain 7), and among its related pathways/superpathways is Nucleotide metabolism. Affiliated tissues include skeletal muscle, pons and subthalamic nucleus, and related phenotypes are emg: myopathic abnormalities and dystonia

Common Targets
FLNC | CAPN3

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