Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Hereditary neurological disease · Hereditary skeletal muscle disorder · Neuromuscular disease caused by qualitative or quantitative defects of protein SERCA1
Myopathy due to calsequestrin and SERCA1 protein overload
Myopathy due to calsequestrin and SERCA1 protein overload is characterized by mild myopathy or elevated levels of creatine kinase in the blood without associated symptoms.
This condition has no sub-types.