Disease Index

myopathy that is characterized by slowly progressive muscle weakness that can involve both proximal muscles and distal muscles

Human disease

Human disease

Human disease

Human disease

Human disease

Human disease

human disease

human disease

human disease

Myopathy due to calsequestrin and SERCA1 protein overload is characterised by mild myopathy or elevated levels of creatine kinase in the blood without associated symptoms

human disease

human disease

Human disease

human disease

human disease

subcutaneous nodular neoplasm arising from myopericytes

visual defect which causes to see the near objects clearly and far objects unclearly

human disease

human disease

muscle tissue disease characterized by increased muscle bulk and strength that has material basis in homozygous mutation in the MSTN gene on chromosome 2q32.2

muscle tissue disease that is characterised by slow muscle relaxation associated with hyperexcitation of the muscle fibres

very rare, persistent and more severe form of potassium-aggravated myotonia

muscular dystrophy characterized by progressive muscle wasting and weakness

long term genetic disorder that affects muscle function

malignant fibroblastic neoplasm arising from the soft tissue. It is characterized by the presence of spindle-shaped cells, cellular pleomorphism, thin-walled blood vessels, fibrous septa, and myxoid stroma

human disease

human disease