Myopathy (Q89563): Difference between revisions
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Revision as of 16:22, 15 August 2026
Disorder of the skeletal muscles associated with disruptions in the structure and metabolic processes of muscle cells as a result of genetic abnormalities, toxins, inflammation, infection, and hormonal and electrolyte imbalances. Characterized by motor symptoms in the absence of any sensory involvement, with weakness often occurring in the proximal muscles.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1870184184 |
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| English | Myopathy |
Disorder of the skeletal muscles associated with disruptions in the structure and metabolic processes of muscle cells as a result of genetic abnormalities, toxins, inflammation, infection, and hormonal and electrolyte imbalances. Characterized by motor symptoms in the absence of any sensory involvement, with weakness often occurring in the proximal muscles. |
Statements
CID11:ID_1870184184
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