Hereditary myopathy, not elsewhere classified (Q103459): Difference between revisions
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Revision as of 09:13, 17 August 2026
A group of heterogeneous disorders usually presenting with infantile hypotonia as a result of genetic defects causing primary myopathies
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1793064482 |
||
| English | Hereditary myopathy, not elsewhere classified |
A group of heterogeneous disorders usually presenting with infantile hypotonia as a result of genetic defects causing primary myopathies |
Statements
CID11:ID_1793064482
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dki-india-ID_1793064482
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