Hereditary myopathy, not elsewhere classified (Q103459): Difference between revisions
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Changed label, description and/or aliases in pt-br, en |
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| description / pt-br | description / pt-br | ||
Um grupo de distúrbios heterogêneos que geralmente se apresentam com hipotonia infantil como resultado de defeitos genéticos que causam miopatias primárias | |||
| description / en | description / en | ||
A group of heterogeneous disorders usually presenting with infantile hypotonia as a result of genetic defects causing primary myopathies | |||
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 |
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| 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 |
