Maternally inherited mitochondrial cardiomyopathy (Q95640): Difference between revisions
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Isso se refere à deterioração mensurável mitocondrial de herança materna da função do miocárdio (o músculo cardíaco) por qualquer motivo, geralmente levando à insuficiência cardíaca; os sintomas comuns são dispneia (falta de ar) e edema periférico (inchaço das pernas). | |||
| description / en | description / en | ||
This refers to the maternally inherited mitochondrial measurable deterioration of the function of the myocardium (the heart muscle) for any reason, usually leading to heart failure; common symptoms are dyspnoea (breathlessness) and peripheral oedema (swelling of the legs). | |||
Revision as of 11:27, 16 August 2026
This refers to the maternally inherited mitochondrial measurable deterioration of the function of the myocardium (the heart muscle) for any reason, usually leading to heart failure; common symptoms are dyspnoea (breathlessness) and peripheral oedema (swelling of the legs).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_338896648 |
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| English | Maternally inherited mitochondrial cardiomyopathy |
This refers to the maternally inherited mitochondrial measurable deterioration of the function of the myocardium (the heart muscle) for any reason, usually leading to heart failure; common symptoms are dyspnoea (breathlessness) and peripheral oedema (swelling of the legs). |
