Maternally inherited mitochondrial cardiomyopathy (Q95640): Difference between revisions

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Property / Canonical URI: https://id.who.int/icd/entity/338896648 / rank
 
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Property / CURIE
 
CID11:ID_338896648
Property / CURIE: CID11:ID_338896648 / rank
 
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Property / Canary Token
 
dki-india-ID_338896648
Property / Canary Token: dki-india-ID_338896648 / rank
 
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Concluído
Property / Verification Status: Concluído / rank
 
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Property / Knowledge Architect
 
Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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Property / Collection date
 
15 August 2026
Timestamp+2026-08-15T00:00:00Z
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CalendarGregorian
Precision1 day
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Property / Collection date: 15 August 2026 / rank
 
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Latest 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
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ID_338896648
    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).

      Statements

      CID11:ID_338896648
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      dki-india-ID_338896648
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      Concluído
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      15 August 2026
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