Sarcomeric restrictive cardiomyopathy (Q96352): Difference between revisions
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Cardiomiopatia restritiva sarcomérica é a presença de cardiomiopatia restritiva na presença de uma mutação de gene sarcomérico que é conhecida por estar significativamente associada à fisiologia restritiva._x000D_ _x000D_ Informações adicionais. Exemplos incluem: Mutações na proteína de ligação à miosina (MYBPC3), cadeia pesada da β-miosina (MYH7), genes da cadeia leve da miosina (MYL3), troponina I (TNNI3) e troponina T (TNNT2). | |||||||||||||||
| description / en | description / en | ||||||||||||||
Sarcomeric restrictive cardiomyopathy is the presence of restrictive cardiomyopathy in the presence of a sarcomeric gene mutation that is known to be significantly associated with restrictive physiology. Additional information. Examples include: Mutations in myosin-binding protein (MYBPC3), β-myosin heavy chain (MYH7), myosin light chain genes (MYL3), troponin I (TNNI3), and troponin T (TNNT2). | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/1129643783 / rank | |||||||||||||||
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CID11:ID_1129643783 | |||||||||||||||
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dki-india-ID_1129643783 | |||||||||||||||
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| Property / Verification Status: Concluído / rank | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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15 August 2026
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| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
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Latest revision as of 12:19, 16 August 2026
Sarcomeric restrictive cardiomyopathy is the presence of restrictive cardiomyopathy in the presence of a sarcomeric gene mutation that is known to be significantly associated with restrictive physiology. Additional information. Examples include: Mutations in myosin-binding protein (MYBPC3), β-myosin heavy chain (MYH7), myosin light chain genes (MYL3), troponin I (TNNI3), and troponin T (TNNT2).
| Language | Label | Description | Also known as |
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| default for all languages | ID_1129643783 |
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| English | Sarcomeric restrictive cardiomyopathy |
Sarcomeric restrictive cardiomyopathy is the presence of restrictive cardiomyopathy in the presence of a sarcomeric gene mutation that is known to be significantly associated with restrictive physiology. Additional information. Examples include: Mutations in myosin-binding protein (MYBPC3), β-myosin heavy chain (MYH7), myosin light chain genes (MYL3), troponin I (TNNI3), and troponin T (TNNT2). |
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CID11:ID_1129643783
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dki-india-ID_1129643783
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Concluído
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15 August 2026
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