Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency

Synonyms

Alternative names recorded for Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency across source vocabularies.

• Combined oxidative phosphorylation defect type 10
• COXPD10 - combined oxidative phosphorylation defect type 10
• defecto combinado de la fosforilación oxidativa tipo 10
• miocardiopatía hipertrófica mitocondrial con acidosis láctica por deficiencia del gen de optimización de traducción del ácido ribonucleico de transferencia mitocondrial 1 (MTO1)
• miocardiopatía hipertrófica mitocondrial con acidosis láctica por deficiencia del gen de optimización de traducción del ácido ribonucleico de transferencia mitocondrial 1 (MTO1) (trastorno)
• miocardiopatía hipertrófica mitocondrial con acidosis láctica por deficiencia de MTO1
• Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to mitochondrial transfer ribonucleic acid translation optimisation 1 deficiency
• Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to mitochondrial transfer ribonucleic acid translation optimization 1 deficiency
• Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to mitochondrial transfer ribonucleic acid translation optimization 1 deficiency (disorder)

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