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8C73.Y Other specified mitochondrial myopathies

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

synonyms

• Other specified mitochondrial myopathies
• Mitochondrial myopathy with cytochrome C oxidase deficiency
• Mitochondrial myopathy with cytochrome C oxidase deficiency, severe infantile form
• Mitochondrial myopathy with coenzyme Q deficiency
• CoQ - [Mitochondrial myopathy with coenzyme Q deficiency]
• CoQ deficiency
• Mitochondrial myopathy with complex I deficiency
• Luft disease
• Mitochondrial neurogastrointestinal encephalopathy
• MNGIE - [Mitochondrial neurogastrointestinal encephalopathy]
• Point mutations of mitochondrial DNA
• Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes
• MELAS - [Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes] syndrome
• MELAS - [Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes]
• Myoclonic epilepsy, ragged red fibres
• Fukuhara syndrome
• MERRF - [Myoclonic epilepsy - ragged red fibres] syndrome
• MERRF - [Myoclonic epilepsy - ragged red fibres]
• Leber hereditary optic neuropathy
• LHON - [Leber hereditary optic neuropathy]
• Leber optic neuropathy
• Leber atrophy
• Leber hereditary optic atrophy
• Leber optic atrophy
• Leber 'plus' disease
• Maternally inherited Leigh syndrome
• MILS - [Maternally inherited Leigh syndrome]
• Maternally inherited mitochondrial dystonia
• Maternally inherited mitochondrial cardiomyopathy
• Maternally inherited mitochondrial myopathy
• Pure mitochondrial myopathy
• Lethal infantile mitochondrial myopathy
• Mitochondrial myopathy with diabetes mellitus
• Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
• Mitochondrial myopathy with reversible COX - [cytochrome C oxidase] deficiency
• Non-syndromic mitochondrial sensorineural deafness
• Isolated mitochondrial neurosensory deafness
• Isolated mitochondrial sensorineural deafness
• Nonsyndromic mitochondrial neurosensory deafness

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