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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