8C73.Y
其他特指的线粒体肌病
Other specified mitochondrial myopathies
- 上级条目
- 8C73 线粒体肌病
- 层级
- 5 级
索引词 可用于检索该条目的同义词与别名
- 其他特指的线粒体肌病
- 线粒体肌病伴细胞色素C氧化酶缺乏
- 线粒体肌病伴细胞色素C氧化酶缺乏，严重婴儿型
- 线粒体肌病伴辅酶Q缺乏
- CoQ缺乏
- CoQ[线粒体肌病伴辅酶Q缺乏]
- 线粒体肌病伴复合物I缺陷
- Luft病
- 勒夫特病
- 线粒体神经胃肠性脑病
- MNGIE[线粒体神经胃肠性脑病]
- 线粒体性脑病，伴乳酸性酸中毒和中风样发作
- MELAS[线粒体性脑病，伴乳酸性酸中毒和中风样发作]综合征
- MELAS[线粒体性脑病，伴乳酸性酸中毒和中风样发作]
- 肌阵挛性癫痫，不整红边纤维
- MERRF[肌阵挛性癫痫，不整红边纤维]综合征
- MERRF[肌阵挛性癫痫，不整红边纤维]
- Fukuhara综合征
- 肌阵挛性癫痫伴破碎红纤维综合征
- 福原综合征
- Leber遗传性视神经病
- Leber萎缩症
- Leber遗传性视神经萎缩
- Leber视神经萎缩
- LHON[leber遗传性视神经病]
- Leber视神经病
- 勒伯尔遗传性视神经病变
- 勒伯尔遗传性视神经萎缩
- 莱伯遗传性视神经病
- Leber+病
- 母体遗传性Leigh综合征
- MILS[母体遗传性Leigh综合征]
- 母体遗传性线粒体肌张力障碍
- 母体遗传性线粒体心肌病
- 母体遗传性线粒体肌病
- 纯线粒体肌病
- 致死性婴儿线粒体肌病
- 线粒体肌病伴糖尿病
- 线粒体肌病伴可逆的细胞色素C氧化酶缺乏
- 线粒体肌病伴可逆的COX[细胞色素氧化酶C]缺乏
- 非综合征型线粒体感音神经性聋
- 孤立性线粒体感音神经性聋
- 孤立性线粒体感音神经性聋
- 非综合征性线粒体神经感觉性聋
英文词条（38）
- 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]
- Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes
- MELAS - [Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes]
- MELAS - [Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes] syndrome
- Myoclonic epilepsy, ragged red fibres
- Fukuhara syndrome
- MERRF - [Myoclonic epilepsy - ragged red fibres]
- MERRF - [Myoclonic epilepsy - ragged red fibres] syndrome
- Leber hereditary optic neuropathy
- LHON - [Leber hereditary optic neuropathy]
- Leber atrophy
- Leber hereditary optic atrophy
- Leber optic atrophy
- Leber optic neuropathy
- 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
后组配轴 Postcoordination
该条目未定义后组配轴，直接使用上面的编码即可。后组配是在主干编码之后追加侧别、具体解剖部位、严重程度、病因等细节的可选组合方式，不是必填项。