121
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Mitochondrially encoded NADH dehydrogenase 1 |
MTND1 |
Alzheimer disease, Attention deficit hyperactivity disorder, Bipolar disorder, Blepharoptosis, Cerebellar ataxia, Cleft palate and bilateral cleft lip, Deafness, aminoglycoside-induced, Deafness, nonsyndromic sensorineural, mitochondrial, Deafness, sensorineural, autosomal-mitochondrial type, Bipolar depression, Developmental regression, Experimental diabetes, Diabetes mellitus type 2, Dysarthria, Dystonia, Global developmental delay, Leber hereditary optic neuropathy, Melas syndrome, Migraine, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy, ataxia, and retinitis pigmentosa, Non-neoplastic peripheral nervous system disease, Obesity, Optic atrophy, Optic neuropathy, Parkinson disease, Hereditary parkinson disease, Peripheral neuropathy, Renal hypertension, Restrictive cardiomyopathy, Rheumatoid arthritis, Rod-cone dystrophy, Toxic shock syndrome, Postaxial polydactyly, Wolfram syndromeView all (21 more) |
122
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- |
- |
Alzheimer disease, Attention deficit hyperactivity disorder, Bipolar disorder, Blepharoptosis, Cerebellar ataxia, Cleft palate and bilateral cleft lip, Deafness, aminoglycoside-induced, Deafness, nonsyndromic sensorineural, mitochondrial, Deafness, sensorineural, autosomal-mitochondrial type, Bipolar depression, Developmental regression, Experimental diabetes, Diabetes mellitus type 2, Dysarthria, Dystonia, Global developmental delay, Leber hereditary optic neuropathy, Melas syndrome, Migraine, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy, ataxia, and retinitis pigmentosa, Non-neoplastic peripheral nervous system disease, Obesity, Optic atrophy, Optic neuropathy, Parkinson disease, Hereditary parkinson disease, Peripheral neuropathy, Renal hypertension, Restrictive cardiomyopathy, Rheumatoid arthritis, Rod-cone dystrophy, Toxic shock syndrome, Postaxial polydactyly, Wolfram syndromeView all (21 more) |
123
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- |
- |
Alzheimer disease, Attention deficit hyperactivity disorder, Bipolar disorder, Blepharoptosis, Cerebellar ataxia, Cleft palate and bilateral cleft lip, Deafness, aminoglycoside-induced, Deafness, nonsyndromic sensorineural, mitochondrial, Deafness, sensorineural, autosomal-mitochondrial type, Bipolar depression, Developmental regression, Experimental diabetes, Diabetes mellitus type 2, Dysarthria, Dystonia, Global developmental delay, Leber hereditary optic neuropathy, Melas syndrome, Migraine, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy, ataxia, and retinitis pigmentosa, Non-neoplastic peripheral nervous system disease, Obesity, Optic atrophy, Optic neuropathy, Parkinson disease, Hereditary parkinson disease, Peripheral neuropathy, Renal hypertension, Restrictive cardiomyopathy, Rheumatoid arthritis, Rod-cone dystrophy, Toxic shock syndrome, Postaxial polydactyly, Wolfram syndromeView all (21 more) |
124
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Mitochondrially encoded NADH dehydrogenase 2 |
MTND2 |
Alzheimer disease, Cerebellar ataxia, Cleft palate and bilateral cleft lip, Developmental delay, Epilepsy, Leigh syndrome, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Multiple sclerosis, Myocardial infarction, Neuropathy, ataxia, and retinitis pigmentosa, Leber hereditary optic neuropathy, Parkinson disease, Rod-cone dystrophy, Postaxial polydactylyView all (1 more) |
125
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- |
- |
Alzheimer disease, Cerebellar ataxia, Cleft palate and bilateral cleft lip, Developmental delay, Epilepsy, Leigh syndrome, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Multiple sclerosis, Myocardial infarction, Neuropathy, ataxia, and retinitis pigmentosa, Leber hereditary optic neuropathy, Parkinson disease, Rod-cone dystrophy, Postaxial polydactylyView all (1 more) |
126
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|
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- |
- |
Alzheimer disease, Cerebellar ataxia, Cleft palate and bilateral cleft lip, Developmental delay, Epilepsy, Leigh syndrome, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Multiple sclerosis, Myocardial infarction, Neuropathy, ataxia, and retinitis pigmentosa, Leber hereditary optic neuropathy, Parkinson disease, Rod-cone dystrophy, Postaxial polydactylyView all (1 more) |
127
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|
|
Mitochondrially encoded NADH dehydrogenase 3 |
MTND3 |
Cerebellar ataxia, Cleft palate and bilateral cleft lip, Leber hereditary optic neuropathy, Leigh syndrome, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy, ataxia, and retinitis pigmentosa, Parkinson disease, Rod-cone dystrophy, Postaxial polydactyly |
128
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|
|
- |
- |
Cerebellar ataxia, Cleft palate and bilateral cleft lip, Leber hereditary optic neuropathy, Leigh syndrome, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy, ataxia, and retinitis pigmentosa, Parkinson disease, Rod-cone dystrophy, Postaxial polydactyly |
129
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|
|
- |
- |
Cerebellar ataxia, Cleft palate and bilateral cleft lip, Leber hereditary optic neuropathy, Leigh syndrome, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy, ataxia, and retinitis pigmentosa, Parkinson disease, Rod-cone dystrophy, Postaxial polydactyly |
130
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|
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Mitochondrially encoded NADH dehydrogenase 4 |
MTND4 |
Cerebellar ataxia, Cleft palate and bilateral cleft lip, Congenital cardiomyopathy, Dementia, Developmental delay, Epilepsy, Hearing impairment, Leber hereditary optic neuropathy, Macular degeneration, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy, ataxia, and retinitis pigmentosa, Optic atrophy, Optic neuritis, Optic neuropathy, Parkinson disease, Peripheral neuropathy, Rod-cone dystrophy, Schizophrenia, Postaxial polydactyly, Venous thromboembolismView all (7 more) |
