8461
|
|
|
Natural killer cell cytotoxicity receptor 3 ligand 1 |
B7-H6, B7H6, DKFZp686O24166 |
|
8462
|
|
|
Neuronal calcium sensor 1 |
FLUP, FREQ |
|
8463
|
|
|
Nicastrin |
ATAG1874 |
|
8464
|
|
|
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, 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, Postaxial polydactyly, Wolfram syndromeView all (19 more) |
8465
|
|
|
- |
- |
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, 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, Postaxial polydactyly, Wolfram syndromeView all (19 more) |
8466
|
|
|
- |
- |
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, 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, Postaxial polydactyly, Wolfram syndromeView all (19 more) |
8467
|
|
|
- |
- |
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) |
8468
|
|
|
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) |
8469
|
|
|
- |
- |
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) |
8470
|
|
|
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 |
