|
491
|
|
|
- |
- |
Cerebellar ataxia, Cleft palate and bilateral cleft lip, Leber hereditary optic neuropathy, Leigh syndrome, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy in association with hereditary ataxia, Parkinson disease, Retinitis pigmentosa, Postaxial polydactyly |
|
492
|
|
|
- |
- |
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, 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, Retinitis pigmentosa, Toxic shock syndrome, Postaxial polydactyly, Wolfram syndromeView all (20 more) |
|
493
|
|
|
- |
- |
Hepatocellular carcinoma, Cerebellar ataxia, Cleft palate and bilateral cleft lip, Congenital cardiomyopathy, Developmental delay, Hearing impairment, Leber hereditary optic neuropathy, Leigh syndrome, Melas syndrome, Myoclonic epilepsy with ragged red fibers, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy, congenital hypomyelinating, Parkinson disease, Retinitis pigmentosa, Postaxial polydactylyView all (1 more) |
|
494
|
|
|
- |
- |
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, Retinitis pigmentosa, Postaxial polydactylyView all (1 more) |
|
495
|
|
|
Neuron navigator 3 |
NEDSFB, POMFIL1, STEERIN3, unc53H3 |
Appendicitis, Autism, Renal cell carcinoma, Cardiac arrhythmia, Cardiac embolism, Cardioembolic stroke, Colorectal cancer, Neurodevelopmental disorder, Diabetic neuropathy, Endometrial cancer, Endometrial neoplasm, Eye disease, Gastroesophageal reflux disease, Hearing impairment, Major depressive disorder, Mood disorder, Neurodevelopmental disorders, Non-specific syndromic intellectual disability, Obesity, Schizophrenia, Sleep apnea, Systemic mastocytosis, TuberculosisView all (8 more) |
|
496
|
|
|
Neuron navigator 1 |
POMFIL3, STEERIN1, UNC53H1 |
Aortic stenosis, Aortic valve disease, Attention deficit hyperactivity disorder, Autism, Cardiovascular disease, Celiac disease, Obstructive pulmonary disease, Color vision deficiency, Colorectal cancer, Gout, Insomnia, Interstitial lung disease, Lung cancer, Metabolic syndrome, Mouth disease, Obesity, Prostate cancer, Schizophrenia, Diabetes mellitus, type 2View all (4 more) |
|
497
|
|
|
Neuron navigator 2 |
HELAD1, POMFIL2, RAINB1, STEERIN2, UNC53H2 |
Alzheimer disease, Autoimmune neurological syndrome, Atrial fibrillation, Atrial flutter, Attention deficit hyperactivity disorder, Autoimmune thrombocytopenic purpura, Central nervous system cancer, Color vision deficiency, Coronary aneurysm, Dementia, Glioblastoma, Glioma, Human immunodeficiency virus infection, Obesity, Paralytic strabismus, Peripheral arterial disease, Scoliosis, Sjogren syndrome, Vascular dementia, Ventricular septal defectView all (5 more) |
|
498
|
|
|
Nucleolar protein 3 |
ARC, FCM, MYOCL1, MYP, NOP, NOP30 |
|
|
499
|
|
|
N-acetyltransferase 1 |
AAC1, MNAT, NAT-1, NATI |
|
|
500
|
|
|
N-acetyltransferase 8 (putative) |
ATase2, CCNAT, CML1, GLA, Hcml1, TSC501, TSC510 |
|
