|
491
|
|
|
- |
- |
Cardiomyopathy, Demyelinating neuropathy, Developmental delay, Developmental regression, Diabetes mellitus, Dyskinetic syndrome, Dysphagia, Epileptic encephalopathy, Hearing loss, Hypertrophic cardiomyopathy, Hypoglycemia, Leber plus disease, Leigh syndrome, Leukodystrophy, Leukoencephalopathy, Liver failure, Maternally inherited leigh syndrome, Microcephaly, Mitochondrial complex deficiency, Mitochondrial myopathy, Myoclonic seizures, Nystagmus, Optic atrophy, Ptosis, Retinitis pigmentosa, Rod-cone dystrophy, Seizure, Sensorimotor neuropathy, Strabismus, West syndromeView all (15 more) |
|
492
|
|
|
- |
- |
Addison`s disease, Wolff-parkinson-white syndrome, Anorexia, Anxiety disorder, Aortic aneurysm, Aortic dissection, Aphasia, Arthrogryposis multiplex congenita, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Cardiomyopathy, Cataract, Central visual impairment, Cerebral cortical atrophy, Congestive heart failure, Dementia, Demyelinating neuropathy, Developmental delay, Developmental regression, Diabetes mellitus, Dwarfism, Dysarthria, Dyskinetic syndrome, Dysphagia, Epileptic encephalopathy, Gastroparesis, Hallucinations, Hearing loss, Heart block, Hematomas, Hemianopsia, Hereditary leber optic atrophy, Hypertension, Hyperthyroidism, Hypertrophic cardiomyopathy, Hypoglycemia, Hypoparathyroidism, Hypopituitarism, Hypothyroidism, Ichthyosis, Intestinal obstruction, Leber plus disease, Left ventricular hypertrophy, Leigh syndrome, Leukodystrophy, Leukoencephalopathy, Liver failure, Malabsorption syndrome, Malformation of cortical development, Maternally inherited leigh syndrome, Melas syndrome, Mental depression, Microcephaly, Migraine, Mitochondrial complex deficiency, Mitochondrial myopathy, Multiple lipomata, Myoclonic seizures, Myopathy, Nephrotic syndrome, Nervous system diseases, Nyctalopia, Nystagmus, Optic atrophy, Optic neuropathy, Pancreatitis, Polyneuropathy, Psychosis, Ptosis, Pulmonary arterial hypertension, Renal glomerular disease, Renal insufficiency, Retinal telangiectasia, Retinitis pigmentosa, Rod-cone dystrophy, Seizure, Sensorimotor neuropathy, Sensorineural hearing loss, Strabismus, Thyroiditis, Ventricular preexcitation, West syndromeView all (68 more) |
|
493
|
|
|
- |
- |
Addison`s disease, Wolff-parkinson-white syndrome, Anorexia, Anxiety disorder, Aortic aneurysm, Aortic dissection, Aphasia, Arthrogryposis multiplex congenita, Attention deficit hyperactivity disorder, Autism, Cardiomyopathy, Cataract, Central visual impairment, Cerebral cortical atrophy, Congestive heart failure, Dementia, Demyelinating neuropathy, Developmental regression, Diabetes mellitus, Dwarfism, Dysarthria, Dyskinetic syndrome, Dysphagia, Epileptic encephalopathy, Gastroparesis, Hallucinations, Hearing loss, Heart block, Hematomas, Hemianopsia, Hereditary leber optic atrophy, Hypertension, Hyperthyroidism, Hypertrophic cardiomyopathy, Hypoparathyroidism, Hypopituitarism, Hypothyroidism, Ichthyosis, Impaired cognition, Intestinal obstruction, Left ventricular hypertrophy, Leigh syndrome, Liver failure, Malabsorption syndrome, Malformation of cortical development, Maternally inherited leigh syndrome, Melas syndrome, Mental depression, Merrf syndrome, Microcephaly, Migraine, Mitochondrial diseases, Mitochondrial myopathy, Movement disorders, Multiple lipomata, Myoclonic seizures, Myopathy, Nephrotic syndrome, Nervous system diseases, Nyctalopia, Nystagmus, Optic atrophy, Pancreatitis, Polyneuropathy, Psychosis, Ptosis, Pulmonary arterial hypertension, Renal glomerular disease, Renal insufficiency, Retinal telangiectasia, Retinitis pigmentosa, Rod-cone dystrophy, Seizure, Sensorimotor neuropathy, Sensorineural hearing loss, Thyroiditis, Ventricular preexcitation, West syndromeView all (63 more) |
|
494
|
|
|
- |
- |
Wolff-parkinson-white syndrome, Cardiomyopathy, Demyelinating neuropathy, Developmental delay, Developmental regression, Diabetes mellitus, Dyskinetic syndrome, Dysphagia, Epileptic encephalopathy, Hearing loss, Hereditary leber optic atrophy, Hypertrophic cardiomyopathy, Hypoglycemia, Leigh syndrome, Leukodystrophy, Leukoencephalopathy, Liver failure, Maternally inherited leigh syndrome, Microcephaly, Mitochondrial complex deficiency, Mitochondrial myopathy, Myoclonic seizures, Myopathy, Nervous system diseases, Nystagmus, Optic atrophy, Polyneuropathy, Ptosis, Retinal telangiectasia, Retinitis pigmentosa, Rod-cone dystrophy, Seizure, Sensorimotor neuropathy, Strabismus, Ventricular preexcitation, West syndromeView all (21 more) |
|
495
|
|
|
Neuron navigator 3 |
NEDSFB, POMFIL1, STEERIN3, unc53H3 |
Arthritis, Autism, Chromophobe carcinoma, Diabetic nephropathy, Endometrial carcinoma, Leukemia, Mental depression, Mood disorder, Myopia, Papillary renal carcinoma, Renal carcinoma |
|
496
|
|
|
Neuron navigator 1 |
POMFIL3, STEERIN1, UNC53H1 |
|
|
497
|
|
|
Neuron navigator 2 |
HELAD1, POMFIL2, RAINB1, STEERIN2, UNC53H2 |
|
|
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 |
|
