|
191
|
|
|
Mitochondrially encoded NADH dehydrogenase 3 |
MTND3 |
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) |
|
192
|
|
|
Mitochondrially encoded NADH dehydrogenase 4 |
MTND4 |
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, Cerebral cortical atrophy, Congestive heart failure, Demyelinating neuropathy, Developmental regression, Diabetes mellitus, Dwarfism, Dysarthria, Dyskinetic syndrome, Dysphagia, Gastroparesis, Hallucinations, Hearing loss, Heart block, Hematomas, Hemianopsia, Hereditary leber optic atrophy, Hereditary optic atrophy, Hypertension, Hyperthyroidism, Hypertrophic cardiomyopathy, Hypoparathyroidism, Hypopituitarism, Hypothyroidism, Ichthyosis, Intestinal obstruction, Leber plus disease, Leigh syndrome, Liver failure, Malabsorption syndrome, Malformation of cortical development, Maternally inherited leigh syndrome, Melas syndrome, Mental depression, Microcephaly, Migraine, Mitochondrial complex deficiency, Mitochondrial diseases, Mitochondrial myopathy, 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, Schizophrenia, Seizure, Sensorimotor neuropathy, Thyroiditis, Ventricular preexcitation, West syndromeView all (59 more) |
|
193
|
|
|
Mitochondrially encoded NADH 4L dehydrogenase |
MTND4L |
|
|
194
|
|
|
Mitochondrially encoded NADH dehydrogenase 5 |
MTND5 |
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) |
|
195
|
|
|
Mitochondrially encoded NADH dehydrogenase 6 |
MTND6 |
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, Hereditary optic atrophy, Hypertension, Hyperthyroidism, Hypertrophic cardiomyopathy, Hypoparathyroidism, Hypopituitarism, Hypothyroidism, Ichthyosis, Intestinal obstruction, Leber plus disease, Left ventricular hypertrophy, Leigh syndrome, Liver failure, Malabsorption syndrome, Malformation of cortical development, Maternally inherited leigh syndrome, Melas syndrome, Mental depression, Microcephaly, Migraine, Mitochondrial myopathy, Multiple lipomata, Myoclonic seizures, Myopathy, Nephrotic syndrome, Nervous system diseases, Nyctalopia, Nystagmus, Optic atrophy, Oxyphilic adenoma, Pancreatitis, Parkinson disease, 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) |
|
196
|
|
|
NGFI-A binding protein 1 |
- |
|
|
197
|
|
|
NGFI-A binding protein 2 |
MADER |
Endometrial neoplasms, Hemangiopericytoma, Solitary fibrous tumor, Hypoinsulinemia, Hypophosphatemic rickets, Leukemia, Liver neoplasms, Lung neoplasms, Soft tissue neoplasms, Neoplasia of the pleura, Nervous system neoplasms, Prostate cancer, Schizophrenia, Vaginal neoplasms |
|
198
|
|
|
Nascent polypeptide associated complex subunit alpha |
HSD48, NAC-alpha, NACA1, skNAC |
|
|
199
|
|
|
Alpha-N-acetylgalactosaminidase |
D22S674, GALB |
Alpha-n-acetylgalactosaminidase deficiency, Amyotrophy, Autism, Cataract, Central visual impairment, Cerebral atrophy, Developmental delay, Developmental regression, Fabry disease, Hearing loss, Hemiplegia/hemiparesis, Hyperkeratosis, Hypertrophic cardiomyopathy, Impaired cognition, Mental retardation, Nervous system diseases, Neuroaxonal dystrophy, Nystagmus, Optic atrophy, Osteopenia, Peripheral axonal neuropathy, StrabismusView all (7 more) |
|
200
|
|
|
N-acetyl-alpha-glucosaminidase |
CMT2V, MPS-IIIB, MPS3B, NAG, UFHSD |
Autism, Bowel incontinence, Brain atrophy, Charcot-marie-tooth disease, Dementia, Developmental regression, Dysmorphic features, Dyssomnia, Hypersexuality, Hypertrichosis, Mental retardation, Legg-calve-perthes disease, Macrotia, Mucopolysaccharidosis, Pfaundler-hurler syndrome, Prostatic neoplasms, Prostate cancer, Repetitive compulsive behavior, Rod-cone dystrophy, Sanfilippo syndrome, Septal hypertrophy, Sleep disorders, SynophrysView all (8 more) |
