|
181
|
|
|
NHL repeat containing 2 |
FINCA |
Brain atrophy, Cerebral atrophy, Developmental delay, Elliptocytosis, Fibrosis, neurodegeneration, and cerebral angiomatosis, Hemolytic anemia, Hypoplasia of corpus callosum, Quadriplegia, Strabismus |
|
182
|
|
|
Negative regulator of reactive oxygen species |
ELLP3030, GARPL1, LRRC33, SENEBAC, UNQ3030 |
|
|
183
|
|
|
NHL repeat containing E3 ubiquitin protein ligase 1 |
EPM2A, EPM2B, MALIN, MELF2, bA204B7.2 |
Absence seizure, Action myoclonus-renal failure syndrome, Apraxia, Bilateral convulsive seizures, Brain atrophy, Cerebral atrophy, Dementia, Dentatorubral pallidoluysian atrophy, Dysarthria, Dyscognitive seizures, Dyssomnia, Glycogen storage disease, Hypotonic seizures, Inclusion-body disease, Lafora disease, Liver failure, Lymphoblastic leukemia, May-white syndrome, Mental depression, Mood swings, Myoclonic epilepsy, Myoclonic seizures, Partial occipital seizures, Psychosis, Seizure, Sleep disorders, Status epilepticus, Visual aurasView all (13 more) |
|
184
|
|
|
Neuropeptide S receptor 1 |
ASRT2, GPR154, GPRA, NPSR, PGR14, VRR1 |
|
|
185
|
|
|
Nuclear GTPase, germinal center associated |
C8orf80, HMFN0672, SLIP-GC, SLIPGC |
|
|
186
|
|
|
Nuclear receptor subfamily 3 group C member 2 |
MCR, MLR, MR, NR3C2VIT |
Cardiomyopathy, Colorectal cancer, Congestive heart failure, Endometrioma, Endometriosis, Heart failure, Hyperaldosteronism, Hyperpotassemia and hypertension, Hypertension, Hypertension with exacerbation in pregnancy, Maternal hypertension, Mental depression, Myocardial infarction, Pseudohypoaldosteronism, Renal pseudohypoaldosteronism |
|
187
|
|
|
NR2F1 regulatory antisense RNA 1 |
NAS1 |
|
|
188
|
|
|
NOTCH regulated ankyrin repeat protein |
- |
|
|
189
|
|
|
Mitochondrially encoded NADH dehydrogenase 1 |
MTND1 |
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) |
|
190
|
|
|
Mitochondrially encoded NADH dehydrogenase 2 |
MTND2 |
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) |
