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421
|
|
|
- |
- |
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) |
|
422
|
|
|
- |
- |
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) |
|
423
|
|
|
- |
- |
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) |
|
424
|
|
|
- |
- |
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) |
|
425
|
|
|
NIMA related kinase 4 |
NRK2, STK2, pp12301 |
|
|
426
|
|
|
Nuclear receptor subfamily 2 group F member 1 |
BBOAS, BBSOAS, COUP-TFI, COUPTF1, EAR-3, EAR3, ERBAL3, SVP44, TCFCOUP1, TFCOUP1 |
Breast cancer, Mammary neoplasms, Breast carcinoma, Central visual impairment, Corpus luteum cyst, Developmental delay, Marfan syndrome, Mental retardation, Nystagmus, Optic atrophy, Optic atrophy, intellectual disability syndrome, Ovarian cysts, Strabismus |
|
427
|
|
|
Nuclear receptor subfamily 2 group F member 2 |
ARP-1, ARP1, CHTD4, COUPTF2, COUPTFB, COUPTFII, NF-E3, SRXX5, SVP40, TFCOUP2 |
Aortic coarctation, Aortic valve sclerosis, Bicuspid aortic valve, Complete atrioventricular septal defect with ventricular hypoplasia, Complete atrioventricular septal defect-tetralogy of fallot, Congenital heart defects, Double outlet right ventricle, Dysmorphic features, Endometrioma, Endometriosis, Hypoplastic left heart syndrome, Multiple congenital anomalies, Partial atrioventricular canal defect, Partial defect of atrioventricular canal, Patent ductus arteriosus, Pulmonary venous return anomaly, Situs ambiguus, Subfertility, Tetralogy of fallot, Transient ischemic attack, Ventricular septal defectView all (6 more) |
|
428
|
|
|
NK2 homeobox 1 |
BCH, BHC, NK-2, NKX2.1, NKX2A, NMTC1, T/EBP, TEBP, TITF1, TTF-1, TTF1 |
Agenesis of corpus callosum, Nonmedullary thyroid carcinoma, Anxiety disorder, Apraxia, Asthma, Atrial septal defect, Benign hereditary chorea, Brain-lung-thyroid syndrome, Congenital alveolar dysplasia, Chorea, Choreoathetosis, Choreoathetosis, hypothyroidism, and neonatal respiratory distress, Compensated hypothyroidism, Congenital hypothyroidism, Developmental delay, Dwarfism, Dysarthria, Dyskinesia, Dyssomnia, Hearing loss, Hereditary chorea, Hirschsprung disease, Huntington disease, Hypersomnia, Hypodontia, Hypoparathyroidism, Hypospadias, Hypothyroidism, Mental retardation, Lung carcinoma, Lung diseases, Macroglossia, Microcephaly, Motor delay, Movement disorders, Neck webbing, Neurodevelopmental disorders, Neuroendocrine cell hyperplasia, Obsessive-compulsive disorder, Papillary thyroid carcinoma, Patent foramen ovale, Pulmonary arterial hypertension, Pulmonary fibrosis, Respiratory failure, Rheumatic chorea, Schizophrenia, Sleep disorders, Thyroid agenesis, Thyroid cancer, Thyroid carcinoma, Thyroid hemiagenesis, Ventricular septal defect, Vesicoureteral refluxView all (38 more) |
|
429
|
|
|
Nuclear receptor subfamily 2 group E member 1 |
TLL, TLX, XTLL |
|
|
430
|
|
|
Nuclear receptor subfamily 2 group C member 1 |
TR2 |
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