|
951
|
|
|
Cytosolic arginine sensor for mTORC1 subunit 1 |
GATSL3 |
|
|
952
|
|
|
Cytochrome P450 family 4 subfamily F member 12 |
CYPIVF12, F22329_1 |
|
|
953
|
|
|
Calpain 15 |
OGIN, SOLH |
|
|
954
|
|
|
- |
- |
Wolff-parkinson-white syndrome, Breast cancer, Central visual impairment, Colorectal cancer, Congestive heart failure, Dementia, Diabetes mellitus, Epileptic encephalopathy, Hemianopsia, Hereditary leber optic atrophy, Histiocytoid cardiomyopathy, Hypertension, Left ventricular hypertrophy, Leigh syndrome, Melas syndrome, Migraine, Mitochondrial encephalomyopathy, Mitochondrial myopathy, Myopathy, Nervous system diseases, Optic atrophy, Ovarian neoplasm, Polyneuropathy, Retinal telangiectasia, Seizure, Sensorineural hearing loss, Ventricular preexcitationView all (12 more) |
|
955
|
|
|
- |
- |
Addison`s disease, Wolff-parkinson-white syndrome, Anorexia, Anxiety disorder, Aortic aneurysm, Aortic dissection, Aphasia, Arthrogryposis multiplex congenita, Attention deficit hyperactivity disorder, Autism, Cataract, Central visual impairment, Cerebral cortical atrophy, Congestive heart failure, Cytochrome-c oxidase deficiency, Dementia, Developmental regression, Diabetes mellitus, Dwarfism, Dysarthria, Epilepsy, Epileptic encephalopathy, Gastroparesis, Hallucinations, Hearing loss, Heart block, Hematomas, Hemianopsia, Hereditary leber optic atrophy, Hypertension, Hyperthyroidism, Hypertrophic cardiomyopathy, Hypoparathyroidism, Hypopituitarism, Hypothyroidism, Ichthyosis, Intestinal obstruction, Left ventricular hypertrophy, Leigh syndrome, Malabsorption syndrome, Malformation of cortical development, Melas syndrome, Mental depression, Microcephaly, Migraine, Mitochondrial encephalopathy, Mitochondrial myopathy, Multiple lipomata, Myopathy, Nephrotic syndrome, Nervous system diseases, Nyctalopia, Optic atrophy, Pancreatitis, Polyneuropathy, Psychosis, Ptosis, Pulmonary arterial hypertension, Renal glomerular disease, Renal insufficiency, Retinal telangiectasia, Seizure, Sensorineural hearing loss, Tetralogy of fallot, Thyroiditis, Ventricular preexcitationView all (51 more) |
|
956
|
|
|
- |
- |
Addison`s disease, Anorexia, Anxiety disorder, Aortic aneurysm, Aortic dissection, Aphasia, Arthrogryposis multiplex congenita, Attention deficit hyperactivity disorder, Autism, Cataract, Central visual impairment, Cerebral cortical atrophy, Colorectal cancer, Congestive heart failure, Cytochrome-c oxidase deficiency, Dementia, Developmental regression, Diabetes mellitus, Dwarfism, Dysarthria, Epileptic encephalopathy, Gastroparesis, Hallucinations, Hearing loss, Heart block, Hematomas, Hemianopsia, Hypertension, Hyperthyroidism, Hypertrophic cardiomyopathy, Hypoparathyroidism, Hypopituitarism, Hypothyroidism, Ichthyosis, Intestinal obstruction, Left ventricular hypertrophy, Malabsorption syndrome, Malformation of cortical development, Melas syndrome, Mental depression, Microcephaly, Migraine, Mitochondrial diseases, Mitochondrial myopathy, Multiple lipomata, Myopathy, Nephrotic syndrome, Neuroblastoma, Nyctalopia, Optic atrophy, Pancreatitis, Psychosis, Ptosis, Pulmonary arterial hypertension, Renal glomerular disease, Renal insufficiency, Seizure, Sensorineural hearing loss, Tetralogy of fallot, Thyroiditis, Wolff-parkinson-white syndromeView all (46 more) |
|
957
|
|
|
- |
- |
Addison`s disease, Anaplastic carcinoma, Wolff-parkinson-white syndrome, Anorexia, Anxiety disorder, Aortic aneurysm, Aortic dissection, Aphasia, Arthrogryposis multiplex congenita, Attention deficit hyperactivity disorder, Autism, Carcinoma, Cardiomyopathy, Cataract, Central visual impairment, Cerebral cortical atrophy, Colorectal cancer, Congestive heart failure, Cytochrome-c oxidase deficiency, Deafness, nonsyndromic sensorineural, mitochondrial, Dementia, Developmental regression, Diabetes mellitus, Dwarfism, Dysarthria, Epileptic encephalopathy, Gastroparesis, Hallucinations, Hearing loss, Heart block, Hematomas, Hemianopsia, Hereditary leber optic atrophy, Hypertension, Hyperthyroidism, Hypertrophic cardiomyopathy, Hypoparathyroidism, Hypopituitarism, Hypothyroidism, Ichthyosis, Intestinal obstruction, Left ventricular hypertrophy, Malabsorption syndrome, Malformation of cortical development, Melas syndrome, Mental depression, Microcephaly, Migraine, Mitochondrial myopathy, Multiple lipomata, Myocardial diseases, Myopathy, Nephrotic syndrome, Nervous system diseases, Nyctalopia, Optic atrophy, Palmoplantar keratoderma with deafness, Pancreatitis, Psychosis, Ptosis, Pulmonary arterial hypertension, Renal glomerular disease, Renal insufficiency, Retinal telangiectasia, Seizure, Sensorineural hearing loss, Tetralogy of fallot, Thyroiditis, Ventricular preexcitationView all (54 more) |
|
958
|
|
|
CD27 antisense RNA 1 |
- |
|
|
959
|
|
|
Cyclin dependent kinase like 5 |
CFAP247, DEE2, EIEE2, ISSX, STK9 |
Angelman syndrome, Autism, Camptodactyly of fingers, Central visual impairment, Cerebellar atrophy, Cerebral cortical atrophy, Choreoathetosis, Clonic seizures, Colorectal cancer, Congenital exomphalos, Cyclin-dependent kinase-like 5 deficiency, Developmental delay, Developmental regression, Dyskinetic syndrome, Dysmorphic features, Dyssomnia, Epilepsy, Epileptic encephalopathy, Episodic ataxia, Febrile seizures, Focal clonic seizures, Focal seizures, Focal tonic seizures, Gastroesophageal reflux disease, Hypoplasia of corpus callosum, Hypotonic seizures, Infantile spasms, Jacksonian seizure, Macrostomia, Macrotia, Mental retardation, Metastatic melanoma, Microcephaly, Movement disorders, Myoclonic seizures, Nephrolithiasis, Neurodevelopmental disorders, Nicolaides baraitser syndrome, Oropharyngeal dysphagia, Ovarian serous adenocarcinoma, Pachygyria, Penis agenesis, Precocious puberty, Renal dysplasia, Retinal dystrophy, Retinoschisis, Retinoschisis, x-linked, Rett syndrome, Scoliosis, Seizure, Sleep disorders, Spasms syndrome, Spasms x-linked, Stereotyped behavior, Stereotypy, Strabismus, Syndactyly of the toes, Ureterocele, Ventricular septal defect, Vesicoureteral reflux, West syndromeView all (46 more) |
|
960
|
|
|
Contactin 2 |
AXT, EPEO5, FAME5, TAG-1, TAX, TAX1 |
|
