|
661
|
|
|
Sodium voltage-gated channel alpha subunit 3 |
DEE62, EIEE62, FFEVF4, NAC3, Nav1.3 |
Arthritis, Attention deficit hyperactivity disorder, Autism, Cerebral atrophy, Cryptogenic partial complex epilepsy, Developmental delay, Developmental regression, Dwarfism, Dysautonomia, Dyskinetic syndrome, Dysphagia, Epilepsy, Epileptic encephalopathy, Gastroesophageal reflux disease, Hypodontia, Hypoplasia of corpus callosum, Mental retardation, Microcephaly, Non-specifi epileptic encephalopathy, Nystagmus, Optic atrophy, Polymicrogyria, Ptosis, Spastic quadriplegia, Status epilepticusView all (10 more) |
|
662
|
|
|
Sodium voltage-gated channel alpha subunit 4 |
CMS16, CMYO22A, CMYP22A, HOKPP2, HYKPP, HYPP, NAC1A, Na(V)1.4, Nav1.4, SkM1 |
Adrenocortical adenoma, Asthma, Atrial septal defect, Blepharospasm, Bowel incontinence, Cerebral palsy, Congenital epicanthus, Myasthenic syndrome, Congenital myopathy, Congenital myotonia, Congestive heart failure, Developmental delay, Dwarfism, Dysphagia, External ophthalmoplegia, Facial paralysis, High palate, Hyperkalemic periodic paralysis, Hypokalemic periodic paralysis, Hypothyroidism, Laryngospasm, Mental retardation, Motor delay, Myasthenia gravis, Myopathy, Myotonia congenita, Myotonia fluctuans, Myotonia levior, Myotonia permanens, Myotonic disorders, Hypotonia, Normokalemic periodic paralysis, Paradoxical myotonia, Paramyotonia congenita, Paramyotonia congenita of von eulenburg, Paramyotonia congenita without cold paralysis, Paramyotonia congenita/myotonia congenita, Periodic hypokalemic paresis, Periodic paralysis, Ptosis, Respiratory failure, Schizophrenia, Ventricular septal defectView all (28 more) |
|
663
|
|
|
Sodium voltage-gated channel beta subunit 4 |
ATFB17, LQT10, Navbeta4 |
|
|
664
|
|
|
Sodium voltage-gated channel alpha subunit 5 |
CDCD2, CMD1E, CMPD2, HB1, HB2, HBBD, HH1, ICCD, IVF, LQT3, Nav1.5, PFHB1, SSS1, VF1 |
Arrhythmogenic right ventricular cardiomyopathy, Arthrogryposis multiplex congenita, Atrial fibrillation, Atrial standstill, Atrioventricular block, Brugada syndrome, Bundle branch block, Cardiac conduction disease, Cardiomyopathy, Congenital long qt syndrome, Congestive heart failure, Dilated cardiomyopathy, Dysautonomia, Hearing loss, Hereditary bundle branch system defect, Idiopathic ventricular fibrillation, Left anterior fascicular block, Left bundle-branch block, Left posterior fascicular block, Left ventricular noncompaction, Lipoatrophy, Lipodystrophy, Long qt syndrome, Long qt syndrome digenic, Multiple congenital anomalies, Myopathy, Nonprogressive cardiac conduction defect, Nonprogressive heart block, Palmoplantar keratoderma, Paroxysmal atrial fibrillation, Paroxysmal ventricular fibrillation, Paroxysmal ventricular tachycardia, Progressive cardiac conduction defect, Romano-ward syndrome, Sick sinus syndrome, Sinus node dysfunction, Stroke, Supraventricular tachycardia, Torsades de pointes, Trifascicular block, Ventricular fibrillation, Ventricular tachycardia, Wolff-parkinson-white syndromeView all (28 more) |
|
665
|
|
|
Sodium voltage-gated channel alpha subunit 7 |
NaG, Nav2.1, Nav2.2, SCN6A |
|
|
666
|
|
|
Sodium voltage-gated channel alpha subunit 8 |
BFIS5, CERIII, CIAT, DEE13, EIEE13, MED, MYOCL2, NaCh6, Nav1.6, PN4 |
Amyotrophic lateral sclerosis, Attention deficit hyperactivity disorder, Autism, Benign epilepsy, Bipolar disorder, Bowel incontinence, Brachycephaly, Bulbar palsy, Cerebellar atrophy, Cerebral atrophy, Choreoathetosis, Cognitive impairment with or without cerebellar ataxia, Convulsions and choreoathetosis, Developmental delay, Developmental regression, Dwarfism, Dyscognitive seizures, Dyskinesia, Dyskinetic syndrome, Dysmorphic features, Dysphagia, Dysphasia, Epilepsy, Epilepsy with encephalopathy, Epileptic encephalopathy, Febrile seizures, Frontal bossing, Gastroesophageal reflux disease, Grand mal status epilepticus, Hallucinations, Hypodontia, Impaired cognition, Infantile convulsions and choreoathetosis, Mental retardation, Keratoconjunctivitis sicca, Leukoencephalopathy, Microcephaly, Micrognathism, Migraine, Movement disorders, Nervous system disorder, Neurodevelopmental disorders, Non-specifi epileptic encephalopathy, Nonconvulsive status epilepticus, Nystagmus, Optic atrophy, Paroxysmal nonkinesigenic dyskinesia, Petit mal status, Precocious puberty, Ptosis, Rubral tremor, Salaam seizures, Seizure, Sleep apnea, Spasms x-linked, Status epilepticus, Stereotyped behavior, Syndactyly of the toesView all (43 more) |
|
667
|
|
|
Sodium voltage-gated channel alpha subunit 9 |
ETHA, FEB3B, GEFSP7, HSAN2D, NE-NA, NENA, Nav1.7, PN1, SFNP |
Acrosteolysis, Anhidrosis, Anxiety disorder, Autism, Bilateral convulsive seizures, Central visual impairment, Cerebral atrophy, Congenital pain insensitivity, Cortical dysplasia, Developmental delay, Developmental regression, Drachtman weinblatt sitarz syndrome, Dravet syndrome, Dysautonomia, Dyscognitive seizures, Dysosteosclerosis, Epilepsy, Epilepsy with febrile seizures plus, Epileptic encephalopathy, Erythermalgia, Erythromelalgia, Febrile seizures, Focal clonic seizures, Gastroesophageal reflux disease, Generalized epilepsy with febrile seizures plus, Hereditary sensory and autonomic neuropathy, Hypohidrosis, Hypotonic seizures, Impaired cognition, Keratoconjunctivitis sicca, Leukemia, Motor delay, Myoclonic astatic epilepsy, Myoclonic encephalopathy, Myoclonic epilepsy, Myoclonic seizures, Myotonia levior, Nervous system diseases, Neuropathy, Obtundation status, Paronychia inflammation, Paroxysmal extreme pain disorder, Seizure, Sensory neuropathy, hereditary, Small fiber neuropathy, Sodium channelopathy-related small fiber neuropathy, Status epilepticus, VasculitisView all (33 more) |
|
668
|
|
|
Sodium voltage-gated channel alpha subunit 10 |
FEPS2, Nav1.8, PN3, SNS |
Atrial fibrillation, Atrioventricular block, Brugada syndrome, Bundle branch block, Cardiac conduction disease, Congenital pain insensitivity, Dysautonomia, Episodic pain syndrome, Erythermalgia, Erythromelalgia, Heart block, Hereditary sensory and autonomic neuropathy, Leukemia, Nervous system diseases, Paroxysmal atrial fibrillation, Paroxysmal extreme pain disorder, Paroxysmal ventricular tachycardia, Romano-ward syndrome, Sick sinus syndrome, Sinus node dysfunction, Small fiber neuropathy, Sodium channelopathy-related small fiber neuropathy, Supraventricular tachycardia, Torsades de pointes, Trifascicular block, Vasculitis, Ventricular fibrillationView all (12 more) |
|
669
|
|
|
Sodium channel epithelial 1 subunit alpha |
BESC2, ENaCa, ENaCalpha, LIDLS3, PHA1B1, SCNEA, SCNN1 |
Bronchiectasis, Brugada syndrome, Neoplasm, Ciliopathies, Cystic fibrosis, Cystic fibrosis of pancreas, Embryonal neoplasm, Bronchitis, Tumor, Hyperaldosteronism, Hyperpotassemia and hypertension, Hypertension, Kidney disease, Liddle syndrome, Lung diseases, Metabolic alkalosis, Myocardial infarction, Sclerocystic ovaries, Polycystic ovary syndrome, Pseudohypoaldosteronism, Pulmonary cystic fibrosis, Renal insufficiencyView all (7 more) |
|
670
|
|
|
Sodium channel epithelial 1 subunit beta |
BESC1, ENaCb, ENaCbeta, LIDLS1, PHA1B2, SCNEB, beta-ENaC, beta-NaCH |
Bartter syndrome, Breast cancer, Bronchiectasis, Ciliopathies, Colorectal cancer, Cystic fibrosis, Cystic fibrosis of pancreas, Bronchitis, Hyperaldosteronism, Hyperpotassemia and hypertension, Hypertension, Hypokalemia, Kidney disease, Liddle syndrome, Lung diseases, Metabolic alkalosis, Myocardial infarction, Pseudohypoaldosteronism, Pulmonary cystic fibrosis, Renal insufficiencyView all (5 more) |
