121
|
|
|
Sodium channel and clathrin linker 1 |
CAP-1A, CAP1A |
Astigmatism, Bardet-biedl syndrome, Obstructive pulmonary disease, Ciliopathy, Color vision deficiency, Cone-rod dystrophy, Global developmental delay, Hyperopia, Nystagmus, Optic atrophy, Orofaciodigital syndrome, Retinitis pigmentosa, Senior-loken syndrome |
122
|
|
|
Selenocysteine lyase |
SCL, hSCL |
|
123
|
|
|
Scm polycomb group protein homolog 1 |
Scml3 |
|
124
|
|
|
Scm polycomb group protein like 2 |
- |
|
125
|
|
|
Scm polycomb group protein like 4 |
dJ47M23.1 |
|
126
|
|
|
Sodium voltage-gated channel alpha subunit 10 |
FEPS2, Nav1.8, PN3, SNS |
Atrial fibrillation, Atrial flutter, Atrioventricular block, Autism, Brugada syndrome, Cardiac arrhythmia, Congenital insensitivity to pain, Episodic pain syndrome, Long qt syndrome, Sick sinus syndrome, Hyperalgesia, Migraine, Orofacial cleft, Paroxysmal extreme pain disorder, Erythromelalgia, Systemic lupus erythematosus, Hypertension, Ventricular fibrillationView all (3 more) |
127
|
|
|
Sodium voltage-gated channel alpha subunit 11 |
FEPS3, HSAN7, NAV1.9, NaN, PN5, SCN12A, SNS-2 |
Hereditary sensory and autonomic neuropathy, Charcot-marie-tooth disease, Congenital insensitivity to pain, Congenital pain insensitivity, Dominantly inherited sensory neuropathy, Episodic pain syndrome, Motor neuron disease, Hyperalgesia, Migraine, Osteoarthritis, Paroxysmal extreme pain disorder, Erythromelalgia, Sensory neuropathy |
128
|
|
|
Sodium voltage-gated channel alpha subunit 1 |
DEE6, DEE6A, DEE6B, DRVT, EIEE6, FEB3, FEB3A, FHM3, GEFSP2, HBSCI, NAC1, Nav1.1, SCN1, SMEI |
Arthrogryposis, Atrial fibrillation, Autism, Clinodactyly, Congenital joint contractures, Developmental and epileptic encephalopathy, Dravet syndrome, Myoclonic epilepsy, Epilepsy, Epilepsy of infancy with migrating focal seizures, Epilepsy with myoclonic atonic seizures, Generalized epilepsy, Rolandic epilepsy, Febrile convulsion, Focal onset epileptic seizure, Generalized epilepsy with febrile seizures plus, Global developmental delay, Hemiplegic migraine, Intellectual developmental disorder, Lennox-gastaut syndrome, Malignant migrating partial seizures of infancy, Migraine, Intellectual disability, Movement disorder, Neurodevelopmental disorder, Obesity, Partial epilepsy, Seizures, West syndromeView all (14 more) |
129
|
|
|
Sodium voltage-gated channel beta subunit 1 |
ATFB13, BRGDA5, DEE52, EIEE52, GEFSP1 |
Atrial fibrillation, Brugada syndrome, Cardiac arrhythmia, Cardiac conduction disease, Cardiomyopathy, Childhood absence epilepsy, Conduction disorder of the heart, Developmental and epileptic encephalopathy, Dravet syndrome, Rolandic epilepsy, Febrile convulsion, Generalized epilepsy with febrile seizures plus, Hereditary atrial fibrillation, Hereditary bundle branch system defect, Long qt syndrome, Seizures, Ventricular fibrillationView all (2 more) |
130
|
|
|
Sodium voltage-gated channel alpha subunit 2 |
BFIC3, BFIS3, BFNIS, DEE11, EA9, EIEE11, HBA, HBSCI, HBSCII, NAC2, Na(v)1.2, Nav1.2, SCN2A1, SCN2A2 |
Attention deficit hyperactivity disorder, Autism, Benign infantile epilepsy, Benign neonatal-infantile seizures, Benign neonatal epilepsy, Bipolar disorder, Neurodevelopmental disorder, Bipolar depression, Developmental and epileptic encephalopathy, Developmental disability, Dravet syndrome, Dystonia, Partial epilepsy, Epilepsy, Epilepsy of infancy with migrating focal seizures, Pyridoxine dependent epilepsy, Rolandic epilepsy, Episodic ataxia, Febrile convulsion, Generalized epilepsy with febrile seizures plus, Global developmental delay, Hemiplegia, Intellectual developmental disorder, Lennox-gastaut syndrome, Malignant migrating partial seizures of infancy, Metabolic syndrome, Movement disorder, Non-specific syndromic intellectual disability, Parkinson disease, Periodontitis, Seizures, Spastic ataxia, Substance abuse, Diabetes mellitus type 2, West syndromeView all (20 more) |
