|
| Entrez Id: |
6323 |
| Gene Symbol: |
SCN1A |
SCN1A
|
0.310 |
Biomarker
|
disease |
CTD_human |
De novo variants in neurodevelopmental disorders with epilepsy.
|
29942082 |
2018 |
|
| Entrez Id: |
6323 |
| Gene Symbol: |
SCN1A |
SCN1A
|
0.310 |
Biomarker
|
disease |
CTD_human |
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.
|
23708187 |
2013 |
|
| Entrez Id: |
6323 |
| Gene Symbol: |
SCN1A |
SCN1A
|
0.310 |
GeneticVariation
|
disease |
BEFREE |
Polymorphisms of the SCN1A gene in children and adolescents with primary headache and idiopathic or cryptogenic epilepsy: is there a linkage?
|
21713554 |
2011 |
|
| Entrez Id: |
6323 |
| Gene Symbol: |
SCN1A |
SCN1A
|
0.310 |
Biomarker
|
disease |
CTD_human |
Differential role of sodium channels SCN1A and SCN2A gene polymorphisms with epilepsy and multiple drug resistance in the north Indian population.
|
19694741 |
2009 |
|
| Entrez Id: |
6323 |
| Gene Symbol: |
SCN1A |
SCN1A
|
0.310 |
Biomarker
|
disease |
CTD_human |
Genetic predictors of the maximum doses patients receive during clinical use of the anti-epileptic drugs carbamazepine and phenytoin.
|
15805193 |
2005 |
|
| Entrez Id: |
3756 |
| Gene Symbol: |
KCNH1 |
KCNH1
|
0.300 |
Biomarker
|
disease |
CTD_human |
De novo variants in neurodevelopmental disorders with epilepsy.
|
29942082 |
2018 |
|
| Entrez Id: |
79868 |
| Gene Symbol: |
ALG13 |
ALG13
|
0.300 |
Biomarker
|
disease |
CTD_human |
De novo variants in neurodevelopmental disorders with epilepsy.
|
29942082 |
2018 |
|
| Entrez Id: |
8243 |
| Gene Symbol: |
SMC1A |
SMC1A
|
0.300 |
Biomarker
|
disease |
CTD_human |
De novo variants in neurodevelopmental disorders with epilepsy.
|
29942082 |
2018 |
|
| Entrez Id: |
1106 |
| Gene Symbol: |
CHD2 |
CHD2
|
0.300 |
Biomarker
|
disease |
CTD_human |
De novo variants in neurodevelopmental disorders with epilepsy.
|
29942082 |
2018 |
|
| Entrez Id: |
80816 |
| Gene Symbol: |
ASXL3 |
ASXL3
|
0.300 |
Biomarker
|
disease |
CTD_human |
De novo variants in neurodevelopmental disorders with epilepsy.
|
29942082 |
2018 |
|
| Entrez Id: |
6812 |
| Gene Symbol: |
STXBP1 |
STXBP1
|
0.300 |
Biomarker
|
disease |
CTD_human |
De novo variants in neurodevelopmental disorders with epilepsy.
|
29942082 |
2018 |
|
| Entrez Id: |
57492 |
| Gene Symbol: |
ARID1B |
ARID1B
|
0.300 |
Biomarker
|
disease |
CTD_human |
De novo variants in neurodevelopmental disorders with epilepsy.
|
29942082 |
2018 |
|
| Entrez Id: |
1654 |
| Gene Symbol: |
DDX3X |
DDX3X
|
0.300 |
Biomarker
|
disease |
CTD_human |
De novo variants in neurodevelopmental disorders with epilepsy.
|
29942082 |
2018 |
|
| Entrez Id: |
1759 |
| Gene Symbol: |
DNM1 |
DNM1
|
0.300 |
Biomarker
|
disease |
CTD_human |
De novo variants in neurodevelopmental disorders with epilepsy.
|
29942082 |
2018 |
|
| Entrez Id: |
8831 |
| Gene Symbol: |
SYNGAP1 |
SYNGAP1
|
0.300 |
Biomarker
|
disease |
CTD_human |
De novo variants in neurodevelopmental disorders with epilepsy.
|
29942082 |
2018 |
|
| Entrez Id: |
6529 |
| Gene Symbol: |
SLC6A1 |
SLC6A1
|
0.300 |
Biomarker
|
disease |
CTD_human |
De novo variants in neurodevelopmental disorders with epilepsy.
|
29942082 |
2018 |
|
| Entrez Id: |
340533 |
| Gene Symbol: |
NEXMIF |
NEXMIF
|
0.300 |
Biomarker
|
disease |
CTD_human |
De novo variants in neurodevelopmental disorders with epilepsy.
|
29942082 |
2018 |
|
| Entrez Id: |
11152 |
| Gene Symbol: |
WDR45 |
WDR45
|
0.300 |
Biomarker
|
disease |
CTD_human |
De novo variants in neurodevelopmental disorders with epilepsy.
|
29942082 |
2018 |
|
| Entrez Id: |
4208 |
| Gene Symbol: |
MEF2C |
MEF2C
|
0.300 |
Biomarker
|
disease |
CTD_human |
De novo variants in neurodevelopmental disorders with epilepsy.
|
29942082 |
2018 |
|
| Entrez Id: |
2775 |
| Gene Symbol: |
GNAO1 |
GNAO1
|
0.300 |
Biomarker
|
disease |
CTD_human |
De novo variants in neurodevelopmental disorders with epilepsy.
|
29942082 |
2018 |
|
| Entrez Id: |
2904 |
| Gene Symbol: |
GRIN2B |
GRIN2B
|
0.300 |
Biomarker
|
disease |
CTD_human |
De novo variants in neurodevelopmental disorders with epilepsy.
|
29942082 |
2018 |
|
| Entrez Id: |
7040 |
| Gene Symbol: |
TGFB1 |
TGFB1
|
0.300 |
Biomarker
|
disease |
CTD_human |
Human TGF-β1 deficiency causes severe inflammatory bowel disease and encephalopathy.
|
29483653 |
2018 |
|
| Entrez Id: |
29123 |
| Gene Symbol: |
ANKRD11 |
ANKRD11
|
0.300 |
Biomarker
|
disease |
CTD_human |
De novo variants in neurodevelopmental disorders with epilepsy.
|
29942082 |
2018 |
|
| Entrez Id: |
1917 |
| Gene Symbol: |
EEF1A2 |
EEF1A2
|
0.300 |
Biomarker
|
disease |
CTD_human |
De novo variants in neurodevelopmental disorders with epilepsy.
|
29942082 |
2018 |
|
| Entrez Id: |
2290 |
| Gene Symbol: |
FOXG1 |
FOXG1
|
0.300 |
Biomarker
|
disease |
CTD_human |
De novo variants in neurodevelopmental disorders with epilepsy.
|
29942082 |
2018 |