EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 1
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
1
|
67
|
0.600 |
strong |
1.000 |
19 |
67
|
1999 |
2016 |
Liver carcinoma
|
disease |
Digestive System Diseases; Neoplasms
|
Neoplastic Process
|
5725
|
942
|
0.500 |
None |
1.000 |
11 |
2
|
2011 |
2019 |
Hepatitis C
|
disease |
Digestive System Diseases; Infections
|
Disease or Syndrome
|
1768
|
347
|
0.050 |
None |
1.000 |
5 |
2
|
2011 |
2019 |
Hepatitis C, Chronic
|
disease |
Digestive System Diseases; Infections
|
Disease or Syndrome
|
430
|
80
|
0.120 |
None |
1.000 |
3 |
2
|
2011 |
2016 |
Intelligence
|
phenotype |
Behavior and Behavior Mechanisms
|
Mental Process
|
645
|
2093
|
0.100 |
None |
1.000 |
1 |
1
|
2012 |
2012 |
Epilepsies, Partial
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
73
|
23
|
0.100 |
None |
0.952 |
21 |
|
2013 |
2020 |
Epilepsy, Partial, with Variable Foci
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
8
|
24
|
0.770 |
definitive |
1.000 |
19 |
24
|
2013 |
2019 |
Seizures
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Sign or Symptom
|
2152
|
553
|
0.150 |
None |
1.000 |
9 |
4
|
2013 |
2020 |
Familial (FPAH)
|
disease |
|
Disease or Syndrome
|
1075
|
276
|
0.060 |
None |
1.000 |
6 |
|
2013 |
2018 |
Autosomal Dominant Nocturnal Frontal Lobe Epilepsy
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
17
|
8
|
0.310 |
None |
1.000 |
3 |
|
2013 |
2014 |
Autosomal Dominant Lateral Temporal Lobe Epilepsy
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders
|
Disease or Syndrome
|
8
|
4
|
0.300 |
None |
1.000 |
2 |
|
2013 |
2013 |
Epilepsy
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
1215
|
339
|
0.100 |
None |
0.929 |
14 |
2
|
2014 |
2020 |
Congenital anomaly of brain
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Nervous System Diseases
|
Congenital Abnormality
|
103
|
7
|
0.040 |
None |
1.000 |
4 |
|
2014 |
2019 |
Malformations of Cortical Development
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Disease or Syndrome
|
60
|
5
|
0.030 |
None |
1.000 |
3 |
|
2014 |
2019 |
Virus Diseases
|
group |
Infections
|
Disease or Syndrome
|
1471
|
42
|
0.020 |
None |
1.000 |
2 |
|
2014 |
2016 |
Congenital Abnormality
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Congenital Abnormality
|
1098
|
73
|
0.020 |
None |
1.000 |
2 |
|
2014 |
2017 |
Temporal epilepsy, familial
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
2
|
|
0.020 |
None |
1.000 |
2 |
|
2014 |
2015 |
Hepatitis B
|
disease |
Digestive System Diseases; Infections
|
Disease or Syndrome
|
1449
|
519
|
0.020 |
None |
1.000 |
2 |
|
2014 |
2015 |
Liver Cirrhosis
|
disease |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases
|
Disease or Syndrome
|
1182
|
189
|
0.020 |
None |
1.000 |
2 |
2
|
2014 |
2016 |
Liver diseases
|
group |
Digestive System Diseases
|
Disease or Syndrome
|
1019
|
100
|
0.020 |
None |
1.000 |
2 |
|
2014 |
2016 |
BAND HETEROTOPIA
|
disease |
|
Disease or Syndrome
|
5
|
4
|
0.010 |
None |
1.000 |
1 |
|
2014 |
2014 |
Fleck corneal dystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
104
|
12
|
0.070 |
None |
1.000 |
7 |
|
2015 |
2020 |
Focal cortical dysplasia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Disease or Syndrome
|
44
|
|
0.050 |
None |
1.000 |
5 |
|
2015 |
2020 |
Neoplasms
|
group |
Neoplasms
|
Neoplastic Process
|
10161
|
1644
|
0.030 |
None |
1.000 |
3 |
|
2015 |
2019 |
Hemimegalencephaly
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
39
|
4
|
0.130 |
None |
1.000 |
3 |
|
2015 |
2019 |