General Paralysis
|
disease |
Infections; Nervous System Diseases
|
Disease or Syndrome
|
12
|
3
|
0.030 |
None |
1.000 |
3 |
|
1996 |
2002 |
Dystonia Disorders
|
group |
Nervous System Diseases
|
Disease or Syndrome
|
167
|
37
|
0.030 |
None |
1.000 |
3 |
|
1997 |
2003 |
Infantile Severe Myoclonic Epilepsy
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
63
|
32
|
0.030 |
None |
1.000 |
3 |
|
2007 |
2019 |
SEIZURES, BENIGN FAMILIAL INFANTILE, 5
|
disease |
|
Disease or Syndrome
|
2
|
6
|
0.700 |
None |
1.000 |
3 |
5
|
2014 |
2016 |
Epileptic Syndromes
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
46
|
2
|
0.030 |
None |
1.000 |
3 |
|
2012 |
2017 |
Absence Epilepsy
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
89
|
17
|
0.020 |
None |
1.000 |
2 |
|
2009 |
2015 |
Epilepsy, Temporal Lobe
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
354
|
33
|
0.020 |
None |
1.000 |
2 |
|
2017 |
2018 |
Status Epilepticus
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Disease or Syndrome
|
533
|
12
|
0.410 |
None |
1.000 |
2 |
|
2009 |
2018 |
Erythema
|
phenotype |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
227
|
8
|
0.020 |
None |
1.000 |
2 |
|
1981 |
2019 |
Epilepsy, Cryptogenic
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
88
|
4
|
0.300 |
None |
1.000 |
2 |
|
2013 |
2018 |
Hyperlipoproteinemia Type IIa
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
201
|
661
|
0.020 |
None |
1.000 |
2 |
|
1996 |
1996 |
Awakening Epilepsy
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
83
|
|
0.300 |
None |
1.000 |
2 |
|
2013 |
2018 |
Sudden unexplained death in epilepsy
|
disease |
|
Disease or Syndrome
|
12
|
|
0.020 |
None |
1.000 |
2 |
|
2012 |
2018 |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
57
|
43
|
0.020 |
None |
1.000 |
2 |
|
2016 |
2019 |
COGNITIVE IMPAIRMENT WITH OR WITHOUT CEREBELLAR ATAXIA
|
disease |
|
Disease or Syndrome
|
1
|
4
|
0.600 |
None |
1.000 |
2 |
4
|
2012 |
2016 |
Epileptic Seizures
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Disease or Syndrome
|
250
|
7
|
0.020 |
None |
1.000 |
2 |
1
|
2014 |
2016 |
Amyotrophic Lateral Sclerosis
|
disease |
Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
1114
|
485
|
0.100 |
None |
1.000 |
1 |
1
|
2007 |
2007 |
Arthrogryposis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Disease or Syndrome
|
198
|
33
|
0.010 |
None |
1.000 |
1 |
|
2006 |
2006 |
Asthma
|
disease |
Respiratory Tract Diseases; Immune System Diseases
|
Disease or Syndrome
|
2096
|
1536
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Atrial Fibrillation
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
939
|
584
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Bone Diseases, Developmental
|
group |
Musculoskeletal Diseases
|
Disease or Syndrome
|
82
|
2
|
0.010 |
None |
1.000 |
1 |
|
2008 |
2008 |
Bronchopulmonary Dysplasia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases
|
Disease or Syndrome
|
423
|
112
|
0.010 |
None |
1.000 |
1 |
|
2008 |
2008 |
Cardiovascular Diseases
|
group |
Cardiovascular Diseases
|
Disease or Syndrome
|
1756
|
711
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Cerebral Palsy
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
241
|
69
|
0.010 |
None |
1.000 |
1 |
|
2015 |
2015 |
Dermatitis
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
496
|
16
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |