Infantile Severe Myoclonic Epilepsy
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
63
|
32
|
0.030 |
None |
1.000 |
3 |
|
2007 |
2019 |
General Paralysis
|
disease |
Infections; Nervous System Diseases
|
Disease or Syndrome
|
12
|
3
|
0.030 |
None |
1.000 |
3 |
|
1996 |
2002 |
Epileptic Syndromes
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
46
|
2
|
0.030 |
None |
1.000 |
3 |
|
2012 |
2017 |
SEIZURES, BENIGN FAMILIAL INFANTILE, 5
|
disease |
|
Disease or Syndrome
|
2
|
6
|
0.700 |
None |
1.000 |
3 |
5
|
2014 |
2016 |
Hypercholesterolemia, Familial
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
203
|
1423
|
0.030 |
None |
1.000 |
3 |
|
1996 |
2007 |
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 |
Tremor
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Sign or Symptom
|
528
|
52
|
0.410 |
None |
0.500 |
2 |
1
|
2009 |
2009 |
Awakening Epilepsy
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
83
|
|
0.300 |
None |
1.000 |
2 |
|
2013 |
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 |
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 |
Impaired cognition
|
disease |
Mental Disorders
|
Mental or Behavioral Dysfunction
|
1630
|
348
|
0.120 |
None |
1.000 |
2 |
1
|
2006 |
2016 |
Global developmental delay
|
disease |
|
Mental or Behavioral Dysfunction
|
1825
|
553
|
0.120 |
None |
1.000 |
2 |
4
|
2016 |
2018 |
Hyperactive behavior
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Mental or Behavioral Dysfunction
|
1263
|
112
|
0.020 |
None |
1.000 |
2 |
1
|
2014 |
2015 |
Developmental delay (disorder)
|
phenotype |
Mental Disorders
|
Mental or Behavioral Dysfunction
|
584
|
68
|
0.020 |
None |
1.000 |
2 |
1
|
2016 |
2018 |
Epilepsy, Cryptogenic
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
88
|
4
|
0.300 |
None |
1.000 |
2 |
|
2013 |
2018 |
Static Tremor
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Sign or Symptom
|
62
|
3
|
0.310 |
None |
1.000 |
2 |
|
2009 |
2009 |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
57
|
43
|
0.020 |
None |
1.000 |
2 |
|
2016 |
2019 |
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 |
Sudden unexplained death in epilepsy
|
disease |
|
Disease or Syndrome
|
12
|
|
0.020 |
None |
1.000 |
2 |
|
2012 |
2018 |
Bipolar Disorder
|
disease |
Mental Disorders
|
Mental or Behavioral Dysfunction
|
1183
|
839
|
0.310 |
None |
1.000 |
2 |
|
2008 |
2010 |
CUI: |
C0236018 |
Disease: |
Aura
|
Aura
|
phenotype |
Nervous System Diseases
|
Finding
|
83
|
|
0.300 |
None |
1.000 |
2 |
|
2013 |
2018 |
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 |
Passive Tremor
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Sign or Symptom
|
9
|
|
0.300 |
None |
1.000 |
1 |
|
2009 |
2009 |