Brugada Syndrome (disorder)
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Disease or Syndrome
|
66
|
201
|
0.800 |
disputed |
0.929 |
14 |
16
|
1998 |
2019 |
Electrocardiogram: P-R interval
|
phenotype |
|
Finding
|
57
|
138
|
0.100 |
None |
1.000 |
11 |
11
|
2010 |
2019 |
Atrial Fibrillation
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
939
|
584
|
0.480 |
None |
0.909 |
11 |
6
|
2010 |
2018 |
Small Fiber Neuropathy
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
35
|
8
|
0.330 |
None |
1.000 |
5 |
2
|
2014 |
2019 |
EPISODIC PAIN SYNDROME, FAMILIAL, 2
|
disease |
|
Disease or Syndrome
|
1
|
2
|
0.700 |
None |
1.000 |
5 |
2
|
2005 |
2016 |
QRS complex feature
|
phenotype |
|
Finding
|
41
|
69
|
0.100 |
None |
1.000 |
2 |
2
|
2010 |
2016 |
Heart Function Tests
|
phenotype |
|
Diagnostic Procedure
|
17
|
27
|
0.100 |
None |
1.000 |
2 |
2
|
2010 |
2010 |
P wave duration (observable entity)
|
phenotype |
|
Clinical Attribute
|
10
|
18
|
0.100 |
None |
1.000 |
2 |
2
|
2014 |
2017 |
Multiple Sclerosis
|
disease |
Immune System Diseases; Nervous System Diseases
|
Disease or Syndrome
|
1800
|
1022
|
0.010 |
None |
1.000 |
1 |
2
|
2016 |
2016 |
CUI: |
C0030193 |
Disease: |
Pain
|
Pain
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
1554
|
196
|
0.030 |
None |
1.000 |
3 |
1
|
2014 |
2018 |
Heart Block
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
58
|
7
|
0.320 |
None |
1.000 |
3 |
1
|
2010 |
2015 |
Neuroblastoma
|
disease |
Neoplasms
|
Neoplastic Process
|
2509
|
386
|
0.020 |
None |
1.000 |
2 |
1
|
2016 |
2018 |
Inflammatory Bowel Diseases
|
group |
Digestive System Diseases
|
Disease or Syndrome
|
1577
|
605
|
0.020 |
None |
1.000 |
2 |
1
|
2018 |
2019 |
Central neuroblastoma
|
disease |
Neoplasms; Nervous System Diseases
|
Neoplastic Process
|
2419
|
231
|
0.020 |
None |
1.000 |
2 |
1
|
2016 |
2018 |
QT interval feature (observable entity)
|
phenotype |
|
Clinical Attribute
|
75
|
226
|
0.100 |
None |
1.000 |
2 |
1
|
2014 |
2019 |
Childhood Neuroblastoma
|
disease |
Neoplasms
|
Neoplastic Process
|
2420
|
231
|
0.020 |
None |
1.000 |
2 |
1
|
2016 |
2018 |
Hypertrophic Cardiomyopathy
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
560
|
635
|
0.010 |
None |
1.000 |
1 |
1
|
2015 |
2015 |
Erythromelalgia
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
14
|
5
|
0.010 |
None |
1.000 |
1 |
1
|
2016 |
2016 |
Electrocardiography
|
phenotype |
|
Diagnostic Procedure
|
8
|
16
|
0.100 |
None |
1.000 |
1 |
1
|
2010 |
2010 |
RESTING HEART RATE
|
phenotype |
|
Finding
|
80
|
134
|
0.100 |
None |
1.000 |
1 |
1
|
2016 |
2016 |
Diabetes Mellitus
|
group |
Nutritional and Metabolic Diseases; Endocrine System Diseases
|
Disease or Syndrome
|
2803
|
824
|
0.010 |
None |
1.000 |
1 |
1
|
2018 |
2018 |
Ventricular Fibrillation
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
96
|
19
|
0.400 |
None |
1.000 |
1 |
1
|
2010 |
2010 |
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder)
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
31
|
121
|
0.010 |
None |
1.000 |
1 |
1
|
2019 |
2019 |
Brugada Syndrome 1
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Disease or Syndrome
|
13
|
234
|
0.500 |
disputed |
1.000 |
9 |
|
1998 |
2017 |
Other specified cardiac arrhythmias
|
phenotype |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
12
|
|
0.300 |
disputed |
1.000 |
8 |
|
1998 |
2017 |