Polymorphic Ventricular Tachycardia by ECG Finding
|
phenotype |
|
Finding
|
1
|
|
0.100 |
None |
|
0 |
|
|
|
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 5, WITH OR WITHOUT MUSCLE WEAKNESS
|
disease |
|
Disease or Syndrome
|
2
|
5
|
0.700 |
None |
1.000 |
3 |
5
|
2012 |
2017 |
Hereditary and idiopathic neuropathy, unspecified
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
3
|
6
|
0.100 |
None |
1.000 |
1 |
1
|
2017 |
2017 |
NEUROPATHY, CONGENITAL HYPOMYELINATING, 3
|
disease |
|
Disease or Syndrome
|
4
|
13
|
0.100 |
None |
1.000 |
1 |
1
|
2017 |
2017 |
NEUROPATHY, CONGENITAL HYPOMYELINATING, 2
|
disease |
|
Disease or Syndrome
|
5
|
9
|
0.100 |
None |
1.000 |
1 |
1
|
2017 |
2017 |
MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA (disorder)
|
disease |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
11
|
20
|
0.010 |
None |
1.000 |
1 |
|
2007 |
2007 |
Ventricular tachycardia, polymorphic
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
11
|
11
|
0.100 |
None |
|
0 |
|
|
|
Multi-core congenital myopathy
|
disease |
Musculoskeletal Diseases; Nervous System Diseases
|
Congenital Abnormality
|
16
|
|
0.010 |
None |
1.000 |
1 |
|
2007 |
2007 |
Abnormal cardiac exercise stress test
|
phenotype |
|
Finding
|
16
|
|
0.100 |
None |
|
0 |
|
|
|
Abnormal T-wave
|
phenotype |
|
Finding
|
20
|
|
0.100 |
None |
|
0 |
|
|
|
Sinus Bradycardia, CTCAE
|
phenotype |
|
Finding
|
20
|
|
0.100 |
None |
|
0 |
|
|
|
continuous electrocardiogram sinus bradycardia (finding)
|
phenotype |
|
Finding
|
20
|
|
0.100 |
None |
|
0 |
|
|
|
Romano-Ward Syndrome
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Disease or Syndrome
|
22
|
17
|
0.300 |
None |
1.000 |
1 |
|
2016 |
2016 |
Sinus bradycardia
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases
|
Pathologic Function
|
22
|
2
|
0.100 |
None |
|
0 |
|
|
|
Abnormality of prenatal development or birth
|
disease |
|
Finding
|
23
|
|
0.100 |
None |
|
0 |
|
|
|
CUI: |
C0036974 |
Disease: |
Shock
|
Shock
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Pathologic Function
|
25
|
|
0.100 |
None |
|
0 |
|
|
|
Prolonged QTc interval
|
phenotype |
|
Pathologic Function
|
25
|
1
|
0.100 |
None |
|
0 |
|
|
|
Prolonged QTc Interval, CTCAE
|
phenotype |
|
Finding
|
25
|
|
0.100 |
None |
|
0 |
|
|
|
Sudden death
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Pathologic Function
|
30
|
3
|
0.100 |
None |
|
0 |
|
|
|
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder)
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
31
|
121
|
0.740 |
strong |
1.000 |
5 |
15
|
2012 |
2020 |
Diabetic Foot
|
disease |
Skin and Connective Tissue Diseases; Endocrine System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
39
|
13
|
0.100 |
None |
1.000 |
1 |
1
|
2017 |
2017 |
Adverse Event Associated with Cardiac Arrhythmia
|
phenotype |
|
Disease or Syndrome
|
42
|
5
|
0.010 |
None |
1.000 |
1 |
|
2012 |
2012 |
Torsades de Pointes
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
51
|
14
|
0.100 |
None |
|
0 |
|
|
|
Heart Failure, Diastolic
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
55
|
9
|
0.300 |
None |
1.000 |
1 |
|
2018 |
2018 |
Premature ventricular contractions
|
phenotype |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
56
|
13
|
0.100 |
None |
|
0 |
|
|
|