Channelopathies
disease
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
94
8
0.040
None
1.000
4
2005
2018
Hyperuricemia
disease
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
196
76
0.030
None
1.000
3
2017
2018
Sudden infant death syndrome
disease
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
140
68
0.020
None
1.000
2
2008
2017
Gliosis
phenotype
Pathological Conditions, Signs and Symptoms
Pathologic Function
102
3
0.300
None
1.000
1
2008
2008
Heartburn
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
139
5
0.010
None
1.000
1
2019
2019
Inflammation
phenotype
Pathological Conditions, Signs and Symptoms
Pathologic Function
467
0.010
None
1.000
1
2008
2008
×
CUI:
C0030193
Disease:
Pain
Pain
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
1554
196
0.010
None
1.000
1
2019
2019
Multiple Chronic Conditions
disease
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
929
42
0.010
None
1.000
1
2018
2018
Astrocytosis
phenotype
Pathological Conditions, Signs and Symptoms
Pathologic Function
37
0.300
None
1.000
1
2008
2008
Atrial Fibrillation
disease
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
Disease or Syndrome
939
584
0.090
None
1.000
9
2011
2019
Cardiac Arrhythmia
phenotype
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
Disease or Syndrome
559
111
0.020
None
1.000
2
2015
2017
Torsades de Pointes
disease
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
Disease or Syndrome
51
14
0.020
None
1.000
2
2005
2017
Chronic atrial fibrillation
disease
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
Disease or Syndrome
31
0.020
None
1.000
2
2015
2017
Ventricular Fibrillation
disease
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
Disease or Syndrome
96
19
0.010
None
1.000
1
2018
2018
Right Ventricular Hypertrophy
disease
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
Disease or Syndrome
160
6
0.010
None
1.000
1
2018
2018
Long QT Syndrome
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
Disease or Syndrome
105
349
0.050
None
1.000
5
1997
2007
Congenital long QT syndrome
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
Disease or Syndrome
30
54
0.020
None
1.000
2
2003
2005
Long QT Syndrome 1
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
Disease or Syndrome
20
240
0.020
None
1.000
2
1997
1998
Romano-Ward Syndrome
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
Disease or Syndrome
22
17
0.010
None
1.000
1
1998
1998
Fetal Growth Retardation
phenotype
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications
Disease or Syndrome
1037
21
0.010
None
1.000
1
2012
2012
Neuralgia
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
767
16
0.010
None
1.000
1
2019
2019
Status Epilepticus
disease
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Disease or Syndrome
533
12
0.200
None
1.000
1
2008
2008
Epileptic Seizures
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Disease or Syndrome
250
7
0.010
None
1.000
1
2017
2017
Cerebral Infarction
disease
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases
Disease or Syndrome
687
123
0.010
None
1.000
1
2010
2010
Deafness
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
Finding
62
37
0.200
None
1.000
1
2007
2007