Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C1623258
Disease: Electrocardiography
Electrocardiography
phenotype Diagnostic Procedure 8 16 0.100 None 1.000 1 1 2010 2010
Abnormal cardiac exercise stress test
phenotype Finding 16 0.100 None 0
CUI: C1261287
Disease: Stenosis
Stenosis
phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 19 1 0.200 None 1.000 1 2011 2011
CUI: C4551647
Disease: Long QT Syndrome 1
Long QT Syndrome 1
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome 20 240 0.010 None 1.000 1 2019 2019
CUI: C1839341
Disease: Abnormal T-wave
Abnormal T-wave
phenotype Finding 20 0.100 None 0
CUI: C1963175
Disease: Sinus Bradycardia, CTCAE
Sinus Bradycardia, CTCAE
phenotype Finding 20 0.100 None 0
continuous electrocardiogram sinus bradycardia (finding)
phenotype Finding 20 0.100 None 0
CUI: C0035828
Disease: Romano-Ward Syndrome
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 2 2009 2010
CUI: C0085610
Disease: Sinus bradycardia
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: C0085119
Disease: Foot Ulcer
Foot Ulcer
disease Skin and Connective Tissue Diseases Disease or Syndrome 25 3 0.010 None 1.000 1 2017 2017
CUI: C1560305
Disease: Prolonged QTc interval
Prolonged QTc interval
phenotype Pathologic Function 25 1 0.100 None 0
CUI: C1963217
Disease: Prolonged QTc Interval, CTCAE
Prolonged QTc Interval, CTCAE
phenotype Finding 25 0.100 None 0
CUI: C1141890
Disease: Congenital long QT syndrome
Congenital long QT syndrome
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome 30 54 0.030 None 0.667 3 2009 2014
Arteriovenous Malformations, Cerebral
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases Congenital Abnormality 35 6 0.010 None 1.000 1 2016 2016
CUI: C0333293
Disease: Healing ulcer
Healing ulcer
disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 43 1 0.010 None 1.000 1 2017 2017
CUI: C0588008
Disease: Severe depression
Severe depression
disease Mental Disorders Mental or Behavioral Dysfunction 46 2 0.010 None 1.000 1 2013 2013
CUI: C0040479
Disease: Torsades de Pointes
Torsades de Pointes
disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 51 14 0.100 None 0
CUI: C0020621
Disease: Hypokalemia
Hypokalemia
phenotype Nutritional and Metabolic Diseases Finding 61 7 0.100 None 0
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome 66 201 0.010 None 1.000 1 1 2014 2014
QT interval feature (observable entity)
phenotype Clinical Attribute 75 226 0.100 None 1.000 10 28 2006 2019
CUI: C0334533
Disease: Arteriovenous hemangioma
Arteriovenous hemangioma
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Cardiovascular Diseases Neoplastic Process 76 14 0.010 None 1.000 1 2016 2016
CUI: C0741923
Disease: cardiac event
cardiac event
phenotype Disease or Syndrome 82 18 0.020 None 1.000 2 1 2010 2015
Amputated structure (morphologic abnormality)
phenotype Wounds and Injuries Acquired Abnormality 94 0.010 None 1.000 1 2017 2017
CUI: C0042514
Disease: Tachycardia, Ventricular
Tachycardia, Ventricular
disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 104 31 0.010 None 1.000 1 2017 2017