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: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		disease Disease or Syndrome 1075 276 0.080 None 1.000 8 3 2003 2017
CUI: C0429087
Disease: Electrocardiogram: P-R interval
Electrocardiogram: P-R interval 		phenotype Finding 57 138 0.100 None 1.000 7 7 2010 2019
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		phenotype Clinical Attribute 75 226 0.100 None 1.000 5 6 2009 2019
CUI: C0741923
Disease: cardiac event
cardiac event 		phenotype Disease or Syndrome 82 18 0.050 None 1.000 5 1998 2018
CUI: C1560249
Disease: Adverse Event Associated with Cardiac Arrhythmia
Adverse Event Associated with Cardiac Arrhythmia 		phenotype Disease or Syndrome 42 5 0.050 None 1.000 5 1995 2013
CUI: C3151464
Disease: ATRIAL FIBRILLATION, FAMILIAL, 10
ATRIAL FIBRILLATION, FAMILIAL, 10 		disease Disease or Syndrome 1 17 0.700 None 1.000 4 17 1995 2012
CUI: C1838527
Disease: LONG QT SYNDROME 3, ACQUIRED, SUSCEPTIBILITY TO (finding)
LONG QT SYNDROME 3, ACQUIRED, SUSCEPTIBILITY TO (finding) 		disease Finding 1 1 0.300 None 1.000 3 1 2001 2012
CUI: C3276240
Disease: LONG QT SYNDROME 2/3, DIGENIC
LONG QT SYNDROME 2/3, DIGENIC 		disease Disease or Syndrome 2 2 0.300 None 1.000 3 1 2001 2012
CUI: C3276241
Disease: LONG QT SYNDROME 3/6, DIGENIC Disorder
LONG QT SYNDROME 3/6, DIGENIC Disorder 		disease Disease or Syndrome 2 2 0.300 None 1.000 3 1 2001 2012
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion 		phenotype Neoplastic Process 6626 169 0.020 None 1.000 2 2010 2012
CUI: C3150852
Disease: EARLY REPOLARIZATION ASSOCIATED WITH VENTRICULAR FIBRILLATION
EARLY REPOLARIZATION ASSOCIATED WITH VENTRICULAR FIBRILLATION 		disease Disease or Syndrome 7 0.020 None 1.000 2 2013 2016
CUI: C0018803
Disease: Heart Function Tests
Heart Function Tests 		phenotype Diagnostic Procedure 17 27 0.100 None 1.000 1 2 2010 2010
CUI: C0391957
Disease: idiopathic epilepsy
idiopathic epilepsy 		disease Disease or Syndrome 30 3 0.010 None 1.000 1 2009 2009
CUI: C0429021
Disease: P wave duration (observable entity)
P wave duration (observable entity) 		phenotype Clinical Attribute 10 18 0.100 None 1.000 1 2 2017 2017
CUI: C0429097
Disease: QRS complex feature
QRS complex feature 		phenotype Finding 41 69 0.100 None 1.000 1 2 2016 2016
CUI: C0741916
Disease: Cardiac defects
Cardiac defects 		group Disease or Syndrome 62 2 0.010 None 1.000 1 2015 2015
CUI: C0748061
Disease: psychiatric hospitalization
psychiatric hospitalization 		disease Mental or Behavioral Dysfunction 5 4 0.010 None 1.000 1 2015 2015
CUI: C0748694
Disease: sick sinus
sick sinus 		disease Disease or Syndrome 1 0.010 None 1.000 1 2012 2012
CUI: C0750194
Disease: Non-sustained ventricular tachycardia
Non-sustained ventricular tachycardia 		disease Disease or Syndrome 5 0.010 None 1.000 1 2019 2019
CUI: C1096378
Disease: Near sudden infant death syndrome
Near sudden infant death syndrome 		phenotype Sign or Symptom 2 0.010 None 1.000 1 2001 2001
CUI: C1397307
Disease: Cardiac fibrosis
Cardiac fibrosis 		disease Disease or Syndrome 297 3 0.010 None 1.000 1 1 2011 2011
CUI: C1623258
Disease: Electrocardiography
Electrocardiography 		phenotype Diagnostic Procedure 8 16 0.100 None 1.000 1 1 2018 2018
CUI: C1821417
Disease: RESTING HEART RATE
RESTING HEART RATE 		phenotype Finding 80 134 0.100 None 1.000 1 1 2016 2016
CUI: C1858430
Disease: Death in infancy
Death in infancy 		phenotype Finding 146 7 0.100 None 1.000 1 2 2016 2016
CUI: C2114320
Disease: preterm contractions
preterm contractions 		phenotype Sign or Symptom 1 0.010 None 1.000 1 2012 2012