Source: BEFREE

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2
potassium voltage-gated channel subfamily H member 2 0.522 0.731 1.00
CUI: C1865020
Disease: Short QT Syndrome 1
Short QT Syndrome 1
disease 0.920 None 1.000 2 0 1995 2018
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2
potassium voltage-gated channel subfamily H member 2 0.522 0.731 1.00
CUI: C3150943
Disease: Long Qt Syndrome 2
Long Qt Syndrome 2
disease 0.800 None 0.989 34 11 1995 2019
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2
potassium voltage-gated channel subfamily H member 2 0.522 0.731 1.00
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
disease 0.700 strong 1.000 14 14 2005 2019
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2
potassium voltage-gated channel subfamily H member 2 0.522 0.731 1.00
CUI: C0023976
Disease: Long QT Syndrome
Long QT Syndrome
disease 0.500 None 0.990 204 42 1995 2020
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2
potassium voltage-gated channel subfamily H member 2 0.522 0.731 1.00
CUI: C0003811
Disease: Cardiac Arrhythmia
Cardiac Arrhythmia
phenotype 0.500 None 1.000 75 10 1995 2020
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2
potassium voltage-gated channel subfamily H member 2 0.522 0.731 1.00
CUI: C0040479
Disease: Torsades de Pointes
Torsades de Pointes
disease 0.500 None 0.968 28 5 1995 2019
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2
potassium voltage-gated channel subfamily H member 2 0.522 0.731 1.00
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
disease 0.450 disputed 1.000 5 1 2002 2020
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2
potassium voltage-gated channel subfamily H member 2 0.522 0.731 1.00
CUI: C0042510
Disease: Ventricular Fibrillation
Ventricular Fibrillation
disease 0.440 strong 1.000 4 1 2004 2019
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2
potassium voltage-gated channel subfamily H member 2 0.522 0.731 1.00
CUI: C0018790
Disease: Cardiac Arrest
Cardiac Arrest
disease 0.420 strong 1.000 2 3 2002 2017
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2
potassium voltage-gated channel subfamily H member 2 0.522 0.731 1.00
CUI: C0027651
Disease: Neoplasms
Neoplasms
group 0.400 None 1.000 13 0 2000 2019
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2
potassium voltage-gated channel subfamily H member 2 0.522 0.731 1.00
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
group 0.380 None 1.000 8 0 2005 2018
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2
potassium voltage-gated channel subfamily H member 2 0.522 0.731 1.00
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
disease 0.370 None 1.000 7 1 2009 2020
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2
potassium voltage-gated channel subfamily H member 2 0.522 0.731 1.00
CUI: C0033975
Disease: Psychotic Disorders
Psychotic Disorders
group 0.320 None 1.000 2 0 2009 2010
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2
potassium voltage-gated channel subfamily H member 2 0.522 0.731 1.00
CUI: C0349204
Disease: Nonorganic psychosis
Nonorganic psychosis
disease 0.320 None 1.000 2 0 2009 2010
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2
potassium voltage-gated channel subfamily H member 2 0.522 0.731 1.00
CUI: C0035828
Disease: Romano-Ward Syndrome
Romano-Ward Syndrome
disease 0.320 None 1.000 2 2 2007 2017
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2
potassium voltage-gated channel subfamily H member 2 0.522 0.731 1.00
CUI: C0235480
Disease: Paroxysmal atrial fibrillation
Paroxysmal atrial fibrillation
disease 0.320 None 1.000 2 0 2001 2018
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2
potassium voltage-gated channel subfamily H member 2 0.522 0.731 1.00
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
disease 0.310 None 1.000 1 0 2004 2005
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2
potassium voltage-gated channel subfamily H member 2 0.522 0.731 1.00
CUI: C1141890
Disease: Congenital long QT syndrome
Congenital long QT syndrome
disease 0.200 None 0.973 49 9 1996 2019
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2
potassium voltage-gated channel subfamily H member 2 0.522 0.731 1.00
CUI: C0039070
Disease: Syncope
Syncope
phenotype 0.200 None 1.000 16 8 2000 2019
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2
potassium voltage-gated channel subfamily H member 2 0.522 0.731 1.00
CUI: C4551647
Disease: Long QT Syndrome 1
Long QT Syndrome 1
disease 0.180 None 1.000 8 4 2004 2018
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2
potassium voltage-gated channel subfamily H member 2 0.522 0.731 1.00
CUI: C0004245
Disease: Atrioventricular Block
Atrioventricular Block
disease 0.160 None 1.000 6 2 2000 2018
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2
potassium voltage-gated channel subfamily H member 2 0.522 0.731 1.00
CUI: C0036572
Disease: Seizures
Seizures
phenotype 0.150 None 1.000 5 0 2009 2018
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2
potassium voltage-gated channel subfamily H member 2 0.522 0.731 1.00
CUI: C2348199
Disease: Short Qt Syndrome
Short Qt Syndrome
disease 0.100 None 1.000 18 2 2004 2019
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2
potassium voltage-gated channel subfamily H member 2 0.522 0.731 1.00
CUI: C0741923
Disease: cardiac event
cardiac event
phenotype 0.100 None 1.000 16 1 1996 2018
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2
potassium voltage-gated channel subfamily H member 2 0.522 0.731 1.00
CUI: C0085612
Disease: Ventricular arrhythmia
Ventricular arrhythmia
disease 0.100 None 0.933 15 2 1997 2020