DSP, desmoplakin, 1832

N. diseases: 28; N. variants: 131
Source: CLINVAR ×
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: C4703660
Disease: Increased troponin I level in blood
Increased troponin I level in blood
phenotype Finding 1 1 0.100 None 0 1
Left ventricular noncompaction cardiomyopathy
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 7 14 0.100 None 0 1
CUI: C2063326
Disease: Right ventricular cardiomyopathy
Right ventricular cardiomyopathy
disease Cardiovascular Diseases Disease or Syndrome 4 4 0.100 None 0 2
Hereditary bundle branch system defect
disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 2 7 0.100 None 0 1
Arrhythmogenic Right Ventricular Dysplasia, Familial, 9
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome 5 61 0.100 None 0 2
CUI: C0855329
Disease: Electrocardiogram change
Electrocardiogram change
phenotype Finding 18 27 0.100 None 0 2
CUI: C0265004
Disease: Dilatation of aorta
Dilatation of aorta
phenotype Cardiovascular Diseases Disease or Syndrome 2 2 0.100 None 0 1
CUI: C0149630
Disease: Bicuspid aortic valve
Bicuspid aortic valve
disease Cardiovascular Diseases Congenital Abnormality 7 7 0.100 None 0 1
CUI: C0018790
Disease: Cardiac Arrest
Cardiac Arrest
disease Cardiovascular Diseases Disease or Syndrome 4 3 0.100 None 0 1
CUI: C0023212
Disease: Left-Sided Heart Failure
Left-Sided Heart Failure
disease Cardiovascular Diseases Disease or Syndrome 4 4 0.100 None 0 1
CUI: C0008031
Disease: Chest Pain
Chest Pain
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 4 5 0.100 None 0 1
CUI: C0023976
Disease: Long QT Syndrome
Long QT Syndrome
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome 16 245 0.100 None 0 1
CUI: C0042510
Disease: Ventricular Fibrillation
Ventricular Fibrillation
disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 2 3 0.100 None 0 1
CUI: C0085298
Disease: Sudden Cardiac Death
Sudden Cardiac Death
phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Pathologic Function 6 5 0.400 None 1.000 0 1 2010 2010
CUI: C0042514
Disease: Tachycardia, Ventricular
Tachycardia, Ventricular
disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 3 4 0.110 None 1.000 0 1 2011 2011
CUI: C0085612
Disease: Ventricular arrhythmia
Ventricular arrhythmia
disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 4 3 0.120 None 1.000 0 1 2011 2014
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure
disease Cardiovascular Diseases Disease or Syndrome 8 9 0.140 None 1.000 0 1 2006 2015
CUI: C0011071
Disease: Sudden death
Sudden death
phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 4 3 0.100 None 1.000 1 1 2016 2016
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
group Cardiovascular Diseases Disease or Syndrome 43 443 0.130 None 1.000 18 30 1999 2017
Cardiomyopathy dilated with Woolly hair and keratoderma
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Cardiovascular Diseases Disease or Syndrome 1 54 0.960 strong 0.971 22 54 1999 2019
Arrhythmogenic Right Ventricular Dysplasia, Familial, 8
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome 1 66 0.900 strong 1.000 22 66 1999 2019
Arrhythmogenic Right Ventricular Dysplasia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome; Congenital Abnormality 11 108 0.200 None 1.000 17 32 1999 2019
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 5 73 0.100 None 1.000 8 1 2008 2019
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
group Cardiovascular Diseases Disease or Syndrome 45 172 0.500 None 0.966 2 13 2002 2019
CUI: C1852127
Disease: KERATOSIS PALMOPLANTARIS STRIATA II
KERATOSIS PALMOPLANTARIS STRIATA II
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 1 4 0.600 strong 1.000 0 4 2011 2019