Source: CLINVAR

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes Num. SNPs
C0007193 Cardiomyopathy, Dilated group Cardiovascular Diseases Disease or Syndrome genetic disease; disease of anatomical entity Abnormality of the cardiovascular system 43 443
C1142166 Brugada Syndrome (disorder) disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome genetic disease; disease of anatomical entity 3 103
C1879286 Hereditary bundle branch system defect disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome genetic disease; disease of anatomical entity 2 7
C0038644 Sudden infant death syndrome disease Pathological Conditions, Signs and Symptoms Disease or Syndrome syndrome 2 5
C4551804 Brugada Syndrome 1 disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome genetic disease; disease of anatomical entity 1 34
C1859062 LONG QT SYNDROME 3 disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome genetic disease; disease of anatomical entity 1 30
C1832680 CARDIOMYOPATHY, DILATED, 1E disease Cardiovascular Diseases Disease or Syndrome genetic disease; disease of anatomical entity 1 11
C3151464 ATRIAL FIBRILLATION, FAMILIAL, 10 disease Disease or Syndrome disease of anatomical entity 1 9
C1837845 SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 1 8
C2751898 Ventricular Fibrillation, Paroxysmal Familial, 1 disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 1 3