Human Diseases

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 Immune system diseases
 Nervous system diseases
 Cardiovascular diseases
   Cardiac diseases
     H00292  Hypertrophic cardiomyopathy [PATH:hsa05410]
     H00293  Arrhythmogenic right ventricular cardiomyopathy [PATH:hsa05412]
     H00294  Dilated cardiomyopathy [PATH:hsa05414]
     H01219  Restrictive cardiomyopathy [PATH:hsa04260]
     H02498  Diabetic cardiomyopathy [PATH:hsa05415]
     H00295  Viral myocarditis [PATH:hsa05416]
     H01216  Left ventricular noncompaction [PATH:hsa04260]
     H00546  Atrial septal defect
     H00547  Atrioventricular septal defect
     H00549  Tetralogy of Fallot [PATH:hsa04330]
     H00550  Complete transposition of the great arteries
     H01786  Congenitally corrected transposition of the great arteries
     H00553  Congenital supravalvar aortic stenosis
     H00555  Char syndrome
     H00654  Barth syndrome [PATH:hsa00564]
     H00669  Naxos disease [PATH:hsa05412]
     H02094  Carvajal syndrome
     H00720  Long QT syndrome [PATH:hsa04261 hsa04921]
     H00725  Short QT syndrome
     H02091  Jervell and Lange-Nielsen syndrome [PATH:hsa04261]
     H00728  Brugada syndrome [PATH:hsa04010 hsa04020 hsa04260 hsa04270 hsa05410 hsa05412 hsa05414]
     H00729  Sick sinus syndrome
     H00730  Familial idiopathic ventricular fibrillation
     H00731  Atrial fibrillation [PATH:hsa04270 hsa04261]
     H00918  Double-outlet right ventricle
     H00939  Darsun syndrome
     H01019  Catecholaminergic polymorphic ventricular tachycardia [PATH:hsa04020 hsa04261 hsa04260]
     H01154  Wolff-Parkinson-White (WPW) syndrome [PATH:hsa04910 hsa04920 hsa05410]
     H01263  Progressive cardiac conduction defect (PCCD)
     H01632  Angina pectoris
     H01729  Premature ventricular complexes
     H01730  Myocardial infarction
     H01736  Persistent truncus arteriosus
     H01783  Ebstein anomaly
     H01785  Tricuspid atresia
     H01787  Univentricular heart
     H01802  Pulmonary atresia with intact ventricular septum
     H01803  Pulmonary atresia with ventricular septal defect
     H01868  Mitral valve prolapse
     H01926  Ventricular septal defect
     H02122  Chronic atrial and intestinal dysrhythmia [PATH:hsa04114]
     H02125  Cardiac conduction disease with dilated cardiomyopathy
     H02269  Familial ventricular tachycardia
   Vascular diseases
   Hematologic diseases
   Hypertensive diseases
 Respiratory diseases
 Endocrine and metabolic diseases
 Digestive system diseases
 Urinary system diseases
 Reproductive system diseases
 Musculoskeletal diseases
 Skin diseases
 Congenital disorders of metabolism
 Congenital malformations
 Other congenital disorders
 Other diseases

Last updated: February 25, 2021

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