CARDIAC CONGENITAL AND VALVULAR DISORDERS WITH MCC - DIAGNOSTIC RELATED GROUP MS-DRG V36.0

The Diagnostic Related Groups (DRGs) are a patient classification scheme which provides a means of relating the type of patients a hospital treats. The DRGs divides all possible principal diagnoses into mutually exclusive principal diagnosis areas referred to as Major Diagnostic Categories (MDC). This is the group for cardiac congenital and valvular disorders with mcc diseases in version MS-DRG V36.0 applicable from 10/01/2018 through 09/30/2019.

  • A52.01 - Syphilitic aneurysm of aorta
  • A52.02 - Syphilitic aortitis
  • B33.21 - Viral endocarditis
  • I01.1 - Acute rheumatic endocarditis
  • I05.0 - Rheumatic mitral stenosis
  • I05.1 - Rheumatic mitral insufficiency
  • I05.2 - Rheumatic mitral stenosis with insufficiency
  • I05.8 - Other rheumatic mitral valve diseases
  • I05.9 - Rheumatic mitral valve disease, unspecified
  • I06.0 - Rheumatic aortic stenosis
  • I06.1 - Rheumatic aortic insufficiency
  • I06.2 - Rheumatic aortic stenosis with insufficiency
  • I06.8 - Other rheumatic aortic valve diseases
  • I06.9 - Rheumatic aortic valve disease, unspecified
  • I07.0 - Rheumatic tricuspid stenosis
  • I07.1 - Rheumatic tricuspid insufficiency
  • I07.2 - Rheumatic tricuspid stenosis and insufficiency
  • I07.8 - Other rheumatic tricuspid valve diseases
  • I07.9 - Rheumatic tricuspid valve disease, unspecified
  • I08.0 - Rheumatic disorders of both mitral and aortic valves
  • I08.1 - Rheumatic disorders of both mitral and tricuspid valves
  • I08.2 - Rheumatic disorders of both aortic and tricuspid valves
  • I08.3 - Comb rheumatic disord of mitral, aortic and tricuspid valves
  • I08.8 - Other rheumatic multiple valve diseases
  • I08.9 - Rheumatic multiple valve disease, unspecified
  • I09.1 - Rheumatic diseases of endocardium, valve unspecified
  • I09.89 - Other specified rheumatic heart diseases
  • I23.4 - Rupture of chord tendne as current comp following AMI
  • I23.5 - Rupture of papillary muscle as current comp following AMI
  • I34.0 - Nonrheumatic mitral (valve) insufficiency
  • I34.1 - Nonrheumatic mitral (valve) prolapse
  • I34.2 - Nonrheumatic mitral (valve) stenosis
  • I34.8 - Other nonrheumatic mitral valve disorders
  • I34.9 - Nonrheumatic mitral valve disorder, unspecified
  • I35.0 - Nonrheumatic aortic (valve) stenosis
  • I35.1 - Nonrheumatic aortic (valve) insufficiency
  • I35.2 - Nonrheumatic aortic (valve) stenosis with insufficiency
  • I35.8 - Other nonrheumatic aortic valve disorders
  • I35.9 - Nonrheumatic aortic valve disorder, unspecified
  • I36.0 - Nonrheumatic tricuspid (valve) stenosis
  • I36.1 - Nonrheumatic tricuspid (valve) insufficiency
  • I36.2 - Nonrheumatic tricuspid (valve) stenosis with insufficiency
  • I36.8 - Other nonrheumatic tricuspid valve disorders
  • I36.9 - Nonrheumatic tricuspid valve disorder, unspecified
  • I37.0 - Nonrheumatic pulmonary valve stenosis
  • I37.1 - Nonrheumatic pulmonary valve insufficiency
  • I37.2 - Nonrheumatic pulmonary valve stenosis with insufficiency
  • I37.8 - Other nonrheumatic pulmonary valve disorders
  • I37.9 - Nonrheumatic pulmonary valve disorder, unspecified
  • I38 - Endocarditis, valve unspecified
  • I39 - Endocarditis and heart valve disord in dis classd elswhr
  • I51.1 - Rupture of chordae tendineae, not elsewhere classified
  • I51.2 - Rupture of papillary muscle, not elsewhere classified
  • Q20.0 - Common arterial trunk
  • Q20.1 - Double outlet right ventricle
  • Q20.2 - Double outlet left ventricle
  • Q20.3 - Discordant ventriculoarterial connection
  • Q20.4 - Double inlet ventricle
  • Q20.5 - Discordant atrioventricular connection
  • Q20.6 - Isomerism of atrial appendages
  • Q20.8 - Oth congenital malform of cardiac chambers and connections
  • Q20.9 - Congenital malform of cardiac chambers and connections, unsp
  • Q21.0 - Ventricular septal defect
  • Q21.1 - Atrial septal defect
  • Q21.2 - Atrioventricular septal defect
  • Q21.3 - Tetralogy of Fallot
  • Q21.4 - Aortopulmonary septal defect
  • Q21.8 - Other congenital malformations of cardiac septa
  • Q21.9 - Congenital malformation of cardiac septum, unspecified
  • Q22.0 - Pulmonary valve atresia
  • Q22.1 - Congenital pulmonary valve stenosis
  • Q22.2 - Congenital pulmonary valve insufficiency
  • Q22.3 - Other congenital malformations of pulmonary valve
  • Q22.4 - Congenital tricuspid stenosis
  • Q22.5 - Ebstein's anomaly
  • Q22.6 - Hypoplastic right heart syndrome
  • Q22.8 - Other congenital malformations of tricuspid valve
  • Q22.9 - Congenital malformation of tricuspid valve, unspecified
  • Q23.0 - Congenital stenosis of aortic valve
  • Q23.1 - Congenital insufficiency of aortic valve
  • Q23.2 - Congenital mitral stenosis
  • Q23.3 - Congenital mitral insufficiency
  • Q23.4 - Hypoplastic left heart syndrome
  • Q23.8 - Other congenital malformations of aortic and mitral valves
  • Q23.9 - Congenital malformation of aortic and mitral valves, unsp
  • Q24.0 - Dextrocardia
  • Q24.1 - Levocardia
  • Q24.2 - Cor triatriatum
  • Q24.3 - Pulmonary infundibular stenosis
  • Q24.4 - Congenital subaortic stenosis
  • Q24.5 - Malformation of coronary vessels
  • Q24.8 - Other specified congenital malformations of heart
  • Q24.9 - Congenital malformation of heart, unspecified
  • Q25.0 - Patent ductus arteriosus
  • Q25.1 - Coarctation of aorta
  • Q25.21 - Interruption of aortic arch
  • Q25.29 - Other atresia of aorta
  • Q25.3 - Supravalvular aortic stenosis
  • Q25.40 - Congenital malformation of aorta unspecified
  • Q25.41 - Absence and aplasia of aorta
  • Q25.42 - Hypoplasia of aorta
  • Q25.43 - Congenital aneurysm of aorta
  • Q25.44 - Congenital dilation of aorta
  • Q25.45 - Double aortic arch
  • Q25.46 - Tortuous aortic arch
  • Q25.47 - Right aortic arch
  • Q25.48 - Anomalous origin of subclavian artery
  • Q25.49 - Other congenital malformations of aorta
  • Q25.5 - Atresia of pulmonary artery
  • Q25.6 - Stenosis of pulmonary artery
  • Q25.71 - Coarctation of pulmonary artery
  • Q25.72 - Congenital pulmonary arteriovenous malformation
  • Q25.79 - Other congenital malformations of pulmonary artery
  • Q25.8 - Other congenital malformations of other great arteries
  • Q25.9 - Congenital malformation of great arteries, unspecified
  • Q26.0 - Congenital stenosis of vena cava
  • Q26.1 - Persistent left superior vena cava
  • Q26.2 - Total anomalous pulmonary venous connection
  • Q26.3 - Partial anomalous pulmonary venous connection
  • Q26.4 - Anomalous pulmonary venous connection, unspecified
  • Q26.8 - Other congenital malformations of great veins
  • Q26.9 - Congenital malformation of great vein, unspecified
  • Q87.40 - Marfan's syndrome, unspecified
  • Q87.410 - Marfan's syndrome with aortic dilation
  • Q87.418 - Marfan's syndrome with other cardiovascular manifestations
  • Q87.42 - Marfan's syndrome with ocular manifestations
  • Q87.43 - Marfan's syndrome with skeletal manifestation
  • R01.0 - Benign and innocent cardiac murmurs
  • R01.1 - Cardiac murmur, unspecified