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ventricle
- Cor triloculare biatriatum
- Single ventricle
- Q20.5 Discordant atrioventricular connection
- Corrected transposition
- Levotransposition
- Ventricular inversion
- Q20.6 Isomerism of atrial appendages
- Isomerism of atrial appendages with asplenia or polysplenia
- Q20.8 Other congenital malformations of cardiac chambers and connections
- Cor binoculare
- Q20.9 Congenital malformation of cardiac chambers and connections, unspecified
Q21 Congenital malformations of cardiac septa
- Excludes1: acquired cardiac septal defect (I51.0)
- Q21.0 Ventricular septal defect
- Roger's disease
- Q21.1 Atrial septal defect
- Coronary sinus defect
- Patent or persistent foramen ovale
- Patent or persistent ostium secundum defect (type II)
- Patent or persistent sinus venosus defect
- Q21.2 Atrioventricular septal defect
- Common atrioventricular canal
- Endocardial cushion defect
- Ostium primum atrial septal defect (type I)
- Q21.3 Tetralogy of Fallot
- Ventricular septal defect with pulmonary stenosis or atresia, dextroposition of aorta and hypertrophy of right ventricle.
- Q21.4 Aortopulmonary septal defect
- Aortic septal defect
- Aortopulmonary window
- Q21.8 Other congenital malformations of cardiac septa
- Eisenmenger's defect
- Pentalogy of Fallot
- Excludes1: Eisenmenger's complex (I27.8)
- Eisenmenger's syndrome (I27.8)
- Q21.9 Congenital malformation of cardiac septum, unspecified
- Septal (heart) defect NOS
Q22 Congenital malformations of pulmonary and tricuspid valves
- Q22.0 Pulmonary valve atresia
- Q22.1 Congenital pulmonary valve stenosis
- Q22.2 Congenital pulmonary valve insufficiency
- Congenital
