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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