Congenital malformations of cardiac septa
Notes: Roger’s disease ; Excludes 2: ostium primum atrial septal defect (type I) (Q21.20) ; Fenestrated atrial septum ; Patent or persistent ostium secundum defect (type II) ; Persistent foramen ovale ; Coronary sinus defect ; Unroofed coronary sinus ; Superior vena cava type atrial septal defect ; Inferior vena cava type atrial septal defect ; Sinus venosus defect, NOS ; Common atrium ; Other specified atrial septal abnormality ; Atrioventricular canal defect ; Endocardial cushion defect ; Ostium primum atrial septal defect (type I) ; Atrioventricular canal, NOS ; Endocardial cushion defect NOS ; Ostium primum atrial septal defect (type I) NOS ; Incomplete atrioventricular canal ; Incomplete atrioventricular septal defect ; Incomplete endocardial cushion defect ; Ostium primum atrial septal defect (type I) with separate atrioventricular valves ; Partial atrioventricular canal ; Partial endocardial cushion defect ; Intermediate atrioventricular canal ; Intermediate atrioventricular septal defect ; Intermediate endocardial cushion defect ; Ostium primum atrial septal defect (type I) with separate atrioventricular valves and a small or restrictive inlet VSD ; Transitional atrioventricular canal ; Transitional endocardial cushion defect ; Common atrioventricular canal ; Common atrioventricular septal defect ; Common endocardial cushion defect ; Ostium primum atrial septal defect (type I) with common atrioventricular valve and a moderate or larger inlet VSD ; Ventricular septal defect with pulmonary stenosis or atresia, dextroposition of aorta and hypertrophy of right ventricle. ; Aortic septal defect ; Aortopulmonary window ; Eisenmenger’s defect ; Pentalogy of Fallot ; Septal (heart) defect NOS ; acquired cardiac septal defect (I51.0)

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dr.kijakarn junda MD. first class hon. , FRCP(t)
Tags: Q21

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