ICD-10-CM Q21: Congenital malformations of cardiac septa

acquired cardiac septal defect (I51.0)

ostium primum atrial septal defect (type I) (Q21.20)

Roger's disease

• 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

• , if applicable:
• Eisenmenger's complex (I27.83)
• Eisenmenger's syndrome (I27.83)