Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Entire right auricular appendage |
Is a |
True |
Structure of right auricular appendage |
Inferred relationship |
Some |
|
A rare heterotaxia characterised by complex congenital heart malformations and abnormal lateralisation of other thoracic and abdominal organs due to embryonic disruption of the left-right axis development. Cardiac defects include dextrocardia or mesocardia, common atrioventricular valve associated with complete atrioventricular septal defect or common atrium, transposition or malposition of the great arteries, and total anomalous pulmonary venous drainage, among others. Cardiac arrhythmias are frequently observed. Typical abnormalities of other organs are bilateral trilobed lungs, midline liver, and asplenia. Patients present in the newborn period with severe cardiac failure and cyanosis. Prognosis is poor. |
Finding site |
True |
Structure of right auricular appendage |
Inferred relationship |
Some |
1 |
Abnormality of right atrial appendage |
Finding site |
False |
Structure of right auricular appendage |
Inferred relationship |
Some |
1 |
Right atrial appendage absent |
Finding site |
False |
Structure of right auricular appendage |
Inferred relationship |
Some |
1 |
Right atrial appendage - left - juxtaposition |
Finding site |
True |
Structure of right auricular appendage |
Inferred relationship |
Some |
1 |
Right atrial appendage aneurysm |
Finding site |
False |
Structure of right auricular appendage |
Inferred relationship |
Some |
1 |
Right atrial appendage aneurysm |
Finding site |
False |
Structure of right auricular appendage |
Inferred relationship |
Some |
2 |
Right atrial appendage aneurysm |
Finding site |
False |
Structure of right auricular appendage |
Inferred relationship |
Some |
2 |
Right atrial appendage aneurysm |
Finding site |
False |
Structure of right auricular appendage |
Inferred relationship |
Some |
1 |
Right atrial appendage aneurysm |
Finding site |
False |
Structure of right auricular appendage |
Inferred relationship |
Some |
2 |
Right atrial appendage aneurysm |
Finding site |
False |
Structure of right auricular appendage |
Inferred relationship |
Some |
1 |
Right atrial appendage aneurysm |
Finding site |
False |
Structure of right auricular appendage |
Inferred relationship |
Some |
1 |
Right atrial appendage aneurysm |
Finding site |
False |
Structure of right auricular appendage |
Inferred relationship |
Some |
2 |
Right atrial appendage aneurysm |
Finding site |
False |
Structure of right auricular appendage |
Inferred relationship |
Some |
1 |
Right atrial appendage aneurysm |
Finding site |
False |
Structure of right auricular appendage |
Inferred relationship |
Some |
2 |
Right atrial appendage aneurysm |
Finding site |
False |
Structure of right auricular appendage |
Inferred relationship |
Some |
2 |
Right atrial appendage aneurysm |
Finding site |
True |
Structure of right auricular appendage |
Inferred relationship |
Some |
1 |
Right atrial appendage - left - juxtaposition |
Finding site |
False |
Structure of right auricular appendage |
Inferred relationship |
Some |
1 |
Right atrial appendage absent |
Finding site |
False |
Structure of right auricular appendage |
Inferred relationship |
Some |
1 |
Abnormality of right atrial appendage |
Finding site |
False |
Structure of right auricular appendage |
Inferred relationship |
Some |
1 |
A rare heterotaxia characterised by complex congenital heart malformations and abnormal lateralisation of other thoracic and abdominal organs due to embryonic disruption of the left-right axis development. Cardiac defects include dextrocardia or mesocardia, common atrioventricular valve associated with complete atrioventricular septal defect or common atrium, transposition or malposition of the great arteries, and total anomalous pulmonary venous drainage, among others. Cardiac arrhythmias are frequently observed. Typical abnormalities of other organs are bilateral trilobed lungs, midline liver, and asplenia. Patients present in the newborn period with severe cardiac failure and cyanosis. Prognosis is poor. |
Finding site |
False |
Structure of right auricular appendage |
Inferred relationship |
Some |
1 |
Repair of total anomalous pulmonary venous connection by insertion of interatrial baffle with reconnection of superior caval vein to right atrial appendage (procedure) |
Procedure site - Direct (attribute) |
True |
Structure of right auricular appendage |
Inferred relationship |
Some |
2 |
Repair of partial anomalous pulmonary venous connection by baffle redirection to left atrium with superior caval vein anastomosis to right atrial appendage (procedure) |
Procedure site - Direct (attribute) |
True |
Structure of right auricular appendage |
Inferred relationship |
Some |
2 |
Right atrial appendage absent |
Finding site |
True |
Structure of right auricular appendage |
Inferred relationship |
Some |
1 |
Abnormality of right atrial appendage |
Finding site |
True |
Structure of right auricular appendage |
Inferred relationship |
Some |
1 |
Ectasia of the right atrial appendage is a rare cardiac malformation characterized by the enlargement of the right auricle without any other associated cardiac lesions. It can be asymptomatic and diagnosed fortuitously, prenatally or during routine clinical examinations or it can present with heart murmur, palpitation, atrial arrhythmia, fatigue, dyspnea or respiratory distress. |
Finding site |
True |
Structure of right auricular appendage |
Inferred relationship |
Some |
1 |