Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Congenital coronary aneurysm |
Is a |
False |
Congenital arterial aneurysm |
Inferred relationship |
Some |
|
Congenital renal artery aneurysm |
Is a |
False |
Congenital arterial aneurysm |
Inferred relationship |
Some |
|
Congenital aneurysm of aorta |
Is a |
False |
Congenital arterial aneurysm |
Inferred relationship |
Some |
|
Congenital aneurysm of anterior communicating artery |
Is a |
False |
Congenital arterial aneurysm |
Inferred relationship |
Some |
|
Congenital retinal aneurysm (disorder) |
Is a |
False |
Congenital arterial aneurysm |
Inferred relationship |
Some |
|
Congenital peripheral aneurysm |
Is a |
False |
Congenital arterial aneurysm |
Inferred relationship |
Some |
|
Congenital brain aneurysm NEC |
Is a |
False |
Congenital arterial aneurysm |
Inferred relationship |
Some |
|
Congenital aneurysm NEC |
Is a |
False |
Congenital arterial aneurysm |
Inferred relationship |
Some |
|
Congenital aneurysm of ascending aorta |
Is a |
False |
Congenital arterial aneurysm |
Inferred relationship |
Some |
|
Congenital pulmonary artery aneurysm |
Is a |
True |
Congenital arterial aneurysm |
Inferred relationship |
Some |
|
Hemorrhage due to ruptured congenital cerebral aneurysm |
Is a |
False |
Congenital arterial aneurysm |
Inferred relationship |
Some |
|
Congenital aneurysm of systemic artery (disorder) |
Is a |
True |
Congenital arterial aneurysm |
Inferred relationship |
Some |
|
A rare, genetic, vascular disorder characterized by severe aneurysmal dilatation, elongation, and tortuosity of the thoracic aorta, its branches and pulmonary arteries with stenosis at various typical locations, typically resulting in infantile demise. Variable associated features may include cutis laxa, long philtrum with thin vermillion border, hypertelorism, sagging cheeks, arachnodactyly, joint laxity and pectus deformities. |
Is a |
True |
Congenital arterial aneurysm |
Inferred relationship |
Some |
|
A rare, genetic, systemic disease characterized by the presence of arterial aneurysms, tortuosity and dissection throughout the arterial tree, associated with early-onset osteoarthritis (predominantly affecting the spine, hands and/or wrists, and knees) and mild craniofacial dysmorphism (including long face, high forehead, flat supraorbital ridges, hypertelorism, malar hypoplasia and, anomalies of the palate and uvula), as well as mild skeletal and cutaneous anomalies. Joint abnormalities, such as osteochondritis dissecans and intervertebral disc degeneration, are frequently associated. Additional cardiovascular anomalies may include mitral valve defects, congenital heart malformations, ventricular hypertrophy and atrial fibrillation. |
Is a |
True |
Congenital arterial aneurysm |
Inferred relationship |
Some |
|