Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Idiopathic polypoidal choroidal vasculopathy |
Is a |
False |
Vascular disorder |
Inferred relationship |
Some |
|
Assessment using Padua Prediction Score for risk of venous thromboembolism |
Has focus |
True |
Vascular disorder |
Inferred relationship |
Some |
1 |
Vascular disorder of testis (disorder) |
Is a |
True |
Vascular disorder |
Inferred relationship |
Some |
|
Intravascular large B-cell lymphoma (IVLBCL) is a very rare form of diffuse large B-cell lymphoma characterized by the selective growth of lymphoma cells within the lumina of small blood vessels (especially the capillaries) that most often presents with a wide range of clinical manifestations (as potentially any tissue can be involved), with patients from Western countries more frequently manifesting with neurological and cutaneous symptoms while patients from Asian countries more frequently displaying hepatosplenomegaly and thrombocytopenia. IVLBCL is characterized by an absence of lymphadenopathy, an aggressive clinical course and a poor prognosis. |
Is a |
True |
Vascular disorder |
Inferred relationship |
Some |
|
Pseudoaneurysm of vascular access site (disorder) |
Is a |
True |
Vascular disorder |
Inferred relationship |
Some |
|
Air embolism complicating intravenous therapy |
Is a |
True |
Vascular disorder |
Inferred relationship |
Some |
|
Air embolism due to surgery |
Is a |
True |
Vascular disorder |
Inferred relationship |
Some |
|
Solitary fibrous tumor |
Is a |
False |
Vascular disorder |
Inferred relationship |
Some |
|
Hypopituitarism due to vascular disorder |
Due to |
True |
Vascular disorder |
Inferred relationship |
Some |
2 |
Benign hemangioma of esophagus |
Is a |
True |
Vascular disorder |
Inferred relationship |
Some |
|
Hemangioma of choroid |
Is a |
True |
Vascular disorder |
Inferred relationship |
Some |
|
Telangiectasia disorder |
Is a |
True |
Vascular disorder |
Inferred relationship |
Some |
|
Telangiectasia due to prolonged vasodilatation (disorder) |
Due to |
True |
Vascular disorder |
Inferred relationship |
Some |
2 |
Vascular lesion of left eyelid |
Is a |
False |
Vascular disorder |
Inferred relationship |
Some |
|
Vascular lesion of right eyelid |
Is a |
False |
Vascular disorder |
Inferred relationship |
Some |
|
Persistent flow of blood into aneurysm sac following endovascular insertion of stent graft (disorder) |
Is a |
True |
Vascular disorder |
Inferred relationship |
Some |
|
Silent white matter disease due to vascular disease |
Due to |
True |
Vascular disorder |
Inferred relationship |
Some |
2 |
ISSVA Classification of Vascular Anomalies ©2018 International Society for the Study of Vascular Anomalies Available at "issva.org/classification" Accessed May 25, 2022. |
Is a |
True |
Vascular disorder |
Inferred relationship |
Some |
|
ISSVA Classification of Vascular Anomalies ©2018 International Society for the Study of Vascular Anomalies Available at "issva.org/classification" Accessed May 11, 2022. |
Is a |
True |
Vascular disorder |
Inferred relationship |
Some |
|
Vascular lesion of eyelid |
Is a |
True |
Vascular disorder |
Inferred relationship |
Some |
|
Iris roseola |
Is a |
False |
Vascular disorder |
Inferred relationship |
Some |
|
Iris papulosa |
Is a |
False |
Vascular disorder |
Inferred relationship |
Some |
|
Myopathy of extraocular muscle due to disorder of blood vessel (disorder) |
Due to |
True |
Vascular disorder |
Inferred relationship |
Some |
2 |
Cauda equina syndrome due to vascular disorder |
Due to |
True |
Vascular disorder |
Inferred relationship |
Some |
2 |
Intravascular hemolysis following ectopic pregnancy |
Is a |
True |
Vascular disorder |
Inferred relationship |
Some |
|
Intravascular hemolysis following molar pregnancy |
Is a |
True |
Vascular disorder |
Inferred relationship |
Some |
|
A disorder characterized by the presence of RPE (retinal pigment epithelium) disruption within the posterior pole over regions of choroidal thickening in eyes, showing no evidence of active or prior CSC (central serous chorioretinopathy). |
Is a |
False |
Vascular disorder |
Inferred relationship |
Some |
|
Anastomosing haemangioma |
Is a |
True |
Vascular disorder |
Inferred relationship |
Some |
|
Intracranial aneurysm |
Is a |
True |
Vascular disorder |
Inferred relationship |
Some |
|
Angiodysplasia of gastrointestinal tract |
Is a |
True |
Vascular disorder |
Inferred relationship |
Some |
|
Disorder of ocular blood vessel (disorder) |
Is a |
True |
Vascular disorder |
Inferred relationship |
Some |
|
Open angle glaucoma of left eye due to vascular disorder (disorder) |
Due to |
True |
Vascular disorder |
Inferred relationship |
Some |
2 |
Open angle glaucoma of bilateral eyes due to vascular disorder (disorder) |
Due to |
True |
Vascular disorder |
Inferred relationship |
Some |
3 |
Open angle glaucoma of right eye due to vascular disorder (disorder) |
Due to |
True |
Vascular disorder |
Inferred relationship |
Some |
2 |
Metastatic malignant neoplasm to blood vessel of perineum |
Is a |
True |
Vascular disorder |
Inferred relationship |
Some |
|
Cervical spondylosis with vascular compression |
Is a |
True |
Vascular disorder |
Inferred relationship |
Some |
|
Cavernous haemangioma of spinal cord |
Is a |
True |
Vascular disorder |
Inferred relationship |
Some |
|
A rare, neurodegenerative disease characterized by progressive dementia and ataxia, widespread cerebral amyloid angiopathy and parenchymal amyloid deposition. Two subtypes have been identified, ABri amyloidosis and ADan amyloidosis. |
Is a |
True |
Vascular disorder |
Inferred relationship |
Some |
|
Secondary systemic amyloid angiopathy of cerebrum (disorder) |
Is a |
True |
Vascular disorder |
Inferred relationship |
Some |
|
A rare type of Ehlers-Danlos syndrome characterised by connective tissue defects (joint laxity of finger joints and knees, small joint hypermotility and tissue fragility), vascular complications (atrioventricular defect, symptomatic cerebral aneurysm, vascular dissection) and frontoparietally accentuated polymicrogyria of the cobblestone variant. Specific brain anomalies (including cerebrocortical dysplasia, cerebellar microcysts and white matter anomalies) are present in all patients. Most of the affected individuals have developmental delay and may develop epilepsy. Additional clinical features include spontaneous intracranial hypotension, idiopathic intracranial hypertension, headache, chronic pain syndrome, peripheral neuropathy, plexopathy, translucent skin and clubfoot. Dysmorphic features such as eye anomalies (strabismus, bilateral hyperopia, esotropia, proptosis), pinched nose, thin upper lip, crowded teeth and retrognathia are also reported. |
Is a |
True |
Vascular disorder |
Inferred relationship |
Some |
|