Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Coronary arteritis |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Thrombophlebitis of vena cava |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Thrombophlebitis of pelvic vein |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Renal vasculitis |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Thrombophlebitis migrans |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Thrombophlebitis of lower extremities |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Thrombophlebitis of central nervous system venous sinuses (disorder) |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Intracranial thrombophlebitis |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Phlebitis of lower limb vein |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Retinal phlebitis |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Thrombophlebitis of upper extremities |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Orbital thrombophlebitis |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Retinal arteritis |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Cerebral arteritis |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Thrombophlebitis of breast |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Aortitis |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Temporal arteritis (disorder) |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Thrombophlebitis of subclavian vein (disorder) |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Primary angiitis of central nervous system |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Thrombophlebitis of left jugular vein |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Thrombophlebitis of right jugular vein (disorder) |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Thrombophlebitis after infusion |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Thrombophlebitis during procedure |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Hughes-Stovin syndrome (HSS) is a life-threatening disorder, believed to be a cardiovascular clinical variant manifestation of Behcet disease. It is characterized by the association of multiple pulmonary artery aneurysms (PAAs) and peripheral venous thrombosis. |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Vasculitis of mesenteric artery (disorder) |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Inflammation of fetal umbilical artery (disorder) |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Phlebitis of intracranial venous sinus |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Lemierre syndrome is a rare, potentially lethal, oropharyngeal infectious disease occurring in immunocompetent adolescents and young adults that is mainly due to Fusobacterium necrophorum and that is characterised by septic thrombophlebitis of the internal jugular vein that leads to septic, usually pulmonary, embolism, associated with ENT (ear, nose, and throat) infection that manifests with fever, neck pain, and tonsillopharyngitis. |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Secondary systemic vasculitis |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Primary systemic vasculitis (disorder) |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Interstitial lung disease co-occurrent and due to systemic vasculitis (disorder) |
Due to |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
1 |
Demyelination due to systemic vasculitis (disorder) |
Due to |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
1 |
Rheumatoid arthritis with systemic vasculitis (disorder) |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Primary systemic arteritis (disorder) |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Phlebitis of iliac vein |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Mondor's phlebitis of the penis |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
Cranial giant cell arteritis |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|
A rare vasculitis characterized by mostly unilateral inflammation of the temporal artery affecting patients up to fifty years of age. Patients typically present with a lump in the temporal region or a prominent temporal artery and often have headaches. Males are more frequently affected than females, and major systemic symptoms, ocular complications, and a biological inflammatory syndrome are usually absent, although peripheral blood eosinophilia may be seen. Histopathological analysis shows arteritis predominantly of the intima with possible extension to the perivascular tissue. The presence of granuloma, giant cells or fibrinoid necrosis is rare. Clinical relapses after one episode are uncommon. |
Is a |
False |
Inflammation of systemic vasculature |
Inferred relationship |
Some |
|