Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Structure of small arteriole of dermis (body structure) |
Is a |
True |
Structure of arteriole |
Inferred relationship |
Some |
|
Entire arteriole |
Is a |
True |
Structure of arteriole |
Inferred relationship |
Some |
|
Structure of afferent arteriole |
Is a |
True |
Structure of arteriole |
Inferred relationship |
Some |
|
Structure of efferent arteriole |
Is a |
True |
Structure of arteriole |
Inferred relationship |
Some |
|
artériole droite |
Is a |
False |
Structure of arteriole |
Inferred relationship |
Some |
|
Structure of splenic arterioles |
Is a |
True |
Structure of arteriole |
Inferred relationship |
Some |
|
All arterioles |
Is a |
True |
Structure of arteriole |
Inferred relationship |
Some |
|
Arteriolar nephritis |
Finding site |
False |
Structure of arteriole |
Inferred relationship |
Some |
1 |
Pericyte of Rouget |
partie de |
False |
Structure of arteriole |
Additional relationship |
Some |
|
Arteriolitis |
Finding site |
False |
Structure of arteriole |
Inferred relationship |
Some |
1 |
Arteriolitis |
Finding site |
True |
Structure of arteriole |
Inferred relationship |
Some |
1 |
Microvascular embolism of arteriole (disorder) |
Finding site |
True |
Structure of arteriole |
Inferred relationship |
Some |
1 |
Disorder of arteriole |
Finding site |
True |
Structure of arteriole |
Inferred relationship |
Some |
1 |
Structure of endometrial spiral arteriole |
Is a |
True |
Structure of arteriole |
Inferred relationship |
Some |
|
Calcific arteriolopathy due to uremia (disorder) |
Finding site |
True |
Structure of arteriole |
Inferred relationship |
Some |
1 |
Non-uremic calcific arteriolopathy |
Finding site |
True |
Structure of arteriole |
Inferred relationship |
Some |
1 |
Dieulafoy vascular malformation of duodenum (disorder) |
Finding site |
False |
Structure of arteriole |
Inferred relationship |
Some |
2 |
Dieulafoy vascular malformation of stomach (disorder) |
Finding site |
False |
Structure of arteriole |
Inferred relationship |
Some |
2 |
Dieulafoy's vascular malformation |
Finding site |
False |
Structure of arteriole |
Inferred relationship |
Some |
2 |
A rare genetic cerebral small vessel disease characterized by an adult-onset primary microangiopathy with severe atherosclerosis of arterioles and secondary leukoencephalopathy. Patients may present with migraine, transient ischemic attacks, stroke with central facial palsy, cognitive dysfunction with impaired concentration, dementia, depression, movement disorder, vertigo, dysphagia, dysarthria, sicca syndrome, impaired REM sleep, and therapy-resistant hypertension, among others. Brain MRI typically shows a leukoencephalopathy that is disproportionately severe and extensive compared to the clinical disease. |
Finding site |
True |
Structure of arteriole |
Inferred relationship |
Some |
1 |
Structure of arteriolae rectae of kidney |
Is a |
True |
Structure of arteriole |
Inferred relationship |
Some |
|
Thrombotic microangiopathy |
Finding site |
True |
Structure of arteriole |
Inferred relationship |
Some |
2 |
Autoimmune thrombotic thrombocytopenic purpura (disorder) |
Finding site |
True |
Structure of arteriole |
Inferred relationship |
Some |
1 |
Acquired thrombotic thrombocytopenic purpura (disorder) |
Finding site |
True |
Structure of arteriole |
Inferred relationship |
Some |
1 |
Drug induced thrombotic thrombocytopenic purpura (disorder) |
Finding site |
True |
Structure of arteriole |
Inferred relationship |
Some |
8 |
Thrombotic thrombocytopenic purpura |
Finding site |
True |
Structure of arteriole |
Inferred relationship |
Some |
6 |
Chronic thrombotic microangiopathy |
Finding site |
True |
Structure of arteriole |
Inferred relationship |
Some |
3 |
Acute intravascular thrombotic microangiopathy |
Finding site |
True |
Structure of arteriole |
Inferred relationship |
Some |
3 |
Upshaw-Schulman syndrome (disorder) |
Finding site |
True |
Structure of arteriole |
Inferred relationship |
Some |
9 |
A rare renal disease characterized by thrombotic microangiopathy developing de novo in kidney transplant recipients with no evidence of occurrence of the disease prior to transplantation. Precipitating factors include antibody-mediated rejection, immunosuppressive medication, viral infections, and genetic abnormalities in the complement cascade, among others. The condition most commonly occurs within the first 3-6 months post-transplantation. Clinical presentation is highly variable and ranges from a limited form confined to the kidney with relatively good prognosis to a systemic variant consisting of the classic triad of thrombocytopenia, microangiopathic hemolytic anemia, and acute kidney injury. |
Finding site |
True |
Structure of arteriole |
Inferred relationship |
Some |
2 |
Thrombotic microangiopathy following hemopoietic stem cell transplant (disorder) |
Finding site |
True |
Structure of arteriole |
Inferred relationship |
Some |
2 |
Hemolytic uremic syndrome, adult type |
Finding site |
True |
Structure of arteriole |
Inferred relationship |
Some |
10 |
Hemolytic uremic syndrome of childhood |
Finding site |
True |
Structure of arteriole |
Inferred relationship |
Some |
11 |
Diarrhea-associated hemolytic uremic syndrome (disorder) |
Finding site |
True |
Structure of arteriole |
Inferred relationship |
Some |
12 |
Diarrhea-negative hemolytic uremic syndrome (disorder) |
Finding site |
True |
Structure of arteriole |
Inferred relationship |
Some |
10 |
Atypical haemolytic uraemic syndrome |
Finding site |
True |
Structure of arteriole |
Inferred relationship |
Some |
11 |
Congenital hemolytic uremic syndrome (disorder) |
Finding site |
True |
Structure of arteriole |
Inferred relationship |
Some |
4 |
Hemolytic uremic syndrome |
Finding site |
True |
Structure of arteriole |
Inferred relationship |
Some |
11 |
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. |
Finding site |
True |
Structure of arteriole |
Inferred relationship |
Some |
6 |
A rare genetic hemolytic uremic syndrome (HUS) characterized by infantile onset of relapsing episodes of microangiopathic hemolytic anemia, thrombocytopenia, and acute kidney injury. The episodes are often preceded by viral infections. Affected individuals typically present persistent hypertension, hematuria, and proteinuria (sometimes in the nephrotic range) and develop chronic kidney disease with age. |
Finding site |
True |
Structure of arteriole |
Inferred relationship |
Some |
10 |
A rare type of hemolytic uremic syndrome (HUS) characterized by the triad of hemolytic anemia due to generalized thrombotic microangiopathy, thrombocytopenia, and acute kidney injury, and most commonly occurring after acute gastroenteritis due to Shiga toxin-producing enterohemorrhagic Escherichia coli or Shigella dysenteriae. Other infectious causes of HUS include Streptococcus pneumoniae, HIV, Mycoplasma pneumoniae, Histoplasmosis, and Coxsackie virus. |
Finding site |
True |
Structure of arteriole |
Inferred relationship |
Some |
11 |
Atypical haemolytic uraemic syndrome with complement gene abnormality |
Finding site |
True |
Structure of arteriole |
Inferred relationship |
Some |
13 |
Atypical haemolytic uraemic syndrome with anti-factor H antibodies |
Finding site |
True |
Structure of arteriole |
Inferred relationship |
Some |
14 |