Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Capillaritis caused by drug (disorder) |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
Nevus anemicus |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
Port-wine stain in proteus syndrome (disorder) |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
Capillary malformation |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
Thrombotic thrombocytopenic purpura |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
2 |
Progressive pigmentary dermatosis of Schamberg |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
2 |
Acquired thrombotic thrombocytopenic purpura (disorder) |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
Autoimmune thrombotic thrombocytopenic purpura (disorder) |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
Drug induced thrombotic thrombocytopenic purpura (disorder) |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
Acquired thrombotic thrombocytopenic purpura (disorder) |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
Drug induced thrombotic thrombocytopenic purpura (disorder) |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
Autoimmune thrombotic thrombocytopenic purpura (disorder) |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
Eczematid-like purpura of Doucas and Kapetanakis |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
Port-wine stain in proteus syndrome (disorder) |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
2 |
Capillary malformation |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
2 |
Salmon patch naevus |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
3 |
Hereditary vascular fragility |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
2 |
Capillary fragility abnormality |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
4 |
Nevus anemicus |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
3 |
Port-wine stain with oculocutaneous melanosis (disorder) |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
2 |
Port-wine stain with associated anomalies (disorder) |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
2 |
Port-wine stain in Rubinstein-Taybi syndrome (disorder) |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
2 |
Port-wine stain associated with spinal dysraphism (disorder) |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
3 |
Salmon patch naevus |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
2 |
Nevus anemicus |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
2 |
Capillary-venous malformation |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
3 |
Capillary-venous-lymphatic malformation |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
6 |
Congenital capillary hemangioma (disorder) |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
Phakomatosis cesioflammea |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
5 |
Phakomatosis spilorosea |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
5 |
Phakomatosis caesiomarmorata |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
5 |
Microcephaly-capillary malformation syndrome |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
3 |
Megalencephaly-capillary malformation syndrome |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
5 |
Pulmonary capillaritis (disorder) |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
A small vessel vasculitis restricted to the lungs that may induce diffuse alveolar hemorrhage without any underlying systemic disease. |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
Capillary-venous malformation |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
2 |
Microcephaly-capillary malformation syndrome |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
2 |
A rare, complex, vascular malformation syndrome characterized by capillary malformation of the lower lip, lymphatic malformation of the face and neck, asymmetry of face and limbs, and partial or generalized overgrowth involving one or more body segments. |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
5 |
Platelet embolism (disorder) |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
A life-threatening, rapidly progressive thrombotic disorder affecting mainly neonates and children that is characterized by purpuric skin lesions and disseminated intravascular coagulation. It may progress rapidly to multi-organ failure caused by thrombotic occlusion of small and medium-sized blood vessels. There are two forms of the disorder that are classified according to triggering mechanisms: acute infectious (the most common form), and idiopathic purpura fulminans. |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
5 |
Senile angioma |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
3 |
Megalencephaly-capillary malformation syndrome |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
Phakomatosis cesioflammea |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
Phakomatosis spilorosea |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
Phakomatosis caesiomarmorata |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
A rare, complex, vascular malformation syndrome characterized by capillary malformation of the lower lip, lymphatic malformation of the face and neck, asymmetry of face and limbs, and partial or generalized overgrowth involving one or more body segments. |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
Pigmented purpuric lichenoid dermatitis of Gougerot and Blum |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
2 |
Pulmonary capillary haemangiomatosis |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
Capillary hemangioma of eyelid |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
2 |
Lichen aureus |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
Capillary hemangioma of orbit |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
2 |
Capillary haemangioma of retina |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
Capillary hemangioma (disorder) |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
à l'examen : nævi angiomateux multiples |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
3 |
Capillary haemangioma of right orbit region |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
Capillary hemangioma of left orbit region (disorder) |
Finding site |
False |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
Megalencephaly capillary malformation |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
2 |
Structure of capillary of lung |
Is a |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
|
Acute intravascular thrombotic microangiopathy |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
Chronic thrombotic microangiopathy |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
Capillary specimen collection |
Procedure site - Indirect (attribute) |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
Heel stick (procedure) |
Procedure site - Indirect (attribute) |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
Ear lobe stick (procedure) |
Procedure site - Indirect (attribute) |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
Thumb-prick sampling |
Procedure site - Indirect (attribute) |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
Finger stick |
Procedure site - Indirect (attribute) |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
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 capillary blood vessel |
Inferred relationship |
Some |
2 |
Capillaroscopy |
Procedure site - Direct (attribute) |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
A life-threatening, rapidly progressive thrombotic disorder affecting mainly neonates and children that is characterized by purpuric skin lesions and disseminated intravascular coagulation. It may progress rapidly to multi-organ failure caused by thrombotic occlusion of small and medium-sized blood vessels. There are two forms of the disorder that are classified according to triggering mechanisms: acute infectious (the most common form), and idiopathic purpura fulminans. |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
2 |
Autoimmune thrombotic thrombocytopenic purpura (disorder) |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
10 |
Acquired thrombotic thrombocytopenic purpura (disorder) |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
10 |
Upshaw-Schulman syndrome (disorder) |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
10 |
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 capillary blood vessel |
Inferred relationship |
Some |
1 |
A rare vascular anomaly characterized by the association of capillary and venous malformations with hypotrophy or shortening of an affected limb due to alterations in bones, muscles, or subcutaneous tissues. In most cases, at least one of the findings is noted shortly after birth, while the other components become evident later in infancy. |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
2 |
Thrombotic microangiopathy following hemopoietic stem cell transplant (disorder) |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
Infantile haemangioma of liver |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
2 |
Giant infantile haemangioma |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
Infantile hemangioma of subglottis (disorder) |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
2 |
Segmental infantile hemangioma |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
Infantile hemangioma (disorder) |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
1 |
Structure of capillary blood vessel of orbital region (body structure) |
Is a |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
|
Hemolytic uremic syndrome, adult type |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
11 |
Hemolytic uremic syndrome of childhood |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
12 |
Diarrhea-associated hemolytic uremic syndrome (disorder) |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
13 |
Diarrhea-negative hemolytic uremic syndrome (disorder) |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
11 |
Atypical haemolytic uraemic syndrome |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
12 |
Congenital hemolytic uremic syndrome (disorder) |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
11 |
Hemolytic uremic syndrome |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
10 |
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 capillary blood vessel |
Inferred relationship |
Some |
2 |
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 capillary blood vessel |
Inferred relationship |
Some |
11 |
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 capillary blood vessel |
Inferred relationship |
Some |
12 |
Atypical haemolytic uraemic syndrome with complement gene abnormality |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
14 |
Atypical haemolytic uraemic syndrome with anti-factor H antibodies |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
13 |
Posterior fossa brain malformation, hemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality syndrome (disorder) |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
2 |
Posterior fossa brain malformation, hemangioma, arterial anomaly, cardiac defect, aortic coarctation, eye abnormality, sternal anomalies syndrome (disorder) |
Finding site |
True |
Structure of capillary blood vessel |
Inferred relationship |
Some |
3 |