Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Accidental heparin overdose |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Intentional heparin overdose (disorder) |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
surdose d'héparine d'intention indéterminée |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Coumarin overdose |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Accidental coumarin overdose |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Intentional coumarin overdose |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Coumarin overdose of undetermined intent |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Accidental warfarin overdose |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
surdose intentionnelle de warfarine sodique |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
surdose de warfarin d'intention indéterminée |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Exhausted platelets |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Thrombocytopenic disorder |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Thrombocytopenic purpura |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Factor V Leiden mutation |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Homozygous Factor V Leiden mutation |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Heterozygous Factor V Leiden mutation |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Thrombocytopenia due to massive blood transfusion |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Idiopathic factor VIII deficiency |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Autoimmune factor VIII deficiency |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Pregnancy-related factor VIII deficiency |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Malignancy-related factor VIII deficiency |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Platelet sequestration |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Thrombocytopenia due to sequestration |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Acquired factor IX deficiency disease |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Purpura hemorrhagica in equine |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Uremic thrombocytopenia (disorder) |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Thrombocytopenic purpura associated with metabolic disorder (disorder) |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Blood coagulation disorder with shortened coagulation time |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Blood coagulation disorder with prolonged coagulation time |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Blood coagulation disorder with shortened bleeding time |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Blood coagulation disorder with prolonged bleeding time (disorder) |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Blood coagulation disorder with impaired clot retraction time |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Amegakaryocytic thrombocytopenia with congenital malformation |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Megakaryocytic aplasia |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
von Willebrand disease, type IIF |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Hemorrhagic disease of the newborn due to vitamin K deficiency |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Pancytopenia |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Blood coagulation disorder, categorised by value of screening test |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Benign gestational thrombocytopenia |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
An autoimmune coagulation disorder characterized by isolated thrombocytopenia (a platelet count <100,000/microL), in the absence of any underlying disorder that may be associated with thrombocytopenia. |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Secondary autoimmune thrombocytopenia |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Alloimmune thrombocytopenia |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Alloimmune platelet transfusion refractoriness |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Acquired platelet function disorder (disorder) |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Hereditary platelet function disorder |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Scott syndrome |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Platelet storage pool defect |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Mixed alpha granule and dense body deficiency |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Platelet factor V deficiency (factor V Quebec) |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Familial alpha>2< adrenergic receptor defect in platelets |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Isolated collagen aggregation defect |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Includes true von Willebrand disease with mutation at the VWF locus, as well as mimicking disorders with other mutations (pseudo VWD) and acquired von Willebrand syndrome. |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
A form of von Willebrand disease (VWD) characterised by a bleeding disorder associated with a partial, quantitative plasmatic deficiency of an otherwise structurally and functionally normal von Willebrand factor (VWF). |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
A form of von Willebrand disease (VWD) characterised by a bleeding disorder associated with a qualitative deficiency and functional anomalies of the Willebrand factor (VWF). Depending on the type of functional abnormalities, this form is classified as type 2A, 2B, 2M or 2N. |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
A form of von Willebrand disease (VWD) characterised by a bleeding disorder associated with a total or near-total absence of Willebrand factor (VWF) in the plasma and cellular compartments, also leading to a profound deficiency of plasmatic factor VIII (FVIII). It is the most severe form of VWD. |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Hereditary von Willebrand disease type 1B |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Hereditary von Willebrand disease type 1C |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
A bleeding disorder characterized by mild to moderate mucocutaneous bleeding, which becomes more pronounced during pregnancy or following ingestion of drugs that have anti-platelet activity. This disease is due to hyperresponsive platelets, resulting in thrombocytopenia. |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Vitamin K deficiency coagulation disorder |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Hereditary von Willebrand disease type 1A |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
von Willebrand disease, type 1^a^ |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
von Willebrand disease type IA |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Hereditary von Willebrand disease type 2A |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
maladie de von Willebrand type 2A |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Hereditary von Willebrand disease type 2B |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
maladie de von Willebrand type 2B |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Acquired hypofibrinogenemia |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Hereditary von Willebrand disease type 2M |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Fibrinogen deficiency |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
maladie de von Willebrand type 2M |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Acquired afibrinogenemia |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Hereditary von Willebrand disease type 2N (disorder) |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
von Willebrand disease Normandy |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Chronic idiopathic thrombocytopenic purpura (disorder) |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Purpura fulminans |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Factor XIII inhibitor disorder |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Acquired factor VIII deficiency disease |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Acquired factor XII deficiency disease |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Protein S deficiency disease |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
dermatite ocra di Favre |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Stasis purpura |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Drug-induced coagulation inhibitor disorder |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
A severe form of hemophilia A characterized by a large deficiency of factor VIII (biological activity <1 IU/dL) leading to frequent spontaneous hemorrhage and abnormal bleeding as a result of minor injuries, or following trauma, surgery or tooth extraction. It primarily affects males but may also be observed in female carriers of disease-causing mutations. |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Hereditary coagulation factor deficiency |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Platelet dysfunction caused by aspirin (disorder) |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Autoimmune pancytopenia |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Factor XIII deficiency disease |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
von Willebrand disease, type IIC |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Lupus anticoagulant disorder |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Drug-induced immune thrombocytopenia |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
von Willebrand disease, type IIB |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Pigmented purpuric lichenoid dermatitis of Gougerot and Blum |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Acquired factor VII deficiency disease |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Vascular hemostatic disease |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Allergic purpura |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Miscarriage with afibrinogenemia (disorder) |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Platelet disorder |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Transient neonatal thrombocytopenia |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
T activation syndrome |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Hemorrhagic disease of the newborn due to factor II deficiency |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
von Willebrand disease, type IIH |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|