Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Accidental heparin overdose |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Intentional heparin overdose |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
overdosis af heparin, uvist med hvilken hensigt |
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 |
|
overdosis af cumarin, uvist med hvilken hensigt |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Accidental warfarin overdose |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
tilsigtet overdosis af warfarinnatrium |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
overdosis af warfarin, uvist med hvilken hensigt |
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 (disorder) |
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 |
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 Willebrands sygdom, 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, categorized by value of screening test |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Benign gestational thrombocytopenia (disorder) |
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 |
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 (disorder) |
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) (disorder) |
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) with characteristics of a bleeding disorder associated with a partial, quantitative plasmatic deficiency of an otherwise structurally and functionally normal von Willebrand factor (VWF). The type 1 disease is considered to be the most common form of VWD, caused by mutations in the VWF gene (12p13.3). Transmitted in an autosomal dominant manner. |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
A form of von Willebrand disease (VWD) with characteristics of 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. The VWF gene (12p13.3) anomalies that lead to type 2 VWD involve the well-defined functional domains of the VWF protein. Most subtypes of type 2 VWD are transmitted in an autosomal dominant manner except for type 2N and some rare forms of type 2A which are autosomal recessive. |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
A total or near-total absence of Willebrand factor (VWF) in the plasma and cellular compartments leading to a profound deficiency of plasmatic factor VIII (FVIII). It is the most severe form of von Willebrand disease. Onset usually occurs during the neonatal period or in infancy, but later onset has been reported. The disease is caused by homozygous or compound heterozygous mutations (mainly missense or large mutations) in the VWF gene (12p13.3) that lead to synthesis of a truncated protein or allele silencing. The pattern of inheritance is autosomal recessive. |
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 with characteristics of 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 Willebrands sygdom, type 1^a^ |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
von Willebrands sygdom 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 |
|
von Willebrands sygdom 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 |
|
von Willebrands sygdom 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 |
|
von Willebrands sygdom 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 Willebrands sygdom type 2N |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Chronic idiopathic thrombocytopenic purpura |
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 |
|
Akroangiodermatit |
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 (disorder) |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|
Severe disease manifests factor VIII activity of less than 1%, except in the U.K. and Italy, where severe disease includes factor VIII activity levels of less than 2% |
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 Willebrands sygdom 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 Willebrands sygdom 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 |
|
Allergisk 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 (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-aktiveringssyndrom |
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 Willebrands sygdom type IIH |
Has definitional manifestation |
False |
Hemostatic system finding |
Inferred relationship |
Some |
|