Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Intentional coumarin overdose |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Coumarin overdose of undetermined intent |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Accidental warfarin overdose |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
surdose intentionnelle de warfarine sodique |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
surdose de warfarin d'intention indéterminée |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Factor V Leiden mutation |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Homozygous Factor V Leiden mutation |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Heterozygous Factor V Leiden mutation |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Idiopathic factor VIII deficiency |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Autoimmune factor VIII deficiency |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Pregnancy-related factor VIII deficiency |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Malignancy-related factor VIII deficiency |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Antibody screen |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Hemolysin detection, cold |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Hemolysin detection, warm |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Acquired factor IX deficiency disease |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
RBC antibody detection, warm with titration |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Blood coagulation disorder with shortened coagulation time |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Blood coagulation disorder with prolonged coagulation time |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Blood coagulation disorder with shortened bleeding time |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Blood coagulation disorder with prolonged bleeding time (disorder) |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Blood coagulation disorder with impaired clot retraction time |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Deficiency of pyruvate kinase |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Deficiency of adenylate kinase (disorder) |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
von Willebrand disease, type IIF |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Hemorrhagic disease of the newborn due to vitamin K deficiency |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
1 |
Infusion of dextran (procedure) |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
1 |
Sickle cell-hemoglobin SS disease |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
1 |
Sickle cell-beta-thalassemia |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
1 |
Sickle cell beta plus thalassaemia |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
1 |
Sickle cell-beta^0^-thalassemia |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
1 |
Sickle cell-delta beta^0^-thalassemia |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
1 |
Sickle cell trait with coexistent alpha-thalassemia |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
1 |
Sickle cell-hemoglobin Lepore disease |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
1 |
Sickle cell-Hemoglobin O Arab disease |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
1 |
Apheresis |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
2 |
Blood coagulation disorder, categorised by value of screening test |
Finding site |
False |
Entire hematological system (body structure) |
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. |
Finding site |
False |
Entire hematological system (body structure) |
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). |
Finding site |
False |
Entire hematological system (body structure) |
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. |
Finding site |
False |
Entire hematological system (body structure) |
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. |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Hereditary von Willebrand disease type 1B |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Hereditary von Willebrand disease type 1C |
Finding site |
False |
Entire hematological system (body structure) |
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. |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Vitamin K deficiency coagulation disorder |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Hereditary von Willebrand disease type 1A |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
von Willebrand disease, type 1^a^ |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
von Willebrand disease type IA |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Hereditary von Willebrand disease type 2A |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
maladie de von Willebrand type 2A |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Hereditary von Willebrand disease type 2B |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
maladie de von Willebrand type 2B |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Acquired hypofibrinogenemia |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Hereditary von Willebrand disease type 2M |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Fibrinogen deficiency |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
maladie de von Willebrand type 2M |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Acquired afibrinogenemia |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Hereditary von Willebrand disease type 2N (disorder) |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
von Willebrand disease Normandy |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Antibody identification, RBC, albumin |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Chronic idiopathic thrombocytopenic purpura (disorder) |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
1 |
Hemolysin detection, cold, quantitative |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Purpura fulminans |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Anti-human globulin test, enzyme technique, titer |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Factor XIII inhibitor disorder |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Acquired factor VIII deficiency disease |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Acquired factor XII deficiency disease |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Protein S deficiency disease |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
dermatite ocra di Favre |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Stasis purpura |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Vitamin B12 absorption test |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
1 |
Vitamin B12 isotope studies (procedure) |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
2 |
Indirect Coombs test |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Drug-induced coagulation inhibitor disorder |
Finding site |
False |
Entire hematological system (body structure) |
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. |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Hereditary coagulation factor deficiency |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Compatibility test, crossmatch, screening for compatible unit, saline and/or high protein |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Blood unit collection for directed donation, donor |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Fresh frozen plasma preparation |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
RBC antibody detection, cold with titration |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Factor XIII deficiency disease |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Packed RBC preparation, sedimentation |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
RBC antibody detection with saline |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
von Willebrand disease, type IIC |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Lupus anticoagulant disorder |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
von Willebrand disease, type IIB |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Therapeutic plasmapheresis using plasma as major replacement fluid (procedure) |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
2 |
Blood typing, ABO, Rho(D) and red blood cell antibody screening (procedure) |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Pigmented purpuric lichenoid dermatitis of Gougerot and Blum |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Acquired factor VII deficiency disease |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Red cell iron utilization study |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
1 |
Antibody detection, RBC, saline, high protein and anti-human globulin technique |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Plasmapheresis |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
2 |
Vascular hemostatic disease |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Allergic purpura |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Blood group typing B |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Miscarriage with afibrinogenemia (disorder) |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Plasma radioiron turnover rate |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
1 |
Hemoglobin S disease without crisis |
Finding site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
1 |
Blood donor rejection, clerical |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|
Antibody detection, red blood cell, enzyme, 1 stage technique, including anti-human globulin (procedure) |
Procedure site |
False |
Entire hematological system (body structure) |
Inferred relationship |
Some |
|