Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Cyclooxygenase deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Thromboxane synthetase deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Giant platelet syndrome |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Acquired platelet disorder |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Amegakaryocytic thrombocytopenia |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Megakaryocytic thrombocytopenia |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
May-Hegglin anomaly |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
2 |
Montreal platelet syndrome (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Mediterranean thrombocytopenia |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Metabolic thrombocytopenic purpura |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Immune thrombocytopenic purpura |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Reactive thrombocytosis |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Post-splenectomy thrombocytosis |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Radionuclide study of neural receptors |
Procedure site |
False |
Body system structure |
Inferred relationship |
Some |
1 |
Whole body counter study with vitamin B12 |
Procedure site |
False |
Body system structure |
Inferred relationship |
Some |
2 |
Red cell mass measurement with Cr51 (procedure) |
Procedure site |
False |
Body system structure |
Inferred relationship |
Some |
1 |
Red cell mass measurement with Tc99m |
Procedure site |
False |
Body system structure |
Inferred relationship |
Some |
1 |
Abortion with afibrinogenemia |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Postpartum afibrinogenaemia with haemorrhage |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
HNSHA due to glutathione synthetase deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
SCID due to absent IL-2 receptor |
Finding site |
True |
Body system structure |
Inferred relationship |
Some |
1 |
Dysfibrinogenemia |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
purpura thrombopénique congénital |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Radionuclide studies in haematology |
Procedure site |
False |
Body system structure |
Inferred relationship |
Some |
1 |
Radionuclide red cell mass measurement |
Procedure site |
False |
Body system structure |
Inferred relationship |
Some |
1 |
Perinatal thrombocytopenia |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Autoimmune neonatal thrombocytopenia |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Anticoagulant-induced bleeding |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Anticoagulant excess without bleeding |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Acquired inhibitor of coagulation |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Acquired storage pool deficiency (platelets) |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Heparin overdose |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Accidental heparin overdose |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Intentional heparin overdose (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
surdose d'héparine d'intention indéterminée |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Coumarin overdose |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Accidental coumarin overdose |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Intentional coumarin overdose |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Coumarin overdose of undetermined intent |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Accidental warfarin overdose |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
surdose intentionnelle de warfarine sodique |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
surdose de warfarin d'intention indéterminée |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Exhausted platelets |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Hereditary nonspherocytic haemolytic anaemia |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Thrombocytopenic disorder |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Thrombocytopenic purpura |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Radionuclide blood cell study |
Procedure site |
False |
Body system structure |
Inferred relationship |
Some |
1 |
Factor V Leiden mutation |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Homozygous Factor V Leiden mutation |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Heterozygous Factor V Leiden mutation |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Thrombocytopenia due to massive blood transfusion |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Idiopathic factor VIII deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Autoimmune factor VIII deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Pregnancy-related factor VIII deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Malignancy-related factor VIII deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Platelet sequestration |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Thrombocytopenia due to sequestration |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Acquired factor IX deficiency disease |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Hereditary disorder of cellular element of blood (disorder) |
Finding site |
True |
Body system structure |
Inferred relationship |
Some |
1 |
Hereditary red blood cell disorder (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Hereditary white blood cell disorder (disorder) |
Finding site |
True |
Body system structure |
Inferred relationship |
Some |
1 |
Blood coagulation disorder with shortened coagulation time |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Blood coagulation disorder with prolonged coagulation time |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Blood coagulation disorder with shortened bleeding time |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Blood coagulation disorder with prolonged bleeding time (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Blood coagulation disorder with impaired clot retraction time |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
von Willebrand disease, type IIF |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Hemorrhagic disease of the newborn due to vitamin K deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Pancytopenia |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Hereditary hemoglobinopathy due to globin chain mutation |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Blood coagulation disorder, categorised by value of screening test |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Benign gestational thrombocytopenia |
Finding site |
False |
Body system structure |
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. |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Secondary autoimmune thrombocytopenia |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Alloimmune thrombocytopenia |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Alloimmune platelet transfusion refractoriness |
Finding site |
False |
Body system 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 |
Body system 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 |
Body system 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 |
Body system 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 |
Body system structure |
Inferred relationship |
Some |
|
Hereditary von Willebrand disease type 1B |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Hereditary von Willebrand disease type 1C |
Finding site |
False |
Body system 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 |
Body system structure |
Inferred relationship |
Some |
|
Vitamin K deficiency coagulation disorder |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Hereditary von Willebrand disease type 1A |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
von Willebrand disease, type 1^a^ |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
von Willebrand disease type IA |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Hereditary von Willebrand disease type 2A |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
maladie de von Willebrand type 2A |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Hereditary von Willebrand disease type 2B |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
maladie de von Willebrand type 2B |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Acquired hypofibrinogenemia |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Hereditary von Willebrand disease type 2M |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Fibrinogen deficiency |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
maladie de von Willebrand type 2M |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Acquired afibrinogenemia |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Hereditary von Willebrand disease type 2N (disorder) |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
von Willebrand disease Normandy |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Factor XIII inhibitor disorder |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|
Acquired factor VIII deficiency disease |
Finding site |
False |
Body system structure |
Inferred relationship |
Some |
|