| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
3 |
| GATA binding protein 1 related thrombocytopenia with dyserythropoiesis (disorder) |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
3 |
| Macrothrombocytopenia with mitral valve insufficiency |
interprète (attribut) |
False |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
3 |
| Failed attempted termination of pregnancy with afibrinogenaemia |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Blood coagulation disorder with prolonged bleeding time |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Mediterranean thrombocytopenia |
interprète (attribut) |
False |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
2 |
| Periodontitis co-occurrent with Chédiak-Higashi syndrome |
interprète (attribut) |
False |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
3 |
| von Willebrand disease type 2M |
interprète (attribut) |
False |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Hereditary factor X deficiency disease |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| von Willebrand disease type 2B |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Blood coagulation disorder complicating childbirth |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Familial multiple factor deficiency syndrome |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Hemophilia |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Chronic acquired pure red cell aplasia |
interprète (attribut) |
False |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
6 |
| Homozygous prothrombin G20210A mutation (disorder) |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Familial multiple factor deficiency syndrome, type I |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Late onset diffuse bleeding diathesis secondary to vitamin K deficient hemorrhagic disease of fetus and newborn (disorder) |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
2 |
| Steroid purpura |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
2 |
| Acquired factor IX deficiency disease |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Haemorrhagic disorder due to increase in anti-10a |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Non-thrombocytopenic purpura |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
2 |
| Postpartum coagulation defects |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Postpartum fibrinolysis with hemorrhage |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
2 |
| Acquired pancytopenia |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
5 |
| von Willebrand disease, type IIE (disorder) |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Fibrinogen abnormality |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Miscarriage with defibrination syndrome |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| von Willebrand disease, type IIA |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Antiprothrombin disorder |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome (disorder) |
interprète (attribut) |
False |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
2 |
| Capillary fragility abnormality |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
3 |
| Thrombocytopenia due to extracorporeal circulation of blood |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
2 |
| von Willebrand disease, type IIF |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Neonatal antiphospholipid syndrome (disorder) |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
2 |
| Acquired PF-3 disease |
interprète (attribut) |
False |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
2 |
| Autosomal dominant deficiency of plasminogen |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| High molecular weight kininogen deficiency |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Pancytopenia-dysmelia |
interprète (attribut) |
False |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
5 |
| Autoimmune factor VIII deficiency |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Secondary non-thrombocytopenic purpura |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
2 |
| Platelet factor V deficiency (factor V Quebec) |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Hyperglobulinemic purpura (disorder) |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
2 |
| Hereditary thrombophilia (disorder) |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Cryofibrinogenemic purpura (disorder) |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
2 |
| Immune thrombocytopenic purpura (disorder) |
interprète (attribut) |
False |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
4 |
| purpura de stase |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
2 |
| Purpura due to increased intravascular pressure (disorder) |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
2 |
| Cryoglobulinemic purpura |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
2 |
| Heterozygous protein S deficiency (disorder) |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Acquired red cell aplasia |
interprète (attribut) |
False |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
6 |
| Early onset diffuse bleeding diathesis secondary to vitamin K deficient hemorrhagic disease of fetus and newborn (disorder) |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
2 |
| Hereditary factor XIII A subunit deficiency (disorder) |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Exhausted platelets |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Alpha-2-antiplasmin deficiency |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Postpartum coagulation defect with haemorrhage |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
2 |
| thrombopénie néonatale auto-immune |
interprète (attribut) |
False |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
3 |
| Blood coagulation disorder with impaired clot retraction time |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Afibrinogenemia following molar AND/OR ectopic pregnancy |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Factor XI deficiency, type II |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Hereditary factor IX deficiency disease without inhibitor (disorder) |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Megakaryocytic aplasia |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
2 |
| Neonatal alloimmune thrombocytopenia |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
2 |
| von Willebrand disease type 2A |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Heterozygous prothrombin G20210A mutation (disorder) |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Hemorrhagic disorder due to increase in anti-11a |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Fibrinolytic bleeding syndrome |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Purpura annularis telangiectodes of Majocchi (disorder) |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
3 |
| Induced termination of pregnancy complicated by defibrination syndrome (disorder) |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| purpura sénile (trouble) |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
2 |
| Familial multiple factor deficiency syndrome, type II |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Qualitative platelet disorder (disorder) |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Constitutional aplastic anemia with malformation |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
6 |
| Factor VIII deficiency |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Combined coagulation factor deficiency |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Fibrinolysis - postpartum |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Hereditary factor IX deficiency disease with inhibitor (disorder) |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Hereditary factor XIII deficiency disease (disorder) |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Familial multiple factor deficiency syndrome, type IV |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Classic onset hemorrhagic disease of newborn due to vitamin K deficiency |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
2 |
| Hereditary elevated factor XI (disorder) |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Factitious purpura |
interprète (attribut) |
False |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
2 |
| Embolic purpura |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
2 |
| Severe hereditary factor VIII deficiency disease without inhibitor (disorder) |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Miscarriage with afibrinogenemia (disorder) |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Autoimmune pancytopenia |
interprète (attribut) |
False |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
5 |
| Posttransfusion purpura |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
3 |
| Systemic fibrinogenolysis |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Hereditary combined coagulation factor deficiency (disorder) |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Postpartum coagulation defects - delivered with postnatal problem |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Hereditary antithrombin III deficiency (disorder) |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Thrombophilia associated with pregnancy |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Platelet type von Willebrand's disease |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Hereditary hyperfibrinogenemia (disorder) |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
2 |
| Moderate hereditary factor VIII deficiency disease with inhibitor (disorder) |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Thrombocytopathy, asplenia and miosis (disorder) |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
3 |
| Hypofibrinogenaemia |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Neonatal thrombocytopenia associated with maternal idiopathic thrombocytopenic purpura |
interprète (attribut) |
False |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
2 |
| purpura thrombopénique thrombotique (trouble) |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
8 |
| Hyperheparinemia |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Hereditary elevated factor VIII (disorder) |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
| Dysplasminogenemia |
interprète (attribut) |
True |
Hemostatic function (observable entity) |
Inferred relationship |
Some |
1 |
FHIR