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74848003: Hemostatic function (observable entity)

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1204583012 Hemostatic function (observable entity) en Fully specified name Active Case insensitive SNOMED CT core
124302017 Hemostatic function en Synonym Active Case insensitive SNOMED CT core
124306019 Blood coagulation en Synonym Active Case insensitive SNOMED CT core
124307011 Blood clotting en Synonym Active Case insensitive SNOMED CT core
124310016 Hemostasis en Synonym Active Case insensitive SNOMED CT core
502831011 Haemostasis en Synonym Active Case insensitive SNOMED CT core
502832016 Haemostatic function en Synonym Active Case insensitive SNOMED CT core

28 descendants. Search Descendants:

Expanded Value Set

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

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Reference Sets

Observable entity foundation reference set

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