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74848003: Hemostatic function (observable entity)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

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

28 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hemostatic function Is a Hematologic function true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Thrombocytopenia due to blood loss Interprets True Hemostatic function Inferred relationship Some 2
Factor IX deficiency (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Hereditary thrombocytopenia with normal platelets Interprets True Hemostatic function Inferred relationship Some 2
von Willebrand disease, type IIB Interprets False Hemostatic function Inferred relationship Some 1
Dysfibrinogenemia Interprets True Hemostatic function Inferred relationship Some 1
Hereditary von Willebrand disease type 2A Interprets True Hemostatic function Inferred relationship Some 1
Mild hereditary factor IX deficiency disease with inhibitor (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Hemorrhagic disorder due to increase in anti-8a (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Platelet disorder Interprets True Hemostatic function Inferred relationship Some 1
Gamma chain defect dysfibrinogenaemia Interprets True Hemostatic function Inferred relationship Some 1
Pseudo von Willebrand disease Interprets True Hemostatic function Inferred relationship Some 1
Passovoy factor deficiency Interprets True Hemostatic function Inferred relationship Some 1
Hereditary von Willebrand disease type 2 Interprets True Hemostatic function Inferred relationship Some 1
Hypoplasminogenaemia Interprets True Hemostatic function Inferred relationship Some 1
Purpura due to prolonged vomiting and/or coughing (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Postpartum afibrinogenemia with hemorrhage Interprets True Hemostatic function Inferred relationship Some 2
Mild hereditary factor IX deficiency disease without inhibitor (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Wiskott-Aldrich autosomal dominant variant syndrome (disorder) Interprets False Hemostatic function Inferred relationship Some 2
Familial multiple factor deficiency syndrome, type VI Interprets True Hemostatic function Inferred relationship Some 1
Familial thrombocytosis (disorder) Interprets False Hemostatic function Inferred relationship Some 2
Moderate hereditary factor VIII deficiency disease without inhibitor (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Itching purpura Interprets True Hemostatic function Inferred relationship Some 3
Kasabach-Merritt syndrome Interprets True Hemostatic function Inferred relationship Some 3
Protein S deficiency disease Interprets True Hemostatic function Inferred relationship Some 1
Thrombocytopenic disorder Interprets True Hemostatic function Inferred relationship Some 2
Hyperfibrinogenemia (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Post infectious thrombocytopenic purpura Interprets True Hemostatic function Inferred relationship Some 3
Thrombocytopenia due to extracorporeal circulation (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Primary non-thrombocytopenic purpura (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Blood coagulation disorder with shortened bleeding time Interprets True Hemostatic function Inferred relationship Some 1
Montreal platelet syndrome (disorder) Interprets False Hemostatic function Inferred relationship Some 2
Deficiency of naturally occurring coagulation factor inhibitor Interprets True Hemostatic function Inferred relationship Some 1
Giant platelet syndrome Interprets True Hemostatic function Inferred relationship Some 1
Factor XI deficiency Interprets True Hemostatic function Inferred relationship Some 1
Platelet membrane defect Interprets True Hemostatic function Inferred relationship Some 1
Blood coagulation disorder Interprets True Hemostatic function Inferred relationship Some 1
Hemorrhagic disorder due to increase in anti-9a Interprets True Hemostatic function Inferred relationship Some 1
Drug induced thrombotic thrombocytopenic purpura (disorder) Interprets False Hemostatic function Inferred relationship Some 8
von Willebrand disease, type 1^a^ Interprets False Hemostatic function Inferred relationship Some 1
Cyclic thrombocytopenia Interprets True Hemostatic function Inferred relationship Some 2
Factor XI deficiency, type III Interprets True Hemostatic function Inferred relationship Some 1
Acquired purpura fulminans (disorder) Interprets True Hemostatic function Inferred relationship Some 4
Prothrombin complex deficiency Interprets True Hemostatic function Inferred relationship Some 1
Moderate hereditary factor VIII deficiency disease (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Factor VII deficiency Interprets True Hemostatic function Inferred relationship Some 1
Illegal abortion with afibrinogenemia Interprets False Hemostatic function Inferred relationship Some 1
Hereditary von Willebrand disease type 3 Interprets True Hemostatic function Inferred relationship Some 1
Blood coagulation disorder complicating pregnancy (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Hereditary hypoplasminogenemia Interprets True Hemostatic function Inferred relationship Some 1
Secondary thrombocytopenia Interprets True Hemostatic function Inferred relationship Some 2
Idiopathic factor VIII deficiency (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Mixed alpha granule and dense body deficiency Interprets True Hemostatic function Inferred relationship Some 1
Stellate pseudoscar in senile purpura (disorder) Interprets True Hemostatic function Inferred relationship Some 3
Hereditary factor II deficiency disease Interprets True Hemostatic function Inferred relationship Some 1
Secondary autoimmune thrombocytopenia Interprets True Hemostatic function Inferred relationship Some 2
Failed attempted abortion with defibrination syndrome (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Familial hemorrhagic diathesis Interprets True Hemostatic function Inferred relationship Some 1
Dermite ocre of Favre Interprets False Hemostatic function Inferred relationship Some 2
Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome Interprets True Hemostatic function Inferred relationship Some 3
GATA binding protein 1 related thrombocytopenia with dyserythropoiesis (disorder) Interprets True Hemostatic function Inferred relationship Some 3
Macrothrombocytopenia with mitral valve insufficiency Interprets False Hemostatic function Inferred relationship Some 3
Failed attempted abortion with afibrinogenemia (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Blood coagulation disorder with prolonged bleeding time Interprets True Hemostatic function Inferred relationship Some 1
Mediterranean thrombocytopenia Interprets False Hemostatic function Inferred relationship Some 2
Periodontitis co-occurrent with Chédiak-Higashi syndrome Interprets False Hemostatic function Inferred relationship Some 3
von Willebrand disease type 2M Interprets False Hemostatic function Inferred relationship Some 1
Hereditary factor X deficiency disease Interprets True Hemostatic function Inferred relationship Some 1
von Willebrand disease type 2B Interprets False Hemostatic function Inferred relationship Some 1
Blood coagulation disorder complicating childbirth Interprets True Hemostatic function Inferred relationship Some 1
Familial multiple factor deficiency syndrome Interprets True Hemostatic function Inferred relationship Some 1
Hemophilia Interprets True Hemostatic function Inferred relationship Some 1
Chronic acquired pure red cell aplasia Interprets False Hemostatic function Inferred relationship Some 6
Homozygous prothrombin G20210A mutation (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Familial multiple factor deficiency syndrome, type I (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Late onset diffuse bleeding diathesis secondary to vitamin K deficient hemorrhagic disease of fetus and newborn (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Steroid purpura Interprets True Hemostatic function Inferred relationship Some 2
Acquired factor IX deficiency disease Interprets True Hemostatic function Inferred relationship Some 1
Haemorrhagic disorder due to increase in anti-10a Interprets True Hemostatic function Inferred relationship Some 1
Non-thrombocytopenic purpura Interprets True Hemostatic function Inferred relationship Some 2
Postpartum coagulation defects Interprets True Hemostatic function Inferred relationship Some 1
Postpartum fibrinolysis with hemorrhage Interprets True Hemostatic function Inferred relationship Some 2
Acquired pancytopenia Interprets True Hemostatic function Inferred relationship Some 5
von Willebrand disease, type IIE Interprets False Hemostatic function Inferred relationship Some 1
Fibrinogen abnormality Interprets True Hemostatic function Inferred relationship Some 1
Miscarriage with defibrination syndrome Interprets True Hemostatic function Inferred relationship Some 1
von Willebrand disease, type IIA Interprets False Hemostatic function Inferred relationship Some 1
Antiprothrombin disorder Interprets True Hemostatic function Inferred relationship Some 1
Radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome (disorder) Interprets False Hemostatic function Inferred relationship Some 2
Capillary fragility abnormality Interprets True Hemostatic function Inferred relationship Some 3
Thrombocytopenia due to extracorporeal circulation of blood Interprets True Hemostatic function Inferred relationship Some 2
von Willebrand disease, type IIF Interprets False Hemostatic function Inferred relationship Some 1
Neonatal antiphospholipid syndrome (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Acquired PF-3 disease Interprets False Hemostatic function Inferred relationship Some 2
Autosomal dominant deficiency of plasminogen Interprets True Hemostatic function Inferred relationship Some 1
High molecular weight kininogen deficiency Interprets True Hemostatic function Inferred relationship Some 1
Pancytopenia-dysmelia Interprets False Hemostatic function Inferred relationship Some 5
Autoimmune factor VIII deficiency Interprets True Hemostatic function Inferred relationship Some 1
Secondary non-thrombocytopenic purpura Interprets True Hemostatic function Inferred relationship Some 2
Platelet factor V deficiency (factor V Quebec) Interprets True Hemostatic function Inferred relationship Some 1
Hyperglobulinemic purpura (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Hereditary thrombophilia (disorder) Interprets True Hemostatic function Inferred relationship Some 1

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