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74848003: Hemostatic function (observable entity)

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

Descriptions:

Id Description Lang Type Status Case? Module
124302017 Hemostatic function en Synonym Active Entire term case insensitive SNOMED CT core module
124304016 Hemostatic function, NOS en Synonym Inactive Only initial character case insensitive SNOMED CT core module
124305015 Hemostasis, NOS en Synonym Inactive Only initial character case insensitive SNOMED CT core module
124306019 Blood coagulation en Synonym Active Entire term case insensitive SNOMED CT core module
124307011 Blood clotting en Synonym Active Entire term case insensitive SNOMED CT core module
124308018 Haemostasis, NOS en Synonym Inactive Only initial character case insensitive SNOMED CT core module
124309014 Haemostatic function, NOS en Synonym Inactive Only initial character case insensitive SNOMED CT core module
124310016 Hemostasis en Synonym Active Entire term case insensitive SNOMED CT core module
502831011 Haemostasis en Synonym Active Entire term case insensitive SNOMED CT core module
502832016 Haemostatic function en Synonym Active Entire term case insensitive SNOMED CT core module
815392011 Hemostatic function (function) en Fully specified name Inactive Only initial character case insensitive SNOMED CT core module
1204583012 Hemostatic function (observable entity) en Fully specified name Active Entire term case insensitive SNOMED CT core module

48 descendants. Search Descendants:

Expanded Value Set

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

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