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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
124304016 Hemostatic function, NOS en Synonym Inactive Initial character case insensitive SNOMED CT core
124305015 Hemostasis, NOS en Synonym Inactive Initial character 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
124308018 Haemostasis, NOS en Synonym Inactive Initial character case insensitive SNOMED CT core
124309014 Haemostatic function, NOS en Synonym Inactive Initial character 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
815392011 Hemostatic function (function) en Fully specified name Inactive Initial character 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
Induced platelet aggregation Is a True Haemostatic function Inferred relationship Some
Dilutional thrombocytopenia Interprets True Haemostatic function Inferred relationship Some 2
Blood coagulation disorder with shortened coagulation time Interprets True Haemostatic function Inferred relationship Some 1
Factor XII deficiency disease Interprets True Haemostatic function Inferred relationship Some 1
Platelet sequestration Interprets True Haemostatic function Inferred relationship Some 1
Isolated thrombocytopaenia Interprets True Haemostatic function Inferred relationship Some 2
Hereditary protein S deficiency Interprets True Haemostatic function Inferred relationship Some 1
Defibrination syndrome following molar AND/OR ectopic pregnancy Interprets True Haemostatic function Inferred relationship Some 1
von Willebrand disease type IC Interprets True Haemostatic function Inferred relationship Some 1
von Willebrand disease, type IID Interprets False Haemostatic function Inferred relationship Some 1
Factor V Leiden mutation Interprets True Haemostatic function Inferred relationship Some 1
Malignancy-related factor VIII deficiency Interprets True Haemostatic function Inferred relationship Some 1
Heparin cofactor II deficiency Interprets True Haemostatic function Inferred relationship Some 1
Moderate hereditary factor IX deficiency disease with inhibitor Interprets True Haemostatic function Inferred relationship Some 1
Blood coagulation disorder with prolonged coagulation time Interprets True Haemostatic function Inferred relationship Some 1
Beta chain defect dysfibrinogenaemia Interprets True Haemostatic function Inferred relationship Some 1
East Texas bleeding disorder Interprets True Haemostatic function Inferred relationship Some 1
Disseminated intravascular coagulation Interprets True Haemostatic function Inferred relationship Some 1
Congenital dysmegakaryopoietic thrombocytopenia, Paris Trousseau type Interprets False Haemostatic function Inferred relationship Some 2
Disorder of haemostatic system Interprets True Haemostatic function Inferred relationship Some 1
Purpuric rash Interprets False Haemostatic function Inferred relationship Some 3
Attenuated Chédiak-Higashi syndrome Interprets False Haemostatic function Inferred relationship Some 3
Contact factor deficiency Interprets True Haemostatic function Inferred relationship Some 1
Factor V deficiency Interprets True Haemostatic function Inferred relationship Some 1
Disorder involving the fibrinolytic system Interprets True Haemostatic function Inferred relationship Some 1
von Willebrand disease type 1 Interprets True Haemostatic function Inferred relationship Some 1
Idiopathic maternal thrombocytopenia Interprets True Haemostatic function Inferred relationship Some 2
Thrombophilia due to vascular anomaly Interprets True Haemostatic function Inferred relationship Some 1
Alloimmune platelet transfusion refractoriness Interprets True Haemostatic function Inferred relationship Some 2
Benign gestational thrombocytopenia Interprets True Haemostatic function Inferred relationship Some 2
Moderate hereditary factor IX deficiency disease without inhibitor Interprets True Haemostatic function Inferred relationship Some 1
Hereditary factor XIII A subunit and B subunit deficiency Interprets True Haemostatic function Inferred relationship Some 1
Mechanical purpura Interprets True Haemostatic function Inferred relationship Some 2
Hereditary protein C deficiency Interprets True Haemostatic function Inferred relationship Some 1
Hereditary thrombophilic dysfibrinogenemia Interprets True Haemostatic function Inferred relationship Some 1
Post-splenectomy thrombocytosis Interprets False Haemostatic function Inferred relationship Some 2
Hereditary factor VIII deficiency disease without inhibitor Interprets True Haemostatic function Inferred relationship Some 1
Heterozygous Factor V Leiden mutation Interprets True Haemostatic function Inferred relationship Some 1
Mediterranean macrothrombocytopenia Interprets True Haemostatic function Inferred relationship Some 2
Prothrombin G20210A mutation Interprets True Haemostatic function Inferred relationship Some 1
Epstein syndrome Interprets False Haemostatic function Inferred relationship Some 4
Fibrinogen deficiency Interprets True Haemostatic function Inferred relationship Some 1
Thrombocytopenia due to blood loss Interprets True Haemostatic function Inferred relationship Some 2
Factor IX deficiency Interprets True Haemostatic function Inferred relationship Some 1
Hereditary thrombocytopenia with normal platelets Interprets True Haemostatic function Inferred relationship Some 2
von Willebrand disease, type IIB Interprets False Haemostatic function Inferred relationship Some 1
Dysfibrinogenaemia Interprets True Haemostatic function Inferred relationship Some 1
Hereditary von Willebrand disease type 2A Interprets True Haemostatic function Inferred relationship Some 1
Mild hereditary factor IX deficiency disease with inhibitor Interprets True Haemostatic function Inferred relationship Some 1
Haemorrhagic disorder due to increase in anti-VIIIa Interprets True Haemostatic function Inferred relationship Some 1
Platelet disorder Interprets True Haemostatic function Inferred relationship Some 1
Gamma chain defect dysfibrinogenaemia Interprets True Haemostatic function Inferred relationship Some 1
Pseudo von Willebrand disease Interprets True Haemostatic function Inferred relationship Some 1
Passovoy factor deficiency Interprets True Haemostatic function Inferred relationship Some 1
von Willebrand disease type 2 Interprets True Haemostatic function Inferred relationship Some 1
Hypoplasminogenaemia Interprets True Haemostatic function Inferred relationship Some 1
Purpura due to prolonged vomiting and/or coughing Interprets True Haemostatic function Inferred relationship Some 2
Postpartum afibrinogenaemia with haemorrhage Interprets True Haemostatic function Inferred relationship Some 2
Mild hereditary factor IX deficiency disease without inhibitor Interprets True Haemostatic function Inferred relationship Some 1
Wiskott-Aldrich autosomal dominant variant syndrome Interprets False Haemostatic function Inferred relationship Some 2
Familial multiple factor deficiency syndrome, type VI Interprets True Haemostatic function Inferred relationship Some 1
Familial thrombocytosis Interprets False Haemostatic function Inferred relationship Some 2
Moderate hereditary factor VIII deficiency disease without inhibitor Interprets True Haemostatic function Inferred relationship Some 1
Itching purpura Interprets True Haemostatic function Inferred relationship Some 3
Kasabach-Merritt syndrome Interprets True Haemostatic function Inferred relationship Some 3
Protein S deficiency disease Interprets True Haemostatic function Inferred relationship Some 1
Thrombocytopenia Interprets True Haemostatic function Inferred relationship Some 2
Hyperfibrinogenemia Interprets True Haemostatic function Inferred relationship Some 2
Post infectious thrombocytopenic purpura Interprets True Haemostatic function Inferred relationship Some 3
Thrombocytopenia due to extracorporeal circulation Interprets True Haemostatic function Inferred relationship Some 2
Primary non-thrombocytopenic purpura Interprets True Haemostatic function Inferred relationship Some 2
Blood coagulation disorder with shortened bleeding time Interprets True Haemostatic function Inferred relationship Some 1
Montreal platelet syndrome Interprets False Haemostatic function Inferred relationship Some 2
Deficiency of naturally occurring coagulation factor inhibitor Interprets True Haemostatic function Inferred relationship Some 1
Giant platelet syndrome Interprets True Haemostatic function Inferred relationship Some 1
Factor XI deficiency Interprets True Haemostatic function Inferred relationship Some 1
Platelet membrane defect Interprets True Haemostatic function Inferred relationship Some 1
Blood coagulation disorder Interprets True Haemostatic function Inferred relationship Some 1
Haemorrhagic disorder due to increase in anti-9a Interprets True Haemostatic function Inferred relationship Some 1
Drug induced thrombotic thrombocytopenic purpura Interprets False Haemostatic function Inferred relationship Some 8
von Willebrand disease, type 1^a^ Interprets False Haemostatic function Inferred relationship Some 1
Cyclic thrombocytopenia Interprets True Haemostatic function Inferred relationship Some 2
Factor XI deficiency, type III Interprets True Haemostatic function Inferred relationship Some 1
Acquired purpura fulminans Interprets True Haemostatic function Inferred relationship Some 4
Prothrombin complex deficiency Interprets True Haemostatic function Inferred relationship Some 1
Moderate hereditary factor VIII deficiency disease Interprets True Haemostatic function Inferred relationship Some 1
Factor VII deficiency Interprets True Haemostatic function Inferred relationship Some 1
Illegal termination of pregnancy with afibrinogenaemia Interprets False Haemostatic function Inferred relationship Some 1
von Willebrand disease type 3 Interprets True Haemostatic function Inferred relationship Some 1
Blood coagulation disorder complicating pregnancy Interprets True Haemostatic function Inferred relationship Some 1
Hereditary hypoplasminogenaemia Interprets True Haemostatic function Inferred relationship Some 1
Secondary thrombocytopenia Interprets True Haemostatic function Inferred relationship Some 2
Idiopathic factor VIII deficiency Interprets True Haemostatic function Inferred relationship Some 1
Mixed alpha granule and dense body deficiency Interprets True Haemostatic function Inferred relationship Some 1
Stellate pseudoscar in senile purpura Interprets True Haemostatic function Inferred relationship Some 3
Hereditary factor II deficiency disease Interprets True Haemostatic function Inferred relationship Some 1
Secondary autoimmune thrombocytopenia Interprets True Haemostatic function Inferred relationship Some 2
Failed attempted termination of pregnancy with defibrination syndrome Interprets True Haemostatic function Inferred relationship Some 1
Familial haemorrhagic diathesis Interprets True Haemostatic function Inferred relationship Some 1
Dermite ocre of Favre Interprets False Haemostatic function Inferred relationship Some 2
Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome Interprets True Haemostatic function Inferred relationship Some 3

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Reference Sets

Observable entity foundation reference set

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