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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
Dysplasminogenaemia Interprets True Haemostatic function Inferred relationship Some 1
Hereditary factor VII deficiency disease Interprets True Haemostatic function Inferred relationship Some 1
Pregnancy-related factor VIII deficiency Interprets True Haemostatic function Inferred relationship Some 1
Eczematid-like purpura of Doucas and Kapetanakis Interprets True Haemostatic function Inferred relationship Some 4
Hereditary factor XII deficiency disease Interprets True Haemostatic function Inferred relationship Some 1
Waldenstrom's hypergammaglobulinaemic purpura Interprets True Haemostatic function Inferred relationship Some 2
Acquired platelet function disorder Interprets True Haemostatic function Inferred relationship Some 1
Dysproteinemic purpura Interprets True Haemostatic function Inferred relationship Some 2
Afibrinogenaemia - postpartum Interprets True Haemostatic function Inferred relationship Some 1
Hereditary factor VIII deficiency disease Interprets True Haemostatic function Inferred relationship Some 1
Purpuric disorder Interprets True Haemostatic function Inferred relationship Some 2
Severe hereditary factor VIII deficiency disease with inhibitor Interprets True Haemostatic function Inferred relationship Some 1
Factor XI deficiency, type I Interprets True Haemostatic function Inferred relationship Some 1
von Willebrand disease, type IIG Interprets False Haemostatic function Inferred relationship Some 1
Legal termination of pregnancy with defibrination syndrome Interprets False Haemostatic function Inferred relationship Some 1
Combined deficiency of factor V and factor VIII Interprets True Haemostatic function Inferred relationship Some 1
MYH9 related disease Interprets True Haemostatic function Inferred relationship Some 2
von Willebrand disease type 2N Interprets True Haemostatic function Inferred relationship Some 1
Thrombocytosis Interprets False Haemostatic function Inferred relationship Some 2
Amegakaryocytic thrombocytopenia Interprets False Haemostatic function Inferred relationship Some 2
Postpartum coagulation defects with postnatal problem Interprets True Haemostatic function Inferred relationship Some 1
Familial thrombomodulin anomalies Interprets True Haemostatic function Inferred relationship Some 1
Familial multiple factor deficiency syndrome, type V Interprets True Haemostatic function Inferred relationship Some 1
Dense body defect Interprets True Haemostatic function Inferred relationship Some 1
Transient neonatal thrombocytopenia due to exchange transfusion Interprets True Haemostatic function Inferred relationship Some 2
Prekallikrein deficiency Interprets True Haemostatic function Inferred relationship Some 1
Anticoagulant-induced bleeding Interprets True Haemostatic function Inferred relationship Some 1
Primary thrombocytopenia Interprets True Haemostatic function Inferred relationship Some 2
Disseminated intravascular coagulation in newborn Interprets True Haemostatic function Inferred relationship Some 1
Protein C deficiency disease Interprets True Haemostatic function Inferred relationship Some 1
Hemorrhagic disorder due to circulating anticoagulants Interprets True Haemostatic function Inferred relationship Some 1
Hypodysfibrinogenaemia Interprets True Haemostatic function Inferred relationship Some 1
Severe hereditary factor VIII deficiency disease Interprets True Haemostatic function Inferred relationship Some 1
Hereditary von Willebrand disease type IA Interprets True Haemostatic function Inferred relationship Some 1
Thrombocythaemia with distal limb defect Interprets True Haemostatic function Inferred relationship Some 4
Congenital amegakaryocytic thrombocytopenia Interprets False Haemostatic function Inferred relationship Some 2
Mild hereditary factor VIII deficiency disease with inhibitor Interprets True Haemostatic function Inferred relationship Some 1
Hereditary dysplasminogenaemia Interprets True Haemostatic function Inferred relationship Some 1
Hereditary factor VIII deficiency disease with inhibitor Interprets True Haemostatic function Inferred relationship Some 1
Aplastic anaemia associated with pregnancy Interprets True Haemostatic function Inferred relationship Some 6
Purpura simplex Interprets True Haemostatic function Inferred relationship Some 2
Benign primary hypergammaglobulinaemic purpura Interprets True Haemostatic function Inferred relationship Some 2
Mild hereditary factor VIII deficiency disease Interprets True Haemostatic function Inferred relationship Some 1
Hereditary platelet function disorder Interprets True Haemostatic function Inferred relationship Some 1
Postinfective immunoglobulin A vasculitis Interprets False Haemostatic function Inferred relationship Some 3
Blood coagulation disorder, categorised by value of screening test Interprets True Haemostatic function Inferred relationship Some 1
Factor X deficiency Interprets True Haemostatic function Inferred relationship Some 1
Thrombocytopenic purpura due to defective platelet production Interprets True Haemostatic function Inferred relationship Some 3
Homozygous protein S deficiency Interprets True Haemostatic function Inferred relationship Some 1
Factor I deficiency disease Interprets True Haemostatic function Inferred relationship Some 1
Transient neonatal thrombocytopenia due to idiopathic maternal thrombocytopenia Interprets True Haemostatic function Inferred relationship Some 2
Thrombocytopenia due to non-immune destruction Interprets True Haemostatic function Inferred relationship Some 2
A disintegrin and metalloproteinase with thrombospondin type 1 motif 13 deficiency (ADAMTS13) Interprets True Haemostatic function Inferred relationship Some 1
P2Y12 defect Interprets True Haemostatic function Inferred relationship Some 2
Gray platelet syndrome Interprets True Haemostatic function Inferred relationship Some 1
Purpura rheumatica Interprets False Haemostatic function Inferred relationship Some 2
Haemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation Interprets True Haemostatic function Inferred relationship Some 1
von Willebrand disease, type IIC Interprets False Haemostatic function Inferred relationship Some 1
Lupus anticoagulant disorder Interprets True Haemostatic function Inferred relationship Some 1
Thrombocytopenic purpura associated with metabolic disorder Interprets True Haemostatic function Inferred relationship Some 3
Antithrombin III deficiency Interprets True Haemostatic function Inferred relationship Some 1
White platelet syndrome Interprets True Haemostatic function Inferred relationship Some 1
Hereditary von Willebrand disease type 2M Interprets True Haemostatic function Inferred relationship Some 1
Hereditary heparin cofactor II deficiency Interprets True Haemostatic function Inferred relationship Some 1
Thromboxane generation defect Interprets True Haemostatic function Inferred relationship Some 1
Pigmented purpuric lichenoid dermatitis of Gougerot and Blum Interprets True Haemostatic function Inferred relationship Some 1
Hereditary von Willebrand disease type 2B Interprets True Haemostatic function Inferred relationship Some 1
Von Voss-Cherstvoy syndrome Interprets True Haemostatic function Inferred relationship Some 2
Amegakaryocytic thrombocytopenia with congenital malformation Interprets True Haemostatic function Inferred relationship Some 3
Hereditary factor V deficiency disease Interprets True Haemostatic function Inferred relationship Some 1
Anti-factor II disorder Interprets True Haemostatic function Inferred relationship Some 1
Anticoagulant excess without bleeding Interprets True Haemostatic function Inferred relationship Some 1
von Willebrand disease type IA Interprets False Haemostatic function Inferred relationship Some 1
Radial aplasia-thrombocytopenia syndrome Interprets True Haemostatic function Inferred relationship Some 2
Factor XIII deficiency disease Interprets True Haemostatic function Inferred relationship Some 1
Blood coagulation disorder due to liver disease Interprets True Haemostatic function Inferred relationship Some 1
Severe hereditary factor IX deficiency disease with inhibitor Interprets True Haemostatic function Inferred relationship Some 1
Haemorrhagic disorder due to antithrombinaemia Interprets True Haemostatic function Inferred relationship Some 1
Alpha chain defect dysfibrinogenaemia Interprets True Haemostatic function Inferred relationship Some 1
Familial multiple factor deficiency syndrome, type III Interprets True Haemostatic function Inferred relationship Some 1
Upshaw-Schulman syndrome Interprets False Haemostatic function Inferred relationship Some 8
Congenital thrombocytopenic purpura Interprets False Haemostatic function Inferred relationship Some 3
von Willebrand disease type IB Interprets True Haemostatic function Inferred relationship Some 1
Factor II deficiency Interprets True Haemostatic function Inferred relationship Some 1
Contact purpura Interprets True Haemostatic function Inferred relationship Some 2
Homozygous protein C deficiency Interprets True Haemostatic function Inferred relationship Some 1
Sex-linked thrombocytopenia Interprets True Haemostatic function Inferred relationship Some 2
Revesz syndrome Interprets False Haemostatic function Inferred relationship Some 8
Mild hereditary factor VIII deficiency disease without inhibitor Interprets True Haemostatic function Inferred relationship Some 1
von Willebrand disorder Interprets True Haemostatic function Inferred relationship Some 1
Megakaryocytic thrombocytopenia Interprets False Haemostatic function Inferred relationship Some 2
Purpura pigmentosa chronica Interprets True Haemostatic function Inferred relationship Some 2
Acute haemorrhagic oedema of childhood Interprets False Haemostatic function Inferred relationship Some 3
Clothing purpura Interprets True Haemostatic function Inferred relationship Some 2
von Willebrand disease, type IIH Interprets False Haemostatic function Inferred relationship Some 1
Legal termination of pregnancy with afibrinogenaemia Interprets False Haemostatic function Inferred relationship Some 1
MYH9 macrothrombocytopenia syndrome Interprets False Haemostatic function Inferred relationship Some 1
Secondary cutaneous vasculitis Interprets True Haemostatic function Inferred relationship Some 3
Afibrinogenaemia Interprets True Haemostatic function Inferred relationship Some 1
Heterozygous protein C deficiency Interprets True Haemostatic function Inferred relationship Some 1
Thrombocytopenic purpura due to platelet consumption Interprets True Haemostatic function Inferred relationship Some 3

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Reference Sets

Observable entity foundation reference set

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