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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
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
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
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
Amegakaryocytic thrombocytopenia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Megakaryocytic thrombocytopenia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
May-Hegglin anomaly Interprets False Hemostatic function Inferred relationship Existential restriction modifier 3
Epstein syndrome Interprets False Hemostatic function Inferred relationship Existential restriction modifier 4
Montreal platelet syndrome Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Mediterranean thrombocytopenia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Post-splenectomy thrombocytosis Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Platelet type pseudo-von Willebrand disease Interprets False Hemostatic function Inferred relationship Existential restriction modifier 3
Pancytopenia-dysmelia Interprets False Hemostatic function Inferred relationship Existential restriction modifier 5
Essential thrombocythemia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Parvoviral aplastic crisis Interprets True Hemostatic function Inferred relationship Existential restriction modifier 7
Thrombocytosis Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Aplastic anemia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 7
Platelet dysfunction associated with uremia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 3
Aplastic anemia due to infection Interprets True Hemostatic function Inferred relationship Existential restriction modifier 8
Hereditary thrombocytopenic disorder Interprets True Hemostatic function Inferred relationship Existential restriction modifier 3
Congenital dysmegakaryopoietic thrombocytopenia, Paris Trousseau type Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Autoimmune neonatal thrombocytopenia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 3
Wiskott-Aldrich autosomal dominant variant syndrome Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Thrombocytopenia due to sequestration Interprets True Hemostatic function Inferred relationship Existential restriction modifier 3
Neonatal thrombocytopenia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 3
Medich giant platelet syndrome Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Attenuated Chédiak-Higashi syndrome Interprets True Hemostatic function Inferred relationship Existential restriction modifier 3
Familial thrombocytosis Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Revesz syndrome Interprets True Hemostatic function Inferred relationship Existential restriction modifier 9
Congenital amegakaryocytic thrombocytopenia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Acquired platelet disorder Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Chronic acquired pure red cell aplasia Interprets False Hemostatic function Inferred relationship Existential restriction modifier 6
Aplastic anemia caused by antineoplastic agent Interprets True Hemostatic function Inferred relationship Existential restriction modifier 7
X-linked dyserythropoietic anemia with abnormal platelets and neutropenia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 7
Pancytopenia due to IKAROS family zinc finger 1 mutations Interprets True Hemostatic function Inferred relationship Existential restriction modifier 6
Macrothrombocytopenia with mitral valve insufficiency Interprets True Hemostatic function Inferred relationship Existential restriction modifier 3
Bleeding disorder due to glycoprotein VI deficiency Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Ataxia pancytopenia syndrome Interprets True Hemostatic function Inferred relationship Existential restriction modifier 6
Thrombocytopenia due to severe acute respiratory syndrome coronavirus 2 Interprets True Hemostatic function Inferred relationship Existential restriction modifier 4
Familial pigmented purpuric eruption Interprets True Hemostatic function Inferred relationship Existential restriction modifier 5
Fetal thrombocytopenia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Fetal hemophilia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Upshaw-Schulman syndrome Interprets False Hemostatic function Inferred relationship Existential restriction modifier 1
Autoimmune thrombotic thrombocytopenic purpura Interprets True Hemostatic function Inferred relationship Existential restriction modifier 5
Acquired thrombotic thrombocytopenic purpura Interprets True Hemostatic function Inferred relationship Existential restriction modifier 5
Drug induced thrombotic thrombocytopenic purpura Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Deficiency of coagulation factor due to vitamin K malabsorption Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Deficiency of coagulation factor due to vitamin K malabsorption in obstructive biliary disease Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Deficiency of factor X due to systemic amyloidosis Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Disorder of fibrinolysis caused by drug Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Disorder of fibrinolysis caused by tissue plasminogen activator Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Disorder of fibrinolysis caused by urokinase Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Pancytopenia caused by anticonvulsant Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Pancytopenia caused by antithyroid drug Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Vaccine-induced prothrombotic immune thrombocytopenia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
X-linked thrombocytopenia with normal platelets Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Acquired prekallikrein deficiency Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Hereditary congenital prekallikrein deficiency Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Diaphanous related formin 1 related sensorineural hearing loss, thrombocytopenia syndrome Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome Interprets True Hemostatic function Inferred relationship Existential restriction modifier 3
Hereditary thrombocytopenia with early-onset myelofibrosis Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Antepartum hemorrhage with afibrinogenemia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Hyperfibrinolysis Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Antepartum hemorrhage with coagulation defect Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Antepartum hemorrhage with hyperfibrinolysis Interprets True Hemostatic function Inferred relationship Existential restriction modifier 3
Antepartum hemorrhage with coagulation defect - delivered Interprets False Hemostatic function Inferred relationship Existential restriction modifier 2
Antepartum hemorrhage with coagulation defect - not delivered Interprets False Hemostatic function Inferred relationship Existential restriction modifier 1
Antepartum hemorrhage with hypofibrinogenemia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Antepartum hemorrhage with disseminated intravascular coagulation Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Maternal perinatal purpura Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Fetal purpura Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Autosomal dominant thrombocytopenia with platelet secretion defect Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Severe autosomal recessive macrothrombocytopenia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly syndrome Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Acquired antithrombin III deficiency Interprets True Hemostatic function Inferred relationship Existential restriction modifier 3
Premature separation of placenta with coagulation defect Interprets True Hemostatic function Inferred relationship Existential restriction modifier 3
Thrombomodulin-related bleeding disorder Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Congenital autosomal recessive small-platelet thrombocytopenia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Acquired protein S deficiency Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Acquired protein C deficiency Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Acquired heparin cofactor II deficiency Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Intrapartum hemorrhage with coagulation defect Interprets True Hemostatic function Inferred relationship Existential restriction modifier 3
Parturient hemorrhage associated with hypofibrinogenemia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 3
Postpartum afibrinogenemia with hemorrhage Interprets True Hemostatic function Inferred relationship Existential restriction modifier 4
Pigmented purpuric dermatosis Interprets True Hemostatic function Inferred relationship Existential restriction modifier 5
Lichen aureus Interprets True Hemostatic function Inferred relationship Existential restriction modifier 6
Progressive pigmentary dermatosis of Schamberg Interprets True Hemostatic function Inferred relationship Existential restriction modifier 6
Upshaw-Schulman syndrome Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Hereditary von Willebrand disease Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Hematopoietic subsyndrome of acute radiation syndrome Interprets True Hemostatic function Inferred relationship Existential restriction modifier 3
Vaccine-induced prothrombotic immune thrombocytopenia Interprets False Hemostatic function Inferred relationship Existential restriction modifier 1
Antithrombin III deficiency type I Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Antithrombin III deficiency type II Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Prothrombin time Is a True Hemostatic function Inferred relationship Existential restriction modifier
Activated partial thromboplastin time Is a True Hemostatic function Inferred relationship Existential restriction modifier

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