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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
Amegakaryocytic thrombocytopenia Interprets True Hemostatic function Inferred relationship Some 2
Megakaryocytic thrombocytopenia Interprets True Hemostatic function Inferred relationship Some 2
May-Hegglin anomaly Interprets False Hemostatic function Inferred relationship Some 3
Epstein syndrome Interprets False Hemostatic function Inferred relationship Some 4
Montreal platelet syndrome (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Mediterranean thrombocytopenia Interprets True Hemostatic function Inferred relationship Some 2
Post-splenectomy thrombocytosis Interprets True Hemostatic function Inferred relationship Some 2
Platelet type pseudo-von Willebrand disease Interprets False Hemostatic function Inferred relationship Some 3
Pancytopenia-dysmelia Interprets False Hemostatic function Inferred relationship Some 5
Essential thrombocythemia (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Parvoviral aplastic crisis Interprets True Hemostatic function Inferred relationship Some 7
Thrombocytosis Interprets True Hemostatic function Inferred relationship Some 2
Aplastic anaemia Interprets True Hemostatic function Inferred relationship Some 7
Platelet dysfunction associated with uremia (disorder) Interprets True Hemostatic function Inferred relationship Some 3
Aplastic anaemia due to infection Interprets True Hemostatic function Inferred relationship Some 8
Hereditary thrombocytopenic disorder (disorder) Interprets True Hemostatic function Inferred relationship Some 3
Congenital dysmegakaryopoietic thrombocytopenia, Paris Trousseau type (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Autoimmune neonatal thrombocytopenia Interprets True Hemostatic function Inferred relationship Some 3
Wiskott-Aldrich autosomal dominant variant syndrome (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Thrombocytopenia due to sequestration Interprets True Hemostatic function Inferred relationship Some 3
Neonatal thrombocytopenia Interprets True Hemostatic function Inferred relationship Some 3
Medich giant platelet syndrome (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Attenuated Chédiak-Higashi syndrome (disorder) Interprets True Hemostatic function Inferred relationship Some 3
Familial thrombocytosis (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Revesz syndrome (disorder) Interprets True Hemostatic function Inferred relationship Some 9
Congenital amegakaryocytic thrombocytopenia (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Acquired platelet disorder Interprets True Hemostatic function Inferred relationship Some 2
Chronic acquired pure red cell aplasia Interprets False Hemostatic function Inferred relationship Some 6
Aplastic anemia caused by antineoplastic agent Interprets True Hemostatic function Inferred relationship Some 7
X-linked dyserythropoietic anemia with abnormal platelets and neutropenia (disorder) Interprets True Hemostatic function Inferred relationship Some 7
Pancytopenia due to IKZF1 mutations Interprets True Hemostatic function Inferred relationship Some 6
Macrothrombocytopenia with mitral valve insufficiency Interprets True Hemostatic function Inferred relationship Some 3
Bleeding disorder due to glycoprotein VI deficiency (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Ataxia pancytopenia syndrome Interprets True Hemostatic function Inferred relationship Some 6
Thrombocytopenia due to COVID-19 Interprets True Hemostatic function Inferred relationship Some 4
Familial pigmented purpuric eruption Interprets True Hemostatic function Inferred relationship Some 5
Fetal thrombocytopenia Interprets True Hemostatic function Inferred relationship Some 2
Fetal hemophilia Interprets True Hemostatic function Inferred relationship Some 1
Upshaw-Schulman syndrome (disorder) Interprets False Hemostatic function Inferred relationship Some 1
Autoimmune thrombotic thrombocytopenic purpura (disorder) Interprets True Hemostatic function Inferred relationship Some 5
Acquired thrombotic thrombocytopenic purpura (disorder) Interprets True Hemostatic function Inferred relationship Some 5
Drug induced thrombotic thrombocytopenic purpura (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Deficiency of coagulation factor due to vitamin K malabsorption (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Deficiency of coagulation factor due to vitamin K malabsorption in obstructive biliary disease (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Factor X deficiency due to systemic amyloidosis Interprets True Hemostatic function Inferred relationship Some 2
Drug-induced fibrinolytic disorder Interprets True Hemostatic function Inferred relationship Some 2
Fibrinolytic disorder caused by tissue plasminogen activator Interprets True Hemostatic function Inferred relationship Some 1
Fibrinolytic disorder caused by urokinase Interprets True Hemostatic function Inferred relationship Some 1
Pancytopenia caused by anticonvulsant Interprets True Hemostatic function Inferred relationship Some 1
Pancytopenia caused by antithyroid drug (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Vaccine-induced prothrombotic immune thrombocytopenia Interprets True Hemostatic function Inferred relationship Some 2
X-linked thrombocytopenia with normal platelets (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Acquired prekallikrein deficiency (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Hereditary congenital prekallikrein deficiency (disorder) Interprets True Hemostatic function Inferred relationship Some 1
DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome Interprets True Hemostatic function Inferred relationship Some 2
Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome Interprets True Hemostatic function Inferred relationship Some 3
Hereditary thrombocytopenia with early-onset myelofibrosis Interprets True Hemostatic function Inferred relationship Some 1
Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Antepartum hemorrhage with afibrinogenemia Interprets True Hemostatic function Inferred relationship Some 2
Hyperfibrinolysis Interprets True Hemostatic function Inferred relationship Some 2
Antepartum hemorrhage with coagulation defect (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Antepartum haemorrhage with hyperfibrinolysis Interprets True Hemostatic function Inferred relationship Some 3
Antepartum hemorrhage with coagulation defect - delivered Interprets False Hemostatic function Inferred relationship Some 2
Antepartum hemorrhage with coagulation defect - not delivered Interprets False Hemostatic function Inferred relationship Some 1
Antepartum hemorrhage with hypofibrinogenemia Interprets True Hemostatic function Inferred relationship Some 2
Antepartum hemorrhage with disseminated intravascular coagulation (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Maternal perinatal purpura (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Fetal purpura (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Autosomal dominant thrombocytopenia with platelet secretion defect Interprets True Hemostatic function Inferred relationship Some 2
Severe autosomal recessive macrothrombocytopenia (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly syndrome (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Acquired antithrombin III deficiency Interprets True Hemostatic function Inferred relationship Some 3
Premature separation of placenta with coagulation defect Interprets True Hemostatic function Inferred relationship Some 3
Thrombomodulin-related bleeding disorder (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Congenital autosomal recessive small-platelet thrombocytopenia (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome Interprets True Hemostatic function Inferred relationship Some 2
Acquired protein S deficiency Interprets True Hemostatic function Inferred relationship Some 1
Acquired protein C deficiency (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Acquired heparin cofactor II deficiency (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Intrapartum hemorrhage with coagulation defect Interprets True Hemostatic function Inferred relationship Some 3
Parturient hemorrhage associated with hypofibrinogenemia Interprets True Hemostatic function Inferred relationship Some 3
Postpartum afibrinogenemia with hemorrhage Interprets True Hemostatic function Inferred relationship Some 4
Pigmented purpuric dermatosis (disorder) Interprets True Hemostatic function Inferred relationship Some 5
Lichen aureus (disorder) Interprets True Hemostatic function Inferred relationship Some 6
Progressive pigmentary dermatosis of Schamberg Interprets True Hemostatic function Inferred relationship Some 6
Upshaw-Schulman syndrome (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Hereditary von Willebrand disease Interprets True Hemostatic function Inferred relationship Some 1
Hematopoietic subsyndrome of acute radiation syndrome (disorder) Interprets True Hemostatic function Inferred relationship Some 3
Afibrinogenemia following molar pregnancy (disorder) Interprets True Hemostatic function Inferred relationship Some 4
Afibrinogenemia following ectopic pregnancy (disorder) Interprets True Hemostatic function Inferred relationship Some 4
Defibrination syndrome following molar pregnancy Interprets True Hemostatic function Inferred relationship Some 1
Defibrination syndrome following ectopic pregnancy (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Postpartum hemolysis-elevated liver enzymes-low platelet count syndrome Interprets True Hemostatic function Inferred relationship Some 3
Fanconi anemia of complementation group C Interprets True Hemostatic function Inferred relationship Some 7
Mild hereditary factor VIII deficiency disease with high response inhibitor (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Mild hereditary factor VIII deficiency disease with low response inhibitor Interprets True Hemostatic function Inferred relationship Some 1
Severe hereditary factor VIII deficiency disease with high response inhibitor (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Severe hereditary factor VIII deficiency disease with low response inhibitor Interprets True Hemostatic function Inferred relationship Some 1
Moderate hereditary factor VIII deficiency disease with high response inhibitor Interprets True Hemostatic function Inferred relationship Some 1
Moderate hereditary factor VIII deficiency disease with low response inhibitor Interprets True Hemostatic function Inferred relationship Some 1

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