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281833003: Entire hematological system (body structure)

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
419941014 Haematological system en Synonym Inactive Only initial character case insensitive SNOMED CT core module
419942019 Hematological system en Synonym Inactive Only initial character case insensitive SNOMED CT core module
675417019 Hematological system (body structure) en Fully specified name Inactive Only initial character case insensitive SNOMED CT core module
2528953015 Entire hematological system (body structure) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2532372011 Entire haematological system en Synonym Active Entire term case insensitive SNOMED CT core module
2532373018 Entire hematological system en Synonym Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Entire hematological system Is a Body system structure false Inferred relationship Existential restriction modifier
Entire hematological system Part of Entire body as a whole false Additional relationship Existential restriction modifier
Entire hematological system Is a Structure of hematological system true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Antibody detection, red blood cell, enzyme, 1 stage technique, including anti-human globulin Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Hemorrhagic disease of the newborn due to factor II deficiency Finding site False Entire hematological system Inferred relationship Existential restriction modifier
von Willebrand disease, type IIH Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Total body iron with chelatable radioiron study Procedure site False Entire hematological system Inferred relationship Existential restriction modifier 1
Whole blood unit collection Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Hereditary spherocytosis due to spectrin deficiency Finding site False Entire hematological system Inferred relationship Existential restriction modifier 1
Acquired coagulation factor deficiency Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Mild hereditary factor VIII deficiency disease Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Fresh frozen plasma thawing Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Antibody identification, leukocyte antibody Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Myelophthisic anemia Finding site False Entire hematological system Inferred relationship Existential restriction modifier 1
Failed attempted abortion with afibrinogenemia Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Blood group typing, RH genotyping, complete Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
High molecular weight kininogen deficiency Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Platelet concentrate, preparation Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Hereditary factor VIII deficiency disease Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Acute idiopathic thrombocytopenic purpura Finding site False Entire hematological system Inferred relationship Existential restriction modifier 1
Blood group typing A>2< Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Reagent red blood cell, preparation A, B or O pool Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Legal abortion with afibrinogenemia Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Special blood bank procedure, explain by report Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Hereditary factor I deficiency disease Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Antibody titration, anti-human globulin technique Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Immune thrombocytopenic purpura Finding site False Entire hematological system Inferred relationship Existential restriction modifier 1
Illegal abortion with afibrinogenemia Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Transient neonatal disorder of coagulation Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Factor XI deficiency, type II Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Hereditary factor II deficiency disease Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Moderate hereditary factor VIII deficiency disease Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Familial hemophagocytic lymphohistiocytosis Finding site False Entire hematological system Inferred relationship Existential restriction modifier 1
Isotope study of blood volume Procedure site False Entire hematological system Inferred relationship Existential restriction modifier 1
Acquired factor X deficiency disease Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Hereditary spherocytosis due to deficiency of protein 4.2 Finding site False Entire hematological system Inferred relationship Existential restriction modifier 1
Disseminated intravascular coagulation in newborn Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Failed attempted abortion with defibrination syndrome Finding site False Entire hematological system Inferred relationship Existential restriction modifier
von Willebrand disease, type IID Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Preparation of antibody sensitized pooled reagent red blood cells Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Frozen blood thawing and processing Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Antibody absorption, red blood cell, cold with autoabsorption Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Abortion with defibrination syndrome Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Acquired factor XI deficiency disease Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Antibody elution, ether Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Acquired factor V deficiency disease Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Antithrombin III deficiency Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Sickle cell-thalassemia disease Finding site False Entire hematological system Inferred relationship Existential restriction modifier 1
Hemolytic uremic syndrome of childhood Finding site False Entire hematological system Inferred relationship Existential restriction modifier 1
Factor VII deficiency Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Hereditary factor X deficiency disease Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Familial multiple factor deficiency syndrome, type V Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Proaccelerin deficiency Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Labile factor deficiency Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Saliva secretor studies Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Factor XI inhibitor disorder Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Antibody elution from red blood cells Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Anti-human globulin test, indirect, titer, non-gamma Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Blood group typing Rho(D) Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Hereditary factor VII deficiency disease Finding site False Entire hematological system Inferred relationship Existential restriction modifier
von Willebrand factor inhibitor disorder Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Antibody elution, alcohol Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Eczematid-like purpura of Doucas and Kapetanakis Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Acquired hypoprothrombinemia Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Factor V inhibitor disorder Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Hereditary factor IX deficiency disease Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Secondary cryofibrinogenemia Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Major crossmatch Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Antibody elution, heat Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Factor V deficiency Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Hereditary factor XII deficiency disease Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Compatibility test, crossmatch, complete standard technique, includes typing and antibody screening of red blood cells Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Anticoagulant overdosage Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Blood group typing Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Hereditary dysfibrinogenemia Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Reagent red blood cell, freeze, liquid nitrogen Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Intrauterine transfusion Procedure site False Entire hematological system Inferred relationship Existential restriction modifier 1
Factor XI deficiency, type III Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Factor XII deficiency disease Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Factor VIII inhibitor disorder Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Preparation of packed red blood cells Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Warfarin overdosage Finding site False Entire hematological system Inferred relationship Existential restriction modifier
White blood cell localization, whole body Procedure site False Entire hematological system Inferred relationship Existential restriction modifier 1
Lymphocyte storage Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Antibody identification, red blood cell antibody panel, enzyme, 2 stage technique including anti-human globulin Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Compatibility test, crossmatch, screening for compatible unit, antiglobulin technique Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Lymphocyte storage, liquid nitrogen Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Prekallikrein deficiency Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Postpartum coagulation defect with hemorrhage Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Hereditary factor XI deficiency disease Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Blood group typing A Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Antibody titration, saline Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Hereditary factor XIII deficiency disease Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Pure red cell aplasia Finding site False Entire hematological system Inferred relationship Existential restriction modifier 1
Miscarriage with defibrination syndrome Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Microangiopathic hemolytic anemia Finding site False Entire hematological system Inferred relationship Existential restriction modifier 3
Antibody identification, red blood cell Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Preparation and centrifugation of packed red blood cells Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
von Willebrand disease, type IIE Finding site False Entire hematological system Inferred relationship Existential restriction modifier
Hemolysin detection Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Hemoglobin Bart's hydrops syndrome Finding site False Entire hematological system Inferred relationship Existential restriction modifier 1
Antibody identification, red blood cell, albumin and anti-human globulin Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Leukocyte poor blood preparation Procedure site False Entire hematological system Inferred relationship Existential restriction modifier
Senile purpura Finding site False Entire hematological system Inferred relationship Existential restriction modifier

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