| Source | us.nlm.vsac#0.11.0:null (v4.0.1) |
| resourceType | ValueSet |
| id | 2.16.840.1.113883.3.3616.200.110.102.6071 |
| canonical | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.3616.200.110.102.6071 |
| version | 20221207 |
| status | active |
| publisher | Clinical Architecture |
| name | COVID19SNOMEDValueSetForCoagulopathies |
| title | COVID19 SNOMED Value Set for Coagulopathies |
| date | 2023-06-21T18:16:37-04:00 |
| experimental | false |
| Usages |
|
This value set contains 232 concepts
| Code | System | Display |
| 10153004 | http://snomed.info/sct | Systemic fibrinogenolysis (disorder) |
| 105604006 | http://snomed.info/sct | Deficiency of naturally occurring coagulation factor inhibitor (disorder) |
| 10934005 | http://snomed.info/sct | Cryofibrinogenemia (disorder) |
| 111588002 | http://snomed.info/sct | Heparin-induced thrombocytopenia with thrombosis (disorder) |
| 111589005 | http://snomed.info/sct | Dysfibrinogenemia (disorder) |
| 1148849001 | http://snomed.info/sct | Disorder of fibrinolysis caused by urokinase (disorder) |
| 1148857003 | http://snomed.info/sct | Disorder of fibrinolysis caused by tissue plasminogen activator (disorder) |
| 1148859000 | http://snomed.info/sct | Disorder of fibrinolysis caused by drug (disorder) |
| 1148862002 | http://snomed.info/sct | Deficiency of factor X due to systemic amyloidosis (disorder) |
| 1148929009 | http://snomed.info/sct | Deficiency of coagulation factor due to vitamin K malabsorption (disorder) |
| 1148930004 | http://snomed.info/sct | Deficiency of coagulation factor due to vitamin K malabsorption in obstructive biliary disease (disorder) |
| 1156746003 | http://snomed.info/sct | Vaccine-induced prothrombotic immune thrombocytopenia (disorder) |
| 1162804003 | http://snomed.info/sct | Hereditary congenital prekallikrein deficiency (disorder) |
| 1162807005 | http://snomed.info/sct | Acquired prekallikrein deficiency (disorder) |
| 1177171004 | http://snomed.info/sct | Hyperfibrinolysis (disorder) |
| 1196942001 | http://snomed.info/sct | Acquired antithrombin III deficiency (disorder) |
| 1197595004 | http://snomed.info/sct | Thrombomodulin-related bleeding disorder (disorder) |
| 12153008 | http://snomed.info/sct | Acquired factor IX deficiency disease (disorder) |
| 1217409009 | http://snomed.info/sct | Acquired protein S deficiency (disorder) |
| 1217410004 | http://snomed.info/sct | Acquired protein C deficiency (disorder) |
| 123786007 | http://snomed.info/sct | Blood coagulation disorder with shortened coagulation time (disorder) |
| 123787003 | http://snomed.info/sct | Blood coagulation disorder with prolonged coagulation time (disorder) |
| 123788008 | http://snomed.info/sct | Blood coagulation disorder with shortened bleeding time (disorder) |
| 123789000 | http://snomed.info/sct | Blood coagulation disorder with prolonged bleeding time (disorder) |
| 123790009 | http://snomed.info/sct | Blood coagulation disorder with impaired clot retraction time (disorder) |
| 128088003 | http://snomed.info/sct | Blood coagulation disorder, categorized by value of screening test (disorder) |
| 128090002 | http://snomed.info/sct | Benign gestational thrombocytopenia (disorder) |
| 128092005 | http://snomed.info/sct | Secondary autoimmune thrombocytopenia (disorder) |
| 128105004 | http://snomed.info/sct | von Willebrand disorder (disorder) |
| 128106003 | http://snomed.info/sct | Hereditary von Willebrand disease type 1 (disorder) |
| 128107007 | http://snomed.info/sct | Hereditary von Willebrand disease type 2 (disorder) |
| 128108002 | http://snomed.info/sct | Hereditary von Willebrand disease type 3 (disorder) |
| 128113003 | http://snomed.info/sct | Hereditary von Willebrand disease type 1B (disorder) |
| 128114009 | http://snomed.info/sct | Hereditary von Willebrand disease type 1C (disorder) |
| 128115005 | http://snomed.info/sct | Pseudo von Willebrand disease (disorder) |
| 1286003 | http://snomed.info/sct | Vitamin K deficiency coagulation disorder (disorder) |
| 13507004 | http://snomed.info/sct | Purpura fulminans (disorder) |
| 13993001 | http://snomed.info/sct | Factor XIII inhibitor disorder (disorder) |
| 14230004 | http://snomed.info/sct | Acquired factor VIII deficiency disease (disorder) |
| 15132005 | http://snomed.info/sct | Acquired factor XII deficiency disease (disorder) |
| 154818001 | http://snomed.info/sct | Congenital afibrinogenemia (disorder) |
| 154826009 | http://snomed.info/sct | Secondary thrombocytopenia (disorder) |
| 1563006 | http://snomed.info/sct | Protein S deficiency disease (disorder) |
| 16773005 | http://snomed.info/sct | Drug-induced coagulation inhibitor disorder (disorder) |
| 16872008 | http://snomed.info/sct | Severe hereditary factor VIII deficiency disease (disorder) |
| 16922007 | http://snomed.info/sct | Hereditary coagulation factor deficiency (disorder) |
| 180481005 | http://snomed.info/sct | Anti-factor II disorder (disorder) |
| 181456001 | http://snomed.info/sct | Antiprothrombin disorder (disorder) |
| 18604004 | http://snomed.info/sct | Factor XIII deficiency disease (disorder) |
| 191296000 | http://snomed.info/sct | Deficiency of coagulation factor due to liver disease (disorder) |
| 191297009 | http://snomed.info/sct | Deficiency of coagulation factor due to vitamin K deficiency (disorder) |
| 191298004 | http://snomed.info/sct | Acquired factor II deficiency (disorder) |
| 191322006 | http://snomed.info/sct | Thrombocytopenia caused by drugs (disorder) |
| 191323001 | http://snomed.info/sct | Thrombocytopenia due to extracorporeal circulation of blood (disorder) |
| 19267009 | http://snomed.info/sct | Lupus anticoagulant disorder (disorder) |
| 19307009 | http://snomed.info/sct | Drug-induced immune thrombocytopenia (disorder) |
| 200173001 | http://snomed.info/sct | Intrapartum hemorrhage with coagulation defect (disorder) |
| 2036003 | http://snomed.info/sct | Acquired factor VII deficiency disease (disorder) |
| 21360006 | http://snomed.info/sct | Miscarriage with afibrinogenemia (disorder) |
| 234440005 | http://snomed.info/sct | Factor VIII deficiency (disorder) |
| 234442002 | http://snomed.info/sct | Hereditary factor VIII deficiency disease with inhibitor (disorder) |
| 234444001 | http://snomed.info/sct | Congenital factor IX deficiency variant (disorder) |
| 234445000 | http://snomed.info/sct | Congenital factor IX deficiency with inhibitor (disorder) |
| 234451005 | http://snomed.info/sct | Acquired von Willebrand disease (disorder) |
| 234452003 | http://snomed.info/sct | Contact factor deficiency (disorder) |
| 234453008 | http://snomed.info/sct | Passovoy factor deficiency (disorder) |
| 234454002 | http://snomed.info/sct | Prothrombin complex deficiency (disorder) |
| 234455001 | http://snomed.info/sct | Fibrinogen abnormality (disorder) |
| 234456000 | http://snomed.info/sct | Congenital fibrinogen abnormality (disorder) |
| 234457009 | http://snomed.info/sct | Hypofibrinogenemia (disorder) |
| 234458004 | http://snomed.info/sct | Hypodysfibrinogenemia (disorder) |
| 234459007 | http://snomed.info/sct | Alpha chain defect dysfibrinogenemia (disorder) |
| 234460002 | http://snomed.info/sct | Beta chain defect dysfibrinogenemia (disorder) |
| 234461003 | http://snomed.info/sct | Gamma chain defect dysfibrinogenemia (disorder) |
| 234462005 | http://snomed.info/sct | Acquired fibrinogen abnormality (disorder) |
| 234463000 | http://snomed.info/sct | Combined coagulation factor deficiency (disorder) |
| 234464006 | http://snomed.info/sct | Fibrinolytic bleeding syndrome (disorder) |
| 234465007 | http://snomed.info/sct | Alpha-2-antiplasmin deficiency (disorder) |
| 234466008 | http://snomed.info/sct | Acquired coagulation disorder (disorder) |
| 239892009 | http://snomed.info/sct | Primary antiphospholipid syndrome (disorder) |
| 239894005 | http://snomed.info/sct | Primary antiphospholipid syndrome with multisystem involvement (disorder) |
| 239895006 | http://snomed.info/sct | Secondary antiphospholipid syndrome (disorder) |
| 239897003 | http://snomed.info/sct | Secondary antiphospholipid syndrome with multisystem involvement (disorder) |
| 25904003 | http://snomed.info/sct | Acquired coagulation factor deficiency (disorder) |
| 26029002 | http://snomed.info/sct | Mild hereditary factor VIII deficiency disease (disorder) |
| 26843008 | http://snomed.info/sct | Antiphospholipid syndrome (disorder) |
| 27312002 | http://snomed.info/sct | High molecular weight kininogen deficiency (disorder) |
| 278365007 | http://snomed.info/sct | Anticoagulant-induced bleeding (disorder) |
| 278366008 | http://snomed.info/sct | Anticoagulant excess without bleeding (disorder) |
| 278504009 | http://snomed.info/sct | Afibrinogenemia (disorder) |
| 282707003 | http://snomed.info/sct | Acquired inhibitor of coagulation (disorder) |
| 28293008 | http://snomed.info/sct | Hereditary factor VIII deficiency disease (disorder) |
| 30182008 | http://snomed.info/sct | Thrombocytopenia due to extracorporeal circulation (disorder) |
| 307342006 | http://snomed.info/sct | Thrombocytopenia due to massive blood transfusion (disorder) |
| 307514008 | http://snomed.info/sct | Idiopathic factor VIII deficiency (disorder) |
| 307515009 | http://snomed.info/sct | Autoimmune factor VIII deficiency (disorder) |
| 31925001 | http://snomed.info/sct | Hereditary factor I deficiency disease (disorder) |
| 33169001 | http://snomed.info/sct | Factor XI deficiency, type II (disorder) |
| 33297000 | http://snomed.info/sct | Hereditary factor II deficiency disease (disorder) |
| 33344008 | http://snomed.info/sct | Moderate hereditary factor VIII deficiency disease (disorder) |
| 33820001 | http://snomed.info/sct | Acquired factor X deficiency disease (disorder) |
| 34395002 | http://snomed.info/sct | Thrombocytopenia caused by hypothermia (disorder) |
| 35554008 | http://snomed.info/sct | Acquired factor XI deficiency disease (disorder) |
| 35913006 | http://snomed.info/sct | Acquired factor V deficiency disease (disorder) |
| 359700009 | http://snomed.info/sct | Hereditary von Willebrand disease type 1A (disorder) |
| 359711001 | http://snomed.info/sct | Hereditary von Willebrand disease type 2A (disorder) |
| 359717002 | http://snomed.info/sct | Hereditary von Willebrand disease type 2B (disorder) |
| 359725000 | http://snomed.info/sct | Hereditary von Willebrand disease type 2M (disorder) |
| 359727008 | http://snomed.info/sct | Fibrinogen deficiency (disorder) |
| 359730001 | http://snomed.info/sct | Acquired afibrinogenemia (disorder) |
| 359732009 | http://snomed.info/sct | Hereditary von Willebrand disease type 2N (disorder) |
| 36351005 | http://snomed.info/sct | Antithrombin III deficiency (disorder) |
| 371074009 | http://snomed.info/sct | Radiation thrombocytopenia (disorder) |
| 37193007 | http://snomed.info/sct | Factor VII deficiency (disorder) |
| 37350004 | http://snomed.info/sct | Hereditary factor X deficiency disease (disorder) |
| 3760002 | http://snomed.info/sct | Familial multiple factor deficiency syndrome, type V (disorder) |
| 38879000 | http://snomed.info/sct | Factor XI inhibitor disorder (disorder) |
| 39191000119103 | http://snomed.info/sct | Disseminated intravascular coagulation due to placental abruption (disorder) |
| 402851000 | http://snomed.info/sct | Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) |
| 402865003 | http://snomed.info/sct | Systemic lupus erythematosus-associated antiphospholipid syndrome (disorder) |
| 40855001 | http://snomed.info/sct | Hereditary factor VII deficiency disease (disorder) |
| 41106001 | http://snomed.info/sct | von Willebrand factor inhibitor disorder (disorder) |
| 41690001 | http://snomed.info/sct | Factor V inhibitor disorder (disorder) |
| 416902009 | http://snomed.info/sct | Uremic thrombocytopenia (disorder) |
| 41788008 | http://snomed.info/sct | Hereditary factor IX deficiency disease (disorder) |
| 41816006 | http://snomed.info/sct | Secondary cryofibrinogenemia (disorder) |
| 425949001 | http://snomed.info/sct | Mild hereditary factor VIII deficiency disease with inhibitor (disorder) |
| 426199009 | http://snomed.info/sct | Congenital factor IX deficiency without inhibitor (disorder) |
| 4320005 | http://snomed.info/sct | Factor V deficiency (disorder) |
| 43217004 | http://snomed.info/sct | Hereditary factor XII deficiency disease (disorder) |
| 438360006 | http://snomed.info/sct | Hereditary factor VIII deficiency disease without inhibitor (disorder) |
| 438372000 | http://snomed.info/sct | Hereditary factor IX deficiency disease with inhibitor (disorder) |
| 438373005 | http://snomed.info/sct | Severe hereditary factor VIII deficiency disease with inhibitor (disorder) |
| 438599002 | http://snomed.info/sct | Moderate hereditary factor VIII deficiency disease with inhibitor (disorder) |
| 438792009 | http://snomed.info/sct | Hereditary factor IX deficiency disease without inhibitor (disorder) |
| 438827002 | http://snomed.info/sct | Hereditary thrombophilic dysfibrinogenemia (disorder) |
| 439000005 | http://snomed.info/sct | Hyperfibrinogenemia (disorder) |
| 439145006 | http://snomed.info/sct | Congenital hypofibrinogenemia (disorder) |
| 439156006 | http://snomed.info/sct | Acquired combined coagulation factor deficiency (disorder) |
| 439157002 | http://snomed.info/sct | Hereditary combined coagulation factor deficiency (disorder) |
| 439274008 | http://snomed.info/sct | Hereditary protein C deficiency (disorder) |
| 439455002 | http://snomed.info/sct | Hereditary factor XIII A subunit deficiency (disorder) |
| 439458000 | http://snomed.info/sct | Factor I deficiency disease (disorder) |
| 439459008 | http://snomed.info/sct | Hereditary factor XIII B subunit deficiency (disorder) |
| 439460003 | http://snomed.info/sct | Hereditary factor XIII A subunit and B subunit deficiency (disorder) |
| 439699000 | http://snomed.info/sct | Hereditary antithrombin III deficiency (disorder) |
| 439702007 | http://snomed.info/sct | Hereditary protein S deficiency (disorder) |
| 440820004 | http://snomed.info/sct | Mild hereditary factor VIII deficiency disease without inhibitor (disorder) |
| 440866009 | http://snomed.info/sct | Severe hereditary factor IX deficiency disease with inhibitor (disorder) |
| 440867000 | http://snomed.info/sct | Moderate hereditary factor IX deficiency disease with inhibitor (disorder) |
| 440868005 | http://snomed.info/sct | Mild hereditary factor IX deficiency disease with inhibitor (disorder) |
| 440924009 | http://snomed.info/sct | Hereditary hyperfibrinogenemia (disorder) |
| 440988005 | http://snomed.info/sct | Heterozygous protein S deficiency (disorder) |
| 440993008 | http://snomed.info/sct | Severe hereditary factor VIII deficiency disease without inhibitor (disorder) |
| 441006000 | http://snomed.info/sct | Moderate hereditary factor VIII deficiency disease without inhibitor (disorder) |
| 441101007 | http://snomed.info/sct | Heterozygous protein C deficiency (disorder) |
| 441188004 | http://snomed.info/sct | Homozygous protein C deficiency (disorder) |
| 441189007 | http://snomed.info/sct | Homozygous protein S deficiency (disorder) |
| 441190003 | http://snomed.info/sct | Severe hereditary factor IX deficiency disease without inhibitor (disorder) |
| 441191004 | http://snomed.info/sct | Moderate hereditary factor IX deficiency disease without inhibitor (disorder) |
| 441192006 | http://snomed.info/sct | Mild hereditary factor IX deficiency disease without inhibitor (disorder) |
| 45366001 | http://snomed.info/sct | Hereditary dysfibrinogenemia (disorder) |
| 45963004 | http://snomed.info/sct | Factor XI deficiency, type III (disorder) |
| 46981006 | http://snomed.info/sct | Factor XII deficiency disease (disorder) |
| 47307007 | http://snomed.info/sct | Factor VIII inhibitor disorder (disorder) |
| 48976006 | http://snomed.info/sct | Prekallikrein deficiency (disorder) |
| 49762007 | http://snomed.info/sct | Hereditary factor XI deficiency disease (disorder) |
| 49886003 | http://snomed.info/sct | Thrombocytopenia due to blood loss (disorder) |
| 50189006 | http://snomed.info/sct | Hereditary factor XIII deficiency disease (disorder) |
| 50770000 | http://snomed.info/sct | Miscarriage with defibrination syndrome (disorder) |
| 51624005 | http://snomed.info/sct | Dilutional thrombocytopenia (disorder) |
| 58327003 | http://snomed.info/sct | Factor I inhibitor disorder (disorder) |
| 609329007 | http://snomed.info/sct | Catastrophic antiphospholipid syndrome (disorder) |
| 61551003 | http://snomed.info/sct | Familial multiple factor deficiency syndrome, type VI (disorder) |
| 61802005 | http://snomed.info/sct | Primary cryofibrinogenemia (disorder) |
| 6364000 | http://snomed.info/sct | Acquired factor XIII deficiency disease (disorder) |
| 64315007 | http://snomed.info/sct | Familial multiple factor deficiency syndrome, type III (disorder) |
| 64509006 | http://snomed.info/sct | Acquired coagulation factor inhibitor disorder (disorder) |
| 64779008 | http://snomed.info/sct | Blood coagulation disorder (disorder) |
| 65768009 | http://snomed.info/sct | Familial multiple factor deficiency syndrome, type II (disorder) |
| 66909001 | http://snomed.info/sct | Familial multiple factor deficiency syndrome, type IV (disorder) |
| 67406007 | http://snomed.info/sct | Disseminated intravascular coagulation (disorder) |
| 6935003 | http://snomed.info/sct | Familial hemorrhagic diathesis (disorder) |
| 69500007 | http://snomed.info/sct | Blood coagulation disorder due to liver disease (disorder) |
| 699208000 | http://snomed.info/sct | Thrombocytopenia caused by alcohol (disorder) |
| 715559004 | http://snomed.info/sct | Combined deficiency of factor V and factor VIII (disorder) |
| 716746003 | http://snomed.info/sct | Congenital alpha-2-antiplasmin deficiency (disorder) |
| 717407006 | http://snomed.info/sct | Congenital plasminogen activator inhibitor deficiency type 1 (disorder) |
| 721304007 | http://snomed.info/sct | Refractory thrombocytopenia (disorder) |
| 724356003 | http://snomed.info/sct | Hereditary combined deficiency of vitamin K-dependent clotting factors (disorder) |
| 724637001 | http://snomed.info/sct | Isolated thrombocytopenia (disorder) |
| 724854007 | http://snomed.info/sct | Purpura of skin and/or skin-associated mucous membrane co-occurrent and due to coagulation disorder (disorder) |
| 725105006 | http://snomed.info/sct | Bleeding disorder due to deficiency of calcium and diacylglycerol-regulated guanine nucleotide exchange factor I (disorder) |
| 725157006 | http://snomed.info/sct | Acquired purpura fulminans (disorder) |
| 725291001 | http://snomed.info/sct | Defect of purinergic receptor p2y G protein-coupled 12 (disorder) |
| 733028000 | http://snomed.info/sct | Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome (disorder) |
| 73397007 | http://snomed.info/sct | Heparin-induced thrombocytopenia (disorder) |
| 73975000 | http://snomed.info/sct | Factor II deficiency (disorder) |
| 74576004 | http://snomed.info/sct | Acquired thrombocytopenia (disorder) |
| 76407009 | http://snomed.info/sct | Protein C deficiency disease (disorder) |
| 76642003 | http://snomed.info/sct | Factor X deficiency (disorder) |
| 76771005 | http://snomed.info/sct | Parturient hemorrhage associated with hypofibrinogenemia (disorder) |
| 767712006 | http://snomed.info/sct | Factor IX deficiency (disorder) |
| 767713001 | http://snomed.info/sct | Factor XI deficiency (disorder) |
| 773422002 | http://snomed.info/sct | East Texas bleeding disorder (disorder) |
| 774084003 | http://snomed.info/sct | Neonatal antiphospholipid syndrome (disorder) |
| 782909004 | http://snomed.info/sct | Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation (disorder) |
| 782934004 | http://snomed.info/sct | Bleeding diathesis due to collagen receptor defect (disorder) |
| 783194008 | http://snomed.info/sct | Bleeding diathesis due to thromboxane synthesis deficiency (disorder) |
| 783256001 | http://snomed.info/sct | Familial thrombomodulin anomalies (disorder) |
| 785308008 | http://snomed.info/sct | Acquired hemophilia (disorder) |
| 789291002 | http://snomed.info/sct | Consumption coagulopathy caused by snake venom (disorder) |
| 79674009 | http://snomed.info/sct | Hyperheparinemia (disorder) |
| 80988005 | http://snomed.info/sct | Mixed cryofibrinogenemia (disorder) |
| 81783000 | http://snomed.info/sct | Familial multiple factor deficiency syndrome (disorder) |
| 84048006 | http://snomed.info/sct | Familial multiple factor deficiency syndrome, type I (disorder) |
| 860725002 | http://snomed.info/sct | Low von Willebrand factor (finding) |
| 86075001 | http://snomed.info/sct | Coagulation factor deficiency syndrome (disorder) |
| 86635005 | http://snomed.info/sct | Kasabach-Merritt syndrome (disorder) |
| 88540000 | http://snomed.info/sct | Factor XI deficiency, type I (disorder) |
| 88776002 | http://snomed.info/sct | Hereditary factor V deficiency disease (disorder) |
| 89729000 | http://snomed.info/sct | Factor IX inhibitor disorder (disorder) |
| 90935002 | http://snomed.info/sct | Hemophilia (disorder) |
| 9489006 | http://snomed.info/sct | Factor X inhibitor disorder (disorder) |
| 95839005 | http://snomed.info/sct | Disorder involving the fibrinolytic system (disorder) |
| 95840007 | http://snomed.info/sct | Hypoplasminogenemia (disorder) |
| 95841006 | http://snomed.info/sct | Hereditary hypoplasminogenemia (disorder) |
| 95842004 | http://snomed.info/sct | Autosomal dominant deficiency of plasminogen (disorder) |
| 95843009 | http://snomed.info/sct | Acquired hypoplasminogenemia (disorder) |
| 95844003 | http://snomed.info/sct | Dysplasminogenemia (disorder) |
| 95845002 | http://snomed.info/sct | Hereditary dysplasminogenemia (disorder) |
| 97571000119109 | http://snomed.info/sct | Thrombocytopenia co-occurrent and due to alcoholism (disorder) |
Produced 08 Sep 2023