| Source | us.nlm.vsac#0.11.0:null (v4.0.1) |
| resourceType | ValueSet |
| id | 2.16.840.1.113762.1.4.1029.285 |
| canonical | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1029.285 |
| version | 20210605 |
| status | active |
| publisher | Joint Commission |
| name | BleedingDisorder |
| title | Bleeding Disorder |
| date | 2021-06-05T01:01:30-04:00 |
| experimental | false |
| Usages | (none) |
This value set contains 198 concepts
| Code | System | Display |
| 105604006 | http://snomed.info/sct | Deficiency of naturally occurring coagulation factor inhibitor (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) |
| 13172003 | http://snomed.info/sct | Chronic idiopathic thrombocytopenic purpura (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) |
| 1563006 | http://snomed.info/sct | Protein S deficiency disease (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) |
| 19267009 | http://snomed.info/sct | Lupus anticoagulant disorder (disorder) |
| 2036003 | http://snomed.info/sct | Acquired factor VII deficiency disease (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) |
| 234482009 | http://snomed.info/sct | Amegakaryocytic thrombocytopenia (disorder) |
| 234483004 | http://snomed.info/sct | Megakaryocytic thrombocytopenia (disorder) |
| 234486007 | http://snomed.info/sct | Montreal platelet syndrome (disorder) |
| 234487003 | http://snomed.info/sct | Mediterranean thrombocytopenia (disorder) |
| 25904003 | http://snomed.info/sct | Acquired coagulation factor deficiency (disorder) |
| 26029002 | http://snomed.info/sct | Mild hereditary factor VIII deficiency disease (disorder) |
| 267534000 | http://snomed.info/sct | Primary thrombocytopenia (disorder) |
| 27312002 | http://snomed.info/sct | High molecular weight kininogen deficiency (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) |
| 2897005 | http://snomed.info/sct | Immune thrombocytopenia (disorder) |
| 302215000 | http://snomed.info/sct | Thrombocytopenic disorder (disorder) |
| 302873008 | http://snomed.info/sct | Thrombocytopenic purpura (disorder) |
| 307514008 | http://snomed.info/sct | Idiopathic factor VIII deficiency (disorder) |
| 307515009 | http://snomed.info/sct | Autoimmune factor VIII deficiency (disorder) |
| 307518006 | http://snomed.info/sct | Malignancy-related factor VIII deficiency (disorder) |
| 31925001 | http://snomed.info/sct | Hereditary factor I deficiency disease (disorder) |
| 323079008 | http://snomed.info/sct | Thrombocytopenia due to sequestration (disorder) |
| 33169001 | http://snomed.info/sct | Factor XI deficiency, type II (disorder) |
| 33183004 | http://snomed.info/sct | Post infectious thrombocytopenic purpura (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) |
| 35554008 | http://snomed.info/sct | Acquired factor XI deficiency disease (disorder) |
| 35913006 | http://snomed.info/sct | Acquired factor V deficiency disease (disorder) |
| 359531004 | http://snomed.info/sct | Amegakaryocytic thrombocytopenia with congenital malformation (disorder) |
| 359536009 | http://snomed.info/sct | Megakaryocytic aplasia (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) |
| 359723007 | http://snomed.info/sct | Acquired hypofibrinogenemia (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) |
| 36070007 | http://snomed.info/sct | Wiskott-Aldrich syndrome (disorder) |
| 36351005 | http://snomed.info/sct | Antithrombin III deficiency (disorder) |
| 371106008 | http://snomed.info/sct | Idiopathic maternal thrombocytopenia (disorder) |
| 37193007 | http://snomed.info/sct | Factor VII deficiency (disorder) |
| 373420004 | http://snomed.info/sct | Upshaw-Schulman syndrome (disorder) |
| 37350004 | http://snomed.info/sct | Hereditary factor X deficiency disease (disorder) |
| 37492005 | http://snomed.info/sct | Sex-linked thrombocytopenia (disorder) |
| 3760002 | http://snomed.info/sct | Familial multiple factor deficiency syndrome, type V (disorder) |
| 38879000 | http://snomed.info/sct | Factor XI inhibitor disorder (disorder) |
| 402653004 | http://snomed.info/sct | Thrombocytopenic purpura due to defective platelet production (disorder) |
| 402654005 | http://snomed.info/sct | Thrombocytopenic purpura due to platelet consumption (disorder) |
| 403837005 | http://snomed.info/sct | Wiskott-Aldrich autosomal dominant variant 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) |
| 417626001 | http://snomed.info/sct | Thrombocytopenic purpura associated with metabolic disorder (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) |
| 438476003 | http://snomed.info/sct | Autoimmune thrombotic thrombocytopenic purpura (disorder) |
| 438492008 | http://snomed.info/sct | Hereditary thrombocytopenic disorder (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) |
| 439007008 | http://snomed.info/sct | Acquired thrombotic thrombocytopenic purpura (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) |
| 441134009 | http://snomed.info/sct | Congenital dysmegakaryopoietic thrombocytopenia, Paris Trousseau type (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) |
| 48788004 | http://snomed.info/sct | Cyclic thrombocytopenia (disorder) |
| 48976006 | http://snomed.info/sct | Prekallikrein deficiency (disorder) |
| 49762007 | http://snomed.info/sct | Hereditary factor XI deficiency disease (disorder) |
| 50189006 | http://snomed.info/sct | Hereditary factor XIII deficiency disease (disorder) |
| 54569005 | http://snomed.info/sct | Bernard Soulier syndrome (disorder) |
| 58327003 | http://snomed.info/sct | Factor I inhibitor disorder (disorder) |
| 60628003 | http://snomed.info/sct | Mediterranean macrothrombocytopenia (disorder) |
| 61551003 | http://snomed.info/sct | Familial multiple factor deficiency syndrome, type VI (disorder) |
| 61802005 | http://snomed.info/sct | Primary cryofibrinogenemia (disorder) |
| 63444004 | http://snomed.info/sct | Thrombocytopenia due to hypersplenism (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) |
| 6935003 | http://snomed.info/sct | Familial hemorrhagic diathesis (disorder) |
| 69500007 | http://snomed.info/sct | Blood coagulation disorder due to liver disease (disorder) |
| 711407000 | http://snomed.info/sct | Thrombocytopathy, asplenia and miosis (disorder) |
| 712922002 | http://snomed.info/sct | Myosin heavy chain 9 non muscle related disease (disorder) |
| 715559004 | http://snomed.info/sct | Combined deficiency of factor V and factor VIII (disorder) |
| 716336002 | http://snomed.info/sct | Congenital amegakaryocytic thrombocytopenia (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) |
| 719021005 | http://snomed.info/sct | DK phocomelia syndrome (disorder) |
| 720521008 | http://snomed.info/sct | Autosomal dominant macrothrombocytopenia (disorder) |
| 721882001 | http://snomed.info/sct | Radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome (disorder) |
| 722401001 | http://snomed.info/sct | Severe fever with thrombocytopenia syndrome virus (disorder) |
| 722475006 | http://snomed.info/sct | X-linked congenital dyserythropoietic anemia with thrombocytopenia (disorder) |
| 73162004 | http://snomed.info/sct | Posttransfusion purpura (disorder) |
| 73975000 | http://snomed.info/sct | Factor II deficiency (disorder) |
| 75331009 | http://snomed.info/sct | Evans syndrome (disorder) |
| 76407009 | http://snomed.info/sct | Protein C deficiency disease (disorder) |
| 76642003 | http://snomed.info/sct | Factor X deficiency (disorder) |
| 78345002 | http://snomed.info/sct | Thrombocytopenia due to diminished platelet production (disorder) |
| 80988005 | http://snomed.info/sct | Mixed cryofibrinogenemia (disorder) |
| 81783000 | http://snomed.info/sct | Familial multiple factor deficiency syndrome (disorder) |
| 82190001 | http://snomed.info/sct | Thrombocytopenia due to defective platelet production (disorder) |
| 84048006 | http://snomed.info/sct | Familial multiple factor deficiency syndrome, type I (disorder) |
| 85589009 | http://snomed.info/sct | Radial aplasia-thrombocytopenia syndrome (disorder) |
| 86075001 | http://snomed.info/sct | Coagulation factor deficiency syndrome (disorder) |
| 86635005 | http://snomed.info/sct | Kasabach-Merritt syndrome (disorder) |
| 87902006 | http://snomed.info/sct | Thrombocytopenia due to non-immune destruction (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) |
Produced 08 Sep 2023