PMH - Bleeding Disorder
Codelist metadata
- Coding system
- SNOMED CT (UK Clinical Edition)
- Coding system release
- unknown
- Author
- Tom Nichols
- Codelist ID
- user/tom-nichols/pmh-bleeding-disorder
- Version ID
- 68d33034
- Number of codes included
- 518
About
No metadata has been provided for this codelist.
Codelists are developed by a broad community of users for individual study purposes, which may or may not meet the needs of other studies. They should not be thought of as universal definitions of a particular condition.
We don't offer any guarantees about what they do or don't identify. Users should carefully check that any codelist meets their needs, and seek clinical input where appropriate.
| code | term |
|---|---|
| 10153004 | Systemic fibrinogenolysis |
| 10278007 | Factitious purpura |
| 105604006 | Deficiency of naturally occurring coagulation factor inhibitor |
| 10749581000119100 | Blood coagulation disorder complicating childbirth |
| 10749641000119106 | Blood coagulation disorder complicating pregnancy |
| 10934005 | Cryofibrinogenemia |
| 109994006 | Essential thrombocythemia |
| 111199007 | Purpura pigmentosa chronica |
| 111396008 | Chédiak-Higashi syndrome |
| 111452009 | Postpartum afibrinogenemia with hemorrhage |
| 111588002 | Heparin-induced thrombocytopenia with thrombosis |
| 111589005 | Dysfibrinogenemia |
| 118791000119106 | Aplastic anemia caused by antineoplastic agent |
| 12153008 | Acquired factor IX deficiency disease |
| 123786007 | Blood coagulation disorder with shortened coagulation time |
| 123787003 | Blood coagulation disorder with prolonged coagulation time |
| 123788008 | Blood coagulation disorder with shortened bleeding time |
| 123789000 | Blood coagulation disorder with prolonged bleeding time |
| 123790009 | Blood coagulation disorder with impaired clot retraction time |
| 12501008 | von Willebrand disease, type IIF |
| 12546009 | Hemorrhagic disease of the newborn due to vitamin K deficiency |
| 127034005 | Pancytopenia |
| 128088003 | Blood coagulation disorder, categorized by value of screening test |
| 128090002 | Benign gestational thrombocytopenia |
| 128091003 | Autoimmune thrombocytopenia |
| 128092005 | Secondary autoimmune thrombocytopenia |
| 128093000 | Alloimmune thrombocytopenia |
| 128094006 | Alloimmune platelet transfusion refractoriness |
| 128095007 | Acquired platelet function disorder |
| 128096008 | Hereditary platelet function disorder |
| 128098009 | Scott syndrome |
| 128099001 | Platelet storage pool defect |
| 128100009 | Mixed alpha granule and dense body deficiency |
| 128101008 | Platelet factor V deficiency (factor V Quebec) |
| 128102001 | Familial alpha>2< adrenergic receptor defect in platelets |
| 128103006 | Isolated collagen aggregation defect |
| 128105004 | von Willebrand disorder |
| 128106003 | von Willebrand disease type 1 |
| 128107007 | von Willebrand disease type 2 |
| 128108002 | von Willebrand disease type 3 |
| 128113003 | von Willebrand disease type IB |
| 128114009 | von Willebrand disease type IC |
| 128115005 | Pseudo von Willebrand disease |
| 1286003 | Vitamin K deficiency coagulation disorder |
| 129654004 | Acquired platelet factor 3 disease |
| 13172003 | Chronic idiopathic thrombocytopenic purpura |
| 13507004 | Purpura fulminans |
| 13993001 | Factor XIII inhibitor disorder |
| 14024008 | Humoral immunologic aplastic anemia |
| 14230004 | Acquired factor VIII deficiency disease |
| 15132005 | Acquired factor XII deficiency disease |
| 154818001 | Congenital afibrinogenemia |
| 154826009 | Secondary thrombocytopenia |
| 1563006 | Protein S deficiency disease |
| 161460007 | History of coagulation defect |
| 16773005 | Drug-induced coagulation inhibitor disorder |
| 16872008 | Severe hereditary factor VIII deficiency disease |
| 16922007 | Hereditary coagulation factor deficiency |
| 17592003 | Platelet dysfunction caused by aspirin |
| 180481005 | Anti-factor II disorder |
| 181456001 | Antiprothrombin disorder |
| 183005 | Autoimmune pancytopenia |
| 18604004 | Factor XIII deficiency disease |
| 1908008 | von Willebrand disease, type IIC |
| 190809001 | Waldenstrom's hypergammaglobulinemic purpura |
| 190810006 | Benign primary hypergammaglobulinemic purpura |
| 190814002 | Cryoglobulinemic purpura |
| 191244003 | Aplastic anemia due to chronic disease |
| 191246001 | Aplastic anemia due to infection |
| 191247005 | Aplastic anemia caused by radiation |
| 191248000 | Aplastic anemia caused by toxic cause |
| 191255003 | Transient acquired pure red cell aplasia |
| 191256002 | Idiopathic aplastic anemia |
| 191287000 | Hemorrhagic disorder due to circulating anticoagulants |
| 191288005 | Hemorrhagic disorder due to antithrombinemia |
| 191289002 | Hemorrhagic disorder due to hyperheparinemia |
| 191290006 | Hemorrhagic disorder due to increase in anti-8a |
| 191291005 | Hemorrhagic disorder due to increase in anti-9a |
| 191292003 | Hemorrhagic disorder due to increase in anti-10a |
| 191293008 | Hemorrhagic disorder due to increase in anti-11a |
| 191296000 | Deficiency of coagulation factor due to liver disease |
| 191297009 | Deficiency of coagulation factor due to vitamin K deficiency |
| 191298004 | Acquired factor II deficiency |
| 191306005 | Immunoglobulin A vasculitis |
| 191322006 | Thrombocytopenia caused by drugs |
| 191323001 | Thrombocytopenia due to extracorporeal circulation of blood |
| 19267009 | Lupus anticoagulant disorder |
| 19307009 | Drug-induced immune thrombocytopenia |
| 19520006 | von Willebrand disease, type IIB |
| 200030007 | Postpartum coagulation defects - delivered with postnatal problem |
| 200031006 | Postpartum coagulation defects with postnatal problem |
| 20343006 | Pigmented purpuric lichenoid dermatitis of Gougerot and Blum |
| 2036003 | Acquired factor VII deficiency disease |
| 206414002 | Perinatal purpura |
| 206510008 | Transient neonatal thrombocytopenia due to exchange transfusion |
| 206511007 | Transient neonatal thrombocytopenia due to idiopathic maternal thrombocytopenia |
| 206512000 | Transient neonatal thrombocytopenia due to isoimmunization |
| 21112004 | Vascular hemostatic disease |
| 21360006 | Miscarriage with afibrinogenemia |
| 22716005 | Platelet disorder |
| 23205009 | Transient neonatal thrombocytopenia |
| 234367000 | Pancytopenia with pancreatitis |
| 234370001 | Pure red cell aplasia, acquired |
| 234376007 | Acquired red cell aplasia |
| 234440005 | Factor VIII deficiency |
| 234442002 | Hereditary factor VIII deficiency disease with inhibitor |
| 234444001 | Congenital factor IX deficiency variant |
| 234445000 | Congenital factor IX deficiency with inhibitor |
| 234446004 | Congenital von Willebrand's disease |
| 234447008 | Congenital von Willebrand's disease type I |
| 234448003 | Congenital von Willebrand's disease type II |
| 234450006 | Congenital von Willebrand's disease type III |
| 234451005 | Acquired von Willebrand's disease |
| 234452003 | Contact factor deficiency |
| 234453008 | Passovoy factor deficiency |
| 234454002 | Prothrombin complex deficiency |
| 234455001 | Fibrinogen abnormality |
| 234456000 | Congenital fibrinogen abnormality |
| 234457009 | Hypofibrinogenemia |
| 234458004 | Hypodysfibrinogenemia |
| 234459007 | Alpha chain defect dysfibrinogenemia |
| 234460002 | Beta chain defect dysfibrinogenemia |
| 234461003 | Gamma chain defect dysfibrinogenemia |
| 234462005 | Acquired fibrinogen abnormality |
| 234463000 | Combined coagulation factor deficiency |
| 234464006 | Fibrinolytic bleeding syndrome |
| 234465007 | Alpha-2-antiplasmin deficiency |
| 234466008 | Acquired coagulation disorder |
| 234467004 | Thrombophilia |
| 234468009 | Heparin cofactor II deficiency |
| 234469001 | Inherited platelet disorder |
| 234470000 | Platelet membrane defect |
| 234471001 | Glycoprotein Ia defect |
| 234472008 | Glycoprotein Ib defect |
| 234473003 | Platelet type von Willebrand's disease |
| 234474009 | Dense body defect |
| 234475005 | Thromboxane generation defect |
| 234476006 | Cyclooxygenase deficiency |
| 234477002 | Thromboxane synthetase deficiency |
| 234478007 | Giant platelet syndrome |
| 234479004 | Acquired platelet disorder |
| 234482009 | Amegakaryocytic thrombocytopenia |
| 234483004 | Megakaryocytic thrombocytopenia |
| 234484005 | May-Hegglin anomaly |
| 234485006 | Epstein syndrome |
| 234486007 | Montreal platelet syndrome |
| 234487003 | Mediterranean thrombocytopenia |
| 234493006 | Non-thrombocytopenic purpura |
| 234494000 | Primary non-thrombocytopenic purpura |
| 234495004 | Secondary non-thrombocytopenic purpura |
| 234496003 | Metabolic purpura |
| 234497007 | Embolic purpura |
| 234500001 | Reactive thrombocytosis |
| 234512002 | Post-splenectomy thrombocytosis |
| 237336007 | Fibrinolysis - postpartum |
| 237337003 | Afibrinogenemia - postpartum |
| 238781005 | Itching purpura |
| 238787009 | Secondary cutaneous vasculitis |
| 239892009 | Primary antiphospholipid syndrome |
| 239893004 | Primary antiphospholipid syndrome with organ/system involvement |
| 239894005 | Primary antiphospholipid syndrome with multisystem involvement |
| 239895006 | Secondary antiphospholipid syndrome |
| 239896007 | Secondary antiphospholipid syndrome with organ/system involvement |
| 239897003 | Secondary antiphospholipid syndrome with multisystem involvement |
| 239946005 | Postinfective immunoglobulin A vasculitis |
| 240305000 | Neonatal thrombocytopenia due to platelet alloimmunization |
| 240486003 | Parvoviral aplastic crisis |
| 24149006 | Hemorrhagic disease of the newborn due to factor II deficiency |
| 24663001 | von Willebrand disease, type IIH |
| 25904003 | Acquired coagulation factor deficiency |
| 26029002 | Mild hereditary factor VIII deficiency disease |
| 267272006 | Postpartum coagulation defects |
| 267524009 | Constitutional aplastic anemia with malformation |
| 267527002 | Aplastic anemia due to drugs |
| 267532001 | Qualitative platelet disorder |
| 267534000 | Primary thrombocytopenia |
| 267535004 | Congenital thrombocytopenic purpura |
| 26843008 | Antiphospholipid syndrome |
| 270117002 | Platelet type pseudo-von Willebrand disease |
| 27068000 | Failed attempted abortion with afibrinogenemia |
| 27312002 | High molecular weight kininogen deficiency |
| 273986001 | Perinatal thrombocytopenia |
| 275446004 | Gardner-Diamond syndrome |
| 275523003 | Pancytopenia-dysmelia |
| 276575001 | Autoimmune neonatal thrombocytopenia |
| 277791008 | Purpura simplex |
| 278365007 | Anticoagulant-induced bleeding |
| 278366008 | Anticoagulant excess without bleeding |
| 278504009 | Afibrinogenemia |
| 281351006 | Arthritis due to bleeding disorder |
| 282707003 | Acquired inhibitor of coagulation |
| 28293008 | Hereditary factor VIII deficiency disease |
| 284078000 | Purpuric rash |
| 28505005 | Acute idiopathic thrombocytopenic purpura |
| 2897005 | Immune thrombocytopenia |
| 28975000 | Constitutional aplastic anemia |
| 296332004 | Acquired storage pool deficiency (platelets) |
| 296926001 | Heparin overdose |
| 296927005 | Accidental heparin overdose |
| 296928000 | Intentional heparin overdose |
| 296929008 | Heparin overdose of undetermined intent |
| 296930003 | Coumarin overdose |
| 296931004 | Accidental coumarin overdose |
| 296932006 | Intentional coumarin overdose |
| 296933001 | Coumarin overdose of undetermined intent |
| 296934007 | Accidental warfarin overdose |
| 296935008 | Intentional warfarin sodium overdose |
| 296936009 | Warfarin overdose of undetermined intent |
| 297307009 | Exhausted platelets |
| 30182008 | Thrombocytopenia due to extracorporeal circulation |
| 302215000 | Thrombocytopenic disorder |
| 302873008 | Thrombocytopenic purpura |
| 30479005 | Legal abortion with afibrinogenemia |
| 30575002 | Fanconi's anemia |
| 306058006 | Aplastic anemia |
| 307091009 | Factor V Leiden mutation |
| 307115002 | Homozygous Factor V Leiden mutation |
| 307116001 | Heterozygous Factor V Leiden mutation |
| 307342006 | Thrombocytopenia due to massive blood transfusion |
| 307514008 | Idiopathic factor VIII deficiency |
| 307515009 | Autoimmune factor VIII deficiency |
| 307517001 | Pregnancy-related factor VIII deficiency |
| 307518006 | Malignancy-related factor VIII deficiency |
| 31925001 | Hereditary factor I deficiency disease |
| 322096003 | Platelet sequestration |
| 32273002 | Immune thrombocytopenic purpura |
| 3230006 | Illegal abortion with afibrinogenemia |
| 323079008 | Thrombocytopenia due to sequestration |
| 32605001 | Transient neonatal disorder of coagulation |
| 328301000119102 | Pancytopenia due to antineoplastic chemotherapy |
| 32942005 | Glanzmann's thrombasthenia |
| 33169001 | Factor XI deficiency, type II |
| 33183004 | Post infectious thrombocytopenic purpura |
| 33297000 | Hereditary factor II deficiency disease |
| 33344008 | Moderate hereditary factor VIII deficiency disease |
| 33820001 | Acquired factor X deficiency disease |
| 34395002 | Thrombocytopenia caused by hypothermia |
| 34417008 | Disseminated intravascular coagulation in newborn |
| 34478009 | Failed attempted abortion with defibrination syndrome |
| 35066007 | von Willebrand disease, type IID |
| 35554008 | Acquired factor XI deficiency disease |
| 35913006 | Acquired factor V deficiency disease |
| 359531004 | Amegakaryocytic thrombocytopenia with congenital malformation |
| 359536009 | Megakaryocytic aplasia |
| 359700009 | Hereditary von Willebrand disease type IA |
| 359704000 | von Willebrand disease, type 1^a^ |
| 359709005 | von Willebrand disease type IA |
| 359711001 | Hereditary von Willebrand disease type 2A |
| 359714009 | von Willebrand disease type 2A |
| 359717002 | Hereditary von Willebrand disease type 2B |
| 359721009 | von Willebrand disease type 2B |
| 359723007 | Acquired hypofibrinogenemia |
| 359725000 | Hereditary von Willebrand disease type 2M |
| 359727008 | Fibrinogen deficiency |
| 359729006 | von Willebrand disease type 2M |
| 359730001 | Acquired afibrinogenemia |
| 359732009 | von Willebrand disease type 2N |
| 36070007 | Wiskott-Aldrich syndrome |
| 361209006 | Dermite ocre of Favre |
| 361210001 | Stasis purpura |
| 362970003 | Disorder of hemostatic system |
| 36351005 | Antithrombin III deficiency |
| 371074009 | Radiation thrombocytopenia |
| 371106008 | Idiopathic maternal thrombocytopenia |
| 37193007 | Factor VII deficiency |
| 373420004 | Upshaw-Schulman syndrome |
| 37350004 | Hereditary factor X deficiency disease |
| 37492005 | Sex-linked thrombocytopenia |
| 3760002 | Familial multiple factor deficiency syndrome, type V |
| 387778001 | Purpuric disorder |
| 38879000 | Factor XI inhibitor disorder |
| 38970002 | Doan-Wright syndrome |
| 39191000119103 | Disseminated intravascular coagulation due to placental abruption |
| 402589000 | Contact purpura |
| 402653004 | Thrombocytopenic purpura due to defective platelet production |
| 402654005 | Thrombocytopenic purpura due to platelet consumption |
| 402848007 | Clothing purpura |
| 402849004 | Purpura due to increased intravascular pressure |
| 402850004 | Purpura due to prolonged vomiting and/or coughing |
| 402851000 | Neonatal purpura fulminans (homozygous protein C deficiency) |
| 402852007 | Hyperglobulinemic purpura |
| 402853002 | Cryofibrinogenemic purpura |
| 402854008 | Dysproteinemic purpura |
| 402856005 | Acute hemorrhagic edema of childhood |
| 402865003 | Systemic lupus erythematosus-associated antiphospholipid syndrome |
| 403393000 | Stellate pseudoscar in senile purpura |
| 403837005 | Wiskott-Aldrich autosomal dominant variant syndrome |
| 40855001 | Hereditary factor VII deficiency disease |
| 41106001 | von Willebrand factor inhibitor disorder |
| 413565006 | Aplastic anemia associated with metabolic alteration |
| 413566007 | Aplastic anemia associated with pancreatitis |
| 413567003 | Aplastic anemia associated with pregnancy |
| 41461004 | Platelet dysfunction caused by drugs |
| 41486008 | Eczematid-like purpura of Doucas and Kapetanakis |
| 41690001 | Factor V inhibitor disorder |
| 416902009 | Uremic thrombocytopenia |
| 417626001 | Thrombocytopenic purpura associated with metabolic disorder |
| 41788008 | Hereditary factor IX deficiency disease |
| 41816006 | Secondary cryofibrinogenemia |
| 421102007 | Aplastic anemia associated with acquired immunodeficiency syndrome |
| 421132004 | Platelet dysfunction associated with uremia |
| 421527008 | Resistance to activated protein C caused by Factor V Leiden |
| 421766003 | Thrombocytopenia associated with acquired immunodeficiency syndrome |
| 425949001 | Mild hereditary factor VIII deficiency disease with inhibitor |
| 426199009 | Congenital factor IX deficiency without inhibitor |
| 4320005 | Factor V deficiency |
| 43217004 | Hereditary factor XII deficiency disease |
| 43302000 | Anticoagulant overdosage |
| 43346008 | Platelet procoagulant activity deficiency |
| 438360006 | Hereditary factor VIII deficiency disease without inhibitor |
| 438372000 | Hereditary factor IX deficiency disease with inhibitor |
| 438373005 | Severe hereditary factor VIII deficiency disease with inhibitor |
| 438476003 | Autoimmune thrombotic thrombocytopenic purpura |
| 438492008 | Hereditary thrombocytopenic disorder |
| 43858000 | Secondary aplastic anemia |
| 438599002 | Moderate hereditary factor VIII deficiency disease with inhibitor |
| 438792009 | Hereditary factor IX deficiency disease without inhibitor |
| 438827002 | Hereditary thrombophilic dysfibrinogenemia |
| 439000005 | Hyperfibrinogenemia |
| 439001009 | Acquired thrombophilia |
| 439002002 | Thrombophilia due to acquired protein C deficiency |
| 439006004 | Hereditary hyperhomocysteinemia |
| 439007008 | Acquired thrombotic thrombocytopenic purpura |
| 439125003 | Thrombophilia due to acquired protein S deficiency |
| 439126002 | Thrombophilia due to acquired antithrombin III deficiency |
| 439145006 | Congenital hypofibrinogenemia |
| 439156006 | Acquired combined coagulation factor deficiency |
| 439157002 | Hereditary combined coagulation factor deficiency |
| 439274008 | Hereditary protein C deficiency |
| 439455002 | Hereditary factor XIII A subunit deficiency |
| 439458000 | Factor I deficiency disease |
| 439459008 | Hereditary factor XIII B subunit deficiency |
| 439460003 | Hereditary factor XIII A subunit and B subunit deficiency |
| 439698008 | Hereditary thrombophilia |
| 439699000 | Hereditary antithrombin III deficiency |
| 439701000 | Hereditary heparin cofactor II deficiency |
| 439702007 | Hereditary protein S deficiency |
| 439725008 | A disintegrin and metalloproteinase with thrombospondin type 1 motif 13 deficiency |
| 440820004 | Mild hereditary factor VIII deficiency disease without inhibitor |
| 440866009 | Severe hereditary factor IX deficiency disease with inhibitor |
| 440867000 | Moderate hereditary factor IX deficiency disease with inhibitor |
| 440868005 | Mild hereditary factor IX deficiency disease with inhibitor |
| 440924009 | Hereditary hyperfibrinogenemia |
| 440988005 | Heterozygous protein S deficiency |
| 440989002 | Prothrombin G20210A mutation |
| 440993008 | Severe hereditary factor VIII deficiency disease without inhibitor |
| 441001005 | Hereditary elevated factor XI |
| 441006000 | Moderate hereditary factor VIII deficiency disease without inhibitor |
| 441042008 | Hereditary elevated factor VIII |
| 441079006 | Thrombophilia due to antiphospholipid antibody |
| 441101007 | Heterozygous protein C deficiency |
| 441134009 | Congenital dysmegakaryopoietic thrombocytopenia, Paris Trousseau type |
| 441188004 | Homozygous protein C deficiency |
| 441189007 | Homozygous protein S deficiency |
| 441190003 | Severe hereditary factor IX deficiency disease without inhibitor |
| 441191004 | Moderate hereditary factor IX deficiency disease without inhibitor |
| 441192006 | Mild hereditary factor IX deficiency disease without inhibitor |
| 441322009 | Drug induced thrombotic thrombocytopenic purpura |
| 441420000 | Homozygous prothrombin G20210A mutation |
| 441421001 | Heterozygous prothrombin G20210A mutation |
| 441697004 | Thrombophilia associated with pregnancy |
| 441762006 | Thrombophilia due to immobilization |
| 441945008 | Thrombophilia due to trauma |
| 441946009 | Thrombophilia due to myeloproliferative disorder |
| 441990004 | Thrombophilia due to paroxysmal nocturnal hemoglobinuria |
| 442078001 | Thrombophilia due to malignant neoplasm |
| 442121006 | Thrombophilia due to vascular anomaly |
| 442197003 | Thrombophilia caused by drug therapy |
| 442363001 | Thrombophilia caused by vascular device |
| 442654007 | Thrombophilia caused by hormone therapy |
| 442760001 | Thrombophilia caused by antineoplastic agent therapy |
| 45366001 | Hereditary dysfibrinogenemia |
| 45963004 | Factor XI deficiency, type III |
| 46760003 | Estren-Dameshek anemia |
| 46981006 | Factor XII deficiency disease |
| 47307007 | Factor VIII inhibitor disorder |
| 47546008 | Warfarin overdosage |
| 48788004 | Cyclic thrombocytopenia |
| 48976006 | Prekallikrein deficiency |
| 49177006 | Postpartum coagulation defect with hemorrhage |
| 49762007 | Hereditary factor XI deficiency disease |
| 49886003 | Thrombocytopenia due to blood loss |
| 50189006 | Hereditary factor XIII deficiency disease |
| 50220002 | Cellular immunologic aplastic anemia |
| 50770000 | Miscarriage with defibrination syndrome |
| 51448009 | Platelet secretory disorder |
| 51624005 | Dilutional thrombocytopenia |
| 51720005 | Gray platelet syndrome |
| 52137009 | von Willebrand disease, type IIE |
| 53751009 | Senile purpura |
| 54569005 | Bernard Soulier syndrome |
| 55907008 | Acquired aplastic anemia |
| 56231002 | Purpura annularis telangiectodes of Majocchi |
| 58327003 | Factor I inhibitor disorder |
| 5876000 | Acquired pancytopenia |
| 60628003 | Mediterranean macrothrombocytopenia |
| 609329007 | Catastrophic antiphospholipid syndrome |
| 609456005 | Induced termination of pregnancy complicated by afibrinogenemia |
| 609462000 | Induced termination of pregnancy complicated by defibrination syndrome |
| 61551003 | Familial multiple factor deficiency syndrome, type VI |
| 61744005 | Neonatal thrombocytopenia due to idiopathic maternal thrombocytopenia |
| 61802005 | Primary cryofibrinogenemia |
| 61810006 | Illegal abortion with defibrination syndrome |
| 62410004 | Postpartum fibrinolysis with hemorrhage |
| 62698000 | Defibrination syndrome following molar AND/OR ectopic pregnancy |
| 63444004 | Thrombocytopenia due to hypersplenism |
| 6364000 | Acquired factor XIII deficiency disease |
| 64315007 | Familial multiple factor deficiency syndrome, type III |
| 64509006 | Acquired coagulation factor inhibitor disorder |
| 64779008 | Blood coagulation disorder |
| 65768009 | Familial multiple factor deficiency syndrome, type II |
| 6631009 | Thrombocytosis |
| 6647006 | Legal abortion with defibrination syndrome |
| 66909001 | Familial multiple factor deficiency syndrome, type IV |
| 67406007 | Disseminated intravascular coagulation |
| 68559009 | May Hegglin syndrome |
| 6935003 | Familial hemorrhagic diathesis |
| 69500007 | Blood coagulation disorder due to liver disease |
| 699208000 | Thrombocytopenia caused by alcohol |
| 7014009 | Mechanical purpura |
| 709465004 | Periodontitis co-occurrent with Chédiak-Higashi syndrome |
| 711407000 | Thrombocytopathy, asplenia and miosis |
| 712922002 | Myosin heavy chain 9 non muscle related disease |
| 713388002 | GATA binding protein 1 related thrombocytopenia with dyserythropoiesis |
| 713508003 | Aplastic anemia co-occurrent with human immunodeficiency virus infection |
| 713910008 | Antibody mediated acquired pure red cell aplasia caused by erythropoiesis stimulating agent |
| 715559004 | Combined deficiency of factor V and factor VIII |
| 716336002 | Congenital amegakaryocytic thrombocytopenia |
| 716746003 | Congenital alpha-2-antiplasmin deficiency |
| 71723006 | von Willebrand disease, type IIG |
| 717407006 | Congenital plasminogen activator inhibitor deficiency type 1 |
| 717769007 | MYH9 macrothrombocytopenia syndrome |
| 717935003 | Early onset diffuse bleeding diathesis secondary to vitamin K deficient hemorrhagic disease of fetus and newborn |
| 717936002 | Classic onset hemorrhagic disease of newborn due to vitamin K deficiency |
| 717937006 | Late onset diffuse bleeding diathesis secondary to vitamin K deficient hemorrhagic disease of fetus and newborn |
| 718195003 | Inherited predisposition to essential thrombocythemia |
| 718553004 | White platelet syndrome |
| 718554005 | Medich giant platelet syndrome |
| 719019000 | WT limb blood syndrome |
| 719021005 | DK phocomelia syndrome |
| 720520009 | Attenuated Chédiak-Higashi syndrome |
| 720521008 | Autosomal dominant macrothrombocytopenia |
| 720950009 | Familial thrombocytosis |
| 721304007 | Refractory thrombocytopenia |
| 72161000119100 | Antiphospholipid syndrome in pregnancy |
| 721882001 | Radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome |
| 722401001 | Severe fever with thrombocytopenia syndrome virus |
| 722475006 | X-linked congenital dyserythropoietic anemia with thrombocytopenia |
| 7226007 | Infection-associated purpura |
| 723011009 | Acute purpuric eruption of skin |
| 723512008 | Revesz syndrome |
| 724344004 | Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency |
| 724356003 | Hereditary combined deficiency of vitamin K-dependent clotting factors |
| 724637001 | Isolated thrombocytopenia |
| 724854007 | Purpura of skin and or skin-associated mucous membrane co-occurrent and due to coagulation disorder |
| 724855008 | Purpura of skin caused by mechanical force |
| 725034002 | Familial platelet syndrome with predisposition to acute myelogenous leukemia |
| 725105006 | Bleeding disorder due to deficiency of calcium and diacylglycerol-regulated guanine nucleotide exchange factor I |
| 725157006 | Acquired purpura fulminans |
| 725291001 | Defect of purinergic receptor p2y G protein-coupled 12 |
| 726513006 | History of hemolysis-elevated liver enzymes-low platelet count syndrome |
| 73162004 | Posttransfusion purpura |
| 733028000 | Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome |
| 733096007 | Thyrocerebrorenal syndrome |
| 73397007 | Heparin-induced thrombocytopenia |
| 736024007 | Pancytopenia caused by medication |
| 737221003 | Congenital thrombocytopenia |
| 737243006 | Purpura of skin co-occurrent and due to vascular fragility |
| 73975000 | Factor II deficiency |
| 74576004 | Acquired thrombocytopenia |
| 75331009 | Evans syndrome |
| 76407009 | Protein C deficiency disease |
| 765748009 | Adult pure red cell aplasia |
| 765977002 | Bleeding disorder due to glycoprotein VI deficiency |
| 76642003 | Factor X deficiency |
| 767712006 | Factor IX deficiency |
| 767713001 | Factor XI deficiency |
| 768556005 | Ataxia pancytopenia syndrome |
| 77084001 | Immunologic aplastic anemia |
| 78129009 | Thrombotic thrombocytopenic purpura |
| 78345002 | Thrombocytopenia due to diminished platelet production |
| 7933002 | Neonatal thrombocytopenia associated with maternal idiopathic thrombocytopenic purpura |
| 79674009 | Hyperheparinemia |
| 80988005 | Mixed cryofibrinogenemia |
| 81500003 | Steroid purpura |
| 81783000 | Familial multiple factor deficiency syndrome |
| 82190001 | Thrombocytopenia due to defective platelet production |
| 82835005 | Neonatal thrombocytopenia |
| 84048006 | Familial multiple factor deficiency syndrome, type I |
| 85589009 | Radial aplasia-thrombocytopenia syndrome |
| 85796009 | Afibrinogenemia following molar AND/OR ectopic pregnancy |
| 86074002 | Purpura rheumatica |
| 86075001 | Coagulation factor deficiency syndrome |
| 86635005 | Kasabach-Merritt syndrome |
| 87397002 | von Willebrand disease, type IIA |
| 87902006 | Thrombocytopenia due to non-immune destruction |
| 88540000 | Factor XI deficiency, type I |
| 88776002 | Hereditary factor V deficiency disease |
| 89729000 | Factor IX inhibitor disorder |
| 89962000 | Neonatal thrombocytopenia due to exchange transfusion |
| 90414007 | Chronic acquired pure red cell aplasia |
| 90935002 | Hemophilia |
| 91304009 | Capillary fragility abnormality |
| 9311003 | Hermansky-Pudlak syndrome |
| 9417000 | Platelet dense granule deficiency |
| 9489006 | Factor X inhibitor disorder |
| 95605009 | Hemolysis-elevated liver enzymes-low platelet count syndrome |
| 95623001 | Neonatal coagulation disorder |
| 95839005 | Disorder involving the fibrinolytic system |
| 95840007 | Hypoplasminogenemia |
| 95841006 | Hereditary hypoplasminogenemia |
| 95842004 | Autosomal dominant deficiency of plasminogen |
| 95843009 | Acquired hypoplasminogenemia |
| 95844003 | Dysplasminogenemia |
| 95845002 | Hereditary dysplasminogenemia |
| 973271000000108 | Antithrombin III deficiency type I |
| 973291000000107 | Antithrombin III deficiency type II |
| 97571000119109 | Thrombocytopenia co-occurrent and due to alcoholism |
This page shows the search terms that were used to build the codelist. Concepts that match the search terms, but which were excluded, are in faint grey.
Bleeding disorder
Included 269 out of 271 matching concepts.
Show matching concepts
-
Accidental coumarin overdose (
296931004) -
Accidental heparin overdose (
296927005) -
Accidental warfarin overdose (
296934007) -
Acquired afibrinogenemia (
359730001) -
Acquired coagulation disorder (
234466008) -
Acquired coagulation factor deficiency (
25904003) -
Acquired coagulation factor inhibitor disorder (
64509006) -
Acquired combined coagulation factor deficiency (
439156006) -
Acquired factor II deficiency (
191298004) -
Acquired factor IX deficiency disease (
12153008) -
Acquired factor V deficiency disease (
35913006) -
Acquired factor VII deficiency disease (
2036003) -
Acquired factor VIII deficiency disease (
14230004) -
Acquired factor X deficiency disease (
33820001) -
Acquired factor XI deficiency disease (
35554008) -
Acquired factor XII deficiency disease (
15132005) -
Acquired factor XIII deficiency disease (
6364000) -
Acquired fibrinogen abnormality (
234462005) -
Acquired hypofibrinogenemia (
359723007) -
Acquired hypoplasminogenemia (
95843009) -
Acquired inhibitor of coagulation (
282707003) -
Acquired purpura fulminans (
725157006) -
Acquired thrombocytopenia (
74576004) -
Acquired von Willebrand's disease (
234451005) -
Afibrinogenemia (
278504009) -
Afibrinogenemia - postpartum (
237337003) -
Afibrinogenemia following molar AND/OR ectopic pregnancy (
85796009) -
Alpha chain defect dysfibrinogenemia (
234459007) -
Alpha-2-antiplasmin deficiency (
234465007) -
Anti-factor II disorder (
180481005) -
Anticoagulant excess without bleeding (
278366008) -
Anticoagulant overdosage (
43302000) -
Anticoagulant-induced bleeding (
278365007) -
Antiprothrombin disorder (
181456001) -
Antithrombin III deficiency (
36351005) -
Antithrombin III deficiency type I (
973271000000108) -
Antithrombin III deficiency type II (
973291000000107) -
Arthritis due to bleeding disorder (
281351006) -
Autoimmune factor VIII deficiency (
307515009) -
Autosomal dominant deficiency of plasminogen (
95842004) -
Benign gestational thrombocytopenia (
128090002) -
Beta chain defect dysfibrinogenemia (
234460002) -
Bleeding disorder due to deficiency of calcium and diacylglycerol-regulated guanine nucleotide exchange factor I (
725105006) -
Bleeding disorder due to glycoprotein VI deficiency (
765977002) -
Blood coagulation disorder (
64779008) -
Blood coagulation disorder complicating childbirth (
10749581000119100) -
Blood coagulation disorder complicating pregnancy (
10749641000119106) -
Blood coagulation disorder due to liver disease (
69500007) -
Blood coagulation disorder with impaired clot retraction time (
123790009) -
Blood coagulation disorder with prolonged bleeding time (
123789000) -
Blood coagulation disorder with prolonged coagulation time (
123787003) -
Blood coagulation disorder with shortened bleeding time (
123788008) -
Blood coagulation disorder with shortened coagulation time (
123786007) -
Blood coagulation disorder, categorized by value of screening test (
128088003) -
Classic onset hemorrhagic disease of newborn due to vitamin K deficiency (
717936002) -
Clotting and bleeding disorders (
191280003) -
Coagulation factor deficiency syndrome (
86075001) -
Combined coagulation factor deficiency (
234463000) -
Combined deficiency of factor V and factor VIII (
715559004) -
Congenital afibrinogenemia (
154818001) -
Congenital alpha-2-antiplasmin deficiency (
716746003) -
Congenital factor IX deficiency variant (
234444001) -
Congenital factor IX deficiency with inhibitor (
234445000) -
Congenital factor IX deficiency without inhibitor (
426199009) -
Congenital fibrinogen abnormality (
234456000) -
Congenital hypofibrinogenemia (
439145006) -
Congenital plasminogen activator inhibitor deficiency type 1 (
717407006) -
Congenital von Willebrand's disease (
234446004) -
Congenital von Willebrand's disease type I (
234447008) -
Congenital von Willebrand's disease type II (
234448003) -
Congenital von Willebrand's disease type III (
234450006) -
Contact factor deficiency (
234452003) -
Coumarin overdose (
296930003) -
Coumarin overdose of undetermined intent (
296933001) -
Cryofibrinogenemia (
10934005) -
Defect of purinergic receptor p2y G protein-coupled 12 (
725291001) -
Defibrination syndrome following molar AND/OR ectopic pregnancy (
62698000) -
Deficiency of coagulation factor due to liver disease (
191296000) -
Deficiency of coagulation factor due to vitamin K deficiency (
191297009) -
Deficiency of naturally occurring coagulation factor inhibitor (
105604006) -
Dilutional thrombocytopenia (
51624005) -
Disorder involving the fibrinolytic system (
95839005) -
Disseminated intravascular coagulation (
67406007) -
Disseminated intravascular coagulation due to placental abruption (
39191000119103) -
Disseminated intravascular coagulation in newborn (
34417008) -
Drug-induced coagulation inhibitor disorder (
16773005) -
Drug-induced immune thrombocytopenia (
19307009) -
Dysfibrinogenemia (
111589005) -
Dysplasminogenemia (
95844003) -
Early onset diffuse bleeding diathesis secondary to vitamin K deficient hemorrhagic disease of fetus and newborn (
717935003) -
Factor I deficiency disease (
439458000) -
Factor I inhibitor disorder (
58327003) -
Factor II deficiency (
73975000) -
Factor IX deficiency (
767712006) -
Factor IX inhibitor disorder (
89729000) -
Factor V deficiency (
4320005) -
Factor V inhibitor disorder (
41690001) -
Factor VII deficiency (
37193007) -
Factor VIII deficiency (
234440005) -
Factor VIII inhibitor disorder (
47307007) -
Factor X deficiency (
76642003) -
Factor X inhibitor disorder (
9489006) -
Factor XI deficiency (
767713001) -
Factor XI deficiency, type I (
88540000) -
Factor XI deficiency, type II (
33169001) -
Factor XI deficiency, type III (
45963004) -
Factor XI inhibitor disorder (
38879000) -
Factor XII deficiency disease (
46981006) -
Factor XIII deficiency disease (
18604004) -
Factor XIII inhibitor disorder (
13993001) -
Failed attempted abortion with afibrinogenemia (
27068000) -
Failed attempted abortion with defibrination syndrome (
34478009) -
Familial hemorrhagic diathesis (
6935003) -
Familial multiple factor deficiency syndrome (
81783000) -
Familial multiple factor deficiency syndrome, type I (
84048006) -
Familial multiple factor deficiency syndrome, type II (
65768009) -
Familial multiple factor deficiency syndrome, type III (
64315007) -
Familial multiple factor deficiency syndrome, type IV (
66909001) -
Familial multiple factor deficiency syndrome, type V (
3760002) -
Familial multiple factor deficiency syndrome, type VI (
61551003) -
Family history of blood coagulation disorder (
108801000119109) -
Fibrinogen abnormality (
234455001) -
Fibrinogen deficiency (
359727008) -
Fibrinolysis - postpartum (
237336007) -
Fibrinolytic bleeding syndrome (
234464006) -
Gamma chain defect dysfibrinogenemia (
234461003) -
Hemolysis-elevated liver enzymes-low platelet count syndrome (
95605009) -
Hemophilia (
90935002) -
Hemorrhagic disease of the newborn due to factor II deficiency (
24149006) -
Hemorrhagic disease of the newborn due to vitamin K deficiency (
12546009) -
Heparin overdose (
296926001) -
Heparin overdose of undetermined intent (
296929008) -
Heparin-induced thrombocytopenia (
73397007) -
Heparin-induced thrombocytopenia with thrombosis (
111588002) -
Hereditary antithrombin III deficiency (
439699000) -
Hereditary coagulation factor deficiency (
16922007) -
Hereditary combined coagulation factor deficiency (
439157002) -
Hereditary combined deficiency of vitamin K-dependent clotting factors (
724356003) -
Hereditary dysfibrinogenemia (
45366001) -
Hereditary dysplasminogenemia (
95845002) -
Hereditary factor I deficiency disease (
31925001) -
Hereditary factor II deficiency disease (
33297000) -
Hereditary factor IX deficiency disease (
41788008) -
Hereditary factor IX deficiency disease with inhibitor (
438372000) -
Hereditary factor IX deficiency disease without inhibitor (
438792009) -
Hereditary factor V deficiency disease (
88776002) -
Hereditary factor VII deficiency disease (
40855001) -
Hereditary factor VIII deficiency disease (
28293008) -
Hereditary factor VIII deficiency disease with inhibitor (
234442002) -
Hereditary factor VIII deficiency disease without inhibitor (
438360006) -
Hereditary factor X deficiency disease (
37350004) -
Hereditary factor XI deficiency disease (
49762007) -
Hereditary factor XII deficiency disease (
43217004) -
Hereditary factor XIII A subunit and B subunit deficiency (
439460003) -
Hereditary factor XIII A subunit deficiency (
439455002) -
Hereditary factor XIII B subunit deficiency (
439459008) -
Hereditary factor XIII deficiency disease (
50189006) -
Hereditary hyperfibrinogenemia (
440924009) -
Hereditary hypoplasminogenemia (
95841006) -
Hereditary protein C deficiency (
439274008) -
Hereditary protein S deficiency (
439702007) -
Hereditary thrombophilic dysfibrinogenemia (
438827002) -
Hereditary von Willebrand disease type 2A (
359711001) -
Hereditary von Willebrand disease type 2B (
359717002) -
Hereditary von Willebrand disease type 2M (
359725000) -
Hereditary von Willebrand disease type IA (
359700009) -
Heterozygous protein C deficiency (
441101007) -
Heterozygous protein S deficiency (
440988005) -
High molecular weight kininogen deficiency (
27312002) -
History of coagulation defect (
161460007) -
History of hemolysis-elevated liver enzymes-low platelet count syndrome (
726513006) -
Homozygous protein C deficiency (
441188004) -
Homozygous protein S deficiency (
441189007) -
Hyperfibrinogenemia (
439000005) -
Hyperheparinemia (
79674009) -
Hypodysfibrinogenemia (
234458004) -
Hypofibrinogenemia (
234457009) -
Hypoplasminogenemia (
95840007) -
Idiopathic factor VIII deficiency (
307514008) -
Illegal abortion with afibrinogenemia (
3230006) -
Illegal abortion with defibrination syndrome (
61810006) -
Induced termination of pregnancy complicated by afibrinogenemia (
609456005) -
Induced termination of pregnancy complicated by defibrination syndrome (
609462000) -
Intentional coumarin overdose (
296932006) -
Intentional heparin overdose (
296928000) -
Intentional warfarin sodium overdose (
296935008) -
Isolated thrombocytopenia (
724637001) -
Kasabach-Merritt syndrome (
86635005) -
Late onset diffuse bleeding diathesis secondary to vitamin K deficient hemorrhagic disease of fetus and newborn (
717937006) -
Legal abortion with afibrinogenemia (
30479005) -
Legal abortion with defibrination syndrome (
6647006) -
Lupus anticoagulant disorder (
19267009) -
Malignancy-related factor VIII deficiency (
307518006) -
Mild hereditary factor IX deficiency disease with inhibitor (
440868005) -
Mild hereditary factor IX deficiency disease without inhibitor (
441192006) -
Mild hereditary factor VIII deficiency disease (
26029002) -
Mild hereditary factor VIII deficiency disease with inhibitor (
425949001) -
Mild hereditary factor VIII deficiency disease without inhibitor (
440820004) -
Miscarriage with afibrinogenemia (
21360006) -
Miscarriage with defibrination syndrome (
50770000) -
Mixed cryofibrinogenemia (
80988005) -
Moderate hereditary factor IX deficiency disease with inhibitor (
440867000) -
Moderate hereditary factor IX deficiency disease without inhibitor (
441191004) -
Moderate hereditary factor VIII deficiency disease (
33344008) -
Moderate hereditary factor VIII deficiency disease with inhibitor (
438599002) -
Moderate hereditary factor VIII deficiency disease without inhibitor (
441006000) -
Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome (
733028000) -
Neonatal coagulation disorder (
95623001) -
Neonatal purpura fulminans (homozygous protein C deficiency) (
402851000) -
Passovoy factor deficiency (
234453008) -
Postpartum afibrinogenemia with hemorrhage (
111452009) -
Postpartum coagulation defect with hemorrhage (
49177006) -
Postpartum coagulation defects (
267272006) -
Postpartum coagulation defects - delivered with postnatal problem (
200030007) -
Postpartum coagulation defects with postnatal problem (
200031006) -
Postpartum fibrinolysis with hemorrhage (
62410004) -
Pregnancy-related factor VIII deficiency (
307517001) -
Prekallikrein deficiency (
48976006) -
Primary cryofibrinogenemia (
61802005) -
Protein C deficiency disease (
76407009) -
Protein S deficiency disease (
1563006) -
Prothrombin complex deficiency (
234454002) -
Pseudo von Willebrand disease (
128115005) -
Purpura fulminans (
13507004) -
Purpura of skin and or skin-associated mucous membrane co-occurrent and due to coagulation disorder (
724854007) -
Radiation thrombocytopenia (
371074009) -
Refractory thrombocytopenia (
721304007) -
Secondary autoimmune thrombocytopenia (
128092005) -
Secondary cryofibrinogenemia (
41816006) -
Secondary thrombocytopenia (
154826009) -
Severe hereditary factor IX deficiency disease with inhibitor (
440866009) -
Severe hereditary factor IX deficiency disease without inhibitor (
441190003) -
Severe hereditary factor VIII deficiency disease (
16872008) -
Severe hereditary factor VIII deficiency disease with inhibitor (
438373005) -
Severe hereditary factor VIII deficiency disease without inhibitor (
440993008) -
Systemic fibrinogenolysis (
10153004) -
Thrombocytopenia associated with acquired immunodeficiency syndrome (
421766003) -
Thrombocytopenia caused by alcohol (
699208000) -
Thrombocytopenia caused by drugs (
191322006) -
Thrombocytopenia caused by hypothermia (
34395002) -
Thrombocytopenia co-occurrent and due to alcoholism (
97571000119109) -
Thrombocytopenia due to blood loss (
49886003) -
Thrombocytopenia due to extracorporeal circulation (
30182008) -
Thrombocytopenia due to extracorporeal circulation of blood (
191323001) -
Thrombocytopenia due to massive blood transfusion (
307342006) -
Transient neonatal disorder of coagulation (
32605001) -
Uremic thrombocytopenia (
416902009) -
Vitamin K deficiency coagulation disorder (
1286003) -
Warfarin overdosage (
47546008) -
Warfarin overdose of undetermined intent (
296936009) -
von Willebrand disease type 1 (
128106003) -
von Willebrand disease type 2 (
128107007) -
von Willebrand disease type 2A (
359714009) -
von Willebrand disease type 2B (
359721009) -
von Willebrand disease type 2M (
359729006) -
von Willebrand disease type 2N (
359732009) -
von Willebrand disease type 3 (
128108002) -
von Willebrand disease type IA (
359709005) -
von Willebrand disease type IB (
128113003) -
von Willebrand disease type IC (
128114009) -
von Willebrand disease, type 1^a^ (
359704000) -
von Willebrand disease, type IIA (
87397002) -
von Willebrand disease, type IIB (
19520006) -
von Willebrand disease, type IIC (
1908008) -
von Willebrand disease, type IID (
35066007) -
von Willebrand disease, type IIE (
52137009) -
von Willebrand disease, type IIF (
12501008) -
von Willebrand disease, type IIG (
71723006) -
von Willebrand disease, type IIH (
24663001) -
von Willebrand disorder (
128105004) -
von Willebrand factor inhibitor disorder (
41106001)
Clotting disorder
Included 265 out of 265 matching concepts.
Show matching concepts
-
Accidental coumarin overdose (
296931004) -
Accidental heparin overdose (
296927005) -
Accidental warfarin overdose (
296934007) -
Acquired afibrinogenemia (
359730001) -
Acquired coagulation disorder (
234466008) -
Acquired coagulation factor deficiency (
25904003) -
Acquired coagulation factor inhibitor disorder (
64509006) -
Acquired combined coagulation factor deficiency (
439156006) -
Acquired factor II deficiency (
191298004) -
Acquired factor IX deficiency disease (
12153008) -
Acquired factor V deficiency disease (
35913006) -
Acquired factor VII deficiency disease (
2036003) -
Acquired factor VIII deficiency disease (
14230004) -
Acquired factor X deficiency disease (
33820001) -
Acquired factor XI deficiency disease (
35554008) -
Acquired factor XII deficiency disease (
15132005) -
Acquired factor XIII deficiency disease (
6364000) -
Acquired fibrinogen abnormality (
234462005) -
Acquired hypofibrinogenemia (
359723007) -
Acquired hypoplasminogenemia (
95843009) -
Acquired inhibitor of coagulation (
282707003) -
Acquired purpura fulminans (
725157006) -
Acquired thrombocytopenia (
74576004) -
Acquired von Willebrand's disease (
234451005) -
Afibrinogenemia (
278504009) -
Afibrinogenemia - postpartum (
237337003) -
Afibrinogenemia following molar AND/OR ectopic pregnancy (
85796009) -
Alpha chain defect dysfibrinogenemia (
234459007) -
Alpha-2-antiplasmin deficiency (
234465007) -
Anti-factor II disorder (
180481005) -
Anticoagulant excess without bleeding (
278366008) -
Anticoagulant overdosage (
43302000) -
Anticoagulant-induced bleeding (
278365007) -
Antiprothrombin disorder (
181456001) -
Antithrombin III deficiency (
36351005) -
Antithrombin III deficiency type I (
973271000000108) -
Antithrombin III deficiency type II (
973291000000107) -
Autoimmune factor VIII deficiency (
307515009) -
Autosomal dominant deficiency of plasminogen (
95842004) -
Benign gestational thrombocytopenia (
128090002) -
Beta chain defect dysfibrinogenemia (
234460002) -
Bleeding disorder due to deficiency of calcium and diacylglycerol-regulated guanine nucleotide exchange factor I (
725105006) -
Blood coagulation disorder (
64779008) -
Blood coagulation disorder complicating childbirth (
10749581000119100) -
Blood coagulation disorder complicating pregnancy (
10749641000119106) -
Blood coagulation disorder due to liver disease (
69500007) -
Blood coagulation disorder with impaired clot retraction time (
123790009) -
Blood coagulation disorder with prolonged bleeding time (
123789000) -
Blood coagulation disorder with prolonged coagulation time (
123787003) -
Blood coagulation disorder with shortened bleeding time (
123788008) -
Blood coagulation disorder with shortened coagulation time (
123786007) -
Blood coagulation disorder, categorized by value of screening test (
128088003) -
Classic onset hemorrhagic disease of newborn due to vitamin K deficiency (
717936002) -
Coagulation factor deficiency syndrome (
86075001) -
Combined coagulation factor deficiency (
234463000) -
Combined deficiency of factor V and factor VIII (
715559004) -
Congenital afibrinogenemia (
154818001) -
Congenital alpha-2-antiplasmin deficiency (
716746003) -
Congenital factor IX deficiency variant (
234444001) -
Congenital factor IX deficiency with inhibitor (
234445000) -
Congenital factor IX deficiency without inhibitor (
426199009) -
Congenital fibrinogen abnormality (
234456000) -
Congenital hypofibrinogenemia (
439145006) -
Congenital plasminogen activator inhibitor deficiency type 1 (
717407006) -
Congenital von Willebrand's disease (
234446004) -
Congenital von Willebrand's disease type I (
234447008) -
Congenital von Willebrand's disease type II (
234448003) -
Congenital von Willebrand's disease type III (
234450006) -
Contact factor deficiency (
234452003) -
Coumarin overdose (
296930003) -
Coumarin overdose of undetermined intent (
296933001) -
Cryofibrinogenemia (
10934005) -
Defect of purinergic receptor p2y G protein-coupled 12 (
725291001) -
Defibrination syndrome following molar AND/OR ectopic pregnancy (
62698000) -
Deficiency of coagulation factor due to liver disease (
191296000) -
Deficiency of coagulation factor due to vitamin K deficiency (
191297009) -
Deficiency of naturally occurring coagulation factor inhibitor (
105604006) -
Dilutional thrombocytopenia (
51624005) -
Disorder involving the fibrinolytic system (
95839005) -
Disseminated intravascular coagulation (
67406007) -
Disseminated intravascular coagulation due to placental abruption (
39191000119103) -
Disseminated intravascular coagulation in newborn (
34417008) -
Drug-induced coagulation inhibitor disorder (
16773005) -
Drug-induced immune thrombocytopenia (
19307009) -
Dysfibrinogenemia (
111589005) -
Dysplasminogenemia (
95844003) -
Early onset diffuse bleeding diathesis secondary to vitamin K deficient hemorrhagic disease of fetus and newborn (
717935003) -
Factor I deficiency disease (
439458000) -
Factor I inhibitor disorder (
58327003) -
Factor II deficiency (
73975000) -
Factor IX deficiency (
767712006) -
Factor IX inhibitor disorder (
89729000) -
Factor V deficiency (
4320005) -
Factor V inhibitor disorder (
41690001) -
Factor VII deficiency (
37193007) -
Factor VIII deficiency (
234440005) -
Factor VIII inhibitor disorder (
47307007) -
Factor X deficiency (
76642003) -
Factor X inhibitor disorder (
9489006) -
Factor XI deficiency (
767713001) -
Factor XI deficiency, type I (
88540000) -
Factor XI deficiency, type II (
33169001) -
Factor XI deficiency, type III (
45963004) -
Factor XI inhibitor disorder (
38879000) -
Factor XII deficiency disease (
46981006) -
Factor XIII deficiency disease (
18604004) -
Factor XIII inhibitor disorder (
13993001) -
Failed attempted abortion with afibrinogenemia (
27068000) -
Failed attempted abortion with defibrination syndrome (
34478009) -
Familial hemorrhagic diathesis (
6935003) -
Familial multiple factor deficiency syndrome (
81783000) -
Familial multiple factor deficiency syndrome, type I (
84048006) -
Familial multiple factor deficiency syndrome, type II (
65768009) -
Familial multiple factor deficiency syndrome, type III (
64315007) -
Familial multiple factor deficiency syndrome, type IV (
66909001) -
Familial multiple factor deficiency syndrome, type V (
3760002) -
Familial multiple factor deficiency syndrome, type VI (
61551003) -
Fibrinogen abnormality (
234455001) -
Fibrinogen deficiency (
359727008) -
Fibrinolysis - postpartum (
237336007) -
Fibrinolytic bleeding syndrome (
234464006) -
Gamma chain defect dysfibrinogenemia (
234461003) -
Hemolysis-elevated liver enzymes-low platelet count syndrome (
95605009) -
Hemophilia (
90935002) -
Hemorrhagic disease of the newborn due to factor II deficiency (
24149006) -
Hemorrhagic disease of the newborn due to vitamin K deficiency (
12546009) -
Heparin overdose (
296926001) -
Heparin overdose of undetermined intent (
296929008) -
Heparin-induced thrombocytopenia (
73397007) -
Heparin-induced thrombocytopenia with thrombosis (
111588002) -
Hereditary antithrombin III deficiency (
439699000) -
Hereditary coagulation factor deficiency (
16922007) -
Hereditary combined coagulation factor deficiency (
439157002) -
Hereditary combined deficiency of vitamin K-dependent clotting factors (
724356003) -
Hereditary dysfibrinogenemia (
45366001) -
Hereditary dysplasminogenemia (
95845002) -
Hereditary factor I deficiency disease (
31925001) -
Hereditary factor II deficiency disease (
33297000) -
Hereditary factor IX deficiency disease (
41788008) -
Hereditary factor IX deficiency disease with inhibitor (
438372000) -
Hereditary factor IX deficiency disease without inhibitor (
438792009) -
Hereditary factor V deficiency disease (
88776002) -
Hereditary factor VII deficiency disease (
40855001) -
Hereditary factor VIII deficiency disease (
28293008) -
Hereditary factor VIII deficiency disease with inhibitor (
234442002) -
Hereditary factor VIII deficiency disease without inhibitor (
438360006) -
Hereditary factor X deficiency disease (
37350004) -
Hereditary factor XI deficiency disease (
49762007) -
Hereditary factor XII deficiency disease (
43217004) -
Hereditary factor XIII A subunit and B subunit deficiency (
439460003) -
Hereditary factor XIII A subunit deficiency (
439455002) -
Hereditary factor XIII B subunit deficiency (
439459008) -
Hereditary factor XIII deficiency disease (
50189006) -
Hereditary hyperfibrinogenemia (
440924009) -
Hereditary hypoplasminogenemia (
95841006) -
Hereditary protein C deficiency (
439274008) -
Hereditary protein S deficiency (
439702007) -
Hereditary thrombophilic dysfibrinogenemia (
438827002) -
Hereditary von Willebrand disease type 2A (
359711001) -
Hereditary von Willebrand disease type 2B (
359717002) -
Hereditary von Willebrand disease type 2M (
359725000) -
Hereditary von Willebrand disease type IA (
359700009) -
Heterozygous protein C deficiency (
441101007) -
Heterozygous protein S deficiency (
440988005) -
High molecular weight kininogen deficiency (
27312002) -
Homozygous protein C deficiency (
441188004) -
Homozygous protein S deficiency (
441189007) -
Hyperfibrinogenemia (
439000005) -
Hyperheparinemia (
79674009) -
Hypodysfibrinogenemia (
234458004) -
Hypofibrinogenemia (
234457009) -
Hypoplasminogenemia (
95840007) -
Idiopathic factor VIII deficiency (
307514008) -
Illegal abortion with afibrinogenemia (
3230006) -
Illegal abortion with defibrination syndrome (
61810006) -
Induced termination of pregnancy complicated by afibrinogenemia (
609456005) -
Induced termination of pregnancy complicated by defibrination syndrome (
609462000) -
Intentional coumarin overdose (
296932006) -
Intentional heparin overdose (
296928000) -
Intentional warfarin sodium overdose (
296935008) -
Isolated thrombocytopenia (
724637001) -
Kasabach-Merritt syndrome (
86635005) -
Late onset diffuse bleeding diathesis secondary to vitamin K deficient hemorrhagic disease of fetus and newborn (
717937006) -
Legal abortion with afibrinogenemia (
30479005) -
Legal abortion with defibrination syndrome (
6647006) -
Lupus anticoagulant disorder (
19267009) -
Malignancy-related factor VIII deficiency (
307518006) -
Mild hereditary factor IX deficiency disease with inhibitor (
440868005) -
Mild hereditary factor IX deficiency disease without inhibitor (
441192006) -
Mild hereditary factor VIII deficiency disease (
26029002) -
Mild hereditary factor VIII deficiency disease with inhibitor (
425949001) -
Mild hereditary factor VIII deficiency disease without inhibitor (
440820004) -
Miscarriage with afibrinogenemia (
21360006) -
Miscarriage with defibrination syndrome (
50770000) -
Mixed cryofibrinogenemia (
80988005) -
Moderate hereditary factor IX deficiency disease with inhibitor (
440867000) -
Moderate hereditary factor IX deficiency disease without inhibitor (
441191004) -
Moderate hereditary factor VIII deficiency disease (
33344008) -
Moderate hereditary factor VIII deficiency disease with inhibitor (
438599002) -
Moderate hereditary factor VIII deficiency disease without inhibitor (
441006000) -
Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome (
733028000) -
Neonatal coagulation disorder (
95623001) -
Neonatal purpura fulminans (homozygous protein C deficiency) (
402851000) -
Passovoy factor deficiency (
234453008) -
Postpartum afibrinogenemia with hemorrhage (
111452009) -
Postpartum coagulation defect with hemorrhage (
49177006) -
Postpartum coagulation defects (
267272006) -
Postpartum coagulation defects - delivered with postnatal problem (
200030007) -
Postpartum coagulation defects with postnatal problem (
200031006) -
Postpartum fibrinolysis with hemorrhage (
62410004) -
Pregnancy-related factor VIII deficiency (
307517001) -
Prekallikrein deficiency (
48976006) -
Primary cryofibrinogenemia (
61802005) -
Protein C deficiency disease (
76407009) -
Protein S deficiency disease (
1563006) -
Prothrombin complex deficiency (
234454002) -
Pseudo von Willebrand disease (
128115005) -
Purpura fulminans (
13507004) -
Purpura of skin and or skin-associated mucous membrane co-occurrent and due to coagulation disorder (
724854007) -
Radiation thrombocytopenia (
371074009) -
Refractory thrombocytopenia (
721304007) -
Secondary autoimmune thrombocytopenia (
128092005) -
Secondary cryofibrinogenemia (
41816006) -
Secondary thrombocytopenia (
154826009) -
Severe hereditary factor IX deficiency disease with inhibitor (
440866009) -
Severe hereditary factor IX deficiency disease without inhibitor (
441190003) -
Severe hereditary factor VIII deficiency disease (
16872008) -
Severe hereditary factor VIII deficiency disease with inhibitor (
438373005) -
Severe hereditary factor VIII deficiency disease without inhibitor (
440993008) -
Systemic fibrinogenolysis (
10153004) -
Thrombocytopenia associated with acquired immunodeficiency syndrome (
421766003) -
Thrombocytopenia caused by alcohol (
699208000) -
Thrombocytopenia caused by drugs (
191322006) -
Thrombocytopenia caused by hypothermia (
34395002) -
Thrombocytopenia co-occurrent and due to alcoholism (
97571000119109) -
Thrombocytopenia due to blood loss (
49886003) -
Thrombocytopenia due to extracorporeal circulation (
30182008) -
Thrombocytopenia due to extracorporeal circulation of blood (
191323001) -
Thrombocytopenia due to massive blood transfusion (
307342006) -
Transient neonatal disorder of coagulation (
32605001) -
Uremic thrombocytopenia (
416902009) -
Vitamin K deficiency coagulation disorder (
1286003) -
Warfarin overdosage (
47546008) -
Warfarin overdose of undetermined intent (
296936009) -
von Willebrand disease type 1 (
128106003) -
von Willebrand disease type 2 (
128107007) -
von Willebrand disease type 2A (
359714009) -
von Willebrand disease type 2B (
359721009) -
von Willebrand disease type 2M (
359729006) -
von Willebrand disease type 2N (
359732009) -
von Willebrand disease type 3 (
128108002) -
von Willebrand disease type IA (
359709005) -
von Willebrand disease type IB (
128113003) -
von Willebrand disease type IC (
128114009) -
von Willebrand disease, type 1^a^ (
359704000) -
von Willebrand disease, type IIA (
87397002) -
von Willebrand disease, type IIB (
19520006) -
von Willebrand disease, type IIC (
1908008) -
von Willebrand disease, type IID (
35066007) -
von Willebrand disease, type IIE (
52137009) -
von Willebrand disease, type IIF (
12501008) -
von Willebrand disease, type IIG (
71723006) -
von Willebrand disease, type IIH (
24663001) -
von Willebrand disorder (
128105004) -
von Willebrand factor inhibitor disorder (
41106001)
Disorder of hemostatic system
Included 515 out of 515 matching concepts.
Show matching concepts
-
A disintegrin and metalloproteinase with thrombospondin type 1 motif 13 deficiency (
439725008) -
Accidental coumarin overdose (
296931004) -
Accidental heparin overdose (
296927005) -
Accidental warfarin overdose (
296934007) -
Acquired afibrinogenemia (
359730001) -
Acquired aplastic anemia (
55907008) -
Acquired coagulation disorder (
234466008) -
Acquired coagulation factor deficiency (
25904003) -
Acquired coagulation factor inhibitor disorder (
64509006) -
Acquired combined coagulation factor deficiency (
439156006) -
Acquired factor II deficiency (
191298004) -
Acquired factor IX deficiency disease (
12153008) -
Acquired factor V deficiency disease (
35913006) -
Acquired factor VII deficiency disease (
2036003) -
Acquired factor VIII deficiency disease (
14230004) -
Acquired factor X deficiency disease (
33820001) -
Acquired factor XI deficiency disease (
35554008) -
Acquired factor XII deficiency disease (
15132005) -
Acquired factor XIII deficiency disease (
6364000) -
Acquired fibrinogen abnormality (
234462005) -
Acquired hypofibrinogenemia (
359723007) -
Acquired hypoplasminogenemia (
95843009) -
Acquired inhibitor of coagulation (
282707003) -
Acquired pancytopenia (
5876000) -
Acquired platelet disorder (
234479004) -
Acquired platelet factor 3 disease (
129654004) -
Acquired platelet function disorder (
128095007) -
Acquired purpura fulminans (
725157006) -
Acquired red cell aplasia (
234376007) -
Acquired storage pool deficiency (platelets) (
296332004) -
Acquired thrombocytopenia (
74576004) -
Acquired thrombophilia (
439001009) -
Acquired thrombotic thrombocytopenic purpura (
439007008) -
Acquired von Willebrand's disease (
234451005) -
Acute hemorrhagic edema of childhood (
402856005) -
Acute idiopathic thrombocytopenic purpura (
28505005) -
Acute purpuric eruption of skin (
723011009) -
Adult pure red cell aplasia (
765748009) -
Afibrinogenemia (
278504009) -
Afibrinogenemia - postpartum (
237337003) -
Afibrinogenemia following molar AND/OR ectopic pregnancy (
85796009) -
Alloimmune platelet transfusion refractoriness (
128094006) -
Alloimmune thrombocytopenia (
128093000) -
Alpha chain defect dysfibrinogenemia (
234459007) -
Alpha-2-antiplasmin deficiency (
234465007) -
Amegakaryocytic thrombocytopenia (
234482009) -
Amegakaryocytic thrombocytopenia with congenital malformation (
359531004) -
Anti-factor II disorder (
180481005) -
Antibody mediated acquired pure red cell aplasia caused by erythropoiesis stimulating agent (
713910008) -
Anticoagulant excess without bleeding (
278366008) -
Anticoagulant overdosage (
43302000) -
Anticoagulant-induced bleeding (
278365007) -
Antiphospholipid syndrome (
26843008) -
Antiphospholipid syndrome in pregnancy (
72161000119100) -
Antiprothrombin disorder (
181456001) -
Antithrombin III deficiency (
36351005) -
Antithrombin III deficiency type I (
973271000000108) -
Antithrombin III deficiency type II (
973291000000107) -
Aplastic anemia (
306058006) -
Aplastic anemia associated with acquired immunodeficiency syndrome (
421102007) -
Aplastic anemia associated with metabolic alteration (
413565006) -
Aplastic anemia associated with pancreatitis (
413566007) -
Aplastic anemia associated with pregnancy (
413567003) -
Aplastic anemia caused by antineoplastic agent (
118791000119106) -
Aplastic anemia caused by radiation (
191247005) -
Aplastic anemia caused by toxic cause (
191248000) -
Aplastic anemia co-occurrent with human immunodeficiency virus infection (
713508003) -
Aplastic anemia due to chronic disease (
191244003) -
Aplastic anemia due to drugs (
267527002) -
Aplastic anemia due to infection (
191246001) -
Ataxia pancytopenia syndrome (
768556005) -
Attenuated Chédiak-Higashi syndrome (
720520009) -
Autoimmune factor VIII deficiency (
307515009) -
Autoimmune neonatal thrombocytopenia (
276575001) -
Autoimmune pancytopenia (
183005) -
Autoimmune thrombocytopenia (
128091003) -
Autoimmune thrombotic thrombocytopenic purpura (
438476003) -
Autosomal dominant deficiency of plasminogen (
95842004) -
Autosomal dominant macrothrombocytopenia (
720521008) -
Benign gestational thrombocytopenia (
128090002) -
Benign primary hypergammaglobulinemic purpura (
190810006) -
Bernard Soulier syndrome (
54569005) -
Beta chain defect dysfibrinogenemia (
234460002) -
Bleeding disorder due to deficiency of calcium and diacylglycerol-regulated guanine nucleotide exchange factor I (
725105006) -
Bleeding disorder due to glycoprotein VI deficiency (
765977002) -
Blood coagulation disorder (
64779008) -
Blood coagulation disorder complicating childbirth (
10749581000119100) -
Blood coagulation disorder complicating pregnancy (
10749641000119106) -
Blood coagulation disorder due to liver disease (
69500007) -
Blood coagulation disorder with impaired clot retraction time (
123790009) -
Blood coagulation disorder with prolonged bleeding time (
123789000) -
Blood coagulation disorder with prolonged coagulation time (
123787003) -
Blood coagulation disorder with shortened bleeding time (
123788008) -
Blood coagulation disorder with shortened coagulation time (
123786007) -
Blood coagulation disorder, categorized by value of screening test (
128088003) -
Capillary fragility abnormality (
91304009) -
Catastrophic antiphospholipid syndrome (
609329007) -
Cellular immunologic aplastic anemia (
50220002) -
Chronic acquired pure red cell aplasia (
90414007) -
Chronic idiopathic thrombocytopenic purpura (
13172003) -
Chédiak-Higashi syndrome (
111396008) -
Classic onset hemorrhagic disease of newborn due to vitamin K deficiency (
717936002) -
Clothing purpura (
402848007) -
Coagulation factor deficiency syndrome (
86075001) -
Combined coagulation factor deficiency (
234463000) -
Combined deficiency of factor V and factor VIII (
715559004) -
Congenital afibrinogenemia (
154818001) -
Congenital alpha-2-antiplasmin deficiency (
716746003) -
Congenital amegakaryocytic thrombocytopenia (
716336002) -
Congenital dysmegakaryopoietic thrombocytopenia, Paris Trousseau type (
441134009) -
Congenital factor IX deficiency variant (
234444001) -
Congenital factor IX deficiency with inhibitor (
234445000) -
Congenital factor IX deficiency without inhibitor (
426199009) -
Congenital fibrinogen abnormality (
234456000) -
Congenital hypofibrinogenemia (
439145006) -
Congenital plasminogen activator inhibitor deficiency type 1 (
717407006) -
Congenital thrombocytopenia (
737221003) -
Congenital thrombocytopenic purpura (
267535004) -
Congenital von Willebrand's disease (
234446004) -
Congenital von Willebrand's disease type I (
234447008) -
Congenital von Willebrand's disease type II (
234448003) -
Congenital von Willebrand's disease type III (
234450006) -
Constitutional aplastic anemia (
28975000) -
Constitutional aplastic anemia with malformation (
267524009) -
Contact factor deficiency (
234452003) -
Contact purpura (
402589000) -
Coumarin overdose (
296930003) -
Coumarin overdose of undetermined intent (
296933001) -
Cryofibrinogenemia (
10934005) -
Cryofibrinogenemic purpura (
402853002) -
Cryoglobulinemic purpura (
190814002) -
Cyclic thrombocytopenia (
48788004) -
Cyclooxygenase deficiency (
234476006) -
DK phocomelia syndrome (
719021005) -
Defect of purinergic receptor p2y G protein-coupled 12 (
725291001) -
Defibrination syndrome following molar AND/OR ectopic pregnancy (
62698000) -
Deficiency of coagulation factor due to liver disease (
191296000) -
Deficiency of coagulation factor due to vitamin K deficiency (
191297009) -
Deficiency of naturally occurring coagulation factor inhibitor (
105604006) -
Dense body defect (
234474009) -
Dermite ocre of Favre (
361209006) -
Dilutional thrombocytopenia (
51624005) -
Disorder involving the fibrinolytic system (
95839005) -
Disorder of hemostatic system (
362970003) -
Disseminated intravascular coagulation (
67406007) -
Disseminated intravascular coagulation due to placental abruption (
39191000119103) -
Disseminated intravascular coagulation in newborn (
34417008) -
Doan-Wright syndrome (
38970002) -
Drug induced thrombotic thrombocytopenic purpura (
441322009) -
Drug-induced coagulation inhibitor disorder (
16773005) -
Drug-induced immune thrombocytopenia (
19307009) -
Dysfibrinogenemia (
111589005) -
Dysplasminogenemia (
95844003) -
Dysproteinemic purpura (
402854008) -
Early onset diffuse bleeding diathesis secondary to vitamin K deficient hemorrhagic disease of fetus and newborn (
717935003) -
Eczematid-like purpura of Doucas and Kapetanakis (
41486008) -
Embolic purpura (
234497007) -
Epstein syndrome (
234485006) -
Essential thrombocythemia (
109994006) -
Estren-Dameshek anemia (
46760003) -
Evans syndrome (
75331009) -
Exhausted platelets (
297307009) -
Factitious purpura (
10278007) -
Factor I deficiency disease (
439458000) -
Factor I inhibitor disorder (
58327003) -
Factor II deficiency (
73975000) -
Factor IX deficiency (
767712006) -
Factor IX inhibitor disorder (
89729000) -
Factor V Leiden mutation (
307091009) -
Factor V deficiency (
4320005) -
Factor V inhibitor disorder (
41690001) -
Factor VII deficiency (
37193007) -
Factor VIII deficiency (
234440005) -
Factor VIII inhibitor disorder (
47307007) -
Factor X deficiency (
76642003) -
Factor X inhibitor disorder (
9489006) -
Factor XI deficiency (
767713001) -
Factor XI deficiency, type I (
88540000) -
Factor XI deficiency, type II (
33169001) -
Factor XI deficiency, type III (
45963004) -
Factor XI inhibitor disorder (
38879000) -
Factor XII deficiency disease (
46981006) -
Factor XIII deficiency disease (
18604004) -
Factor XIII inhibitor disorder (
13993001) -
Failed attempted abortion with afibrinogenemia (
27068000) -
Failed attempted abortion with defibrination syndrome (
34478009) -
Familial alpha>2< adrenergic receptor defect in platelets (
128102001) -
Familial hemorrhagic diathesis (
6935003) -
Familial multiple factor deficiency syndrome (
81783000) -
Familial multiple factor deficiency syndrome, type I (
84048006) -
Familial multiple factor deficiency syndrome, type II (
65768009) -
Familial multiple factor deficiency syndrome, type III (
64315007) -
Familial multiple factor deficiency syndrome, type IV (
66909001) -
Familial multiple factor deficiency syndrome, type V (
3760002) -
Familial multiple factor deficiency syndrome, type VI (
61551003) -
Familial platelet syndrome with predisposition to acute myelogenous leukemia (
725034002) -
Familial thrombocytosis (
720950009) -
Fanconi's anemia (
30575002) -
Fibrinogen abnormality (
234455001) -
Fibrinogen deficiency (
359727008) -
Fibrinolysis - postpartum (
237336007) -
Fibrinolytic bleeding syndrome (
234464006) -
GATA binding protein 1 related thrombocytopenia with dyserythropoiesis (
713388002) -
Gamma chain defect dysfibrinogenemia (
234461003) -
Gardner-Diamond syndrome (
275446004) -
Giant platelet syndrome (
234478007) -
Glanzmann's thrombasthenia (
32942005) -
Glycoprotein Ia defect (
234471001) -
Glycoprotein Ib defect (
234472008) -
Gray platelet syndrome (
51720005) -
Hemolysis-elevated liver enzymes-low platelet count syndrome (
95605009) -
Hemophilia (
90935002) -
Hemorrhagic disease of the newborn due to factor II deficiency (
24149006) -
Hemorrhagic disease of the newborn due to vitamin K deficiency (
12546009) -
Hemorrhagic disorder due to antithrombinemia (
191288005) -
Hemorrhagic disorder due to circulating anticoagulants (
191287000) -
Hemorrhagic disorder due to hyperheparinemia (
191289002) -
Hemorrhagic disorder due to increase in anti-10a (
191292003) -
Hemorrhagic disorder due to increase in anti-11a (
191293008) -
Hemorrhagic disorder due to increase in anti-8a (
191290006) -
Hemorrhagic disorder due to increase in anti-9a (
191291005) -
Heparin cofactor II deficiency (
234468009) -
Heparin overdose (
296926001) -
Heparin overdose of undetermined intent (
296929008) -
Heparin-induced thrombocytopenia (
73397007) -
Heparin-induced thrombocytopenia with thrombosis (
111588002) -
Hereditary antithrombin III deficiency (
439699000) -
Hereditary coagulation factor deficiency (
16922007) -
Hereditary combined coagulation factor deficiency (
439157002) -
Hereditary combined deficiency of vitamin K-dependent clotting factors (
724356003) -
Hereditary dysfibrinogenemia (
45366001) -
Hereditary dysplasminogenemia (
95845002) -
Hereditary elevated factor VIII (
441042008) -
Hereditary elevated factor XI (
441001005) -
Hereditary factor I deficiency disease (
31925001) -
Hereditary factor II deficiency disease (
33297000) -
Hereditary factor IX deficiency disease (
41788008) -
Hereditary factor IX deficiency disease with inhibitor (
438372000) -
Hereditary factor IX deficiency disease without inhibitor (
438792009) -
Hereditary factor V deficiency disease (
88776002) -
Hereditary factor VII deficiency disease (
40855001) -
Hereditary factor VIII deficiency disease (
28293008) -
Hereditary factor VIII deficiency disease with inhibitor (
234442002) -
Hereditary factor VIII deficiency disease without inhibitor (
438360006) -
Hereditary factor X deficiency disease (
37350004) -
Hereditary factor XI deficiency disease (
49762007) -
Hereditary factor XII deficiency disease (
43217004) -
Hereditary factor XIII A subunit and B subunit deficiency (
439460003) -
Hereditary factor XIII A subunit deficiency (
439455002) -
Hereditary factor XIII B subunit deficiency (
439459008) -
Hereditary factor XIII deficiency disease (
50189006) -
Hereditary heparin cofactor II deficiency (
439701000) -
Hereditary hyperfibrinogenemia (
440924009) -
Hereditary hyperhomocysteinemia (
439006004) -
Hereditary hypoplasminogenemia (
95841006) -
Hereditary platelet function disorder (
128096008) -
Hereditary protein C deficiency (
439274008) -
Hereditary protein S deficiency (
439702007) -
Hereditary thrombocytopenic disorder (
438492008) -
Hereditary thrombophilia (
439698008) -
Hereditary thrombophilic dysfibrinogenemia (
438827002) -
Hereditary von Willebrand disease type 2A (
359711001) -
Hereditary von Willebrand disease type 2B (
359717002) -
Hereditary von Willebrand disease type 2M (
359725000) -
Hereditary von Willebrand disease type IA (
359700009) -
Hermansky-Pudlak syndrome (
9311003) -
Heterozygous Factor V Leiden mutation (
307116001) -
Heterozygous protein C deficiency (
441101007) -
Heterozygous protein S deficiency (
440988005) -
Heterozygous prothrombin G20210A mutation (
441421001) -
High molecular weight kininogen deficiency (
27312002) -
Homozygous Factor V Leiden mutation (
307115002) -
Homozygous protein C deficiency (
441188004) -
Homozygous protein S deficiency (
441189007) -
Homozygous prothrombin G20210A mutation (
441420000) -
Humoral immunologic aplastic anemia (
14024008) -
Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency (
724344004) -
Hyperfibrinogenemia (
439000005) -
Hyperglobulinemic purpura (
402852007) -
Hyperheparinemia (
79674009) -
Hypodysfibrinogenemia (
234458004) -
Hypofibrinogenemia (
234457009) -
Hypoplasminogenemia (
95840007) -
Idiopathic aplastic anemia (
191256002) -
Idiopathic factor VIII deficiency (
307514008) -
Idiopathic maternal thrombocytopenia (
371106008) -
Illegal abortion with afibrinogenemia (
3230006) -
Illegal abortion with defibrination syndrome (
61810006) -
Immune thrombocytopenia (
2897005) -
Immune thrombocytopenic purpura (
32273002) -
Immunoglobulin A vasculitis (
191306005) -
Immunologic aplastic anemia (
77084001) -
Induced termination of pregnancy complicated by afibrinogenemia (
609456005) -
Induced termination of pregnancy complicated by defibrination syndrome (
609462000) -
Infection-associated purpura (
7226007) -
Inherited platelet disorder (
234469001) -
Inherited predisposition to essential thrombocythemia (
718195003) -
Intentional coumarin overdose (
296932006) -
Intentional heparin overdose (
296928000) -
Intentional warfarin sodium overdose (
296935008) -
Isolated collagen aggregation defect (
128103006) -
Isolated thrombocytopenia (
724637001) -
Itching purpura (
238781005) -
Kasabach-Merritt syndrome (
86635005) -
Late onset diffuse bleeding diathesis secondary to vitamin K deficient hemorrhagic disease of fetus and newborn (
717937006) -
Legal abortion with afibrinogenemia (
30479005) -
Legal abortion with defibrination syndrome (
6647006) -
Lupus anticoagulant disorder (
19267009) -
MYH9 macrothrombocytopenia syndrome (
717769007) -
Malignancy-related factor VIII deficiency (
307518006) -
May Hegglin syndrome (
68559009) -
May-Hegglin anomaly (
234484005) -
Mechanical purpura (
7014009) -
Medich giant platelet syndrome (
718554005) -
Mediterranean macrothrombocytopenia (
60628003) -
Mediterranean thrombocytopenia (
234487003) -
Megakaryocytic aplasia (
359536009) -
Megakaryocytic thrombocytopenia (
234483004) -
Metabolic purpura (
234496003) -
Mild hereditary factor IX deficiency disease with inhibitor (
440868005) -
Mild hereditary factor IX deficiency disease without inhibitor (
441192006) -
Mild hereditary factor VIII deficiency disease (
26029002) -
Mild hereditary factor VIII deficiency disease with inhibitor (
425949001) -
Mild hereditary factor VIII deficiency disease without inhibitor (
440820004) -
Miscarriage with afibrinogenemia (
21360006) -
Miscarriage with defibrination syndrome (
50770000) -
Mixed alpha granule and dense body deficiency (
128100009) -
Mixed cryofibrinogenemia (
80988005) -
Moderate hereditary factor IX deficiency disease with inhibitor (
440867000) -
Moderate hereditary factor IX deficiency disease without inhibitor (
441191004) -
Moderate hereditary factor VIII deficiency disease (
33344008) -
Moderate hereditary factor VIII deficiency disease with inhibitor (
438599002) -
Moderate hereditary factor VIII deficiency disease without inhibitor (
441006000) -
Montreal platelet syndrome (
234486007) -
Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome (
733028000) -
Myosin heavy chain 9 non muscle related disease (
712922002) -
Neonatal coagulation disorder (
95623001) -
Neonatal purpura fulminans (homozygous protein C deficiency) (
402851000) -
Neonatal thrombocytopenia (
82835005) -
Neonatal thrombocytopenia associated with maternal idiopathic thrombocytopenic purpura (
7933002) -
Neonatal thrombocytopenia due to exchange transfusion (
89962000) -
Neonatal thrombocytopenia due to idiopathic maternal thrombocytopenia (
61744005) -
Neonatal thrombocytopenia due to platelet alloimmunization (
240305000) -
Non-thrombocytopenic purpura (
234493006) -
Pancytopenia (
127034005) -
Pancytopenia caused by medication (
736024007) -
Pancytopenia due to antineoplastic chemotherapy (
328301000119102) -
Pancytopenia with pancreatitis (
234367000) -
Pancytopenia-dysmelia (
275523003) -
Parvoviral aplastic crisis (
240486003) -
Passovoy factor deficiency (
234453008) -
Perinatal purpura (
206414002) -
Perinatal thrombocytopenia (
273986001) -
Periodontitis co-occurrent with Chédiak-Higashi syndrome (
709465004) -
Pigmented purpuric lichenoid dermatitis of Gougerot and Blum (
20343006) -
Platelet dense granule deficiency (
9417000) -
Platelet disorder (
22716005) -
Platelet dysfunction associated with uremia (
421132004) -
Platelet dysfunction caused by aspirin (
17592003) -
Platelet dysfunction caused by drugs (
41461004) -
Platelet factor V deficiency (factor V Quebec) (
128101008) -
Platelet membrane defect (
234470000) -
Platelet procoagulant activity deficiency (
43346008) -
Platelet secretory disorder (
51448009) -
Platelet sequestration (
322096003) -
Platelet storage pool defect (
128099001) -
Platelet type pseudo-von Willebrand disease (
270117002) -
Platelet type von Willebrand's disease (
234473003) -
Post infectious thrombocytopenic purpura (
33183004) -
Post-splenectomy thrombocytosis (
234512002) -
Postinfective immunoglobulin A vasculitis (
239946005) -
Postpartum afibrinogenemia with hemorrhage (
111452009) -
Postpartum coagulation defect with hemorrhage (
49177006) -
Postpartum coagulation defects (
267272006) -
Postpartum coagulation defects - delivered with postnatal problem (
200030007) -
Postpartum coagulation defects with postnatal problem (
200031006) -
Postpartum fibrinolysis with hemorrhage (
62410004) -
Posttransfusion purpura (
73162004) -
Pregnancy-related factor VIII deficiency (
307517001) -
Prekallikrein deficiency (
48976006) -
Primary antiphospholipid syndrome (
239892009) -
Primary antiphospholipid syndrome with multisystem involvement (
239894005) -
Primary antiphospholipid syndrome with organ/system involvement (
239893004) -
Primary cryofibrinogenemia (
61802005) -
Primary non-thrombocytopenic purpura (
234494000) -
Primary thrombocytopenia (
267534000) -
Protein C deficiency disease (
76407009) -
Protein S deficiency disease (
1563006) -
Prothrombin G20210A mutation (
440989002) -
Prothrombin complex deficiency (
234454002) -
Pseudo von Willebrand disease (
128115005) -
Pure red cell aplasia, acquired (
234370001) -
Purpura annularis telangiectodes of Majocchi (
56231002) -
Purpura due to increased intravascular pressure (
402849004) -
Purpura due to prolonged vomiting and/or coughing (
402850004) -
Purpura fulminans (
13507004) -
Purpura of skin and or skin-associated mucous membrane co-occurrent and due to coagulation disorder (
724854007) -
Purpura of skin caused by mechanical force (
724855008) -
Purpura of skin co-occurrent and due to vascular fragility (
737243006) -
Purpura pigmentosa chronica (
111199007) -
Purpura rheumatica (
86074002) -
Purpura simplex (
277791008) -
Purpuric disorder (
387778001) -
Purpuric rash (
284078000) -
Qualitative platelet disorder (
267532001) -
Radial aplasia-thrombocytopenia syndrome (
85589009) -
Radiation thrombocytopenia (
371074009) -
Radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome (
721882001) -
Reactive thrombocytosis (
234500001) -
Refractory thrombocytopenia (
721304007) -
Resistance to activated protein C caused by Factor V Leiden (
421527008) -
Revesz syndrome (
723512008) -
Scott syndrome (
128098009) -
Secondary antiphospholipid syndrome (
239895006) -
Secondary antiphospholipid syndrome with multisystem involvement (
239897003) -
Secondary antiphospholipid syndrome with organ/system involvement (
239896007) -
Secondary aplastic anemia (
43858000) -
Secondary autoimmune thrombocytopenia (
128092005) -
Secondary cryofibrinogenemia (
41816006) -
Secondary cutaneous vasculitis (
238787009) -
Secondary non-thrombocytopenic purpura (
234495004) -
Secondary thrombocytopenia (
154826009) -
Senile purpura (
53751009) -
Severe fever with thrombocytopenia syndrome virus (
722401001) -
Severe hereditary factor IX deficiency disease with inhibitor (
440866009) -
Severe hereditary factor IX deficiency disease without inhibitor (
441190003) -
Severe hereditary factor VIII deficiency disease (
16872008) -
Severe hereditary factor VIII deficiency disease with inhibitor (
438373005) -
Severe hereditary factor VIII deficiency disease without inhibitor (
440993008) -
Sex-linked thrombocytopenia (
37492005) -
Stasis purpura (
361210001) -
Stellate pseudoscar in senile purpura (
403393000) -
Steroid purpura (
81500003) -
Systemic fibrinogenolysis (
10153004) -
Systemic lupus erythematosus-associated antiphospholipid syndrome (
402865003) -
Thrombocytopathy, asplenia and miosis (
711407000) -
Thrombocytopenia associated with acquired immunodeficiency syndrome (
421766003) -
Thrombocytopenia caused by alcohol (
699208000) -
Thrombocytopenia caused by drugs (
191322006) -
Thrombocytopenia caused by hypothermia (
34395002) -
Thrombocytopenia co-occurrent and due to alcoholism (
97571000119109) -
Thrombocytopenia due to blood loss (
49886003) -
Thrombocytopenia due to defective platelet production (
82190001) -
Thrombocytopenia due to diminished platelet production (
78345002) -
Thrombocytopenia due to extracorporeal circulation (
30182008) -
Thrombocytopenia due to extracorporeal circulation of blood (
191323001) -
Thrombocytopenia due to hypersplenism (
63444004) -
Thrombocytopenia due to massive blood transfusion (
307342006) -
Thrombocytopenia due to non-immune destruction (
87902006) -
Thrombocytopenia due to sequestration (
323079008) -
Thrombocytopenic disorder (
302215000) -
Thrombocytopenic purpura (
302873008) -
Thrombocytopenic purpura associated with metabolic disorder (
417626001) -
Thrombocytopenic purpura due to defective platelet production (
402653004) -
Thrombocytopenic purpura due to platelet consumption (
402654005) -
Thrombocytosis (
6631009) -
Thrombophilia (
234467004) -
Thrombophilia associated with pregnancy (
441697004) -
Thrombophilia caused by antineoplastic agent therapy (
442760001) -
Thrombophilia caused by drug therapy (
442197003) -
Thrombophilia caused by hormone therapy (
442654007) -
Thrombophilia caused by vascular device (
442363001) -
Thrombophilia due to acquired antithrombin III deficiency (
439126002) -
Thrombophilia due to acquired protein C deficiency (
439002002) -
Thrombophilia due to acquired protein S deficiency (
439125003) -
Thrombophilia due to antiphospholipid antibody (
441079006) -
Thrombophilia due to immobilization (
441762006) -
Thrombophilia due to malignant neoplasm (
442078001) -
Thrombophilia due to myeloproliferative disorder (
441946009) -
Thrombophilia due to paroxysmal nocturnal hemoglobinuria (
441990004) -
Thrombophilia due to trauma (
441945008) -
Thrombophilia due to vascular anomaly (
442121006) -
Thrombotic thrombocytopenic purpura (
78129009) -
Thromboxane generation defect (
234475005) -
Thromboxane synthetase deficiency (
234477002) -
Thyrocerebrorenal syndrome (
733096007) -
Transient acquired pure red cell aplasia (
191255003) -
Transient neonatal disorder of coagulation (
32605001) -
Transient neonatal thrombocytopenia (
23205009) -
Transient neonatal thrombocytopenia due to exchange transfusion (
206510008) -
Transient neonatal thrombocytopenia due to idiopathic maternal thrombocytopenia (
206511007) -
Transient neonatal thrombocytopenia due to isoimmunization (
206512000) -
Upshaw-Schulman syndrome (
373420004) -
Uremic thrombocytopenia (
416902009) -
Vascular hemostatic disease (
21112004) -
Vitamin K deficiency coagulation disorder (
1286003) -
WT limb blood syndrome (
719019000) -
Waldenstrom's hypergammaglobulinemic purpura (
190809001) -
Warfarin overdosage (
47546008) -
Warfarin overdose of undetermined intent (
296936009) -
White platelet syndrome (
718553004) -
Wiskott-Aldrich autosomal dominant variant syndrome (
403837005) -
Wiskott-Aldrich syndrome (
36070007) -
X-linked congenital dyserythropoietic anemia with thrombocytopenia (
722475006) -
von Willebrand disease type 1 (
128106003) -
von Willebrand disease type 2 (
128107007) -
von Willebrand disease type 2A (
359714009) -
von Willebrand disease type 2B (
359721009) -
von Willebrand disease type 2M (
359729006) -
von Willebrand disease type 2N (
359732009) -
von Willebrand disease type 3 (
128108002) -
von Willebrand disease type IA (
359709005) -
von Willebrand disease type IB (
128113003) -
von Willebrand disease type IC (
128114009) -
von Willebrand disease, type 1^a^ (
359704000) -
von Willebrand disease, type IIA (
87397002) -
von Willebrand disease, type IIB (
19520006) -
von Willebrand disease, type IIC (
1908008) -
von Willebrand disease, type IID (
35066007) -
von Willebrand disease, type IIE (
52137009) -
von Willebrand disease, type IIF (
12501008) -
von Willebrand disease, type IIG (
71723006) -
von Willebrand disease, type IIH (
24663001) -
von Willebrand disorder (
128105004) -
von Willebrand factor inhibitor disorder (
41106001)
coagulopathy
Included 265 out of 267 matching concepts.
Show matching concepts
-
Accidental coumarin overdose (
296931004) -
Accidental heparin overdose (
296927005) -
Accidental warfarin overdose (
296934007) -
Acquired afibrinogenemia (
359730001) -
Acquired coagulation disorder (
234466008) -
Acquired coagulation factor deficiency (
25904003) -
Acquired coagulation factor inhibitor disorder (
64509006) -
Acquired combined coagulation factor deficiency (
439156006) -
Acquired factor II deficiency (
191298004) -
Acquired factor IX deficiency disease (
12153008) -
Acquired factor V deficiency disease (
35913006) -
Acquired factor VII deficiency disease (
2036003) -
Acquired factor VIII deficiency disease (
14230004) -
Acquired factor X deficiency disease (
33820001) -
Acquired factor XI deficiency disease (
35554008) -
Acquired factor XII deficiency disease (
15132005) -
Acquired factor XIII deficiency disease (
6364000) -
Acquired fibrinogen abnormality (
234462005) -
Acquired hypofibrinogenemia (
359723007) -
Acquired hypoplasminogenemia (
95843009) -
Acquired inhibitor of coagulation (
282707003) -
Acquired purpura fulminans (
725157006) -
Acquired thrombocytopenia (
74576004) -
Acquired von Willebrand's disease (
234451005) -
Afibrinogenemia (
278504009) -
Afibrinogenemia - postpartum (
237337003) -
Afibrinogenemia following molar AND/OR ectopic pregnancy (
85796009) -
Alpha chain defect dysfibrinogenemia (
234459007) -
Alpha-2-antiplasmin deficiency (
234465007) -
Anti-factor II disorder (
180481005) -
Anticoagulant excess without bleeding (
278366008) -
Anticoagulant overdosage (
43302000) -
Anticoagulant-induced bleeding (
278365007) -
Antiprothrombin disorder (
181456001) -
Antithrombin III deficiency (
36351005) -
Antithrombin III deficiency type I (
973271000000108) -
Antithrombin III deficiency type II (
973291000000107) -
Autoimmune factor VIII deficiency (
307515009) -
Autosomal dominant deficiency of plasminogen (
95842004) -
Benign gestational thrombocytopenia (
128090002) -
Beta chain defect dysfibrinogenemia (
234460002) -
Bite of unidentified snake with coagulopathy (
241815008) -
Bleeding disorder due to deficiency of calcium and diacylglycerol-regulated guanine nucleotide exchange factor I (
725105006) -
Blood coagulation disorder (
64779008) -
Blood coagulation disorder complicating childbirth (
10749581000119100) -
Blood coagulation disorder complicating pregnancy (
10749641000119106) -
Blood coagulation disorder due to liver disease (
69500007) -
Blood coagulation disorder with impaired clot retraction time (
123790009) -
Blood coagulation disorder with prolonged bleeding time (
123789000) -
Blood coagulation disorder with prolonged coagulation time (
123787003) -
Blood coagulation disorder with shortened bleeding time (
123788008) -
Blood coagulation disorder with shortened coagulation time (
123786007) -
Blood coagulation disorder, categorized by value of screening test (
128088003) -
Blood coagulation panel, disseminated intravascular coagulation (
53643002) -
Classic onset hemorrhagic disease of newborn due to vitamin K deficiency (
717936002) -
Coagulation factor deficiency syndrome (
86075001) -
Combined coagulation factor deficiency (
234463000) -
Combined deficiency of factor V and factor VIII (
715559004) -
Congenital afibrinogenemia (
154818001) -
Congenital alpha-2-antiplasmin deficiency (
716746003) -
Congenital factor IX deficiency variant (
234444001) -
Congenital factor IX deficiency with inhibitor (
234445000) -
Congenital factor IX deficiency without inhibitor (
426199009) -
Congenital fibrinogen abnormality (
234456000) -
Congenital hypofibrinogenemia (
439145006) -
Congenital plasminogen activator inhibitor deficiency type 1 (
717407006) -
Congenital von Willebrand's disease (
234446004) -
Congenital von Willebrand's disease type I (
234447008) -
Congenital von Willebrand's disease type II (
234448003) -
Congenital von Willebrand's disease type III (
234450006) -
Contact factor deficiency (
234452003) -
Coumarin overdose (
296930003) -
Coumarin overdose of undetermined intent (
296933001) -
Cryofibrinogenemia (
10934005) -
Defect of purinergic receptor p2y G protein-coupled 12 (
725291001) -
Defibrination syndrome following molar AND/OR ectopic pregnancy (
62698000) -
Deficiency of coagulation factor due to liver disease (
191296000) -
Deficiency of coagulation factor due to vitamin K deficiency (
191297009) -
Deficiency of naturally occurring coagulation factor inhibitor (
105604006) -
Dilutional thrombocytopenia (
51624005) -
Disorder involving the fibrinolytic system (
95839005) -
Disseminated intravascular coagulation (
67406007) -
Disseminated intravascular coagulation due to placental abruption (
39191000119103) -
Disseminated intravascular coagulation in newborn (
34417008) -
Drug-induced coagulation inhibitor disorder (
16773005) -
Drug-induced immune thrombocytopenia (
19307009) -
Dysfibrinogenemia (
111589005) -
Dysplasminogenemia (
95844003) -
Early onset diffuse bleeding diathesis secondary to vitamin K deficient hemorrhagic disease of fetus and newborn (
717935003) -
Factor I deficiency disease (
439458000) -
Factor I inhibitor disorder (
58327003) -
Factor II deficiency (
73975000) -
Factor IX deficiency (
767712006) -
Factor IX inhibitor disorder (
89729000) -
Factor V deficiency (
4320005) -
Factor V inhibitor disorder (
41690001) -
Factor VII deficiency (
37193007) -
Factor VIII deficiency (
234440005) -
Factor VIII inhibitor disorder (
47307007) -
Factor X deficiency (
76642003) -
Factor X inhibitor disorder (
9489006) -
Factor XI deficiency (
767713001) -
Factor XI deficiency, type I (
88540000) -
Factor XI deficiency, type II (
33169001) -
Factor XI deficiency, type III (
45963004) -
Factor XI inhibitor disorder (
38879000) -
Factor XII deficiency disease (
46981006) -
Factor XIII deficiency disease (
18604004) -
Factor XIII inhibitor disorder (
13993001) -
Failed attempted abortion with afibrinogenemia (
27068000) -
Failed attempted abortion with defibrination syndrome (
34478009) -
Familial hemorrhagic diathesis (
6935003) -
Familial multiple factor deficiency syndrome (
81783000) -
Familial multiple factor deficiency syndrome, type I (
84048006) -
Familial multiple factor deficiency syndrome, type II (
65768009) -
Familial multiple factor deficiency syndrome, type III (
64315007) -
Familial multiple factor deficiency syndrome, type IV (
66909001) -
Familial multiple factor deficiency syndrome, type V (
3760002) -
Familial multiple factor deficiency syndrome, type VI (
61551003) -
Fibrinogen abnormality (
234455001) -
Fibrinogen deficiency (
359727008) -
Fibrinolysis - postpartum (
237336007) -
Fibrinolytic bleeding syndrome (
234464006) -
Gamma chain defect dysfibrinogenemia (
234461003) -
Hemolysis-elevated liver enzymes-low platelet count syndrome (
95605009) -
Hemophilia (
90935002) -
Hemorrhagic disease of the newborn due to factor II deficiency (
24149006) -
Hemorrhagic disease of the newborn due to vitamin K deficiency (
12546009) -
Heparin overdose (
296926001) -
Heparin overdose of undetermined intent (
296929008) -
Heparin-induced thrombocytopenia (
73397007) -
Heparin-induced thrombocytopenia with thrombosis (
111588002) -
Hereditary antithrombin III deficiency (
439699000) -
Hereditary coagulation factor deficiency (
16922007) -
Hereditary combined coagulation factor deficiency (
439157002) -
Hereditary combined deficiency of vitamin K-dependent clotting factors (
724356003) -
Hereditary dysfibrinogenemia (
45366001) -
Hereditary dysplasminogenemia (
95845002) -
Hereditary factor I deficiency disease (
31925001) -
Hereditary factor II deficiency disease (
33297000) -
Hereditary factor IX deficiency disease (
41788008) -
Hereditary factor IX deficiency disease with inhibitor (
438372000) -
Hereditary factor IX deficiency disease without inhibitor (
438792009) -
Hereditary factor V deficiency disease (
88776002) -
Hereditary factor VII deficiency disease (
40855001) -
Hereditary factor VIII deficiency disease (
28293008) -
Hereditary factor VIII deficiency disease with inhibitor (
234442002) -
Hereditary factor VIII deficiency disease without inhibitor (
438360006) -
Hereditary factor X deficiency disease (
37350004) -
Hereditary factor XI deficiency disease (
49762007) -
Hereditary factor XII deficiency disease (
43217004) -
Hereditary factor XIII A subunit and B subunit deficiency (
439460003) -
Hereditary factor XIII A subunit deficiency (
439455002) -
Hereditary factor XIII B subunit deficiency (
439459008) -
Hereditary factor XIII deficiency disease (
50189006) -
Hereditary hyperfibrinogenemia (
440924009) -
Hereditary hypoplasminogenemia (
95841006) -
Hereditary protein C deficiency (
439274008) -
Hereditary protein S deficiency (
439702007) -
Hereditary thrombophilic dysfibrinogenemia (
438827002) -
Hereditary von Willebrand disease type 2A (
359711001) -
Hereditary von Willebrand disease type 2B (
359717002) -
Hereditary von Willebrand disease type 2M (
359725000) -
Hereditary von Willebrand disease type IA (
359700009) -
Heterozygous protein C deficiency (
441101007) -
Heterozygous protein S deficiency (
440988005) -
High molecular weight kininogen deficiency (
27312002) -
Homozygous protein C deficiency (
441188004) -
Homozygous protein S deficiency (
441189007) -
Hyperfibrinogenemia (
439000005) -
Hyperheparinemia (
79674009) -
Hypodysfibrinogenemia (
234458004) -
Hypofibrinogenemia (
234457009) -
Hypoplasminogenemia (
95840007) -
Idiopathic factor VIII deficiency (
307514008) -
Illegal abortion with afibrinogenemia (
3230006) -
Illegal abortion with defibrination syndrome (
61810006) -
Induced termination of pregnancy complicated by afibrinogenemia (
609456005) -
Induced termination of pregnancy complicated by defibrination syndrome (
609462000) -
Intentional coumarin overdose (
296932006) -
Intentional heparin overdose (
296928000) -
Intentional warfarin sodium overdose (
296935008) -
Isolated thrombocytopenia (
724637001) -
Kasabach-Merritt syndrome (
86635005) -
Late onset diffuse bleeding diathesis secondary to vitamin K deficient hemorrhagic disease of fetus and newborn (
717937006) -
Legal abortion with afibrinogenemia (
30479005) -
Legal abortion with defibrination syndrome (
6647006) -
Lupus anticoagulant disorder (
19267009) -
Malignancy-related factor VIII deficiency (
307518006) -
Mild hereditary factor IX deficiency disease with inhibitor (
440868005) -
Mild hereditary factor IX deficiency disease without inhibitor (
441192006) -
Mild hereditary factor VIII deficiency disease (
26029002) -
Mild hereditary factor VIII deficiency disease with inhibitor (
425949001) -
Mild hereditary factor VIII deficiency disease without inhibitor (
440820004) -
Miscarriage with afibrinogenemia (
21360006) -
Miscarriage with defibrination syndrome (
50770000) -
Mixed cryofibrinogenemia (
80988005) -
Moderate hereditary factor IX deficiency disease with inhibitor (
440867000) -
Moderate hereditary factor IX deficiency disease without inhibitor (
441191004) -
Moderate hereditary factor VIII deficiency disease (
33344008) -
Moderate hereditary factor VIII deficiency disease with inhibitor (
438599002) -
Moderate hereditary factor VIII deficiency disease without inhibitor (
441006000) -
Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome (
733028000) -
Neonatal coagulation disorder (
95623001) -
Neonatal purpura fulminans (homozygous protein C deficiency) (
402851000) -
Passovoy factor deficiency (
234453008) -
Postpartum afibrinogenemia with hemorrhage (
111452009) -
Postpartum coagulation defect with hemorrhage (
49177006) -
Postpartum coagulation defects (
267272006) -
Postpartum coagulation defects - delivered with postnatal problem (
200030007) -
Postpartum coagulation defects with postnatal problem (
200031006) -
Postpartum fibrinolysis with hemorrhage (
62410004) -
Pregnancy-related factor VIII deficiency (
307517001) -
Prekallikrein deficiency (
48976006) -
Primary cryofibrinogenemia (
61802005) -
Protein C deficiency disease (
76407009) -
Protein S deficiency disease (
1563006) -
Prothrombin complex deficiency (
234454002) -
Pseudo von Willebrand disease (
128115005) -
Purpura fulminans (
13507004) -
Purpura of skin and or skin-associated mucous membrane co-occurrent and due to coagulation disorder (
724854007) -
Radiation thrombocytopenia (
371074009) -
Refractory thrombocytopenia (
721304007) -
Secondary autoimmune thrombocytopenia (
128092005) -
Secondary cryofibrinogenemia (
41816006) -
Secondary thrombocytopenia (
154826009) -
Severe hereditary factor IX deficiency disease with inhibitor (
440866009) -
Severe hereditary factor IX deficiency disease without inhibitor (
441190003) -
Severe hereditary factor VIII deficiency disease (
16872008) -
Severe hereditary factor VIII deficiency disease with inhibitor (
438373005) -
Severe hereditary factor VIII deficiency disease without inhibitor (
440993008) -
Systemic fibrinogenolysis (
10153004) -
Thrombocytopenia associated with acquired immunodeficiency syndrome (
421766003) -
Thrombocytopenia caused by alcohol (
699208000) -
Thrombocytopenia caused by drugs (
191322006) -
Thrombocytopenia caused by hypothermia (
34395002) -
Thrombocytopenia co-occurrent and due to alcoholism (
97571000119109) -
Thrombocytopenia due to blood loss (
49886003) -
Thrombocytopenia due to extracorporeal circulation (
30182008) -
Thrombocytopenia due to extracorporeal circulation of blood (
191323001) -
Thrombocytopenia due to massive blood transfusion (
307342006) -
Transient neonatal disorder of coagulation (
32605001) -
Uremic thrombocytopenia (
416902009) -
Vitamin K deficiency coagulation disorder (
1286003) -
Warfarin overdosage (
47546008) -
Warfarin overdose of undetermined intent (
296936009) -
von Willebrand disease type 1 (
128106003) -
von Willebrand disease type 2 (
128107007) -
von Willebrand disease type 2A (
359714009) -
von Willebrand disease type 2B (
359721009) -
von Willebrand disease type 2M (
359729006) -
von Willebrand disease type 2N (
359732009) -
von Willebrand disease type 3 (
128108002) -
von Willebrand disease type IA (
359709005) -
von Willebrand disease type IB (
128113003) -
von Willebrand disease type IC (
128114009) -
von Willebrand disease, type 1^a^ (
359704000) -
von Willebrand disease, type IIA (
87397002) -
von Willebrand disease, type IIB (
19520006) -
von Willebrand disease, type IIC (
1908008) -
von Willebrand disease, type IID (
35066007) -
von Willebrand disease, type IIE (
52137009) -
von Willebrand disease, type IIF (
12501008) -
von Willebrand disease, type IIG (
71723006) -
von Willebrand disease, type IIH (
24663001) -
von Willebrand disorder (
128105004) -
von Willebrand factor inhibitor disorder (
41106001)