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Type one disease * AllRare coagulation disorderRare thrombotic disease of hematologic originRare thrombotic disorder due to a coagulation factors defectRare thrombotic disorder due to a constitutional coagulation factors defectCongenital factor XII deficiencyFamilial thrombomodulin anomaliesHypercoagulability syndrome due to glycosylphosphatidylinositol deficiencyRare hereditary thrombophiliaHereditary thrombophilia due to congenital protein S deficiencyHereditary thrombophilia due to congenital protein C deficiencyHereditary thrombophilia due to congenital antithrombin deficiencyHereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiencyRare thrombotic disorder due to an acquired coagulation factors defectCatastrophic antiphospholipid syndromeHeparin-induced thrombocytopeniaProtein S acquired deficiencyAcquired purpura fulminansGaisböck syndromeSimple cryoglobulinemiaRare thrombotic disorder due to a platelet anomalyThrombotic thrombocytopenic purpuraCongenital thrombotic thrombocytopenic purpuraAcquired thrombotic thrombocytopenic purpuraRare thrombotic disorder due to a constitutional platelet anomalyFamilial thrombocytosisHereditary thrombocytosis with transverse limb defectRare thrombotic disorder due to an acquired platelet anomalyEssential thrombocythemiaRare hemorrhagic disorderRare hemorrhagic disorder due to a coagulation factors defectRare hemorrhagic disorder due to a constitutional coagulation factors defectMultiple sclerosis-ichthyosis-factor VIII deficiency syndromeHemophiliaHemophilia ASevere hemophilia AModerately severe hemophilia AMild hemophilia ASymptomatic form of hemophilia A in female carriersHemophilia BSevere hemophilia BModerately severe hemophilia BMild hemophilia BSymptomatic form of hemophilia B in female carriersCongenital factor V deficiencyCongenital fibrinogen deficiencyFamilial afibrinogenemiaFamilial dysfibrinogenemiaFamilial hypofibrinogenemiaFamilial hypodysfibrinogenemiaCongenital alpha2-antiplasmin deficiencyCongenital factor XIII deficiencyVon Willebrand diseaseVon Willebrand disease type 1Von Willebrand disease type 2Von Willebrand disease type 2AVon Willebrand disease type 2BVon Willebrand disease type 2MVon Willebrand disease type 2NVon Willebrand disease type 3Congenital factor XI deficiencyCongenital plasminogen activator inhibitor type 1 deficiencyCongenital high-molecular-weight kininogen deficiencyCongenital prekallikrein deficiencyCombined deficiency of factor V and factor VIIICongenital vitamin K-dependent coagulation factors deficiencyCongenital factor VII deficiencyCongenital factor II deficiencyCongenital factor X deficiencyHereditary combined deficiency of vitamin K-dependent clotting factorsHemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutationEast Texas bleeding disorderThrombomodulin-related bleeding disorderRare hemorrhagic disorder due to an acquired coagulation factor defectAcquired prothrombin deficiencyAcquired hemophiliaAcquired von Willebrand syndromeRare hemorrhagic disorder due to a platelet anomalyRare hemorrhagic disorder due to a constitutional platelet anomalyRare hemorrhagic disorder due to a constitutional thrombocytopeniaSyndromic constitutional thrombocytopeniaHereditary thrombocytopenia with early-onset myelofibrosisStormorken-Sjaastad-Langslet syndromeThrombocytopenia-absent radius syndromeRadio-ulnar synostosis-amegakaryocytic thrombocytopenia syndromeMYH9-related diseaseGNE myopathyJacobsen syndromeMacrothrombocytopenia with mitral valve insufficiencyAlpha delta granule deficiencyDense granule diseaseWiskott-Aldrich syndromeChédiak-Higashi syndromeHereditary thrombocytopenia with normal platelets-hematological cancer predisposition syndromeHermansky-Pudlak syndromeHermansky-Pudlak syndrome with neutropeniaHermansky-Pudlak syndrome with pulmonary fibrosisHermansky-Pudlak syndrome without pulmonary fibrosisHermansky-Pudlak syndrome type 7Hermansky-Pudlak syndrome type 8Hermansky-Pudlak syndrome type 9Isolated constitutional thrombocytopeniaIsolated hereditary giant platelet disorderSevere autosomal recessive macrothrombocytopeniaBernard-Soulier syndromeThrombocytopenia with congenital dyserythropoietic anemiaAutosomal dominant macrothrombocytopeniaAlpha granule diseaseGray platelet syndromeQuebec platelet disorderMedich giant platelet syndromeWhite platelet syndromeParis-Trousseau thrombocytopeniaX-linked dyserythropoetic anemia with abnormal platelets and neutropeniaHereditary thrombocytopenia with normal plateletsX-linked thrombocytopenia with normal plateletsAutosomal thrombocytopenia with normal plateletsCongenital amegakaryocytic thrombocytopeniaBleeding diathesis due to thromboxane synthesis deficiencyIsolated delta-storage pool diseaseAutosomal dominant thrombocytopenia with platelet secretion defectRare hemorrhagic disorder due to a qualitative platelet defectGlanzmann thrombastheniaCytosolic phospholipase-A2 alpha deficiency associated bleeding disorderEhlers-Danlos syndrome, fibronectinemic typeScott syndromeP2Y12 defectPseudo-von Willebrand diseaseBleeding diathesis due to a collagen receptor defectBleeding diathesis due to glycoprotein VI deficiencyBleeding diathesis due to integrin alpha2-beta1 deficiencyBleeding disorder due to CalDAG-GEFI deficiencyRare hemorrhagic disorder due to an acquired platelet anomalyMultifocal lymphangioendotheliomatosis-thrombocytopenia syndromeTAFRO syndromeHELLP syndromeFetal and neonatal alloimmune thrombocytopeniaAutoimmune thrombocytopeniaImmune thrombocytopenic purpuraEvans syndromeSTAT3-related early-onset multisystem autoimmune diseaseKasabach-Merritt syndromeRare anemiaRare hemolytic anemiaRare constitutional hemolytic anemiaAtypical hemolytic-uremic syndromeAtypical hemolytic-uremic syndrome with DGKE deficiencyAtypical hemolytic-uremic syndrome with C3 anomalyAtypical hemolytic-uremic syndrome with MCP/CD46 anomalyAtypical hemolytic-uremic syndrome with B factor anomalyAtypical hemolytic-uremic syndrome with H factor anomalyAtypical hemolytic-uremic syndrome with I factor anomalyAtypical hemolytic-uremic syndrome with anti-factor H antibodiesAtypical hemolytic-uremic syndrome with thrombomodulin anomalyRare acquired hemolytic anemiaTypical hemolytic-uremic syndromeParoxysmal nocturnal hemoglobinuriaAplastic anemiaRare constitutional aplastic anemiaBlackfan-Diamond anemiaDyskeratosis congenitaFanconi anemiaRevesz syndromeHoyeraal-Hreidarsson syndromeWT limb-blood syndromeShwachman-Diamond syndromeAutosomal dominant aplasia and myelodysplasiaHereditary isolated aplastic anemiaPancytopenia-developmental delay syndromeRare acquired aplastic anemiaPrimary myelofibrosisIdiopathic aplastic anemiaRed cell aplasiaTransient erythroblastopenia of childhoodAdult pure red cell aplasiaMonocytopenia with susceptibility to infectionsRare deficiency anemiaConstitutional deficiency anemiaConstitutional megaloblastic anemia due to vitamin B12 metabolism disorderMethylmalonic acidemia with homocystinuriaMethylmalonic acidemia with homocystinuria, type cblCMethylmalonic acidemia with homocystinuria, type cblDMethylmalonic acidemia with homocystinuria type cblFMethylmalonic acidemia with homocystinuria, type cblJMethylmalonic acidemia with homocystinuria, type cblXTranscobalamin deficiencyCongenital intrinsic factor deficiencyHomocystinuria without methylmalonic aciduriaMethylcobalamin deficiency type cblEMethylcobalamin deficiency type cblGMethylcobalamin deficiency type cblDv1Gräsbeck-Imerslund diseaseConstitutional megaloblastic anemia due to folate metabolism disorderFormiminoglutamic aciduriaHereditary folate malabsorptionConstitutional megaloblastic anemia with severe neurologic diseaseVitamin B12- and folate-independent constitutional megaloblastic anemiaHereditary orotic aciduriaThiamine-responsive megaloblastic anemia syndromeHypoxanthine-guanine phosphoribosyltransferase deficiencyLesch-Nyhan syndromeHypoxanthine guanine phosphoribosyltransferase partial deficiencyConstitutional dyserythropoietic anemiaCongenital dyserythropoietic anemiaCongenital dyserythropoietic anemia type ICongenital dyserythropoietic anemia type IIICongenital dyserythropoietic anemia type IICongenital dyserythropoietic anemia type IVMajeed syndromePancreatic insufficiency-anemia-hyperostosis syndromeSideroblastic anemiaAcquired idiopathic sideroblastic anemiaConstitutional sideroblastic anemiaPearson syndromeMitochondrial myopathy and sideroblastic anemiaX-linked sideroblastic anemia and ataxiaX-linked sideroblastic anemiaAdult-onset autosomal recessive sideroblastic anemiaAutosomal recessive sideroblastic anemiaSevere congenital hypochromic anemia with ringed sideroblastsCongenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndromeConstitutional anemia due to iron metabolism disorderCongenital atransferrinemiaAceruloplasminemiaMicrocytic anemia with liver iron overloadIRIDA syndromeRare acquired deficiency anemiaPlummer-Vinson syndromeRare iron overloadRare hereditary hemochromatosisHFE related hereditary hemochromatosis (Symptomatic form of hemochromatosis type 1) - OMIM 235200HJV related hereditary hemochromatosis - OMIM 602390 (Hemochromatosis type 2A)HAMP related hereditary hemochromatosis - OMIM 613313 (Hemochromatosis type 2B)TFR2 related hereditary hemochromatosis OMIM 604250 (Hemochromatosis type 3)FTH related hereditary hemochromatosis - OMIM 615517 (Hemochromatosis type 5)SLC40A1 related hereditary hemochromatosis - OMIM 606069 (Hemochromatosis type 4A)Ferroportin Disease (Hemochromatosis type 4B)​Rare FerritinopathyL-ferritin deficiencyHereditary Hyperferritinemia with or without cataractHereditary hyperferritinemia with congenital cataractsGenetic hyperferritinemia without iron overloadNeuroferritinopathyPorphyriasAutosomal erythropoietic protoporphyriaX-linked erythropoietic protoporphyriaErythropoietic uroporphyria associated with myeloid malignancyPorphyria cutanea tardaSporadic porphyria cutanea tarda (OMOM176090)Familial porphyria cutanea tarda (OMIM176100)Hepatoerythropoietic porphyriaHereditary coproporphyriaPorphyria variegata (OMIM176200)Congenital erythropoietic porphyriaAcute Intermitent porphyriaPorphyria due to ALA dehydratase deficiencyTumor of hematopoietic and lymphoid tissuesLymphoid hemopathyHistiocytic and dendritic cell tumorMacrophage or histiocytic tumorHistiocytic sarcomaDendritic cell tumorLangerhans cell histiocytosisLetterer-Siwe diseaseEosinophilic granulomaHashimoto-Pritzker syndromeHand-Schüller-Christian diseaseAdult pulmonary Langerhans cell histiocytosisLangerhans cell sarcomaInterdigitating dendritic cell sarcomaFollicular dendritic cell sarcomaDendritic cell sarcoma not otherwise specifiedDeafness-lymphedema-leukemia syndromeAutoimmune lymphoproliferative syndromePlasma cell tumorPOEMS syndromeMultiple myelomaAL amyloidosisPrimary systemic amyloidosisPrimary localized amyloidosisPlasmacytomaPrimary plasmacytoma of the boneExtramedullary soft tissue plasmacytomaNon-amyloid monoclonal immunoglobulin deposition diseaseHeavy chain deposition diseaseLight and heavy chain deposition diseaseLight chain deposition diseaseHeavy chain diseaseMu-heavy chain diseaseAlpha-heavy chain diseaseGamma-heavy chain diseasePlasma cell leukemiaImmunodeficiency-associated lymphoproliferative diseasePost-transplant lymphoproliferative diseaseMethotrexate-associated lymphoproliferative disordersLymphoproliferative disease associated with primary immune diseaseLymphomaNon-Hodgkin lymphomaAcute lymphoblastic leukemiaPrecursor B-cell acute lymphoblastic leukemiaPrecursor T-cell acute lymphoblastic leukemiaMature B-cell acute lymphoblastic leukemiaB-cell non-Hodgkin lymphomaIndolent B-cell non-Hodgkin lymphomaFollicular lymphomaWaldenström macroglobulinemiaHairy cell leukemiaB-cell chronic lymphocytic leukemiaIndolent primary cutaneous B-cell lymphomaPrimary cutaneous marginal zone B-cell lymphomaPrimary cutaneous follicle center lymphomaHairy cell leukemia variantMarginal zone lymphomaMALT lymphomaSplenic marginal zone lymphomaNodal marginal zone B-cell lymphomaSplenic diffuse red pulp small B-cell lymphomaLymphoplasmacytic lymphoma without IgM productionAggressive B-cell non-Hodgkin lymphomaBurkitt lymphomaDiffuse large B-cell lymphomaLymphomatoid granulomatosisPrimary mediastinal large B-cell lymphomaIntravascular large B-cell lymphomaEpstein-Barr virus-positive diffuse large B-cell lymphoma of the elderlyDiffuse large B-cell lymphoma of the central nervous systemT-cell/histiocyte rich large B cell lymphomaDiffuse large B-cell lymphoma with chronic inflammationALK-positive large B-cell lymphomaPrimary effusion lymphomaMantle cell lymphomaB-cell prolymphocytic leukemiaAggressive primary cutaneous B-cell lymphomaPrimary cutaneous diffuse large B-cell lymphoma, leg typePlasmablastic lymphomaT-cell non-Hodgkin lymphomaCD4+/CD56+ hematodermic neoplasmT-cell prolymphocytic leukemiaT-cell large granular lymphocyte leukemiaAggressive NK-cell leukemiaAdult T-cell leukemia/lymphomaExtranodal nasal NK/T cell lymphomaEnteropathy-associated T-cell lymphomaHepatosplenic T-cell lymphomaAngioimmunoblastic T-cell lymphomaAnaplastic large cell lymphomaALK-positive anaplastic large cell lymphomaALK-negative anaplastic large cell lymphomaPrimary cutaneous T-cell lymphomaIndolent primary cutaneous T-cell lymphomaPrimary cutaneous CD30+ T-cell lymphoproliferative diseaseLymphomatoid papulosisPrimary cutaneous anaplastic large cell lymphomaSubcutaneous panniculitis-like T-cell lymphomaPrimary cutaneous CD4+ small/medium-sized pleomorphic T-cell lymphomaMycosis fungoides and variantsClassic mycosis fungoidesGranulomatous slack skinFolliculotropic mycosis fungoidesLocalized pagetoid reticulosisAggressive primary cutaneous T-cell lymphomaSézary syndromePrimary cutaneous peripheral T-cell lymphoma not otherwise specifiedPrimary cutaneous aggressive epidermotropic CD8+ T-cell lymphomaPrimary cutaneous gamma/delta-positive T-cell lymphomaSystemic Epstein-Barr virus-positive T-cell lymphoproliferative disease of childhoodHydroa vacciniforme-like lymphomaPeripheral T-cell lymphoma NOSHodgkin lymphomaClassic Hodgkin lymphomaClassic Hodgkin lymphoma, nodular sclerosis typeClassic Hodgkin lymphoma, mixed cellularity typeClassic Hodgkin lymphoma, lymphocyte-rich typeClassic Hodgkin lymphoma, lymphocyte-depleted typeNodular lymphocyte predominant Hodgkin lymphomaComposite lymphomaPrimary organ-specific lymphomaPrimary pulmonary lymphomaPrimary cutaneous lymphomaPrimary cutaneous B-cell lymphomaPrimary central nervous system lymphomaThyroid lymphomaPrimary oculocerebral lymphomaPrimary intraocular lymphomaPrimary bone lymphomaPrimary lymphoma of the conjunctivaRAS-associated autoimmune leukoproliferative diseasePersistent polyclonal B-cell lymphocytosisCastleman diseasePediatric Castleman diseaseLocalized Castleman diseaseMulticentric Castleman diseaseBloom syndromeMastocytosisSystemic mastocytosisIndolent systemic mastocytosisSmouldering systemic mastocytosisIsolated bone marrow mastocytosisSystemic mastocytosis with an associated clonal hematologic non-mast cell lineage diseaseAggressive systemic mastocytosisLymphoadenopathic mastocytosis with eosinophiliaMast cell leukemiaClassic mast cell leukemiaAleukemic mast cell leukemiaCutaneous mastocytosisCutaneous mastocytomaDiffuse cutaneous mastocytosisBullous diffuse cutaneous mastocytosisPseudoxanthomatous diffuse cutaneous mastocytosisMaculopapular cutaneous mastocytosisTelangiectasia macularis eruptiva perstansTypical urticaria pigmentosaPlaque-form urticaria pigmentosaNodular urticaria pigmentosaMast cell sarcomaExtracutaneous mastocytomaMyeloid hemopathyAcute myeloid leukemiaAcute myeloid leukemia with multilineage dysplasiaTherapy related acute myeloid leukemia and myelodysplastic syndromeAcute myeloid leukemia and myelodysplastic syndromes related to alkylating agentAcute myeloid leukemia and myelodysplastic syndromes related to topoisomerase type 2 inhibitorAcute myeloid leukemia and myelodysplastic syndromes related to radiationAcute leukemia of ambiguous lineageAcute undifferentiated leukemiaBilineal acute leukemiaAcute biphenotypic leukemiaAcute myeloid leukemia with recurrent genetic anomalyAcute promyelocytic leukemiaAcute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)Acute myeloid leukemia with 11q23 abnormalitiesAcute myeloid leukemia with t(8;21)(q22;q22) translocationAcute myeloid leukemia with CEBPA somatic mutationsAcute myeloid leukemia with t(8;16)(p11;p13) translocationAcute myeloid leukemia with t(6;9)(p23;q34)Acute myeloid leukemia with t(9;11)(p22;q23)Acute myeloid leukemia with inv3(p21;q26.2) or t(3;3)(p21;q26.2)Megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13)Acute myeloid leukemia with NPM1 somatic mutationsUnclassified acute myeloid leukemiaAcute erythroid leukemiaAcute megakaryoblastic leukemiaAcute megakaryoblastic leukemia in Down syndromeAcute megakaryoblastic leukemia without Down syndromeAcute panmyelosis with myelofibrosisAcute basophilic leukemiaMyeloid sarcomaAcute myeloid leukemia with minimal differentiationAcute myeloblastic leukemia without maturationAcute myeloblastic leukemia with maturationAcute myelomonocytic leukemiaAcute monoblastic leukemiaInherited acute myeloid leukemiaInherited acute myeloid leukemia with presdisposing GAT2 mutationInherited acute myeloid leukemia with presdisposing RUNX1 mutationInherited acute myeloid leukemia with presdisposing DDX41 mutationMyelodysplastic syndromeRefractory cytopenia with multilineage dysplasiaRefractory anemiaUnclassified myelodysplastic syndromeAregenerative anemiaRefractory anemia with excess blastsRefractory anemia with excess blasts type 1Refractory anemia with excess blasts type 2Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormalityRefractory anemia with excess blasts in transformationMyeloproliferative neoplasmChronic myeloid leukemiaPolycythemia veraChronic neutrophilic leukemiaChronic myeloproliferative disease, unclassifiableChronic eosinophilic leukemiaHypereosinophilic syndromeIdiopathic hypereosinophilic syndromePrimary hypereosinophilic syndromeSecondary hypereosinophilic syndromeLymphocytic hypereosinophilic syndromeTransient myeloproliferative syndromeMyelodysplastic/myeloproliferative diseaseJuvenile myelomonocytic leukemiaChronic myelomonocytic leukemiaAtypical chronic myeloid leukemiaUnclassified myelodysplastic/myeloproliferative diseaseMyeloid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB or FGFR1Myeloid neoplasm associated with PDGFRA rearrangementMyeloid neoplasm associated with PDGFRB rearrangementMyeloid neoplasm associated with FGFR1 rearrangementPolycythemiaPrimary familial polycythemiaSecondary polycythemiaCongenital secondary polycythemiaChuvash erythrocytosisAutosomal recessive secondary polycythemia not associated with VHL geneAutosomal dominant secondary polycythemiaAcquired secondary polycythemiaHemoglobinopathyHemoglobin E diseaseHemoglobin D diseaseUnstable hemoglobin diseaseAlpha-thalassemia and related diseasesAlpha-thalassemiaHemoglobin H diseaseHb Bart's hydrops fetalisAlpha-thalassemia-related diseasesAlpha-thalassemia-X-linked intellectual disability syndromeAlpha-thalassemia-intellectual disability syndrome linked to chromosome 16Alpha-thalassemia-myelodysplastic syndromeBeta-thalassemia and related diseasesBeta-thalassemiaBeta-thalassemia majorBeta-thalassemia intermediaDominant beta-thalassemiaBeta-thalassemia associated with another hemoglobin anomalyHereditary persistence of fetal hemoglobin-beta-thalassemia syndromeDelta-beta-thalassemiaHemoglobin C-beta-thalassemia syndromeHemoglobin E-beta-thalassemia syndromeHemoglobin Lepore-beta-thalassemia syndromeBeta-thalassemia with other manifestationsBeta-thalassemia-X-linked thrombocytopenia syndromeSickle cell disease and related diseasesSickle cell anemiaSickle cell disease associated with an other hemoglobin anomalySickle cell-beta-thalassemia disease syndromeSickle cell-hemoglobin C disease syndromeSickle cell-hemoglobin D disease syndromeSickle cell-hemoglobin E disease syndromeHereditary persistence of fetal hemoglobin-sickle cell disease syndromeHemoglobinopathy Toms RiverHereditary methemoglobinemiaHemoglobin C diseaseHemoglobin M diseaseAcquired methemoglobinemiaRare constitutional hemolytic anemia due to a red cell membrane anomalyHereditary spherocytosisHereditary elliptocytosisDistal renal tubular acidosis with anemiaHereditary stomatocytosisOverhydrated hereditary stomatocytosisDehydrated hereditary stomatocytosisRh deficiency syndromeFamilial pseudohyperkalemiaSoutheast Asian ovalocytosisHereditary cryohydrocytosis with reduced stomatinHereditary cryohydrocytosis with normal stomatinConstitutional hemolytic anemia due to acanthocytosisAbetalipoproteinemiaMcLeod neuroacanthocytosis syndromePrimary CD59 deficiencyRare constitutional hemolytic anemia due to an enzyme disorderHemolytic anemia due to hexose monophosphate shunt and glutathione metabolism anomaliesGlutathione synthetase deficiencyGlutathione synthetase deficiency with 5-oxoprolinuriaGlutathione synthetase deficiency without 5-oxoprolinuriaGamma-glutamylcysteine synthetase deficiencyHemolytic anemia due to glutathione reductase deficiency6-phosphogluconate dehydrogenase deficiencyHemolytic anemia due to a disorder of glycolytic enzymesGlycogen storage disease due to muscle phosphofructokinase deficiencyTriose phosphate-isomerase deficiencyGlycogen storage disease due to aldolase A deficiencyGlycogen storage disease due to phosphoglycerate kinase 1 deficiencyHemolytic anemia due to red cell pyruvate kinase deficiencyHemolytic anemia due to glucophosphate isomerase deficiencyHemolytic anemia due to diphosphoglycerate mutase deficiencyNon-spherocytic hemolytic anemia due to hexokinase deficiencyHemolytic anemia due to glyceraldehyde-3-phosphate dehydrogenase deficiencyClass I glucose-6-phosphate dehydrogenase deficiencyHemolytic anemia due to an erythrocyte nucleotide metabolism disorderHemolytic anemia due to pyrimidine 5' nucleotidase deficiencyHemolytic anemia due to adenylate kinase deficiencyHemolytic anemia due to erythrocyte adenosine deaminase overproductionHeinz body anemia

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