{
  "concept_id": 4151,
  "concept_version_id": 11511,
  "coding_system": {
    "id": 9,
    "name": "SNOMED  CT codes",
    "description": "SNOMED CT codes"
  },
  "name": "Non-malignant haematological (SNOMED-CT)",
  "description": null,
  "author": "",
  "entry_date": "2025-01-19",
  "validation_performed": false,
  "validation_description": null,
  "publication_doi": "",
  "publication_link": "",
  "secondary_publication_links": null,
  "paper_published": false,
  "source_reference": "",
  "citation_requirements": null,
  "owner_access": 3,
  "group_access": 1,
  "world_access": 1,
  "tags": null,
  "collections": null,
  "created_by": null,
  "modified_by": null,
  "owner": null,
  "group": null,
  "phenotype_owner": "PH1705",
  "phenotype_owner_history_id": 3630,
  "requested_entity_id": null,
  "components": [
    {
      "id": 9978,
      "name": "Inclusion 1",
      "logical_type": "INCLUDE",
      "source_type": "FILE_IMPORT",
      "source": "text/csv",
      "codes": [
        {
          "id": 534120,
          "code": "10180006",
          "description": "Focal hemosiderosis (disorder)"
        },
        {
          "id": 534121,
          "code": "105599000",
          "description": "Anemia related to disturbed deoxyribonucleic acid synthesis (disorder)"
        },
        {
          "id": 534122,
          "code": "105601003",
          "description": "Quantitative disorder of neutrophils (disorder)"
        },
        {
          "id": 534123,
          "code": "105604006",
          "description": "Deficiency of naturally occurring coagulation factor inhibitor (disorder)"
        },
        {
          "id": 534124,
          "code": "10564005",
          "description": "Severe hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin (disorder)"
        },
        {
          "id": 534125,
          "code": "10749581000119100",
          "description": "Blood coagulation disorder complicating childbirth (disorder)"
        },
        {
          "id": 534126,
          "code": "10749641000119106",
          "description": "Blood coagulation disorder complicating pregnancy (disorder)"
        },
        {
          "id": 534127,
          "code": "10759351000119103",
          "description": "Sickle cell anemia in mother complicating childbirth (disorder)"
        },
        {
          "id": 534128,
          "code": "10806241000119108",
          "description": "Thalassemia in mother complicating childbirth (disorder)"
        },
        {
          "id": 534129,
          "code": "111199007",
          "description": "Purpura pigmentosa chronica (disorder)"
        },
        {
          "id": 534130,
          "code": "111575000",
          "description": "Anemia due to membrane defect (disorder)"
        },
        {
          "id": 534131,
          "code": "111576004",
          "description": "Acquired stomatocytosis (disorder)"
        },
        {
          "id": 534132,
          "code": "111577008",
          "description": "Anemia due to enzyme deficiency (disorder)"
        },
        {
          "id": 534133,
          "code": "111578003",
          "description": "Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency (disorder)"
        },
        {
          "id": 534134,
          "code": "111579006",
          "description": "Hereditary nonspherocytic hemolytic anemia due to glutathione synthetase deficiency (disorder)"
        },
        {
          "id": 534135,
          "code": "111585004",
          "description": "Neutropenia associated with autoimmune disease (disorder)"
        },
        {
          "id": 534136,
          "code": "111589005",
          "description": "Dysfibrinogenemia (disorder)"
        },
        {
          "id": 534137,
          "code": "115963009",
          "description": "Regenerative anemia (disorder)"
        },
        {
          "id": 534138,
          "code": "11603001",
          "description": "Sickle cell retinopathy (disorder)"
        },
        {
          "id": 534139,
          "code": "11888009",
          "description": "Hyperviscosity syndrome (disorder)"
        },
        {
          "id": 534140,
          "code": "123728005",
          "description": "Recurrent bone marrow hyperplasia (disorder)"
        },
        {
          "id": 534141,
          "code": "123772008",
          "description": "Homozygous hemoglobinopathy (disorder)"
        },
        {
          "id": 534142,
          "code": "123773003",
          "description": "Heterozygous hemoglobinopathy (disorder)"
        },
        {
          "id": 534143,
          "code": "123786007",
          "description": "Blood coagulation disorder with shortened coagulation time (disorder)"
        },
        {
          "id": 534144,
          "code": "123787003",
          "description": "Blood coagulation disorder with prolonged coagulation time (disorder)"
        },
        {
          "id": 534145,
          "code": "123788008",
          "description": "Blood coagulation disorder with shortened bleeding time (disorder)"
        },
        {
          "id": 534146,
          "code": "123789000",
          "description": "Blood coagulation disorder with prolonged bleeding time (disorder)"
        },
        {
          "id": 534147,
          "code": "123790009",
          "description": "Blood coagulation disorder with impaired clot retraction time (disorder)"
        },
        {
          "id": 534148,
          "code": "124134002",
          "description": "Deficiency of glucose-6-phosphate dehydrogenase (disorder)"
        },
        {
          "id": 534149,
          "code": "124297004",
          "description": "Deficiency of hexokinase (disorder)"
        },
        {
          "id": 534150,
          "code": "124340003",
          "description": "Deficiency of adenylate kinase (disorder)"
        },
        {
          "id": 534151,
          "code": "124437004",
          "description": "Deficiency of glucose-6-phosphatase (disorder)"
        },
        {
          "id": 534152,
          "code": "12501008",
          "description": "von Willebrand disease, type IIF (disorder)"
        },
        {
          "id": 534153,
          "code": "127038008",
          "description": "Hereditary hemoglobinopathy due to globin chain mutation (disorder)"
        },
        {
          "id": 534154,
          "code": "127039000",
          "description": "Acquired hemoglobinopathy (disorder)"
        },
        {
          "id": 534155,
          "code": "127040003",
          "description": "Sickle cell-hemoglobin SS disease (disorder)"
        },
        {
          "id": 534156,
          "code": "127041004",
          "description": "Sickle cell-beta-thalassemia (disorder)"
        },
        {
          "id": 534157,
          "code": "127042006",
          "description": "Sickle cell beta plus thalassemia (disorder)"
        },
        {
          "id": 534158,
          "code": "127043001",
          "description": "Sickle cell-beta^0^-thalassemia (disorder)"
        },
        {
          "id": 534159,
          "code": "127044007",
          "description": "Sickle cell-delta beta^0^-thalassemia (disorder)"
        },
        {
          "id": 534160,
          "code": "127045008",
          "description": "Sickle cell anemia with coexistent alpha-thalassemia (disorder)"
        },
        {
          "id": 534161,
          "code": "127046009",
          "description": "Sickle cell trait with coexistent alpha-thalassemia (disorder)"
        },
        {
          "id": 534162,
          "code": "127047000",
          "description": "Sickle cell-hemoglobin Lepore disease (disorder)"
        },
        {
          "id": 534163,
          "code": "127048005",
          "description": "Sickle cell-Hemoglobin O Arab disease (disorder)"
        },
        {
          "id": 534164,
          "code": "127062003",
          "description": "Erythrocytosis (disorder)"
        },
        {
          "id": 534165,
          "code": "127065001",
          "description": "Familial erythrocytosis due to diphosphoglycerate mutase deficiency (disorder)"
        },
        {
          "id": 534166,
          "code": "127066000",
          "description": "Familial polycythemia vera (disorder)"
        },
        {
          "id": 534167,
          "code": "128088003",
          "description": "Blood coagulation disorder, categorized by value of screening test (disorder)"
        },
        {
          "id": 534168,
          "code": "128091003",
          "description": "Autoimmune thrombocytopenia (disorder)"
        },
        {
          "id": 534169,
          "code": "128092005",
          "description": "Secondary autoimmune thrombocytopenia (disorder)"
        },
        {
          "id": 534170,
          "code": "128093000",
          "description": "Alloimmune thrombocytopenia (disorder)"
        },
        {
          "id": 534171,
          "code": "128094006",
          "description": "Alloimmune platelet transfusion refractoriness (disorder)"
        },
        {
          "id": 534172,
          "code": "128095007",
          "description": "Acquired platelet function disorder (disorder)"
        },
        {
          "id": 534173,
          "code": "128096008",
          "description": "Hereditary platelet function disorder (disorder)"
        },
        {
          "id": 534174,
          "code": "128098009",
          "description": "Scott syndrome (disorder)"
        },
        {
          "id": 534175,
          "code": "128099001",
          "description": "Platelet storage pool defect (disorder)"
        },
        {
          "id": 534176,
          "code": "128100009",
          "description": "Mixed alpha granule and dense body deficiency (disorder)"
        },
        {
          "id": 534177,
          "code": "128101008",
          "description": "Platelet factor V deficiency (factor V Quebec) (disorder)"
        },
        {
          "id": 534178,
          "code": "128102001",
          "description": "Familial alpha>2< adrenergic receptor defect in platelets (disorder)"
        },
        {
          "id": 534179,
          "code": "128103006",
          "description": "Isolated collagen aggregation defect (disorder)"
        },
        {
          "id": 534180,
          "code": "128105004",
          "description": "von Willebrand disorder (disorder)"
        },
        {
          "id": 534181,
          "code": "128106003",
          "description": "von Willebrand disease type 1 (disorder)"
        },
        {
          "id": 534182,
          "code": "128107007",
          "description": "von Willebrand disease type 2 (disorder)"
        },
        {
          "id": 534183,
          "code": "128108002",
          "description": "von Willebrand disease type 3 (disorder)"
        },
        {
          "id": 534184,
          "code": "128113003",
          "description": "von Willebrand disease type IB (disorder)"
        },
        {
          "id": 534185,
          "code": "128114009",
          "description": "von Willebrand disease type IC (disorder)"
        },
        {
          "id": 534186,
          "code": "128115005",
          "description": "Pseudo von Willebrand disease (disorder)"
        },
        {
          "id": 534187,
          "code": "129640007",
          "description": "Benign granulocytopenia in childhood (disorder)"
        },
        {
          "id": 534188,
          "code": "129641006",
          "description": "Chronic benign neutropenia of childhood (disorder)"
        },
        {
          "id": 534189,
          "code": "129642004",
          "description": "Chronic idiopathic immunoneutropenia in adults (disorder)"
        },
        {
          "id": 534190,
          "code": "129643009",
          "description": "Chronic hypoplastic neutropenia (disorder)"
        },
        {
          "id": 534191,
          "code": "129645002",
          "description": "Adult glucose-6-phosphate dehydrogenase deficiency of leukocytes syndrome (disorder)"
        },
        {
          "id": 534192,
          "code": "129654004",
          "description": "Acquired platelet factor 3 disease (disorder)"
        },
        {
          "id": 534193,
          "code": "13172003",
          "description": "Chronic idiopathic thrombocytopenic purpura (disorder)"
        },
        {
          "id": 534194,
          "code": "13886001",
          "description": "Sickle cell nephropathy (disorder)"
        },
        {
          "id": 534195,
          "code": "13993001",
          "description": "Factor XIII inhibitor disorder (disorder)"
        },
        {
          "id": 534196,
          "code": "14087004",
          "description": "Hereditary stomatocytosis (disorder)"
        },
        {
          "id": 534197,
          "code": "14126008",
          "description": "Autosomal-linked pyridoxine refractory sideroblastic anemia (disorder)"
        },
        {
          "id": 534198,
          "code": "143101000119101",
          "description": "Hemochromatosis following repeated red blood cell transfusion (disorder)"
        },
        {
          "id": 534199,
          "code": "14514008",
          "description": "Anemia due to disturbance of hemoglobin synthesis (disorder)"
        },
        {
          "id": 534200,
          "code": "15121005",
          "description": "Hereditary elliptocytosis due to glycophorin C deficiency (disorder)"
        },
        {
          "id": 534201,
          "code": "154818001",
          "description": "Congenital afibrinogenemia (disorder)"
        },
        {
          "id": 534202,
          "code": "154826009",
          "description": "Secondary thrombocytopenia (disorder)"
        },
        {
          "id": 534203,
          "code": "1563006",
          "description": "Protein S deficiency disease (disorder)"
        },
        {
          "id": 534204,
          "code": "16360009",
          "description": "Delta beta thalassemia (disorder)"
        },
        {
          "id": 534205,
          "code": "16427007",
          "description": "Delta thalassemia (disorder)"
        },
        {
          "id": 534206,
          "code": "16773005",
          "description": "Drug-induced coagulation inhibitor disorder (disorder)"
        },
        {
          "id": 534207,
          "code": "16872008",
          "description": "Severe hereditary factor VIII deficiency disease (disorder)"
        },
        {
          "id": 534208,
          "code": "16922007",
          "description": "Hereditary coagulation factor deficiency (disorder)"
        },
        {
          "id": 534209,
          "code": "16964007",
          "description": "Hereditary persistence of fetal hemoglobin thalassemia (disorder)"
        },
        {
          "id": 534210,
          "code": "17342003",
          "description": "Familial erythrocytosis (disorder)"
        },
        {
          "id": 534211,
          "code": "1801000119106",
          "description": "Anemia, pre-end stage renal disease on erythropoietin protocol (disorder)"
        },
        {
          "id": 534212,
          "code": "180481005",
          "description": "Anti-factor II disorder (disorder)"
        },
        {
          "id": 534213,
          "code": "181456001",
          "description": "Antiprothrombin disorder (disorder)"
        },
        {
          "id": 534214,
          "code": "18273004",
          "description": "Unstable hemoglobin disease (disorder)"
        },
        {
          "id": 534215,
          "code": "18604004",
          "description": "Factor XIII deficiency disease (disorder)"
        },
        {
          "id": 534216,
          "code": "18662002",
          "description": "Acquired Heinz body anemia (disorder)"
        },
        {
          "id": 534217,
          "code": "1908008",
          "description": "von Willebrand disease, type IIC (disorder)"
        },
        {
          "id": 534218,
          "code": "190846002",
          "description": "Hemosiderosis, primary (disorder)"
        },
        {
          "id": 534219,
          "code": "190847006",
          "description": "Hemosiderosis, acquired (disorder)"
        },
        {
          "id": 534220,
          "code": "191169008",
          "description": "Hereditary elliptocytosis (disorder)"
        },
        {
          "id": 534221,
          "code": "191170009",
          "description": "Hemolytic anemia due to glutathione metabolism disorder (disorder)"
        },
        {
          "id": 534222,
          "code": "191172001",
          "description": "Favism (disorder)"
        },
        {
          "id": 534223,
          "code": "191177007",
          "description": "Hemolytic anemia due to hexokinase deficiency (disorder)"
        },
        {
          "id": 534224,
          "code": "191178002",
          "description": "Hemolytic anemia due to pyruvate kinase deficiency (disorder)"
        },
        {
          "id": 534225,
          "code": "191179005",
          "description": "Hemolytic anemia due to triose phosphate isomerase deficiency (disorder)"
        },
        {
          "id": 534226,
          "code": "191180008",
          "description": "Anemia due to disorders of nucleotide metabolism (disorder)"
        },
        {
          "id": 534227,
          "code": "191202009",
          "description": "Hemoglobin Zurich disease (disorder)"
        },
        {
          "id": 534228,
          "code": "191260004",
          "description": "Pyridoxine-responsive sideroblastic anemia (disorder)"
        },
        {
          "id": 534229,
          "code": "191261000",
          "description": "Secondary sideroblastic anemia due to disease (disorder)"
        },
        {
          "id": 534230,
          "code": "191296000",
          "description": "Deficiency of coagulation factor due to liver disease (disorder)"
        },
        {
          "id": 534231,
          "code": "191297009",
          "description": "Deficiency of coagulation factor due to vitamin K deficiency (disorder)"
        },
        {
          "id": 534232,
          "code": "191338000",
          "description": "Primary splenic neutropenia (disorder)"
        },
        {
          "id": 534233,
          "code": "191347008",
          "description": "Cyclical neutropenia (disorder)"
        },
        {
          "id": 534234,
          "code": "191382009",
          "description": "Chronic congestive splenomegaly (disorder)"
        },
        {
          "id": 534235,
          "code": "191388008",
          "description": "Familial methemoglobinemia (disorder)"
        },
        {
          "id": 534236,
          "code": "191389000",
          "description": "Idiopathic methemoglobinemia (disorder)"
        },
        {
          "id": 534237,
          "code": "19267009",
          "description": "Lupus anticoagulant disorder (disorder)"
        },
        {
          "id": 534238,
          "code": "193370005",
          "description": "Proliferative retinopathy due to sickle cell disease (disorder)"
        },
        {
          "id": 534239,
          "code": "19520006",
          "description": "von Willebrand disease, type IIB (disorder)"
        },
        {
          "id": 534240,
          "code": "203486002",
          "description": "Osteonecrosis due to hemoglobinopathy (disorder)"
        },
        {
          "id": 534241,
          "code": "21112004",
          "description": "Vascular hemostatic disease (disorder)"
        },
        {
          "id": 534242,
          "code": "21412009",
          "description": "X chromosome-linked pyridoxine refractory sideroblastic anemia (disorder)"
        },
        {
          "id": 534243,
          "code": "21914002",
          "description": "Anemia of thyroid dysfunction (disorder)"
        },
        {
          "id": 534244,
          "code": "22347002",
          "description": "Anemia of gonadal dysfunction (disorder)"
        },
        {
          "id": 534245,
          "code": "22716005",
          "description": "Platelet disorder (disorder)"
        },
        {
          "id": 534246,
          "code": "22933009",
          "description": "Glucose-6-phosphate dehydrogenase deficiency class I variant anemia (disorder)"
        },
        {
          "id": 534247,
          "code": "232033003",
          "description": "Sickle cell-hemoglobin C retinopathy (disorder)"
        },
        {
          "id": 534248,
          "code": "23269001",
          "description": "Double heterozygous sickling disorder (disorder)"
        },
        {
          "id": 534249,
          "code": "23371004",
          "description": "Epsilon gamma delta beta thalassemia (disorder)"
        },
        {
          "id": 534250,
          "code": "234345001",
          "description": "von Jaksch's anemia (disorder)"
        },
        {
          "id": 534251,
          "code": "234365008",
          "description": "Thiamine-responsive macrocytosis (disorder)"
        },
        {
          "id": 534252,
          "code": "234366009",
          "description": "Alcohol-related sideroblastic anemia (disorder)"
        },
        {
          "id": 534253,
          "code": "234367000",
          "description": "Pancytopenia with pancreatitis (disorder)"
        },
        {
          "id": 534254,
          "code": "234373004",
          "description": "Constitutional red cell hypoplasia (disorder)"
        },
        {
          "id": 534255,
          "code": "234383000",
          "description": "Homozygous alpha thalassemia (disorder)"
        },
        {
          "id": 534256,
          "code": "234388009",
          "description": "Delta-beta-Lepore thalassemia (disorder)"
        },
        {
          "id": 534257,
          "code": "234389001",
          "description": "Alpha-beta thalassemia (disorder)"
        },
        {
          "id": 534258,
          "code": "234390005",
          "description": "Gamma thalassemia (disorder)"
        },
        {
          "id": 534259,
          "code": "234391009",
          "description": "Sickle cell anemia with high hemoglobin F (disorder)"
        },
        {
          "id": 534260,
          "code": "234392002",
          "description": "Hemoglobin E/beta thalassemia disease (disorder)"
        },
        {
          "id": 534261,
          "code": "234394001",
          "description": "High affinity hemoglobin (disorder)"
        },
        {
          "id": 534262,
          "code": "234395000",
          "description": "Congenital methemoglobinaema with defective methemoglobin-reducing system (disorder)"
        },
        {
          "id": 534263,
          "code": "234396004",
          "description": "Congenital methemoglobinemia with abnormal methemoglobins (disorder)"
        },
        {
          "id": 534264,
          "code": "234401000",
          "description": "Erythrocyte enzyme deficiency (disorder)"
        },
        {
          "id": 534265,
          "code": "234402007",
          "description": "Chronic non-spherocytic hemolytic anemia (disorder)"
        },
        {
          "id": 534266,
          "code": "234404008",
          "description": "Glucose phosphate isomerase deficiency (disorder)"
        },
        {
          "id": 534267,
          "code": "234405009",
          "description": "Triose phosphate isomerase deficiency (disorder)"
        },
        {
          "id": 534268,
          "code": "234407001",
          "description": "Uridine monophosphate hydrolase deficiency (disorder)"
        },
        {
          "id": 534269,
          "code": "234408006",
          "description": "Adenosine deaminase overproduction (disorder)"
        },
        {
          "id": 534270,
          "code": "234410008",
          "description": "Hereditary elliptocytosis with transient poikilocytosis (disorder)"
        },
        {
          "id": 534271,
          "code": "234411007",
          "description": "Blood group deletion syndrome (disorder)"
        },
        {
          "id": 534272,
          "code": "234418001",
          "description": "Chronic benign granulocytopenia (disorder)"
        },
        {
          "id": 534273,
          "code": "234423001",
          "description": "Chronic benign neutropenia (disorder)"
        },
        {
          "id": 534274,
          "code": "234424007",
          "description": "Metabolic neutropenia (disorder)"
        },
        {
          "id": 534275,
          "code": "234425008",
          "description": "Autoimmune neutropenia (disorder)"
        },
        {
          "id": 534276,
          "code": "234440005",
          "description": "Factor VIII deficiency (disorder)"
        },
        {
          "id": 534277,
          "code": "234441009",
          "description": "Carrier of hereditary factor VIII deficiency disease (finding)"
        },
        {
          "id": 534278,
          "code": "234442002",
          "description": "Hereditary factor VIII deficiency disease with inhibitor (disorder)"
        },
        {
          "id": 534279,
          "code": "234444001",
          "description": "Congenital factor IX deficiency variant (disorder)"
        },
        {
          "id": 534280,
          "code": "234445000",
          "description": "Congenital factor IX deficiency with inhibitor (disorder)"
        },
        {
          "id": 534281,
          "code": "234446004",
          "description": "Congenital von Willebrand's disease (disorder)"
        },
        {
          "id": 534282,
          "code": "234447008",
          "description": "Congenital von Willebrand's disease type I (disorder)"
        },
        {
          "id": 534283,
          "code": "234448003",
          "description": "Congenital von Willebrand's disease type II (disorder)"
        },
        {
          "id": 534284,
          "code": "234450006",
          "description": "Congenital von Willebrand's disease type III (disorder)"
        },
        {
          "id": 534285,
          "code": "234451005",
          "description": "Acquired von Willebrand's disease (disorder)"
        },
        {
          "id": 534286,
          "code": "234453008",
          "description": "Passovoy factor deficiency (disorder)"
        },
        {
          "id": 534287,
          "code": "234454002",
          "description": "Prothrombin complex deficiency (disorder)"
        },
        {
          "id": 534288,
          "code": "234455001",
          "description": "Fibrinogen abnormality (disorder)"
        },
        {
          "id": 534289,
          "code": "234456000",
          "description": "Congenital fibrinogen abnormality (disorder)"
        },
        {
          "id": 534290,
          "code": "234457009",
          "description": "Hypofibrinogenemia (disorder)"
        },
        {
          "id": 534291,
          "code": "234458004",
          "description": "Hypodysfibrinogenemia (disorder)"
        },
        {
          "id": 534292,
          "code": "234459007",
          "description": "Alpha chain defect dysfibrinogenemia (disorder)"
        },
        {
          "id": 534293,
          "code": "234460002",
          "description": "Beta chain defect dysfibrinogenemia (disorder)"
        },
        {
          "id": 534294,
          "code": "234461003",
          "description": "Gamma chain defect dysfibrinogenemia (disorder)"
        },
        {
          "id": 534295,
          "code": "234463000",
          "description": "Combined coagulation factor deficiency (disorder)"
        },
        {
          "id": 534296,
          "code": "234466008",
          "description": "Acquired coagulation disorder (disorder)"
        },
        {
          "id": 534297,
          "code": "234467004",
          "description": "Thrombophilia (disorder)"
        },
        {
          "id": 534298,
          "code": "234468009",
          "description": "Heparin cofactor II deficiency (disorder)"
        },
        {
          "id": 534299,
          "code": "234470000",
          "description": "Platelet membrane defect (disorder)"
        },
        {
          "id": 534300,
          "code": "234471001",
          "description": "Glycoprotein Ia defect (disorder)"
        },
        {
          "id": 534301,
          "code": "234472008",
          "description": "Glycoprotein Ib defect (disorder)"
        },
        {
          "id": 534302,
          "code": "234473003",
          "description": "Platelet type von Willebrand's disease (disorder)"
        },
        {
          "id": 534303,
          "code": "234474009",
          "description": "Dense body defect (disorder)"
        },
        {
          "id": 534304,
          "code": "234475005",
          "description": "Thromboxane generation defect (disorder)"
        },
        {
          "id": 534305,
          "code": "234476006",
          "description": "Cyclooxygenase deficiency (disorder)"
        },
        {
          "id": 534306,
          "code": "234477002",
          "description": "Thromboxane synthetase deficiency (disorder)"
        },
        {
          "id": 534307,
          "code": "234478007",
          "description": "Giant platelet syndrome (disorder)"
        },
        {
          "id": 534308,
          "code": "234479004",
          "description": "Acquired platelet disorder (disorder)"
        },
        {
          "id": 534309,
          "code": "234482009",
          "description": "Amegakaryocytic thrombocytopenia (disorder)"
        },
        {
          "id": 534310,
          "code": "234483004",
          "description": "Megakaryocytic thrombocytopenia (disorder)"
        },
        {
          "id": 534311,
          "code": "234485006",
          "description": "Epstein syndrome (disorder)"
        },
        {
          "id": 534312,
          "code": "234486007",
          "description": "Montreal platelet syndrome (disorder)"
        },
        {
          "id": 534313,
          "code": "234487003",
          "description": "Mediterranean thrombocytopenia (disorder)"
        },
        {
          "id": 534314,
          "code": "234496003",
          "description": "Metabolic purpura (disorder)"
        },
        {
          "id": 534315,
          "code": "234511009",
          "description": "Post-splenectomy disorder (disorder)"
        },
        {
          "id": 534316,
          "code": "234513007",
          "description": "Post-splenectomy leukocytosis (disorder)"
        },
        {
          "id": 534317,
          "code": "234576008",
          "description": "Chronic familial neutropenia (disorder)"
        },
        {
          "id": 534318,
          "code": "234605000",
          "description": "Factor B deficiency (disorder)"
        },
        {
          "id": 534319,
          "code": "234621005",
          "description": "Factor I deficiency (disorder)"
        },
        {
          "id": 534320,
          "code": "236422008",
          "description": "Fechtner syndrome (disorder)"
        },
        {
          "id": 534321,
          "code": "23761004",
          "description": "Hyposplenism (disorder)"
        },
        {
          "id": 534322,
          "code": "237985009",
          "description": "Pearson's syndrome (disorder)"
        },
        {
          "id": 534323,
          "code": "239892009",
          "description": "Primary antiphospholipid syndrome (disorder)"
        },
        {
          "id": 534324,
          "code": "239894005",
          "description": "Primary antiphospholipid syndrome with multisystem involvement (disorder)"
        },
        {
          "id": 534325,
          "code": "239895006",
          "description": "Secondary antiphospholipid syndrome (disorder)"
        },
        {
          "id": 534326,
          "code": "239897003",
          "description": "Secondary antiphospholipid syndrome with multisystem involvement (disorder)"
        },
        {
          "id": 534327,
          "code": "24661004",
          "description": "Glucose-6-phosphate dehydrogenase deficiency class III variant anemia (disorder)"
        },
        {
          "id": 534328,
          "code": "24663001",
          "description": "von Willebrand disease, type IIH (disorder)"
        },
        {
          "id": 534329,
          "code": "247860002",
          "description": "Familial neutropenia (disorder)"
        },
        {
          "id": 534330,
          "code": "248693006",
          "description": "Chronic idiopathic neutropenia (disorder)"
        },
        {
          "id": 534331,
          "code": "24974008",
          "description": "Myelokathexis (disorder)"
        },
        {
          "id": 534332,
          "code": "24975009",
          "description": "Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin (disorder)"
        },
        {
          "id": 534333,
          "code": "25065001",
          "description": "Hemoglobin E disease (disorder)"
        },
        {
          "id": 534334,
          "code": "25251008",
          "description": "Hereditary nonspherocytic hemolytic anemia due to gamma glutamyl cysteine synthetase deficiency (disorder)"
        },
        {
          "id": 534335,
          "code": "25266006",
          "description": "Hereditary spherocytosis due to spectrin deficiency (disorder)"
        },
        {
          "id": 534336,
          "code": "25443007",
          "description": "X chromosome-linked pyridoxine responsive sideroblastic anemia (disorder)"
        },
        {
          "id": 534337,
          "code": "25472008",
          "description": "Sickle cell-hemoglobin D disease (disorder)"
        },
        {
          "id": 534338,
          "code": "26029002",
          "description": "Mild hereditary factor VIII deficiency disease (disorder)"
        },
        {
          "id": 534339,
          "code": "26409005",
          "description": "Congenital dyserythropoietic anemia, type III (disorder)"
        },
        {
          "id": 534340,
          "code": "267524009",
          "description": "Constitutional aplastic anemia with malformation (disorder)"
        },
        {
          "id": 534341,
          "code": "267525005",
          "description": "Constitutional red cell aplasia and hypoplasia (disorder)"
        },
        {
          "id": 534342,
          "code": "267532001",
          "description": "Qualitative platelet disorder (disorder)"
        },
        {
          "id": 534343,
          "code": "267534000",
          "description": "Primary thrombocytopenia (disorder)"
        },
        {
          "id": 534344,
          "code": "267535004",
          "description": "Congenital thrombocytopenic purpura (disorder)"
        },
        {
          "id": 534345,
          "code": "267540007",
          "description": "Neutropenia caused by irradiation (disorder)"
        },
        {
          "id": 534346,
          "code": "267550008",
          "description": "Congenital methemoglobinemia (disorder)"
        },
        {
          "id": 534347,
          "code": "26843008",
          "description": "Antiphospholipid syndrome (disorder)"
        },
        {
          "id": 534348,
          "code": "2694001",
          "description": "Myelophthisic anemia (disorder)"
        },
        {
          "id": 534349,
          "code": "270117002",
          "description": "Platelet type pseudo-von Willebrand disease (disorder)"
        },
        {
          "id": 534350,
          "code": "275325009",
          "description": "Arthropathy secondary to hemoglobinopathy (disorder)"
        },
        {
          "id": 534351,
          "code": "275523003",
          "description": "Pancytopenia-dysmelia (disorder)"
        },
        {
          "id": 534352,
          "code": "276448005",
          "description": "Idiopathic sideroblastic anemia (disorder)"
        },
        {
          "id": 534353,
          "code": "278504009",
          "description": "Afibrinogenemia (disorder)"
        },
        {
          "id": 534354,
          "code": "282707003",
          "description": "Acquired inhibitor of coagulation (disorder)"
        },
        {
          "id": 534355,
          "code": "28293008",
          "description": "Hereditary factor VIII deficiency disease (disorder)"
        },
        {
          "id": 534356,
          "code": "2897005",
          "description": "Immune thrombocytopenia (disorder)"
        },
        {
          "id": 534357,
          "code": "28975000",
          "description": "Constitutional aplastic anemia (disorder)"
        },
        {
          "id": 534358,
          "code": "29177004",
          "description": "Anemia due to pentose phosphate pathway defect (disorder)"
        },
        {
          "id": 534359,
          "code": "295315008",
          "description": "Acquired methemoglobinemia (disorder)"
        },
        {
          "id": 534360,
          "code": "29551000",
          "description": "Anemia caused by oxygen (disorder)"
        },
        {
          "id": 534361,
          "code": "296332004",
          "description": "Acquired storage pool deficiency (platelets) (disorder)"
        },
        {
          "id": 534362,
          "code": "301317008",
          "description": "Hereditary nonspherocytic hemolytic anemia (disorder)"
        },
        {
          "id": 534363,
          "code": "302215000",
          "description": "Thrombocytopenic disorder (disorder)"
        },
        {
          "id": 534364,
          "code": "302873008",
          "description": "Thrombocytopenic purpura (disorder)"
        },
        {
          "id": 534365,
          "code": "303011007",
          "description": "Neutropenic disorder (disorder)"
        },
        {
          "id": 534366,
          "code": "303266002",
          "description": "Aplastic bone marrow (disorder)"
        },
        {
          "id": 534367,
          "code": "304132006",
          "description": "Hematopoietic aplasia (disorder)"
        },
        {
          "id": 534368,
          "code": "30418008",
          "description": "Anemia of adrenal dysfunction (disorder)"
        },
        {
          "id": 534369,
          "code": "30575002",
          "description": "Fanconi's anemia (disorder)"
        },
        {
          "id": 534370,
          "code": "306058006",
          "description": "Aplastic anemia (disorder)"
        },
        {
          "id": 534371,
          "code": "307091009",
          "description": "Factor V Leiden mutation (disorder)"
        },
        {
          "id": 534372,
          "code": "307115002",
          "description": "Homozygous Factor V Leiden mutation (disorder)"
        },
        {
          "id": 534373,
          "code": "307116001",
          "description": "Heterozygous Factor V Leiden mutation (disorder)"
        },
        {
          "id": 534374,
          "code": "307343001",
          "description": "Acquired hemoglobin H disease (disorder)"
        },
        {
          "id": 534375,
          "code": "307514008",
          "description": "Idiopathic factor VIII deficiency (disorder)"
        },
        {
          "id": 534376,
          "code": "307515009",
          "description": "Autoimmune factor VIII deficiency (disorder)"
        },
        {
          "id": 534377,
          "code": "307517001",
          "description": "Pregnancy-related factor VIII deficiency (disorder)"
        },
        {
          "id": 534378,
          "code": "307518006",
          "description": "Malignancy-related factor VIII deficiency (disorder)"
        },
        {
          "id": 534379,
          "code": "30913008",
          "description": "Disorder of iron metabolism (disorder)"
        },
        {
          "id": 534380,
          "code": "31820007",
          "description": "Anemia of endocrine disorder (disorder)"
        },
        {
          "id": 534381,
          "code": "31925001",
          "description": "Hereditary factor I deficiency disease (disorder)"
        },
        {
          "id": 534382,
          "code": "322699009",
          "description": "Intracorpuscular hemolytic anemia (disorder)"
        },
        {
          "id": 534383,
          "code": "32273002",
          "description": "Idiopathic thrombocytopenic purpura (disorder)"
        },
        {
          "id": 534384,
          "code": "323666000",
          "description": "Anemia due to intrinsic red cell abnormality (disorder)"
        },
        {
          "id": 534385,
          "code": "32648007",
          "description": "Mild hereditary spherocytosis due to spectrin deficiency (disorder)"
        },
        {
          "id": 534386,
          "code": "32942005",
          "description": "Glanzmann's thrombasthenia (disorder)"
        },
        {
          "id": 534387,
          "code": "33169001",
          "description": "Factor XI deficiency, type II (disorder)"
        },
        {
          "id": 534388,
          "code": "33297000",
          "description": "Hereditary factor II deficiency disease (disorder)"
        },
        {
          "id": 534389,
          "code": "33344008",
          "description": "Moderate hereditary factor VIII deficiency disease (disorder)"
        },
        {
          "id": 534390,
          "code": "33905008",
          "description": "Hereditary spherocytosis due to deficiency of protein 4.2 (disorder)"
        },
        {
          "id": 534391,
          "code": "34194007",
          "description": "Hereditary nonspherocytic hemolytic anemia due to pyrimidine-5'-nucleotidase deficiency (disorder)"
        },
        {
          "id": 534392,
          "code": "343570008",
          "description": "Latent hemochromatosis (disorder)"
        },
        {
          "id": 534393,
          "code": "34395002",
          "description": "Thrombocytopenia caused by hypothermia (disorder)"
        },
        {
          "id": 534394,
          "code": "344587002",
          "description": "Precirrhotic hemochromatosis (disorder)"
        },
        {
          "id": 534395,
          "code": "34852006",
          "description": "Glucose-6-phosphate dehydrogenase deficiency class II variant anemia (disorder)"
        },
        {
          "id": 534396,
          "code": "35066007",
          "description": "von Willebrand disease, type IID (disorder)"
        },
        {
          "id": 534397,
          "code": "35400008",
          "description": "Hereditary hemochromatosis (disorder)"
        },
        {
          "id": 534398,
          "code": "35434009",
          "description": "Sickle cell-hemoglobin C disease (disorder)"
        },
        {
          "id": 534399,
          "code": "35554008",
          "description": "Acquired factor XI deficiency disease (disorder)"
        },
        {
          "id": 534400,
          "code": "359531004",
          "description": "Amegakaryocytic thrombocytopenia with congenital malformation (disorder)"
        },
        {
          "id": 534401,
          "code": "359536009",
          "description": "Megakaryocytic aplasia (disorder)"
        },
        {
          "id": 534402,
          "code": "359700009",
          "description": "Hereditary von Willebrand disease type IA (disorder)"
        },
        {
          "id": 534403,
          "code": "359704000",
          "description": "von Willebrand disease, type 1^a^ (disorder)"
        },
        {
          "id": 534404,
          "code": "359709005",
          "description": "von Willebrand disease type IA (disorder)"
        },
        {
          "id": 534405,
          "code": "359711001",
          "description": "Hereditary von Willebrand disease type 2A (disorder)"
        },
        {
          "id": 534406,
          "code": "359714009",
          "description": "von Willebrand disease type 2A (disorder)"
        },
        {
          "id": 534407,
          "code": "359717002",
          "description": "Hereditary von Willebrand disease type 2B (disorder)"
        },
        {
          "id": 534408,
          "code": "359721009",
          "description": "von Willebrand disease type 2B (disorder)"
        },
        {
          "id": 534409,
          "code": "359725000",
          "description": "Hereditary von Willebrand disease type 2M (disorder)"
        },
        {
          "id": 534410,
          "code": "359727008",
          "description": "Fibrinogen deficiency (disorder)"
        },
        {
          "id": 534411,
          "code": "359732009",
          "description": "von Willebrand disease type 2N (disorder)"
        },
        {
          "id": 534412,
          "code": "361209006",
          "description": "Dermite ocre of Favre (disorder)"
        },
        {
          "id": 534413,
          "code": "362970003",
          "description": "Disorder of hemostatic system (disorder)"
        },
        {
          "id": 534414,
          "code": "363041004",
          "description": "Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (disorder)"
        },
        {
          "id": 534415,
          "code": "36351005",
          "description": "Antithrombin III deficiency (disorder)"
        },
        {
          "id": 534416,
          "code": "36467003",
          "description": "Alpha plus thalassemia (disorder)"
        },
        {
          "id": 534417,
          "code": "36472007",
          "description": "Sickle cell-thalassemia disease (disorder)"
        },
        {
          "id": 534418,
          "code": "367061000119107",
          "description": "Priapism due to sickle cell disease (disorder)"
        },
        {
          "id": 534419,
          "code": "36799008",
          "description": "Glutamate-cysteine ligase deficiency (disorder)"
        },
        {
          "id": 534420,
          "code": "371074009",
          "description": "Radiation thrombocytopenia (disorder)"
        },
        {
          "id": 534421,
          "code": "371104006",
          "description": "Hand-foot syndrome in sickle cell anemia (disorder)"
        },
        {
          "id": 534422,
          "code": "37193007",
          "description": "Factor VII deficiency (disorder)"
        },
        {
          "id": 534423,
          "code": "372146004",
          "description": "Acute chest syndrome (disorder)"
        },
        {
          "id": 534424,
          "code": "37272000",
          "description": "Rh deficiency syndrome (disorder)"
        },
        {
          "id": 534425,
          "code": "37350004",
          "description": "Hereditary factor X deficiency disease (disorder)"
        },
        {
          "id": 534426,
          "code": "37492005",
          "description": "Sex-linked thrombocytopenia (disorder)"
        },
        {
          "id": 534427,
          "code": "3760002",
          "description": "Familial multiple factor deficiency syndrome, type V (disorder)"
        },
        {
          "id": 534428,
          "code": "38589006",
          "description": "Mixed hemoglobin disorder (disorder)"
        },
        {
          "id": 534429,
          "code": "387778001",
          "description": "Purpuric disorder (disorder)"
        },
        {
          "id": 534430,
          "code": "38911009",
          "description": "Hereditary hemolytic anemia (disorder)"
        },
        {
          "id": 534431,
          "code": "38959009",
          "description": "Methemoglobinemia (disorder)"
        },
        {
          "id": 534432,
          "code": "39011001",
          "description": "Hemosiderosis (disorder)"
        },
        {
          "id": 534433,
          "code": "3947004",
          "description": "High oxygen affinity hemoglobin polycythemia (disorder)"
        },
        {
          "id": 534434,
          "code": "39586009",
          "description": "Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia (disorder)"
        },
        {
          "id": 534435,
          "code": "39784009",
          "description": "Secondary hemosiderosis (disorder)"
        },
        {
          "id": 534436,
          "code": "399053004",
          "description": "Idiopathic hemochromatosis (disorder)"
        },
        {
          "id": 534437,
          "code": "399126000",
          "description": "Bronze cirrhosis (disorder)"
        },
        {
          "id": 534438,
          "code": "399144008",
          "description": "Bronze diabetes (disorder)"
        },
        {
          "id": 534439,
          "code": "399170009",
          "description": "Primary hemochromatosis (disorder)"
        },
        {
          "id": 534440,
          "code": "399187006",
          "description": "Hemochromatosis (disorder)"
        },
        {
          "id": 534441,
          "code": "40108008",
          "description": "Thalassemia (disorder)"
        },
        {
          "id": 534442,
          "code": "402653004",
          "description": "Thrombocytopenic purpura due to defective platelet production (disorder)"
        },
        {
          "id": 534443,
          "code": "402854008",
          "description": "Dysproteinemic purpura (disorder)"
        },
        {
          "id": 534444,
          "code": "402865003",
          "description": "Systemic lupus erythematosus-associated antiphospholipid syndrome (disorder)"
        },
        {
          "id": 534445,
          "code": "402920006",
          "description": "Papular purpuric gloves and socks syndrome (disorder)"
        },
        {
          "id": 534446,
          "code": "403261006",
          "description": "Skin pigmentation due to hemosiderosis (disorder)"
        },
        {
          "id": 534447,
          "code": "40855001",
          "description": "Hereditary factor VII deficiency disease (disorder)"
        },
        {
          "id": 534448,
          "code": "41106001",
          "description": "von Willebrand factor inhibitor disorder (disorder)"
        },
        {
          "id": 534449,
          "code": "413566007",
          "description": "Aplastic anemia associated with pancreatitis (disorder)"
        },
        {
          "id": 534450,
          "code": "413567003",
          "description": "Aplastic anemia associated with pregnancy (disorder)"
        },
        {
          "id": 534451,
          "code": "41387000",
          "description": "Hereditary nonspherocytic hemolytic anemia due to phosphofructokinase deficiency (disorder)"
        },
        {
          "id": 534452,
          "code": "414127000",
          "description": "Erythrocytosis due to polycythemia vera (disorder)"
        },
        {
          "id": 534453,
          "code": "41614006",
          "description": "Hypoplastic anemia (disorder)"
        },
        {
          "id": 534454,
          "code": "416180004",
          "description": "Hemoglobin SS disease without crisis (disorder)"
        },
        {
          "id": 534455,
          "code": "416214006",
          "description": "Sickle cell-hemoglobin D disease without crisis (disorder)"
        },
        {
          "id": 534456,
          "code": "416290001",
          "description": "Hemoglobin S sickling disorder without crisis (disorder)"
        },
        {
          "id": 534457,
          "code": "416484003",
          "description": "Sickle cell-hemoglobin E disease with crisis (disorder)"
        },
        {
          "id": 534458,
          "code": "416638004",
          "description": "Sickle cell-hemoglobin E disease without crisis (disorder)"
        },
        {
          "id": 534459,
          "code": "416826005",
          "description": "Sickle cell-thalassemia disease with crisis (disorder)"
        },
        {
          "id": 534460,
          "code": "41690001",
          "description": "Factor V inhibitor disorder (disorder)"
        },
        {
          "id": 534461,
          "code": "416902009",
          "description": "Uremic thrombocytopenia (disorder)"
        },
        {
          "id": 534462,
          "code": "417048006",
          "description": "Sickle cell-thalassemia disease without crisis (disorder)"
        },
        {
          "id": 534463,
          "code": "417279003",
          "description": "Hemoglobin S sickling disorder with crisis (disorder)"
        },
        {
          "id": 534464,
          "code": "417357006",
          "description": "Sickling disorder due to hemoglobin S (disorder)"
        },
        {
          "id": 534465,
          "code": "417425009",
          "description": "Hemoglobin SS disease with crisis (disorder)"
        },
        {
          "id": 534466,
          "code": "417517009",
          "description": "Sickle cell-hemoglobin C disease with crisis (disorder)"
        },
        {
          "id": 534467,
          "code": "417626001",
          "description": "Thrombocytopenic purpura associated with metabolic disorder (disorder)"
        },
        {
          "id": 534468,
          "code": "417672002",
          "description": "Granulocytopenic disorder (disorder)"
        },
        {
          "id": 534469,
          "code": "417683006",
          "description": "Sickle cell-hemoglobin C disease without crisis (disorder)"
        },
        {
          "id": 534470,
          "code": "417748003",
          "description": "Sickle cell-hemoglobin D disease with crisis (disorder)"
        },
        {
          "id": 534471,
          "code": "41788008",
          "description": "Hereditary factor IX deficiency disease (disorder)"
        },
        {
          "id": 534472,
          "code": "41814009",
          "description": "Neutropenia with dysgranulopoiesis (disorder)"
        },
        {
          "id": 534473,
          "code": "41841004",
          "description": "Sideroblastic anemia (disorder)"
        },
        {
          "id": 534474,
          "code": "421102007",
          "description": "Aplastic anemia associated with acquired immunodeficiency syndrome (disorder)"
        },
        {
          "id": 534475,
          "code": "421132004",
          "description": "Platelet dysfunction associated with uremia (disorder)"
        },
        {
          "id": 534476,
          "code": "421527008",
          "description": "Resistance to activated protein C caused by Factor V Leiden (disorder)"
        },
        {
          "id": 534477,
          "code": "421766003",
          "description": "Thrombocytopenia associated with acquired immunodeficiency syndrome (disorder)"
        },
        {
          "id": 534478,
          "code": "42484009",
          "description": "Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency (disorder)"
        },
        {
          "id": 534479,
          "code": "425949001",
          "description": "Mild hereditary factor VIII deficiency disease with inhibitor (disorder)"
        },
        {
          "id": 534480,
          "code": "42601008",
          "description": "Congenital hemolytic anemia (disorder)"
        },
        {
          "id": 534481,
          "code": "426199009",
          "description": "Congenital factor IX deficiency without inhibitor (disorder)"
        },
        {
          "id": 534482,
          "code": "427306008",
          "description": "Hereditary hemoglobinopathy (disorder)"
        },
        {
          "id": 534483,
          "code": "4320005",
          "description": "Factor V deficiency (disorder)"
        },
        {
          "id": 534484,
          "code": "43346008",
          "description": "Platelet procoagulant activity deficiency (disorder)"
        },
        {
          "id": 534485,
          "code": "438360006",
          "description": "Hereditary factor VIII deficiency disease without inhibitor (disorder)"
        },
        {
          "id": 534486,
          "code": "438372000",
          "description": "Hereditary factor IX deficiency disease with inhibitor (disorder)"
        },
        {
          "id": 534487,
          "code": "438373005",
          "description": "Severe hereditary factor VIII deficiency disease with inhibitor (disorder)"
        },
        {
          "id": 534488,
          "code": "438492008",
          "description": "Hereditary thrombocytopenic disorder (disorder)"
        },
        {
          "id": 534489,
          "code": "43858000",
          "description": "Secondary aplastic anemia (disorder)"
        },
        {
          "id": 534490,
          "code": "438599002",
          "description": "Moderate hereditary factor VIII deficiency disease with inhibitor (disorder)"
        },
        {
          "id": 534491,
          "code": "438792009",
          "description": "Hereditary factor IX deficiency disease without inhibitor (disorder)"
        },
        {
          "id": 534492,
          "code": "438827002",
          "description": "Hereditary thrombophilic dysfibrinogenemia (disorder)"
        },
        {
          "id": 534493,
          "code": "439000005",
          "description": "Hyperfibrinogenemia (disorder)"
        },
        {
          "id": 534494,
          "code": "439001009",
          "description": "Acquired thrombophilia (disorder)"
        },
        {
          "id": 534495,
          "code": "439002002",
          "description": "Thrombophilia due to acquired protein C deficiency (disorder)"
        },
        {
          "id": 534496,
          "code": "439125003",
          "description": "Thrombophilia due to acquired protein S deficiency (disorder)"
        },
        {
          "id": 534497,
          "code": "439126002",
          "description": "Thrombophilia due to acquired antithrombin III deficiency (disorder)"
        },
        {
          "id": 534498,
          "code": "439145006",
          "description": "Congenital hypofibrinogenemia (disorder)"
        },
        {
          "id": 534499,
          "code": "439156006",
          "description": "Acquired combined coagulation factor deficiency (disorder)"
        },
        {
          "id": 534500,
          "code": "439157002",
          "description": "Hereditary combined coagulation factor deficiency (disorder)"
        },
        {
          "id": 534501,
          "code": "439274008",
          "description": "Hereditary protein C deficiency (disorder)"
        },
        {
          "id": 534502,
          "code": "439455002",
          "description": "Hereditary factor XIII A subunit deficiency (disorder)"
        },
        {
          "id": 534503,
          "code": "439458000",
          "description": "Factor I deficiency disease (disorder)"
        },
        {
          "id": 534504,
          "code": "439459008",
          "description": "Hereditary factor XIII B subunit deficiency (disorder)"
        },
        {
          "id": 534505,
          "code": "439460003",
          "description": "Hereditary factor XIII A subunit and B subunit deficiency (disorder)"
        },
        {
          "id": 534506,
          "code": "439698008",
          "description": "Hereditary thrombophilia (disorder)"
        },
        {
          "id": 534507,
          "code": "439699000",
          "description": "Hereditary antithrombin III deficiency (disorder)"
        },
        {
          "id": 534508,
          "code": "439701000",
          "description": "Hereditary heparin cofactor II deficiency (disorder)"
        },
        {
          "id": 534509,
          "code": "439702007",
          "description": "Hereditary protein S deficiency (disorder)"
        },
        {
          "id": 534510,
          "code": "440206000",
          "description": "Hemoglobin SS disease with vasoocclusive crisis (disorder)"
        },
        {
          "id": 534511,
          "code": "440820004",
          "description": "Mild hereditary factor VIII deficiency disease without inhibitor (disorder)"
        },
        {
          "id": 534512,
          "code": "440866009",
          "description": "Severe hereditary factor IX deficiency disease with inhibitor (disorder)"
        },
        {
          "id": 534513,
          "code": "440867000",
          "description": "Moderate hereditary factor IX deficiency disease with inhibitor (disorder)"
        },
        {
          "id": 534514,
          "code": "440868005",
          "description": "Mild hereditary factor IX deficiency disease with inhibitor (disorder)"
        },
        {
          "id": 534515,
          "code": "440924009",
          "description": "Hereditary hyperfibrinogenemia (disorder)"
        },
        {
          "id": 534516,
          "code": "440988005",
          "description": "Heterozygous protein S deficiency (disorder)"
        },
        {
          "id": 534517,
          "code": "440989002",
          "description": "Prothrombin G20210A mutation (disorder)"
        },
        {
          "id": 534518,
          "code": "440993008",
          "description": "Severe hereditary factor VIII deficiency disease without inhibitor (disorder)"
        },
        {
          "id": 534519,
          "code": "441001005",
          "description": "Hereditary elevated factor XI (disorder)"
        },
        {
          "id": 534520,
          "code": "441006000",
          "description": "Moderate hereditary factor VIII deficiency disease without inhibitor (disorder)"
        },
        {
          "id": 534521,
          "code": "441042008",
          "description": "Hereditary elevated factor VIII (disorder)"
        },
        {
          "id": 534522,
          "code": "441079006",
          "description": "Thrombophilia due to antiphospholipid antibody (disorder)"
        },
        {
          "id": 534523,
          "code": "441101007",
          "description": "Heterozygous protein C deficiency (disorder)"
        },
        {
          "id": 534524,
          "code": "441134009",
          "description": "Congenital dysmegakaryopoietic thrombocytopenia, Paris Trousseau type (disorder)"
        },
        {
          "id": 534525,
          "code": "441188004",
          "description": "Homozygous protein C deficiency (disorder)"
        },
        {
          "id": 534526,
          "code": "441189007",
          "description": "Homozygous protein S deficiency (disorder)"
        },
        {
          "id": 534527,
          "code": "441190003",
          "description": "Severe hereditary factor IX deficiency disease without inhibitor (disorder)"
        },
        {
          "id": 534528,
          "code": "441191004",
          "description": "Moderate hereditary factor IX deficiency disease without inhibitor (disorder)"
        },
        {
          "id": 534529,
          "code": "441192006",
          "description": "Mild hereditary factor IX deficiency disease without inhibitor (disorder)"
        },
        {
          "id": 534530,
          "code": "441420000",
          "description": "Homozygous prothrombin G20210A mutation (disorder)"
        },
        {
          "id": 534531,
          "code": "441421001",
          "description": "Heterozygous prothrombin G20210A mutation (disorder)"
        },
        {
          "id": 534532,
          "code": "441762006",
          "description": "Thrombophilia due to immobilization (disorder)"
        },
        {
          "id": 534533,
          "code": "441945008",
          "description": "Thrombophilia due to trauma (disorder)"
        },
        {
          "id": 534534,
          "code": "441990004",
          "description": "Thrombophilia due to paroxysmal nocturnal hemoglobinuria (disorder)"
        },
        {
          "id": 534535,
          "code": "442078001",
          "description": "Thrombophilia due to malignant neoplasm (disorder)"
        },
        {
          "id": 534536,
          "code": "442121006",
          "description": "Thrombophilia due to vascular anomaly (disorder)"
        },
        {
          "id": 534537,
          "code": "442197003",
          "description": "Thrombophilia caused by drug therapy (disorder)"
        },
        {
          "id": 534538,
          "code": "442363001",
          "description": "Thrombophilia caused by vascular device (disorder)"
        },
        {
          "id": 534539,
          "code": "442654007",
          "description": "Thrombophilia caused by hormone therapy (disorder)"
        },
        {
          "id": 534540,
          "code": "442760001",
          "description": "Thrombophilia caused by antineoplastic agent therapy (disorder)"
        },
        {
          "id": 534541,
          "code": "443230004",
          "description": "Myeloid metaplasia (disorder)"
        },
        {
          "id": 534542,
          "code": "444108000",
          "description": "Acute sickle cell splenic sequestration crisis (disorder)"
        },
        {
          "id": 534543,
          "code": "444271000",
          "description": "Erythropoietin resistance in anemia of chronic kidney disease (disorder)"
        },
        {
          "id": 534544,
          "code": "44641000",
          "description": "Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder)"
        },
        {
          "id": 534545,
          "code": "447117006",
          "description": "Hemoglobin H constant spring thalassemia (disorder)"
        },
        {
          "id": 534546,
          "code": "45366001",
          "description": "Hereditary dysfibrinogenemia (disorder)"
        },
        {
          "id": 534547,
          "code": "45963004",
          "description": "Factor XI deficiency, type III (disorder)"
        },
        {
          "id": 534548,
          "code": "46760003",
          "description": "Estren-Dameshek anemia (disorder)"
        },
        {
          "id": 534549,
          "code": "47024008",
          "description": "Sickle cell-hemoglobin E disease (disorder)"
        },
        {
          "id": 534550,
          "code": "47047009",
          "description": "Thalassemia with other hemoglobinopathy (disorder)"
        },
        {
          "id": 534551,
          "code": "471863000",
          "description": "Disorder of myocardium due to sickle cell hemoglobinopathy (disorder)"
        },
        {
          "id": 534552,
          "code": "47307007",
          "description": "Factor VIII inhibitor disorder (disorder)"
        },
        {
          "id": 534553,
          "code": "47516005",
          "description": "Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin (disorder)"
        },
        {
          "id": 534554,
          "code": "47526003",
          "description": "Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder)"
        },
        {
          "id": 534555,
          "code": "47844003",
          "description": "Megaloblastic anemia due to chronic hemolytic anemia (disorder)"
        },
        {
          "id": 534556,
          "code": "48250002",
          "description": "Gaisbock's syndrome (disorder)"
        },
        {
          "id": 534557,
          "code": "48553001",
          "description": "Hemoglobin H disease (disorder)"
        },
        {
          "id": 534558,
          "code": "48788004",
          "description": "Cyclic thrombocytopenia (disorder)"
        },
        {
          "id": 534559,
          "code": "48983004",
          "description": "X chromosome-linked sideroblastic anemia (disorder)"
        },
        {
          "id": 534560,
          "code": "49762007",
          "description": "Hereditary factor XI deficiency disease (disorder)"
        },
        {
          "id": 534561,
          "code": "50189006",
          "description": "Hereditary factor XIII deficiency disease (disorder)"
        },
        {
          "id": 534562,
          "code": "50855007",
          "description": "Juvenile hemochromatosis (disorder)"
        },
        {
          "id": 534563,
          "code": "51053007",
          "description": "Hemoglobin C disease (disorder)"
        },
        {
          "id": 534564,
          "code": "51448009",
          "description": "Platelet secretory disorder (disorder)"
        },
        {
          "id": 534565,
          "code": "51720005",
          "description": "Gray platelet syndrome (disorder)"
        },
        {
          "id": 534566,
          "code": "52137009",
          "description": "von Willebrand disease, type IIE (disorder)"
        },
        {
          "id": 534567,
          "code": "52212006",
          "description": "Hereditary nonspherocytic hemolytic anemia due to glutathione reductase deficiency (disorder)"
        },
        {
          "id": 534568,
          "code": "52413004",
          "description": "Hereditary nonspherocytic hemolytic anemia due to glucose phosphate isomerase deficiency (disorder)"
        },
        {
          "id": 534569,
          "code": "52951008",
          "description": "Congenital dyserythropoietic anemia (disorder)"
        },
        {
          "id": 534570,
          "code": "5300004",
          "description": "Hemoglobin Bart's hydrops syndrome (disorder)"
        },
        {
          "id": 534571,
          "code": "5315003",
          "description": "Hereditary nonspherocytic hemolytic anemia due to increased adenosine deaminase activity (disorder)"
        },
        {
          "id": 534572,
          "code": "53836006",
          "description": "Secondary hemochromatosis (disorder)"
        },
        {
          "id": 534573,
          "code": "54006005",
          "description": "Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder)"
        },
        {
          "id": 534574,
          "code": "54569005",
          "description": "Bernard Soulier syndrome (disorder)"
        },
        {
          "id": 534575,
          "code": "55995005",
          "description": "Hereditary spherocytosis (disorder)"
        },
        {
          "id": 534792,
          "code": "95845002",
          "description": "Hereditary dysplasminogenemia (disorder)"
        },
        {
          "id": 534576,
          "code": "56941009",
          "description": "Restrictive cardiomyopathy secondary to hemochromatosis (disorder)"
        },
        {
          "id": 534577,
          "code": "57020009",
          "description": "Stokvis' disease (disorder)"
        },
        {
          "id": 534578,
          "code": "58327003",
          "description": "Factor I inhibitor disorder (disorder)"
        },
        {
          "id": 534579,
          "code": "58381000",
          "description": "Hypersplenism (disorder)"
        },
        {
          "id": 534580,
          "code": "58639003",
          "description": "Doan-Wiseman syndrome (disorder)"
        },
        {
          "id": 534581,
          "code": "5876000",
          "description": "Acquired pancytopenia (disorder)"
        },
        {
          "id": 534582,
          "code": "59106005",
          "description": "Anemia due to decreased red cell production (disorder)"
        },
        {
          "id": 534583,
          "code": "59548005",
          "description": "Congenital dyserythropoietic anemia, type I (disorder)"
        },
        {
          "id": 534584,
          "code": "59644002",
          "description": "Hereditary nonspherocytic hemolytic anemia due to phosphoglycerate kinase deficiency (disorder)"
        },
        {
          "id": 534585,
          "code": "5967006",
          "description": "A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis (disorder)"
        },
        {
          "id": 534586,
          "code": "5994005",
          "description": "Hereditary elliptocytosis due to deficiency of protein 4.1 (disorder)"
        },
        {
          "id": 534587,
          "code": "60138009",
          "description": "Anemia of pituitary deficiency (disorder)"
        },
        {
          "id": 534588,
          "code": "60628003",
          "description": "Mediterranean macrothrombocytopenia (disorder)"
        },
        {
          "id": 534589,
          "code": "60737008",
          "description": "Iron overload (disorder)"
        },
        {
          "id": 534590,
          "code": "60805002",
          "description": "Hemolytic anemia with emphysema AND cutis laxa (disorder)"
        },
        {
          "id": 534591,
          "code": "609329007",
          "description": "Catastrophic antiphospholipid syndrome (disorder)"
        },
        {
          "id": 534592,
          "code": "61261009",
          "description": "Hemolytic anemia (disorder)"
        },
        {
          "id": 534593,
          "code": "61395005",
          "description": "Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia (disorder)"
        },
        {
          "id": 534594,
          "code": "61551003",
          "description": "Familial multiple factor deficiency syndrome, type VI (disorder)"
        },
        {
          "id": 534595,
          "code": "6160004",
          "description": "Neonatal hemochromatosis (disorder)"
        },
        {
          "id": 534596,
          "code": "61777009",
          "description": "Thalassemia-hemoglobin C disease (disorder)"
        },
        {
          "id": 534597,
          "code": "61802005",
          "description": "Primary cryofibrinogenemia (disorder)"
        },
        {
          "id": 534598,
          "code": "62074008",
          "description": "Delta zero thalassemia (disorder)"
        },
        {
          "id": 534599,
          "code": "62268000",
          "description": "Hereditary nonspherocytic hemolytic anemia due to diphosphoglycerate mutase deficiency (disorder)"
        },
        {
          "id": 534600,
          "code": "62403005",
          "description": "Glucose-6-phosphate dehydrogenase deficiency anemia (disorder)"
        },
        {
          "id": 534601,
          "code": "63444004",
          "description": "Thrombocytopenia due to hypersplenism (disorder)"
        },
        {
          "id": 534602,
          "code": "64315007",
          "description": "Familial multiple factor deficiency syndrome, type III (disorder)"
        },
        {
          "id": 534603,
          "code": "64779008",
          "description": "Blood coagulation disorder (disorder)"
        },
        {
          "id": 534604,
          "code": "65623009",
          "description": "Immune neutropenia (disorder)"
        },
        {
          "id": 534605,
          "code": "65768009",
          "description": "Familial multiple factor deficiency syndrome, type II (disorder)"
        },
        {
          "id": 534606,
          "code": "66055002",
          "description": "Alpha zero thalassemia (disorder)"
        },
        {
          "id": 534607,
          "code": "66262001",
          "description": "Hereditary elliptocytosis due to beta spectrin-ankyrin interaction (disorder)"
        },
        {
          "id": 534608,
          "code": "66576001",
          "description": "African nutritional hemochromatosis (disorder)"
        },
        {
          "id": 534609,
          "code": "66729008",
          "description": "Hemoglobin D disease (disorder)"
        },
        {
          "id": 534610,
          "code": "66909001",
          "description": "Familial multiple factor deficiency syndrome, type IV (disorder)"
        },
        {
          "id": 534611,
          "code": "68870007",
          "description": "Congenital dyserythropoietic anemia, type II (disorder)"
        },
        {
          "id": 534612,
          "code": "68913001",
          "description": "Alpha thalassemia (disorder)"
        },
        {
          "id": 534613,
          "code": "691401000119104",
          "description": "Anemia co-occurrent and due to chronic kidney disease stage 4 (disorder)"
        },
        {
          "id": 534614,
          "code": "691411000119101",
          "description": "Anemia co-occurrent and due to chronic kidney disease stage 5 (disorder)"
        },
        {
          "id": 534615,
          "code": "691421000119108",
          "description": "Anemia co-occurrent and due to chronic kidney disease stage 3 (disorder)"
        },
        {
          "id": 534616,
          "code": "69216008",
          "description": "Hb Lepore thalassemia (disorder)"
        },
        {
          "id": 534617,
          "code": "6935003",
          "description": "Familial hemorrhagic diathesis (disorder)"
        },
        {
          "id": 534618,
          "code": "69574002",
          "description": "Anemia of parathyroid dysfunction (disorder)"
        },
        {
          "id": 534619,
          "code": "697908003",
          "description": "Pulmonary arterial hypertension associated with chronic hemolytic anemia (disorder)"
        },
        {
          "id": 534620,
          "code": "697919000",
          "description": "Pulmonary hypertension due to post-splenectomy hematological disorder (disorder)"
        },
        {
          "id": 534621,
          "code": "699208000",
          "description": "Thrombocytopenia caused by alcohol (disorder)"
        },
        {
          "id": 534622,
          "code": "69981004",
          "description": "Hereditary spherocytosis due to beta spectrin defect (disorder)"
        },
        {
          "id": 534623,
          "code": "700052007",
          "description": "Post-splenectomy sepsis (disorder)"
        },
        {
          "id": 534624,
          "code": "703135009",
          "description": "Anemia in malignant neoplastic disease (disorder)"
        },
        {
          "id": 534625,
          "code": "703148008",
          "description": "Periodontitis associated with chronic familial neutropenia (disorder)"
        },
        {
          "id": 534626,
          "code": "703280000",
          "description": "Hemosiderosis of lower limb due to venous insufficiency (disorder)"
        },
        {
          "id": 534627,
          "code": "703540008",
          "description": "Chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anemia and neutrophilic dermatosis (disorder)"
        },
        {
          "id": 534628,
          "code": "707323002",
          "description": "Anemia co-occurrent and due to chronic kidney disease (disorder)"
        },
        {
          "id": 534629,
          "code": "707324008",
          "description": "Anemia co-occurrent and due to end stage renal disease (disorder)"
        },
        {
          "id": 534630,
          "code": "707480001",
          "description": "Chronic hemolytic anemia (disorder)"
        },
        {
          "id": 534631,
          "code": "709142003",
          "description": "Arthropathy due to sickle cell disease (disorder)"
        },
        {
          "id": 534632,
          "code": "709535007",
          "description": "Periodontitis co-occurrent with infantile genetic agranulocytosis (disorder)"
        },
        {
          "id": 534633,
          "code": "709608008",
          "description": "Periodontitis co-occurrent with acquired neutropenia (disorder)"
        },
        {
          "id": 534634,
          "code": "710926008",
          "description": "Periodontitis co-occurrent with familial neutropenia (disorder)"
        },
        {
          "id": 534635,
          "code": "710927004",
          "description": "Periodontitis co-occurrent with cyclical neutropenia (disorder)"
        },
        {
          "id": 534636,
          "code": "711407000",
          "description": "Thrombocytopathy, asplenia and miosis (disorder)"
        },
        {
          "id": 534637,
          "code": "712922002",
          "description": "Myosin heavy chain 9 non muscle related disease (disorder)"
        },
        {
          "id": 534638,
          "code": "713388002",
          "description": "GATA binding protein 1 related thrombocytopenia with dyserythropoiesis (disorder)"
        },
        {
          "id": 534639,
          "code": "713508003",
          "description": "Aplastic anemia co-occurrent with human immunodeficiency virus infection (disorder)"
        },
        {
          "id": 534640,
          "code": "715342005",
          "description": "Alpha thalassemia X-linked intellectual disability syndrome (disorder)"
        },
        {
          "id": 534641,
          "code": "715526002",
          "description": "Dehydrated hereditary stomatocytosis (disorder)"
        },
        {
          "id": 534642,
          "code": "715559004",
          "description": "Combined deficiency of factor V and factor VIII (disorder)"
        },
        {
          "id": 534643,
          "code": "716336002",
          "description": "Congenital amegakaryocytic thrombocytopenia (disorder)"
        },
        {
          "id": 534644,
          "code": "716746003",
          "description": "Congenital alpha-2-antiplasmin deficiency (disorder)"
        },
        {
          "id": 534645,
          "code": "717050005",
          "description": "Autosomal recessive sideroblastic anemia (disorder)"
        },
        {
          "id": 534646,
          "code": "71723006",
          "description": "von Willebrand disease, type IIG (disorder)"
        },
        {
          "id": 534647,
          "code": "717254007",
          "description": "Familial pseudohyperkalemia (disorder)"
        },
        {
          "id": 534648,
          "code": "717407006",
          "description": "Congenital plasminogen activator inhibitor deficiency type 1 (disorder)"
        },
        {
          "id": 534649,
          "code": "717769007",
          "description": "MYH9 macrothrombocytopenia syndrome (disorder)"
        },
        {
          "id": 534650,
          "code": "717901001",
          "description": "Hypoparathyroidism due to hemochromatosis (disorder)"
        },
        {
          "id": 534651,
          "code": "717941005",
          "description": "Body skin hyperlaxity due to vitamin K dependent coagulation factor deficiency (disorder)"
        },
        {
          "id": 534652,
          "code": "718553004",
          "description": "White platelet syndrome (disorder)"
        },
        {
          "id": 534653,
          "code": "718554005",
          "description": "Medich giant platelet syndrome (disorder)"
        },
        {
          "id": 534654,
          "code": "718882006",
          "description": "X-linked severe congenital neutropenia (disorder)"
        },
        {
          "id": 534655,
          "code": "719019000",
          "description": "WT limb blood syndrome (disorder)"
        },
        {
          "id": 534656,
          "code": "719402008",
          "description": "Lethal hemolytic anemia and genital anomaly syndrome (disorder)"
        },
        {
          "id": 534657,
          "code": "719453009",
          "description": "Congenital dyserythropoietic anemia type IV (disorder)"
        },
        {
          "id": 534658,
          "code": "719816006",
          "description": "X-linked sideroblastic anemia with spinocerebellar ataxia (disorder)"
        },
        {
          "id": 534659,
          "code": "71988008",
          "description": "Aase syndrome (disorder)"
        },
        {
          "id": 534660,
          "code": "719974003",
          "description": "Hemochromatosis type 3 (disorder)"
        },
        {
          "id": 534661,
          "code": "719975002",
          "description": "Autosomal dominant hereditary hemochromatosis (disorder)"
        },
        {
          "id": 534662,
          "code": "720465002",
          "description": "Adult-onset autosomal recessive sideroblastic anemia (disorder)"
        },
        {
          "id": 534663,
          "code": "720521008",
          "description": "Autosomal dominant macrothrombocytopenia (disorder)"
        },
        {
          "id": 534664,
          "code": "720950009",
          "description": "Familial thrombocytosis (disorder)"
        },
        {
          "id": 534665,
          "code": "721303001",
          "description": "Refractory neutropenia (disorder)"
        },
        {
          "id": 534666,
          "code": "721304007",
          "description": "Refractory thrombocytopenia (disorder)"
        },
        {
          "id": 534667,
          "code": "72161000119100",
          "description": "Antiphospholipid syndrome in pregnancy (disorder)"
        },
        {
          "id": 534668,
          "code": "721840000",
          "description": "Hyperuricemia, anemia, renal failure syndrome (disorder)"
        },
        {
          "id": 534669,
          "code": "722085003",
          "description": "Renal papillary necrosis due to sickle cell disease (disorder)"
        },
        {
          "id": 534670,
          "code": "722125003",
          "description": "Overhydrated hereditary stomatocytosis (disorder)"
        },
        {
          "id": 534671,
          "code": "722147003",
          "description": "Focal segmental glomerulosclerosis due to sickle cell disease (disorder)"
        },
        {
          "id": 534672,
          "code": "722207000",
          "description": "Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome (disorder)"
        },
        {
          "id": 534673,
          "code": "722475006",
          "description": "X-linked congenital dyserythropoietic anemia with thrombocytopenia (disorder)"
        },
        {
          "id": 534674,
          "code": "72331000119105",
          "description": "Thalassemia in mother complicating pregnancy (disorder)"
        },
        {
          "id": 534675,
          "code": "723512008",
          "description": "Revesz syndrome (disorder)"
        },
        {
          "id": 534676,
          "code": "723623002",
          "description": "Southeast Asian ovalocytosis (disorder)"
        },
        {
          "id": 534677,
          "code": "723829000",
          "description": "Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome (disorder)"
        },
        {
          "id": 534678,
          "code": "724138007",
          "description": "Mitochondrial myopathy with sideroblastic anemia syndrome (disorder)"
        },
        {
          "id": 534679,
          "code": "724356003",
          "description": "Hereditary combined deficiency of vitamin K-dependent clotting factors (disorder)"
        },
        {
          "id": 534680,
          "code": "724639003",
          "description": "Asplenia following surgical procedure (disorder)"
        },
        {
          "id": 534681,
          "code": "724854007",
          "description": "Purpura of skin and or skin-associated mucous membrane co-occurrent and due to coagulation disorder (disorder)"
        },
        {
          "id": 534682,
          "code": "725034002",
          "description": "Familial platelet syndrome with predisposition to acute myelogenous leukemia (disorder)"
        },
        {
          "id": 534683,
          "code": "725057008",
          "description": "Nonspherocytic hemolytic anemia due to deficiency of adenosinetriphosphatase (disorder)"
        },
        {
          "id": 534684,
          "code": "725105006",
          "description": "Bleeding disorder due to deficiency of calcium and diacylglycerol-regulated guanine nucleotide exchange factor I (disorder)"
        },
        {
          "id": 534685,
          "code": "725137007",
          "description": "Neutropenia, monocytopenia, deafness syndrome (disorder)"
        },
        {
          "id": 534686,
          "code": "725291001",
          "description": "Defect of purinergic receptor p2y G protein-coupled 12 (disorder)"
        },
        {
          "id": 534687,
          "code": "725463007",
          "description": "Severe congenital hypochromic anemia with ringed sideroblasts (disorder)"
        },
        {
          "id": 534688,
          "code": "73073009",
          "description": "Hereditary elliptocytosis due to beta spectrin defect in self-association (disorder)"
        },
        {
          "id": 534689,
          "code": "73190000",
          "description": "epsilon gamma delta beta^0^ Thalassemia (disorder)"
        },
        {
          "id": 534690,
          "code": "733028000",
          "description": "Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome (disorder)"
        },
        {
          "id": 534691,
          "code": "733064004",
          "description": "Osteosarcoma, limb anomalies, erythroid macrocytosis syndrome (disorder)"
        },
        {
          "id": 534692,
          "code": "734349003",
          "description": "Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder)"
        },
        {
          "id": 534693,
          "code": "737221003",
          "description": "Congenital thrombocytopenia (disorder)"
        },
        {
          "id": 534694,
          "code": "737243006",
          "description": "Purpura of skin co-occurrent and due to vascular fragility (disorder)"
        },
        {
          "id": 534695,
          "code": "73975000",
          "description": "Factor II deficiency (disorder)"
        },
        {
          "id": 534696,
          "code": "74703006",
          "description": "Hereditary nonspherocytic hemolytic anemia due to pyruvate kinase deficiency (disorder)"
        },
        {
          "id": 534697,
          "code": "74789008",
          "description": "Coombs positive hemolytic anemia (disorder)"
        },
        {
          "id": 534698,
          "code": "74912001",
          "description": "Hereditary methemoglobinemia due to globin chain mutation (disorder)"
        },
        {
          "id": 534699,
          "code": "75063005",
          "description": "Hemoglobinopathy with erythrocytosis (disorder)"
        },
        {
          "id": 534700,
          "code": "75331009",
          "description": "Evans syndrome (disorder)"
        },
        {
          "id": 534701,
          "code": "75443009",
          "description": "Hereditary elliptocytosis due to abnormal protein 4.1 (disorder)"
        },
        {
          "id": 534702,
          "code": "763096004",
          "description": "Disorder of liver due to sickle cell disease (disorder)"
        },
        {
          "id": 534703,
          "code": "76336008",
          "description": "Delta beta zero thalassemia (disorder)"
        },
        {
          "id": 534704,
          "code": "76407009",
          "description": "Protein C deficiency disease (disorder)"
        },
        {
          "id": 534705,
          "code": "765327005",
          "description": "Congenital sideroblastic anemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome (disorder)"
        },
        {
          "id": 534706,
          "code": "765977002",
          "description": "Bleeding disorder due to glycoprotein VI deficiency (disorder)"
        },
        {
          "id": 534707,
          "code": "76642003",
          "description": "Factor X deficiency (disorder)"
        },
        {
          "id": 534708,
          "code": "766982000",
          "description": "Hemolytic anemia due to adenylate kinase deficiency (disorder)"
        },
        {
          "id": 534709,
          "code": "767497003",
          "description": "Autosomal recessive congenital methemoglobinemia (disorder)"
        },
        {
          "id": 534710,
          "code": "767498008",
          "description": "Autosomal recessive congenital methemoglobinemia type II (disorder)"
        },
        {
          "id": 534711,
          "code": "767499000",
          "description": "Autosomal recessive congenital methemoglobinemia type I (disorder)"
        },
        {
          "id": 534712,
          "code": "767712006",
          "description": "Factor IX deficiency (disorder)"
        },
        {
          "id": 534713,
          "code": "767713001",
          "description": "Factor XI deficiency (disorder)"
        },
        {
          "id": 534714,
          "code": "768556005",
          "description": "Ataxia pancytopenia syndrome (disorder)"
        },
        {
          "id": 534715,
          "code": "769167005",
          "description": "Vaso-occlusive pain co-occurrent and due to sickle cell disease (disorder)"
        },
        {
          "id": 534716,
          "code": "770407006",
          "description": "Chuvash erythrocytosis (disorder)"
        },
        {
          "id": 534717,
          "code": "770942003",
          "description": "Kostmann syndrome (disorder)"
        },
        {
          "id": 534718,
          "code": "770947009",
          "description": "Autosomal dominant severe congenital neutropenia (disorder)"
        },
        {
          "id": 534719,
          "code": "771075004",
          "description": "Macrothrombocytopenia with mitral valve insufficiency (disorder)"
        },
        {
          "id": 534720,
          "code": "773422002",
          "description": "East Texas bleeding disorder (disorder)"
        },
        {
          "id": 534721,
          "code": "773489008",
          "description": "Hereditary cryohydrocytosis with normal stomatin (disorder)"
        },
        {
          "id": 534722,
          "code": "774071007",
          "description": "Pancytopenia with developmental delay syndrome (disorder)"
        },
        {
          "id": 534723,
          "code": "774084003",
          "description": "Neonatal antiphospholipid syndrome (disorder)"
        },
        {
          "id": 534724,
          "code": "77413008",
          "description": "Severe hereditary spherocytosis due to spectrin deficiency (disorder)"
        },
        {
          "id": 534725,
          "code": "775909002",
          "description": "Congenital neutropenia, myelofibrosis, nephromegaly syndrome (disorder)"
        },
        {
          "id": 534726,
          "code": "7772007",
          "description": "Erythropoietic hemochromatosis (disorder)"
        },
        {
          "id": 534727,
          "code": "778006008",
          "description": "Autosomal dominant aplasia and myelodysplasia (disorder)"
        },
        {
          "id": 534728,
          "code": "782759001",
          "description": "X-linked dyserythropoietic anemia with abnormal platelets and neutropenia (disorder)"
        },
        {
          "id": 534729,
          "code": "782880001",
          "description": "Hemoglobinopathy Toms River (disorder)"
        },
        {
          "id": 534730,
          "code": "782909004",
          "description": "Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation (disorder)"
        },
        {
          "id": 534731,
          "code": "782911008",
          "description": "Hereditary cryohydrocytosis with reduced stomatin (disorder)"
        },
        {
          "id": 534732,
          "code": "782934004",
          "description": "Bleeding diathesis due to collagen receptor defect (disorder)"
        },
        {
          "id": 534733,
          "code": "783058007",
          "description": "Autosomal recessive severe congenital neutropenia due to glucose-6-phosphatase catalytic subunit 3 deficiency (disorder)"
        },
        {
          "id": 534734,
          "code": "783194008",
          "description": "Bleeding diathesis due to thromboxane synthesis deficiency (disorder)"
        },
        {
          "id": 534735,
          "code": "783199003",
          "description": "Autosomal recessive severe congenital neutropenia due to jagunal homolog 1 deficiency (disorder)"
        },
        {
          "id": 534736,
          "code": "783200000",
          "description": "Autosomal recessive severe congenital neutropenia due to C-X-C motif chemokine receptor 2 deficiency (disorder)"
        },
        {
          "id": 534737,
          "code": "783201001",
          "description": "Autosomal recessive severe congenital neutropenia due to colony stimulating factor 3 receptor deficiency (disorder)"
        },
        {
          "id": 534738,
          "code": "783202008",
          "description": "Autosomal dominant secondary polycythemia (disorder)"
        },
        {
          "id": 534739,
          "code": "783250007",
          "description": "Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency (disorder)"
        },
        {
          "id": 534740,
          "code": "783251006",
          "description": "Hereditary thrombocytopenia with normal platelets (disorder)"
        },
        {
          "id": 534741,
          "code": "783254003",
          "description": "Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome (disorder)"
        },
        {
          "id": 534742,
          "code": "783255002",
          "description": "Hereditary isolated aplastic anemia (disorder)"
        },
        {
          "id": 534743,
          "code": "783256001",
          "description": "Familial thrombomodulin anomalies (disorder)"
        },
        {
          "id": 534744,
          "code": "78345002",
          "description": "Thrombocytopenia due to diminished platelet production (disorder)"
        },
        {
          "id": 534745,
          "code": "784392009",
          "description": "Adult chronic idiopathic neutropenia (disorder)"
        },
        {
          "id": 534746,
          "code": "785308008",
          "description": "Acquired hemophilia (disorder)"
        },
        {
          "id": 534747,
          "code": "788865000",
          "description": "Anemia due to chronic infectious disease (disorder)"
        },
        {
          "id": 534748,
          "code": "788944005",
          "description": "Gamma delta beta thalassemia (disorder)"
        },
        {
          "id": 534749,
          "code": "78908001",
          "description": "Hereditary nonspherocytic hemolytic anemia due to decreased adenosine deaminase activity (disorder)"
        },
        {
          "id": 534750,
          "code": "80141007",
          "description": "Hemoglobinopathy (disorder)"
        },
        {
          "id": 534751,
          "code": "80813006",
          "description": "Hemophilic arthropathy (disorder)"
        },
        {
          "id": 534752,
          "code": "80963002",
          "description": "Glucose-6-phosphate dehydrogenase deficiency class V variant anemia (disorder)"
        },
        {
          "id": 534753,
          "code": "81783000",
          "description": "Familial multiple factor deficiency syndrome (disorder)"
        },
        {
          "id": 534754,
          "code": "82003006",
          "description": "Glucose-6-phosphate dehydrogenase deficiency class IV variant anemia (disorder)"
        },
        {
          "id": 534755,
          "code": "8209004",
          "description": "Dilated cardiomyopathy secondary to hemochromatosis (disorder)"
        },
        {
          "id": 534756,
          "code": "82190001",
          "description": "Thrombocytopenia due to defective platelet production (disorder)"
        },
        {
          "id": 534757,
          "code": "82893001",
          "description": "Splenic atrophy (disorder)"
        },
        {
          "id": 534758,
          "code": "838361004",
          "description": "Arthropathy due to hemochromatosis (disorder)"
        },
        {
          "id": 534759,
          "code": "84048006",
          "description": "Familial multiple factor deficiency syndrome, type I (disorder)"
        },
        {
          "id": 534760,
          "code": "84188003",
          "description": "Thalassemia syndrome (disorder)"
        },
        {
          "id": 534761,
          "code": "84260001",
          "description": "Hemoglobinopathy with cyanosis (disorder)"
        },
        {
          "id": 534762,
          "code": "85422000",
          "description": "alpha^+^ Thalassemia, nondeletion type (disorder)"
        },
        {
          "id": 534763,
          "code": "860725002",
          "description": "Low von Willebrand factor (disorder)"
        },
        {
          "id": 534764,
          "code": "86075001",
          "description": "Coagulation factor deficiency syndrome (disorder)"
        },
        {
          "id": 534765,
          "code": "86242003",
          "description": "alpha^+^ Thalassemia, deletion type (disorder)"
        },
        {
          "id": 534766,
          "code": "86325007",
          "description": "Non megaloblastic anemia due to alcoholism (disorder)"
        },
        {
          "id": 534767,
          "code": "86859003",
          "description": "Glucose-6-phosphate dehydrogenase variant enzyme deficiency anemia (disorder)"
        },
        {
          "id": 534768,
          "code": "87397002",
          "description": "von Willebrand disease, type IIA (disorder)"
        },
        {
          "id": 534769,
          "code": "87902006",
          "description": "Thrombocytopenia due to non-immune destruction (disorder)"
        },
        {
          "id": 534770,
          "code": "87994004",
          "description": "Xerocytosis (disorder)"
        },
        {
          "id": 534771,
          "code": "88540000",
          "description": "Factor XI deficiency, type I (disorder)"
        },
        {
          "id": 534772,
          "code": "8857001",
          "description": "Hereditary elliptocytosis due to alpha spectrin defect (disorder)"
        },
        {
          "id": 534773,
          "code": "88776002",
          "description": "Hereditary factor V deficiency disease (disorder)"
        },
        {
          "id": 534774,
          "code": "88854002",
          "description": "Congenital hypoplastic anemia (disorder)"
        },
        {
          "id": 534775,
          "code": "89112009",
          "description": "Aregenerative anemia (disorder)"
        },
        {
          "id": 534776,
          "code": "89454001",
          "description": "Shwachman syndrome (disorder)"
        },
        {
          "id": 534777,
          "code": "89459006",
          "description": "Hereditary persistence of fetal hemoglobin linked to beta-globulin gene cluster (disorder)"
        },
        {
          "id": 534778,
          "code": "89655007",
          "description": "Congenital neutropenia (disorder)"
        },
        {
          "id": 534779,
          "code": "89729000",
          "description": "Factor IX inhibitor disorder (disorder)"
        },
        {
          "id": 534780,
          "code": "89810003",
          "description": "^A^gamma delta beta^0^ thalassemia (disorder)"
        },
        {
          "id": 534781,
          "code": "90175006",
          "description": "Secondary acquired sideroblastic anemia (disorder)"
        },
        {
          "id": 534782,
          "code": "90501009",
          "description": "Erythrocytosis due to defective oxygen transport (disorder)"
        },
        {
          "id": 534783,
          "code": "90935002",
          "description": "Hemophilia (disorder)"
        },
        {
          "id": 534784,
          "code": "9417000",
          "description": "Platelet dense granule deficiency (disorder)"
        },
        {
          "id": 534785,
          "code": "9434008",
          "description": "Hereditary pyropoikilocytosis (disorder)"
        },
        {
          "id": 534786,
          "code": "9489006",
          "description": "Factor X inhibitor disorder (disorder)"
        },
        {
          "id": 534787,
          "code": "95839005",
          "description": "Disorder involving the fibrinolytic system (disorder)"
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        {
          "id": 534788,
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          "description": "Hypoplasminogenemia (disorder)"
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          "description": "Hereditary hypoplasminogenemia (disorder)"
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        {
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          "code": "95842004",
          "description": "Autosomal dominant deficiency of plasminogen (disorder)"
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        {
          "id": 534791,
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          "description": "Dysplasminogenemia (disorder)"
        },
        {
          "id": 534793,
          "code": "97571000119109",
          "description": "Thrombocytopenia co-occurrent and due to alcoholism (disorder)"
        },
        {
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          "code": "9764001",
          "description": "Anemia caused by radiation (disorder)"
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      ]
    }
  ],
  "version_history": [
    {
      "version_id": 11511,
      "version_name": "Non-malignant haematological (SNOMED-CT)",
      "version_date": "2025-01-19T16:17:21.911250Z",
      "is_published": true,
      "is_latest": true
    }
  ]
}