{
  "concept_id": 4150,
  "concept_version_id": 11510,
  "coding_system": {
    "id": 5,
    "name": "Read codes v2",
    "description": "Read codes v2"
  },
  "name": "Non-malignant haematological (Read v2)",
  "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": 9977,
      "name": "Inclusion 1",
      "logical_type": "INCLUDE",
      "source_type": "FILE_IMPORT",
      "source": "text/csv",
      "codes": [
        {
          "id": 533914,
          "code": "C310.12",
          "description": "Glucose-6-phosphate deficiency"
        },
        {
          "id": 533915,
          "code": "C310212",
          "description": "Glucose-6-phosphatase deficiency"
        },
        {
          "id": 533916,
          "code": "C310213",
          "description": "Glycogenosis, type 1"
        },
        {
          "id": 533917,
          "code": "C350.00",
          "description": "Disorders of iron metabolism"
        },
        {
          "id": 533918,
          "code": "C350000",
          "description": "Haemochromatosis"
        },
        {
          "id": 533919,
          "code": "C350011",
          "description": "Bronzed diabetes"
        },
        {
          "id": 533920,
          "code": "C350012",
          "description": "Pigmentary cirrhosis of liver"
        },
        {
          "id": 533921,
          "code": "C350013",
          "description": "Von Recklinghausen - Applebaum disease"
        },
        {
          "id": 533922,
          "code": "C350100",
          "description": "Haemosiderosis, primary"
        },
        {
          "id": 533923,
          "code": "C350200",
          "description": "Haemosiderosis, acquired"
        },
        {
          "id": 533924,
          "code": "C350400",
          "description": "Haemosiderosis NOS"
        },
        {
          "id": 533925,
          "code": "C350y00",
          "description": "Other specified disorder of iron metabolism"
        },
        {
          "id": 533926,
          "code": "C350z00",
          "description": "Disorder of iron metabolism NOS"
        },
        {
          "id": 533927,
          "code": "D1...00",
          "description": "Haemolytic anaemias"
        },
        {
          "id": 533928,
          "code": "D10..00",
          "description": "Hereditary haemolytic anaemias"
        },
        {
          "id": 533929,
          "code": "D100.00",
          "description": "Hereditary spherocytosis"
        },
        {
          "id": 533930,
          "code": "D100.11",
          "description": "Acholuric familial jaundice"
        },
        {
          "id": 533931,
          "code": "D100.12",
          "description": "Minkowski - Chauffard syndrome"
        },
        {
          "id": 533932,
          "code": "D102.00",
          "description": "Haemolytic anaemia due to glutathione metabolism disorder"
        },
        {
          "id": 533933,
          "code": "D102000",
          "description": "Glucose-6-phosphate dehydrogenase deficiency anaemia"
        },
        {
          "id": 533934,
          "code": "D102100",
          "description": "Favism"
        },
        {
          "id": 533935,
          "code": "D102y00",
          "description": "Other specified haemolytic anaemia due to glutathione metabolism disorder"
        },
        {
          "id": 533936,
          "code": "D102z00",
          "description": "Haemolytic anaemia due to glutathione metabolism disorder NOS"
        },
        {
          "id": 533937,
          "code": "D103.00",
          "description": "Other enzyme deficiency haemolytic anaemia"
        },
        {
          "id": 533938,
          "code": "D103000",
          "description": "Haemolytic anaemia due to hexokinase deficiency"
        },
        {
          "id": 533939,
          "code": "D103100",
          "description": "Haemolytic anaemia due to pyruvate kinase deficiency"
        },
        {
          "id": 533940,
          "code": "D103200",
          "description": "Haemolytic anaemia due to triose phosphate isomerase deficiency"
        },
        {
          "id": 533941,
          "code": "D103300",
          "description": "Anaemia due to disorders of nucleotide metabolism"
        },
        {
          "id": 533942,
          "code": "D103z00",
          "description": "Enzyme deficiency haemolytic anaemia NOS"
        },
        {
          "id": 533943,
          "code": "D104.00",
          "description": "Thalassaemia"
        },
        {
          "id": 533944,
          "code": "D104.11",
          "description": "Leptocytosis, hereditary"
        },
        {
          "id": 533945,
          "code": "D104.12",
          "description": "Mediterranean anaemia"
        },
        {
          "id": 533946,
          "code": "D104200",
          "description": "Thalassaemia with haemoglobin S disease"
        },
        {
          "id": 533947,
          "code": "D104211",
          "description": "Sickle-cell thalassaemia"
        },
        {
          "id": 533948,
          "code": "D104300",
          "description": "Alpha thalassaemia"
        },
        {
          "id": 533949,
          "code": "D104311",
          "description": "Homozygous alpha thalassaemia"
        },
        {
          "id": 533950,
          "code": "D104900",
          "description": "Delta-beta thalassaemia"
        },
        {
          "id": 533951,
          "code": "D104A00",
          "description": "Hereditary leptocytosis"
        },
        {
          "id": 533952,
          "code": "D104z00",
          "description": "Thalassaemia NOS"
        },
        {
          "id": 533953,
          "code": "D104z11",
          "description": "Mediterranean anaemia"
        },
        {
          "id": 533954,
          "code": "D106.00",
          "description": "Sickle-cell anaemia"
        },
        {
          "id": 533955,
          "code": "D106000",
          "description": "Sickle-cell anaemia of unspecified type"
        },
        {
          "id": 533956,
          "code": "D106100",
          "description": "Sickle-cell anaemia with no crisis"
        },
        {
          "id": 533957,
          "code": "D106200",
          "description": "Sickle-cell anaemia with crisis"
        },
        {
          "id": 533958,
          "code": "D106300",
          "description": "Sickle-cell anaemia with haemoglobin C disease"
        },
        {
          "id": 533959,
          "code": "D106400",
          "description": "Sickle-cell anaemia with haemoglobin D disease"
        },
        {
          "id": 533960,
          "code": "D106500",
          "description": "Sickle-cell anaemia with haemoglobin E disease"
        },
        {
          "id": 533961,
          "code": "D106z00",
          "description": "Sickle-cell anaemia NOS"
        },
        {
          "id": 533962,
          "code": "D107.00",
          "description": "Other haemoglobinopathies"
        },
        {
          "id": 533963,
          "code": "D107000",
          "description": "Congenital Heinz-body anaemia"
        },
        {
          "id": 533964,
          "code": "D107200",
          "description": "Haemoglobin Bart's disease"
        },
        {
          "id": 533965,
          "code": "D107300",
          "description": "Haemoglobin-C disease"
        },
        {
          "id": 533966,
          "code": "D107400",
          "description": "Haemoglobin-D disease"
        },
        {
          "id": 533967,
          "code": "D107600",
          "description": "Haemoglobin Zurich disease"
        },
        {
          "id": 533968,
          "code": "D107700",
          "description": "Haemoglobin-H disease"
        },
        {
          "id": 533969,
          "code": "D107y00",
          "description": "Other specified other haemoglobinopathy"
        },
        {
          "id": 533970,
          "code": "D107z00",
          "description": "Other haemoglobinopathy NOS"
        },
        {
          "id": 533971,
          "code": "D10y.00",
          "description": "Other specified hereditary haemolytic anaemias"
        },
        {
          "id": 533972,
          "code": "D10yz00",
          "description": "Other specified hereditary haemolytic anaemia NOS"
        },
        {
          "id": 533973,
          "code": "D10z.00",
          "description": "Hereditary haemolytic anaemia NOS"
        },
        {
          "id": 533974,
          "code": "D1y..00",
          "description": "Other specified haemolytic anaemias"
        },
        {
          "id": 533975,
          "code": "D1z..00",
          "description": "Haemolytic anaemias NOS"
        },
        {
          "id": 533976,
          "code": "D20..00",
          "description": "Aplastic anaemia"
        },
        {
          "id": 533977,
          "code": "D200.00",
          "description": "Constitutional aplastic anaemia"
        },
        {
          "id": 533978,
          "code": "D200.12",
          "description": "Pancytopenia with malformations"
        },
        {
          "id": 533979,
          "code": "D200.13",
          "description": "Blackfan - Diamond syndrome"
        },
        {
          "id": 533980,
          "code": "D200.15",
          "description": "Hypoplastic anaemia - familial"
        },
        {
          "id": 533981,
          "code": "D200000",
          "description": "Congenital hypoplastic anaemia"
        },
        {
          "id": 533982,
          "code": "D200011",
          "description": "Constitutional aplastic anaemia without mention of malformation"
        },
        {
          "id": 533983,
          "code": "D200100",
          "description": "Fanconi's familial refractory anaemia"
        },
        {
          "id": 533984,
          "code": "D200111",
          "description": "Fanconi's hypoplastic anaemia"
        },
        {
          "id": 533985,
          "code": "D200200",
          "description": "Constitutional aplastic anaemia with malformation"
        },
        {
          "id": 533986,
          "code": "D200211",
          "description": "Pancytopenia-dysmelia"
        },
        {
          "id": 533987,
          "code": "D200300",
          "description": "Constitutional red cell aplasia and hypoplasia"
        },
        {
          "id": 533988,
          "code": "D200311",
          "description": "Blackfan - Diamond syndrome"
        },
        {
          "id": 533989,
          "code": "D200312",
          "description": "Congenital pure red cell aplasia"
        },
        {
          "id": 533990,
          "code": "D200313",
          "description": "Constitutional red cell hypoplasia"
        },
        {
          "id": 533991,
          "code": "D200314",
          "description": "Congenital red cell hypoplasia"
        },
        {
          "id": 533992,
          "code": "D200400",
          "description": "Erythrogenesis imperfecta"
        },
        {
          "id": 533993,
          "code": "D200y00",
          "description": "Other specified constitutional aplastic anaemia"
        },
        {
          "id": 533994,
          "code": "D200z00",
          "description": "Constitutional aplastic anaemia NOS"
        },
        {
          "id": 533995,
          "code": "D201500",
          "description": "Pancytopenia - acquired"
        },
        {
          "id": 533996,
          "code": "D201611",
          "description": "Pancytopenia with malformation"
        },
        {
          "id": 533997,
          "code": "D201612",
          "description": "Pancytopenia with pancreatitis"
        },
        {
          "id": 533998,
          "code": "D20z.00",
          "description": "Aplastic anaemia NOS"
        },
        {
          "id": 533999,
          "code": "D210.00",
          "description": "Sideroblastic anaemia"
        },
        {
          "id": 534000,
          "code": "D210000",
          "description": "Congenital sideroblastic anaemia"
        },
        {
          "id": 534001,
          "code": "D210100",
          "description": "Acquired sideroblastic anaemia"
        },
        {
          "id": 534002,
          "code": "D210200",
          "description": "Pyridoxine-responsive sideroblastic anaemia"
        },
        {
          "id": 534003,
          "code": "D210300",
          "description": "Secondary sideroblastic anaemia due to disease"
        },
        {
          "id": 534004,
          "code": "D210z00",
          "description": "Sideroblastic anaemia NOS"
        },
        {
          "id": 534005,
          "code": "D21y.11",
          "description": "Von Jaksch's anaemia"
        },
        {
          "id": 534006,
          "code": "D21y000",
          "description": "Congenital dyshaematopoietic anaemia"
        },
        {
          "id": 534007,
          "code": "D21y011",
          "description": "Congenital dyserythropoietic anaemia"
        },
        {
          "id": 534008,
          "code": "D21y012",
          "description": "Congenital dyserythropoiesis NEC"
        },
        {
          "id": 534009,
          "code": "D21y200",
          "description": "Leukoerythroblastic anaemia"
        },
        {
          "id": 534010,
          "code": "D21y300",
          "description": "Hereditary erythroblast multinuclearity with positive acid serum test"
        },
        {
          "id": 534011,
          "code": "D3...00",
          "description": "Clotting and bleeding disorders"
        },
        {
          "id": 534012,
          "code": "D30..00",
          "description": "Coagulation defects"
        },
        {
          "id": 534013,
          "code": "D30..11",
          "description": "Bleeding disorders"
        },
        {
          "id": 534014,
          "code": "D300.00",
          "description": "Haemophilia-A (factor VIII deficiency)"
        },
        {
          "id": 534015,
          "code": "D300.11",
          "description": "Antihaemophilic globulin deficiency"
        },
        {
          "id": 534016,
          "code": "D300.12",
          "description": "Haemophilia A"
        },
        {
          "id": 534017,
          "code": "D301.00",
          "description": "Haemophilia-B (factor IX deficiency)"
        },
        {
          "id": 534018,
          "code": "D301.11",
          "description": "Christmas disease"
        },
        {
          "id": 534019,
          "code": "D301.12",
          "description": "Haemophilia B"
        },
        {
          "id": 534020,
          "code": "D302.00",
          "description": "Haemophilia-C (factor XI deficiency)"
        },
        {
          "id": 534021,
          "code": "D302.11",
          "description": "Haemophilia C"
        },
        {
          "id": 534022,
          "code": "D302.12",
          "description": "Rosenthal's disease"
        },
        {
          "id": 534023,
          "code": "D303.00",
          "description": "Congenital deficiency of other clotting factors"
        },
        {
          "id": 534024,
          "code": "D303000",
          "description": "Congenital afibrinogenaemia"
        },
        {
          "id": 534025,
          "code": "D303100",
          "description": "Deficiency of factor II or prothrombin"
        },
        {
          "id": 534026,
          "code": "D303111",
          "description": "Hypoprothrombinaemia"
        },
        {
          "id": 534027,
          "code": "D303200",
          "description": "Deficiency of factor V or labile factor"
        },
        {
          "id": 534028,
          "code": "D303300",
          "description": "Deficiency of factor VII or stable factor"
        },
        {
          "id": 534029,
          "code": "D303400",
          "description": "Deficiency of factor X or Stuart-Prower factor"
        },
        {
          "id": 534030,
          "code": "D303500",
          "description": "Deficiency of factor XII or Hageman factor"
        },
        {
          "id": 534031,
          "code": "D303600",
          "description": "Deficiency of factor XIII or fibrin stabilizing factor"
        },
        {
          "id": 534032,
          "code": "D303611",
          "description": "Fibrin stabilising factor deficiency"
        },
        {
          "id": 534033,
          "code": "D303700",
          "description": "Factor V Leiden mutation"
        },
        {
          "id": 534034,
          "code": "D303800",
          "description": "Homozygous factor V Leiden mutation"
        },
        {
          "id": 534035,
          "code": "D303900",
          "description": "Heterozygous factor V Leiden mutation"
        },
        {
          "id": 534036,
          "code": "D303y00",
          "description": "Other specified congenital deficiency of other clotting factor"
        },
        {
          "id": 534037,
          "code": "D303z00",
          "description": "Congenital deficiency of other clotting factor NOS"
        },
        {
          "id": 534038,
          "code": "D304.00",
          "description": "Von Willebrand's disease"
        },
        {
          "id": 534039,
          "code": "D307000",
          "description": "Deficiency of coagulation factor due to liver disease"
        },
        {
          "id": 534040,
          "code": "D307100",
          "description": "Deficiency of coagulation factor due to vitamin K deficiency"
        },
        {
          "id": 534041,
          "code": "D307z00",
          "description": "Acquired coagulation factor deficiency NOS"
        },
        {
          "id": 534042,
          "code": "D309.00",
          "description": "Protein S deficiency"
        },
        {
          "id": 534043,
          "code": "D30A.00",
          "description": "Thrombophilia"
        },
        {
          "id": 534044,
          "code": "D30A000",
          "description": "Primary thrombophilia"
        },
        {
          "id": 534045,
          "code": "D30B.00",
          "description": "Protein C deficiency"
        },
        {
          "id": 534046,
          "code": "D30C.00",
          "description": "Hypofibrinogenaemia"
        },
        {
          "id": 534047,
          "code": "D30z.00",
          "description": "Coagulation defect NOS"
        },
        {
          "id": 534048,
          "code": "D311.00",
          "description": "Qualitative platelet defects"
        },
        {
          "id": 534049,
          "code": "D311.11",
          "description": "Bernard - Soulier thrombopathy"
        },
        {
          "id": 534050,
          "code": "D311000",
          "description": "Hereditary haemorrhagic thrombasthenia"
        },
        {
          "id": 534051,
          "code": "D311011",
          "description": "Glanzmann's syndrome"
        },
        {
          "id": 534052,
          "code": "D311z00",
          "description": "Qualitative platelet deficiency NOS"
        },
        {
          "id": 534053,
          "code": "D313.00",
          "description": "Primary thrombocytopenia"
        },
        {
          "id": 534054,
          "code": "D313.11",
          "description": "Evan's syndrome"
        },
        {
          "id": 534055,
          "code": "D313.12",
          "description": "Idiopathic thrombocytopenic purpura"
        },
        {
          "id": 534056,
          "code": "D313.14",
          "description": "Megakaryocytic hypoplasia"
        },
        {
          "id": 534057,
          "code": "D313.15",
          "description": "Thrombocytopenic purpura"
        },
        {
          "id": 534058,
          "code": "D313000",
          "description": "Idiopathic thrombocytopenic purpura"
        },
        {
          "id": 534059,
          "code": "D313012",
          "description": "ITP - idiopathic thrombocytopenic purpura"
        },
        {
          "id": 534060,
          "code": "D313100",
          "description": "Congenital thrombocytopenic purpura"
        },
        {
          "id": 534061,
          "code": "D313111",
          "description": "Hereditary thrombocytopenia NEC"
        },
        {
          "id": 534062,
          "code": "D313300",
          "description": "[X]Essential thrombocytopenia NOS"
        },
        {
          "id": 534063,
          "code": "D313y00",
          "description": "Other specified primary thrombocytopenia"
        },
        {
          "id": 534064,
          "code": "D313z00",
          "description": "Primary thrombocytopenia NOS"
        },
        {
          "id": 534065,
          "code": "D313z11",
          "description": "Essential thrombocytopenia NOS"
        },
        {
          "id": 534066,
          "code": "D314.00",
          "description": "Secondary thrombocytopenia"
        },
        {
          "id": 534067,
          "code": "D31y.00",
          "description": "Other specified haemorrhagic conditions"
        },
        {
          "id": 534068,
          "code": "D31yz00",
          "description": "Other specified haemorrhagic condition NOS"
        },
        {
          "id": 534069,
          "code": "D3y..00",
          "description": "Other specified disorders of clotting or bleeding"
        },
        {
          "id": 534070,
          "code": "D3z..00",
          "description": "Clotting or bleeding disorder NOS"
        },
        {
          "id": 534071,
          "code": "D400.11",
          "description": "Kostmann's syndrome"
        },
        {
          "id": 534072,
          "code": "D400000",
          "description": "Idiopathic agranulocytosis"
        },
        {
          "id": 534073,
          "code": "D400011",
          "description": "Idiopathic neutropenia"
        },
        {
          "id": 534074,
          "code": "D400100",
          "description": "Primary splenic neutropenia"
        },
        {
          "id": 534075,
          "code": "D400300",
          "description": "Agranulocytosis due to irradiation"
        },
        {
          "id": 534076,
          "code": "D400311",
          "description": "Radiation agranulocytosis"
        },
        {
          "id": 534077,
          "code": "D400312",
          "description": "Neutropenia due to irradiation"
        },
        {
          "id": 534078,
          "code": "D400500",
          "description": "Congenital neutropenia"
        },
        {
          "id": 534079,
          "code": "D400511",
          "description": "Congenital agranulocytosis NEC"
        },
        {
          "id": 534080,
          "code": "D400800",
          "description": "Acquired neutropenia NEC"
        },
        {
          "id": 534081,
          "code": "D400811",
          "description": "Acquired agranulocytosis NEC"
        },
        {
          "id": 534082,
          "code": "D400900",
          "description": "Cyclical neutropenia"
        },
        {
          "id": 534083,
          "code": "D400y00",
          "description": "Other specified agranulocytosis"
        },
        {
          "id": 534084,
          "code": "D400z00",
          "description": "Agranulocytosis NOS"
        },
        {
          "id": 534085,
          "code": "D414.00",
          "description": "Hypersplenism"
        },
        {
          "id": 534086,
          "code": "D415100",
          "description": "Chronic congestive splenamegaly"
        },
        {
          "id": 534087,
          "code": "D415400",
          "description": "Splenic atrophy"
        },
        {
          "id": 534088,
          "code": "D415A00",
          "description": "Hyposplenism"
        },
        {
          "id": 534089,
          "code": "D416.00",
          "description": "Familial polycythaemia"
        },
        {
          "id": 534090,
          "code": "D417.00",
          "description": "Methaemoglobinaemia"
        },
        {
          "id": 534091,
          "code": "D417.11",
          "description": "Stokvis' disease"
        },
        {
          "id": 534092,
          "code": "D417000",
          "description": "Congenital methaemoglobinaemia"
        },
        {
          "id": 534093,
          "code": "D417011",
          "description": "Congenital methaemoglobinaemia with abnormal methaemoglobins"
        },
        {
          "id": 534094,
          "code": "D417012",
          "description": "Congenital methaemoglobinaema with defective methaemoglobin-reducing system"
        },
        {
          "id": 534095,
          "code": "D417100",
          "description": "Familial methaemoglobinaemia"
        },
        {
          "id": 534096,
          "code": "D417200",
          "description": "Idiopathic methaemoglobinaemia"
        },
        {
          "id": 534097,
          "code": "D417500",
          "description": "Acquired methaemoglobinaemia"
        },
        {
          "id": 534098,
          "code": "D417z00",
          "description": "Methaemoglobinaemia NOS"
        },
        {
          "id": 534099,
          "code": "Dyu1.00",
          "description": "[X]Haemolytic anaemias"
        },
        {
          "id": 534100,
          "code": "Dyu1100",
          "description": "[X]Other thalassaemias"
        },
        {
          "id": 534101,
          "code": "Dyu1200",
          "description": "[X]Other sickle-cell disorders"
        },
        {
          "id": 534102,
          "code": "Dyu1300",
          "description": "[X]Other haemoglobinopathies"
        },
        {
          "id": 534103,
          "code": "Dyu1400",
          "description": "[X]Other specified hereditary haemolytic anaemias"
        },
        {
          "id": 534104,
          "code": "Dyu2100",
          "description": "[X]Other specified aplastic anaemias"
        },
        {
          "id": 534105,
          "code": "Dyu2300",
          "description": "[X]Other sideroblastic anaemias"
        },
        {
          "id": 534106,
          "code": "Dyu3.00",
          "description": "[X]Coagulation defects, purpura and other haemorrhagic conditions"
        },
        {
          "id": 534107,
          "code": "Dyu3000",
          "description": "[X]Other specified coagulation defects"
        },
        {
          "id": 534108,
          "code": "Dyu3200",
          "description": "[X]Other primary thrombocytopenia"
        },
        {
          "id": 534109,
          "code": "Dyu4200",
          "description": "[X]Other methaemoglobinaemias"
        },
        {
          "id": 534110,
          "code": "F100100",
          "description": "Schulz's disease"
        },
        {
          "id": 534111,
          "code": "F422100",
          "description": "Proliferative retinopathy due to sickle cell disease"
        },
        {
          "id": 534112,
          "code": "K0G..00",
          "description": "Sickle cell nephropathy"
        },
        {
          "id": 534113,
          "code": "N006.00",
          "description": "Antiphospholipid syndrome"
        },
        {
          "id": 534114,
          "code": "N032000",
          "description": "Arthropathy due to haemophilia"
        },
        {
          "id": 534115,
          "code": "N068.00",
          "description": "Haemophilic arthropathy"
        },
        {
          "id": 534116,
          "code": "N334C00",
          "description": "Osteonecrosis due to haemoglobinopathy"
        },
        {
          "id": 534117,
          "code": "NyuCB00",
          "description": "[X]Osteonecrosis due to haemoglobinopathy classified elsewhere"
        },
        {
          "id": 534118,
          "code": "PJ53500",
          "description": "Shwachman-Diamond syndrome"
        },
        {
          "id": 534119,
          "code": "R105B00",
          "description": "[D]Hyperferritinaemia"
        }
      ]
    }
  ],
  "version_history": [
    {
      "version_id": 11510,
      "version_name": "Non-malignant haematological (Read v2)",
      "version_date": "2025-01-19T16:17:16.944911Z",
      "is_published": true,
      "is_latest": true
    }
  ]
}