{
  "concept_id": 4168,
  "concept_version_id": 11528,
  "coding_system": {
    "id": 5,
    "name": "Read codes v2",
    "description": "Read codes v2"
  },
  "name": "Metabolic (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": "PH1711",
  "phenotype_owner_history_id": 3636,
  "requested_entity_id": null,
  "components": [
    {
      "id": 9995,
      "name": "Inclusion 1",
      "logical_type": "INCLUDE",
      "source_type": "FILE_IMPORT",
      "source": "text/csv",
      "codes": [
        {
          "id": 537886,
          "code": "C30..00",
          "description": "Disorders of amino-acid transport and metabolism"
        },
        {
          "id": 537887,
          "code": "C30..00",
          "description": "Disorders of amino-acid transport and metabolism"
        },
        {
          "id": 537888,
          "code": "C300.00",
          "description": "Disorders of amino-acid transport"
        },
        {
          "id": 537889,
          "code": "C300000",
          "description": "Cystinosis"
        },
        {
          "id": 537890,
          "code": "C300200",
          "description": "Cystinaemia"
        },
        {
          "id": 537891,
          "code": "C300300",
          "description": "Fanconi-de-Toni syndrome"
        },
        {
          "id": 537892,
          "code": "C300311",
          "description": "Cystine storage disease"
        },
        {
          "id": 537893,
          "code": "C300500",
          "description": "Succinic semialdehyde dehydrogenase deficiency"
        },
        {
          "id": 537894,
          "code": "C300800",
          "description": "Juvenile nephropathic cystinosis"
        },
        {
          "id": 537895,
          "code": "C300811",
          "description": "Adolescent cystinosis"
        },
        {
          "id": 537896,
          "code": "C300B00",
          "description": "Dibasic aminoaciduria - type I"
        },
        {
          "id": 537897,
          "code": "C300C00",
          "description": "Lysinuric protein intolerance"
        },
        {
          "id": 537898,
          "code": "C300C11",
          "description": "Dibasic aminoaciduria - type II"
        },
        {
          "id": 537899,
          "code": "C300D00",
          "description": "Infantile nephropathic cystinosis"
        },
        {
          "id": 537900,
          "code": "C300E00",
          "description": "Dibasic aminoaciduria"
        },
        {
          "id": 537901,
          "code": "C300y00",
          "description": "Other specified amino-acid transport disorder"
        },
        {
          "id": 537902,
          "code": "C300y11",
          "description": "Glycinuria"
        },
        {
          "id": 537903,
          "code": "C300y12",
          "description": "Hypophosphataemic rickets with nephrotic-glycosuric dwarfism"
        },
        {
          "id": 537904,
          "code": "C300z00",
          "description": "Amino-acid transport disorder NOS"
        },
        {
          "id": 537905,
          "code": "C301.00",
          "description": "Phenylketonuria"
        },
        {
          "id": 537906,
          "code": "C302.00",
          "description": "Other disturbances of aromatic amino-acid metabolism"
        },
        {
          "id": 537907,
          "code": "C302.11",
          "description": "Albinism"
        },
        {
          "id": 537908,
          "code": "C302000",
          "description": "Alkaptonuria"
        },
        {
          "id": 537909,
          "code": "C302011",
          "description": "Homogentisic acid defect"
        },
        {
          "id": 537910,
          "code": "C302100",
          "description": "Hydroxykynureninuria"
        },
        {
          "id": 537911,
          "code": "C302200",
          "description": "Indicanuria"
        },
        {
          "id": 537912,
          "code": "C302300",
          "description": "Tyrosinosis"
        },
        {
          "id": 537913,
          "code": "C302400",
          "description": "Tyrosinuria"
        },
        {
          "id": 537914,
          "code": "C302500",
          "description": "Lowe disease"
        },
        {
          "id": 537915,
          "code": "C302511",
          "description": "Oculocerebrorenal syndrome"
        },
        {
          "id": 537916,
          "code": "C302512",
          "description": "Oculocerebrorenal dystrophy"
        },
        {
          "id": 537917,
          "code": "C302600",
          "description": "Hypertyrosinaemia"
        },
        {
          "id": 537918,
          "code": "C302611",
          "description": "Tyrosinaemia"
        },
        {
          "id": 537919,
          "code": "C302700",
          "description": "Albinism"
        },
        {
          "id": 537920,
          "code": "C302712",
          "description": "Albino"
        },
        {
          "id": 537921,
          "code": "C302713",
          "description": "Albinismus"
        },
        {
          "id": 537922,
          "code": "C302800",
          "description": "Chediak-Higashi syndrome"
        },
        {
          "id": 537923,
          "code": "C302900",
          "description": "Hermansky-Pudlak syndrome"
        },
        {
          "id": 537924,
          "code": "C302A00",
          "description": "Partial albinism"
        },
        {
          "id": 537925,
          "code": "C302y00",
          "description": "Other specified disturbance of aromatic amino-acid metabolism"
        },
        {
          "id": 537926,
          "code": "C302y11",
          "description": "Oasthouse urine disease"
        },
        {
          "id": 537927,
          "code": "C302z00",
          "description": "Disturbance of aromatic amino-acid metabolism NOS"
        },
        {
          "id": 537928,
          "code": "C303.00",
          "description": "Disturbances of branched-chain amino-acid metabolism"
        },
        {
          "id": 537929,
          "code": "C303000",
          "description": "Leucinosis"
        },
        {
          "id": 537930,
          "code": "C303011",
          "description": "Leucine sensitivity"
        },
        {
          "id": 537931,
          "code": "C303100",
          "description": "Isoleucinosis"
        },
        {
          "id": 537932,
          "code": "C303200",
          "description": "Hypervalinaemia"
        },
        {
          "id": 537933,
          "code": "C303211",
          "description": "Valinosis"
        },
        {
          "id": 537934,
          "code": "C303300",
          "description": "Maple syrup urine disease"
        },
        {
          "id": 537935,
          "code": "C303400",
          "description": "Hypervalinaemia"
        },
        {
          "id": 537936,
          "code": "C303y00",
          "description": "Other specified disturbance of branched chain amino-acid metabolism"
        },
        {
          "id": 537937,
          "code": "C303z00",
          "description": "Disturbance of branched-chain amino-acid metabolism NOS"
        },
        {
          "id": 537938,
          "code": "C304.00",
          "description": "Disturbance of sulphur-bearing amino-acid metabolism"
        },
        {
          "id": 537939,
          "code": "C304200",
          "description": "Methioninaemia"
        },
        {
          "id": 537940,
          "code": "C304211",
          "description": "Hypermethioninaemia"
        },
        {
          "id": 537941,
          "code": "C304300",
          "description": "Homocystinuria"
        },
        {
          "id": 537942,
          "code": "C304400",
          "description": "Sulphite oxidase deficiency"
        },
        {
          "id": 537943,
          "code": "C304500",
          "description": "Hyperhomocysteinaemia"
        },
        {
          "id": 537944,
          "code": "C304y00",
          "description": "Other specified disturbance of sulphur-bearing amino-acid metabolism"
        },
        {
          "id": 537945,
          "code": "C304z00",
          "description": "Disturbance of sulphur-bearing amino-acid metabolism NOS"
        },
        {
          "id": 537946,
          "code": "C304z11",
          "description": "Methionine malabsorption syndrome"
        },
        {
          "id": 537947,
          "code": "C305.00",
          "description": "Disturbance of histidine metabolism"
        },
        {
          "id": 537948,
          "code": "C305000",
          "description": "Histidinaemia"
        },
        {
          "id": 537949,
          "code": "C305100",
          "description": "Imidazole aminoaciduria"
        },
        {
          "id": 537950,
          "code": "C305200",
          "description": "Histidinuria"
        },
        {
          "id": 537951,
          "code": "C305y00",
          "description": "Other specified disturbance of histidine metabolism"
        },
        {
          "id": 537952,
          "code": "C305z00",
          "description": "Disturbance of histidine metabolism NOS"
        },
        {
          "id": 537953,
          "code": "C306.00",
          "description": "Disturbance of urea cycle metabolism"
        },
        {
          "id": 537954,
          "code": "C306000",
          "description": "Hyperornithinaemia"
        },
        {
          "id": 537955,
          "code": "C306100",
          "description": "Citrullinaemia"
        },
        {
          "id": 537956,
          "code": "C306200",
          "description": "Argininosuccinic aciduria"
        },
        {
          "id": 537957,
          "code": "C306300",
          "description": "Hyperargininaemia"
        },
        {
          "id": 537958,
          "code": "C306y00",
          "description": "Other specified disturbance of urea cycle metabolism"
        },
        {
          "id": 537959,
          "code": "C306z00",
          "description": "Disturbance of urea cycle metabolism NOS"
        },
        {
          "id": 538162,
          "code": "Cyu8900",
          "description": "[X]Other lipid storage disorders"
        },
        {
          "id": 537960,
          "code": "C307.00",
          "description": "Disturbance of other straight-chain amino-acid metabolism"
        },
        {
          "id": 537961,
          "code": "C307100",
          "description": "Disturbance of threonine metabolism"
        },
        {
          "id": 537962,
          "code": "C307200",
          "description": "Disturbance of serine metabolism"
        },
        {
          "id": 537963,
          "code": "C307300",
          "description": "Disturbance of glutamine metabolism"
        },
        {
          "id": 537964,
          "code": "C307400",
          "description": "Hyperlysinaemia"
        },
        {
          "id": 537965,
          "code": "C307500",
          "description": "Pipecolic acidaemia"
        },
        {
          "id": 537966,
          "code": "C307600",
          "description": "Saccharopinuria"
        },
        {
          "id": 537967,
          "code": "C307y00",
          "description": "Other specified disturbance of other straight-chain amino-acid metabolism"
        },
        {
          "id": 537968,
          "code": "C307y11",
          "description": "Methylmalonic acidaemia"
        },
        {
          "id": 537969,
          "code": "C307z00",
          "description": "Disturbance of other straight-chain amino-acid metabolism NOS"
        },
        {
          "id": 537970,
          "code": "C308.00",
          "description": "Disorders of fatty-acid metabolism"
        },
        {
          "id": 537971,
          "code": "C308000",
          "description": "Medium chain acyl-CoA dehydrogenase deficiency"
        },
        {
          "id": 537972,
          "code": "C308100",
          "description": "Multiple acyl-CoA dehydrogenase deficiencies"
        },
        {
          "id": 537973,
          "code": "C308200",
          "description": "X-linked adrenoleucodystrophy"
        },
        {
          "id": 537974,
          "code": "C309.00",
          "description": "Glutaryl CoA dehydrogenase deficiency"
        },
        {
          "id": 537975,
          "code": "C30A.00",
          "description": "Tryptophan malabsorption syndrome"
        },
        {
          "id": 537976,
          "code": "C30A.11",
          "description": "Blue diaper syndrome"
        },
        {
          "id": 537977,
          "code": "C30y.00",
          "description": "Disturbance of other specified amino-acid metabolism"
        },
        {
          "id": 537978,
          "code": "C30y000",
          "description": "Alaninaemia"
        },
        {
          "id": 537979,
          "code": "C30y100",
          "description": "Ethanolaminuria"
        },
        {
          "id": 537980,
          "code": "C30y300",
          "description": "Hydroxyprolinaemia"
        },
        {
          "id": 537981,
          "code": "C30y400",
          "description": "Hyperprolinaemia"
        },
        {
          "id": 537982,
          "code": "C30y600",
          "description": "Iminoacidopathy"
        },
        {
          "id": 537983,
          "code": "C30y700",
          "description": "Sarcosinaemia"
        },
        {
          "id": 537984,
          "code": "C30y800",
          "description": "Glutaric aciduria Type 1"
        },
        {
          "id": 537985,
          "code": "C30yy00",
          "description": "Other specified disturbance of amino-acid metabolism"
        },
        {
          "id": 537986,
          "code": "C30yy00",
          "description": "Other specified disturbance of amino-acid metabolism"
        },
        {
          "id": 537987,
          "code": "C30yz00",
          "description": "Disturbance of other specified amino-acid metabolism NOS"
        },
        {
          "id": 537988,
          "code": "C30yz00",
          "description": "Disturbance of other specified amino-acid metabolism NOS"
        },
        {
          "id": 537989,
          "code": "C30z.00",
          "description": "Disturbance of amino-acid transport or metabolism NOS"
        },
        {
          "id": 537990,
          "code": "C30z.00",
          "description": "Disturbance of amino-acid transport or metabolism NOS"
        },
        {
          "id": 537991,
          "code": "C310.00",
          "description": "Glycogenosis - glycogen storage disease"
        },
        {
          "id": 537992,
          "code": "C310.11",
          "description": "Amylopectinosis"
        },
        {
          "id": 537993,
          "code": "C310.13",
          "description": "Glycogen storage disease"
        },
        {
          "id": 537994,
          "code": "C310000",
          "description": "McArdle's disease"
        },
        {
          "id": 537995,
          "code": "C310011",
          "description": "Myophosphorylase deficiency"
        },
        {
          "id": 537996,
          "code": "C310012",
          "description": "Glycogenosis, type 5"
        },
        {
          "id": 537997,
          "code": "C310100",
          "description": "Generalised glycogenosis"
        },
        {
          "id": 537998,
          "code": "C310112",
          "description": "Pompe's disease"
        },
        {
          "id": 537999,
          "code": "C310113",
          "description": "Glycogenosis, type 2"
        },
        {
          "id": 538000,
          "code": "C310211",
          "description": "Von Gierke's disease"
        },
        {
          "id": 538001,
          "code": "C310300",
          "description": "Glycogenosis of liver and muscle"
        },
        {
          "id": 538002,
          "code": "C310311",
          "description": "Glycogenosis of liver and muscle"
        },
        {
          "id": 538003,
          "code": "C310400",
          "description": "Glycogenosis with hepatic cirrhosis"
        },
        {
          "id": 538004,
          "code": "C310411",
          "description": "Glycogenosis, type 4"
        },
        {
          "id": 538005,
          "code": "C310412",
          "description": "Andersen's disease"
        },
        {
          "id": 538006,
          "code": "C310y00",
          "description": "Other specified glycogenosis"
        },
        {
          "id": 538007,
          "code": "C310z00",
          "description": "Glycogenosis NOS"
        },
        {
          "id": 538008,
          "code": "C311.00",
          "description": "Galactosaemia"
        },
        {
          "id": 538009,
          "code": "C311000",
          "description": "Galactose-1-phosphate uridyl transferase deficiency"
        },
        {
          "id": 538010,
          "code": "C311100",
          "description": "Galactokinase deficiency"
        },
        {
          "id": 538011,
          "code": "C311y00",
          "description": "Other specified galactosaemia"
        },
        {
          "id": 538012,
          "code": "C311z00",
          "description": "Galactosaemia NOS"
        },
        {
          "id": 538013,
          "code": "C312.00",
          "description": "Hereditary fructose intolerance"
        },
        {
          "id": 538014,
          "code": "C312.11",
          "description": "Fructosaemia"
        },
        {
          "id": 538015,
          "code": "C314.00",
          "description": "Renal glycosuria"
        },
        {
          "id": 538016,
          "code": "C315.00",
          "description": "Disorders of pyruvate metabolism and gluconeogenesis"
        },
        {
          "id": 538017,
          "code": "C315000",
          "description": "Pyruvate dehydrogenase deficiency"
        },
        {
          "id": 538018,
          "code": "C31y000",
          "description": "Essential benign pentosuria"
        },
        {
          "id": 538019,
          "code": "C31y100",
          "description": "Fucosidosis"
        },
        {
          "id": 538020,
          "code": "C31y200",
          "description": "Oxalosis"
        },
        {
          "id": 538021,
          "code": "C31y300",
          "description": "Mannosidosis"
        },
        {
          "id": 538022,
          "code": "C31y400",
          "description": "Xylosuria"
        },
        {
          "id": 538023,
          "code": "C31y500",
          "description": "Primary oxaluria"
        },
        {
          "id": 538024,
          "code": "C31y600",
          "description": "Oxaluria NEC"
        },
        {
          "id": 538025,
          "code": "C31y700",
          "description": "Aspartylglucosaminuria"
        },
        {
          "id": 538026,
          "code": "C31y800",
          "description": "Glycerol kinase deficiency"
        },
        {
          "id": 538027,
          "code": "C31yX00",
          "description": "Disorder of glycoprotein metabolism, unspecified"
        },
        {
          "id": 538028,
          "code": "C320.00",
          "description": "Pure hypercholesterolaemia"
        },
        {
          "id": 538029,
          "code": "C320.11",
          "description": "Familial hypercholesterolaemia"
        },
        {
          "id": 538030,
          "code": "C320.12",
          "description": "Fredrickson type IIa lipidaemia"
        },
        {
          "id": 538031,
          "code": "C320.13",
          "description": "Low density lipoproteinaemia"
        },
        {
          "id": 538032,
          "code": "C320000",
          "description": "Familial hypercholesterolaemia"
        },
        {
          "id": 538033,
          "code": "C320100",
          "description": "Hyperbetalipoproteinaemia"
        },
        {
          "id": 538034,
          "code": "C320200",
          "description": "Hyperlipidaemia, group A"
        },
        {
          "id": 538035,
          "code": "C320300",
          "description": "Low-density-lipoprotein-type (LDL) hyperlipoproteinaemia"
        },
        {
          "id": 538036,
          "code": "C320400",
          "description": "Fredrickson's hyperlipoproteinaemia, type IIa"
        },
        {
          "id": 538037,
          "code": "C320500",
          "description": "Familial defective apolipoprotein B-100"
        },
        {
          "id": 538038,
          "code": "C320600",
          "description": "Polygenic hypercholesterolaemia"
        },
        {
          "id": 538039,
          "code": "C320y00",
          "description": "Other specified pure hypercholesterolaemia"
        },
        {
          "id": 538040,
          "code": "C320z00",
          "description": "Pure hypercholesterolaemia NOS"
        },
        {
          "id": 538041,
          "code": "C321.00",
          "description": "Pure hyperglyceridaemia"
        },
        {
          "id": 538042,
          "code": "C321.11",
          "description": "Fredrickson type IV lipidaemia"
        },
        {
          "id": 538043,
          "code": "C321.12",
          "description": "Very low density lipoprotinaemia"
        },
        {
          "id": 538044,
          "code": "C321000",
          "description": "Hypertriglyceridaemia"
        },
        {
          "id": 538045,
          "code": "C322.11",
          "description": "Fredrickson type IIb lipidaemia"
        },
        {
          "id": 538046,
          "code": "C322.12",
          "description": "Fredrickson type III lipidaemia"
        },
        {
          "id": 538047,
          "code": "C322000",
          "description": "Familial combined hyperlipidaemia"
        },
        {
          "id": 538048,
          "code": "C323.00",
          "description": "Hyperchylomicronaemia"
        },
        {
          "id": 538049,
          "code": "C323.11",
          "description": "Burger - Grute syndrome"
        },
        {
          "id": 538050,
          "code": "C323.13",
          "description": "Fredrickson type V lipaemia"
        },
        {
          "id": 538051,
          "code": "C325000",
          "description": "High density lipoid deficiency"
        },
        {
          "id": 538052,
          "code": "C327.00",
          "description": "Lipidoses"
        },
        {
          "id": 538053,
          "code": "C327.11",
          "description": "Anderson's disease"
        },
        {
          "id": 538054,
          "code": "C327.12",
          "description": "Fabry's disease"
        },
        {
          "id": 538055,
          "code": "C327.13",
          "description": "Pseudo - Hurler's disease"
        },
        {
          "id": 538056,
          "code": "C327100",
          "description": "Gaucher's disease"
        },
        {
          "id": 538057,
          "code": "C327200",
          "description": "Niemann-Pick disease"
        },
        {
          "id": 538058,
          "code": "C327300",
          "description": "Wolman disease"
        },
        {
          "id": 538059,
          "code": "C327311",
          "description": "Primary familial xanthomatosis"
        },
        {
          "id": 538060,
          "code": "C327400",
          "description": "Alpha-galactosidase A deficiency"
        },
        {
          "id": 538061,
          "code": "C327411",
          "description": "Fabry's disease"
        },
        {
          "id": 538062,
          "code": "C327412",
          "description": "Anderson's disease"
        },
        {
          "id": 538063,
          "code": "C327413",
          "description": "Anderson-Fabry disease"
        },
        {
          "id": 538064,
          "code": "C327z00",
          "description": "Lipidoses NOS"
        },
        {
          "id": 538065,
          "code": "C329.00",
          "description": "Hypercholesterolaemia"
        },
        {
          "id": 538066,
          "code": "C33y000",
          "description": "Hypoproteinaemia"
        },
        {
          "id": 538067,
          "code": "C351.00",
          "description": "Disorders of copper metabolism"
        },
        {
          "id": 538068,
          "code": "C351000",
          "description": "Hepatolenticular degeneration (Wilson's disease)"
        },
        {
          "id": 538069,
          "code": "C351011",
          "description": "Wilson's disease"
        },
        {
          "id": 538070,
          "code": "C351z00",
          "description": "Disorder of copper metabolism NOS"
        },
        {
          "id": 538071,
          "code": "C371.00",
          "description": "Disorders of porphyrin metabolism"
        },
        {
          "id": 538072,
          "code": "C371000",
          "description": "Congenital porphyria"
        },
        {
          "id": 538073,
          "code": "C371100",
          "description": "Erythropoietic protoporphyria"
        },
        {
          "id": 538074,
          "code": "C371200",
          "description": "Acute intermittent porphyria"
        },
        {
          "id": 538075,
          "code": "C371300",
          "description": "Protocoproporphyria"
        },
        {
          "id": 538076,
          "code": "C371400",
          "description": "Porphyria cutanea tarda"
        },
        {
          "id": 538077,
          "code": "C371500",
          "description": "Coproporphyria"
        },
        {
          "id": 538078,
          "code": "C371600",
          "description": "Pseudoporphyria"
        },
        {
          "id": 538079,
          "code": "C371z00",
          "description": "Porphyria NOS"
        },
        {
          "id": 538080,
          "code": "C372.00",
          "description": "Other disorders of purine and pyrimidine metabolism"
        },
        {
          "id": 538081,
          "code": "C372.11",
          "description": "Lesch - Nyhan syndrome"
        },
        {
          "id": 538082,
          "code": "C372000",
          "description": "Hypoxanthine-guanine-phosphoribosyltransferase deficiency"
        },
        {
          "id": 538083,
          "code": "C372011",
          "description": "Lesch - Nyhan syndrome"
        },
        {
          "id": 538084,
          "code": "C372100",
          "description": "Xanthinuria"
        },
        {
          "id": 538085,
          "code": "C372300",
          "description": "Lesch-Nyhan syndrome"
        },
        {
          "id": 538086,
          "code": "C372z00",
          "description": "Other disorder of purine or pyrimidine metabolism NOS"
        },
        {
          "id": 538087,
          "code": "C373.00",
          "description": "Amyloidosis"
        },
        {
          "id": 538088,
          "code": "C373000",
          "description": "Sporadic primary amyloidosis"
        },
        {
          "id": 538089,
          "code": "C373100",
          "description": "Familial Mediterranean fever"
        },
        {
          "id": 538090,
          "code": "C373111",
          "description": "Familial periodic peritonitis"
        },
        {
          "id": 538091,
          "code": "C373112",
          "description": "Recurrent polyserositis"
        },
        {
          "id": 538092,
          "code": "C373200",
          "description": "Familial neuropathic amyloid"
        },
        {
          "id": 538093,
          "code": "C373300",
          "description": "Familial cardiac amyloid"
        },
        {
          "id": 538094,
          "code": "C373411",
          "description": "Muckle-Wells syndrome"
        },
        {
          "id": 538095,
          "code": "C373412",
          "description": "Amyloid nephropathy with deafness and urticaria"
        },
        {
          "id": 538096,
          "code": "C373600",
          "description": "Nephropathic amyloidosis"
        },
        {
          "id": 538097,
          "code": "C373700",
          "description": "Primary amyloidosis NEC"
        },
        {
          "id": 538098,
          "code": "C373800",
          "description": "Familial periodic fever"
        },
        {
          "id": 538099,
          "code": "C373900",
          "description": "Organ limited non-hereditary amyloidosis"
        },
        {
          "id": 538100,
          "code": "C373A00",
          "description": "Hereditary periodic fever"
        },
        {
          "id": 538101,
          "code": "C373B00",
          "description": "Tumor necrosis factor receptor associated periodic syndrome"
        },
        {
          "id": 538102,
          "code": "C373C00",
          "description": "AL amyloidosis"
        },
        {
          "id": 538103,
          "code": "C373D00",
          "description": "Senile systemic amyloidosis"
        },
        {
          "id": 538104,
          "code": "C373E00",
          "description": "Amyloid polyneuropathy type I"
        },
        {
          "id": 538105,
          "code": "C373E11",
          "description": "Swedish type amyloid polyneuropathy"
        },
        {
          "id": 538106,
          "code": "C373E12",
          "description": "Andrade type amyloid polyneuropathy"
        },
        {
          "id": 538107,
          "code": "C373F00",
          "description": "Familial amyloid polyneuropathy type II"
        },
        {
          "id": 538108,
          "code": "C373F11",
          "description": "Swiss type amyloid polyneuropathy"
        },
        {
          "id": 538109,
          "code": "C373G00",
          "description": "Senile cardiac amyloidosis"
        },
        {
          "id": 538110,
          "code": "C373H00",
          "description": "Amyloid A amyloidosis"
        },
        {
          "id": 538111,
          "code": "C373J00",
          "description": "Beta-2 microglobulin amyloidosis"
        },
        {
          "id": 538112,
          "code": "C373K00",
          "description": "Familial amyloid polyneuropathy, Iowa type"
        },
        {
          "id": 538113,
          "code": "C373K11",
          "description": "Van Allen type amyloid polyneuropathy"
        },
        {
          "id": 538114,
          "code": "C373K12",
          "description": "British type amyloid polyneuropathy"
        },
        {
          "id": 538115,
          "code": "C373K13",
          "description": "Familial amyloid polyneuropathy type III"
        },
        {
          "id": 538116,
          "code": "C373L00",
          "description": "Amyloid nephropathy of Ostertag"
        },
        {
          "id": 538117,
          "code": "C373X00",
          "description": "Heredofamilial amyloidosis, unspecified"
        },
        {
          "id": 538118,
          "code": "C373y00",
          "description": "Other specified amyloidosis"
        },
        {
          "id": 538119,
          "code": "C373z00",
          "description": "Amyloidosis NOS"
        },
        {
          "id": 538120,
          "code": "C375.00",
          "description": "Mucopolysaccharidosis"
        },
        {
          "id": 538121,
          "code": "C375.11",
          "description": "Gargoylism"
        },
        {
          "id": 538122,
          "code": "C375.12",
          "description": "Hunter's syndrome"
        },
        {
          "id": 538123,
          "code": "C375.13",
          "description": "Hurler's syndrome"
        },
        {
          "id": 538124,
          "code": "C375.14",
          "description": "Lipochondrodystrophy"
        },
        {
          "id": 538125,
          "code": "C375.15",
          "description": "Maroteaux - Lamy syndrome"
        },
        {
          "id": 538126,
          "code": "C375.16",
          "description": "Morquio - Brailsford disease"
        },
        {
          "id": 538127,
          "code": "C375.17",
          "description": "Osteochondrodystrophy"
        },
        {
          "id": 538128,
          "code": "C375.18",
          "description": "Sanfilippo's syndrome"
        },
        {
          "id": 538129,
          "code": "C375.19",
          "description": "Scheie's syndrome"
        },
        {
          "id": 538130,
          "code": "C375.1A",
          "description": "Dysostosis multiplex"
        },
        {
          "id": 538131,
          "code": "C375000",
          "description": "Mannosidosis"
        },
        {
          "id": 538132,
          "code": "C375011",
          "description": "A-fucosidase deficiency"
        },
        {
          "id": 538133,
          "code": "C375100",
          "description": "Mucopolysaccharidosis, type 1"
        },
        {
          "id": 538134,
          "code": "C375111",
          "description": "Gargoylism"
        },
        {
          "id": 538135,
          "code": "C375112",
          "description": "Hurler's syndrome"
        },
        {
          "id": 538136,
          "code": "C375113",
          "description": "Scheie's syndrome"
        },
        {
          "id": 538137,
          "code": "C375200",
          "description": "Mucopolysaccharidosis, type II"
        },
        {
          "id": 538138,
          "code": "C375211",
          "description": "Hunter's syndrome"
        },
        {
          "id": 538139,
          "code": "C375300",
          "description": "Mucopolysaccharidosis, type III"
        },
        {
          "id": 538140,
          "code": "C375311",
          "description": "Sanfilippo syndrome"
        },
        {
          "id": 538141,
          "code": "C375400",
          "description": "Mucopolysaccharidosis, type IV"
        },
        {
          "id": 538142,
          "code": "C375411",
          "description": "Morquio - Brailsford syndrome"
        },
        {
          "id": 538143,
          "code": "C375600",
          "description": "Mucopolysaccharidosis, type VI"
        },
        {
          "id": 538144,
          "code": "C375611",
          "description": "Maroteaux - Lamy syndrome"
        },
        {
          "id": 538145,
          "code": "C375700",
          "description": "Mucopolysaccharidosis, type VII"
        },
        {
          "id": 538146,
          "code": "C375711",
          "description": "Beta-glucuronidase deficiency"
        },
        {
          "id": 538147,
          "code": "C375712",
          "description": "Sly syndrome"
        },
        {
          "id": 538148,
          "code": "C375800",
          "description": "Multiple sulphatase deficiency"
        },
        {
          "id": 538149,
          "code": "C375X00",
          "description": "Disorder of glucosaminoglycan metabolism, unspecified"
        },
        {
          "id": 538150,
          "code": "C375y00",
          "description": "Other specified mucopolysaccharidosis"
        },
        {
          "id": 538151,
          "code": "C375z00",
          "description": "Mucopolysaccharidosis NOS"
        },
        {
          "id": 538152,
          "code": "C376100",
          "description": "Alpha-1-antitrypsin hepatitis"
        },
        {
          "id": 538153,
          "code": "C376200",
          "description": "Alpha-1-antitrypsin deficiency"
        },
        {
          "id": 538154,
          "code": "C377.00",
          "description": "Disorders of glycoprotein metabolism"
        },
        {
          "id": 538155,
          "code": "C377100",
          "description": "Mucolipidosis type III"
        },
        {
          "id": 538156,
          "code": "C377111",
          "description": "Pseudo - Hurler's disease"
        },
        {
          "id": 538157,
          "code": "Cyu8100",
          "description": "[X]Other disorders of aromatic amino-acid metabolism"
        },
        {
          "id": 538158,
          "code": "Cyu8200",
          "description": "[X]Other disorders of branched-chain amino-acid metabolism"
        },
        {
          "id": 538159,
          "code": "Cyu8300",
          "description": "[X]Other specified disorders of amino-acid metabolism"
        },
        {
          "id": 538160,
          "code": "Cyu8700",
          "description": "[X]Other gangliosidosis"
        },
        {
          "id": 538161,
          "code": "Cyu8800",
          "description": "[X]Other sphingolipidosis"
        },
        {
          "id": 538163,
          "code": "Cyu8A00",
          "description": "[X]Other mucopolysaccharidoses"
        },
        {
          "id": 538164,
          "code": "Cyu8B00",
          "description": "[X]Other disorders of glucosaminoglycan metabolism"
        },
        {
          "id": 538165,
          "code": "Cyu8C00",
          "description": "[X]Other glycoprotein metabolism disorders"
        },
        {
          "id": 538166,
          "code": "Cyu8F00",
          "description": "[X]Other disorders of purine and pyrimidine metabolism"
        },
        {
          "id": 538167,
          "code": "Cyu8H00",
          "description": "[X]Other porphyria"
        },
        {
          "id": 538168,
          "code": "Cyu8L00",
          "description": "[X]Other amyloidosis"
        },
        {
          "id": 538169,
          "code": "Cyu8R00",
          "description": "[X]Disorder of glucosaminoglycan metabolism, unspecified"
        },
        {
          "id": 538170,
          "code": "Cyu8S00",
          "description": "[X]Disorder of glycoprotein metabolism, unspecified"
        },
        {
          "id": 538171,
          "code": "Cyu8U00",
          "description": "[X]Heredofamilial amyloidosis, unspecified"
        },
        {
          "id": 538172,
          "code": "D014100",
          "description": "Oroticaciduria"
        },
        {
          "id": 538173,
          "code": "D402.12",
          "description": "Chediak - Steinbrinck anomaly"
        },
        {
          "id": 538174,
          "code": "D402.17",
          "description": "Chediak-Higashi syndrome"
        },
        {
          "id": 538175,
          "code": "F100.00",
          "description": "Leucodystrophy"
        },
        {
          "id": 538176,
          "code": "F100000",
          "description": "Krabbe's disease"
        },
        {
          "id": 538177,
          "code": "F100200",
          "description": "Pelizaeus-Merzbacher disease"
        },
        {
          "id": 538178,
          "code": "F100300",
          "description": "Metachromatic leucodystrophy"
        },
        {
          "id": 538179,
          "code": "F100z00",
          "description": "Leucodystrophy NOS"
        },
        {
          "id": 538180,
          "code": "F101.00",
          "description": "Cerebral lipidoses"
        },
        {
          "id": 538181,
          "code": "F101000",
          "description": "Jansky-Bielschowsky disease"
        },
        {
          "id": 538182,
          "code": "F101100",
          "description": "Kuf's disease"
        },
        {
          "id": 538183,
          "code": "F101200",
          "description": "Spielmeyer-Vogt (Batten) disease"
        },
        {
          "id": 538184,
          "code": "F101211",
          "description": "Batten's disease of retina"
        },
        {
          "id": 538185,
          "code": "F101300",
          "description": "Tay-Sach's disease"
        },
        {
          "id": 538186,
          "code": "F101400",
          "description": "Gangliosidosis"
        },
        {
          "id": 538187,
          "code": "F101500",
          "description": "Retinal dystrophy in cerebroretinal lipidosis"
        },
        {
          "id": 538188,
          "code": "F101600",
          "description": "Sandhoff disease"
        },
        {
          "id": 538189,
          "code": "F102000",
          "description": "Cerebral degeneration in Gaucher's disease"
        },
        {
          "id": 538190,
          "code": "F102100",
          "description": "Cerebral degeneration in Niemann-Pick disease"
        },
        {
          "id": 538191,
          "code": "F103000",
          "description": "Cerebral degeneration in Hunter's disease"
        },
        {
          "id": 538192,
          "code": "F103100",
          "description": "Cerebral degeneration in mucopolysaccharidoses"
        },
        {
          "id": 538193,
          "code": "F374000",
          "description": "Polyneuropathy in amyloidosis"
        },
        {
          "id": 538194,
          "code": "F374800",
          "description": "Polyneuropathy in porphyria"
        },
        {
          "id": 538195,
          "code": "F396000",
          "description": "Myopathy due to amyloid"
        },
        {
          "id": 538196,
          "code": "F398.00",
          "description": "Myopathy in metabolic diseases"
        },
        {
          "id": 538197,
          "code": "F427K00",
          "description": "Lipofuscinosis NOS"
        },
        {
          "id": 538198,
          "code": "F427K11",
          "description": "Lipofuscinosis NEC"
        },
        {
          "id": 538199,
          "code": "F435800",
          "description": "Generalised gyrate choroid atrophy"
        },
        {
          "id": 538200,
          "code": "F4C5700",
          "description": "Conjunctival amyloidosis"
        },
        {
          "id": 538201,
          "code": "F4K2F00",
          "description": "Amyloid of vitreous"
        },
        {
          "id": 538202,
          "code": "F4K2F11",
          "description": "Vitreous amyloid"
        },
        {
          "id": 538203,
          "code": "Fyu8800",
          "description": "[X]Myopathy in metabolic diseases classified elsewhere"
        },
        {
          "id": 538204,
          "code": "G557000",
          "description": "Amyloid heart disease"
        },
        {
          "id": 538205,
          "code": "G557011",
          "description": "Cardiac amyloidosis"
        },
        {
          "id": 538206,
          "code": "G557200",
          "description": "Cardiac glycogenosis"
        },
        {
          "id": 538207,
          "code": "G557400",
          "description": "Mucopolysaccharidosis cardiomyopathy"
        },
        {
          "id": 538208,
          "code": "G674000",
          "description": "Cerebral amyloid angiopathy"
        },
        {
          "id": 538209,
          "code": "H57y000",
          "description": "Pulmonary amyloidosis"
        },
        {
          "id": 538210,
          "code": "J57B000",
          "description": "Amyloidosis of small intestine"
        },
        {
          "id": 538211,
          "code": "J57B011",
          "description": "Amyloid of small intestine"
        },
        {
          "id": 538212,
          "code": "K01x000",
          "description": "Nephrotic syndrome in amyloidosis"
        },
        {
          "id": 538213,
          "code": "K08yH00",
          "description": "Familial renal hypouricaemia"
        },
        {
          "id": 538214,
          "code": "K168.00",
          "description": "Amyloid of bladder"
        },
        {
          "id": 538215,
          "code": "K199.00",
          "description": "Amyloid disease of the urethra"
        },
        {
          "id": 538216,
          "code": "M2y9000",
          "description": "Bullous cutaneous amyloidosis"
        },
        {
          "id": 538217,
          "code": "M2y9011",
          "description": "Bullous cutaneous amyloid"
        },
        {
          "id": 538218,
          "code": "N030200",
          "description": "Arthropathy in amyloidosis"
        },
        {
          "id": 538219,
          "code": "N030211",
          "description": "Articular amyloid"
        },
        {
          "id": 538220,
          "code": "N030212",
          "description": "Amyloid arthropathy"
        },
        {
          "id": 538221,
          "code": "N039.00",
          "description": "Beta-2 microglobulin arthropathy"
        },
        {
          "id": 538222,
          "code": "N067.00",
          "description": "Ochronotic arthropathy"
        },
        {
          "id": 538223,
          "code": "P3y0.00",
          "description": "Ocular albinism"
        },
        {
          "id": 538224,
          "code": "PKy9200",
          "description": "Menke's syndrome"
        },
        {
          "id": 538225,
          "code": "PKy9211",
          "description": "Kinky hair syndrome"
        },
        {
          "id": 538226,
          "code": "PKy9212",
          "description": "Congenital kinking hair"
        },
        {
          "id": 538227,
          "code": "Q433800",
          "description": "Neonatal jaundice with porphyria"
        },
        {
          "id": 538228,
          "code": "Q435100",
          "description": "Perinatal jaundice due to galactosaemia"
        },
        {
          "id": 538229,
          "code": "R11z500",
          "description": "[D]Hyperuricuria"
        }
      ]
    }
  ],
  "version_history": [
    {
      "version_id": 11528,
      "version_name": "Metabolic (Read v2)",
      "version_date": "2025-01-19T16:48:54.301953Z",
      "is_published": true,
      "is_latest": true
    }
  ]
}