{
  "concept_id": 4574,
  "concept_version_id": 11938,
  "coding_system": {
    "id": 4,
    "name": "ICD10 codes",
    "description": "ICD10 Codes"
  },
  "name": "ICD10 - EuroLinkCAT CA Identification",
  "description": null,
  "author": "",
  "entry_date": "2025-06-25",
  "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": "PH1909",
  "code_attribute_header": [
    "group"
  ],
  "phenotype_owner_history_id": 4235,
  "requested_entity_id": null,
  "components": [
    {
      "id": 10438,
      "name": "CODES - ICD10 - EuroLinkCAT CA Identification",
      "logical_type": "INCLUDE",
      "source_type": "FILE_IMPORT",
      "source": null,
      "codes": [
        {
          "id": 614516,
          "code": "Q00",
          "description": "Anencephaly and similar malformations",
          "attributes": {
            "group": "Anencephaly"
          }
        },
        {
          "id": 614517,
          "code": "Q01",
          "description": "Encephalocele",
          "attributes": {
            "group": "Encephalocele"
          }
        },
        {
          "id": 614518,
          "code": "Q05",
          "description": "Spina bifida",
          "attributes": {
            "group": "Spina Bifida (isolated cases with or without hydrocephalus)"
          }
        },
        {
          "id": 614519,
          "code": "Q03",
          "description": "Congenital hydrocephalus",
          "attributes": {
            "group": "Hydrocephalus"
          }
        },
        {
          "id": 614520,
          "code": "Q02",
          "description": "Microcephaly",
          "attributes": {
            "group": "Severe microcephaly"
          }
        },
        {
          "id": 614521,
          "code": "Q041",
          "description": "Arhinencephaly",
          "attributes": {
            "group": "Arhinencephaly/holoprosencephaly"
          }
        },
        {
          "id": 614522,
          "code": "Q042",
          "description": "Holoprosencephaly",
          "attributes": {
            "group": "Arhinencephaly/holoprosencephaly"
          }
        },
        {
          "id": 614523,
          "code": "Q20",
          "description": "Congenital malformations of cardiac chambers and connections",
          "attributes": {
            "group": "Congenital heart defect (CHD)"
          }
        },
        {
          "id": 614524,
          "code": "Q21",
          "description": "Congenital malformations of cardiac septa",
          "attributes": {
            "group": "Congenital heart defect (CHD)"
          }
        },
        {
          "id": 614525,
          "code": "Q22",
          "description": "Congenital malformations of pulmonary and tricuspid valves",
          "attributes": {
            "group": "Congenital heart defect (CHD)"
          }
        },
        {
          "id": 614526,
          "code": "Q23",
          "description": "Congenital malformations of aortic and mitral valves",
          "attributes": {
            "group": "Congenital heart defect (CHD)"
          }
        },
        {
          "id": 614527,
          "code": "Q24",
          "description": "Other congenital malformations of heart",
          "attributes": {
            "group": "Congenital heart defect (CHD)"
          }
        },
        {
          "id": 614528,
          "code": "Q25",
          "description": "Congenital malformations of great arteries",
          "attributes": {
            "group": "Congenital heart defect (CHD)"
          }
        },
        {
          "id": 614529,
          "code": "Q200",
          "description": "Common arterial trunk",
          "attributes": {
            "group": "Common arterial truncus"
          }
        },
        {
          "id": 614530,
          "code": "Q201",
          "description": "Double outlet right ventricle",
          "attributes": {
            "group": "Double outlet right ventricle"
          }
        },
        {
          "id": 614531,
          "code": "Q203",
          "description": "Discordant ventriculoarterial connection",
          "attributes": {
            "group": "Transposition of great vessels (Only severe CHD)"
          }
        },
        {
          "id": 614532,
          "code": "Q204",
          "description": "Double inlet ventricle",
          "attributes": {
            "group": "Single ventricle"
          }
        },
        {
          "id": 614533,
          "code": "Q210",
          "description": "Ventricular septal defect",
          "attributes": {
            "group": "Ventricular Septal Defect (without severe CHD)"
          }
        },
        {
          "id": 614534,
          "code": "Q211",
          "description": "Atrial septal defect",
          "attributes": {
            "group": "Atrial septal defect (without severe CHD)"
          }
        },
        {
          "id": 614535,
          "code": "Q212",
          "description": "Atrioventricular septal defect",
          "attributes": {
            "group": "Atrioventricular septal defect"
          }
        },
        {
          "id": 614536,
          "code": "Q213",
          "description": "Tetralogy of Fallot",
          "attributes": {
            "group": "Tetralogy of Fallot"
          }
        },
        {
          "id": 614537,
          "code": "Q221",
          "description": "Congenital pulmonary valve stenosis",
          "attributes": {
            "group": "Pulmonary valve stenosis"
          }
        },
        {
          "id": 614538,
          "code": "Q220",
          "description": "Pulmonary valve atresia",
          "attributes": {
            "group": "Pulmonary valve atresia"
          }
        },
        {
          "id": 614539,
          "code": "Q230",
          "description": "Congenital stenosis of aortic valve",
          "attributes": {
            "group": "Aortic valve atresia/stenosis"
          }
        },
        {
          "id": 614540,
          "code": "Q232",
          "description": "Congenital mitral stenosis",
          "attributes": {
            "group": "Mitral valve anomalies"
          }
        },
        {
          "id": 614541,
          "code": "Q233",
          "description": "Congenital mitral insufficiency",
          "attributes": {
            "group": "Mitral valve anomalies"
          }
        },
        {
          "id": 614542,
          "code": "Q234",
          "description": "Hypoplastic left heart syndrome",
          "attributes": {
            "group": "Hypoplastic left heart"
          }
        },
        {
          "id": 614543,
          "code": "Q226",
          "description": "Hypoplastic right heart syndrome",
          "attributes": {
            "group": "Hypoplastic right heart"
          }
        },
        {
          "id": 614544,
          "code": "Q251",
          "description": "Coarctation of aorta",
          "attributes": {
            "group": "Coarctation of aorta"
          }
        },
        {
          "id": 614545,
          "code": "Q262",
          "description": "Total anomalous pulmonary venous connection",
          "attributes": {
            "group": "Total anomalous pulmonary venous return"
          }
        },
        {
          "id": 614546,
          "code": "Q250",
          "description": "Patent ductus arteriosus",
          "attributes": {
            "group": "PDA as only CHD in term infants (GA +37 weeks)"
          }
        },
        {
          "id": 614547,
          "code": "Q300",
          "description": "Choanal atresia",
          "attributes": {
            "group": "Choanal atresia"
          }
        },
        {
          "id": 614548,
          "code": "Q3380",
          "description": "Other congenital malformations of lung",
          "attributes": {
            "group": "Cystic adenomatous malformation of lung"
          }
        },
        {
          "id": 614549,
          "code": "Q36",
          "description": "Cleft lip",
          "attributes": {
            "group": "Cleft lip with or without cleft palate"
          }
        },
        {
          "id": 614550,
          "code": "Q37",
          "description": "Cleft palate with cleft lip",
          "attributes": {
            "group": "Cleft lip with or without cleft palate"
          }
        },
        {
          "id": 614551,
          "code": "Q35",
          "description": "Cleft palate",
          "attributes": {
            "group": "Cleft palate"
          }
        },
        {
          "id": 614552,
          "code": "Q390",
          "description": "Atresia of oesophagus without fistula",
          "attributes": {
            "group": "Oesophageal atresia with or without trachea-oesophageal fistula"
          }
        },
        {
          "id": 614553,
          "code": "Q410",
          "description": "Congenital absence, atresia and stenosis of duodenum",
          "attributes": {
            "group": "Duodenal atresia or stenosis"
          }
        },
        {
          "id": 614554,
          "code": "Q420",
          "description": "Congenital absence, atresia and stenosis of rectum with fistula",
          "attributes": {
            "group": "Ano-rectal atresia and stenosis"
          }
        },
        {
          "id": 614555,
          "code": "Q421",
          "description": "Congenital absence, atresia and stenosis of rectum without fistula",
          "attributes": {
            "group": "Ano-rectal atresia and stenosis"
          }
        },
        {
          "id": 614556,
          "code": "Q422",
          "description": "Congenital absence, atresia and stenosis of anus with fistula",
          "attributes": {
            "group": "Ano-rectal atresia and stenosis"
          }
        },
        {
          "id": 614557,
          "code": "Q431",
          "description": "Hirschsprung disease",
          "attributes": {
            "group": "Hirschsprung's disease"
          }
        },
        {
          "id": 614558,
          "code": "Q442",
          "description": "Atresia of bile ducts",
          "attributes": {
            "group": "Atresia of bile ducts"
          }
        },
        {
          "id": 614559,
          "code": "Q790",
          "description": "Congenital diaphragmatic hernia",
          "attributes": {
            "group": "Diaphragmatic hernia"
          }
        },
        {
          "id": 614560,
          "code": "Q793",
          "description": "Gastroschisis",
          "attributes": {
            "group": "Gastroschisis"
          }
        },
        {
          "id": 614561,
          "code": "Q792",
          "description": "Exomphalos",
          "attributes": {
            "group": "Omphalocele"
          }
        },
        {
          "id": 614562,
          "code": "Q601",
          "description": "Renal agenesis, bilateral",
          "attributes": {
            "group": "Bilateral renal agenesis"
          }
        },
        {
          "id": 614563,
          "code": "Q606",
          "description": "Potter syndrome",
          "attributes": {
            "group": "Bilateral renal agenesis"
          }
        },
        {
          "id": 614564,
          "code": "Q614",
          "description": "Renal dysplasia",
          "attributes": {
            "group": "Multicystic renal dysplasia"
          }
        },
        {
          "id": 614565,
          "code": "Q620",
          "description": "Congenital hydronephrosis",
          "attributes": {
            "group": "Cong hydronephrosis"
          }
        },
        {
          "id": 614566,
          "code": "Q71",
          "description": "Reduction defects of upper limb",
          "attributes": {
            "group": "Limb reduction defects"
          }
        },
        {
          "id": 614567,
          "code": "Q72",
          "description": "Reduction defects of lower limb",
          "attributes": {
            "group": "Limb reduction defects"
          }
        },
        {
          "id": 614568,
          "code": "Q750",
          "description": "Craniosynostosis",
          "attributes": {
            "group": "Craniosynostosis"
          }
        },
        {
          "id": 614569,
          "code": "Q8726",
          "description": "Congenital malformation syndromes predominantly involving limbs",
          "attributes": {
            "group": "VATER/VACTERL"
          }
        },
        {
          "id": 614570,
          "code": "Q90",
          "description": "Down syndrome",
          "attributes": {
            "group": "Down syndrome"
          }
        },
        {
          "id": 614571,
          "code": "Q914",
          "description": "Trisomy 13, meiotic nondisjunction",
          "attributes": {
            "group": "Trisomy 13"
          }
        },
        {
          "id": 614572,
          "code": "Q915",
          "description": "Trisomy 13, mosaicism (mitotic nondisjunction)",
          "attributes": {
            "group": "Trisomy 13"
          }
        },
        {
          "id": 614573,
          "code": "Q916",
          "description": "Trisomy 13, translocation",
          "attributes": {
            "group": "Trisomy 13"
          }
        },
        {
          "id": 614574,
          "code": "Q910",
          "description": "Trisomy 18, meiotic nondisjunction",
          "attributes": {
            "group": "Trisomy 18"
          }
        },
        {
          "id": 614575,
          "code": "Q911",
          "description": "Trisomy 18, mosaicism (mitotic nondisjunction)",
          "attributes": {
            "group": "Trisomy 18"
          }
        },
        {
          "id": 614576,
          "code": "Q912",
          "description": "Trisomy 18, translocation",
          "attributes": {
            "group": "Trisomy 18"
          }
        }
      ]
    }
  ],
  "version_history": [
    {
      "version_id": 11938,
      "version_name": "ICD10 - EuroLinkCAT CA Identification",
      "version_date": "2025-06-25T23:19:01.710027Z",
      "is_published": true,
      "is_latest": true
    }
  ]
}