FHIR IG Statistics: ValueSet/2.16.840.1.113883.2.4.3.11.60.90.77.11.298--20200824133956

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{
  "resourceType": "ValueSet",
  "id": "2.16.840.1.113883.2.4.3.11.60.90.77.11.298--20200824133956",
  "meta": {
    "profile": [
      "http://hl7.org/fhir/StructureDefinition/shareablevalueset"
    ]
  },
  "extension": [
    {
      "url": "http://hl7.org/fhir/StructureDefinition/resource-effectivePeriod",
      "valuePeriod": {
        "start": "2020-08-24T13:39:56Z"
      }
    }
  ],
  "url": "http://decor.nictiz.nl/fhir/ValueSet/2.16.840.1.113883.2.4.3.11.60.90.77.11.298--20200824133956",
  "identifier": [
    {
      "use": "official",
      "system": "urn:ietf:rfc:3986",
      "value": "urn:oid:2.16.840.1.113883.2.4.3.11.60.90.77.11.298"
    }
  ],
  "version": "2020-08-24T13:39:56",
  "name": "ProbleemNaam_CongenitaleAfwijkingPediatrie",
  "title": "ProbleemNaam CongenitaleAfwijking Pediatrie",
  "status": "active",
  "experimental": false,
  "publisher": "Nictiz",
  "contact": [
    {
      "name": "Nictiz",
      "telecom": [
        {
          "system": "phone",
          "value": "070-3173450"
        }
      ]
    }
  ],
  "description": "ProbleemNaam CongenitaleAfwijking Pediatrie",
  "immutable": false,
  "copyright": "This artefact includes content from SNOMED Clinical Terms® (SNOMED CT®) which is copyright of the International Health Terminology Standards Development Organisation (IHTSDO). Implementers of these artefacts must have the appropriate SNOMED CT Affiliate license - for more information contact http://www.snomed.org/snomed-ct/getsnomed-ct or info@snomed.org.",
  "compose": {
    "include": [
      {
        "system": "http://hl7.org/fhir/v3/NullFlavor",
        "concept": [
          {
            "code": "NI",
            "display": "geen informatie"
          },
          {
            "code": "OTH",
            "display": "overig"
          },
          {
            "code": "UNK",
            "display": "onbekend"
          }
        ]
      },
      {
        "system": "http://snomed.info/sct",
        "concept": [
          {
            "code": "88425004",
            "display": "congenitale misvorming van zenuwstelsel (aandoening)"
          },
          {
            "code": "89369001",
            "display": "anencefalie (aandoening)"
          },
          {
            "code": "1829003",
            "display": "microcefalie (aandoening)"
          },
          {
            "code": "76916001",
            "display": "spina bifida occulta (aandoening)"
          },
          {
            "code": "414667000",
            "display": "meningomyelocele (aandoening)"
          },
          {
            "code": "171131006",
            "display": "meningocele (aandoening)"
          },
          {
            "code": "55999004",
            "display": "encephalocele (aandoening)"
          },
          {
            "code": "30023002",
            "display": "hydranencefalie (aandoening)"
          },
          {
            "code": "47032000",
            "display": "congenitale hydrocefalus (aandoening)"
          },
          {
            "code": "30915001",
            "display": "holoprosencefalie (aandoening)"
          },
          {
            "code": "4945003",
            "display": "polymicrogyrie (aandoening)"
          },
          {
            "code": "9904008",
            "display": "congenitale afwijking van tractus circulatorius (aandoening)"
          },
          {
            "code": "204470001",
            "display": "enkele navelstrengarterie (aandoening)"
          },
          {
            "code": "30288003",
            "display": "ventrikelseptumdefect (aandoening)"
          },
          {
            "code": "61959006",
            "display": "truncus arteriosus communis (aandoening)"
          },
          {
            "code": "204296002",
            "display": "discordante ventriculoarteriële verbinding (aandoening)"
          },
          {
            "code": "86299006",
            "display": "tetralogie van Fallot (aandoening)"
          },
          {
            "code": "45503006",
            "display": "monoventrikel (aandoening)"
          },
          {
            "code": "7484005",
            "display": "'double-outlet' rechter ventrikel (aandoening)"
          },
          {
            "code": "360481003",
            "display": "gemeenschappelijk atrioventriculair kanaal (aandoening)"
          },
          {
            "code": "253591008",
            "display": "pulmonale atresie met ventrikelseptumdefect (aandoening)"
          },
          {
            "code": "63042009",
            "display": "tricuspidalisklepatresie (aandoening)"
          },
          {
            "code": "62067003",
            "display": "hypoplastisch-linkerhartsyndroom (aandoening)"
          },
          {
            "code": "218728005",
            "display": "onderbroken aortaboog (aandoening)"
          },
          {
            "code": "111323005",
            "display": "abnormale volledige verbinding van venae pulmonales (aandoening)"
          },
          {
            "code": "281587000",
            "display": "pentalogie van Cantrell (aandoening)"
          },
          {
            "code": "7305005",
            "display": "aortacoarctatie (aandoening)"
          },
          {
            "code": "4374004",
            "display": "congenitale misvorming van tricuspidalisklep (aandoening)"
          },
          {
            "code": "94702005",
            "display": "multipele congenitale hartdefecten (aandoening)"
          },
          {
            "code": "95470009",
            "display": "congenitale afwijking van tractus digestivus (aandoening)"
          },
          {
            "code": "449790007",
            "display": "cheilognathopalatoschisis (aandoening)"
          },
          {
            "code": "87979003",
            "display": "palatoschisis (aandoening)"
          },
          {
            "code": "80281008",
            "display": "cheiloschisis (aandoening)"
          },
          {
            "code": "77414002",
            "display": "cheilognathoschisis (aandoening)"
          },
          {
            "code": "66948001",
            "display": "cheilopalatoschisis (aandoening)"
          },
          {
            "code": "337471007",
            "display": "schisis van bovenlip, bovenkaak en palatum (aandoening)"
          },
          {
            "code": "69771008",
            "display": "congenitale misvorming van oesofagus (aandoening)"
          },
          {
            "code": "60983006",
            "display": "congenitale tracheo-oesofageale fistel (aandoening)"
          },
          {
            "code": "26179002",
            "display": "congenitale atresie van oesofagus (aandoening)"
          },
          {
            "code": "204659003",
            "display": "oesofagusatresie met tracheo-oesofageale fistel (aandoening)"
          },
          {
            "code": "93032003",
            "display": "congenitale atresie van darm (aandoening)"
          },
          {
            "code": "84296002",
            "display": "congenitale atresie van dunne darm (aandoening)"
          },
          {
            "code": "51118003",
            "display": "duodenumatresie (aandoening)"
          },
          {
            "code": "360491009",
            "display": "atresie van jejunum (aandoening)"
          },
          {
            "code": "25896009",
            "display": "atresie van ileum (aandoening)"
          },
          {
            "code": "37054000",
            "display": "colonatresie (aandoening)"
          },
          {
            "code": "204711007",
            "display": "atresie van dikke darm (aandoening)"
          },
          {
            "code": "33225004",
            "display": "anorectale malformatie (aandoening)"
          },
          {
            "code": "204712000",
            "display": "congenitale atresie van anus (aandoening)"
          },
          {
            "code": "204739008",
            "display": "ziekte van Hirschsprung (aandoening)"
          },
          {
            "code": "29980002",
            "display": "congenitale malrotatie van darm (aandoening)"
          },
          {
            "code": "9707006",
            "display": "intestinale volvulus (aandoening)"
          },
          {
            "code": "18735004",
            "display": "omfalocele (aandoening)"
          },
          {
            "code": "72951007",
            "display": "gastroschisis (aandoening)"
          },
          {
            "code": "77480004",
            "display": "atresie van galwegen (aandoening)"
          },
          {
            "code": "287085006",
            "display": "congenitale afwijking van tractus urogenitalis (aandoening)"
          },
          {
            "code": "41962002",
            "display": "syndroom van Potter (aandoening)"
          },
          {
            "code": "82525005",
            "display": "congenitale polycysteuze nierziekte (aandoening)"
          },
          {
            "code": "204949001",
            "display": "dysplasie van nier (aandoening)"
          },
          {
            "code": "28770003",
            "display": "autosomaal recessieve polycysteuze nierziekte (aandoening)"
          },
          {
            "code": "765330003",
            "display": "autosomaal dominante polycysteuze nierziekte (aandoening)"
          },
          {
            "code": "7163005",
            "display": "obstructie van urinewegen (aandoening)"
          },
          {
            "code": "61758007",
            "display": "exstrofie van blaas (aandoening)"
          },
          {
            "code": "416010008",
            "display": "hypospadie (aandoening)"
          },
          {
            "code": "406476007",
            "display": "epispadie (aandoening)"
          },
          {
            "code": "204878001",
            "display": "niet-ingedaalde testis (aandoening)"
          },
          {
            "code": "39179006",
            "display": "stoornis in geslachtelijke ontwikkeling (aandoening)"
          },
          {
            "code": "74345006",
            "display": "congenitale aandoening door chromosoomafwijking (aandoening)"
          },
          {
            "code": "21111006",
            "display": "trisomie 13 (aandoening)"
          },
          {
            "code": "51500006",
            "display": "trisomie 18 (aandoening)"
          },
          {
            "code": "41040004",
            "display": "Down-syndroom (aandoening)"
          },
          {
            "code": "66651005",
            "display": "syndroom door triploïdie (aandoening)"
          },
          {
            "code": "275260000",
            "display": "congenitale afwijking van ademhalingsstelsel (aandoening)"
          },
          {
            "code": "53189005",
            "display": "congenitale atresie van trachea (aandoening)"
          },
          {
            "code": "111318005",
            "display": "congenitale cysteuze adenomatoïde malformatie van long (aandoening)"
          },
          {
            "code": "204508009",
            "display": "choanale atresie (aandoening)"
          },
          {
            "code": "14532008",
            "display": "congenitale malformatie van trachea (aandoening)"
          },
          {
            "code": "80825009",
            "display": "congenitale hypoplasie van long (aandoening)"
          },
          {
            "code": "66987001",
            "display": "congenitaal lobair emfyseem (aandoening)"
          },
          {
            "code": "111318005",
            "display": "congenitale cysteuze adenomatoïde malformatie van long (aandoening)"
          },
          {
            "code": "79231000",
            "display": "hydrothorax (aandoening)"
          },
          {
            "code": "83035003",
            "display": "chylothorax (aandoening)"
          },
          {
            "code": "21524000",
            "display": "relaxatie van diafragma (aandoening)"
          },
          {
            "code": "17101000146103",
            "display": "congenitale neuromusculaire afwijking (aandoening)"
          },
          {
            "code": "19416009",
            "display": "congenitale afwijking van oog (aandoening)"
          },
          {
            "code": "61142002",
            "display": "microftalmie (aandoening)"
          },
          {
            "code": "275259005",
            "display": "congenitale malformatie van oor (aandoening)"
          },
          {
            "code": "199879009",
            "display": "congenitale misvorming van huid (aandoening)"
          },
          {
            "code": "93471006",
            "display": "hemangioom van huid (aandoening)"
          },
          {
            "code": "398943008",
            "display": "naevus naevocellularis van huid (aandoening)"
          },
          {
            "code": "81336004",
            "display": "congenitale afwijking van buikwand (aandoening)"
          },
          {
            "code": "18735004",
            "display": "omfalocele (aandoening)"
          },
          {
            "code": "429200006",
            "display": "congenitale hernia inguinalis (aandoening)"
          },
          {
            "code": "72951007",
            "display": "gastroschisis (aandoening)"
          },
          {
            "code": "396347007",
            "display": "hernia umbilicalis (aandoening)"
          },
          {
            "code": "73573004",
            "display": "congenitale afwijking van bewegingsstelsel (aandoening)"
          },
          {
            "code": "105986008",
            "display": "skeletdysplasie (aandoening)"
          },
          {
            "code": "367506006",
            "display": "polydactylie (aandoening)"
          },
          {
            "code": "373413006",
            "display": "syndactylie (aandoening)"
          },
          {
            "code": "302297009",
            "display": "congenitale deformiteit van voet (aandoening)"
          },
          {
            "code": "45806008",
            "display": "reductiedefect van bovenste extremiteit (aandoening)"
          },
          {
            "code": "77595004",
            "display": "congenitaal lengtedefect van gehele onderste extremiteit (aandoening)"
          },
          {
            "code": "36172001",
            "display": "congenitale subluxatie van heup (aandoening)"
          },
          {
            "code": "276654001",
            "display": "congenitale malformatie (aandoening)"
          },
          {
            "code": "17190001",
            "display": "congenitale hernia diaphragmatica (aandoening)"
          },
          {
            "code": "276508000",
            "display": "hydrops foetalis (aandoening)"
          },
          {
            "code": "59566000",
            "display": "oligohydramnion (aandoening)"
          },
          {
            "code": "240104008",
            "display": "congenitale myotone dystrofie (aandoening)"
          },
          {
            "code": "41337007",
            "display": "Siamese tweeling (aandoening)"
          },
          {
            "code": "276720006",
            "display": "dysmorfie (aandoening)"
          },
          {
            "code": "43876007",
            "display": "situs inversus viscerum (aandoening)"
          },
          {
            "code": "82354003",
            "display": "malformatiesyndroom met betrokkenheid van meerdere systemen (aandoening)"
          },
          {
            "code": "400038003",
            "display": "congenitaal malformatiesyndroom (aandoening)"
          },
          {
            "code": "217710005",
            "display": "congenitale-jodiumdeficiëntiesyndroom (aandoening)"
          },
          {
            "code": "151801000146100",
            "display": "congenitaal maligne neoplasma (aandoening)"
          },
          {
            "code": "86095007",
            "display": "aangeboren defect van stofwisseling (aandoening)"
          },
          {
            "code": "20957000",
            "display": "stoornis van koolhydraatmetabolisme (aandoening)"
          },
          {
            "code": "29633007",
            "display": "glycogeenstapelingsziekte (aandoening)"
          },
          {
            "code": "7265005",
            "display": "glycogeenstapelingsziekte type 1 (aandoening)"
          },
          {
            "code": "444707001",
            "display": "glycogeenstapelingsziekte type 1a (aandoening)"
          },
          {
            "code": "30102006",
            "display": "glycogeenstapelingsziekte type 1b (aandoening)"
          },
          {
            "code": "274864009",
            "display": "glycogeenstapelingsziekte type II (aandoening)"
          },
          {
            "code": "66937008",
            "display": "glycogeenstapelingsziekte type 3 (aandoening)"
          },
          {
            "code": "190745006",
            "display": "galactosemie (aandoening)"
          },
          {
            "code": "190694001",
            "display": "stoornis van aminozuurmetabolisme (aandoening)"
          },
          {
            "code": "7573000",
            "display": "klassieke fenylketonurie (aandoening)"
          },
          {
            "code": "85020001",
            "display": "cystinurie (aandoening)"
          },
          {
            "code": "190694001",
            "display": "tyrosinemie (aandoening)"
          },
          {
            "code": "410056006",
            "display": "tyrosinemie type 1 (aandoening)"
          },
          {
            "code": "4887000",
            "display": "tyrosinemie type 2 (aandoening)"
          },
          {
            "code": "11282001",
            "display": "homocystinurie (aandoening)"
          },
          {
            "code": "13144005",
            "display": "3-methylcrotonylglycinurie (aandoening)"
          },
          {
            "code": "76175005",
            "display": "glutaaracidurie type 1 (aandoening)"
          },
          {
            "code": "116021002",
            "display": "stoornis van metabolisme van organisch zuur (aandoening)"
          },
          {
            "code": "69080001",
            "display": "propionacidurie (aandoening)"
          },
          {
            "code": "42393006",
            "display": "methylmalonzuuracidemie (aandoening)"
          },
          {
            "code": "87827003",
            "display": "deficiëntie van isovaleryl-co-enzym A-dehydrogenase (aandoening)"
          },
          {
            "code": "27718001",
            "display": "maple syrup urine disease (aandoening)"
          },
          {
            "code": "28987007",
            "display": "glutaaracidurie (aandoening)"
          },
          {
            "code": "76175005",
            "display": "glutaaracidurie type 1 (aandoening)"
          },
          {
            "code": "22886006",
            "display": "glutaaracidurie type 2 (aandoening)"
          },
          {
            "code": "124611007",
            "display": "deficiëntie van hydroxymethylglutaryl-co-enzyme-A-lyase (aandoening)"
          },
          {
            "code": "36444000",
            "display": "stoornis van metabolisme van ureumcyclus (aandoening)"
          },
          {
            "code": "80908008",
            "display": "deficiëntie van ornithinecarbamoyltransferase (aandoening)"
          },
          {
            "code": "39929009",
            "display": "stoornis van vetzuurmetabolisme (aandoening)"
          },
          {
            "code": "128596003",
            "display": "deficiëntie van middenketenacyl-co-enzym A-dehydrogenase (aandoening)"
          },
          {
            "code": "307127004",
            "display": "geïsoleerde deficiëntie van langeketen-hydroxyacyl-co-enzym A-dehydrogenase (aandoening)"
          },
          {
            "code": "237997005",
            "display": "deficiëntie van zeerlangeketen-acyl-co-enzym-A-dehydrogenase (aandoening)"
          },
          {
            "code": "23585005",
            "display": "lysosomale enzymafwijking (aandoening)"
          },
          {
            "code": "11380006",
            "display": "mucopolysacharidose (aandoening)"
          },
          {
            "code": "43916004",
            "display": "mucopolysacharidose type 7 (aandoening)"
          },
          {
            "code": "190794006",
            "display": "ziekte van Gaucher (aandoening)"
          },
          {
            "code": "240096000",
            "display": "mitochondriale cytopathie (aandoening)"
          },
          {
            "code": "237988006",
            "display": "ademhalingsketen-complex-1-deficiëntie (aandoening)"
          },
          {
            "code": "237989003",
            "display": "ademhalingsketen-complex-2-deficiëntie (aandoening)"
          },
          {
            "code": "237990007",
            "display": "ademhalingsketen-complex-3-deficiëntie (aandoening)"
          },
          {
            "code": "67434000",
            "display": "ademhalingsketen-complex-4-deficiëntie (aandoening)"
          },
          {
            "code": "16851005",
            "display": "mitochondriale myopathie (aandoening)"
          },
          {
            "code": "39925003",
            "display": "mitochondriale encefalomyopathie met lactaatacidose en stroke-like episodes (aandoening)"
          },
          {
            "code": "238059005",
            "display": "stoornis van peroxisomale functie (aandoening)"
          },
          {
            "code": "238006008",
            "display": "stoornis van purine- en pyrimidinemetabolisme (aandoening)"
          },
          {
            "code": "124275001",
            "display": "deficiëntie van hypoxanthinefosforibosyltransferase (aandoening)"
          },
          {
            "code": "45744005",
            "display": "stoornis van mineraalstofwisseling (aandoening)"
          },
          {
            "code": "79886009",
            "display": "stoornis van kopermetabolisme (aandoening)"
          },
          {
            "code": "30913008",
            "display": "stoornis van ijzermetabolisme (aandoening)"
          },
          {
            "code": "399187006",
            "display": "hemochromatose (aandoening)"
          },
          {
            "code": "46727001",
            "display": "stoornis van zinkmetabolisme (aandoening)"
          },
          {
            "code": "59178007",
            "display": "Menke's kroeshaarsyndroom (aandoening)"
          },
          {
            "code": "238049009",
            "display": "congenitaal defect in glycosylering (aandoening)"
          },
          {
            "code": "85670002",
            "display": "vitaminedeficiëntie (aandoening)"
          },
          {
            "code": "386080007",
            "display": "pyridoxinedeficiëntie (aandoening)"
          },
          {
            "code": "190634004",
            "display": "cobalaminedeficiëntie (aandoening)"
          },
          {
            "code": "8808004",
            "display": "biotinidasedeficiëntie (aandoening)"
          },
          {
            "code": "360369003",
            "display": "deficiëntie van holocarboxylasesynthase (aandoening)"
          },
          {
            "code": "1821000146108",
            "display": "hereditaire stoornis van metabolisme (aandoening)"
          }
        ]
      }
    ]
  }
}