Resource ValueSet/FHIR Server from package nictiz.fhir.nl.stu3.geboortezorg#1.3.3-rc4 (47 ms)
Resources that use this resource
Resources that this resource uses
Source
{
"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" : "draft",
"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)"
}
]
}
]
},
"text" : {
}
}
XIG built as of ??metadata-date??. Found ??metadata-resources?? resources in ??metadata-packages?? packages.
FHIR