{
"description": "A Condition profile describing child disorders, such as chromosomal and congenital abnormalities or other problems, as defined by BabyConnect.",
"_filename": "bc-DisorderOfChild.json",
"package_name": "nictiz.fhir.nl.stu3.geboortezorg",
"date": null,
"derivation": "constraint",
"publisher": null,
"fhirVersion": "3.0.2",
"name": "bc-DisorderOfChild",
"mapping": [ {
"uri": "https://zibs.nl/wiki/ConcernForTransfer-v1.2(2015EN)",
"name": "HCIM ConcernForTransfer-v1.2(2015EN)",
"identity": "hcim-concernfortransfer-v1.2-2015EN"
}, {
"uri": "https://zibs.nl/wiki/ConcernForTransfer-v3.0(2016EN)",
"name": "HCIM ConcernForTransfer-v3.0(2016EN)",
"identity": "hcim-concernfortransfer-v3.0-2016EN"
}, {
"uri": "https://zibs.nl/wiki/Problem-v4.1(2017EN)",
"name": "HCIM Problem-v4.1(2017EN)",
"comment": "ConcernForTransfer is renamed to Problem with release 2017 of the HCIMs.",
"identity": "hcim-problem-v1.2-2017EN"
}, {
"uri": "https://zibs.nl/wiki/BasicElements-v1.0(2017EN)",
"name": "HCIM BasicElements-v1.0(2017EN)",
"identity": "hcim-basicelements-v1.0-2017EN"
}, {
"uri": "https://decor.nictiz.nl/art-decor/decor-datasets--peri20-?id=2.16.840.1.113883.2.4.3.11.60.90.77.1.6&effectiveDate=2016-09-08T00%3A00%3A00&conceptId=2.16.840.1.113883.2.4.3.11.60.90.77.2.6.40050&conceptEffectiveDate=2016-09-08T00%3A00%3A00",
"name": "Geboortezorg Perinatologie 2.3",
"identity": "gebz-peri-v2.3"
} ],
"abstract": false,
"type": "Condition",
"experimental": null,
"resourceType": "StructureDefinition",
"title": null,
"package_version": "0.1.0",
"status": "draft",
"id": "0cdf1012-2654-406f-bb7d-f62ca0238423",
"kind": "resource",
"url": "http://nictiz.nl/fhir/StructureDefinition/bc-DisorderOfChild",
"version": null,
"differential": {
"element": [ {
"id": "Condition.verificationStatus",
"path": "Condition.verificationStatus",
"comment": "A ConceptMap (https://simplifier.net/resolve?canonical=http://nictiz.nl/fhir/ConceptMap/UncertaintyCode-to-VerificationStatus) is available.",
"mapping": [ {
"map": "peri23-dataelement-40100",
"comment": "Waarschijnlijkheid congenitale afwijking",
"identity": "gebz-peri-v2.3"
}, {
"map": "peri23-dataelement-40130",
"comment": "Waarschijnlijkheid chromosomale afwijking",
"identity": "gebz-peri-v2.3"
} ]
}, {
"id": "Condition.category",
"path": "Condition.category",
"slicing": {
"rules": "open",
"discriminator": [ {
"path": "coding",
"type": "value"
} ]
}
}, {
"id": "Condition.category:disorderOfChild",
"max": "1",
"path": "Condition.category",
"sliceName": "disorderOfChild"
}, {
"id": "Condition.category:disorderOfChild.coding",
"max": "1",
"path": "Condition.category.coding",
"slicing": {
"rules": "open",
"discriminator": [ {
"path": "$this",
"type": "value"
} ]
}
}, {
"id": "Condition.category:disorderOfChild.coding:disorderOfChild",
"max": "1",
"path": "Condition.category.coding",
"sliceName": "disorderOfChild",
"patternCoding": {
"code": "414025005",
"system": "http://snomed.info/sct",
"display": "Disorder of fetus or newborn (disorder)"
}
}, {
"id": "Condition.category:disorderOfChild.coding:disorderOfChild.system",
"path": "Condition.category.coding.system",
"fixedUri": "http://snomed.info/sct"
}, {
"id": "Condition.category:disorderOfChild.coding:disorderOfChild.code",
"path": "Condition.category.coding.code",
"fixedCode": "414025005"
}, {
"id": "Condition.category:disorderOfChild.coding:disorderOfChild.display",
"path": "Condition.category.coding.display",
"defaultValueString": "Disorder of fetus or newborn (disorder)"
}, {
"id": "Condition.code.coding",
"path": "Condition.code.coding",
"slicing": {
"rules": "open",
"discriminator": [ {
"path": "code",
"type": "value"
} ]
}
}, {
"id": "Condition.code.coding:CongenitalDisorder",
"path": "Condition.code.coding",
"binding": {
"strength": "extensible",
"description": "CongenitaleAfwijkingen",
"valueSetUri": "http://decor.nictiz.nl/fhir/ValueSet/2.16.840.1.113883.2.4.11.196--20191010091229"
},
"mapping": [ {
"map": "peri23-dataelement-40090",
"comment": "Specificatie congenitale afwijking",
"identity": "gebz-peri-v2.3"
} ],
"sliceName": "CongenitalDisorder"
}, {
"id": "Condition.code.coding:ChromosomalDisorder",
"path": "Condition.code.coding",
"binding": {
"strength": "extensible",
"description": "ChromosomaleAfwijking",
"valueSetUri": "http://decor.nictiz.nl/fhir/ValueSet/2.16.840.1.113883.2.4.11.198--20161026164418"
},
"mapping": [ {
"map": "peri23-dataelement-40120",
"comment": "Specificatie chromosomale afwijking",
"identity": "gebz-peri-v2.3"
} ],
"sliceName": "ChromosomalDisorder"
}, {
"id": "Condition.code.coding:ProblemChild",
"path": "Condition.code.coding",
"binding": {
"strength": "extensible",
"description": "ProblematiekKind",
"valueSetUri": "http://decor.nictiz.nl/fhir/ValueSet/2.16.840.1.113883.2.4.3.11.60.90.77.11.12--20191009125104"
},
"mapping": [ {
"map": "peri23-dataelement-80789",
"comment": "Problematiek kind",
"identity": "gebz-peri-v2.3"
} ],
"sliceName": "ProblemChild"
}, {
"id": "Condition.subject",
"path": "Condition.subject",
"type": [ {
"code": "Reference",
"targetProfile": "http://nictiz.nl/fhir/StructureDefinition/bc-Child"
} ]
}, {
"id": "Condition.context",
"path": "Condition.context",
"type": [ {
"code": "Reference",
"targetProfile": "http://nictiz.nl/fhir/StructureDefinition/bc-Encounter"
}, {
"code": "Reference",
"targetProfile": "http://nictiz.nl/fhir/StructureDefinition/bc-MaternalRecord"
} ],
"mapping": [ {
"map": "peri23-dataelement-4",
"comment": "Zorgverlening",
"identity": "gebz-peri-v2.3"
} ]
} ]
},
"baseDefinition": "http://nictiz.nl/fhir/StructureDefinition/zib-Problem"
}