HL7 PT FHIR Implementation Guide: Noticia de Nascimento, published by HL7 Portugal. This guide is not an authorized publication; it is the continuous build for version 0.0.1 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/hl7-pt/obs-neonat-ig/ and changes regularly. See the Directory of published versions
: Tipos de doença congénita ValueSet - TTL Representation
Raw ttl | Download
@prefix fhir: <http://hl7.org/fhir/> .
@prefix owl: <http://www.w3.org/2002/07/owl#> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
# - resource -------------------------------------------------------------------
a fhir:ValueSet ;
fhir:nodeRole fhir:treeRoot ;
fhir:id [ fhir:v "newborn-congenital-anomalies-vs"] ; #
fhir:text [
fhir:status [ fhir:v "generated" ] ;
fhir:div "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p class=\"res-header-id\"><b>Generated Narrative: ValueSet newborn-congenital-anomalies-vs</b></p><a name=\"newborn-congenital-anomalies-vs\"> </a><a name=\"hcnewborn-congenital-anomalies-vs\"> </a><a name=\"newborn-congenital-anomalies-vs-pt-PT\"> </a><ul><li>Include these codes as defined in <a href=\"http://www.snomed.org/\"><code>http://snomed.info/sct</code></a><table class=\"none\"><tr><td style=\"white-space:nowrap\"><b>Code</b></td><td><b>Display</b></td></tr><tr><td><a href=\"http://snomed.info/id/89369001\">89369001</a></td><td>Anencephalus</td></tr><tr><td><a href=\"http://snomed.info/id/67531005\">67531005</a></td><td>Meningomyelocele/Spina bifida</td></tr><tr><td><a href=\"http://snomed.info/id/12770006\">12770006</a></td><td>Cyanotic congenital heart disease</td></tr><tr><td><a href=\"http://snomed.info/id/17190001\">17190001</a></td><td>Congenital diaphragmatic hernia</td></tr><tr><td><a href=\"http://snomed.info/id/18735004\">18735004</a></td><td>Congenital omphalocele</td></tr><tr><td><a href=\"http://snomed.info/id/72951007\">72951007</a></td><td>Gastroschisis</td></tr><tr><td><a href=\"http://snomed.info/id/67341007\">67341007</a></td><td>Longitudinal deficiency of limb - Limb reduction defect (excluding congenital amputation and dwarfing syndromes)</td></tr><tr><td><a href=\"http://snomed.info/id/80281008\">80281008</a></td><td>Cleft Lip with or without Cleft Palate</td></tr><tr><td><a href=\"http://snomed.info/id/87979003\">87979003</a></td><td>Cleft palate</td></tr><tr><td><a href=\"http://snomed.info/id/70156005\">70156005</a></td><td>Anomaly of chromosome pair 21</td></tr><tr><td><a href=\"http://snomed.info/id/409709004\">409709004</a></td><td>Chromosomal disorder</td></tr><tr><td><a href=\"http://snomed.info/id/416010008\">416010008</a></td><td>Hypospadias</td></tr><tr><td><a href=\"http://snomed.info/id/282332003\">282332003</a></td><td>No abnormality detected - examination result</td></tr></table></li></ul></div>"
] ; #
fhir:url [ fhir:v "https://hl7.pt/fhir/NoticiaNascimento/ValueSet/newborn-congenital-anomalies-vs"^^xsd:anyURI] ; #
fhir:version [ fhir:v "0.0.1"] ; #
fhir:name [ fhir:v "NewbornCongenitalAnomaliesVS"] ; #
fhir:title [ fhir:v "Tipos de doença congénita ValueSet"] ; #
fhir:status [ fhir:v "active"] ; #
fhir:experimental [ fhir:v "false"^^xsd:boolean] ; #
fhir:date [ fhir:v "2024-12-04T15:23:35+00:00"^^xsd:dateTime] ; #
fhir:publisher [ fhir:v "HL7 Portugal"] ; #
fhir:contact ( [
fhir:name [ fhir:v "HL7 Portugal" ] ;
( fhir:telecom [
fhir:system [ fhir:v "url" ] ;
fhir:value [ fhir:v "http://hl7.pt" ] ] [
fhir:system [ fhir:v "email" ] ;
fhir:value [ fhir:v "info@hl7.pt" ] ] )
] [
fhir:name [ fhir:v "HL7 Portugal" ] ;
( fhir:telecom [
fhir:system [ fhir:v "email" ] ;
fhir:value [ fhir:v "geral@hl7.pt" ] ;
fhir:use [ fhir:v "work" ] ] )
] ) ; #
fhir:description [ fhir:v "Tipos de doença congénita ValueSet"] ; #
fhir:jurisdiction ( [
( fhir:coding [
fhir:system [ fhir:v "urn:iso:std:iso:3166"^^xsd:anyURI ] ;
fhir:code [ fhir:v "PT" ] ;
fhir:display [ fhir:v "Portugal" ] ] )
] ) ; #
fhir:compose [
( fhir:include [
fhir:system [ fhir:v "http://snomed.info/sct"^^xsd:anyURI ] ;
( fhir:concept [
fhir:code [ fhir:v "89369001" ] ;
fhir:display [ fhir:v "Anencephalus" ] ] [
fhir:code [ fhir:v "67531005" ] ;
fhir:display [ fhir:v "Meningomyelocele/Spina bifida" ] ] [
fhir:code [ fhir:v "12770006" ] ;
fhir:display [ fhir:v "Cyanotic congenital heart disease" ] ] [
fhir:code [ fhir:v "17190001" ] ;
fhir:display [ fhir:v "Congenital diaphragmatic hernia" ] ] [
fhir:code [ fhir:v "18735004" ] ;
fhir:display [ fhir:v "Congenital omphalocele" ] ] [
fhir:code [ fhir:v "72951007" ] ;
fhir:display [ fhir:v "Gastroschisis" ] ] [
fhir:code [ fhir:v "67341007" ] ;
fhir:display [ fhir:v "Longitudinal deficiency of limb - Limb reduction defect (excluding congenital amputation and dwarfing syndromes)" ] ] [
fhir:code [ fhir:v "80281008" ] ;
fhir:display [ fhir:v "Cleft Lip with or without Cleft Palate" ] ] [
fhir:code [ fhir:v "87979003" ] ;
fhir:display [ fhir:v "Cleft palate" ] ] [
fhir:code [ fhir:v "70156005" ] ;
fhir:display [ fhir:v "Anomaly of chromosome pair 21" ] ] [
fhir:code [ fhir:v "409709004" ] ;
fhir:display [ fhir:v "Chromosomal disorder" ] ] [
fhir:code [ fhir:v "416010008" ] ;
fhir:display [ fhir:v "Hypospadias" ] ] [
fhir:code [ fhir:v "282332003" ] ;
fhir:display [ fhir:v "No abnormality detected - examination result" ] ] ) ] )
] . #
