FHIR IG Statistics: ValueSet/newborn-congenital-anomalies-vs
Resources that use this resource
StructureDefinition |
Congenital | Perfil de informação clinicas - Rastreio Cardiopatias Congénitas |
Resources that this resource uses
CodeSystem |
sct | SNOMED CT (all versions) |
sct | SNOMED codes used in this IG |
sct | veri |
Narrative
Note: links and images are rebased to the (stated) source
Source
{
"resourceType": "ValueSet",
"id": "newborn-congenital-anomalies-vs",
"text": {
"status": "generated",
"div": "<!-- snip (see above) -->"
},
"url": "https://hl7.pt/fhir/NoticiaNascimento/ValueSet/newborn-congenital-anomalies-vs",
"version": "0.0.1",
"name": "NewbornCongenitalAnomaliesVS",
"title": "Tipos de doença congénita ValueSet",
"status": "active",
"experimental": false,
"date": "2025-05-12T10:05:07+00:00",
"publisher": "HL7 Portugal",
"contact": [
{
"name": "HL7 Portugal",
"telecom": [
{
"system": "url",
"value": "http://hl7.pt"
},
{
"system": "email",
"value": "info@hl7.pt"
}
]
},
{
"name": "HL7 Portugal",
"telecom": [
{
"system": "email",
"value": "geral@hl7.pt",
"use": "work"
}
]
}
],
"description": "Tipos de doença congénita ValueSet",
"jurisdiction": [
{
"coding": [
{
"system": "urn:iso:std:iso:3166",
"code": "PT",
"display": "Portugal"
}
]
}
],
"compose": {
"include": [
{
"system": "http://snomed.info/sct",
"concept": [
{
"code": "89369001",
"display": "Anencephalus"
},
{
"code": "67531005",
"display": "Meningomyelocele/Spina bifida"
},
{
"code": "12770006",
"display": "Cyanotic congenital heart disease"
},
{
"code": "17190001",
"display": "Congenital diaphragmatic hernia"
},
{
"code": "18735004",
"display": "Congenital omphalocele"
},
{
"code": "72951007",
"display": "Gastroschisis"
},
{
"code": "67341007",
"display": "Longitudinal deficiency of limb - Limb reduction defect (excluding congenital amputation and dwarfing syndromes)"
},
{
"code": "80281008",
"display": "Cleft Lip with or without Cleft Palate"
},
{
"code": "87979003",
"display": "Cleft palate"
},
{
"code": "70156005",
"display": "Anomaly of chromosome pair 21"
},
{
"code": "409709004",
"display": "Chromosomal disorder"
},
{
"code": "416010008",
"display": "Hypospadias"
},
{
"code": "282332003",
"display": "No abnormality detected - examination result"
}
]
}
]
}
}