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FHIR IG Statistics: ValueSet/newborn-congenital-anomalies-vs

Packagehl7.fhir.pt.obs-neonat
TypeValueSet
Idnewborn-congenital-anomalies-vs
FHIR VersionR4
Sourcehttps://hl7.pt/fhir/NoticiaNascimento/https://build.fhir.org/ig/hl7-pt/obs-neonat-ig/ValueSet-newborn-congenital-anomalies-vs.html
URLhttps://hl7.pt/fhir/NoticiaNascimento/ValueSet/newborn-congenital-anomalies-vs
Version0.0.1
Statusactive
Date2025-05-12T10:05:07+00:00
NameNewbornCongenitalAnomaliesVS
TitleTipos de doença congénita ValueSet
Realmpt
Authorityhl7
DescriptionTipos de doença congénita ValueSet

Resources that use this resource

StructureDefinition
CongenitalPerfil de informação clinicas - Rastreio Cardiopatias Congénitas

Resources that this resource uses

CodeSystem
sctSNOMED CT (all versions)
sctSNOMED codes used in this IG
sctveri

Narrative

Note: links and images are rebased to the (stated) source

Generated Narrative: ValueSet newborn-congenital-anomalies-vs


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"
          }
        ]
      }
    ]
  }
}