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FHIR IG Statistics: ValueSet/2.16.840.1.114222.4.11.7122

Packageus.cdc.phinvads
Resource TypeValueSet
Id2.16.840.1.114222.4.11.7122
FHIR VersionR4
Sourcehttp://fhir.org/packages/us.cdc.phinvads
URLhttp://phinvads.cdc.gov/fhir/ValueSet/2.16.840.1.114222.4.11.7122
Version1
Statusactive
Date2013-01-28T00:06:00+11:00
NamePHVS_NewbornCongenitalAnomalies_NCHS
TitleNewborn Congenital Anomalies (NCHS)
Realmus
DescriptionThe value set contain the list of values use to specify malformations of the newborn diagnosed prenatally or after delivery.

Resources that use this resource

StructureDefinition
Condition-congenital-anomaly-of-newbornCondition - Congenital Anomaly of Newborn

Resources that this resource uses

CodeSystem
sctSNOMED CT (all versions)

Narrative

No narrative content found in resource


Source

{
  "resourceType": "ValueSet",
  "id": "2.16.840.1.114222.4.11.7122",
  "meta": {
    "source": "https://phinvads.cdc.gov/vads/ViewValueSet.action?oid=2.16.840.1.114222.4.11.7122"
  },
  "url": "http://phinvads.cdc.gov/fhir/ValueSet/2.16.840.1.114222.4.11.7122",
  "version": "1",
  "name": "PHVS_NewbornCongenitalAnomalies_NCHS",
  "title": "Newborn Congenital Anomalies (NCHS)",
  "status": "active",
  "date": "2013-01-28T00:06:00+11:00",
  "description": "The value set contain the list of values use to specify malformations of the newborn diagnosed prenatally or after delivery.",
  "compose": {
    "include": [
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20200901",
        "concept": [
          {
            "code": "89369001",
            "display": "Anencephaly"
          },
          {
            "code": "67531005",
            "display": "Meningomyelocele/Spina bifida"
          },
          {
            "code": "12770006",
            "display": "Cyanotic congenital heart disease"
          },
          {
            "code": "17190001",
            "display": "Congenital diaphragmatic hernia"
          },
          {
            "code": "18735004",
            "display": "Omphalocele"
          },
          {
            "code": "72951007",
            "display": "Gastroschisis"
          },
          {
            "code": "67341007",
            "display": "Limb reduction defect (excluding congenital amputation and dwarfing syndromes)"
          },
          {
            "code": "80281008",
            "display": "Cleft Lip with or without Cleft Palate"
          },
          {
            "code": "87979003",
            "display": "Cleft Palate alone"
          },
          {
            "code": "70156005",
            "display": "Down Syndrome"
          },
          {
            "code": "409709004",
            "display": "Suspected chromosomal disorder"
          },
          {
            "code": "416010008",
            "display": "Hypospadias"
          },
          {
            "code": "260413007",
            "display": "None of the specified items in this value set (including concept codes: 89369001, 67531005, 12770006,  17190001, 18735004, 72951007, 67341007, 67341007, 80281008, 87979003, 70156005, 409709004, 416010008) for Newborn Congenital Anomalies"
          }
        ]
      }
    ]
  }
}