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Packagehl7.fhir.us.bfdr.r4
Resource TypeValueSet
IdValueSet-ValueSet-newborn-congenital-anomalies.json
FHIR VersionR4

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Narrative

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

Generated Narrative: ValueSet ValueSet-newborn-congenital-anomalies

This value set includes codes based on the following rules:

  • Include these codes as defined in http://snomed.info/sct
    CodeDisplay
    89369001Anencephalus
    67531005Meningomyelocele/Spina bifida
    12770006Cyanotic congenital heart disease
    17190001Congenital diaphragmatic hernia
    18735004Congenital omphalocele
    72951007Gastroschisis
    67341007Longitudinal deficiency of limb - Limb reduction defect (excluding congenital amputation and dwarfing syndromes)
    80281008Cleft Lip with or without Cleft Palate
    87979003Cleft palate
    70156005Anomaly of chromosome pair 21
    409709004Chromosomal disorder
    416010008Hypospadias
  • Include these codes as defined in http://terminology.hl7.org/CodeSystem/v3-NullFlavor
    CodeDisplayDefinition
    OTHOther**Description:**The actual value is not a member of the set of permitted data values in the constrained value domain of a variable. (e.g., concept not provided by required code system).

    **Usage Notes**: This flavor and its specializations are most commonly used with the CD datatype and its flavors. However, it may apply to \*any\* datatype where the constraints of the type are tighter than can be conveyed. For example, a PQ that is for a true measured amount whose units are not supported in UCUM, a need to convey a REAL when the type has been constrained to INT, etc.

    With coded datatypes, this null flavor may only be used if the vocabulary binding has a coding strength of CNE. By definition, all local codes and original text are part of the value set if the coding strength is CWE.

Source1

{
  "resourceType": "ValueSet",
  "id": "ValueSet-newborn-congenital-anomalies",
  "text": {
    "status": "extensions",
    "div": "<!-- snip (see above) -->"
  },
  "extension": [
    {
      "url": "http://hl7.org/fhir/StructureDefinition/structuredefinition-wg",
      "valueCode": "pher"
    }
  ],
  "url": "http://hl7.org/fhir/us/bfdr/ValueSet/ValueSet-newborn-congenital-anomalies",
  "identifier": [
    {
      "system": "urn:ietf:rfc:3986",
      "value": "urn:oid:2.16.840.1.113883.4.642.40.13.48.17"
    }
  ],
  "version": "2.0.0",
  "name": "NewbornCongenitalAnomaliesVS",
  "title": "Newborn Congenital Anomalies",
  "status": "active",
  "experimental": false,
  "date": "2024-10-15T15:43:14+00:00",
  "publisher": "HL7 International / Public Health",
  "contact": [
    {
      "name": "HL7 International / Public Health",
      "telecom": [
        {
          "system": "url",
          "value": "http://www.hl7.org/Special/committees/pher"
        }
      ]
    }
  ],
  "description": "The valueset contains codes to represent newborn congenital anomalies. Includes 'Other' value for general utility, although #OTH is not allowed for birth submissions to NCHS.\n\nMapping to IJE codes [here](ConceptMap-NewbornCongenitalAnomaliesCM.html).",
  "jurisdiction": [
    {
      "coding": [
        {
          "system": "urn:iso:std:iso:3166",
          "code": "US",
          "display": "United States of America"
        }
      ]
    }
  ],
  "copyright": "This value set includes content from SNOMED CT, which is copyright © 2002+ International Health Terminology Standards Development Organisation (IHTSDO), and distributed by agreement between IHTSDO and HL7. Implementer use of SNOMED CT is not covered by this agreement",
  "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"
          }
        ]
      },
      {
        "system": "http://terminology.hl7.org/CodeSystem/v3-NullFlavor",
        "concept": [
          {
            "code": "OTH",
            "display": "Other"
          }
        ]
      }
    ]
  }
}