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Resource ValueSet/FHIR Server from package hl7.fhir.us.bfdr#current (47 ms)

Package hl7.fhir.us.bfdr
Type ValueSet
Id Id
FHIR Version R4
Source http://hl7.org/fhir/us/bfdr/https://build.fhir.org/ig/HL7/fhir-bfdr/ValueSet-ValueSet-newborn-congenital-anomalies.html
Url http://hl7.org/fhir/us/bfdr/ValueSet/ValueSet-newborn-congenital-anomalies
Version 2.0.0-Preview1
Status active
Date 2024-07-11T19:37:53+00:00
Name NewbornCongenitalAnomaliesVS
Title Newborn Congenital Anomalies
Experimental False
Realm us
Authority hl7
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. Mapping to IJE codes [here](ConceptMap-NewbornCongenitalAnomaliesCM.html).
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

Resources that use this resource

ConceptMap
NewbornCongenitalAnomaliesCM NewbornCongenitalAnomalies Concept Map
http://hl7.org/fhir/us/bfdr/StructureDefinition/Condition-congenital-anomaly-of-newborn Condition - Congenital Anomaly of Newborn

Resources that this resource uses

CodeSystem
http://snomed.info/sct SNOMED CT (all versions)
http://terminology.hl7.org/CodeSystem/v3-NullFlavor NullFlavor
http://snomed.info/sct SNOMED codes used in this IG
http://snomed.info/sct SNOMED CT Canada Immunizations


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.

Source

{
  "resourceType" : "ValueSet",
  "id" : "ValueSet-newborn-congenital-anomalies",
  "text" : {
    "status" : "extensions",
    "div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p class=\"res-header-id\"><b>Generated Narrative: ValueSet ValueSet-newborn-congenital-anomalies</b></p><a name=\"ValueSet-newborn-congenital-anomalies\"> </a><a name=\"hcValueSet-newborn-congenital-anomalies\"> </a><a name=\"hcValueSet-newborn-congenital-anomalies-en-US\"> </a><p>This value set includes codes based on the following rules:</p><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></table></li><li>Include these codes as defined in <a href=\"http://terminology.hl7.org/5.5.0/CodeSystem-v3-NullFlavor.html\"><code>http://terminology.hl7.org/CodeSystem/v3-NullFlavor</code></a><table class=\"none\"><tr><td style=\"white-space:nowrap\"><b>Code</b></td><td><b>Display</b></td><td><b>Definition</b></td></tr><tr><td><a href=\"http://terminology.hl7.org/5.5.0/CodeSystem-v3-NullFlavor.html#v3-NullFlavor-OTH\">OTH</a></td><td>Other</td><td>**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).<br/><br/>**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.<br/><br/>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.</td></tr></table></li></ul></div>"
  },
  "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:2.16.840.1.113883.4.642.40.13.48.16"
    }
  ],
  "version" : "2.0.0-Preview1",
  "name" : "NewbornCongenitalAnomaliesVS",
  "title" : "Newborn Congenital Anomalies",
  "status" : "active",
  "experimental" : false,
  "date" : "2024-07-11T19:37:53+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"
          }
        ]
      }
    ]
  }
}

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