Birth And Fetal Death (BFDR) FHIR Implementation Guide
2.0.0 - STU2
Birth And Fetal Death (BFDR) FHIR Implementation Guide
2.0.0 - STU2
Birth And Fetal Death (BFDR) FHIR Implementation Guide, published by HL7 International / Public Health. This guide is not an authorized publication; it is the continuous build for version 2.0.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/fhir-bfdr/ and changes regularly. See the Directory of published versions
| Active as of 2024-10-15 |
{
"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=\"ValueSet-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/6.0.2/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/6.0.2/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:2.16.840.1.113883.4.642.40.13.48.17"
}
],
"version" : "2.0.0",
"name" : "NewbornCongenitalAnomaliesVS",
"title" : "Newborn Congenital Anomalies",
"status" : "active",
"experimental" : false,
"date" : "2024-10-15T13:57:58+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"
}
]
}
]
}
}
IG © 2023+ HL7 International / Public Health. Package hl7.fhir.us.bfdr#2.0.0 based on FHIR 4.0.1. Generated 2024-10-15
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