Birth And Fetal Death (BFDR) - STU2-ballot
2.0.0-ballot - ballot
Birth And Fetal Death (BFDR) - STU2-ballot
2.0.0-ballot - ballot
This page is part of the Vital Records Birth and Fetal Death Reporting (v2.0.0-ballot: STU 2 Ballot 1) based on FHIR (HL7® FHIR® Standard) R4. The current version which supersedes this version is 1.1.0. For a full list of available versions, see the Directory of published versions
| Official URL: http://hl7.org/fhir/us/bfdr/ValueSet/ValueSet-newborn-congenital-anomalies | Version: 2.0.0-ballot | |||
| Draft as of 2023-12-18 | Computable Name: NewbornCongenitalAnomaliesVS | |||
Copyright/Legal: 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 |
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The valueset contains codes to represent newborn congenital anomalies. This valueset is based on PHVS_NewbornCongenitalAnomalies_NCHS
References
http://snomed.info/sct| Code | Display |
| 89369001 | Anencephalus |
| 67531005 | Meningomyelocele/Spina bifida |
| 12770006 | Cyanotic congenital heart disease |
| 17190001 | Congenital diaphragmatic hernia |
| 18735004 | Congenital omphalocele |
| 72951007 | Gastroschisis |
| 67341007 | Longitudinal deficiency of limb - Limb reduction defect (excluding congenital amputation and dwarfing syndromes) |
| 80281008 | Cleft Lip with or without Cleft Palate |
| 87979003 | Cleft palate |
| 70156005 | Anomaly of chromosome pair 21 |
| 409709004 | Chromosomal disorder |
| 416010008 | Hypospadias |
| 260413007 | None |
Expansion based on:
This value set contains 13 concepts
| Code | System | Display |
| 89369001 | http://snomed.info/sct | Anencephalus |
| 67531005 | http://snomed.info/sct | Meningomyelocele/Spina bifida |
| 12770006 | http://snomed.info/sct | Cyanotic congenital heart disease |
| 17190001 | http://snomed.info/sct | Congenital diaphragmatic hernia |
| 18735004 | http://snomed.info/sct | Congenital omphalocele |
| 72951007 | http://snomed.info/sct | Gastroschisis |
| 67341007 | http://snomed.info/sct | Longitudinal deficiency of limb - Limb reduction defect (excluding congenital amputation and dwarfing syndromes) |
| 80281008 | http://snomed.info/sct | Cleft Lip with or without Cleft Palate |
| 87979003 | http://snomed.info/sct | Cleft palate |
| 70156005 | http://snomed.info/sct | Anomaly of chromosome pair 21 |
| 409709004 | http://snomed.info/sct | Chromosomal disorder |
| 416010008 | http://snomed.info/sct | Hypospadias |
| 260413007 | http://snomed.info/sct | None |
Explanation of the columns that may appear on this page:
| Level | A few code lists that FHIR defines are hierarchical - each code is assigned a level. In this scheme, some codes are under other codes, and imply that the code they are under also applies |
| System | The source of the definition of the code (when the value set draws in codes defined elsewhere) |
| Code | The code (used as the code in the resource instance) |
| Display | The display (used in the display element of a Coding). If there is no display, implementers should not simply display the code, but map the concept into their application |
| Definition | An explanation of the meaning of the concept |
| Comments | Additional notes about how to use the code |
IG © 2023+ HL7 International / Public Health. Package hl7.fhir.us.bfdr#2.0.0-ballot based on FHIR 4.0.1. Generated 2023-12-18
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