Error | ValueSet.version | Values for version differ: '2.0.0-ballot' vs '2.0.0' |
Information | ValueSet.title | Values for title differ: 'ValueSet - Newborn Congenital Anomalies' vs 'Newborn Congenital Anomalies' |
Information | ValueSet.status | Values for status differ: 'draft' vs 'active' |
Information | ValueSet.date | Values for date differ: '2023-12-18T14:34:58+00:00' vs '2024-10-15T13:57:58+00:00' |
Error | ValueSet.compose.exclude[0] | Code 260413007 removed |
Name | Value | Comments | |
---|---|---|---|
compose.inactive | |||
compose.lockedDate | |||
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 | ||
date | 2023-12-18T14:34:58+00:00 | 2024-10-15T13:57:58+00:00 |
|
description | The valueset contains codes to represent newborn congenital anomalies. This valueset is based on [PHVS_NewbornCongenitalAnomalies_NCHS](https://phinvads.cdc.gov/vads/ViewValueSet.action?id=BC64CB23-8210-4CE0-B2AE-F45169BBDC51) | 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). |
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experimental | false | ||
immutable | |||
jurisdiction | |||
jurisdiction[0] | urn:iso:std:iso:3166#US | ||
name | NewbornCongenitalAnomaliesVS | ||
publisher | HL7 International / Public Health | ||
purpose | |||
status | draft | active |
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title | ValueSet - Newborn Congenital Anomalies | Newborn Congenital Anomalies |
|
url | http://hl7.org/fhir/us/bfdr/ValueSet/ValueSet-newborn-congenital-anomalies | ||
version | 2.0.0-ballot | 2.0.0 |
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Item | Property | Value | Comments | ||
---|---|---|---|---|---|
include | http://snomed.info/sct | ||||
Concept | 89369001 | Anencephalus | |||
Concept | 67531005 | Meningomyelocele/Spina bifida | |||
Concept | 12770006 | Cyanotic congenital heart disease | |||
Concept | 17190001 | Congenital diaphragmatic hernia | |||
Concept | 18735004 | Congenital omphalocele | |||
Concept | 72951007 | Gastroschisis | |||
Concept | 67341007 | Longitudinal deficiency of limb - Limb reduction defect (excluding congenital amputation and dwarfing syndromes) | |||
Concept | 80281008 | Cleft Lip with or without Cleft Palate | |||
Concept | 87979003 | Cleft palate | |||
Concept | 70156005 | Anomaly of chromosome pair 21 | |||
Concept | 409709004 | Chromosomal disorder | |||
Concept | 416010008 | Hypospadias | |||
Concept | 260413007 | Version: None |
| ||
include | http://terminology.hl7.org/CodeSystem/v3-NullFlavor |
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Unable to generate expansion - see errors