Package | us.cdc.phinvads |
Resource Type | ValueSet |
Id | 1.3.6.1.4.1.19376.1.7.3.1.1.13.8.61 |
FHIR Version | R4 |
Source | http://fhir.org/packages/us.cdc.phinvads |
URL | http://phinvads.cdc.gov/fhir/ValueSet/1.3.6.1.4.1.19376.1.7.3.1.1.13.8.61 |
Version | 2 |
Status | active |
Date | 2014-01-22T00:09:00+11:00 |
Name | PHVS_DownSyndrome_NCHS |
Title | Down Syndrome (NCHS) |
Realm | us |
Description | To reflect Down Syndrome as an anomaly of the newborn |
No resources found
CodeSystem | |
sct | SNOMED CT (all versions) |
No narrative content found in resource
{ "resourceType": "ValueSet", "id": "1.3.6.1.4.1.19376.1.7.3.1.1.13.8.61", "meta": { "source": "https://phinvads.cdc.gov/vads/ViewValueSet.action?oid=1.3.6.1.4.1.19376.1.7.3.1.1.13.8.61" }, "url": "http://phinvads.cdc.gov/fhir/ValueSet/1.3.6.1.4.1.19376.1.7.3.1.1.13.8.61", "version": "2", "name": "PHVS_DownSyndrome_NCHS", "title": "Down Syndrome (NCHS)", "status": "active", "date": "2014-01-22T00:09:00+11:00", "description": "To reflect Down Syndrome as an anomaly of the newborn", "compose": { "include": [ { "system": "http://snomed.info/sct", "version": "http://snomed.info/sct/731000124108/version/20200901", "concept": [ { "code": "70156005", "display": "Anomaly of chromosome pair 21" }, { "code": "41040004", "display": "Complete trisomy 21 syndrome" }, { "code": "205615000", "display": "Trisomy 21- meiotic nondisjunction" }, { "code": "205616004", "display": "Trisomy 21- mitotic nondisjunction mosaicism" }, { "code": "254264002", "display": "Partial trisomy 21 in Down's syndrome" }, { "code": "371045000", "display": "Translocation Down syndrome" } ] } ] } }