Package | us.cdc.phinvads |
Resource Type | ValueSet |
Id | 2.16.840.1.114222.4.11.7608 |
FHIR Version | R4 |
Source | http://fhir.org/packages/us.cdc.phinvads |
URL | http://phinvads.cdc.gov/fhir/ValueSet/2.16.840.1.114222.4.11.7608 |
Version | 4 |
Status | active |
Date | 2017-01-25T00:10:00+11:00 |
Name | PHVS_Complications_CRS |
Title | Type Of Complication (CRS) |
Realm | us |
Description | Complications associated with the illness being reported |
No resources found
CodeSystem | |
sct | SNOMED CT (all versions) |
v3-NullFlavor | NullFlavor |
No narrative content found in resource
{ "resourceType": "ValueSet", "id": "2.16.840.1.114222.4.11.7608", "meta": { "source": "https://phinvads.cdc.gov/vads/ViewValueSet.action?oid=2.16.840.1.114222.4.11.7608" }, "url": "http://phinvads.cdc.gov/fhir/ValueSet/2.16.840.1.114222.4.11.7608", "version": "4", "name": "PHVS_Complications_CRS", "title": "Type Of Complication (CRS)", "status": "active", "date": "2017-01-25T00:10:00+11:00", "description": "Complications associated with the illness being reported", "compose": { "include": [ { "system": "http://snomed.info/sct", "version": "http://snomed.info/sct/731000124108/version/20200901", "concept": [ { "code": "128306009", "display": "Cataract" }, { "code": "15188001", "display": "Hearing Impairment" }, { "code": "13213009", "display": "Congenital heart disease" }, { "code": "83330001", "display": "Patent ductus arteriosus" }, { "code": "415582006", "display": "Stenosis" }, { "code": "204113001", "display": "Congenital glaucoma" }, { "code": "13225007", "display": "Meningoencephalitis" }, { "code": "12393003", "display": "Purpura" }, { "code": "16294009", "display": "Enlarged spleen" }, { "code": "80515008", "display": "Enlarged liver" }, { "code": "387712008", "display": "Neonatal jaundice" } ] }, { "system": "urn:oid:2.16.840.1.114222.4.5.232", "version": "20200528", "concept": [ { "code": "CRS021", "display": "Other congenital heart disease, specify" }, { "code": "INV345", "display": "Peripheral pulmonic stenosis" }, { "code": "INV347", "display": "Pigmentary retinopathy" }, { "code": "INV348", "display": "Developmental delay or Mental retardation" }, { "code": "INV350", "display": "Microencephaly" }, { "code": "INV354", "display": "Radiolucent bone disease" }, { "code": "INV356", "display": "Low platelets" }, { "code": "INV357", "display": "Dermal erythropoieses (Blueberry Muffin Syndrome)" } ] }, { "system": "http://terminology.hl7.org/CodeSystem/v3-NullFlavor", "version": "20090501", "concept": [ { "code": "OTH", "display": "Other" }, { "code": "UNK", "display": "Unknown" } ] } ] } }