FHIR IG Statistics: ValueSet/2.16.840.1.113762.1.4.1235.299
Package | us.nlm.vsac |
Resource Type | ValueSet |
Id | 2.16.840.1.113762.1.4.1235.299 |
FHIR Version | R4 |
Source | http://fhir.org/packages/us.nlm.vsac/https://vsac.nlm.nih.gov/valueset/2.16.840.1.113762.1.4.1235.299/expansion |
URL | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1235.299 |
Version | 20230518 |
Status | active |
Date | 2023-05-18T01:12:46-04:00 |
Name | FITDNATest_Lab_Grouping |
Title | FIT DNA Test_Lab_Grouping |
Realm | us |
Authority | hl7 |
Description | b.well created value set by Sr. Clinical Business Analyst for FIT DNA Test. |
Purpose | (Clinical Focus: This value set's intent is to define the clinical codes that constitute the FIT DNA Test utilization in patients/users connected health.),(Data Element Scope: This value set's intent is to define the clinical codes that constitute the FIT DNA Test utilization in patients/users connected health.),(Inclusion Criteria: This value set's intent is to define the clinical codes that constitute the FIT DNA Test utilization in patients/users connected health.),(Exclusion Criteria: This value set's intent is to define the clinical codes that constitute the FIT DNA Test utilization in patients/users connected health.) |
Resources that use this resource
No resources found
Resources that this resource uses
CodeSystem |
loinc.org | LOINC Code System |
sct | SNOMED CT (all versions) |
cpt | Current Procedural Terminology (CPT®) |
Narrative
No narrative content found in resource
Source
{
"resourceType": "ValueSet",
"id": "2.16.840.1.113762.1.4.1235.299",
"meta": {
"versionId": "6",
"lastUpdated": "2023-12-21T17:43:03.000-05:00",
"profile": [
"http://hl7.org/fhir/StructureDefinition/shareablevalueset",
"http://hl7.org/fhir/us/cqfmeasures/StructureDefinition/computable-valueset-cqfm",
"http://hl7.org/fhir/us/cqfmeasures/StructureDefinition/publishable-valueset-cqfm"
]
},
"extension": [
{
"url": "http://hl7.org/fhir/StructureDefinition/valueset-author",
"valueContactDetail": {
"name": "B.well Connected Health Author"
}
},
{
"url": "http://hl7.org/fhir/StructureDefinition/resource-lastReviewDate",
"valueDate": "2024-06-04"
},
{
"url": "http://hl7.org/fhir/StructureDefinition/valueset-effectiveDate",
"valueDate": "2023-05-18"
}
],
"url": "http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1235.299",
"identifier": [
{
"system": "urn:ietf:rfc:3986",
"value": "urn:oid:2.16.840.1.113762.1.4.1235.299"
}
],
"version": "20230518",
"name": "FITDNATest_Lab_Grouping",
"title": "FIT DNA Test_Lab_Grouping",
"status": "active",
"date": "2023-05-18T01:12:46-04:00",
"publisher": "B.well Connected Health Steward",
"description": "b.well created value set by Sr. Clinical Business Analyst for FIT DNA Test.",
"jurisdiction": [
{
"coding": [
{
"system": "urn:iso:std:iso:3166",
"code": "US"
}
]
}
],
"purpose": "(Clinical Focus: This value set's intent is to define the clinical codes that constitute the FIT DNA Test utilization in patients/users connected health.),(Data Element Scope: This value set's intent is to define the clinical codes that constitute the FIT DNA Test utilization in patients/users connected health.),(Inclusion Criteria: This value set's intent is to define the clinical codes that constitute the FIT DNA Test utilization in patients/users connected health.),(Exclusion Criteria: This value set's intent is to define the clinical codes that constitute the FIT DNA Test utilization in patients/users connected health.)",
"compose": {
"include": [
{
"valueSet": [
"http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1235.295"
]
},
{
"valueSet": [
"http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1235.296"
]
},
{
"valueSet": [
"http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1235.297"
]
},
{
"valueSet": [
"http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1235.298"
]
}
]
},
"expansion": {
"identifier": "urn:uuid:581b09aa-b82a-444e-84b9-d1f49fb00352",
"timestamp": "2025-05-23T20:22:09-04:00",
"total": 4,
"contains": [
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "708699002",
"display": "Colorectal cancer detected by DNA-based stool screening (finding)"
},
{
"system": "http://loinc.org",
"version": "2.80",
"code": "77353-1",
"display": "Noninvasive colorectal cancer DNA and occult blood screening [Interpretation] in Stool Narrative"
},
{
"system": "http://loinc.org",
"version": "2.80",
"code": "77354-9",
"display": "Noninvasive colorectal cancer DNA and occult blood screening [Presence] in Stool"
},
{
"system": "http://www.ama-assn.org/go/cpt",
"version": "2025",
"code": "81528",
"display": "Oncology (colorectal) screening, quantitative real-time target and signal amplification of 10 DNA markers (KRAS mutations, promoter methylation of NDRG4 and BMP3) and fecal hemoglobin, utilizing stool, algorithm reported as a positive or negative result"
}
]
}
}