FHIR IG Statistics: ValueSet/2.16.840.1.113762.1.4.1222.742
| Package | us.nlm.vsac |
| Resource Type | ValueSet |
| Id | 2.16.840.1.113762.1.4.1222.742 |
| FHIR Version | R4 |
| Source | http://fhir.org/packages/us.nlm.vsac/https://vsac.nlm.nih.gov/valueset/2.16.840.1.113762.1.4.1222.742/expansion |
| URL | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1222.742 |
| Version | 20240712 |
| Status | active |
| Date | 2024-07-12T01:03:21-04:00 |
| Name | Hypertriglyceridemia |
| Title | Hypertriglyceridemia |
| Realm | us |
| Authority | hl7 |
| Description | This value set may undergo changes until the HL7 Multiple Chronic Care FHIR IG is formally published in 2024. |
| Purpose | (Clinical Focus: This set of values addresses terms representing Hypertriglyceridemia.),(Data Element Scope: The intent of this set of values is to identify patients who have a/an documented diagnosis of hypertriglyceridemia.),(Inclusion Criteria: Includes GROUP codes for Hypertriglyceridemia.),(Exclusion Criteria: Terms not representative of observable encoded terms that may have values indicating Hypertriglyceridemia.) |
Resources that use this resource
No resources found
Resources that this resource uses
| CodeSystem |
| sct | SNOMED CT (all versions) |
| icd-10-cm | International Classification of Diseases, 10th Revision, Clinical Modification (ICD-10-CM) |
Narrative
No narrative content found in resource
Source
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"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "267435002",
"display": "Familial hyperchylomicronemia (disorder)"
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{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "302870006",
"display": "Hypertriglyceridemia (disorder)"
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{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "34349009",
"display": "Familial type 5 hyperlipoproteinemia (disorder)"
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"system": "http://snomed.info/sct",
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"display": "Sporadic primary hypertriglyceridemia (disorder)"
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"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "403827000",
"display": "Familial lipoprotein lipase deficiency with type I phenotype (disorder)"
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"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "773649005",
"display": "Transient infantile hypertriglyceridemia and hepatosteatosis (disorder)"
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{
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"version": "2025",
"code": "E78.1",
"display": "Pure hyperglyceridemia"
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FHIR