FHIR IG analytics
| Package | us.nlm.vsac |
| Resource Type | ValueSet |
| Id | ValueSet-2.16.840.1.113762.1.4.1047.85.json |
| FHIR Version | R4 |
| Source | https://vsac.nlm.nih.gov/valueset/2.16.840.1.113762.1.4.1047.85/expansion |
| URL | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1047.85 |
| Version | 20230217 |
| Status | active |
| Date | 2023-02-17T01:03:27-05:00 |
| Name | FamilialHypercholesterolemia |
| Title | Familial Hypercholesterolemia |
| Realm | us |
| Authority | hl7 |
| Purpose | (Clinical Focus: The purpose of this value set is to represent concepts for familial hypercholesterolemia.),(Data Element Scope: This value set may use a model element related to Diagnosis.),(Inclusion Criteria: Includes concepts that represent a diagnosis of familial hypercholesterolemia.),(Exclusion Criteria: No exclusions.) |
Resources that use this resource
Resources that this resource uses
| CodeSystem |
| sct | SNOMED codes used in this IG |
Narrative
No narrative content found in resource
Source1
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"name": "FamilialHypercholesterolemia",
"title": "Familial Hypercholesterolemia",
"status": "active",
"date": "2023-02-17T01:03:27-05:00",
"publisher": "American Institutes for Research Steward",
"jurisdiction": [
{
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{
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"code": "US"
}
]
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],
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"compose": {
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{
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{
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"display": "Polygenic hypercholesterolemia (disorder)"
},
{
"code": "238078005",
"display": "Familial hypercholesterolemia - homozygous (disorder)"
},
{
"code": "238079002",
"display": "Familial hypercholesterolemia - heterozygous (disorder)"
},
{
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"display": "Familial hypercholesterolemia (disorder)"
},
{
"code": "398796005",
"display": "Familial type 3 hyperlipoproteinemia (disorder)"
},
{
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"display": "Familial hypercholesterolemia due to heterozygous low density lipoprotein receptor mutation (disorder)"
},
{
"code": "403830007",
"display": "Familial hypercholesterolemia due to homozygous low density lipoprotein receptor mutation (disorder)"
},
{
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"timestamp": "2025-05-23T17:35:45-04:00",
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"display": "Familial hypercholesterolemia due to homozygous low density lipoprotein receptor mutation (disorder)"
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}