Package | us.nlm.vsac |
Type | ValueSet |
Id | Id |
FHIR Version | R4 |
Source | http://fhir.org/packages/us.nlm.vsac/https://vsac.nlm.nih.gov/valueset/2.16.840.1.113762.1.4.1196.1139/expansion |
Url | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1196.1139 |
Version | 20220826 |
Status | active |
Date | 2022-08-26T01:03:06-04:00 |
Name | S4GHyperlipidemia |
Title | S4G Hyperlipidemia |
Experimental | False |
Realm | us |
Authority | hl7 |
Description | (This is a sync for genes test value set. This is only a test value set.) |
Purpose | (Clinical Focus: ),(Data Element Scope: ),(Inclusion Criteria: SNOMED hyperlipidemia codes),(Exclusion Criteria: ) |
No resources found
CodeSystem | |
http://snomed.info/sct ![]() | SNOMED CT (all versions) |
http://snomed.info/sct ![]() | Nutrition Care Process Terminology module |
http://snomed.info/sct ![]() | veri |
{
"resourceType" : "ValueSet",
"id" : "2.16.840.1.113762.1.4.1196.1139",
"meta" : {
"versionId" : "8",
"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" : "Elimu Informatics Author"
}
},
{
"url" : "http://hl7.org/fhir/StructureDefinition/resource-lastReviewDate",
"valueDate" : "2024-02-14"
},
{
"url" : "http://hl7.org/fhir/StructureDefinition/valueset-effectiveDate",
"valueDate" : "2022-08-26"
}
],
"url" : "http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1196.1139",
"identifier" : [
{
"system" : "urn:ietf:rfc:3986",
"value" : "urn:oid:2.16.840.1.113762.1.4.1196.1139"
}
],
"version" : "20220826",
"name" : "S4GHyperlipidemia",
"title" : "S4G Hyperlipidemia",
"status" : "active",
"experimental" : false,
"date" : "2022-08-26T01:03:06-04:00",
"publisher" : "Elimu Informatics Steward",
"description" : "(This is a sync for genes test value set. This is only a test value set.)",
"jurisdiction" : [
{
"coding" : [
{
"system" : "urn:iso:std:iso:3166",
"code" : "US"
}
]
}
],
"purpose" : "(Clinical Focus: ),(Data Element Scope: ),(Inclusion Criteria: SNOMED hyperlipidemia codes),(Exclusion Criteria: )",
"compose" : {
"include" : [
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"filter" : [
{
"property" : "concept",
"op" : "is-a",
"value" : "55822004"
}
]
}
]
},
"expansion" : {
"identifier" : "urn:uuid:561b3e2c-27d5-4047-b31b-992d1b001251",
"timestamp" : "2024-12-10T07:34:45-05:00",
"total" : 64,
"contains" : [
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "114831000119107",
"display" : "Hyperlipidemia caused by steroid (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "1197489003",
"display" : "Familial chylomicronemia syndrome (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "1208738002",
"display" : "Transmembrane protein 199 congenital disorder of glycosylation (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "1256066001",
"display" : "Xanthoma due to secondary hyperlipidemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "1256071008",
"display" : "Xanthoma due to primary hypertriglyceridemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "1256073006",
"display" : "Xanthoma due to primary combined hyperlipidemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "1256075004",
"display" : "Xanthoma due to primary hypercholesterolemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "1258977001",
"display" : "Xanthoma due to primary chylomicronemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "129589009",
"display" : "Endogenous hyperlipidemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "129590000",
"display" : "Exogenous hyperlipidemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "129591001",
"display" : "Mixed hypercholesterolemia and hypertriglyceridemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "13644009",
"display" : "Hypercholesterolemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "137931000119102",
"display" : "Hyperlipidemia due to type 2 diabetes mellitus (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "137941000119106",
"display" : "Hyperlipidemia due to type 1 diabetes mellitus (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "1571000119104",
"display" : "Mixed hyperlipidemia due to type 1 diabetes mellitus (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "15771000119109",
"display" : "Familial hyperalphalipoproteinemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "190774002",
"display" : "Hyperlipidemia, group A (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "238040008",
"display" : "Familial combined hyperlipidemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "238076009",
"display" : "Primary hypercholesterolemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "238077000",
"display" : "Polygenic hypercholesterolemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "238078005",
"display" : "Familial hypercholesterolemia - homozygous (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "238079002",
"display" : "Familial hypercholesterolemia - heterozygous (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "238080004",
"display" : "Hyperalphalipoproteinemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "238081000",
"display" : "Familial defective apolipoprotein B-100 (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "238082007",
"display" : "Secondary hypercholesterolemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "238083002",
"display" : "Primary hypertriglyceridemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "238084008",
"display" : "Very low density lipoprotinemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "238085009",
"display" : "Fredrickson type IV hyperlipoproteinemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "238087001",
"display" : "Secondary hypertriglyceridemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "238088006",
"display" : "Primary combined hyperlipidemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "238089003",
"display" : "Secondary combined hyperlipidemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "267432004",
"display" : "Pure hypercholesterolemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "267433009",
"display" : "Pure hyperglyceridemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "267434003",
"display" : "Mixed hyperlipidemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "267435002",
"display" : "Familial hyperchylomicronemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "275598004",
"display" : "Familial lipoprotein lipase deficiency (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "299465007",
"display" : "Familial multiple lipoprotein-type hyperlipidemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "302870006",
"display" : "Hypertriglyceridemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "33513003",
"display" : "Familial apolipoprotein C-II deficiency (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "34349009",
"display" : "Familial type 5 hyperlipoproteinemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "34528009",
"display" : "Familial hypertriglyceridemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "397915002",
"display" : "Fredrickson type IIa hyperlipoproteinemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "398036000",
"display" : "Familial hypercholesterolemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "402473001",
"display" : "Sporadic primary hypertriglyceridemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "402474007",
"display" : "Primary polygenic type IIb combined hyperlipidemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "402475008",
"display" : "Primary acquired chylomicronemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "402725005",
"display" : "Hyperlipidemia with lipid deposition in skin (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "402726006",
"display" : "Primary chylomicronemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "402727002",
"display" : "Secondary hyperlipidemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "402785008",
"display" : "Primary genetic hyperlipidemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "402786009",
"display" : "Chylomicronemia syndrome (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "402787000",
"display" : "Primary genetic mixed hyperlipidemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "403827000",
"display" : "Familial lipoprotein lipase deficiency with type I phenotype (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "403828005",
"display" : "Familial lipoprotein lipase deficiency with type V phenotype (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "403829002",
"display" : "Familial hypercholesterolemia due to heterozygous low density lipoprotein receptor mutation (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "403830007",
"display" : "Familial hypercholesterolemia due to homozygous low density lipoprotein receptor mutation (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "403831006",
"display" : "Familial hypercholesterolemia due to genetic defect of apolipoprotein B (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "426161002",
"display" : "Chemically induced hyperlipidemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "445261005",
"display" : "Posttransplant hyperlipidemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "55822004",
"display" : "Hyperlipidemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "701000119103",
"display" : "Mixed hyperlipidemia due to type 2 diabetes mellitus (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "767133009",
"display" : "Familial hypercholesterolemia co-occurrent and due to combined heterozygous low density lipoprotein receptor and low density lipoprotein receptor adaptor protein 1 mutations (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "773649005",
"display" : "Transient infantile hypertriglyceridemia and hepatosteatosis (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "773726000",
"display" : "Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency (disorder)"
}
]
},
"text" : {
}
}
XIG built as of ??metadata-date??. Found ??metadata-resources?? resources in ??metadata-packages?? packages.