FHIR IG analytics| Package | us.nlm.vsac |
| Resource Type | ValueSet |
| Id | ValueSet-2.16.840.1.113762.1.4.1251.36.json |
| FHIR Version | R4 |
| Source | https://vsac.nlm.nih.gov/valueset/2.16.840.1.113762.1.4.1251.36/expansion |
| URL | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1251.36 |
| Version | 20231001 |
| Status | active |
| Date | 2023-10-01T01:01:17-04:00 |
| Name | Dyslipidemia |
| Title | Dyslipidemia |
| Realm | us |
| Authority | hl7 |
| Description | SNOMED CT intensional (rule-based) value set for defining dyslipidemia diagnoses, available for a range of potential uses including problem-oriented views of relevant clinical information, clinical decision support rules, electronic patient registries, and data analytics. |
| Purpose | (Clinical Focus: Broad grouper of concepts for dyslipidemias (all types) including hyperlipidemia, as well as concepts for associated abnormal lab values.),(Data Element Scope: Employs SNOMED CT concept hierarchies primarily in the Disorder (Clinical finding) branch, though some can be in the Situation with Explicit Context branch or the Procedure branch.),(Inclusion Criteria: Includes dyslipidemias of all types, hyperlipidemias (primary or secondary), and concepts for abnormal lipid values.),(Exclusion Criteria: Excludes findings of normal lipid levels.) |
No resources found
| CodeSystem | |
| sct | SNOMED codes used in this IG |
No narrative content found in resource
FHIR
FHIRsmith{
"resourceType": "ValueSet",
"id": "2.16.840.1.113762.1.4.1251.36",
"meta": {
"versionId": "9",
"lastUpdated": "2024-01-13T09:16:45.000-05:00",
"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": "UTSW Clinical Informatics Center Author"
}
},
{
"url": "http://hl7.org/fhir/StructureDefinition/resource-lastReviewDate",
"valueDate": "2024-01-13"
},
{
"url": "http://hl7.org/fhir/StructureDefinition/valueset-effectiveDate",
"valueDate": "2023-10-01"
}
],
"url": "http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1251.36",
"identifier": [
{
"system": "urn:ietf:rfc:3986",
"value": "urn:oid:2.16.840.1.113762.1.4.1251.36"
}
],
"version": "20231001",
"name": "Dyslipidemia",
"title": "Dyslipidemia",
"status": "active",
"date": "2023-10-01T01:01:17-04:00",
"publisher": "UTSW Clinical Informatics Center Steward",
"description": "SNOMED CT intensional (rule-based) value set for defining dyslipidemia diagnoses, available for a range of potential uses including problem-oriented views of relevant clinical information, clinical decision support rules, electronic patient registries, and data analytics.",
"jurisdiction": [
{
"coding": [
{
"system": "urn:iso:std:iso:3166",
"code": "US"
}
]
}
],
"purpose": "(Clinical Focus: Broad grouper of concepts for dyslipidemias (all types) including hyperlipidemia, as well as concepts for associated abnormal lab values.),(Data Element Scope: Employs SNOMED CT concept hierarchies primarily in the Disorder (Clinical finding) branch, though some can be in the Situation with Explicit Context branch or the Procedure branch.),(Inclusion Criteria: Includes dyslipidemias of all types, hyperlipidemias (primary or secondary), and concepts for abnormal lipid values.),(Exclusion Criteria: Excludes findings of normal lipid levels.)",
"compose": {
"include": [
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "238037008"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "370992007"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "363140000"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "267436001"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "43465001"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "365793008"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "55822004"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "124040006"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "124054003"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "124041005"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "124055002"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "166853009"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "365798004"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "365795001"
}
]
}
],
"exclude": [
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "365746001"
}
]
}
]
},
"expansion": {
"identifier": "urn:uuid:f919c8b2-cddb-411b-a0d4-4ba8662e6774",
"timestamp": "2025-05-23T21:00:51-04:00",
"total": 138,
"contains": [
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "109041000119107",
"display": "Complex dyslipidemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "111231000119109",
"display": "Dyslipidemia with high density lipoprotein below reference range and triglyceride above reference range due to type 2 diabetes mellitus (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "114831000119107",
"display": "Hyperlipidemia caused by steroid (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1162800007",
"display": "Cholesterol esters within reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1172654005",
"display": "High density lipoprotein below reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1172655006",
"display": "Low density lipoprotein cholesterol below reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1172656007",
"display": "Low density lipoprotein cholesterol within reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1172683008",
"display": "Microcephaly, congenital cataract, psoriasiform dermatitis syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1197489003",
"display": "Familial chylomicronemia syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1208738002",
"display": "Transmembrane protein 199 congenital disorder of glycosylation (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "124040006",
"display": "Lipoprotein above reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "124041005",
"display": "Lipoprotein below reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "124054003",
"display": "Cholesterol esters above reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "124055002",
"display": "Cholesterol esters below reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1256066001",
"display": "Xanthoma due to secondary hyperlipidemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1256071008",
"display": "Xanthoma due to primary hypertriglyceridemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1256073006",
"display": "Xanthoma due to primary combined hyperlipidemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1256075004",
"display": "Xanthoma due to primary hypercholesterolemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1258977001",
"display": "Xanthoma due to primary chylomicronemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1264212004",
"display": "Lipoprotein (a) hyperlipoproteinemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1264565005",
"display": "Familial lecithin cholesterol acyltransferase deficiency (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "129589009",
"display": "Endogenous hyperlipidemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "129590000",
"display": "Exogenous hyperlipidemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "129591001",
"display": "Mixed hypercholesterolemia and hypertriglyceridemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "13644009",
"display": "Hypercholesterolemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "137931000119102",
"display": "Hyperlipidemia due to type 2 diabetes mellitus (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "137941000119106",
"display": "Hyperlipidemia due to type 1 diabetes mellitus (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "15346004",
"display": "Familial hypoalphalipoproteinemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1571000119104",
"display": "Mixed hyperlipidemia due to type 1 diabetes mellitus (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "15771000119109",
"display": "Familial hyperalphalipoproteinemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "166814000",
"display": "Serum lipids within reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "166816003",
"display": "Serum lipids above reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "166828006",
"display": "Serum cholesterol within reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "166830008",
"display": "Serum cholesterol above reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "166846000",
"display": "Serum triglycerides within reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "166848004",
"display": "Serum triglycerides above reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "166853009",
"display": "Lipoprotein electrophoresis outside reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "190773008",
"display": "Hyperbetalipoproteinemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "190774002",
"display": "Hyperlipidemia, group A (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "190785000",
"display": "Hypoalphalipoproteinemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "190786004",
"display": "Hypo-beta-lipoproteinemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "190787008",
"display": "Abetalipoproteinemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "238037008",
"display": "Disorder of lipoprotein storage and metabolism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "238038003",
"display": "Familial hyperlipoproteinemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "238040008",
"display": "Familial combined hyperlipidemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "238041007",
"display": "Familial hypolipoproteinemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "238076009",
"display": "Primary hypercholesterolemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "238077000",
"display": "Polygenic hypercholesterolemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "238078005",
"display": "Familial hypercholesterolemia - homozygous (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "238079002",
"display": "Familial hypercholesterolemia - heterozygous (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "238080004",
"display": "Hyperalphalipoproteinemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "238081000",
"display": "Familial defective apolipoprotein B-100 (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "238082007",
"display": "Secondary hypercholesterolemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "238083002",
"display": "Primary hypertriglyceridemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "238084008",
"display": "Very low density lipoprotinemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "238085009",
"display": "Fredrickson type IV hyperlipoproteinemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "238087001",
"display": "Secondary hypertriglyceridemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "238088006",
"display": "Primary combined hyperlipidemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "238089003",
"display": "Secondary combined hyperlipidemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "238090007",
"display": "Hypolipidemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "238091006",
"display": "Lecithin cholesterol acyltransferase deficiency (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "238092004",
"display": "Fish-eye disease (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "238093009",
"display": "Familial hypobetalipoproteinemia - homozygous form (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "238094003",
"display": "Familial hypobetalipoproteinemia - heterozygous form (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "238095002",
"display": "Apolipoprotein A-I deficiency (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "238096001",
"display": "Apolipoprotein A-I variant disorder (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "238097005",
"display": "Apo A-I Milano variant (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "238098000",
"display": "Apo A-I Marburg variant (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "238099008",
"display": "ApoA-I Munster variant 1 (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "238100000",
"display": "ApoA-I Munster variant 2 (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "238101001",
"display": "ApoA-I Munster variant 3 (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "238102008",
"display": "Apo A-I Giessen variant (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "238103003",
"display": "Apo A-I variant fisheye-like syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "238104009",
"display": "Sitosterolemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "267432004",
"display": "Pure hypercholesterolemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "267433009",
"display": "Pure hyperglyceridemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "267434003",
"display": "Mixed hyperlipidemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "267435002",
"display": "Familial hyperchylomicronemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "267436001",
"display": "Lipoprotein deficiency disorder (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "275598004",
"display": "Familial lipoprotein lipase deficiency (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "299465007",
"display": "Familial multiple lipoprotein-type hyperlipidemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "302870006",
"display": "Hypertriglyceridemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "33513003",
"display": "Familial apolipoprotein C-II deficiency (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "34349009",
"display": "Familial type 5 hyperlipoproteinemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "34528009",
"display": "Familial hypertriglyceridemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "363140000",
"display": "Hypolipoproteinemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "365793008",
"display": "Finding of cholesterol level (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "365794002",
"display": "Finding of serum cholesterol level (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "365795001",
"display": "Finding of triglyceride level (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "365796000",
"display": "Finding of serum triglyceride levels (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "365798004",
"display": "Finding of serum lipid levels (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "368551000119104",
"display": "Dyslipidemia due to type 1 diabetes mellitus (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "370992007",
"display": "Dyslipidemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "3744001",
"display": "Hyperlipoproteinemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "397915002",
"display": "Fredrickson type IIa hyperlipoproteinemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "398036000",
"display": "Familial hypercholesterolemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "398796005",
"display": "Familial type 3 hyperlipoproteinemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "402473001",
"display": "Sporadic primary hypertriglyceridemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "402474007",
"display": "Primary polygenic type IIb combined hyperlipidemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "402475008",
"display": "Primary acquired chylomicronemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "402725005",
"display": "Hyperlipidemia with lipid deposition in skin (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "402726006",
"display": "Primary chylomicronemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "402727002",
"display": "Secondary hyperlipidemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "402785008",
"display": "Primary genetic hyperlipidemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "402786009",
"display": "Chylomicronemia syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "402787000",
"display": "Primary genetic mixed hyperlipidemia (disorder)"
},
{
"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)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "403828005",
"display": "Familial lipoprotein lipase deficiency with type V phenotype (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"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/20250301",
"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/20250301",
"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/20250301",
"code": "426161002",
"display": "Chemically induced hyperlipidemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "428014009",
"display": "Homozygous sitosterolemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "428530009",
"display": "Heterozygous sitosterolemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "43465001",
"display": "Inborn error of lipoprotein metabolism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "443835004",
"display": "High density lipoprotein above reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "445010006",
"display": "Low density lipoprotein receptor mutation (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "445261005",
"display": "Posttransplant hyperlipidemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "445445006",
"display": "Low density lipoprotein cholesterol above reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "446923008",
"display": "Lipoprotein glomerulopathy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "448834003",
"display": "High density lipoprotein deficiency (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "49973006",
"display": "Familial lipoprotein deficiency (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "55822004",
"display": "Hyperlipidemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "58618005",
"display": "Familial disease with storage of sterols (other than cholesterol) (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "60193003",
"display": "Familial hypobetalipoproteinemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "61336008",
"display": "Hypocholesterolemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "65419005",
"display": "Sitosterolemia with xanthomatosis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "67991000119104",
"display": "Serum cholesterol outside reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "701000119103",
"display": "Mixed hyperlipidemia due to type 2 diabetes mellitus (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "720940008",
"display": "Hepatic lipase deficiency (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "723579009",
"display": "Tangier disease (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "724770001",
"display": "Ataxia co-occurrent and due to abetalipoproteinemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "761000119102",
"display": "Dyslipidemia due to type 2 diabetes mellitus (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"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/20250301",
"code": "767134003",
"display": "Low density lipoprotein receptor adaptor protein 1 mutation (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "767139008",
"display": "Combined heterozygous low density lipoprotein receptor co-occurrent with low density lipoprotein receptor adaptor protein 1 mutations (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "773649005",
"display": "Transient infantile hypertriglyceridemia and hepatosteatosis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "773726000",
"display": "Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency (disorder)"
}
]
}
}