| Source | us.nlm.vsac#0.11.0:null (v4.0.1) |
| resourceType | ValueSet |
| id | 2.16.840.1.113762.1.4.1078.430 |
| canonical | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1078.430 |
| version | 20230324 |
| status | active |
| publisher | Optum Steward |
| name | Hypercholesterolemia |
| title | Hypercholesterolemia |
| date | 2023-03-24T01:02:43-04:00 |
| Usages | (none) |
This value set contains 36 concepts
| Code | System | Display |
| 1208738002 | http://snomed.info/sct | Transmembrane protein 199 congenital disorder of glycosylation (disorder) |
| 13644009 | http://snomed.info/sct | Hypercholesterolemia (disorder) |
| 15771000119109 | http://snomed.info/sct | Familial hyperalphalipoproteinemia (disorder) |
| 166830008 | http://snomed.info/sct | Serum cholesterol above reference range (finding) |
| 190774002 | http://snomed.info/sct | Hyperlipidemia, group A (disorder) |
| 238076009 | http://snomed.info/sct | Primary hypercholesterolemia (disorder) |
| 238077000 | http://snomed.info/sct | Polygenic hypercholesterolemia (disorder) |
| 238078005 | http://snomed.info/sct | Familial hypercholesterolemia - homozygous (disorder) |
| 238079002 | http://snomed.info/sct | Familial hypercholesterolemia - heterozygous (disorder) |
| 238080004 | http://snomed.info/sct | Hyperalphalipoproteinemia (disorder) |
| 238081000 | http://snomed.info/sct | Familial defective apolipoprotein B-100 (disorder) |
| 238082007 | http://snomed.info/sct | Secondary hypercholesterolemia (disorder) |
| 267432004 | http://snomed.info/sct | Pure hypercholesterolemia (disorder) |
| 397915002 | http://snomed.info/sct | Fredrickson type IIa hyperlipoproteinemia (disorder) |
| 398036000 | http://snomed.info/sct | Familial hypercholesterolemia (disorder) |
| 403829002 | http://snomed.info/sct | Familial hypercholesterolemia due to heterozygous low density lipoprotein receptor mutation (disorder) |
| 403830007 | http://snomed.info/sct | Familial hypercholesterolemia due to homozygous low density lipoprotein receptor mutation (disorder) |
| 403831006 | http://snomed.info/sct | Familial hypercholesterolemia due to genetic defect of apolipoprotein B (disorder) |
| 767133009 | http://snomed.info/sct | Familial hypercholesterolemia co-occurrent and due to combined heterozygous low density lipoprotein receptor and low density lipoprotein receptor adaptor protein 1 mutations (disorder) |
| 773726000 | http://snomed.info/sct | Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency (disorder) |
| E78.00 | http://hl7.org/fhir/sid/icd-10-cm | Pure hypercholesterolemia, unspecified |
| E78.01 | http://hl7.org/fhir/sid/icd-10-cm | Familial hypercholesterolemia |
| E78.1 | http://hl7.org/fhir/sid/icd-10-cm | Pure hyperglyceridemia |
| E78.2 | http://hl7.org/fhir/sid/icd-10-cm | Mixed hyperlipidemia |
| E78.3 | http://hl7.org/fhir/sid/icd-10-cm | Hyperchylomicronemia |
| E78.41 | http://hl7.org/fhir/sid/icd-10-cm | Elevated Lipoprotein(a) |
| E78.49 | http://hl7.org/fhir/sid/icd-10-cm | Other hyperlipidemia |
| E78.5 | http://hl7.org/fhir/sid/icd-10-cm | Hyperlipidemia, unspecified |
| E78.6 | http://hl7.org/fhir/sid/icd-10-cm | Lipoprotein deficiency |
| E78.70 | http://hl7.org/fhir/sid/icd-10-cm | Disorder of bile acid and cholesterol metabolism, unspecified |
| E78.71 | http://hl7.org/fhir/sid/icd-10-cm | Barth syndrome |
| E78.72 | http://hl7.org/fhir/sid/icd-10-cm | Smith-Lemli-Opitz syndrome |
| E78.79 | http://hl7.org/fhir/sid/icd-10-cm | Other disorders of bile acid and cholesterol metabolism |
| E78.81 | http://hl7.org/fhir/sid/icd-10-cm | Lipoid dermatoarthritis |
| E78.89 | http://hl7.org/fhir/sid/icd-10-cm | Other lipoprotein metabolism disorders |
| E78.9 | http://hl7.org/fhir/sid/icd-10-cm | Disorder of lipoprotein metabolism, unspecified |
Produced 08 Sep 2023