Rekord LOINC: 93201-2
Dostępne tłumaczenie polskie ACTIVE
Tłumaczenie polskie
Szczegóły rekordu LOINC
Informacje podstawowe
| Kod LOINC: |
93201-2
FHIR
|
| Long Common Name: | Coronary heart disease multigene analysis in Blood or Tissue by Molecular genetics method |
| Short Name: | CHD Multigene Anl Bld/T |
| Status: | ACTIVE |
| Class Type: | 1 |
Fully Specified Name (FSN)
Klasyfikacja
| Class: |
PLpatologia molekularna
ENMOLPATH
|
| Consumer Name: | - |
| Order/Observation: | Both |
| Panel Type: | - |
Informacje dodatkowe
| Units Required: | - |
| Example Units: | - |
| UCUM Units: | - |
| Version Last Changed: | 2.67 |
Definicja i opis
This test includes analysis of alleles at multiple genetic loci associated with coronary heart disease (CHD). Testing is performed to determine an individual's genetic-based risk for CHD, particularly in patients at intermediate risk for atherosclerotic cardiovascular disease (ASCVD) and those with family history of ASCVD. An overall genetic risk score (GRS) [LOINC: 93306-9] and interpretation (high/low) [LOINC: 93307-7] may be provided to improve risk estimates and aid in the prevention of CHD. The GRS is based on the genotype of multiple genetic variants associated with CHD. Additionally, a patient's overall 10-year probability of CHD may be calculated by multiply the 10-year ASCVD score from the Pooled Cohort Equations by the GRS.
Powiązane nazwy
Analiza wielogenowa w kierunku choroby niedokrwiennej serca diagnostyka molekularna