93201-2
Coronary heart disease multigene analysis in Blood or Tissue by Molecular genetics method
Active
Term Description
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.
LOINC Names Get Info
- Fully-Specified Name
- Coronary heart disease multigene analysis:
Find: Pt: Bld/Tiss: Doc: Molgen - Long Common Name
- Coronary heart disease multigene analysis in Blood or Tissue by Molecular genetics method
- Short Name
- CHD Multigene Anl Bld/T
- Display Name
- Coronary heart disease multigene analysis Molgen Doc (Bld/Tiss)
- Consumer Name Alpha Get Info
- Coronary heart disease multigene analysis, Blood or tissue specimen
Part Model Get Info
- Component
- Coronary heart disease multigene analysis
LP410958-5
- Analyte
- Coronary heart disease multigene analysis
LP410958-5
- Component Numerator
- Coronary heart disease multigene analysis
LP410958-5
- Component Numerator Core
- Coronary heart disease multigene analysis
LP410958-5
- Component Numerator Core Suffix
- NULL
- Component Denominator
- NULL
- Component Denominator Core
- NULL
- Component Denominator Core Suffix
- NULL
- Challenge
- NULL
- Adjustment
- NULL
- Count
- NULL
- Property
- Find
LP6813-2
- Time
- Pt
LP6960-1
- Time Core
- Pt
LP6960-1
- Time Modifier
- NULL
- System
- Bld/Tiss
LP7061-7
- System Core
- Bld/Tiss
LP7061-7
- Super System
- NULL
- Scale
- Doc
LP32888-7
- Method
- Molgen
LP6404-0
Basic Attributes
- Class
- MOLPATH
- Type
- Laboratory
- First Released
- Version 2.67
- Last Updated
- Version 2.67 (ADD)
- Order vs. Observation
- Both
Language Variants Get Info
| Tag | Language | Translation |
|---|---|---|
| cs-CZ | Czech (Czechia) | Ischemická choroba srdeční multigenová analýza: |
| el-GR | Greek (Greece) | Πολυγονιδιακή ανάλυση στεφανιαίας νόσου: Synonyms: Doc MOLPATH Pt Αίμα Αίμα/Ιστός Εύρεση Ιστός Μοριακή γενετική Πολυγονιδιακή ανάλυση στεφανιαίας νόσου |
| es-ES | Spanish (Spain) | Análisis multigénico de enfermedades coronarias: |
| es-MX | Spanish (Mexico) | Análisis multigénico de enfermedades coronarias: |
| fr-FR | French (France) | Analyse multigénique d'une maladie coronarienne: |
| it-IT | Italian (Italy) | Analisi multigenica della malattia coronarica: Synonyms: Genetica molecolare Osservazione Patologia molecolare Punto nel tempo (episodio) Sangue Sangue o Tessuto Tessuto & |
| nl-NL | Dutch (Netherlands) | multigen-analyse op coronaire hartziekte: Synonyms: coronaire arteriosclerose molgen |
| pl-PL | Polish (Poland) | Analiza wielogenowa choroby niedokrwiennej serca: Synonyms: Analiza wielogenowa w kierunku choroby niedokrwiennej serca diagnostyka molekularna |
| zh-CN | Chinese (China) | 冠心病多基因分析: Synonyms: 临床文档型; |
LOINC Terminology Service (API) using HL7® FHIR® Get Info
Requests to this service require a free LOINC username and password. Below is a sample of the possible capabilities. See the LOINC Terminology Service documentation for more information.
LOINC Copyright
Copyright © Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://