Coronary heart disease multigene analysis in Blood or Tissue by Molecular genetics method   93201-2

LOINC Code


LOINC code93201-2
nameCoronary heart disease multigene analysis in Blood or Tissue by Molecular genetics method
descriptionThis 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.
statusACTIVE

Fully-Specified Name

componentCoronary heart disease multigene analysis
propertyFind  =  Finding
timePt  =  Point in time:  To identify measures at a point in time. This is a synonym for “spot” or “random” as applied to urine measurements.
systemBld/Tiss
    Bld  =  Whole blood
    Tiss  =  Tissue, unspecified
scaleDoc  =  Document:  A document that could be in many formats (XML, narrative, etc.)
methodMolgen  =  Molecular Genetics:  General class of methods used to detect genetic attributes on a molecular basis including RFL, PCR and other methods.

Additional Names

short nameCHD Multigene Anl Bld/T

Basic Attributes

classMOLPATH
type1  Laboratory
order vs. observationBoth

Associated Observations

LOINC codes that represent optional associated observation(s) for a clinical observation or laboratory test. A LOINC term may represent a single associated observation or panel containing several associated observations.

History/Usage

first released
last updated2.67
last change typeADD  - added

Related Names

Blood
CHD Multigene Anl
Dis
Diseases
Document
Dz
Finding
Findings
Gene
Gene panel
Molecular genetics
Molecular pathology
MOLPATH
Multi-gene study
Multiple-gene panel test
PCR
Point in time
Random
Tissue
Tissue, unspecified
WB
Whole blood
Whole blood or Tissue

Copyright © 2024 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2024, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://loinc.org/license for the full LOINC copyright and license.

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