AutoICD API

93306-9

Clinical

Genetic risk score for coronary heart disease

Definition

An overall genetic risk score (GRS) for developing coronary heart disease (CHD) that may be based on a number of factors, including family history (pedigree) and genetic testing. The GRS-based risk classification (high risk/low risk) [LOINC: 93307-7] for developing CHD may also be reported.

LOINC 6-Axis Classification

Component

Genetic risk score for coronary heart disease

Property

Score

Time Aspect

Lifetime

System

^Patient

Scale Type

Qn

Method Type

N/A

Details

Class

CLIN.RISK

Order/Observation

Observation

Short Name

GRS for CHD

Related Names

CLINCLIN.RISKCoronary Artery DiseasesDisDisease, Coronary ArteryDiseasesDzGeneticsGenomicGenomic risk scoreGRS for CHDPolygenic risk scoreQNTQuanQuantQuantitativeScaleScre

Frequently Asked Questions

What is LOINC code 93306-9?

LOINC code 93306-9 identifies "Genetic risk score for coronary heart disease". An overall genetic risk score (GRS) for developing coronary heart disease (CHD) that may be based on a number of factors, including family history (pedigree) and genetic testing. The GRS-based risk classification (high risk/low risk) [LOINC: 93307-7] for developing CHD may also be reported.

What does 93306-9 measure?

This code measures Genetic risk score for coronary heart disease in ^Patient. It belongs to the CLIN.RISK class in the LOINC classification.

What is LOINC?

LOINC (Logical Observation Identifiers Names and Codes) is a universal standard for identifying laboratory and clinical observations. It is maintained by the Regenstrief Institute and used worldwide for health data exchange.