LOINC Code 93788-8: F5 gene HR2 haplotype genotype Molgen (Bld)

What is this code?

LOINC codes identify tests, measurements, observations, survey items, and clinical questions in a standardized way. It is associated with the component F5 gene HR2 haplotype. It is commonly used with the system or sample type Bld.

When is it used?

• Used in lab systems, EHRs, and clinical data exchange.
• May identify a test, observation, survey item, or clinical document request rather than a diagnosis.
• Status: ACTIVE
• Order vs observation: Both
• Method: Molgen

What it does not mean

• The code identifies the observation or test, not the actual result.

Key facts

• F5 gene HR2 haplotype [Genotype] in Blood by Molecular genetics method Nominal
• F5 gene HR2 haplotype
• Factor V HR2 Allele, DNA Mutation Analysis is useful in patients who are carriers of Factor V Mutation (Leiden)as coinheritance of Factor V Mutation (Leiden) is associated with a 3-4-fold increased risk of venous thrombosis compared to inheritance of Factor V Mutation (Leiden) alone. As a result the result of the HR2 haplotype analysis is interpreted in the context of knowledge of the Leiden mutation.
• Activated protein C cofactor; APC; Blood; Coagulation Factor V - Leiden gene; coagulation factor V (proaccelerin, labile factor); F5 HR2; Factor V gene HR2 allele; FVL; Labile factor; Molecular genetics; Molecular pathology; MOLPATH; Nominal; PCCF; PCR; Point in time; Proaccelerin gene; Random; RPRGL1; THPH2; Thrombophilia; WB; Whole blood

Where you may see this code

You may see this code in lab systems, lab reports, EHR exports, interoperability feeds, or other structured clinical data exchanges.

Common synonyms

Frequently asked questions