AutoICD API

21669-7

Laboratory

F5 gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal

LOINC 6-Axis Classification

Component

F5 gene mutations tested for

Property

Prid

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Nom

Method Type

Molgen

Details

Class

MOLPATH.MUT

Order/Observation

Observation

Short Name

F5 gene Mut Tested Bld/T

Display Name

F5 gene mutations tested for Molgen Nom (Bld/Tiss)

Related Names

Activated protein C cofactorAPCBloodCoagulation Factor V - Leiden genecoagulation factor V (proaccelerin, labile factor)FVLGene mut testedGeneticsHeredityHeritableIdentity or presenceInheritedLabile factorMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut TestedMutationMutsNominalPCCFPCRPoint in timeProaccelerin geneRandomRPRGL1THPH2ThrombophiliaTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 21669-7?

LOINC code 21669-7 identifies "F5 gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal". It measures F5 gene mutations tested for in Bld/Tiss.

What does 21669-7 measure?

This code measures F5 gene mutations tested for in Bld/Tiss. It belongs to the MOLPATH.MUT 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.