AutoICD API

21665-5

Laboratory

EGFR gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

LOINC 6-Axis Classification

Component

EGFR gene targeted mutation analysis

Property

Prid

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Nom

Method Type

Molgen

Details

Class

MOLPATH.MUT

Order/Observation

Both

Short Name

EGFR gene Mut Anl Bld/T

Display Name

EGFR gene targeted mutation analysis Molgen Nom (Bld/Tiss)

Related Names

Bloodepidermal growth factor receptorEpidermal growth factor receptor geneERBBERBB1GeneticsHER1HeredityHeritableIdentity or presenceInheritedmENAMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsNISBD2NominalOncogene ERBBOncologyPCRPIG61Point in timeRandomTissueTissue, unspecifiedUniversalLabOrdersV-ERB-B avian erythroblastic leukemia viral oncogene homologWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 21665-5?

LOINC code 21665-5 identifies "EGFR gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal". It measures EGFR gene targeted mutation analysis in Bld/Tiss.

What does 21665-5 measure?

This code measures EGFR gene targeted mutation analysis 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.