AutoICD API

21660-6

Laboratory

CTNNB1 gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal

LOINC 6-Axis Classification

Component

CTNNB1 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

CTNNB1 gene Mut Tested Bld/T

Display Name

CTNNB1 gene mutations tested for Molgen Nom (Bld/Tiss)

Related Names

armadilloBeta-catenin geneBloodCadherin associated protein beta genecatenin (cadherin-associated protein), beta 1, 88kDaColorectal cancerCTNNBGene mut testedGeneticsHepatoblastomaHeredityHeritableIdentity or presenceInheritedMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMRD19MutMut TestedMutationMutsNominalPCRPilomatricomaPoint in timeRandomTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 21660-6?

LOINC code 21660-6 identifies "CTNNB1 gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal". It measures CTNNB1 gene mutations tested for in Bld/Tiss.

What does 21660-6 measure?

This code measures CTNNB1 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.