AutoICD API

32630-6

Laboratory

MSH2 gene+MLH1 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

LOINC 6-Axis Classification

Component

MSH2 gene+MLH1 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

MSH2+MLH1 gene Mut Anl Bld/T

Display Name

MSH2 gene+MLH1 gene targeted mutation analysis Molgen Nom (Bld/Tiss)

Related Names

BAT-26BloodCOCA1COCA2Colon cancer nonpolyposis type 1FCC1FCC2GeneticsHeredityHeritablehMLH1HNPCCHNPCC1HNPCC2Identity or presenceInheritedLCFS2Lynch syndromeMGC5172Molecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMSH2+MLH1 geneMutMut AnlMutationsmutL homolog 1MutL homolog 1, colon cancer, nonpolyposis type 2mutS homolog 2NominalPCRPoint in timeRandomTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 32630-6?

LOINC code 32630-6 identifies "MSH2 gene+MLH1 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal". It measures MSH2 gene+MLH1 gene targeted mutation analysis in Bld/Tiss.

What does 32630-6 measure?

This code measures MSH2 gene+MLH1 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.