LOINCActiveBoth

LOINC Code 76063-7: MSH2 gene+MLH1 gene+MSH6 gene familial mut analysis Molgen Doc (Bld/Tiss)

76063-7 is a LOINC code used to identify MSH2 gene+MLH1 gene+MSH6 gene familial mut analysis Molgen Doc (Bld/Tiss) in laboratory and clinical observation data. You may see this code in lab systems, lab reports, EHR exports, interoperability feeds, or other structured clinical data exchanges. LOINC codes identify tests, measurements, observations, survey items, and clinical questions in a standardized way. It is associated with the component MSH2 gene+MLH1 gene+MSH6 gene mutation analysis limited to known familial mutations. It is commonly used with the system or sample type Bld/Tiss.

Reviewed by HealthAssure Clinical TeamUpdated 21 May 2026

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 MSH2 gene+MLH1 gene+MSH6 gene mutation analysis limited to known familial mutations. It is commonly used with the system or sample type Bld/Tiss.

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

  • MSH2 gene+MLH1 gene+MSH6 gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method
  • MSH2 gene+MLH1 gene+MSH6 gene mutation analysis limited to known familial mutations
  • This term is used for carrier or diagnostic testing for at-risk or presymptomatic relatives of an affected individual who has a previously identified known genetic mutation within the MLH1, MSH2 or MSH6 genes. Mutations in these genes cause hereditary nonpolyposis colorectal cancer (HNPCC). Mutation analysis only includes testing for the known familial mutation.
  • BAT-26; Blood; COCA1; COCA2; Colon cancer nonpolyposis type 1; Document; Fam Mut Anl; FCC1; FCC2; Finding; Findings; G/T mismatch-binding protein gene; Genetics; GTBP; GTMBP; Hereditary Nonpolyposis Colorectal Cancer; Heredity; Heritable; hMLH1; HNPCC; HNPCC1; HNPCC2; HNPCC5; HSAP; Inherited; LCFS2; LMTED; LTD; Lynch syndrome; MGC5172; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; MSH2+MLH1 gene; MSH2+MLH1+MSH6 gene; Mut; Mutation; Mutations; mutL homolog 1; MutL homolog 1, colon cancer, nonpolyposis type 2; Muts; mutS homolog 2; mutS homolog 6; p160; PCR; Point in time; Random; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue

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

MSH2 gene+MLH1 gene+MSH6 gene familial mut analysis Molgen Doc (Bld/Tiss)MSH2 gene+MLH1 gene+MSH6 gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics methodMSH2+MLH1+MSH6 gene Fam Mut Anl Bld/TMSH2 gene+MLH1 gene+MSH6 gene mutation analysis limited to known familial mutationsMOLPATH.MUTMSH2 gene+MLH1 gene+MSH6 gene familial variant analysis, Blood or tissue specimenFind

Frequently asked questions

Code details

Code76063-7
SystemLOINC
Display nameMSH2 gene+MLH1 gene+MSH6 gene familial mut analysis Molgen Doc (Bld/Tiss)
DescriptionMSH2 gene+MLH1 gene+MSH6 gene mutation analysis limited to known familial mutations
Short nameMSH2+MLH1+MSH6 gene Fam Mut Anl Bld/T
ComponentMSH2 gene+MLH1 gene+MSH6 gene mutation analysis limited to known familial mutations
PropertyFind
TimingPt
System (specimen)Bld/Tiss
ScaleDoc
MethodMolgen
ClassMOLPATH.MUT
StatusACTIVE
Order/ObservationBoth

Flags

BillableNo
Valid clinical useNo

Source

SourceLOINC
Version2.82
Releasemain
First released2.50
Last changed2.66

Consumer names

MSH2 gene+MLH1 gene+MSH6 gene familial variant analysis, Blood or tissue specimen

Part names

MSH2 gene+MLH1 gene+MSH6 gene mutation analysis limited to known familial mutationsFindPtBld/TissDocMolgenFindingPoint in time (spot)Blood or TissueMolecular genetics

About this content

This page is prepared by HealthAssure's clinical team using official coding standards from LOINC. AI tools assist with drafting explanations, which are then reviewed and verified by healthcare professionals for accuracy. This content is for informational purposes and does not replace professional medical advice. Meet our team.