LOINC Code 89039-2: MSH2 gene deletion+duplication and full mutation analysis and EPCAM gene exons 8 and 9 del and dup mutation analysis Molgen Doc (Bld/Tiss)
89039-2 is a LOINC code used to identify MSH2 gene deletion+duplication and full mutation analysis and EPCAM gene exons 8 and 9 del and dup mutation 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 deletion+duplication & full mutation analysis & EPCAM gene exons 8 & 9 deletion+duplication. It is commonly used with the system or sample type Bld/Tiss.
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 deletion+duplication & full mutation analysis & EPCAM gene exons 8 & 9 deletion+duplication. 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 deletion+duplication and full mutation analysis and EPCAM gene exons 8 and 9 deletion and duplication mutation analysis in Blood or Tissue by Molecular genetics method
- MSH2 gene deletion+duplication & full mutation analysis & EPCAM gene exons 8 & 9 deletion+duplication
- This test includes full sequencing analysis of the MSH2 gene as well as deletions and/or duplication analysis of one or more exons in the MSH2 gene and exons 8 and 9 in the EPCAM gene. Testing is performed for the diagnosis of Lynch syndrome (also known as hereditary nonpolyposis colorectal cancer (HNPCC)) and for predictive diagnosis and potential early intervention for at risk family members.
- Amplification; BAT-26; Blood; COCA1; Colon cancer nonpolyposis type 1; Del; Del+Dup; Deletions; DIAR5; Document; Dp; EGP-2; EGP314; EGP40; EPCAM Exons 8 + 9; epithelial cell adhesion molecule; ESA; FCC1; Finding; Findings; HNPCC; HNPCC1; HNPCC8; KS1/4; KSA; LCFS2; Lynch syndrome; M4S1; MIC18; MK-1; Molecular genetics; Molecular pathology; MOLPATH; MSH2 Del+Dup+Full EPCAM 8+9; MSH2 DelDup+Full + EPCAM Ex8+9 DelDup; Mut; Mutations; mutS homolog 2; PCR; Point in time; Random; TACSTD1; Tissue; Tissue, unspecified; TROP1; 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
Frequently asked questions
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.