LOINCActiveBoth

LOINC Code 89037-6: CDKN2A gene del+dup and full mutation analysis Molgen Doc (Bld/Tiss)

89037-6 is a LOINC code used to identify CDKN2A gene del+dup and full 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 CDKN2A gene deletion+duplication & full mutation analysis. 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 CDKN2A gene deletion+duplication & full mutation analysis. 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

  • CDKN2A gene deletion+duplication and full mutation analysis in Blood or Tissue by Molecular genetics method
  • CDKN2A gene deletion+duplication & full mutation analysis
  • Amplification; ARF; Blood; CDK4 inhibitor; CDK4I; CDKN2; CMM2; Cyclin-dependent kinase 4 inhibitor A gene; cyclin-dependent kinase inhibitor 2A; Cyclin-dependent kinase inhibitor 2A gene; Del; Del+Dup; Del+Dup + Full Mut Anl; Deletions; Document; Dp; Finding; Findings; full gene sequencing; Full Mut Anl; Genetics; Heredity; Heritable; Inherited; INK4; INK4a; Melanoma; MLM; Molecular genetics; Molecular pathology; MOLPATH; MTS1; MTS-1; Multiple tumor suppressor 1; Mut; Mutations; P14; P14ARF; p16; P16INK4; P16INK4A; P16-INK4A; P19; P19ARF; PCR; Point in time; Random; sequencing of entire coding region; Tissue; Tissue, unspecified; TP16; 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

CDKN2A gene del+dup and full mutation analysis Molgen Doc (Bld/Tiss)CDKN2A gene deletion+duplication and full mutation analysis in Blood or Tissue by Molecular genetics methodCDKN2A Del+Dup + Full Mut Anl Bld/TCDKN2A gene deletion+duplication & full mutation analysisMOLPATHCDKN2A gene variant analysis, Blood or tissue specimenFind

Frequently asked questions

Code details

Code89037-6
SystemLOINC
Display nameCDKN2A gene del+dup and full mutation analysis Molgen Doc (Bld/Tiss)
DescriptionCDKN2A gene deletion+duplication & full mutation analysis
Short nameCDKN2A Del+Dup + Full Mut Anl Bld/T
ComponentCDKN2A gene deletion+duplication & full mutation analysis
PropertyFind
TimingPt
System (specimen)Bld/Tiss
ScaleDoc
MethodMolgen
ClassMOLPATH
StatusACTIVE
Order/ObservationBoth

Flags

BillableNo
Valid clinical useNo

Source

SourceLOINC
Version2.82
Releasemain
First released2.64
Last changed2.65

Consumer names

CDKN2A gene variant analysis, Blood or tissue specimen

Part names

CDKN2A gene deletion+duplication & full mutation analysisFindPtBld/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.