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LOINC Code 69384-6: AGXT gene familial mut analysis Molgen Doc (Bld/Tiss)

69384-6 is a LOINC code used to identify AGXT 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 AGXT 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 AGXT 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

AGXT gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method
AGXT gene mutation analysis limited to known familial mutations
This term is used for carrier, diagnostic, or prenatal testing for at-risk relatives of an affected individual who has a previously identified known genetic mutation within the AGXT gene. Mutation analysis only includes testing for the known familial mutation(s).
2q37.3; AGT; AGT1; AGXT1; alanine-glyoxylate aminotransferase; Blood; Document; Fam Mut Anl; Finding; Findings; Genetics; Heredity; Heritable; Inherited; L-alanineglyoxylate aminotransferase 1; LMTED; LTD; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mutation; Mutations; Muts; oxalosis I; PCR; PH1; Point in time; primary hyperoxaluria type 1; Random; serine:pyruvate aminotransferase; SPAT; SPT; Tissue; Tissue, unspecified; TLH6; 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

AGXT gene familial mut analysis Molgen Doc (Bld/Tiss)AGXT gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics methodAGXT gene Fam Mut Anl Bld/TAGXT gene mutation analysis limited to known familial mutationsMOLPATH.MUTAGXT gene familial variant analysis, Blood or tissue specimenFind

Frequently asked questions

Code details

Code69384-6
SystemLOINC
Display nameAGXT gene familial mut analysis Molgen Doc (Bld/Tiss)
DescriptionAGXT gene mutation analysis limited to known familial mutations
Short nameAGXT gene Fam Mut Anl Bld/T
ComponentAGXT 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 released2.40
Last changed2.66

Consumer names

AGXT gene familial variant analysis, Blood or tissue specimen

Part names

AGXT 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.

LOINC Code 69384-6 | HealthAssure