What does this LOINC code represent?

This LOINC code identifies a lab observation, measurement, question, or clinical concept in a standardized format.

Is this enough to understand my test result?

No. The code identifies the test or observation, but the interpretation depends on the actual result, reference range, and clinical context.

LOINCActiveBoth

LOINC Code 82528-1: VHL gene full mutation analysis Sequencing Doc (Bld/Tiss)

Name: LOINC Code 82528-1: VHL gene full mutation analysis Sequencing Doc (Bld/Tiss)
Creator: HealthAssure Clinical Team
Published: 2026-05-21T09:00:08.165Z

82528-1 is a LOINC code used to identify VHL gene full mutation analysis Sequencing 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 VHL gene 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 VHL gene 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: Sequencing

What it does not mean

The code identifies the observation or test, not the actual result.

Key facts

VHL gene full mutation analysis in Blood or Tissue by Sequencing

VHL gene full mutation analysis

Full sequencing analysis of the three coding exons and intron/exon boundaries of the VHL gene.[OMIM608537][NCBI Gene ID: 7428] This test is performed for patients with suspected hereditary erythrocytosis, or familial erythrocytosis, type 2 (ECYT2)[OMIM: 263400], associated with lifelong increased RBC mass, elevated RBC count, hemoglobin, and hematocrit. Mutations in the VHL gene that cause ECYT2 are inherited in an autosomal recessive fashion and associated with normal to increased serum erythropoietin (EPO) levels. For genetic testing for von Hippel-Lindau (VHL) disease, see VHL gene deletion+duplication & full mutation analysis [LOINC: 82533-1].

Blood; Document; Finding; Findings; full gene sequencing; Full Mut Anl; Genetics; Heredity; Heritable; high-throughput sequencing; HRCA1; HTS; Inherited; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mutations; Next generation sequencing; NGS; Point in time; pVHL; Random; RCA1; sequencing of entire coding region; Tissue; Tissue, unspecified; VHL1; von Hippel-Lindau syndrome; von Hippel-Lindau tumor suppressor, E3 ubiquitin protein ligase; 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

VHL gene full mutation analysis Sequencing Doc (Bld/Tiss)VHL gene full mutation analysis in Blood or Tissue by SequencingVHL gene Full Mut Anl Bld/T SeqVHL gene full mutation analysisMOLPATH.MUTVHL gene variant analysis, Blood or tissue specimenFind

Frequently asked questions

Code details

Code82528-1

SystemLOINC

Display nameVHL gene full mutation analysis Sequencing Doc (Bld/Tiss)

DescriptionVHL gene full mutation analysis

Short nameVHL gene Full Mut Anl Bld/T Seq

ComponentVHL gene full mutation analysis

PropertyFind

TimingPt

System (specimen)Bld/Tiss

ScaleDoc

MethodSequencing

ClassMOLPATH.MUT

StatusACTIVE

Order/ObservationBoth

Flags

BillableNo

Valid clinical useNo

Source

SourceLOINC

Version2.82

Releasemain

First released2.58

Last changed2.65

Consumer names

VHL gene variant analysis, Blood or tissue specimen

Part names

VHL gene full mutation analysisFindPtBld/TissDocSequencingFindingPoint in time (spot)Blood or Tissue

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.