LOINCActiveBoth

LOINC Code 82532-3: SDHB and SDHC and SDHD gene del+dup and full mutation analysis Molgen Doc (Bld/Tiss)

82532-3 is a LOINC code used to identify SDHB and SDHC and SDHD 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 SDHB & SDHC & SDHD 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 SDHB & SDHC & SDHD 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

  • SDHB and SDHC and SDHD gene deletion+duplication and full mutation analysis in Blood or Tissue by Molecular genetics method
  • SDHB & SDHC & SDHD gene deletion+duplication & full mutation analysis
  • Full sequencing analysis of all coding exons and intron/exon boundaries of the SDHB, SDHC and SDHD genes is performed along with large deletion/duplication analysis by methods such as multiplex ligation-dependent probe amplification (MLPA). This test is performed to aid in the diagnosis of hereditary paraganglioma-pheochromocytoma syndrome associated with pathogenic variants in one of these genes.
  • Amplification; Blood; CBT1; CII-4; CWS3; cybS; Del; Del+Dup; Del+Dup + Full Mut Anl; Deletions; Document; Dp; Finding; Findings; full gene sequencing; Full Mut Anl; Genetics; Heredity; Heritable; Inherited; Molecular genetics; Molecular pathology; MOLPATH; Mut; Mutations; paraganglioma or familial glomus tumors 1; PCR; PGL; PGL1; Point in time; QPs3; Random; SDH4; SDHB+SDHC+SDHD; sequencing of entire coding region; succinate dehydrogenase complex, subunit D, integral membrane protein; 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

SDHB and SDHC and SDHD gene del+dup and full mutation analysis Molgen Doc (Bld/Tiss)SDHB and SDHC and SDHD gene deletion+duplication and full mutation analysis in Blood or Tissue by Molecular genetics methodSDHB+SDHC+SDHD Del+Dup + Full Mut Bld/TSDHB & SDHC & SDHD gene deletion+duplication & full mutation analysisMOLPATHSDHB and SDHC and SDHD gene variant analysis, Blood or tissue specimenFind

Frequently asked questions

Code details

Code82532-3
SystemLOINC
Display nameSDHB and SDHC and SDHD gene del+dup and full mutation analysis Molgen Doc (Bld/Tiss)
DescriptionSDHB & SDHC & SDHD gene deletion+duplication & full mutation analysis
Short nameSDHB+SDHC+SDHD Del+Dup + Full Mut Bld/T
ComponentSDHB & SDHC & SDHD 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 released2.58
Last changed2.65

Consumer names

SDHB and SDHC and SDHD gene variant analysis, Blood or tissue specimen

Part names

SDHB & SDHC & SDHD 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.