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.
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
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.