82529-9
LaboratorySDHD gene deletion+duplication and full mutation analysis in Blood or Tissue by Molecular genetics method
Definition
Full sequencing analysis of all 4 coding exons and intron/exon boundaries of the SDHD gene is performed along with large deletion/duplication analysis.[OMIM: 602690][NCBI Gene ID: 6392] This test is performed to aid in the diagnosis of hereditary paraganglioma-pheochromocytoma syndrome associated with pathogenic SDHD gene variants.
LOINC 6-Axis Classification
Component
SDHD gene deletion+duplication & full mutation analysis
Property
Find
Time Aspect
Pt
System
Bld/Tiss
Scale Type
Doc
Method Type
Molgen
Details
Class
MOLPATH.MUT
Order/Observation
Both
Short Name
SDHD gene Del+Dup + Full Mut Anl Bld/T
Display Name
SDHD gene del+dup and full mutation analysis Molgen Doc (Bld/Tiss)
Related Names
Frequently Asked Questions
What is LOINC code 82529-9?
LOINC code 82529-9 identifies "SDHD gene deletion+duplication and full mutation analysis in Blood or Tissue by Molecular genetics method". Full sequencing analysis of all 4 coding exons and intron/exon boundaries of the SDHD gene is performed along with large deletion/duplication analysis.[OMIM: 602690][NCBI Gene ID: 6392] This test is performed to aid in the diagnosis of hereditary paraganglioma-pheochromocytoma syndrome associated with pathogenic SDHD gene variants.
What does 82529-9 measure?
This code measures SDHD gene deletion+duplication & full mutation analysis in Bld/Tiss. It belongs to the MOLPATH.MUT class in the LOINC classification.
What is LOINC?
LOINC (Logical Observation Identifiers Names and Codes) is a universal standard for identifying laboratory and clinical observations. It is maintained by the Regenstrief Institute and used worldwide for health data exchange.