69488-5
LaboratoryTNFRSF13B gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method
Definition
This term is used for diagnostic testing for symptomatic relatives of an affected individual who has a previously identified known genetic mutation within the TNFRSF13B gene (also known as TACI gene). Mutation analysis only includes testing for the known familial mutation(s).
LOINC 6-Axis Classification
Component
TNFRSF13B gene mutation analysis limited to known familial mutations
Property
Find
Time Aspect
Pt
System
Bld/Tiss
Scale Type
Doc
Method Type
Molgen
Details
Class
MOLPATH.MUT
Order/Observation
Both
Short Name
TNFRSF13B gene Fam Mut Anl Bld/T
Display Name
TNFRSF13B gene familial mut analysis Molgen Doc (Bld/Tiss)
Related Names
Frequently Asked Questions
What is LOINC code 69488-5?
LOINC code 69488-5 identifies "TNFRSF13B gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method". This term is used for diagnostic testing for symptomatic relatives of an affected individual who has a previously identified known genetic mutation within the TNFRSF13B gene (also known as TACI gene). Mutation analysis only includes testing for the known familial mutation(s).
What does 69488-5 measure?
This code measures TNFRSF13B gene mutation analysis limited to known familial mutations 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.