92992-7
LaboratoryFGA, FGB, and FGG gene full mutation analysis in Blood or Tissue by Sequencing
Definition
This test detects pathogenic alterations within the FGA, FGB, and FGG genes to delineate the underlying molecular defect in a patient with a laboratory diagnosis of congenital afibrinogenemia/hypofibrinogenemia or dysfibrinogenemia/hypodysfibrinogenemia.
LOINC 6-Axis Classification
Component
FGA gene & FGB gene & FGG gene full mutation analysis
Property
Find
Time Aspect
Pt
System
Bld/Tiss
Scale Type
Doc
Method Type
Sequencing
Details
Class
MOLPATH
Order/Observation
Both
Short Name
FGA + FGB + FGG Full Mut Anl Bld/T Seq
Display Name
FGA, FGB, and FGG gene full mutation analysis Sequencing Doc (Bld/Tiss)
Related Names
Frequently Asked Questions
What is LOINC code 92992-7?
LOINC code 92992-7 identifies "FGA, FGB, and FGG gene full mutation analysis in Blood or Tissue by Sequencing". This test detects pathogenic alterations within the FGA, FGB, and FGG genes to delineate the underlying molecular defect in a patient with a laboratory diagnosis of congenital afibrinogenemia/hypofibrinogenemia or dysfibrinogenemia/hypodysfibrinogenemia.
What does 92992-7 measure?
This code measures FGA gene & FGB gene & FGG gene full mutation analysis in Bld/Tiss. It belongs to the MOLPATH 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.