92991-9
LaboratoryF13A1 and F13B gene full mutation analysis in Blood or Tissue by Sequencing
Definition
This test detects pathogenic alterations within the F13A1 and F13B genes to delineate the underlying molecular defect in a patient with a laboratory diagnosis of factor XIII deficiency.
LOINC 6-Axis Classification
Component
F13A1 gene & F13B 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
F13A1 + F13B Full Mut Anl Bld/T Seq
Display Name
F13A1 and F13B gene full mutation analysis Sequencing Doc (Bld/Tiss)
Related Names
Frequently Asked Questions
What is LOINC code 92991-9?
LOINC code 92991-9 identifies "F13A1 and F13B gene full mutation analysis in Blood or Tissue by Sequencing". This test detects pathogenic alterations within the F13A1 and F13B genes to delineate the underlying molecular defect in a patient with a laboratory diagnosis of factor XIII deficiency.
What does 92991-9 measure?
This code measures F13A1 gene & F13B 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.