94219-3
LaboratoryVWF gene full mutation analysis in Blood or Tissue by Sequencing
Definition
Full gene sequence analysis, such as by next-generation sequencing and/or Sanger sequencing, are performed to detect pathogenic variants within the VWF gene for the diagnosis of von Willebrand disease (VWD).[GHR gene: VWF]
LOINC 6-Axis Classification
Component
VWF 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
VWF gene Full Mut Anl Bld/T Seq
Display Name
VWF gene full mutation analysis Sequencing Doc (Bld/Tiss)
Related Names
Frequently Asked Questions
What is LOINC code 94219-3?
LOINC code 94219-3 identifies "VWF gene full mutation analysis in Blood or Tissue by Sequencing". Full gene sequence analysis, such as by next-generation sequencing and/or Sanger sequencing, are performed to detect pathogenic variants within the VWF gene for the diagnosis of von Willebrand disease (VWD).[GHR gene: VWF]
What does 94219-3 measure?
This code measures VWF 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.