94215-1
LaboratoryPRSS1 gene full mutation analysis in Blood or Tissue by Sequencing
Definition
Full sequence analysis to test for the presence of a mutation in all coding regions and intron/exon boundaries of the PRSS1 gene. Testing is used to confirm the diagnosis of hereditary pancreatitis (HP) in patients with chronic pancreatitis and allow for predictive and diagnostic testing in affected family members.
LOINC 6-Axis Classification
Component
PRSS1 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
PRSS1 gene Full Mut Anl Bld/T Seq
Display Name
PRSS1 gene full mutation analysis Sequencing Doc (Bld/Tiss)
Related Names
Frequently Asked Questions
What is LOINC code 94215-1?
LOINC code 94215-1 identifies "PRSS1 gene full mutation analysis in Blood or Tissue by Sequencing". Full sequence analysis to test for the presence of a mutation in all coding regions and intron/exon boundaries of the PRSS1 gene. Testing is used to confirm the diagnosis of hereditary pancreatitis (HP) in patients with chronic pancreatitis and allow for predictive and diagnostic testing in affected family members.
What does 94215-1 measure?
This code measures PRSS1 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.