AutoICD API

22066-5

Laboratory

PRSS1 gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal

LOINC 6-Axis Classification

Component

PRSS1 gene mutations tested for

Property

Prid

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Nom

Method Type

Molgen

Details

Class

MOLPATH.MUT

Order/Observation

Observation

Short Name

PRSS1 gene Mut Tested Bld/T

Display Name

PRSS1 gene mutations tested for Molgen Nom (Bld/Tiss)

Related Names

BloodCationic trypsinogenGene mut testedGeneticsHereditary pancreatitisHeredityHeritableHPCIdentity or presenceInheritedMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut TestedMutationMutsNominalPCRPCTTPoint in timeprotease, serine, 1 (trypsin 1)RandomTissueTissue, unspecifiedTRP1TRY1TRY4TRYP1Trypsin 1 precursorTrypsinogen 1WBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 22066-5?

LOINC code 22066-5 identifies "PRSS1 gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal". It measures PRSS1 gene mutations tested for in Bld/Tiss.

What does 22066-5 measure?

This code measures PRSS1 gene mutations tested for 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.