AutoICD API

21692-9

Laboratory

PRSS1 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

LOINC 6-Axis Classification

Component

PRSS1 gene targeted mutation analysis

Property

Prid

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Nom

Method Type

Molgen

Details

Class

MOLPATH.MUT

Order/Observation

Both

Short Name

PRSS1 gene Mut Anl Bld/T

Display Name

PRSS1 gene targeted mutation analysis Molgen Nom (Bld/Tiss)

Related Names

BloodCationic trypsinogenGeneticsHereditary pancreatitisHeredityHeritableHPCIdentity or presenceInheritedMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsNominalPCRPCTTPoint in timeprotease, serine, 1 (trypsin 1)RandomTissueTissue, unspecifiedTRP1TRY1TRY4TRYP1Trypsin 1 precursorTrypsinogen 1WBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 21692-9?

LOINC code 21692-9 identifies "PRSS1 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal". It measures PRSS1 gene targeted mutation analysis in Bld/Tiss.

What does 21692-9 measure?

This code measures PRSS1 gene targeted mutation analysis 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.