AutoICD API

21693-7

Laboratory

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

LOINC 6-Axis Classification

Component

Hereditary pancreatitis 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

HP gene Mut Tested Bld/T

Display Name

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

Related Names

BloodGene mut testedGeneticsHeredityHeritableHP geneIdentity or presenceInheritedMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut TestedMutationMutsNominalPCRPoint in timeRandomTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 21693-7?

LOINC code 21693-7 identifies "HP gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal". It measures Hereditary pancreatitis gene mutations tested for in Bld/Tiss.

What does 21693-7 measure?

This code measures Hereditary pancreatitis 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.