AutoICD API

47997-2

Laboratory

Genetic variant clinical significance [Interpretation] in Blood or Tissue by Molecular genetics method

LOINC 6-Axis Classification

Component

Genetic variant clinical significance

Property

Imp

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Nom

Method Type

Molgen

Details

Class

MOLPATH.MISC

Order/Observation

Observation

Short Name

Genetic variant clin sig Bld/T-Imp

Display Name

Genetic variant clinical significance Molgen (Bld/Tiss) [Interp]

Related Names

BloodGenetic variant clin sigGeneticsGenomicImpressionImpression/interpretation of studyImpressionsInterpInterpretationMISCMiscellaneous molecular pathologyMolecular geneticsMolecular pathologyMOLPATHNominalPCRPoint in timeRandomTissueTissue, unspecifiedVariant InterpretationWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 47997-2?

LOINC code 47997-2 identifies "Genetic variant clinical significance [Interpretation] in Blood or Tissue by Molecular genetics method". It measures Genetic variant clinical significance in Bld/Tiss.

What does 47997-2 measure?

This code measures Genetic variant clinical significance in Bld/Tiss. It belongs to the MOLPATH.MISC 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.