AutoICD API

53045-1

Laboratory

Reference sequence alteration [Identifier]

Definition

Human Genome Variation Society (HGVS) nomenclature for conveying an alteration to the associated reference sequences used to define the genome as a basis for comparison with actual results.

LOINC 6-Axis Classification

Component

Reference sequence alteration

Property

Prid

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Nom

Method Type

Molgen

Details

Class

HL7.GENETICS

Order/Observation

Observation

Short Name

Ref sequence alteration

Display Name

Reference sequence alteration Molgen Nom (Bld/Tiss)

Related Names

BloodGeneticGeneticsGenomicHL7.GENETICSIdentity or presenceMolecular geneticsMOLPATH.GENERALNominalPCRPoint in timeRandomRef SequenceRef sequence alterationRefSeqTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 53045-1?

LOINC code 53045-1 identifies "Reference sequence alteration [Identifier]". Human Genome Variation Society (HGVS) nomenclature for conveying an alteration to the associated reference sequences used to define the genome as a basis for comparison with actual results.

What does 53045-1 measure?

This code measures Reference sequence alteration in Bld/Tiss. It belongs to the HL7.GENETICS 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.