HL7 genetics   LP70593-6

LOINC Hierarchy


Select the title to see children of the section (▸) or the LOINC code. Select a code to view information about the section/code.

Allele name   LP62065-5

Allelic state   LP69969-1

Amino acid change   LP62062-2

Amino acid change type   LP62063-0

Amino acid marker assessed   LP71012-6

DNA change   LP62061-4

DNA change type   LP62077-0

DNA marker assessed   LP69970-9

DNA sequence variation identifier   LP66913-2

DNA sequence variation display name   LP66914-0

Drug efficacy analysis overall interpretation   LP66897-7

Drug efficacy sequence variation interpretation   LP66894-4

Drug metabolism sequence variation interpretation   LP69975-8

Filler DNA analysis test identifier   LP69971-7

Genetic disease analysis overall carrier interpretation   LP69974-1

Genetic disease analysis overall interpretation   LP66901-7

Genetic analysis narrative report   LP66902-5

Genetic disease assessed   LP66900-9

Genetic disease sequence variation interpretation   LP69972-5

Genetic knowledge reference   LP136541-2

Genetic variant assessment   LP136540-4

Genomic source class   LP66917-3

Individual allele identifier   LP66903-3

Medication assessed   LP66896-9

Pharmacogenetic analysis report   LP66898-5

Placer DNA analysis test identifier   LP66890-2

Reason for study additional note   LP70577-9

Reference nucleotide   LP136539-6

Reference sequence alteration   LP69979-0

Transcript reference sequence identifier   LP66891-0


Copyright © 2024 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2024, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://loinc.org/license for the full LOINC copyright and license.

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