HL7 genetics LP70593-6
LOINC Hierarchy
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▸ 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 © 2023 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2023, 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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