HL7.GENETICS LP70593-6

LOINC Hierarchy

LOINC part code	LP70593-6
name	HL7.GENETICS
type	CLASS
status	ACTIVE
children	LOINC Home {component} LP432695-7 Laboratory LP29693-6 Molecular pathology LP7822-2 Genetics results LP70194-3 HL7 genetics LP70593-6 ▸ 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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LOINC Home

{component} LP432695-7

Laboratory LP29693-6

Molecular pathology LP7822-2

Genetics results LP70194-3

HL7.GENETICS LP70593-6

LOINC Hierarchy

▸ 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