LOINC Home

{component}   LP432695-7

Laboratory   LP29693-6

Lab terms not yet categorized   LP248770-2

Hypertrophic cardiomyopathy gene targeted mutation analysis in Blood or Tissue by Sequencing   81860-9

LOINC Code


LOINC code81860-9
nameHypertrophic cardiomyopathy gene targeted mutation analysis in Blood or Tissue by Sequencing
descriptionMulti-gene analysis by sequencing methods for variants known to be associated with hypertrophic cardiomyopathy (HCM). The genes/variants included and detection rates will vary across laboratories. To report the genes included in the test, use a "gene mutations tested for" code (e.g. [LOINC: 36908-2]).
statusACTIVE

Fully-Specified Name

componentHypertrophic cardiomyopathy gene targeted mutation analysis
propertyFind  =  Finding
timePt  =  Point in time:  To identify measures at a point in time. This is a synonym for “spot” or “random” as applied to urine measurements.
systemBld/Tiss
    Bld  =  Whole blood
    Tiss  =  Tissue, unspecified
scaleDoc  =  Document:  A document that could be in many formats (XML, narrative, etc.)
methodSequencing

Additional Names

short nameHCM Mut Anl Bld/T Seq

Basic Attributes

classMOLPATH.MUT
type1  Laboratory
order vs. observationBoth

Ask At Order Entry

Ask at Order Entry (AOE) observations for a clinical observation or laboratory test. A LOINC term may represent a single AOE observation or a panel containing several AOE observations.

81247-9Master HL7 genetic variant reporting panel

Associated Observations

LOINC codes that represent optional associated observation(s) for a clinical observation or laboratory test. A LOINC term may represent a single associated observation or panel containing several associated observations.

History/Usage

first released
last updated2.65
last change typeMIN  - change to field other than name

Related Names

Blood
Document
Finding
Findings
Genetics
HCM
HCM gene
Heredity
Heritable
high-throughput sequencing
HTS
Hypertrophic cardiomyopathy
Inherited
Molecular pathology
 MOLPATH
MOLPATH.MUTATIONS
Mut
Mut Anl
Mutations
Next generation sequencing
NGS
Point in time
Random
Tissue
Tissue, unspecified
WB
Whole blood
Whole blood or Tissue

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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