MYH9 gene full mutation analysis in Blood by Molecular genetics method   105332-1

LOINC Code


LOINC code105332-1
nameMYH9 gene full mutation analysis in Blood by Molecular genetics method
statusACTIVE

Fully-Specified Name

componentMYH9 gene full 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  =  Whole blood
scaleDoc  =  Document:  A document that could be in many formats (XML, narrative, etc.)
methodMolgen  =  Molecular Genetics:  General class of methods used to detect genetic attributes on a molecular basis including RFL, PCR and other methods.

Additional Names

short nameMYH9 gene Full Mut Anl Bld

Basic Attributes

classMOLPATH
type1  Laboratory
order vs. observationOrder

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 updated2.78
last change typeADD  - added

Related Names

Blood
Document
Finding
Findings
full gene sequencing
Full Mut Anl
Molecular genetics
Molecular pathology
MOLPATH
Mut
Mutations
MYH9 gene full mut anl
Myosin heavy chain 9
PCR
Point in time
Random
sequencing of entire coding region
WB
Whole blood

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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