GP1BB full mutation analysis in Blood or Tissue by Molecular genetics method   101388-7

LOINC Code


LOINC code101388-7
nameGP1BB full mutation analysis in Blood or Tissue by Molecular genetics method
statusACTIVE

Fully-Specified Name

componentGP1BB 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/Tiss
    Bld  =  Whole blood
    Tiss  =  Tissue, unspecified
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 nameGP1BB Full Mut Anl Bld/T

Basic Attributes

classMOLPATH
type1  Laboratory
order vs. observationBoth

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 updated2.75
last change typeMIN  - change to field other than name

Related Names

Bernard Soulier syndrome
beta polypeptide
Blood
CD42c
Document
Finding
Findings
full gene sequencing
Full Mut Anl
GP1BB full mutation analysis
GPIbbeta
Molecular genetics
Molecular pathology
MOLPATH
Mut
Mutations
PCR
platelet glycoprotein Ib beta chain
Point in time
Random
sequencing of entire coding region
Tissue
Tissue, unspecified
WB
Whole blood
Whole blood or Tissue

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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