F12 gene mutations found [Type] in Blood or Tissue by Molecular genetics method   58937-4

LOINC Code


LOINC code58937-4
nameF12 gene mutations found [Type] in Blood or Tissue by Molecular genetics method
statusACTIVE

Fully-Specified Name

componentF12 gene targeted mutation analysis
propertyType  =  Type:  The Property Type is used for assays that identify the specific analyte in cases when the baseline presence of the analyte is known.
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
scaleNom  =  Nominal:  Nominal or categorical responses that do not have a natural ordering. (e.g., names of bacteria, reported as answers, categories of appearance that do not have a natural ordering, such as, yellow, clear, bloody.
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 nameF12 gene Mut Anl Bld/T

Basic Attributes

classMOLPATH.MUT
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 updated2.63
last change typeMIN  - change to field other than name
change reasonBased on LOINC Committee review (June 2016), "targeted" was added to the Component to clarify that this test is looking for a specific set of mutations as described in the LOINC User Guide under the Molecular Genetics section.

Related Names

beta-factor XIIa part 1
Blood
coagulation factor XII
coagulation factor XII (Hageman factor)
coagulation factor XIIa heavy chain
coagulation factor XIIa light chain
EC 3.4.21.38
Genetics
HAE3
HAEX
HAF
Hageman factor
Heredity
Heritable
Inherited
Molecular genetics
Molecular pathology
MOLPATH
MOLPATH.MUTATIONS
Mut
Mut Anl
Mutations
Nominal
PCR
Point in time
Random
Tissue
Tissue, unspecified
Typ
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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