BRCA2 gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method   79208-5

LOINC Code


LOINC code79208-5
nameBRCA2 gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method
descriptionThis test is for detection of known familial mutations of the BCRA2 gene. Known family mutations are variants that have been previously identified in other members of the patient's biological family.
statusACTIVE

Fully-Specified Name

componentBRCA2 gene mutation analysis limited to known familial mutations
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 nameBRCA2 gene Fam Mut Anl Bld/T

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

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BRCA
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BROVCA2
Document
FACD
FAD
FAD1
Fam Mut Anl
FANCB
FANCD
FANCD1
Finding
Findings
Genetics
GLM3
Heredity
Heritable
Inherited
LMTED
LTD
Molecular genetics
Molecular pathology
MOLPATH
MOLPATH.MUTATIONS
Mut
Mutation
Mutations
Muts
Oncology
PCR
PNCA2
Point in time
Random
Tissue
Tissue, unspecified
WB
Whole blood
Whole blood or Tissue
XRCC11

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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