Chromosome 12 trisomy and chromosome region 11q22.3 and 13q14 and 17p13.1 deletion in Blood or Tissue by FISH   82256-9

LOINC Code


LOINC code82256-9
nameChromosome 12 trisomy and chromosome region 11q22.3 and 13q14 and 17p13.1 deletion in Blood or Tissue by FISH
descriptionMulti-chromosome analysis by FISH for variants known to be associated with chronic lymphocytic leukemia (CLL). This term was created for, but is not limited in use to, the submitter's Vysis CLL FISH probe kit.
statusACTIVE

Fully-Specified Name

componentChromosome 12 trisomy & chromosome region 11q22.3 & 13q14 & 17p13.1 deletion
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.)
methodFISH

Additional Names

short name12Ts+11p22.3+13q14+17p13.1 Del Bl/T FISH

Basic Attributes

classMOLPATH.MISC
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
change reasonChanged "11p22.3" in Component to "11q22.3", the correct location (long arm of the chromosome).

Related Names

Blood
Chr 12 Ts
Chr 12 Ts + Chr 11q22.3 + 13q14 + 17p13.1 del
Chr 12Ts + 11q22.3+13q14+17p13.1
Chromosom
Chromosomes
Chronic lymphocytic leukemia
Cyto loc
Del
Deletions
Document
Finding
Findings
Fluorescent in situ hybridization
Genetics
Heredity
Heritable
Inherited
MISC
Miscellaneous molecular pathology
Molecular pathology
MOLPATH
Point in time
Random
Tissue
Tissue, unspecified
Ts
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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