6p25 and 6q23 and 11q and 8q24 and 9p21 chromosome partial aneuploidy in Blood or Tissue by FISH   76065-2

LOINC Code


LOINC code76065-2
name6p25 and 6q23 and 11q and 8q24 and 9p21 chromosome partial aneuploidy in Blood or Tissue by FISH
descriptionMalignant melanoma often exhibits abnormal copy number of certain chromosomal regions. The assessment of gains and losses in 6p25, 6q23 11q, 8q24 and 9p21 by fluorescent in situ hybridization (FISH) has been found to be helpful in distinguishing benign from malignant melanocytic lesions. This term was created for the submitter's assay which uses three commercially available probes sets: RREB1/D6Z1/MYB/CCND1 (assessing chromosomes 6 and 11), CDKN2A/D9Z1 (assessing chromosome 9p), and D8Z2/MYC (assessing chromosome 8q). The chromosomal abnormalities in melanoma can be varied, so the combined assay has been found to have a better chance to aid in diagnosis. The findings have some mechanistic implications, with tumor suppressor genes on 9p and oncogene (MYC) on 8q.
statusACTIVE

Fully-Specified Name

component6p25 & 6q23 & 11q & 8q24 & 9p21 chromosome partial aneuploidy
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 name6p25+6q23+11q+8q24+9p21 aneup Bld/T FISH

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 updated2.66
last change typeMAJ  - change to name field other than Component;
change reasonBased on LOINC Committee review (June 2019), updated the Property from "Prid" to "Find" and Scale from "Nar" to "Doc" to align with the current LOINC model for naming collections of information reported in narrative and/or structured formats.

Related Names

6p25+6q23+11q+8q24+9p21 aneup
Blood
Chromosom
Chromosomes
Document
Finding
Findings
Fluorescent in situ hybridization
Genetics
Heredity
Heritable
Inherited
Melanoma
Molecular pathology
MOLPATH
MOLPATH.MUTATIONS
Point in time
Random
Tissue
Tissue, unspecified
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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