FGFR1 gene rearrangements [Presence] in Blood or Tissue by FISH   78915-6

LOINC Code


LOINC code78915-6
nameFGFR1 gene rearrangements [Presence] in Blood or Tissue by FISH
descriptionThis term was created for, but is not limited in use to, the MetaSystems XL FGFR1 break apart FISH probe, which is intended to detect chromosomal rearrangements at the FGFR1 locus on chromosome region 8p11.
statusACTIVE

Fully-Specified Name

componentFGFR1 gene rearrangements
propertyPrThr  =  Present or threshold:  The Property PrThr stands for “Presence or Threshold”, meaning either a) the actual presence or absence of an analyte, or b) that the amount of analyte detected is over some predetermined threshold.
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
scaleOrd  =  Ordinal:  Ordered categorical responses, e.g., 1+, 2+, 3+; positive, negative; reactive, indeterminate, nonreactive.
methodFISH

Additional Names

short nameFGFR1 gene rearr Bld/T Ql FISH

Basic Attributes

classMOLPATH.REARRANGE
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 updated2.61
last change typeMIN  - change to field other than name
change reasonThe PrThr property is used for LOINC terms whose results are reported using an ordered categorical scale, regardless of whether or not an internal threshold was used to make that determination. This change was approved by the Laboratory LOINC Committee in June 2016.

Related Names

Basic fibroblast growth factor receptor 1 precursor
BFGFR
bFGF-R-1
Blood
CD331
CEK
C-FGR
FGFBR
FGFR-1
fibroblast growth factor receptor 1
fibroblast growth factor receptor 1 (fms-related tyrosine kinase 2, Pfeiffer syndrome)
FLG
FLT2
FLT-2
Fluorescent in situ hybridization
Genetics
H2
H3
H4
H5
HBGFR
Heredity
Heritable
HH2
HRTFDS
Inherited
KAL2
Molecular pathology
MOLPATH
MOLPATH.REARRANGEMENTS
N-SAM
OGD
Ordinal
Point in time
PR
QL
Qual
Qualitative
Random
Rearr
Rearrangement
Screen
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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