LOINC Home

{component}   LP432695-7

Laboratory   LP29693-6

Molecular pathology   LP7822-2

Genetics results   LP70194-3

HL7 genetics   LP70593-6

Genomic source class   LP66917-3

Genomic source class | Blood or Tissue | HL7 genetics   LP410560-9

Genomic source class [Type]   48002-0

LOINC Code


LOINC code48002-0
nameGenomic source class [Type]
descriptionThe genomic class of the specimen being analyzed: Germline for inherited genome, somatic for cancer genome, and prenatal for fetal genome.
statusACTIVE

Fully-Specified Name

componentGenomic source class
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 nameGenomic source class

Basic Attributes

classHL7.GENETICS
type1  Laboratory
order vs. observationObservation

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.

Member of these Panels

62386-8Chromosome analysis summary panel
62386-8Chromosome analysis summary panel
62386-8Chromosome analysis summary panel
62386-8Chromosome analysis summary panel
81250-3Discrete genetic variant panel
81250-3Discrete genetic variant panel
81250-3Discrete genetic variant panel
55208-3DNA analysis discrete sequence variation panel
51960-3DNA marker results panel
55232-3Genetic analysis summary panel
51966-0Genetic disease DNA analysis panel
51975-1Individual allele results panel
51962-9Pharmacogenetic DNA analysis panel
48014-5Sequence variation panel - Blood or Tissue by Molecular genetics method

History/Usage

test rank14631 of 2000 most commonly performed tests by labs in USA
first released
last updated2.73
last change typeMIN  - change to field other than name

Related Names

Blood
Genetic
Genetic variant source
Genetics
Genomic
Heredity
Heritable
HL7.GENETICS
Inherited
Molecular genetics
MOLPATH.GENERAL
 Nominal
PCR
Point in time
Random
Srce
Tissue
Tissue, unspecified
Typ
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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