PPOX gene full mutation analysis in Blood or Tissue by Sequencing   94213-6

LOINC Code


LOINC code94213-6
namePPOX gene full mutation analysis in Blood or Tissue by Sequencing
descriptionFull sequence analysis of all coding regions and intron/exon boundaries of the PPOX gene is performed as part of a clinical work-up for individuals with variegate porphyria.
statusACTIVE

Fully-Specified Name

componentPPOX gene full mutation analysis
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.)
methodSequencing

Additional Names

short namePPOX Full Mut Anl Bld/T Seq

Basic Attributes

classMOLPATH
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 updated2.68
last change typeADD  - added

Related Names

Blood
Document
Finding
Findings
full gene sequencing
Full Mut Anl
Genetics
Heredity
Heritable
high-throughput sequencing
HTS
hypocretin neuropeptide precursor
Inherited
Molecular pathology
MOLPATH
Mut
Mutations
Next generation sequencing
NGS
NRCLP1
OX
Point in time
PPOX
Random
sequencing of entire coding region
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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