ATP5A1 gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method   77073-5

LOINC Code


LOINC code77073-5
nameATP5A1 gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method
statusACTIVE

Fully-Specified Name

componentATP5A1 gene mutation analysis limited to known familial mutations
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.)
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 nameATP5A1 Fam Mut Anl Bld/T

Basic Attributes

classMOLPATH.MUT
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

Related Names

ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1, cardiac muscle
ATP5A
ATP5AL2
ATPM
Blood
Combined oxidative phosphorylation deficiency-22
COXPD22
Document
Fam Mut Anl
Finding
Findings
Genetics
hATP1
HEL-S-123m
Heredity
Heritable
Inherited
LMTED
LTD
MC5DN4
Mitochondrial ATP synthase
Mitochondrial complex V deficiency nuclear type 4
Molecular genetics
Molecular pathology
MOLPATH
MOLPATH.MUTATIONS
MOM2
Mut
Mutation
Mutations
Muts
OMR
ORM
PCR
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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