94189-8

LOINC Code


LOINC code94189-8
name
descriptionFull gene sequence analysis of the APOA2 gene to detect mutations associated with apolipoprotein A-II-associated familial amyloidosis or familial hypercholesterolemia.[OMIM: 107670]
statusACTIVE

Fully-Specified Name

componentAPOA2 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 nameapoAII; Apo-AII; apolipoprotein A2; Blood; Document; Finding; Findings; full gene sequencing; Full Mut Anl; Genetics; Heredity; Heritable; high-throughput sequencing; HTS; Inherited; Molecular pathology; MOLPATH; Mut; Mutations; Next generation sequencing

Basic Attributes

classMOLPATH
type1  Laboratory
order vs. observationAPOA2 Full Mut

History/Usage

first released
last updated2.72
last change typeMIN  - change to field other than name

Related Names



Copyright © 2026 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2026, 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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