APOA1 gene full mutation analysis in Blood or Tissue by Sequencing 93420-8
LOINC Code
LOINC code | 93420-8 | ||
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name | APOA1 gene full mutation analysis in Blood or Tissue by Sequencing | ||
description | The test includes sequence analysis of variants in all coding regions and intron/exon boundaries of the Apolipoprotein A-I (APOA1) gene. Testing is performed for the diagnosis of individuals suspected of having APOA1 gene-associated familial amyloidosis. The overall result summary (positive/negative) along with information about variant(s) identified, interpretation, testing method(s) and recommendations are typically included in the report. | ||
status | ACTIVE | ||
Fully-Specified Name | |||
component | APOA1 gene full mutation analysis | ||
property | Find = Finding | ||
time | Pt = Point in time: To identify measures at a point in time. This is a synonym for “spot” or “random” as applied to urine measurements. | ||
system | Bld/Tiss Bld = Whole blood Tiss = Tissue, unspecified | ||
scale | Doc = Document: A document that could be in many formats (XML, narrative, etc.) | ||
method | Sequencing | ||
Additional Names | |||
short name | APOA1 Full Mut Anl Bld/T Seq | ||
Basic Attributes | |||
class | MOLPATH | ||
type | 1 Laboratory | ||
order vs. observation | Both | ||
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 updated | 2.67 | ||
last change type | ADD - added | ||
Related Names | |||
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