APOA1 gene full mutation analysis:Find:Pt:Bld/Tiss:Doc:Sequencing

Preferred Label : APOA1 gene full mutation analysis:Find:Pt:Bld/Tiss:Doc:Sequencing;

LOINC status : ACTIVE;

LOINC display name : APOA1 gene full mutation analysis Sequencing Doc (Bld/Tiss);

LOINC long common name : APOA1 gene full mutation analysis in Blood or Tissue by Sequencing;

LOINC short name : APOA1 Full Mut Anl Bld/T Seq;

LOINC 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.;

Details

Origin ID

93420-8;

UMLS CUI

C5211942;

Has component
- APOA1 gene [LOINC component]
- APOA1 gene full mutation analysis [LOINC component]
- Gene [LOINC component]
Has method
- Sequencing [LOINC method]
Has property
- Finding [LOINC Property]
Has scale
- Doc [LOINC scale]
Has system
- Blood [LOINC System]
- Blood or Tissue [LOINC System]
- Tissue and Smears [LOINC System]
Has time aspect
- Point in time (spot) [LOINC time aspect]
Semantic type(s)
- Clinical Attribute [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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