FGA gene & FGB gene & FGG gene full mutation analysis:Find:Pt:Bld/Tiss:Doc:Sequencing

Preferred Label : FGA gene & FGB gene & FGG gene full mutation analysis:Find:Pt:Bld/Tiss:Doc:Sequencing;

LOINC status : ACTIVE;

LOINC display name : FGA, FGB, and FGG gene full mutation analysis Sequencing Doc (Bld/Tiss);

LOINC long common name : FGA, FGB, and FGG gene full mutation analysis in Blood or Tissue by Sequencing;

LOINC short name : FGA FGB FGG Full Mut Anl Bld/T Seq;

LOINC description : This test detects pathogenic alterations within the FGA, FGB, and FGG genes to delineate the underlying molecular defect in a patient with a laboratory diagnosis of congenital afibrinogenemia/hypofibrinogenemia or dysfibrinogenemia/hypodysfibrinogenemia.;

Details

Origin ID

92992-7;

UMLS CUI

C5144867;

Has component
- FGA gene [LOINC component]
- FGA gene & FGB gene & FGG gene full mutation analysis [LOINC component]
- FGA, FGB, and FGG gene [LOINC component]
- FGB gene [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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