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

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

LOINC status : ACTIVE;

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

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

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

LOINC description : Full gene sequence analysis, such as by next-generation sequencing and/or Sanger sequencing, are performed to detect pathogenic variants within the VWF gene for the diagnosis of von Willebrand disease (VWD).[GHR gene: VWF];

Details

Origin ID

94219-3;

UMLS CUI

C5381143;

Has component
- Gene [LOINC component]
- VWF gene [LOINC component]
- VWF gene full mutation analysis [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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