Genetic variant assessment:Find:Pt:Bld/Tiss:Nom:Molgen

Preferred Label : Genetic variant assessment:Find:Pt:Bld/Tiss:Nom:Molgen;

LOINC status : ACTIVE;

LOINC display name : Genetic variant assessment Molgen Nom (Bld/Tiss);

LOINC long common name : Genetic variant assessment;

LOINC short name : Genetic var assess;

LOINC description : Where testing scenarios are intended to assess the prescence or absence of a known set of DNA variants (e.g. tumor profiling using genotyping technology), then the Genetic Variant Assessment is used in conjunction with answer list supports structured communication of these findings. Of note, 'No Call' is different from 'Absent', because 'No Call' did not result in the determination of the marker's presents or absents. This may be due to test failure or specimen specific context which renders the test ineffective.;

Détails

Origin ID

69548-6;

UMLS CUI

C3263353;

Has component
- Assessment [LOINC component]
- Genetic variant assessment [LOINC component]
Has method
- Molecular genetics [LOINC method]
Has property
- Finding [LOINC Property]
Has scale
- Nom [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]
Part of panel
- DNA analysis discrete sequence variation panel:-:Pt:Bld/Tiss:-:Molgen [LOINC code]
- Simple variant panel:-:Pt:^Patient:-: [LOINC code]
Semantic type(s)
- Clinical Attribute [UMLS semantic type]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients