Genetic variant clinical significance:Imp:Pt:Bld/Tiss:Nom:Molgen

Preferred Label : Genetic variant clinical significance:Imp:Pt:Bld/Tiss:Nom:Molgen;

LOINC status : ACTIVE;

LOINC display name : Genetic variant clinical significance Molgen (Bld/Tiss) [Interp];

LOINC long common name : Genetic variant clinical significance [Interpretation] in Blood or Tissue by Molecular genetics method;

LOINC short name : Genetic variant clin sig Bld/T-Imp;

Details

Origin ID

47997-2;

UMLS CUI

C1953336;

Has component
- Genetic variant clinical significance [LOINC component]
Has method
- Molecular genetics [LOINC method]
Has property
- Impression/interpretation of study [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
- Sequence variation panel:-:Pt:Bld/Tiss:-:Molgen [LOINC code]
Semantic type(s)
- Clinical Attribute [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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