Reference sequence alteration:Prid:Pt:Bld/Tiss:Nom:Molgen

Preferred Label : Reference sequence alteration:Prid:Pt:Bld/Tiss:Nom:Molgen;

LOINC status : ACTIVE;

LOINC display name : Reference sequence alteration Molgen Nom (Bld/Tiss);

LOINC long common name : Reference sequence alteration [Identifier];

LOINC short name : Ref sequence alteration;

LOINC description : Human Genome Variation Society (HGVS) nomenclature for conveying an alteration to the associated reference sequences used to define the genome as a basis for comparison with actual results.;

Details

Origin ID

53045-1;

UMLS CUI

C2361532;

Has component
- Reference sequence [LOINC component]
- Reference sequence alteration [LOINC component]
Has method
- Molecular genetics [LOINC method]
Has property
- Presence or Identity [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 marker assessed panel:-:Pt:Bld/Tiss:-:Molgen [LOINC code]
- DNA marker identified 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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