DNA sequence variation identifier:ID:Pt:Bld/Tiss:Nom:Molgen

Preferred Label : DNA sequence variation identifier:ID:Pt:Bld/Tiss:Nom:Molgen;

LOINC status : ACTIVE;

LOINC display name : DNA sequence variation identifier Molgen Nom (Bld/Tiss) [ID];

LOINC long common name : DNA sequence variation identifier [Identifier];

LOINC short name : DNA seq var ID;

LOINC description : A DNA Marker identifier conveys a universal or standard repository identifier for definitive characterstics of a DNA Marker. (recommend using NCBI dbSNP ids - rs#);

Details

Origin ID

48003-8;

UMLS CUI

C1953348;

Has component
- DNA [LOINC component]
- DNA sequence variation [LOINC component]
- DNA sequence variation identifier [LOINC component]
- Identifier [LOINC component]
Has method
- Molecular genetics [LOINC method]
Has property
- Identifier [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]
- DNA marker assessed panel:-:Pt:Bld/Tiss:-:Molgen [LOINC code]
- DNA marker identified panel:-:Pt:Bld/Tiss:-:Molgen [LOINC code]
- 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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