Sequence variation panel:-:Pt:Bld/Tiss:-:Molgen

Preferred Label : Sequence variation panel:-:Pt:Bld/Tiss:-:Molgen;

LOINC status : ACTIVE;

LOINC display name : Sequence variation panel Molgen (Bld/Tiss);

LOINC long common name : Sequence variation panel - Blood or Tissue by Molecular genetics method;

LOINC short name : Sequence Variation Panel Bld/T;

Details

Origin ID

48014-5;

UMLS CUI

C1953370;

Has component
- Sequence variation panel [LOINC component]
Has method
- Molecular genetics [LOINC method]
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]
Panel of LOINC codes
- Amino acid change type:Type:Pt:Bld/Tiss:Nom:Molgen [LOINC code]
- Amino acid change:Find:Pt:Bld/Tiss:Nom:Molgen [LOINC code]
- Chromosome region:ID:Pt:Bld/Tiss:Nom:Molgen [LOINC code]
- Chromosome:ID:Pt:Bld/Tiss:Nom:Molgen [LOINC code]
- DNA change type:Type:Pt:Bld/Tiss:Nom:Molgen [LOINC code]
- DNA change:Find:Pt:Bld/Tiss:Nom:Molgen [LOINC code]
- DNA region name:ID:Pt:Bld/Tiss:Nom:Molgen [LOINC code]
- DNA sequence variation display name:Txt:Pt:Bld/Tiss:Nar:Molgen [LOINC code]
- DNA sequence variation identifier:ID:Pt:Bld/Tiss:Nom:Molgen [LOINC code]
- Gene identifier:ID:Pt:Bld/Tiss:Nom: [LOINC code]
- Genetic variant allelic state:Type:Pt:Bld/Tiss:Nom:Molgen [LOINC code]
- Genetic variant clinical significance:Imp:Pt:Bld/Tiss:Nom:Molgen [LOINC code]
- Genomic source class:Type:Pt:Bld/Tiss:Nom:Molgen [LOINC code]
Semantic type(s)
- Clinical Attribute [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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