Variables that apply to the overall study:-:Pt: Patient:-:

Preferred Label : Variables that apply to the overall study:-:Pt: Patient:-:;

LOINC status : TRIAL;

LOINC display name : Variables that apply to the overall study;

LOINC long common name : Variables that apply to the overall study;

LOINC short name : Overall study variables type;

Details

Origin ID

81306-3;

UMLS CUI

C4265522;

Has component
- Overall [LOINC component]
- Study [LOINC component]
- Variables that apply to the overall study [LOINC component]
Has system
- Patient [LOINC System]
- ^Patient [LOINC System]
Has time aspect
- Point in time (spot) [LOINC time aspect]
Panel of LOINC codes
- COSMIC version:ID:Pt:^Patient:Nom: [LOINC code]
- ClinVar version:ID:Pt:^Patient:Nom: [LOINC code]
- DNA region of interest:NumRange:Pt:Bld/Tiss:Nom:Molgen [LOINC code]
- Deletion-duplication overall interpretation:Imp:Pt:^Patient:Nom: [LOINC code]
- Gene identifier:ID:Pt:Bld/Tiss:Nom: [LOINC code]
- Gene mutations tested for:Prid:Pt:Bld/Tiss:Nom:Molgen [LOINC code]
- Genetic analysis summary report:Find:Pt:Bld/Tiss:Doc:Molgen [LOINC code]
- Genetic disease analysis overall interpretation:Imp:Pt:Bld/Tiss:Nom:Molgen [LOINC code]
- Genetic disease assessed:ID:Pt:Bld/Tiss:Nom:Molgen [LOINC code]
- HGVS version:ID:Pt:^Patient:Nom: [LOINC code]
- Human reference sequence assembly release number:ID:Pt:Bld/Tiss:Nom:Molgen [LOINC code]
- Medication assessed:ID:Pt:Bld/Tiss:Nom:Molgen [LOINC code]
- Range(s) of DNA sequences examined:Txt:Pt:^Patient:Nar: [LOINC code]
- Reason for study additional note:Txt:Pt:Bld/Tiss:Nar:Molgen [LOINC code]
- Structural variant ISCN name:Find:Pt:^Patient:Nom: [LOINC code]
- dbSNP version:ID:Pt:^Patient:Nom: [LOINC code]
Part of panel
- Master HL7 genetic variant reporting panel:-:Pt:^Patient:-: [LOINC code]
Semantic type(s)
- Clinical Attribute [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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