Pharmacogenomics result panel:-:Pt: Patient:-:

Preferred Label : Pharmacogenomics result panel:-:Pt: Patient:-:;

LOINC status : TRIAL;

LOINC display name : Pharmacogenomics result panel;

LOINC long common name : Pharmacogenomics result panel;

LOINC short name : Pharmg result pnl;

Details

Origin ID

82118-1;

UMLS CUI

C4255498;

Has component
- Pharmacogenomics [LOINC component]
- Pharmacogenomics result panel [LOINC component]
Has system
- Patient [LOINC System]
- ^Patient [LOINC System]
Has time aspect
- Point in time (spot) [LOINC time aspect]
Panel of LOINC codes
- Drug efficacy sequence variation interpretation:Imp:Pt:Bld/Tiss:Ord:Molgen [LOINC code]
- Drug metabolism sequence variation interpretation:Imp:Pt:Bld/Tiss:Ord:Molgen [LOINC code]
- Gene identifier:ID:Pt:Bld/Tiss:Nom: [LOINC code]
- Genetic variation effect on high-risk allele:Imp:Pt:^Patient:Ord: [LOINC code]
- Genotype display name:Find:Pt:^Patient:Nom: [LOINC code]
- Medication usage implications panel:-:Pt:^Patient:-: [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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