Genetic variation effect on high-risk allele:Imp:Pt: Patient:Ord:

Preferred Label : Genetic variation effect on high-risk allele:Imp:Pt: Patient:Ord:;

LOINC status : TRIAL;

LOINC display name : Genetic variation effect on high-risk allele Ql [Interp];

LOINC long common name : Genetic variation's effect on high-risk allele;

LOINC short name : Genetic var eff high-risk allele;

Details

Origin ID

83009-1;

UMLS CUI

C4298294;

Has component
- Genetic variation effect on high-risk allele [LOINC component]
Has property
- Impression/interpretation of study [LOINC Property]
Has scale
- Ord [LOINC scale]
Has system
- Patient [LOINC System]
- ^Patient [LOINC System]
Has time aspect
- Point in time (spot) [LOINC time aspect]
Part of panel
- Pharmacogenomics result panel:-:Pt:^Patient:-: [LOINC code]
Semantic type(s)
- Clinical Attribute [UMLS semantic type]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients