Associated phenotype:Find:Pt: Patient:Nom:

Preferred Label : Associated phenotype:Find:Pt: Patient:Nom:;

LOINC status : TRIAL;

LOINC display name : Associated phenotype;

LOINC long common name : Associated phenotype;

LOINC short name : Prob assoc phenotype;

LOINC description : The possible phenotype associated with the genetic variant found in this study.;

Détails

Origin ID

81259-4;

UMLS CUI

C4255287;

Has component
- Associated phenotype [LOINC component]
Has property
- Finding [LOINC Property]
Has scale
- Nom [LOINC scale]
Has system
- Patient [LOINC System]
- ^Patient [LOINC System]
Has time aspect
- Point in time (spot) [LOINC time aspect]
Part of panel
- Complex variant panel:-:Pt:^Patient:-: [LOINC code]
- Simple variant panel:-:Pt:^Patient:-: [LOINC code]
Semantic type(s)
- Clinical Attribute [UMLS semantic type]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients