Complex variant panel:-:Pt: Patient:-:

Preferred Label : Complex variant panel:-:Pt: Patient:-:;

LOINC status : TRIAL;

LOINC display name : Complex variant panel;

LOINC long common name : Complex genetic variant panel;

LOINC short name : Comp var pnl;

LOINC description : This panel is used to report information related to a complex genetic variant and includes a repeating subpanel for reporting specific information for each simple variation that the complex variant includes.;

Détails

Origin ID

81251-1;

UMLS CUI

C4255290;

Has component
- Complex variant [LOINC component]
- Complex variant 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
- Allelic state:Find:Pt:Bld/Tiss:Nom:Molgen [LOINC code]
- Associated phenotype:Find:Pt:^Patient:Nom: [LOINC code]
- Basis for allelic phase:Type:Pt:^Patient:Nom:* [LOINC code]
- Complex variant HGVS name:Find:Pt:^Patient:Nom: [LOINC code]
- Complex variant type:Type:Pt:^Patient:Nom: [LOINC code]
- Complex variant:ID:Pt:^Patient:Nom: [LOINC code]
- Genetic disease sequence variation interpretation:Imp:Pt:Bld/Tiss:Nom:Molgen [LOINC code]
- Simple variant 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]

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

Vous pouvez consulter :

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documents for patients