Complex variant:ID:Pt: Patient:Nom:

Preferred Label : Complex variant:ID:Pt: Patient:Nom:;

LOINC status : TRIAL;

LOINC display name : Complex variant Nom [ID];

LOINC long common name : Complex genetic variant [ID];

LOINC short name : Comp var ID;

LOINC description : This term is used to report the unique identifier of the complex variant found in this study. The identifier may come from various sources, including NCBI's ClinVar and Ensembl. For example, the variant NM_000106.5(CYP2D6):c.[886C T;457G C] - Haplotype has the ClinVar ID 16895. [http://www.ncbi.nlm.nih.gov/clinvar/variation/16895/];

Détails

Origin ID

81260-2;

UMLS CUI

C4265554;

Has component
- Complex variant [LOINC component]
Has property
- Identifier [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]
Semantic type(s)
- Clinical Attribute [UMLS semantic type]

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

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