Structural variant ISCN name:Find:Pt: Patient:Nom:

Preferred Label : Structural variant ISCN name:Find:Pt: Patient:Nom:;

LOINC status : TRIAL;

LOINC display name : Structural variant ISCN name Nom;

LOINC long common name : Variant ISCN;

LOINC short name : Struct var ISCN name;

LOINC description : ISCN is a syntax for describing cytogenetic findings, from classical karyotypes to details that can be observed with copy number methodologies. Using ISCN nomenclature is highly recommended for reporting structural variants.;

Détails

Origin ID

81291-7;

UMLS CUI

C4255115;

Has component
- Name [LOINC component]
- Structural variant [LOINC component]
- Structural variant ISCN name [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
- Variables that apply to the overall study:-: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