Structural variant cytogenetic location:ID:Pt: Patient:Nom:

Preferred Label : Structural variant cytogenetic location:ID:Pt: Patient:Nom:;

LOINC status : TRIAL;

LOINC display name : Structural variant cytogenetic location Nom [ID];

LOINC long common name : Structural variant cytogenetic location [Identifier];

LOINC short name : Struct var cyto loc ID;

LOINC description : The chromosome region where the structural variant was found, for example, 17p12. This term may be used when more specific information, such as the structural variant reported start-end [LOINC: 81287-5], precision of boundaries [LOINC: 81288-3] and inner and outer start-end [LOINC: 81302-2] and [LOINC: 81301-4], respectively, cannot be or are not reported.;

Details

Origin ID

81298-2;

UMLS CUI

C4265529;

Has component
- Location [LOINC component]
- Structural variant [LOINC component]
- Structural variant cytogenetic location [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]
Semantic type(s)
- Clinical Attribute [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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