Genomic structural variant copy number:Num:Pt: Patient:Qn:

Preferred Label : Genomic structural variant copy number:Num:Pt: Patient:Qn:;

LOINC status : TRIAL;

LOINC display name : Genomic structural variant copy number [#];

LOINC long common name : Genomic structural variant copy number;

LOINC short name : Gen struct var copy num;

Details

Origin ID

82155-3;

UMLS CUI

C4255301;

Has component
- Genomic structural variant copy number [LOINC component]
- Number [LOINC component]
- Structural variant [LOINC component]
Has property
- Number (count) [LOINC Property]
Has system
- Patient [LOINC System]
- ^Patient [LOINC System]
Has time aspect
- Point in time (spot) [LOINC time aspect]
Part of panel
- Structural variant panel:-:Pt:^Patient:-: [LOINC code]
Semantic type(s)
- Clinical Attribute [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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