Structural variant analysis method:Type:Pt: Patient:Nom:*

Preferred Label : Structural variant analysis method:Type:Pt: Patient:Nom:*;

LOINC status : TRIAL;

LOINC display name : Structural variant analysis method Nom;

LOINC long common name : Variant analysis method [Type];

LOINC short name : Struct var analysis method;

LOINC description : The method used for analyzing chromosome structural variation, such as FISH, arrCGH, sequencing, and MLPA.;

Details

Origin ID

81304-8;

UMLS CUI

C4265524;

Has component
- Analysis method [LOINC component]
- Method [LOINC component]
- Structural variant [LOINC component]
- Structural variant analysis method [LOINC component]
Has property
- Type [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
- Simple variant panel:-:Pt:^Patient:-: [LOINC code]
Semantic type(s)
- Clinical Attribute [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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