Gene mutations tested for:Prid:Pt:Bld/Tiss:Nom:Molgen

Preferred Label : Gene mutations tested for:Prid:Pt:Bld/Tiss:Nom:Molgen;

LOINC status : ACTIVE;

LOINC display name : Gene mutations tested for Molgen Nom (Bld/Tiss);

LOINC long common name : Gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal;

LOINC short name : Gene Mut Tested Bld/T;

LOINC description : For targeted mutation analysis, report the discrete mutations the study is designed to detect. In HL7 V2 they can be reported in one observation as a list separated by repeat delimiters OR as a series of separate OBX segments, one per mutation tested for. In FHIR, multiple coded entries can not be reported as a list in one observation value field. They must be reported as the values of separate observations.;

Details

Origin ID

36908-2;

UMLS CUI

C1508048;

Has component
- Gene [LOINC component]
- Gene mutations tested for [LOINC component]
- Mutations [LOINC component]
Has method
- Molecular genetics [LOINC method]
Has property
- Presence or Identity [LOINC Property]
Has scale
- Nom [LOINC scale]
Has system
- Blood [LOINC System]
- Blood or Tissue [LOINC System]
- Tissue and Smears [LOINC System]
Has time aspect
- Point in time (spot) [LOINC time aspect]
Part of panel
- DNA analysis discrete sequence variation basic associated observations panel:-:Pt:Bld/Tiss:-:Molgen [LOINC code]
- Variables that apply to the overall study:-:Pt:^Patient:-: [LOINC code]
Semantic type(s)
- Clinical Attribute [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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