UGT2B15 gene targeted mutation analysis:Prid:Pt:Bld/Tiss:Nom:Molgen

Preferred Label : UGT2B15 gene targeted mutation analysis:Prid:Pt:Bld/Tiss:Nom:Molgen;

LOINC status : ACTIVE;

LOINC display name : UGT2B15 gene targeted mutation analysis Molgen Nom (Bld/Tiss);

LOINC long common name : UGT2B15 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal;

LOINC short name : UGT2B15 Mut Anl Bld/T;

LOINC description : A patient's genotype for the UGT2B15 gene is typically reported as *A/*B where A is the allele from one chromosome and B is the allele from the other chromosome. The genotype is determined by the analysis of specific single nucleotide polymorphisms (SNPs) within the gene by various molecular techniques, including PCR and microarray. In some cases, SNP results are analyzed by bioinformatics computer software to determine a patient's overall genotype.;

Détails

Origin ID

72881-6;

UMLS CUI

C3655042;

Has component
- Gene [LOINC component]
- UGT2B15 gene [LOINC component]
- UGT2B15 gene targeted mutation analysis [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]
Semantic type(s)
- Clinical Attribute [UMLS semantic type]

Position du mot-clé dans l'(les) arborescence(s) :

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