LP31754-2
CYP2D6 gene deletion
Active
Description
Deletion of the entire CYP2D6 gene (CYP2D6*5 allele) results in defective CYP2D6 enzymatic activity and therefore impaired ability to metabolize various drugs for CYP2D6, such as debrisoquine and sparteine. PMID: 16272752 Individuals with this variant are classified as poor metabolizers (PM).[OMIM: 124030] Source: Regenstrief LOINC
Basic Part Properties
- Part Name
- CYP2D6 gene deletion
- Part Display Name
- CYP2D6 gene deletion
- Part Type
- Component (Describes the core component or analyte measured)
- Created On
- 2003-05-13
- Construct for LOINC Short Name
- CYP2D6 gene Del
LOINC Terminology Service (API) using HL7® FHIR® Get Info
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Language Variants Get Info
| Tag | Language | Translation |
|---|---|---|
| zh-CN | Chinese (China) | CYP2D6 基因突变分析 缺失 Synonyms: CYP2D6 基因突变分析 基因缺失; |
| es-ES | Spanish (Spain) | Gen CYP2D6 Del |
| it-IT | Italian (Italy) | CYP2D6, analisi mutazione gene per delezione Synonyms: Gene CYP2D6 Delezione |
| tr-TR | Turkish (Turkey) | CYP2D6 geni mutation analizi del |
| ru-RU | Russian (Russian Federation) | CYP2D6 ген мутация анализ делеция |
| fr-FR | French (France) | CYP2D6 gène délétion |
LOINC Copyright
Copyright © Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://