MeSH Browser

MeSH Heading: Pharmacogenomic Testing
Tree Number(s): E01.370.225.562.500; E05.200.562.500; E05.393.435.500; N02.421.308.430.500; N02.421.726.233.221.500
Unique ID: D000071185
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D000071185
Scope Note: The detection of genetic variability (e.g., PHARMACOGENOMIC VARIANTS) relevant to PHARMACOGENETICS and PRECISION MEDICINE. The purpose of such genetic testing is to help determine the most effective treatment options and their optimum dosages with least potential risks for DRUG-RELATED SIDE EFFECTS AND ADVERSE REACTIONS.
Entry Term(s): Pharmacogenetic Analysis; Pharmacogenetic Screening; Pharmacogenetic Study; Pharmacogenetic Testing; Pharmacogenomic Analysis; Pharmacogenomic Screening; Pharmacogenomic Study
Previous Indexing: Genetic Testing (2001-2016); Pharmacogenetics (2001-2016)
Public MeSH Note: 2017
History Note: 2017
Date Established: 2017/01/01
Date of Entry: 2016/07/05
Revision Date: 2016/06/16

Allowable Qualifiers: classification (CL)

economics (EC)

ethics (ES)

history (HI)

instrumentation (IS)

legislation & jurisprudence (LJ)

methods (MT)

standards (ST)

statistics & numerical data (SN)

trends (TD)

veterinary (VE)

Concept UI: M000613505
Terms: Pharmacogenomic Analysis Preferred Term
Term UI T000893559
Date01/13/2016
LexicalTag NON
ThesaurusID NLM (2017); Pharmacogenetic Study
Term UI T000893564
Date01/13/2016
LexicalTag NON
ThesaurusID NLM (2017); Pharmacogenetic Analysis
Term UI T000893560
Date01/13/2016
LexicalTag NON
ThesaurusID NLM (2017); Pharmacogenomic Study
Term UI T000893462
Date01/11/2016
LexicalTag NON
ThesaurusID NLM (2017)

Pharmacogenomic Testing MeSH Descriptor Data 2024