Drug Metabolism, Poor, Cyp2d6-related

Clinical Features

Phenotypes and symptoms related to Drug Metabolism, Poor, Cyp2d6-related

  • Neoplasm
  • Hypertension
  • Abnormality of metabolism/homeostasis
  • Depressivity
  • Hypotension
  • Schizophrenia

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
No data available about the known clinical features onset.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Drug Metabolism, Poor, Cyp2d6-related Recommended genes panels

Panel Name, Specifity and genes Tested/covered
CYP2D6 Genotyping.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States).

CYP2D6
Specificity
100 %
Genes
100 %
Psychiatry Pharmacogenetics Expanded Panel.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center (United States).

CYP2C19, CYP2D6
Specificity
50 %
Genes
100 %
Cytochrome P450 Genotype Panel.

By ARUP Laboratories, Molecular Genetics and Genomics (United States).

CYP2C19, CYP2C9, CYP2D6
Specificity
34 %
Genes
100 %
Cytochrome P450 (6 alleles of CYP2D6, CYP2C9, CYP2C19 and CYP3A4).

By CGC Genetics (Portugal).

CYP2C19, CYP2C9, CYP2D6, CYP3A4
Specificity
25 %
Genes
100 %
Cytochrome P450 (13 alleles).

By CGC Genetics (Portugal).

CYP2C19, CYP2C9, CYP2D6, CYP3A4
Specificity
25 %
Genes
100 %
Antidepressants and antipsychotics pharmacogenetics.

By CGC Genetics (Portugal).

CYP2C19, CYP2D6
Specificity
50 %
Genes
100 %
Pharmacogenetic panel for cardiology.

By CGC Genetics (Portugal).

VKORC1, CYP2C19, CYP2C9, CYP2D6
Specificity
25 %
Genes
100 %
Tamoxifen pharmacogenetics.

By CGC Genetics (Portugal).

CYP2D6
Specificity
100 %
Genes
100 %

You can get up to 72 more panels with our dedicated tool

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Sources and references

You can check the following sources for additional information.

MESH OMIM Genetic Syndrome Finder

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