Disorders


 

Dihydropyrimidinase Deficiency


 

OMIM

GeneLocusProtein
DPYS8q22Dihydropyrimidinase

Laboratory Test Method Prenatal Carrier *
University of Amsterdam Academic Medical Center, Laboratory Genetic Metabolic Diseases - Amsterdam, Netherlands• Analyte
• Enzyme assay
  

* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.

Loading...