Term Name: dihydropyrimidine dehydrogenase deficiency
Synonyms: Dihydrouracil Dehydrogenase deficiency, familial pyrimidinaemia, thymine-uracilurea
Definition: A purine-pyrimidine metabolic disorder that is an autosomal recessive metabolic disorder in which there is absent or significantly decreased activity of dihydropyrimidine dehydrogenase, an enzyme involved in the metabolism of uracil and thymine.
Ontology: Human Disease [DOID:14218]   ( DOID:14218 )

Relationships
is a type of: purine-pyrimidine metabolic disorder