Showing entry for Dihydropyrimidine Dehydrogenase Deficiency



                               
General Disease Information
BXGD IdBXGD016643
Disease NameDihydropyrimidine Dehydrogenase Deficiency
Disease CUI IdC1959620
MeSH Codes C16   C18  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id HP:0001939  
Human Phenotype Ontology TermAbnormality of metabolism/homeostasis
Disease Ontology Id DOID:0014667   DOID:630  
Disease Ontology Class Namedisease of metabolism; genetic disease
Disorder Network disorder-protein-compound-food associations