Skip to main content

Medical Subject Headings (thesaurus)

Search from vocabulary

Concept information

Preferred term

Urea Cycle Disorders, Inborn  

Type

  • mesh:Descriptor

Definition

  • Rare congenital metabolism disorders of the urea cycle. The disorders are due to mutations that result in complete (neonatal onset) or partial (childhood or adult onset) inactivity of an enzyme, involved in the urea cycle. Neonatal onset results in clinical features that include irritability, vomiting, lethargy, seizures, NEONATAL HYPOTONIA; RESPIRATORY ALKALOSIS; HYPERAMMONEMIA; coma, and death. Survivors of the neonatal onset and childhood/adult onset disorders share common risks for ENCEPHALOPATHIES, METABOLIC, INBORN; and RESPIRATORY ALKALOSIS due to HYPERAMMONEMIA.

Entry terms

  • Inborn Urea Cycle Disorder
  • Urea Cycle Disorders

In other languages

  • French

  • Anomalies du cycle de l'urée
  • Erreurs innées du métabolisme du cycle de l'urée
  • Trouble congénital du cycle de l'urée
  • Troubles congénitaux du cycle de l'urée
  • Troubles du cycle de l'urée

URI

http://data.loterre.fr/ark:/67375/JVR-H79L77V9-9

Download this concept:

RDF/XML TURTLE JSON-LD Created 7/6/09