Skip to main

Medical Subject Headings (thesaurus)

Search from vocabulary

Concept information

Término preferido

Urea Cycle Disorders, Inborn  

Notice: Undefined index: in /var/www/html/model/Concept.php on line 545

Tipo

  • mesh:Descriptor

Definición

  • 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.

Etiquetas alternativas

  • Inborn Urea Cycle Disorder
  • Urea Cycle Disorders

En otras lenguas

  • francés

  • 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

Descargue este concepto:

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