Concept information
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
...
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Término preferido
Urea Cycle Disorders, Inborn
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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.
Concepto genérico
Conceptos específicos
Etiquetas alternativas
- Inborn Urea Cycle Disorder
- Urea Cycle Disorders
En otras lenguas
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francés
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Anomalies du cycle de l'urée
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Erreurs innées du métabolisme du cycle de l'urée
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Trouble congénital du cycle de l'urée
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Troubles congénitaux du cycle de l'urée
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Troubles du cycle de l'urée
URI
http://data.loterre.fr/ark:/67375/JVR-H79L77V9-9
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