Concept information
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Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Urea Cycle Disorders, Inborn
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Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Urea Cycle Disorders, Inborn
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Genetic Diseases, Inborn
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Urea Cycle Disorders, Inborn
...
Metabolic Diseases
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Urea Cycle Disorders, Inborn
Término preferido
Citrullinemia
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Tipo
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mesh:Descriptor
Definición
- A group of diseases related to a deficiency of the enzyme ARGININOSUCCINATE SYNTHASE which causes an elevation of serum levels of CITRULLINE. In neonates, clinical manifestations include lethargy, hypotonia, and SEIZURES. Milder forms also occur. Childhood and adult forms may present with recurrent episodes of intermittent weakness, lethargy, ATAXIA, behavioral changes, and DYSARTHRIA. (From Menkes, Textbook of Child Neurology, 5th ed, p49)
Concepto genérico
Etiquetas alternativas
- Argininosuccinate Synthase Deficiency Disease
- Argininosuccinate Synthetase Deficiency
- Argininosuccinic Acid Synthase Deficiency Disease
- Argininosuccinic Acid Synthetase Deficiency
- Argininosuccinic Acid Synthetase Deficiency Disease
- ASS Deficiency
- Citrullinuria
- Deficiency Disease, Argininosuccinate Synthase
- Deficiency Disease, Argininosuccinic Acid Synthase
En otras lenguas
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francés
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Déficit en argininosuccinate synthase
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Déficit en argininosuccinate synthétase
URI
http://data.loterre.fr/ark:/67375/JVR-N94FJG70-H
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