Neurological conditions associated with aminoacylase 1 deficiency (Q105263)
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Aminoacylase 1 deficiency (ACY1D) is an inborn error of metabolism marked by a characteristic pattern of urinary N-acetyl amino acid excretion and variable neurologic symptoms. (delayed psychomotor development or seizures).
| Language | Label | Description | Also known as |
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| default for all languages | ID_620694696 |
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| English | Neurological conditions associated with aminoacylase 1 deficiency |
Aminoacylase 1 deficiency (ACY1D) is an inborn error of metabolism marked by a characteristic pattern of urinary N-acetyl amino acid excretion and variable neurologic symptoms. (delayed psychomotor development or seizures). |
Statements
CID11:ID_620694696
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