Neurological conditions associated with aminoacylase 1 deficiency (Q105263): Difference between revisions
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Revision as of 11:21, 17 August 2026
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).
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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). |
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CID11:ID_620694696
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dki-india-ID_620694696
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