Aminoacylase 1 deficiency
MONDO:0012368Aminoacylase 1 deficiency (ACY1D) is an inborn error of metabolism marked by a characteristic pattern of urinary N-acetyl amino acid excretion and neurologic symptoms.
Also known as: ACY1D, N-acyl-L-amino acid amidohydrolase deficiency, aminoacylase 1 deficiency, neurological conditions associated with aminoacylase 1 deficiency, ACY1 deficiency, deficiency of the aminoacylase-1 enzyme
0 clinical trials for this condition and its sub-types, 0 tagged with Aminoacylase 1 deficiency itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.