Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Inborn disorder of amino acid metabolism · Inborn aminoacylase deficiency
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 neurologic symptoms.
This condition has no sub-types.