Defects in Amino Acid Metabolism

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Phenylketonuria

Type I Tyrosinemia -Tyrosinosis

Type II Tyrosinnemia -Richner-Hanhart Syndrome

Type III Tyrosinemia

Alkaptonuria

Homocystinuria

Histidinemia

Maple Syrup Urine Disease, MSUD

Methylmalonic Aciduria

Glycine encephalopathy, GCE - Non-ketotic hyperglycinemia, NKH

Hyperlysinemia

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Michael W. King, Ph.D / IU School of Medicine / miking at iupui.edu

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Last modified: June 11, 2009