Defects in Amino Acid Metabolism
Cystinuria
Glycine encephalopathy, GCE - Non-ketotic hyperglycinemia, NKH
Histidinemia
Homocystinuria
Hyperlysinemia
MethylmalonicAciduria
Type I Tyrosinemia -Tyrosinosis
Type II Tyrosinnemia -Richner-Hanhart Syndrome
Type III Tyrosinemia
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Last modified: February 8, 2013