Amino Acid and Organic Acid Disorders

Defects in Amino Acid Metabolism



Alkaptonuria

Cystinuria

Glycine encephalopathy, GCE - Non-ketotic hyperglycinemia, NKH

Hartnup Disorder

Histidinemia

Homocystinurias

Hyperlysinemia

Maple Syrup Urine Disease, MSUD

Methylmalonic acidemia/aciduria

Phenylketonuria

Type I Tyrosinemia -Tyrosinosis
Type II Tyrosinnemia -Richner-Hanhart Syndrome
Type III Tyrosinemia

 

 

 

 

 

 

 

 

 

 


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Last modified: November 7, 2013