Defects in Amino Acid Metabolism
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Alkaptonuria
CystinuriaGlycine encephalopathy, GCE - Non-ketotic hyperglycinemia, NKH
Histidinemia
Homocystinuria
Hyperlysinemia
Maple Syrup Urine Disease, MSUD
MethylmalonicAciduriaPhenylketonuria
Type I Tyrosinemia -TyrosinosisType II Tyrosinnemia -Richner-Hanhart Syndrome
Type III Tyrosinemia
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Michael W King, PhD | © 1996–2012 themedicalbiochemistrypage.org, LLC | info @ themedicalbiochemistrypage.org
Last modified: March 10, 2012
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