Defects in Amino Acid Metabolism

---

Alkaptonuria

Cystinuria
Glycine encephalopathy, GCE - Non-ketotic hyperglycinemia, NKH
Histidinemia
Homocystinuria
Hyperlysinemia

Maple Syrup Urine Disease, MSUD

MethylmalonicAciduria

Phenylketonuria

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

 

 

 

 

 

 

 

 

 

 

---

back to Inborn Errors Page

---

Return to The Medical Biochemistry Page

---

Michael W King, PhD | © 1996–2013 themedicalbiochemistrypage.org, LLC | info @ themedicalbiochemistrypage.org

---

Last modified: February 8, 2013