1.1.d

Disorders of phenylalanine and tyrosine metabolism

  • Phenylalanine hydroxylase deficiency (Phenylketonuria)
  • Tyrosinase deficiency (Oculocutaneous albinism type 1)
  • Tyrosine aminotransferase deficiency (Tyrosinemia type 2; Richner-Hanhart syndrome)
  • 4-hydroxyphenylpyruvate dioxygenase deficiency (Tyrosinemia type 3)
  • Hawkinsinuria (Tyrosinemia type 3)
  • Homogentisic acid oxidase deficiency (Alkaptonuria)
  • Maleylacetoacetate isomerase deficiency (Benign hypersuccinylacetonemia)
  • Fumarylacetoacetase deficiency (Tyrosinemia type 1)

Subnetworks

AOA 1

AOA

Aminoacid and organic acids related disorders

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