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Hawkinsinuria
Hawkinsinuria
Overview
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Inborn errors of metabolism
3 methylcrotonyl-coa carboxylase deficiency
2-Methylbutyryl-CoA dehydrogenase deficiency
Tyrosinemia
Genetic disorder
6-pyruvoyl- tetrahydropterin synthase deficiency
2-Methylbutyryl-CoA dehydrogenase deficiency
Genetic disorders
3 methylcrotonyl-coa carboxylase deficiency
6-pyruvoyl- tetrahydropterin synthase deficiency
2-Methylbutyryl-CoA dehydrogenase deficiency
Tyrosinemia
Medical condition
6-pyruvoyl- tetrahydropterin synthase deficiency
Tyrosinemia
Tyrosinemia
Ochronosis
Type I tyrosinemia
Type III tyrosinemia
Tyrosinemia type II
See also
Diseases and disorders
Hawkinsin
Tyrosine metabolism
4-Hydroxyp- henylpyruvate dioxygenase
Amino acid
Alkaptonuria