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Hyperprolinemia
Hyperprolinemia
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Inborn errors of metabolism
3-hydroxy-- 3-methylglutaryl-CoA lyase deficiency
Hypermethioninemia
2-Methylbutyryl-CoA dehydrogenase deficiency
3 methylcrotonyl-coa carboxylase deficiency
Inborn error of metabolism
Autosomal recessive disorders
Hypermethioninemia
3 methylcrotonyl-coa carboxylase deficiency
Genetic disorders
6-pyruvoyl- tetrahydropterin synthase deficiency
Genetic disorder
Neurofibromatosis type II
3-hydroxy-- 3-methylglutaryl-CoA lyase deficiency
Hypermethioninemia
2-Methylbutyryl-CoA dehydrogenase deficiency
3 methylcrotonyl-coa carboxylase deficiency
Medical condition
Mild mental retardation
6-pyruvoyl- tetrahydropterin synthase deficiency
Inborn error of metabolism
Neurofibromatosis type II
Metabolism
Amino acid metabolism
Enzyme
Inborn error of metabolism
See also
(12)
Diseases and disorders
Proline oxidase
Pyrroline-- 5-carboxylate
ALDH4A1
Proline dehydrogenase
Proline dehydrogenase
Proline
Endocrine diseases
List of amino acid metabolism disorders
7700
Heredity
Carnosinemia
Histidinemia
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