Misplaced Pages

The following pages link to 3-Methylcrotonyl-CoA carboxylase deficiency

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Showing 50 items.

• Oculocerebrorenal syndrome (links | edit)
• 2-Methylbutyryl-CoA dehydrogenase deficiency (links | edit)
• Histidinemia (links | edit)
• Succinic semialdehyde dehydrogenase deficiency (links | edit)
• N-Acetylglutamate synthase deficiency (links | edit)
• Hyperhomocysteinemia (links | edit)
• Isobutyryl-coenzyme A dehydrogenase deficiency (links | edit)
• Carbamoyl phosphate synthetase I deficiency (links | edit)
• Ethylmalonic encephalopathy (links | edit)
• Sarcosinemia (links | edit)
• 3-methylcrotonyl-CoA carboxylase deficiency (redirect page) (links | edit)
  • Talk:3-Methylcrotonyl-CoA carboxylase deficiency (links | edit)
• Ornithine translocase deficiency (links | edit)
• Methylcrotonyl-CoA carboxylase (links | edit)
• Prolidase deficiency (links | edit)
• Pipecolic acidemia (links | edit)
• 3-methyl crotonyl-coa carboxylase deficiency (redirect page) (links | edit)
  • List of diseases (0–9) (links | edit)
  • Misplaced Pages talk:WikiProject Missing encyclopedic articles/Missing diseases (links | edit)
• 3-Methylcrotonylglycinuria type 1 (redirect page) (links | edit)
• 3MCC deficiency (redirect page) (links | edit)
• Hypermethioninemia (links | edit)
• Cystathioninuria (links | edit)
• Hyperprolinemia (links | edit)
• Brunner syndrome (links | edit)
• Hypervalinemia (links | edit)
• Organic acidemia (links | edit)
• Urocanic aciduria (links | edit)
• Carnosinemia (links | edit)
• Congenital disorders of amino acid metabolism (links | edit)
• Amino acid transport disorder (links | edit)
• Inborn errors of renal tubular transport (links | edit)
• Ocular albinism (links | edit)
• Tyrosinemia type III (links | edit)
• Ocular albinism type 1 (links | edit)
• Hypertryptophanemia (links | edit)
• Iminoglycinuria (links | edit)
• Dopamine beta hydroxylase deficiency (links | edit)
• Tyrosinemia type II (links | edit)
• List of causes of hypoglycemia (links | edit)
• D-Glyceric acidemia (links | edit)
• Beta-methyl crotonyl carboxylase deficiency (redirect page) (links | edit)
  • List of disorders included in newborn screening programs (links | edit)
• Fanconi syndrome (links | edit)
• Argininemia (links | edit)
• List of disorders included in newborn screening programs (links | edit)
• Aminoacylase 1 deficiency (links | edit)
• 3-Methylcrotonylglycinuria (redirect page) (links | edit)
  • Β-Hydroxy β-methylbutyric acid (links | edit)
• Tyrosinemia type I (links | edit)
• Branched-chain keto acid dehydrogenase kinase deficiency (links | edit)
• 3 alpha methylcrotonyl-Coa carboxylase 1 deficiency (redirect page) (links | edit)
  • List of diseases (0–9) (links | edit)
• Talk:3-Methylcrotonyl-CoA carboxylase deficiency (transclusion) (links | edit)
• Talk:Branched-chain amino acid (links | edit)
• User:Madhero88/OthersBM (links | edit)