Pages that link to "Trimethylaminuria"
From WikiMD.com Medical Encyclopedia
The following pages link to Trimethylaminuria:
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- Template:Amino acid metabolic pathology (← links | edit)
- Fish malodor syndrome (redirect page) (← links | edit)
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- Homocystinuria due to CBS deficiency (← links | edit)
- Mild phenylketonuria (← links | edit)
- Carbamoyl phosphate synthetase 1 deficiency (← links | edit)
- Fetor (← links | edit)
- Hermansky Pudlak syndrome 2 (← links | edit)
- Prolidase deficiency (← links | edit)
- 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency (← links | edit)
- Glutaric aciduria type 1 (← links | edit)
- Inborn errors of renal tubular transport (← links | edit)
- Isobutyryl-coenzyme A dehydrogenase deficiency (← links | edit)
- Succinic semialdehyde dehydrogenase deficiency (← links | edit)
- 2-methylbutyryl-CoA dehydrogenase deficiency (← links | edit)
- 3-methylglutaconyl-CoA hydratase deficiency (AUH defect) (← links | edit)
- Tyrosinemia type 2 (← links | edit)
- Ornithine translocase deficiency syndrome (← links | edit)
- Hyperprolinemia type 2 (← links | edit)
- Tyrosinemia type 3 (← links | edit)
- T (← links | edit)
- Hypermethioninemia due to S-adenosylhomocysteine hydrolase deficiency (← links | edit)
- Dictionary-T (← links | edit)
- Flavin-containing monooxygenase 3 (← links | edit)
- List of top 5000 medicine articles (← links | edit)
- Dictionary of pediatrics (← links | edit)