Pages that link to "Saccharopinuria"
From WikiMD's Wellness Encyclopedia
The following pages link to Saccharopinuria:
Displaying 39 items.
- List of diseases (S) (← links | edit)
- Homocystinuria (← links | edit)
- Fanconi syndrome (← links | edit)
- Isovaleric acidemia (← links | edit)
- Waardenburg syndrome (← links | edit)
- Inborn errors of metabolism (← links | edit)
- Cystinuria (← links | edit)
- Histidinemia (← links | edit)
- Miscellaneous (← links | edit)
- Fumarase deficiency (← links | edit)
- List of rare diseases-S (← links | edit)
- List of rare metabolic disorders (← links | edit)
- Genetic diseases-S (← links | edit)
- Health-encyclopedia-S (← links | edit)
- Diseases-and-disorders-S (← links | edit)
- Lysinuric protein intolerance (← links | edit)
- Ethylmalonic encephalopathy (← links | edit)
- Dopamine beta hydroxylase deficiency (← links | edit)
- Carnosinemia (← links | edit)
- Alkaptonuria (← links | edit)
- Homocystinuria due to CBS deficiency (← links | edit)
- Mild phenylketonuria (← links | edit)
- Carbamoyl phosphate synthetase 1 deficiency (← 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)
- Hypermethioninemia due to S-adenosylhomocysteine hydrolase deficiency (← links | edit)
- Dictionary-S (← links | edit)
- Template:Amino acid metabolic pathology (← links | edit)
