Pages that link to "Isovaleric acidemia"
From WikiMD.com Medical Encyclopedia
The following pages link to Isovaleric acidemia:
Displayed 50 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- List of OMIM disorder codes (← links | edit)
- Genetic disorder (← links | edit)
- Homocystinuria (← links | edit)
- Pediatric glossary of terms (← links | edit)
- Pediatric glossary of terms expanded (← links | edit)
- Fanconi syndrome (← links | edit)
- Waardenburg syndrome (← links | edit)
- Carglumic acid (← links | edit)
- Inborn errors of metabolism (← links | edit)
- Cystinuria (← links | edit)
- Histidinemia (← links | edit)
- Fumarase deficiency (← links | edit)
- Health topics a-z (← links | edit)
- 6-Pyruvoyltetrahydropterin synthase deficiency (← links | edit)
- List of rare diseases-I (← links | edit)
- List of rare metabolic disorders (← links | edit)
- Health-encyclopedia-I (← links | edit)
- Diseases-and-disorders-I (← links | edit)
- Template:Amino acid metabolic pathology (← links | edit)
- Saccharopinuria (← links | edit)
- Oculocutaneous albinism (← links | edit)
- Organic acidemia (← links | edit)
- Lysinuric protein intolerance (← links | edit)
- Ethylmalonic encephalopathy (← links | edit)
- Dopamine beta hydroxylase deficiency (← links | edit)
- Carnosinemia (← links | edit)
- Alkaptonuria (← links | edit)
- Newborn screening (← 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)
- Methylmalonyl-CoA mutase 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-I (← links | edit)
- Isovaleryl-CoA (← links | edit)
- Isovaleryl-CoA dehydrogenase (← links | edit)
- Isovaleric acid (← links | edit)
