Pages that link to "Template:Amino acid metabolic pathology"
From WikiMD's Food, Medicine & Wellness Encyclopedia
The following pages link to Template:Amino acid metabolic pathology:
Displayed 50 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Homocystinuria (transclusion) (← links | edit)
- Fanconi syndrome (transclusion) (← links | edit)
- Isovaleric acidemia (transclusion) (← links | edit)
- Waardenburg syndrome (transclusion) (← links | edit)
- Inborn errors of metabolism (transclusion) (← links | edit)
- Cystinuria (transclusion) (← links | edit)
- Histidinemia (transclusion) (← links | edit)
- Cystinosis (transclusion) (← links | edit)
- Fumarase deficiency (transclusion) (← links | edit)
- 6-Pyruvoyltetrahydropterin synthase deficiency (transclusion) (← links | edit)
- 2-Hydroxyglutaric aciduria (transclusion) (← links | edit)
- N-Acetylglutamate synthase deficiency (transclusion) (← links | edit)
- Metabolic diseases (transclusion) (← links | edit)
- Beta ketothiolase deficiency (transclusion) (← links | edit)
- Saccharopinuria (transclusion) (← links | edit)
- Oculocutaneous albinism (transclusion) (← links | edit)
- Organic acidemia (transclusion) (← links | edit)
- Ornithine transcarbamylase deficiency (transclusion) (← links | edit)
- Lysinuric protein intolerance (transclusion) (← links | edit)
- Hermansky-Pudlak syndrome (transclusion) (← links | edit)
- Ethylmalonic encephalopathy (transclusion) (← links | edit)
- Dopamine beta hydroxylase deficiency (transclusion) (← links | edit)
- Carnosinemia (transclusion) (← links | edit)
- Citrullinemia type II (transclusion) (← links | edit)
- Alkaptonuria (transclusion) (← links | edit)
- Aminoacylase 1 deficiency (transclusion) (← links | edit)
- Arginase deficiency (transclusion) (← links | edit)
- Argininosuccinic aciduria (transclusion) (← links | edit)
- Homocystinuria due to CBS deficiency (transclusion) (← links | edit)
- Methylmalonic acidemia with homocystinuria (transclusion) (← links | edit)
- Mild phenylketonuria (transclusion) (← links | edit)
- N-acetylglutamate synthase deficiency (transclusion) (← links | edit)
- Phenylketonuria (transclusion) (← links | edit)
- Carbamoyl phosphate synthetase 1 deficiency (transclusion) (← links | edit)
- Hermansky Pudlak syndrome 2 (transclusion) (← links | edit)
- Prolidase deficiency (transclusion) (← links | edit)
- 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency (transclusion) (← links | edit)
- Glutaric aciduria type 1 (transclusion) (← links | edit)
- Inborn errors of renal tubular transport (transclusion) (← links | edit)
- Isobutyryl-coenzyme A dehydrogenase deficiency (transclusion) (← links | edit)
- Succinic semialdehyde dehydrogenase deficiency (transclusion) (← links | edit)
- 3-Methylcrotonyl-CoA carboxylase deficiency (transclusion) (← links | edit)
- Lowe oculocerebrorenal syndrome (transclusion) (← links | edit)
- 2-methylbutyryl-CoA dehydrogenase deficiency (transclusion) (← links | edit)
- 3-methylglutaconyl-CoA hydratase deficiency (AUH defect) (transclusion) (← links | edit)
- Glutaric acidemia type II (transclusion) (← links | edit)
- Tyrosinemia type 2 (transclusion) (← links | edit)
- Ornithine translocase deficiency syndrome (transclusion) (← links | edit)
- Hyperprolinemia type 2 (transclusion) (← links | edit)
- Tyrosinemia type 3 (transclusion) (← links | edit)