The following pages link to Template:Amino acid metabolic pathology
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View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Phenylketonuria (transclusion) (links | edit)
- Alkaptonuria (transclusion) (links | edit)
- Methylmalonic acidemias (transclusion) (links | edit)
- Propionic acidemia (transclusion) (links | edit)
- Hyperammonemia (transclusion) (links | edit)
- Waardenburg syndrome (transclusion) (links | edit)
- Homocystinuria (transclusion) (links | edit)
- Cystinuria (transclusion) (links | edit)
- Ornithine transcarbamylase deficiency (transclusion) (links | edit)
- Inborn errors of metabolism (transclusion) (links | edit)
- Trimethylaminuria (transclusion) (links | edit)
- Isovaleric acidemia (transclusion) (links | edit)
- Maple syrup urine disease (transclusion) (links | edit)
- Cystinosis (transclusion) (links | edit)
- Citrullinemia (transclusion) (links | edit)
- Beta-ketothiolase deficiency (transclusion) (links | edit)
- 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency (transclusion) (links | edit)
- Tyrosinemia (transclusion) (links | edit)
- Hartnup disease (transclusion) (links | edit)
- Glutaric aciduria type 1 (transclusion) (links | edit)
- Saccharopinuria (transclusion) (links | edit)
- Ochronosis (transclusion) (links | edit)
- Lysinuric protein intolerance (transclusion) (links | edit)
- Hyperlysinemia (transclusion) (links | edit)
- Tetrahydrobiopterin deficiency (transclusion) (links | edit)
- Hermansky–Pudlak syndrome (transclusion) (links | edit)
- Argininosuccinic aciduria (transclusion) (links | edit)
- Oculocutaneous albinism (transclusion) (links | edit)
- Glutaric acidemia type 2 (transclusion) (links | edit)
- List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders (transclusion) (links | edit)
- 2-Hydroxyglutaric aciduria (transclusion) (links | edit)
- 3-Methylglutaconic aciduria (transclusion) (links | edit)
- 6-Pyruvoyltetrahydropterin synthase deficiency (transclusion) (links | edit)
- 3-Methylcrotonyl-CoA carboxylase deficiency (transclusion) (links | edit)
- Methylmalonyl-CoA mutase deficiency (transclusion) (links | edit)
- Glycine encephalopathy (transclusion) (links | edit)
- Hawkinsinuria (transclusion) (links | edit)
- Fumarase deficiency (transclusion) (links | edit)
- Aminoaciduria (transclusion) (links | edit)
- Oculocerebrorenal syndrome (transclusion) (links | edit)
- 2-Methylbutyryl-CoA dehydrogenase deficiency (transclusion) (links | edit)
- Histidinemia (transclusion) (links | edit)
- Succinic semialdehyde dehydrogenase deficiency (transclusion) (links | edit)
- N-Acetylglutamate synthase deficiency (transclusion) (links | edit)
- Hyperhomocysteinemia (transclusion) (links | edit)
- Isobutyryl-coenzyme A dehydrogenase deficiency (transclusion) (links | edit)
- Carbamoyl phosphate synthetase I deficiency (transclusion) (links | edit)
- Ethylmalonic encephalopathy (transclusion) (links | edit)
- Sarcosinemia (transclusion) (links | edit)
- Ornithine translocase deficiency (transclusion) (links | edit)