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