methylmalonyl-coa mutase
81Beta-ketothiolase deficiency — Classification and external resources Isoleucine OMIM 203750 …
82Ochronosis — Classification and external resources Homogentisic acid ICD 10 E …
83Lysinuric protein intolerance — Classification and external resources Lysine ICD 10 E …
84Oculocutaneous albinism — Classification and external resources ICD 10 E70.3 ICD 9 270.2 …
85Glutaric acidemia type 2 — Classification and external resources Glutaric acid ICD 10 E …
86Fanconi syndrome — Not to be confused with Fanconi anemia. Fanconi syndrome Classification and external resources ICD 10 E72.0 ICD 9 …
872-Hydroxyglutaric aciduria — Classification and external resources Alpha Hydroxyglutaric acid OMIM 600721 …
88D-Glyceric acidemia — Classification and external resources OMIM 220120 D Glyceric Acidemia (a.k.a. D Glyceric Aciduria) is an inherited disease, in the category of inborn errors of metabolism. It is caused by a mutation in the gene GLYCTK, which encodes the for the… …
89Oculocerebrorenal syndrome — Classification and external resources ICD 10 E72.0 ICD 9 270.8 …
90Glutathione synthetase deficiency — Classification and external resources Glutathione OMIM 266130 …