cystinuria
81Medical genetics — Clinical genetics redirects here. For the journal, see Clinical Genetics (journal). For a non technical introduction to the topic, see Introduction to Genetics. Part of a series on Genetics Key components Chromosome …
82Oculocutaneous albinism — Classification and external resources ICD 10 E70.3 ICD 9 270.2 …
83Glutaric acidemia type 2 — Classification and external resources Glutaric acid ICD 10 E …
84Cysteamine — Cysteamine …
85Fanconi syndrome — Not to be confused with Fanconi anemia. Fanconi syndrome Classification and external resources ICD 10 E72.0 ICD 9 …
862-Hydroxyglutaric aciduria — Classification and external resources Alpha Hydroxyglutaric acid OMIM 600721 …
873-Methylglutaconic aciduria — Classification and external resources 3 methylglutaconic acid DiseasesDB …
883-Methylcrotonyl-CoA carboxylase deficiency — Classification and external resources Methylcrotonyl CoA OMIM 210200 …
89Methylmalonyl-CoA mutase deficiency — Classification and external resources OMIM 251000 DiseasesDB 29509 Methylmalonyl CoA mutase deficiency ( MUT ) is an inborn error of organ …
90D-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… …