Searched for "Amino Acid Metabolism, Inborn Errors".
31
results
found
on Genetics Home Reference.
Showing results 1 to 20.
- isobutyryl-CoA dehydrogenase deficiency condition summary
Related classification: Amino Acid Metabolism, Inborn Errors
- 2-methylbutyryl-CoA dehydrogenase deficiency condition summary
Related classification: Amino Acid Metabolism, Inborn Errors
- 3-hydroxy-3-methylglutaryl-CoA lyase deficiency condition summary
Related classification: Amino Acid Metabolism, Inborn Errors
- alkaptonuria condition summary
Related classification: Amino Acid Metabolism, Inborn Errors
- arginase deficiency condition summary
Related classification: Amino Acid Metabolism, Inborn Errors
- argininosuccinic aciduria condition summary
Related classification: Amino Acid Metabolism, Inborn Errors
- biotinidase deficiency condition summary
Related classification: Amino Acid Metabolism, Inborn Errors
- carbamoyl phosphate synthetase I deficiency condition summary
Related classification: Amino Acid Metabolism, Inborn Errors
- citrullinemia condition summary
Related classification: Amino Acid Metabolism, Inborn Errors
- glutaric acidemia type I condition summary
Related classification: Amino Acid Metabolism, Inborn Errors
- glycine encephalopathy condition summary
Related classification: Amino Acid Metabolism, Inborn Errors
- histidinemia condition summary
Related classification: Amino Acid Metabolism, Inborn Errors
- Hermansky-Pudlak syndrome condition summary
Related classification: Amino Acid Metabolism, Inborn Errors
- holocarboxylase synthetase deficiency condition summary
Related classification: Amino Acid Metabolism, Inborn Errors
- homocystinuria condition summary
Related classification: Amino Acid Metabolism, Inborn Errors
- hyperlysinemia condition summary
Related classification: Amino Acid Metabolism, Inborn Errors
- hypermethioninemia condition summary
Related classification: Amino Acid Metabolism, Inborn Errors
- hyperprolinemia condition summary
Related classification: Amino Acid Metabolism, Inborn Errors
- isovaleric acidemia condition summary
Related classification: Amino Acid Metabolism, Inborn Errors
- maple syrup urine disease condition summary
Related classification: Amino Acid Metabolism, Inborn Errors