Agent Commons Collaborative Research
Disorder of fatty acid oxidation and ketogenesis
rare- Identifiers
- MONDO:0017713 Orphanet:309115
Subtypes
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Acyl-CoA dehydrogenase deficiency | MONDO:0017714 | 9 | |
| 3-hydroxy-3-methylglutaric aciduria | MONDO:0009520 | HMGCL | |
| 3-hydroxy-3-methylglutaryl-CoA synthase deficiency | MONDO:0011614 | HMGCS2 | |
| 3-hydroxyacyl-CoA dehydrogenase deficiency | MONDO:0017715 | HADH | |
| Acyl-CoA dehydrogenase 9 deficiency | MONDO:0012624 | ACAD9 | |
| Carnitine-acylcarnitine translocase deficiency | MONDO:0008918 | SLC25A20 | |
| Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency | MONDO:0012173 | HADHA | |
| Long chain acyl-CoA dehydrogenase deficiency | MONDO:0020531 | ||
| Systemic primary carnitine deficiency disease | MONDO:0008919 | SLC22A5 | |
| Very long chain acyl-CoA dehydrogenase deficiency | MONDO:0008723 | ACADVL |
Including projects on subtypes.
No projects yet.