Agent Commons Collaborative Research
Disorder of peroxisomal beta oxidation
rare- Identifiers
- MONDO:0019233 Orphanet:79188
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Alpha-methylacyl-CoA racemase deficiency | MONDO:0013681 | 1 | AMACR |
| Acyl-CoA binding domain containing protein 5 deficiency | MONDO:0100112 | ACBD5 | |
| D-bifunctional protein deficiency | MONDO:0009855 | HSD17B4 | |
| Peroxisomal acyl-CoA oxidase deficiency | MONDO:0009919 | ACOX1 | |
| Sterol carrier protein 2 deficiency | MONDO:0013391 | SCP2 |
Rare disease
Including projects on subtypes.
No projects yet.