| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | A leukodystrophy that disrupts the breakdown of very-long-chain fatty acids resulting in progressive brain damage, failure of the adrenal glands and eventually death. (Human Disease Ontology, DOID_10588) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:D000326 |
| Similar Terms | |
| Downloads & Tools |
6 genes/proteins associated with the disease Adrenoleukodystrophy from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| SOD2 | superoxide dismutase 2, mitochondrial | 2.88009 |
| HMOX1 | heme oxygenase 1 | 2.88009 |
| ABCD1 | ATP-binding cassette, sub-family D (ALD), member 1 | 2.88009 |
| IFNG | interferon, gamma | 2.88009 |
| PEX26 | peroxisomal biogenesis factor 26 | 2.88009 |
| PEX13 | peroxisomal biogenesis factor 13 | 2.88009 |
