| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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://www.omim.org/entry/300100 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the adrenoleukodystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| ABCD1 | ATP-binding cassette, sub-family D (ALD), member 1 |
