Adrenoleukodystrophy Gene Set

Dataset ClinVar Gene-Phenotype 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
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Genes

2 genes associated with the Adrenoleukodystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
ABCD1 ATP-binding cassette, sub-family D (ALD), member 1
BCAP31 B-cell receptor-associated protein 31