adrenoleukodystrophy Gene Set

Dataset	GeneRIF Biological Term Annotations
Category	structural or functional annotations
Type	biological term
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)
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Genes

13 genes co-occuring with the biological term adrenoleukodystrophy in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Symbol	Name
ABCD1	ATP-binding cassette, sub-family D (ALD), member 1
ABCD2	ATP-binding cassette, sub-family D (ALD), member 2
ABCD3	ATP-binding cassette, sub-family D (ALD), member 3
ABCD4	ATP-binding cassette, sub-family D (ALD), member 4
ACSBG1	acyl-CoA synthetase bubblegum family member 1
ACSBG2	acyl-CoA synthetase bubblegum family member 2
BCAP31	B-cell receptor-associated protein 31
CBS	cystathionine-beta-synthase
CHIT1	chitinase 1 (chitotriosidase)
EIF2B2	eukaryotic translation initiation factor 2B, subunit 2 beta, 39kDa
F8	coagulation factor VIII, procoagulant component
PEX12	peroxisomal biogenesis factor 12
PEX19	peroxisomal biogenesis factor 19