Alexander Disease Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A leukodystrophy that is characterized by the destruction of white matter and the formation of Rosenthal fibers consisting of abnormal clumps of protein that accumulate in astrocytes. (Human Disease Ontology, DOID_4252)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D038261
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Genes

2 genes/proteins associated with the disease Alexander Disease from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
GFAP glial fibrillary acidic protein 2.88009
NDUFV1 NADH dehydrogenase (ubiquinone) flavoprotein 1, 51kDa 2.88009