Alexander's disease Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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://www.omim.org/entry/203450
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Genes

1 genes associated with the Alexander's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
GFAP glial fibrillary acidic protein