A malignant form of astrocytoma histologically characterized by pleomorphism of cells, nuclear atypia, microhemorrhage, and necrosis. They may arise in any region of the central nervous system, with a predilection for the cerebral hemispheres, basal ganglia, and commissural pathways. Clinical presentation most frequently occurs in the fifth or sixth decade of life with focal neurologic signs or seizures (MeSH).
Disease Interacts with Genes
Disease Interacts with Substances
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Processes Associated With Disease
Molecular Function Associated With Disease
Biological Processes Associated With Disease
Pathways Associated With Disease