meningioma Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A central nervous system cancer that are manifested in the central nervous system and arise from the arachnoid cap cells of the arachnoid villi in the meninges. (Human Disease Ontology, DOID_3565)
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1 genes associated with the meningioma phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
MN1 meningioma (disrupted in balanced translocation) 1