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meningioma

Disease Summary
Associated Targets (19)
Tbio

15

Tclin

3

Tchem

1


GARD Rare
Mondo Description A generally slow growing tumor attached to the dura mater. It is composed of neoplastic meningothelial (arachnoidal) cells. It typically occurs in adults, often women and it has a wide range of histopathological appearances. Of the various subtypes, meningothelial, fibrous and transitional meningiomas are the most common. Most meningiomas are WHO grade I tumors, and some are WHO grade II or III tumors. Most subtypes share a common clinical behavior, although some subtypes are more likely to recur and follow a more aggressive clinical course. (Adapted from WHO)
Uniprot Description A common neoplasm of the central nervous system derived from arachnoidal cells. The majority of meningiomas are well differentiated vascular tumors which grow slowly and have a low potential to be invasive, although malignant subtypes occur. Most cases are sporadic. Familial occurrence of meningioma is rare.
Disease Ontology 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.
Mondo Term and Equivalent IDs
MONDO:0016642:  meningioma
GARD:0007015: 
MESH:D008579: 
NCIT:C3230: 
ONCOTREE:MNG: 
Orphanet:2495: 
SCTID:302820008: 
UMLS:C0025286: