Diseases

Meningioma

meningioma

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Entity Type: Diseases
Relation Groups: 2
Relation Preview: 16

Basic Information

Grouped by core information, identifiers, and descriptions.

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Core Information

Disease Name: Meningioma
Standard Disease Name: meningioma
MeSH Tree: No data
ICD-10: D32.9

Identifiers

DO ID: No data
MeSH ID: D008579
OMIM ID: MTHU003590|601728|190040|MTHU036996
UMLS ID: C0025286
HPO ID: No data

Description and Extensions

Description: NCI2016_NICHD_1602D:A usually benign tumor that develops in the meninges.|NCI2016_NCI-GLOSS_1602D:A type of slow-growing tumor that forms in the meninges (thin layers of tissue that cover and protect the brain and spinal cord). Meningiomas usually occur in adults.|NCI2016_CDISC_1602D:A neoplasm of the meninges, for which the status of malignancy has not been determined.|NCI2016_02D: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)|MSH2017_2016_08_12:A relatively common neoplasm of the CENTRAL NERVOUS SYSTEM that arises from arachnoidal cells. The majority are well differentiated vascular tumors which grow slowly and have a low potential to be invasive, although malignant subtypes occur. Meningiomas have a predilection to arise from the parasagittal region, cerebral convexity, sphenoidal ridge, olfactory groove, and SPINAL CANAL. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2056-7)|HPO2016_07_04:The presence of a meningioma, i.e., a benign tumor originating from the dura mater or arachnoid mater. [HPO:probinson]|CSP2006:relatively common neoplasm of the central nervous system that arises from arachnoidal cells; the majority are well differentiated vascular tumors which grow slowly and have a low potential to be invasive, although malignant subtypes occur; they have a predilection to arise from the parasagittal region, cerebral convexity, sphenoidal ridge, olfactory groove, and spinal canal.|CHV2011_02:tumor of the membranes that cover and protect the brain and spinal cord|CHV2011_02:tumor of the membranes that cover and protect the brain and spinal cord|CHV2011_02:tumor of the membranes that cover and protect the brain and spinal cord|CHV2011_02:tumor of the membranes that cover and protect the brain and spinal cord|CHV2011_02:tumor of the membranes that cover and protect the brain and spinal cord|CHV2011_02:tumor of the membranes that cover and protect the brain and spinal cord|CHV2011_02:tumor of the membranes that cover and protect the brain and spinal cord

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