Meningioma, Familial (MNGMA)

Alias:

Meningioma

Familial Meningioma

Meningioma, Familial, Susceptibility to

Meningeal Neoplasms

Meningeal Neoplasm

Meningiomas

Meningothelial Sarcoma of Unspecified Site

Meningeal Sarcoma of Unspecified Site

Meningioma, Benign, No Icd-O Subtype

Primary Neoplasm of Spinal Meninges

Meningioma, Nf2-Related, Somatic

Familial Multiple Meningioma

Meningothelial Cell Neoplasm

Supratentorial Meningioma

Meningothelial Cell Tumor

Neoplasm of the Meninges

Meningioma, Sis-Related

Intracranial Meningioma

Primary Meningeal Tumor

Meningeal Tumours

Mngma

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Meningioma, Familial, also known as meningioma, is related to spinal meningioma and intracranial meningioma, and has symptoms including headache and seizures. An important gene associated with Meningioma, Familial is SMARCE1 (SWI/SNF Related, Matrix Associated, Actin Dependent Regulator Of Chromatin, Subfamily E, Member 1), and among its related pathways/superpathways are Signal Transduction and PI3K-Akt signaling pathway. The drugs Cytarabine and Methotrexate have been mentioned in the context of this disorder. Affiliated tissues include brain and spinal cord, and related phenotypes are chromosomal breakage induced by ionizing radiation and increased sensitivity to ionizing radiation

Related ID：

MALACARDS：MNN043

OMIM：607174

MESH：C537443

ICD11：1478862889