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
Basic Information
Medical Symptom
Gene & Mutation
Drugs
Disease Model
References
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
Basic Information
Inheritance
Age Of Onset
Prevalence
Related Gene
Related Models
Reference
MALACARDS
AD
All ages
1-9/100000
13
195
62
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available
Gene & Mutation
#
Gene
Function
Score
Count
No data available
Drugs
Name
CAS Number
Status
Phase
No data available
Disease Model
Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available
References
Title
PMID
Journal
Year
IF
No Data Found!
Comparison
Al agent
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