Rare Disease
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
Neuronal diseases
Endocrine diseases
Basic Information
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
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MALACARD
Medical Symptom
Even among those with the same illness, each patient's condition and symptoms are unique. To provide patient-centered medical care, medical professionals must carefully evaluate individual differences between patients. This involves thorough assessment of medical details when diagnosing and developing treatment plans. To achieve personalized and maximally effective care, practitioners refer to the latest research and standards of care to tailor treatment strategies for each patient.
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Categorization
Description
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Gene & Mutation
Diseases are frequently associated with anomalies or mutations in certain genes. These genes and mutations can disrupt cellular functioning and induce physiological imbalances, resulting in illnesses. In-depth research on illness genes and mutations can help us better understand disease etiology and give new ideas and approaches for disease prevention, diagnosis, and therapy.
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Gene
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Drugs
Gene target medications are a novel form of treatment that can alter genes or proteins while also blocking disease processes. It precisely detects and chooses target proteins in order to induce therapeutic effects. Target medications are categorized into several groups based on disease causes and molecular foundation, and numerous ways are employed to treat illnesses.
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Disease Model
The mouse disease model refers to the manipulation of the mouse genome through gene editing and other techniques, enabling it to carry a specific disease gene or lack an important gene. This provides an experimental platform for researching the mechanism of disease occurrence, drug development, and treatment efficacy.
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MGI
Related Gene
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References
Disease literature reviews provide a wide spectrum of research findings and clinical data, giving vital information for our comprehensive understanding of illnesses. By researching this material, we may gain a better understanding of the illness's pathophysiology and treatment strategies, as well as give a scientific foundation for disease prevention and management.
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BioGPT