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Ontology Browser

Parent Terms Term With Siblings Child Terms
angiomatous meningioma 
benign meningioma 
bilateral meningioma of optic nerve 
Birt-Hogg-Dube syndrome  
brain meningioma +  
Brooke-Spiegler syndrome  
Capillary Hemangioma, Infantile  
cavernous sinus meningioma 
cerebellopontine angle meningioma 
choroid plexus meningioma 
clear cell meningioma +  
Diaphyseal Medullary Stenosis with Malignant Fibrous Histiocytoma  
dysplastic nevus syndrome +   
ethmoid sinus ectopic meningioma 
familial adenomatous polyposis +   
Familial Cancer with In Vitro Radioresistance 
familial chronic myelocytic leukemia-like syndrome  
Familial Cutaneous Collagenoma  
familial meningioma +   
Familial Multiple Trichodiscomas 
fibrous meningioma 
foramen magnum meningioma +  
Gasserian ganglion meningioma 
hereditary breast ovarian cancer syndrome  
Hereditary Leiomyomatosis and Renal Cell Cancer  
hereditary multiple exostoses +   
Hereditary Paraganglioma-Pheochromocytoma Syndromes  
Hunter-Macdonald Syndrome 
internal auditory canal meningioma 
intraorbital meningioma 
juvenile polyposis syndrome +   
Li-Fraumeni syndrome +   
lung meningioma 
lymphoplasmacyte-rich meningioma 
Lynch syndrome +   
malignant leptomeningeal tumor +  
Melanoma-Pancreatic Cancer Syndrome  
meninges hemangiopericytoma 
meninges sarcoma +  
meningothelial meningioma 
microcystic meningioma 
Multiple Endocrine Neoplasia +   
Multiple Hamartoma Syndrome +   
nephroblastoma +   
neurofibromatosis +   
nevoid basal cell carcinoma syndrome +   
Paragangliomas 2  
Paragangliomas 3  
parapharyngeal meningioma 
pediatric meningioma +  
periocular meningioma 
petrous apex meningioma 
Peutz-Jeghers syndrome  
pituitary stalk meningioma 
posterior cranial fossa meningioma +  
psammomatous meningioma 
Radiation Induced Meningioma 
rhabdoid meningioma +  
secretory meningioma 
skin meningioma 
skull base meningioma +  
spinal canal and spinal cord meningioma +  
spinal meningioma 
suprasellar meningioma 
transitional meningioma 
tuberous sclerosis +   
Turcot Syndrome  

Primary IDs: MESH:C537443 ;   RDO:0003286
Alternate IDs: OMIM:607174
Xrefs: NCI:C5301

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.