Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Glioma of spinal cord |
Is a |
True |
Glioma of central nervous system (disorder) |
Inferred relationship |
Some |
|
Malignant glioma of central nervous system |
Is a |
True |
Glioma of central nervous system (disorder) |
Inferred relationship |
Some |
|
Glial tumor of brain |
Is a |
True |
Glioma of central nervous system (disorder) |
Inferred relationship |
Some |
|
Optic nerve glioma |
Is a |
True |
Glioma of central nervous system (disorder) |
Inferred relationship |
Some |
|
Chiasmal glioma (disorder) |
Is a |
False |
Glioma of central nervous system (disorder) |
Inferred relationship |
Some |
|
Optic nerve glioma of orbit (disorder) |
Is a |
False |
Glioma of central nervous system (disorder) |
Inferred relationship |
Some |
|
Benign papilloma of choroid plexus (disorder) |
Is a |
False |
Glioma of central nervous system (disorder) |
Inferred relationship |
Some |
|
Pilocytic astrocytoma is a rare subtype of low-grade glioma of the central nervous system characterized by a well circumscribed, often cystic, brain tumor with a discrete mural nodule and long, hair-like projections that extend from the neoplastic astrocytes. Depending on the primary localization and the size of the tumor, patients can present with signs of raised intracranial pressure (headache, vomiting, papilledema), blurred vision, decreased visual acuity, ataxia and/or nystagmus, among others. It is most commonly located in the cerebellum, but occurrence in the hypothalamus, brain stem, optic chiasma, and hemispheres has also been reported. |
Is a |
True |
Glioma of central nervous system (disorder) |
Inferred relationship |
Some |
|
Ependymoma of central nervous system (disorder) |
Is a |
True |
Glioma of central nervous system (disorder) |
Inferred relationship |
Some |
|
Desmoplastic infantile astrocytoma/ganglioglioma are mixed neuronal-glial tumors representing a histological spectrum of the same tumor. They are usually supratentorially located, large, cystic masses with a peripheral solid component, characterized by prominent desmoplastic stroma and pleomorphic populations of neoplastic cells with either astrocytic or ganglionic differentiation and poorly differentiated cells in variable proportions. They usually present in the first 18 months of age with rapid head growth, bulging anterior fontanel and bone structures over the tumor, signs of raised intracranial pressure (headache, vomiting, papilledema), focal neurological signs and sometimes seizures. |
Is a |
False |
Glioma of central nervous system (disorder) |
Inferred relationship |
Some |
|
An extremely rare slow-growing glial neoplasm of the central nervous system, usually arising in a superficial location in the cerebrum, affecting all ages and both sexes, and characterized by intractable seizures and headaches, with most cases being cured by surgical incision alone and therefore having a good prognosis. |
Is a |
True |
Glioma of central nervous system (disorder) |
Inferred relationship |
Some |
|
A very rare type of choroid plexus tumor that, contrary to papilloma of the choroid plexus, has an increased likelihood of progression to carcinoma and of recurrence. It displays brisk mitoses, nuclear pleomorphism, raised cellular density, obscurity of the papillary growth pattern, and cell necrosis. |
Is a |
False |
Glioma of central nervous system (disorder) |
Inferred relationship |
Some |
|
Dysembryoplastic neuroepithelial neoplasm of brain |
Is a |
False |
Glioma of central nervous system (disorder) |
Inferred relationship |
Some |
|