1217383007: RELA fusion-positive supratentorial ependymoma (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Head finding (finding)\Mass of head (finding)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Head finding (finding)\Mass of head (finding)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Head finding (finding)\Mass of head (finding)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Head finding (finding)\Mass of head (finding)\Intracranial mass\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Head finding (finding)\Mass of head (finding)\Intracranial mass\Mass lesion of brain (finding)\Neoplasm of brain\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Head finding (finding)\Mass of head (finding)\Intracranial mass\Mass lesion of brain (finding)\Neoplasm of brain\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Head finding (finding)\Mass of head (finding)\Intracranial mass\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Head finding (finding)\Mass of head (finding)\Intracranial mass\Intracranial neoplasm\Neoplasm of brain\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Head finding (finding)\Mass of head (finding)\Intracranial mass\Intracranial neoplasm\Neoplasm of brain\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Head finding (finding)\Finding of brain\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Head finding (finding)\Finding of brain\Mass lesion of brain (finding)\Neoplasm of brain\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Head finding (finding)\Finding of brain\Mass lesion of brain (finding)\Neoplasm of brain\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Head finding (finding)\Finding of brain\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Head finding (finding)\Finding of brain\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Head finding (finding)\Finding of brain\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Head finding (finding)\Disorder of head (disorder)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Head finding (finding)\Disorder of head (disorder)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Head finding (finding)\Disorder of head (disorder)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.

\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Intracranial mass\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Intracranial mass\Mass lesion of brain (finding)\Neoplasm of brain\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Intracranial mass\Mass lesion of brain (finding)\Neoplasm of brain\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Intracranial mass\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Intracranial mass\Intracranial neoplasm\Neoplasm of brain\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Intracranial mass\Intracranial neoplasm\Neoplasm of brain\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Neoplasm of head and neck\Malignant neoplasm of head and/or neck (disorder)\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Neoplasm of head and neck\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Neoplasm of head and neck\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Neoplasm of head and neck\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Mass of body structure\Space-occupying lesion of nervous system\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Mass of body structure\Space-occupying lesion of nervous system\Mass lesion of brain (finding)\Neoplasm of brain\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Mass of body structure\Space-occupying lesion of nervous system\Mass lesion of brain (finding)\Neoplasm of brain\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant glioma of central nervous system\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Glioma of central nervous system (disorder)\Ependymoma of central nervous system (disorder)\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Glioma of central nervous system (disorder)\Malignant glioma of central nervous system\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Glioma of central nervous system (disorder)\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Glioma of central nervous system (disorder)\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant glioma of central nervous system\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.

\Neurological lesion\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Neurological lesion\Lesion of brain\Neoplasm of brain\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Neurological lesion\Lesion of brain\Neoplasm of brain\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Neurological lesion\Space-occupying lesion of nervous system\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Neurological lesion\Space-occupying lesion of nervous system\Mass lesion of brain (finding)\Neoplasm of brain\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Neurological lesion\Space-occupying lesion of nervous system\Mass lesion of brain (finding)\Neoplasm of brain\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant glioma of central nervous system\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Glioma of central nervous system (disorder)\Ependymoma of central nervous system (disorder)\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Glioma of central nervous system (disorder)\Malignant glioma of central nervous system\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Glioma of central nervous system (disorder)\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Glioma of central nervous system (disorder)\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant glioma of central nervous system\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.

\Central nervous system finding\Finding of brain\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Central nervous system finding\Finding of brain\Mass lesion of brain (finding)\Neoplasm of brain\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Central nervous system finding\Finding of brain\Mass lesion of brain (finding)\Neoplasm of brain\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Central nervous system finding\Finding of brain\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Central nervous system finding\Finding of brain\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Central nervous system finding\Finding of brain\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Glioma of central nervous system (disorder)\Ependymoma of central nervous system (disorder)\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Glioma of central nervous system (disorder)\Malignant glioma of central nervous system\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Glioma of central nervous system (disorder)\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Glioma of central nervous system (disorder)\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant glioma of central nervous system\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Neoplasm of brain\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Neoplasm of brain\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.

\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Glioma\Glioma of central nervous system (disorder)\Ependymoma of central nervous system (disorder)\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Glioma\Glioma of central nervous system (disorder)\Malignant glioma of central nervous system\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Glioma\Glioma of central nervous system (disorder)\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Glioma\Glioma of central nervous system (disorder)\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Glioma\Ependymoma (disorder)\Ependymoma of central nervous system (disorder)\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Malignant neoplastic disease (disorder)\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant glioma of central nervous system\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Malignant neoplastic disease (disorder)\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Malignant neoplastic disease (disorder)\Malignant neoplasm of head and/or neck (disorder)\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of head and neck\Malignant neoplasm of head and/or neck (disorder)\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of head and neck\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of head and neck\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of head and neck\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant glioma of central nervous system\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Neoplasm of central nervous system\Glioma of central nervous system (disorder)\Ependymoma of central nervous system (disorder)\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Neoplasm of central nervous system\Glioma of central nervous system (disorder)\Malignant glioma of central nervous system\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Neoplasm of central nervous system\Glioma of central nervous system (disorder)\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Neoplasm of central nervous system\Glioma of central nervous system (disorder)\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant glioma of central nervous system\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant glioma of central nervous system\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Neoplasm of central nervous system\Glioma of central nervous system (disorder)\Ependymoma of central nervous system (disorder)\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Neoplasm of central nervous system\Glioma of central nervous system (disorder)\Malignant glioma of central nervous system\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Neoplasm of central nervous system\Glioma of central nervous system (disorder)\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Neoplasm of central nervous system\Glioma of central nervous system (disorder)\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant glioma of central nervous system\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Glioma of central nervous system (disorder)\Ependymoma of central nervous system (disorder)\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Glioma of central nervous system (disorder)\Malignant glioma of central nervous system\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Glioma of central nervous system (disorder)\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Glioma of central nervous system (disorder)\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant glioma of central nervous system\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Neoplasm of brain\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Neoplasm of brain\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Disorder of head (disorder)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Disorder of head (disorder)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Disorder of head (disorder)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Disorder of head (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Disorder of head (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Glial tumor of brain\Malignant glioma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.
\Disease\Disorder of head (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Glial tumor of brain\Ependymoma of brain\A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Apr 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

5036103017 A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

5036104011 A rare ependymal tumour characterised by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

5036100019 RELA fusion-positive supratentorial ependymoma (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

5036102010 RELA fusion-positive supratentorial ependymoma en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

7753801000241110 épendymome supratentoriel avec fusion RELA (RELA proto-oncogene, NF-kB subunit) fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

3392831001000115 RELA-Fusion-positives Ependymom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.	Is a	Ependymoma of central nervous system (disorder)	false	Inferred relationship	Some
A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.	Is a	Malignant glioma of central nervous system	false	Inferred relationship	Some
A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.	Is a	Primary malignant neoplasm of brain	false	Inferred relationship	Some
A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.	Finding site	Supratentorial brain	true	Inferred relationship	Some	1
A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.	Associated morphology	RELA fusion-positive ependymoma (morphologic abnormality)	true	Inferred relationship	Some	1
A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.	Is a	Malignant neoplasm of brain (disorder)	false	Inferred relationship	Some
A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.	Is a	Ependymoma of brain	true	Inferred relationship	Some
A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.	Is a	Malignant glioma of brain	true	Inferred relationship	Some

Inbound Relationships

Type

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Refinability

Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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Id	Description	Lang	Type	Status	Case?	Module
5036103017	A rare ependymal tumor characterized by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5036104011	A rare ependymal tumour characterised by the presence of a RELA fusion gene. This supratentorial grade II or III ependymoma most often occurs in children and young adults. Histopathological features are variable, but a distinctive vascular pattern of branching capillaries or clear-cell change are common. Patients may present with focal neurological deficits, seizures, or features of raised intracranial pressure. Prognosis is worse than in other supratentorial ependymomas.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5036100019	RELA fusion-positive supratentorial ependymoma (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5036102010	RELA fusion-positive supratentorial ependymoma	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
7753801000241110	épendymome supratentoriel avec fusion RELA (RELA proto-oncogene, NF-kB subunit)	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3392831001000115	RELA-Fusion-positives Ependymom	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module