Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Epidural supratentorial pyogenic abscess |
Is a |
True |
Inflammatory disease of the central nervous system |
Inferred relationship |
Some |
|
Multiple intracranial pyogenic abscesses |
Is a |
False |
Inflammatory disease of the central nervous system |
Inferred relationship |
Some |
|
Tuberculous abscess of brain |
Is a |
False |
Inflammatory disease of the central nervous system |
Inferred relationship |
Some |
|
Multiple sclerosis |
Is a |
True |
Inflammatory disease of the central nervous system |
Inferred relationship |
Some |
|
Extradural infratentorial pyogenic abscess |
Is a |
True |
Inflammatory disease of the central nervous system |
Inferred relationship |
Some |
|
Tuberculous abscess of epidural space (disorder) |
Is a |
False |
Inflammatory disease of the central nervous system |
Inferred relationship |
Some |
|
Phlebitis of lateral venous sinus |
Is a |
True |
Inflammatory disease of the central nervous system |
Inferred relationship |
Some |
|
Granuloma of brain caused by Schistosoma mansoni (disorder) |
Is a |
True |
Inflammatory disease of the central nervous system |
Inferred relationship |
Some |
|
Granuloma of brain caused by Schistosoma haematobium |
Is a |
True |
Inflammatory disease of the central nervous system |
Inferred relationship |
Some |
|
Granuloma of brain caused by Schistosoma japonicum (disorder) |
Is a |
True |
Inflammatory disease of the central nervous system |
Inferred relationship |
Some |
|
Parasitic infection of central nervous system |
Is a |
False |
Inflammatory disease of the central nervous system |
Inferred relationship |
Some |
|
Encephalopathy with sepsis |
Is a |
True |
Inflammatory disease of the central nervous system |
Inferred relationship |
Some |
|
Myelin oligodendrocyte glycoprotein antibody-associated disease |
Is a |
True |
Inflammatory disease of the central nervous system |
Inferred relationship |
Some |
|
Chronic inflammatory demyelinating disease of peripheral nervous system and central nervous system (disorder) |
Is a |
True |
Inflammatory disease of the central nervous system |
Inferred relationship |
Some |
|
Limbic encephalitis |
Is a |
True |
Inflammatory disease of the central nervous system |
Inferred relationship |
Some |
|
Hypophysitis |
Is a |
True |
Inflammatory disease of the central nervous system |
Inferred relationship |
Some |
|
A rare, potentially fatal, epileptic encephalopathy characterized by explosive-onset of recurrent multifocal and bilateral tonic-clonic seizures following an unspecific febrile illness. The syndrome develops without a clear acute structural, toxic or metabolic cause, in a patient without previous epilepsy. FIRES is a subgroup of new-onset refractory status epilepticus (NORSE) and requires a preceding febrile infection as a mandatory feature. |
Is a |
True |
Inflammatory disease of the central nervous system |
Inferred relationship |
Some |
|
Cerebral sarcoidosis |
Is a |
True |
Inflammatory disease of the central nervous system |
Inferred relationship |
Some |
|
Cerebral pyogenic abscess |
Is a |
True |
Inflammatory disease of the central nervous system |
Inferred relationship |
Some |
|
Cerebellar pyogenic abscess |
Is a |
True |
Inflammatory disease of the central nervous system |
Inferred relationship |
Some |
|
Granuloma of cerebral hemispheric lobe (disorder) |
Is a |
True |
Inflammatory disease of the central nervous system |
Inferred relationship |
Some |
|
A rare neurologic disease characterized by a rapid onset of seizures, an altered state of consciousness, neurologic decline, and variable degrees of hepatic dysfunction following a respiratory or gastrointestinal infection (e.g. mycoplasma, influenza virus) in a previously healthy child. Brain MRI of patients reveals bilateral, multiple, symmetrical lesions predominantly observed in thalami and brainstem, but also in periventricular white matter and cerebellum in some cases. |
Is a |
True |
Inflammatory disease of the central nervous system |
Inferred relationship |
Some |
|
Cerebellar granuloma |
Is a |
True |
Inflammatory disease of the central nervous system |
Inferred relationship |
Some |
|
Autoimmune inflammation of cerebellum (disorder) |
Is a |
True |
Inflammatory disease of the central nervous system |
Inferred relationship |
Some |
|
Brainstem pyogenic abscess |
Is a |
True |
Inflammatory disease of the central nervous system |
Inferred relationship |
Some |
|
Granuloma of brainstem (disorder) |
Is a |
True |
Inflammatory disease of the central nervous system |
Inferred relationship |
Some |
|
Brown-Séquard syndrome due to multiple sclerosis |
Is a |
True |
Inflammatory disease of the central nervous system |
Inferred relationship |
Some |
|
A rare cerebellar ataxia characterized by cerebellar inflammation caused by viral or bacterial infection-triggered, immune-mediated mechanisms. It mainly affects young children following an episode of usually viral infection (notably varicella), but sometimes also adults, mostly upon Epstein-Barr virus or mycoplasma infection. Affected individuals mainly present with acute-onset afebrile gait ataxia, meningeal signs, high intracranial pressure with or without extracerebellar manifestations (such as clouding of consciousness, seizures and altered mental status) or extracerebellar focal signs. Mild behavioral changes can also be present. Pleocytosis in cerebrospinal fluid is reported in the majority of the patients. |
Is a |
True |
Inflammatory disease of the central nervous system |
Inferred relationship |
Some |
|