Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Allergic encephalitis |
Is a |
False |
Autoimmune encephalitis |
Inferred relationship |
Some |
|
Acute hemorrhagic leukoencephalitis |
Is a |
False |
Autoimmune encephalitis |
Inferred relationship |
Some |
|
Systemic lupus erythematosus encephalitis |
Is a |
True |
Autoimmune encephalitis |
Inferred relationship |
Some |
|
Autoimmune hypophysitis |
Is a |
False |
Autoimmune encephalitis |
Inferred relationship |
Some |
|
Acute disseminated encephalomyelitis |
Is a |
True |
Autoimmune encephalitis |
Inferred relationship |
Some |
|
Limbic encephalitis with contactin-associated protein-like 2 antibodies (disorder) |
Is a |
False |
Autoimmune encephalitis |
Inferred relationship |
Some |
|
Limbic encephalitis with leucine-rich glioma-inactivated 1 antibodies |
Is a |
False |
Autoimmune encephalitis |
Inferred relationship |
Some |
|
A rare neurologic disorder characterized by a unique non-REM and REM parasomnia with sleep breathing dysfunction, gait instability and repetitive episodes of respiratory insufficiency, as well as autoantibodies against IgLON5. Patients may present stridor, chorea, limb ataxia, abnormal ocular movements, and bulbar symptoms (i.e. dysphagia, dysarthria, episodic central hypoventilation) with normal brain MRI. Excessive day sleepiness and cognitive deterioration have also been reported. |
Is a |
True |
Autoimmune encephalitis |
Inferred relationship |
Some |
|
Steroid-responsive encephalopathy associated with autoimmune thyroiditis (SREAT) is a rare, acquired, neurological disease characterized by encephalopathy associated with elevated antithyroid antibodies, in the absence of other causes. Clinical presentation varies from minor cognitive impairment to status epilepticus and coma, and frequently includes seizures, confusion, speech disorder, memory impairment, ataxia and psychiatric manifestations. |
Is a |
True |
Autoimmune encephalitis |
Inferred relationship |
Some |
|
Limbic encephalitis with neurexin-3 antibodies (disorder) |
Is a |
False |
Autoimmune encephalitis |
Inferred relationship |
Some |
|
Autoimmune acquired autonomic encephalomyelitis |
Is a |
True |
Autoimmune encephalitis |
Inferred relationship |
Some |
|
Autoimmune encephalitis caused by N-methyl-D-aspartate receptor antibody (disorder) |
Is a |
True |
Autoimmune encephalitis |
Inferred relationship |
Some |
|
Autoimmune inflammation of cerebellum (disorder) |
Is a |
False |
Autoimmune encephalitis |
Inferred relationship |
Some |
|
Autonomic disorder due to autoimmune encephalitis |
Due to |
True |
Autoimmune encephalitis |
Inferred relationship |
Some |
2 |
Dementia due to autoimmune encephalitis (disorder) |
Due to |
True |
Autoimmune encephalitis |
Inferred relationship |
Some |
3 |
A rare autoimmune encephalitis involving the mesial temporal lobes and clinically characterised by subacute onset (rapid progression of less than three months) of short-term memory deficits, seizures or psychiatric symptoms, such as behavioural changes, anxiety, depression, and psychosis. Further diagnostic criteria are bilateral abnormalities restricted to the mesial temporal lobes in brain MRI, cerebrospinal fluid pleocytosis and/or epileptic or slow-wave activity involving the temporal lobes in EEG, and reasonable exclusion of alternative causes. Paraneoplastic or non-paraneoplastic antibodies against neuronal antigens may be found in serum and/or cerebrospinal fluid. |
Is a |
True |
Autoimmune encephalitis |
Inferred relationship |
Some |
|
A rare autoimmune encephalitis characterized by various phenotypes depending on the region of the brainstem that is involved; patients present with gaze palsies (in midbrain involvement), facial palsy or vertical gaze palsies (in pontine involvement), dysarthria, dysphagia or central hypoventilation (in medullary involvement). Additional clinical features may also involve pyramidal symptoms and gait impairment. |
Is a |
True |
Autoimmune encephalitis |
Inferred relationship |
Some |
|