Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Demyelinating sensorimotor neuropathy |
Is a |
True |
Peripheral demyelinating neuropathy |
Inferred relationship |
Some |
|
Subacute inflammatory demyelinating polyradiculoneuropathy |
Is a |
True |
Peripheral demyelinating neuropathy |
Inferred relationship |
Some |
|
Chronic inflammatory demyelinating polyradiculoneuropathy |
Is a |
True |
Peripheral demyelinating neuropathy |
Inferred relationship |
Some |
|
Canine polyradiculoneuritis |
Is a |
False |
Peripheral demyelinating neuropathy |
Inferred relationship |
Some |
|
Guillain-Barré syndrome |
Is a |
True |
Peripheral demyelinating neuropathy |
Inferred relationship |
Some |
|
kronisk inflammatorisk demyeliniserende polyneurit |
Is a |
False |
Peripheral demyelinating neuropathy |
Inferred relationship |
Some |
|
Acute inflammatory demyelinating polyneuropathy (disorder) |
Is a |
True |
Peripheral demyelinating neuropathy |
Inferred relationship |
Some |
|
A demyelinating polyneuropathy characterized clinically by sensory ataxia, tremor, paresthesia, and impaired gait. |
Is a |
True |
Peripheral demyelinating neuropathy |
Inferred relationship |
Some |
|
This syndrome is characterized by the association of sensorineural hearing impairment and peripheral neuropathy. |
Is a |
True |
Peripheral demyelinating neuropathy |
Inferred relationship |
Some |
|
Peripheral demyelinating neuropathy-central dysmyelinating leucodystrophy-Waardenburg syndrome-Hirschsprung disease (PCWH) is a systemic disease characterised by the association of the features of Waardenburg-Shah syndrome (WSS) with neurological features of variable severity. |
Is a |
True |
Peripheral demyelinating neuropathy |
Inferred relationship |
Some |
|
Hypertrophic interstitial neuropathy |
Is a |
True |
Peripheral demyelinating neuropathy |
Inferred relationship |
Some |
|
Acquired demyelinating disorder of peripheral nerve (disorder) |
Is a |
True |
Peripheral demyelinating neuropathy |
Inferred relationship |
Some |
|
A rare genetic neurological disorder with characteristics of childhood to adolescence onset of progressive demyelination occurring in episodes, sensorimotor polyneuropathy, and hearing loss. Disease progression and severity is variable. In general, in an increasing and decreasing course, patients eventually develop respiratory insufficiency, loss of motor skills and ambulation, ataxia, and cognitive decline. Vision problems and skin rashes are commonly reported. |
Is a |
True |
Peripheral demyelinating neuropathy |
Inferred relationship |
Some |
|