loading...| Preferred Name |
Guillain-Barre Syndrome [Disease/Finding] |
|
| Synonyms |
Acute Inflammatory Polyneuropathy |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000004093 |
|
| altLabel |
Acute Inflammatory Polyneuropathy Guillain-Barre Syndrome, Familial Guillain-Barré Syndrome Polyneuropathy, Inflammatory Demyelinating, Acute Acute Autoimmune Neuropathy Acute Inflammatory Polyradiculoneuropathy Polyradiculoneuropathy, Acute Inflammatory Inflammatory Polyneuropathy Acute Inflammatory Demyelinating Polyradiculoneuropathy, Acute Polyneuropathy, Acute Inflammatory Demyelinating Polyradiculoneuropathy, Acute Inflammatory Guillaine-Barre Syndrome Acute Inflammatory Demyelinating Polyneuropathy Acute Inflammatory Demyelinating Polyradiculoneuropathy Polyradiculoneuropathy, Acute Inflammatory Demyelinating Landry-Guillain-Barre Syndrome Guillain-Barre Syndrome Acute Infectious Polyneuritis |
|
| cui |
C0018378 C3542501 |
|
| May be treated by | ||
| MESH DEFINITION |
An acute inflammatory autoimmune neuritis caused by T cell- mediated cellular immune response directed towards peripheral myelin. Demyelination occurs in peripheral nerves and nerve roots. The process is often preceded by a viral or bacterial infection, surgery, immunization, lymphoma, or exposure to toxins. Common clinical manifestations include progressive weakness, loss of sensation, and loss of deep tendon reflexes. Weakness of respiratory muscles and autonomic dysfunction may occur. (From Adams et al., Principles of Neurology, 6th ed, pp1312-1314) |
|
| MESH DUI |
D020275 |
|
| MeSH name |
Guillain-Barre Syndrome |
|
| MESH UI |
M0017242 |
|
| NDFRT kind |
DISEASE_KIND |
|
| notation |
N0000004093 |
|
| NUI |
N0000004093 |
|
| prefLabel |
Guillain-Barre Syndrome [Disease/Finding] |
|
| SNOMED CID |
40956001 128085000 129131007 193174005 |
|
| tui |
T047 |
|
| subClassOf |