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National Drug File - Reference Terminology
Last uploaded:
July 6, 2018
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| Id | http://purl.bioontology.org/ontology/NDFRT/N0000003960
http://purl.bioontology.org/ontology/NDFRT/N0000003960
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|---|---|
| Preferred Name | Miller Fisher Syndrome [Disease/Finding] |
| Synonyms |
Guillain-Barre Syndrome, Miller Fisher Variant
Miller Fisher Variant of Guillain Barre Syndrome
Ophthalmoplegia, Ataxia and Areflexia Syndrome
Miller-Fisher Syndrome
Miller Fisher Syndrome
Fisher Syndrome
Guillain Barre Syndrome, Miller Fisher Variant
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
Guillain-Barre Syndrome, Miller Fisher Variant
Miller Fisher Variant of Guillain Barre Syndrome
Ophthalmoplegia, Ataxia and Areflexia Syndrome
Miller-Fisher Syndrome
Miller Fisher Syndrome
Fisher Syndrome
Guillain Barre Syndrome, Miller Fisher Variant
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|---|---|
| prefLabel |
Miller Fisher Syndrome [Disease/Finding]
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| notation |
N0000003960
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| MESH DEFINITION |
A variant of the GUILLAIN-BARRE SYNDROME characterized by the acute onset of oculomotor dysfunction, ataxia, and loss of deep tendon reflexes with relative sparing of strength in the extremities and trunk. The ataxia is produced by peripheral sensory nerve dysfunction and not by cerebellar injury. Facial weakness and sensory loss may also occur. The process is mediated by autoantibodies directed against a component of myelin found in peripheral nerves. (Adams et al., Principles of Neurology, 6th ed, p1313; Neurology 1987 Sep;37(9):1493-8)
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| MESH UI |
M0029456
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| subClassOf | |
| Semantic type UMLS property | |
| MeSH name |
Miller Fisher Syndrome
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| NDFRT kind |
DISEASE_KIND
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| type | |
| SNOMED CID |
1767005
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| tui |
T047
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| NUI |
N0000003960
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| cui |
C0393799
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| MESH DUI |
D019846
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