loading...| Preferred Name |
Horner Syndrome [Disease/Finding] |
|
| Synonyms |
Claude Bernard-Horner Syndrome Sympathetic Ocular-Ophthalmoplegia Oculosympathetic Syndrome Bernard's Syndrome Ophthalmoplegia, Sympathetic Ocular Horner's Syndrome Horner Syndrome Bernard Syndrome |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000001555 |
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| altLabel |
Claude Bernard-Horner Syndrome Sympathetic Ocular-Ophthalmoplegia Oculosympathetic Syndrome Bernard's Syndrome Ophthalmoplegia, Sympathetic Ocular Horner's Syndrome Horner Syndrome Bernard Syndrome |
|
| cui |
C0019937 |
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| MESH DEFINITION |
A syndrome associated with defective sympathetic innervation to one side of the face, including the eye. Clinical features include MIOSIS; mild BLEPHAROPTOSIS; and hemifacial ANHIDROSIS (decreased sweating)(see HYPOHIDROSIS). Lesions of the BRAIN STEM; cervical SPINAL CORD; first thoracic nerve root; apex of the LUNG; CAROTID ARTERY; CAVERNOUS SINUS; and apex of the ORBIT may cause this condition. (From Miller et al., Clinical Neuro-Ophthalmology, 4th ed, pp500-11) |
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| MESH DUI |
D006732 |
|
| MeSH name |
Horner Syndrome |
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| MESH UI |
M0010542 |
|
| NDFRT kind |
DISEASE_KIND |
|
| notation |
N0000001555 |
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| NUI |
N0000001555 |
|
| prefLabel |
Horner Syndrome [Disease/Finding] |
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| SNOMED CID |
192915005 |
|
| tui |
T047 |
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| subClassOf |