| General Information | |||
|---|---|---|---|
| Term | Horner's syndrome | ID (Ontology) | DOID:11486 (Human Disease) |
| Definition | An autonomic neuropathy that is characterized by the classic triad of unilateral ptosis, unilateral miosis with anisocoria, and ipsilateral facial anhidrosis, resulting from unilateral paralysis of the cervical sympathetics. | ||
| Also Known As | "Bernard Horner syndrome" ; "cervical sympathetic paralysis" ; "Horner syndrome" | ||
| Comment | |||
| Links to External Ontologies | |||
| DO.org | |||
| Annotations | |||
| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
|
|||
|
No relevant statements available
|
|||
|
||||||
autonomic nervous system disease |__autonomic neuropathy |__Horner's syndrome |
| Spanning Tree View Settings | |||
|---|---|---|---|
| Parents/Children View Depth |
|||
Relationships
|
|||
| Is a | autonomic neuropathy | ||
| Part of | |||
Synonyms & Secondary IDs
|
|||
| Synonyms | |||
|
|||
| Secondary IDs | |||
|
|
|||
External Crossreferences & Linkouts
|
|||
|
GARD:6670 ICD10CM:G90.2 MESH:D006732 MIM:143000 NCI:C28155 SNOMEDCT_US_2023_03_01:192922002 UMLS_CUI:C0019937 |
|||