Horner Syndrome
Disease ID: disease_node_4032
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| Dbxref | GARD:6670, ICD10CM:G90.2, MESH:D006732, MIM:143000, NCI:C28155, SNOMEDCT_US_2023_03_01:192922002, UMLS_CUI:C0019937 |
|---|---|
| Subclassof | DOID_11504 |
| Data Source | DOID, MESH |
| Synonyms | Bernard Horner syndrome, Horner syndrome, cervical sympathetic paralysis |
| Mesh Id | D006732 |
| Mesh Label | Horner Syndrome |
| Mesh Subclassof | D015877, D000096826, D001342 |
| Doid Label | Horner's syndrome |
| Doid Description | 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. |
| Disease Node Id | disease_node_4032 |
| Doid Id | DOID_11486 |
| Label | Horner Syndrome |
- Outgoing r'ship
SUBCLASS_OFto/from Autonomic Neuropathy(ID:disease_node_14269) (Disease)