DISEASES

Disease-gene associations mined from literature

Human genes for Horner's syndrome

Horner's syndrome [DOID:11486]

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.

Synonyms:  Horner's syndrome,  DOID:11486,  Horners syndrome,  Horner's disease,  Horner's disorder ...

Linkouts:  OMIM