Horner syndrome https://github.com/monarch-initiative/mondo/issues/9097 https://rarediseases.info.nih.gov/diseases/6670/horners-syndrome https://www.malacards.org/card/horners_syndrome ICD10CM:G90.2 UMLS:C0019937 Bernard-Horner syndrome DOID:11486 MESH:D006732 ICD9:337.09 Horner syndrome MEDGEN:5616 NCIT:C28155 oculosympathetic palsy SCTID:192915005 icd11.foundation:178756462 MONDO:0001294 Horner's syndrome is a rare condition characterized by miosis (constriction of thepupil), ptosis (drooping of the upper eyelid), and anhidrosis (absence of sweating of the face). It iscaused by damage to the sympathetic nerves of the face. The underlying causes of Horner's syndrome vary greatly and may include a tumor, stroke, or other damage to a part of the brain called the brain stem ; injury to the carotid artery ;and trauma to the brachial plexus. In rare cases, Horner's syndrome is congenital (present from birth) and associated with a lack of pigmentation of the iris (colored part of the eye). Treatment of Horner's syndrome depends on the underlying cause. Horner's syndrome autonomic neuropathy