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1281810006: Horner syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Jun 2023. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5238773015 Horner syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5238774014 Horner syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core


4 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Horner syndrome Is a Segmental autonomic dysfunction true Inferred relationship Some
Horner syndrome Is a Disorder of sympathetic nervous system true Inferred relationship Some
Horner syndrome Finding site Sympathetic nerve structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital Horner syndrome is a rare neurological disorder characterized by relative pupillary miosis and blepharoptosis, evident at birth, caused by interruption of the oculosympathetic innervation at any point along the neural pathway from the hypothalamus to the orbit. Often additional symptoms, such as enophthalmos, facial anhidrosis, iris heterochromia, conjunctival congestion, transient hypotonia and/or pupillary dilation lag, may be present. Association with birth trauma, neoplasms or vascular malformations has been reported. Is a True Horner syndrome Inferred relationship Some
Acquired Horner syndrome (disorder) Is a True Horner syndrome Inferred relationship Some
History of Horner syndrome (situation) Associated finding True Horner syndrome Inferred relationship Some 1

This concept is not in any reference sets

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