271730003: Horner's syndrome pupil (disorder)

Status: retired, 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

406624019 Horner's syndrome pupil en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

406626017 Miosis innervational defect en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

664166018 Horner's syndrome pupil (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

2838260011 Horner syndrome pupil en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

2400151000005116 Horners syndrom-pupil da Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Danish module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Horners syndrom-pupil	Is a	Persistent miosis	false	Inferred relationship	Some
Horners syndrom-pupil	Is a	Segmental autonomic dysfunction	false	Inferred relationship	Some
Horners syndrom-pupil	Finding site	Autonomic nerve structure	false	Inferred relationship	Some	3
Horners syndrom-pupil	Finding site	Iris structure	false	Inferred relationship	Some
Horners syndrom-pupil	Finding site	Pupil structure (body structure)	false	Inferred relationship	Some	1
Horners syndrom-pupil	Is a	Peripheral nerve finding	false	Inferred relationship	Some
Horners syndrom-pupil	Interprets	Pupil constriction (observable entity)	false	Inferred relationship	Some	2
Horners syndrom-pupil	Finding site	Autonomic nervous system structure	false	Inferred relationship	Some
Horners syndrom-pupil	Interprets	Size of pupil	false	Inferred relationship	Some	4

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	False	Horners syndrom-pupil	Inferred relationship	Some

Reference Sets

Concept inactivation indicator reference set

POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)