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770626007: Congenital Horner syndrome (disorder)


Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3701687013 Congenital Horner syndrome (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
3701688015 Congenital Horner syndrome en Synonym Active Initial character case insensitive SNOMED CT core
3701689011 Congenital Claude Bernard Horner syndrome en Synonym Active Initial character case insensitive SNOMED CT core
3701690019 A rare neurological disorder with characteristics of 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. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital Horner syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
Congenital Horner syndrome Pathological process Pathological developmental process true Inferred relationship Some 3
Congenital Horner syndrome Pathological process Pathological developmental process true Inferred relationship Some 2
Congenital Horner syndrome Associated morphology Prolapse true Inferred relationship Some 1
Congenital Horner syndrome Is a Developmental hereditary disorder true Inferred relationship Some
Congenital Horner syndrome Occurrence Congenital true Inferred relationship Some 2
Congenital Horner syndrome Is a Horner's syndrome pupil true Inferred relationship Some
Congenital Horner syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Congenital Horner syndrome Is a Inherited autonomic nervous system disorder true Inferred relationship Some
Congenital Horner syndrome Is a Congenital ptosis true Inferred relationship Some
Congenital Horner syndrome Is a Hereditary disorder of the visual system true Inferred relationship Some
Congenital Horner syndrome Interprets Pupil constriction true Inferred relationship Some 4
Congenital Horner syndrome Occurrence Congenital true Inferred relationship Some 1
Congenital Horner syndrome Occurrence Congenital true Inferred relationship Some 3
Congenital Horner syndrome Finding site Upper eyelid structure true Inferred relationship Some 1
Congenital Horner syndrome Finding site Pupil structure true Inferred relationship Some 3
Congenital Horner syndrome Finding site Autonomic nerve structure true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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