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770626007: Congenital Horner syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module Reference Sets
3701687013 Congenital Horner syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
3701688015 Congenital Horner syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
3701689011 Congenital Claude Bernard Horner syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
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 Entire term case sensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
907681000172119 syndrome de Horner congénital fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept) Belgian French language reference set (foundation metadata concept): Preferred (foundation metadata concept)
927951000172112 syndrome congénital de Claude-Bernard-Horner fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept) Belgian French language reference set (foundation metadata concept): Acceptable (foundation metadata concept)
2240261000172119 syndrome de Claude Bernard-Horner fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept) Belgian GP French language reference set (foundation metadata concept): Preferred (foundation metadata concept)
945101000172117 congenitaal syndroom van Claude-Bernard-Horner nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept) Belgian Dutch language reference set (foundation metadata concept): Acceptable (foundation metadata concept)
981031000172118 congenitaal syndroom van Horner nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept) Belgian Dutch language reference set (foundation metadata concept): Preferred (foundation metadata concept)
2240271000172111 Claude Bernard-Horner syndroom nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept) Belgian GP Dutch language reference set (foundation metadata concept): Preferred (foundation metadata concept)

0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Belgian GP subset (foundation metadata concept)

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