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770626007: syndrome de Horner congénital (trouble)


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
3701687013 Congenital Horner syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3701688015 Congenital Horner syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3701689011 Congenital Claude Bernard Horner syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
769541000241117 syndrome de Horner congénital (trouble) fr Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
907681000172119 syndrome de Horner congénital fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
927951000172112 syndrome congénital de Claude-Bernard-Horner fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core 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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
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) morphologie associée (attribut) Prolapse true Inferred relationship Some 1
Congenital Horner syndrome (disorder) est un(e) (attribut) Developmental hereditary disorder true Inferred relationship Some
Congenital Horner syndrome (disorder) survenue (attribut) congénital true Inferred relationship Some 2
Congenital Horner syndrome (disorder) est un(e) (attribut) Horner's syndrome pupil true Inferred relationship Some
Congenital Horner syndrome (disorder) est un(e) (attribut) Autosomal dominant hereditary disorder true Inferred relationship Some
Congenital Horner syndrome (disorder) est un(e) (attribut) Inherited autonomic nervous system disorder (disorder) true Inferred relationship Some
Congenital Horner syndrome (disorder) est un(e) (attribut) Congenital ptosis of upper eyelid true Inferred relationship Some
Congenital Horner syndrome (disorder) est un(e) (attribut) Hereditary disorder of the visual system true Inferred relationship Some
Congenital Horner syndrome (disorder) interprète (attribut) Pupil constriction (observable entity) true Inferred relationship Some 4
Congenital Horner syndrome (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Congenital Horner syndrome (disorder) survenue (attribut) congénital true Inferred relationship Some 3
Congenital Horner syndrome (disorder) localisation d'une constatation (attribut) paupière supérieure (structure corporelle) true Inferred relationship Some 1
Congenital Horner syndrome (disorder) localisation d'une constatation (attribut) Pupil structure (body structure) true Inferred relationship Some 3
Congenital Horner syndrome (disorder) localisation d'une constatation (attribut) Autonomic nerve structure true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

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