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232093001: Infantile esotropia (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
347765016 Congenital esotropia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
347766015 Essential infantile esotropia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2579192018 Infantile esotropia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4034914011 Infantile esotropia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4034915012 Infantile esotropia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
347765016 Congenital esotropia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
347765016 Congenital esotropia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
347766015 Essential infantile esotropia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
347766015 Essential infantile esotropia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
620113012 Congenital esotropia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
620113012 Congenital esotropia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2579192018 Infantile esotropia syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2579192018 Infantile esotropia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4034914011 Infantile esotropia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4034915012 Infantile esotropia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
576991000274118 Infantile Esotropie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
637041000274118 Kongenitale Esotropie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
76881000077110 ésotropie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
76881000077110 ésotropie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
576991000274118 Infantile Esotropie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
637041000274118 Kongenitale Esotropie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


6 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Infantile esotropia (disorder) Is a Esotropia false Inferred relationship Existential restriction modifier (core metadata concept)
Infantile esotropia (disorder) Finding site Eye structure false Inferred relationship Existential restriction modifier (core metadata concept)
Infantile esotropia (disorder) Finding site Eye region structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Infantile esotropia (disorder) Is a Congenital disease false Inferred relationship Existential restriction modifier (core metadata concept)
Infantile esotropia (disorder) Associated morphology Misalignment (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Infantile esotropia (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
Infantile esotropia (disorder) Finding site The eye, ocular adnexa, afferent visual pathways, efferent visual pathways, and pupil innervation pathways false Inferred relationship Existential restriction modifier (core metadata concept) 2
Infantile esotropia (disorder) Interprets Ocular muscle balance false Inferred relationship Existential restriction modifier (core metadata concept) 1
Infantile esotropia (disorder) Interprets Ocular motility observable (observable entity) false Inferred relationship Existential restriction modifier (core metadata concept)
Infantile esotropia (disorder) Has interpretation Abnormal false Inferred relationship Existential restriction modifier (core metadata concept) 1
Infantile esotropia (disorder) Has interpretation Abnormal false Inferred relationship Existential restriction modifier (core metadata concept) 1
Infantile esotropia (disorder) Interprets Ocular muscle balance false Inferred relationship Existential restriction modifier (core metadata concept) 1
Infantile esotropia (disorder) Finding site The eye, ocular adnexa, afferent visual pathways, efferent visual pathways, and pupil innervation pathways true Inferred relationship Existential restriction modifier (core metadata concept) 1
Infantile esotropia (disorder) Is a Acquired esotropia true Inferred relationship Existential restriction modifier (core metadata concept)
Infantile esotropia (disorder) Occurrence Infancy true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Esotropia with dissociated vertical deviation Is a True Infantile esotropia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Esotropia with nystagmus Is a True Infantile esotropia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Esotropia with nystagmus block (disorder) Is a True Infantile esotropia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
A rare syndrome characterised by the association of blepharophimosis and ptosis, V-esotropia, and weakness of extraocular and frontal muscles with syndactyly of the toes, short stature, prognathism, and hypertrophy and fusion of the eyebrows. Is a False Infantile esotropia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Bilateral infantile esotropia of eyes Is a False Infantile esotropia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Infantile esotropia of right eye Is a True Infantile esotropia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Infantile esotropia of left eye Is a True Infantile esotropia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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