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1217207008: Congenital oculomotor nerve palsy (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Apr 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5399906012 A rare ophthalmic disorder with cranial nerve involvement characterized by partial or complete ptosis and ophthalmoplegia with impaired ability to elevate, depress, or adduct the eyeball, causing strabismus and amblyopia. The pupils can also be dilated. The condition is typically unilateral and may present with or without aberrant regeneration. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399907015 A rare ophthalmic disorder with cranial nerve involvement characterised by partial or complete ptosis and ophthalmoplegia with impaired ability to elevate, depress, or adduct the eyeball, causing strabismus and amblyopia. The pupils can also be dilated. The condition is typically unilateral and may present with or without aberrant regeneration. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5035130015 Congenital third cranial nerve palsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5035131016 Congenital oculomotor nerve palsy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5035132011 Congenital oculomotor nerve palsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
7752531000241113 paralysie congénitale du troisième nerf crânien fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
7752541000241115 paralysie congénitale du nerf crânien III fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
7752551000241117 paralysie congénitale du nerf oculomoteur fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
592901000274118 Kongenitale Lähmung des Nervus oculomotorius de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
592911000274116 Kongenitale Okulomotoriusparese de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
A rare ophthalmic disorder with cranial nerve involvement characterized by partial or complete ptosis and ophthalmoplegia with impaired ability to elevate, depress, or adduct the eyeball, causing strabismus and amblyopia. The pupils can also be dilated. The condition is typically unilateral and may present with or without aberrant regeneration. Is a Third cranial nerve weakness (disorder) true Inferred relationship Some
A rare ophthalmic disorder with cranial nerve involvement characterized by partial or complete ptosis and ophthalmoplegia with impaired ability to elevate, depress, or adduct the eyeball, causing strabismus and amblyopia. The pupils can also be dilated. The condition is typically unilateral and may present with or without aberrant regeneration. Is a Congenital disease true Inferred relationship Some
A rare ophthalmic disorder with cranial nerve involvement characterized by partial or complete ptosis and ophthalmoplegia with impaired ability to elevate, depress, or adduct the eyeball, causing strabismus and amblyopia. The pupils can also be dilated. The condition is typically unilateral and may present with or without aberrant regeneration. Occurrence Congenital true Inferred relationship Some 1
A rare ophthalmic disorder with cranial nerve involvement characterized by partial or complete ptosis and ophthalmoplegia with impaired ability to elevate, depress, or adduct the eyeball, causing strabismus and amblyopia. The pupils can also be dilated. The condition is typically unilateral and may present with or without aberrant regeneration. Finding site Oculomotor nerve structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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