1217207008: Congenital oculomotor nerve palsy (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \General finding of soft tissue\Peripheral nerve finding\Peripheral nerve disease\Third cranial nerve disease\Third cranial nerve weakness (disorder)\Congenital oculomotor nerve palsy (disorder)
• \General finding of soft tissue\Disorder of soft tissue\Peripheral nerve disease\Third cranial nerve disease\Third cranial nerve weakness (disorder)\Congenital oculomotor nerve palsy (disorder)
• \Eye / vision finding\Visual system disorder\Disorder of oculomotor system (disorder)\Third cranial nerve disease\Third cranial nerve weakness (disorder)\Congenital oculomotor nerve palsy (disorder)
• \Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital oculomotor nerve palsy (disorder)
• \Disease\Disorder of body system\Visual system disorder\Disorder of oculomotor system (disorder)\Third cranial nerve disease\Third cranial nerve weakness (disorder)\Congenital oculomotor nerve palsy (disorder)
• \Disease\Disorder of body system\Disease of nervous system (disorder)\Neuropathy\Peripheral nerve disease\Third cranial nerve disease\Third cranial nerve weakness (disorder)\Congenital oculomotor nerve palsy (disorder)
• \Disease\Disorder of body system\Disease of nervous system (disorder)\Neuropathy\Cranial nerve disorder (disorder)\Third cranial nerve disease\Third cranial nerve weakness (disorder)\Congenital oculomotor nerve palsy (disorder)
• \Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the peripheral nervous system (disorder)\Peripheral nerve disease\Third cranial nerve disease\Third cranial nerve weakness (disorder)\Congenital oculomotor nerve palsy (disorder)
• \Disease\Disorder of soft tissue\Peripheral nerve disease\Third cranial nerve disease\Third cranial nerve weakness (disorder)\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
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
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
5035133018	A rare ophthalmic disorder with cranial nerve involvement and characteristics of 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
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
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
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
3415641001000113	Okulomotoriusparese, kongenitale	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Reference Sets

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

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