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1217207008: Congenital oculomotor nerve palsy (disorder)


Status: current, Defined. Date: 30-Apr 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5035130015 Congenital third cranial nerve palsy en Synonym Active Case insensitive SNOMED CT core
5035131016 Congenital oculomotor nerve palsy (disorder) en Fully specified name Active Case insensitive SNOMED CT core
5035132011 Congenital oculomotor nerve palsy en Synonym Active Case insensitive 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 Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital oculomotor nerve palsy Is a Oculomotor nerve paresis true Inferred relationship Some
Congenital oculomotor nerve palsy Is a Congenital disease true Inferred relationship Some
Congenital oculomotor nerve palsy Occurrence Congenital true Inferred relationship Some 1
Congenital oculomotor nerve palsy Finding site Oculomotor nerve structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

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