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782679002: Familial congenital palsy of trochlear nerve (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3755126019 Familial congenital palsy of trochlear nerve (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3755127011 Familial congenital palsy of trochlear nerve en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3755128018 A rare genetic neuro-ophthalmological disease with characteristics of congenital fourth cranial nerve palsy, manifesting with hypertropia in side gaze, unexplained head tilt, acquired vertical diplopia and progressive increase in vertical fusional vergence amplitudes with prolonged occlusion. Facial asymmetry (for example hemifacial retrusion, upward slanting of mouth on the side of the head tilt, mild enophthalmos of paretic eye) and superior oblique tendon abnormalities (such as absence, redundance, misdirection) are frequently associated. Some asymptomatic cases have been reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3755126019 Familial congenital palsy of trochlear nerve (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3755127011 Familial congenital palsy of trochlear nerve en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3755128018 A rare genetic neuro-ophthalmological disease with characteristics of congenital fourth cranial nerve palsy, manifesting with hypertropia in side gaze, unexplained head tilt, acquired vertical diplopia and progressive increase in vertical fusional vergence amplitudes with prolonged occlusion. Facial asymmetry (for example hemifacial retrusion, upward slanting of mouth on the side of the head tilt, mild enophthalmos of paretic eye) and superior oblique tendon abnormalities (such as absence, redundance, misdirection) are frequently associated. Some asymptomatic cases have been reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
545731000274113 Kongenitale Trochlearislähmung, familiäre Form de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3413441001000110 Trochlearislähmung, kongenitale, familiäre Form de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6208161000241110 paralysie congénitale familiale du quatrième nerf crânien fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6208171000241119 paralysie congénitale familiale du nerf crânien IV fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6208181000241117 paralysie congénitale familiale du nerf trochléaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6208161000241110 paralysie congénitale familiale du quatrième nerf crânien fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6208171000241119 paralysie congénitale familiale du nerf crânien IV fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6208181000241117 paralysie congénitale familiale du nerf trochléaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
545731000274113 Kongenitale Trochlearislähmung, familiäre Form de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3413441001000110 Trochlearislähmung, kongenitale, familiäre Form 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
Familial congenital palsy of trochlear nerve (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial congenital palsy of trochlear nerve (disorder) Is a Fourth nerve palsy (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Familial congenital palsy of trochlear nerve (disorder) Is a Congenital disease false Inferred relationship Existential restriction modifier (core metadata concept)
Familial congenital palsy of trochlear nerve (disorder) Is a Familial disease true Inferred relationship Existential restriction modifier (core metadata concept)
Familial congenital palsy of trochlear nerve (disorder) Finding site Trochlear nerve structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial congenital palsy of trochlear nerve (disorder) Is a Congenital palsy of trochlear nerve (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Familial congenital palsy of trochlear nerve (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Familial congenital palsy of trochlear nerve (disorder) Is a Hereditary disorder of nervous system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Familial congenital palsy of trochlear nerve (disorder) Is a Hereditary disorder of the visual system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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