722990003: Congenital atrophy of optic nerve (disorder)

SNOMED CT Concept\constatation clinique\...

\constatation à propos du système nerveux central\Disorder of the central nervous system (disorder)\...

\maladie dégénérative du système nerveux central\Optic atrophy\Congenital atrophy of optic nerve (disorder)

\Disorder of visual pathways (disorder)\Disorder of optic nerve\Optic atrophy\Congenital atrophy of optic nerve (disorder)

\constatation à propos des yeux ou de la vue\affection du système visuel\Disorder of visual pathways (disorder)\Disorder of optic nerve\Optic atrophy\Congenital atrophy of optic nerve (disorder)

\Disease\affection dégénérative\maladie dégénérative du système nerveux central\Optic atrophy\Congenital atrophy of optic nerve (disorder)
\Disease\affection d'un système corporel\affection du système visuel\Disorder of visual pathways (disorder)\Disorder of optic nerve\Optic atrophy\Congenital atrophy of optic nerve (disorder)
\Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Neuropathy (disorder)\Cranial nerve disorder\Disorder of optic nerve\Optic atrophy\Congenital atrophy of optic nerve (disorder)
\Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\maladie dégénérative du système nerveux central\Optic atrophy\Congenital atrophy of optic nerve (disorder)
\Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of visual pathways (disorder)\Disorder of optic nerve\Optic atrophy\Congenital atrophy of optic nerve (disorder)
\Disease\Congenital disease\Congenital atrophy of optic nerve (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3334096018 Congenital atrophy of optic nerve (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3334097010 Congenital atrophy of optic nerve en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3334098017 Congenital optic atrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital atrophy of optic nerve (disorder)	est un(e) (attribut)	Congenital disease	true	Inferred relationship	Some
Congenital atrophy of optic nerve (disorder)	est un(e) (attribut)	Optic atrophy	true	Inferred relationship	Some
Congenital atrophy of optic nerve (disorder)	morphologie associée (attribut)	atrophie (anomalie morphologique)	true	Inferred relationship	Some	1
Congenital atrophy of optic nerve (disorder)	survenue (attribut)	congénital	true	Inferred relationship	Some	1
Congenital atrophy of optic nerve (disorder)	localisation d'une constatation (attribut)	Optic nerve structure	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
SPOAN and SPOAN-related disorder	est un(e) (attribut)	False	Congenital atrophy of optic nerve (disorder)	Inferred relationship	Some
Late congenital syphilitic optic atrophy	est un(e) (attribut)	True	Congenital atrophy of optic nerve (disorder)	Inferred relationship	Some
Leber plus disease (disorder)	est un(e) (attribut)	True	Congenital atrophy of optic nerve (disorder)	Inferred relationship	Some
Early-onset X-linked optic atrophy (disorder)	est un(e) (attribut)	True	Congenital atrophy of optic nerve (disorder)	Inferred relationship	Some
Severe X-linked intellectual disability Gustavson type (disorder)	est un(e) (attribut)	True	Congenital atrophy of optic nerve (disorder)	Inferred relationship	Some
Spastic paraplegia, optic atrophy, neuropathy syndrome (disorder)	est un(e) (attribut)	False	Congenital atrophy of optic nerve (disorder)	Inferred relationship	Some
syndrome d'ataxie cérébelleuse, déficience intellectuelle, atrophie optique, anomalies cutanées	est un(e) (attribut)	True	Congenital atrophy of optic nerve (disorder)	Inferred relationship	Some
Wolfram-like syndrome (disorder)	est un(e) (attribut)	True	Congenital atrophy of optic nerve (disorder)	Inferred relationship	Some
Combined immunodeficiency with faciooculoskeletal anomalies syndrome (disorder)	est un(e) (attribut)	True	Congenital atrophy of optic nerve (disorder)	Inferred relationship	Some

Reference Sets

Canada English language reference set (foundation metadata concept)

Description inactivation indicator reference set