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722990003: 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
11346161000172118 atrophie congénitale du deuxième nerf crânien fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
11346171000172110 atrophie congénitale du nerf crânien II fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
11346181000172113 atrophie congénitale du nerf optique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
4618471000172114 aangeboren atrofie van nervus opticus nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
4618481000172112 congenitale atrofie van tweede hersenzenuw nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
4618491000172110 congenitale atrofie van nervus opticus nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
4618501000172117 congenitale atrofie van hersenzenuw II nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)


8 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital atrophy of optic nerve (disorder) Is a Congenital disease (disorder) true Inferred relationship Some
Congenital atrophy of optic nerve (disorder) Is a Optic atrophy true Inferred relationship Some
Congenital atrophy of optic nerve (disorder) Associated morphology Atrophy true Inferred relationship Some 1
Congenital atrophy of optic nerve (disorder) Occurrence Congenital true Inferred relationship Some 1
Congenital atrophy of optic nerve (disorder) Finding site Optic nerve structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Leber plus disease (disorder) Is a True Congenital atrophy of optic nerve (disorder) Inferred relationship Some
Early-onset X-linked optic atrophy (disorder) Is a True Congenital atrophy of optic nerve (disorder) Inferred relationship Some
Severe X-linked intellectual disability Gustavson type (disorder) Is a True Congenital atrophy of optic nerve (disorder) Inferred relationship Some
Spastic paraplegia, optic atrophy, neuropathy syndrome (disorder) Is a False Congenital atrophy of optic nerve (disorder) Inferred relationship Some
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) Is a True Congenital atrophy of optic nerve (disorder) Inferred relationship Some
Wolfram-like syndrome (disorder) Is a True Congenital atrophy of optic nerve (disorder) Inferred relationship Some
Combined immunodeficiency with faciooculoskeletal anomalies syndrome (disorder) Is a True Congenital atrophy of optic nerve (disorder) Inferred relationship Some
SPOAN and SPOAN-related disorder Is a False Congenital atrophy of optic nerve (disorder) Inferred relationship Some
Late congenital syphilitic optic atrophy Is a True Congenital atrophy of optic nerve (disorder) Inferred relationship Some
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome (disorder) Is a True Congenital atrophy of optic nerve (disorder) Inferred relationship Some

Reference Sets

GB English

US English

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