FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

76976005: Optic atrophy (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2005. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
127783019 Optic atrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
200625011 Optic nerve atrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
503423016 OA - Optic atrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
817755012 Optic atrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
127783019 Optic atrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
127783019 Optic atrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
200625011 Optic nerve atrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
200625011 Optic nerve atrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
503423016 OA - Optic atrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
817755012 Optic atrophy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
817755012 Optic atrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
391771000274119 Optikusatrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
648281000274119 Sehnervenatrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
71961000077119 atrophie optique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
312811000172119 atrophie du nerf optique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
71961000077119 atrophie optique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
312811000172119 atrophie du nerf optique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
391771000274119 Optikusatrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
648281000274119 Sehnervenatrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

75 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Optic atrophy Is a Disorder of optic nerve true Inferred relationship Existential restriction modifier (core metadata concept)
Optic atrophy Associated morphology Atrophy false Inferred relationship Existential restriction modifier (core metadata concept) 1
Optic atrophy Finding site Optic nerve structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Optic atrophy Is a Degenerative disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Optic atrophy Is a Neurological lesion false Inferred relationship Existential restriction modifier (core metadata concept)
Optic atrophy Finding site Optic nerve structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Optic atrophy Associated morphology Atrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Optic atrophy Is a Degenerative disease of the central nervous system true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Optic atrophy secondary to retinal disease Is a True Optic atrophy Inferred relationship Existential restriction modifier (core metadata concept)
Post-compressive optic atrophy Is a False Optic atrophy Inferred relationship Existential restriction modifier (core metadata concept)
Odontotrichomelic syndrome Is a False Optic atrophy Inferred relationship Existential restriction modifier (core metadata concept)
Partial optic atrophy Is a True Optic atrophy Inferred relationship Existential restriction modifier (core metadata concept)
Compressive optic atrophy Is a True Optic atrophy Inferred relationship Existential restriction modifier (core metadata concept)
Glaucomatous atrophy of optic disc (disorder) Is a False Optic atrophy Inferred relationship Existential restriction modifier (core metadata concept)
Secondary optic atrophy Is a True Optic atrophy Inferred relationship Existential restriction modifier (core metadata concept)
Complete optic atrophy Is a True Optic atrophy Inferred relationship Existential restriction modifier (core metadata concept)
Optic atrophy associated with retinal dystrophy Is a True Optic atrophy Inferred relationship Existential restriction modifier (core metadata concept)
Primary optic atrophy Is a True Optic atrophy Inferred relationship Existential restriction modifier (core metadata concept)
Wolfram syndrome (disorder) Is a False Optic atrophy Inferred relationship Existential restriction modifier (core metadata concept)
Atrophy of optic disc (disorder) Is a True Optic atrophy Inferred relationship Existential restriction modifier (core metadata concept)
Retrobulbar optic nerve atrophy Is a True Optic atrophy Inferred relationship Existential restriction modifier (core metadata concept)
Unspecified optic atrophy Is a False Optic atrophy Inferred relationship Existential restriction modifier (core metadata concept)
Optic atrophy NOS Is a False Optic atrophy Inferred relationship Existential restriction modifier (core metadata concept)
Behr syndrome Is a False Optic atrophy Inferred relationship Existential restriction modifier (core metadata concept)
Congenital atrophy of optic nerve (disorder) Is a True Optic atrophy Inferred relationship Existential restriction modifier (core metadata concept)
Optic atrophy of left eye Is a True Optic atrophy Inferred relationship Existential restriction modifier (core metadata concept)
Optic atrophy of right eye Is a True Optic atrophy Inferred relationship Existential restriction modifier (core metadata concept)
Syphilitic optic atrophy Is a True Optic atrophy Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome Is a True Optic atrophy Inferred relationship Existential restriction modifier (core metadata concept)
Optic atrophy due to late syphilis (disorder) Is a True Optic atrophy Inferred relationship Existential restriction modifier (core metadata concept)
History of optic atrophy Associated finding True Optic atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Ocular anomalies, axonal neuropathy, developmental delay syndrome (disorder) Is a True Optic atrophy Inferred relationship Existential restriction modifier (core metadata concept)
A rare mitochondrial disease characterized by bilateral auditory neuropathy and optic atrophy. Patients present hearing and visual impairment in the first or second decade of life, while psychomotor development is normal. Bilateral retinitis pigmentosa has been reported in association. Is a True Optic atrophy Inferred relationship Existential restriction modifier (core metadata concept)
Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome (disorder) Is a True Optic atrophy Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

Back to Start