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15632891000119109: Optic atrophy of bilateral eyes (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
3706285012 Optic atrophy of bilateral eyes en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3706286013 Optic atrophy of both eyes en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3706287016 Optic atrophy of bilateral eyes (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3706288014 Bilateral optic atrophy of eyes en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

10 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Optic atrophy of bilateral eyes (disorder) Is a Optic atrophy of right eye true Inferred relationship Some
Optic atrophy of bilateral eyes (disorder) Is a Optic atrophy of left eye true Inferred relationship Some
Optic atrophy of bilateral eyes (disorder) Associated morphology Atrophy (morphologic abnormality) true Inferred relationship Some 2
Optic atrophy of bilateral eyes (disorder) Associated morphology Atrophy (morphologic abnormality) true Inferred relationship Some 1
Optic atrophy of bilateral eyes (disorder) Finding site Structure of right optic nerve (body structure) true Inferred relationship Some 2
Optic atrophy of bilateral eyes (disorder) Finding site Structure of left optic nerve (body structure) true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary bilateral optic atrophy (disorder) Is a False Optic atrophy of bilateral eyes (disorder) Inferred relationship Some
Bilateral partial optic atrophy Is a True Optic atrophy of bilateral eyes (disorder) Inferred relationship Some
A rare genetic endocrine disorder with characteristics of type 1 diabetes mellitus (DM), diabetes insipidus (DI), sensorineural deafness (D), bilateral optical atrophy (OA) and neurological signs. Two types of Wolfram syndrome may be distinguished: type 1 (WS1) and type 2 (WS2). Two causative genes have been identified: WFS1 (4p16.1) and CISD2 (4q24). The clinical criteria for Wolfram syndrome diagnosis are juvenile-onset diabetes mellitus and optic atrophy, family history of Wolfram syndrome or diabetes mellitus and deafness. Transmission is autosomal recessive. Is a True Optic atrophy of bilateral eyes (disorder) Inferred relationship Some
Bilateral atrophy of optic nerves following inflammation Is a True Optic atrophy of bilateral eyes (disorder) Inferred relationship Some
Primary optic atrophy of bilateral eyes (disorder) Is a True Optic atrophy of bilateral eyes (disorder) Inferred relationship Some
A rare hereditary optic atrophy characterised by an early onset of bilateral optic nerve degeneration without other systemic features. Clinical manifestations include pallor of the optic discs, severe but slowly progressing visual impairment, and in some patients also paracentral scotoma, photophobia and dyschromatopsia. Is a True Optic atrophy of bilateral eyes (disorder) Inferred relationship Some
Atrophy of optic disc of bilateral eyes due to glaucoma Is a True Optic atrophy of bilateral eyes (disorder) Inferred relationship Some

Reference Sets

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