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838307002: Childhood-onset autosomal dominant optic atrophy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3896439011 Childhood-onset autosomal dominant optic atrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3896440013 Childhood-onset autosomal dominant optic atrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3896439011 Childhood-onset autosomal dominant optic atrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3896440013 Childhood-onset autosomal dominant optic atrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
508361000274119 Im Kindesalter beginnende autosomal-dominante Sehnervenatrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
589691000274114 Im Kindesalter beginnende autosomal-dominante Optikusatrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5797371000241114 atrophie optique autosomique dominante débutant dans l'enfance fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5797371000241114 atrophie optique autosomique dominante débutant dans l'enfance fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
508361000274119 Im Kindesalter beginnende autosomal-dominante Sehnervenatrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
589691000274114 Im Kindesalter beginnende autosomal-dominante Optikusatrophie 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
Childhood-onset autosomal dominant optic atrophy (disorder) Occurrence Childhood true Inferred relationship Existential restriction modifier (core metadata concept) 1
Childhood-onset autosomal dominant optic atrophy (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Childhood-onset autosomal dominant optic atrophy (disorder) Is a Hereditary optic atrophy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Childhood-onset autosomal dominant optic atrophy (disorder) Associated morphology Primary atrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Childhood-onset autosomal dominant optic atrophy (disorder) Finding site Optic nerve structure true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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