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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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Childhood-onset autosomal dominant optic atrophy survenue (attribut) enfance true Inferred relationship Some 1
Childhood-onset autosomal dominant optic atrophy est un(e) (attribut) Autosomal dominant hereditary disorder true Inferred relationship Some
Childhood-onset autosomal dominant optic atrophy est un(e) (attribut) Hereditary optic atrophy true Inferred relationship Some
Childhood-onset autosomal dominant optic atrophy morphologie associée (attribut) Primary atrophy true Inferred relationship Some 1
Childhood-onset autosomal dominant optic atrophy localisation d'une constatation (attribut) Optic nerve structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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