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


Status: current, Primitive. 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 Active Case insensitive SNOMED CT core
3896440013 Childhood-onset autosomal dominant optic atrophy (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Childhood-onset autosomal dominant optic atrophy Occurrence Childhood true Inferred relationship Some 1
Childhood-onset autosomal dominant optic atrophy Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Childhood-onset autosomal dominant optic atrophy Is a Hereditary optic atrophy true Inferred relationship Some
Childhood-onset autosomal dominant optic atrophy Associated morphology Primary atrophy true Inferred relationship Some 1
Childhood-onset autosomal dominant optic atrophy Finding site Optic nerve structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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