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838345001: Autosomal recessive optic atrophy type 6 (disorder)


Status: current, Primitive. Date: 31-Jul 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3896534015 Autosomal recessive optic atrophy type 6 en Synonym Active Case insensitive SNOMED CT core
3896535019 Autosomal recessive optic atrophy type 6 (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
Autosomal recessive optic atrophy type 6 Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Autosomal recessive optic atrophy type 6 Is a Hereditary optic atrophy true Inferred relationship Some
Autosomal recessive optic atrophy type 6 Associated morphology Primary atrophy true Inferred relationship Some 1
Autosomal recessive optic atrophy type 6 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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