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715374003: Autosomal dominant optic atrophy plus syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3302395011 Autosomal dominant optic atrophy plus syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3302396012 Autosomal dominant optic atrophy plus syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
5048275014 ADOA (autosomal dominant optic atrophy) plus en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant optic atrophy plus syndrome Is a Dominant hereditary optic atrophy true Inferred relationship Existential restriction modifier
Autosomal dominant optic atrophy plus syndrome Is a Mitochondrial cytopathy true Inferred relationship Existential restriction modifier
Autosomal dominant optic atrophy plus syndrome Associated morphology Primary atrophy true Inferred relationship Existential restriction modifier 1
Autosomal dominant optic atrophy plus syndrome Finding site Optic nerve structure true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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