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717336005: Autosomal dominant optic atrophy classic form (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
3309090013 Autosomal dominant optic atrophy classic form (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3309091012 Autosomal dominant optic atrophy classic form en Synonym Active Entire term case insensitive SNOMED CT core module
3309092017 Autosomal dominant optic atrophy Kjer type en Synonym Active Only initial character case insensitive SNOMED CT core module
3309093010 Kjer optic atrophy en Synonym Active Entire term case sensitive SNOMED CT core module
3309094016 Optic atrophy type 1 en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant optic atrophy classic form Is a Dominant hereditary optic atrophy true Inferred relationship Existential restriction modifier
Autosomal dominant optic atrophy classic form Associated morphology Primary atrophy true Inferred relationship Existential restriction modifier 1
Autosomal dominant optic atrophy classic form 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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