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715647007: Bothnia retinal dystrophy (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
3303283016 Bothnia retinal dystrophy (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3303284010 Bothnia retinal dystrophy en Synonym Active Entire term case sensitive SNOMED CT core module
3303285011 Vasterbotten dystrophy 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
Bothnia retinal dystrophy Is a Hereditary retinal dystrophy true Inferred relationship Existential restriction modifier
Bothnia retinal dystrophy Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Bothnia retinal dystrophy Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Bothnia retinal dystrophy Finding site Retinal 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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