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699299001: Neuroferritinopathy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2014. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
2983562016 Adult onset basal ganglia disease en Synonym Active Entire term case insensitive SNOMED CT core module
2983627019 Neuroferritinopathy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2983630014 Ferritin related neurodegeneration en Synonym Active Entire term case insensitive SNOMED CT core module
2983654016 Neuroferritinopathy 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
Neuroferritinopathy Is a Iron overload true Inferred relationship Existential restriction modifier
Neuroferritinopathy Is a Disorder of basal ganglia true Inferred relationship Existential restriction modifier
Neuroferritinopathy Is a Disorder presenting primarily with chorea true Inferred relationship Existential restriction modifier
Neuroferritinopathy Causative agent Iron AND/OR iron compound false Inferred relationship Existential restriction modifier
Neuroferritinopathy Finding site Basal ganglion structure true Inferred relationship Existential restriction modifier 2
Neuroferritinopathy Causative agent Iron and/or iron compound true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Chorea due to neuroferritinopathy Due to True Neuroferritinopathy Inferred relationship Existential restriction modifier 2

This concept is not in any reference sets

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