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699299001: Neuroferritinopathy (disorder)


Status: current, Primitive. Date: 31-Jan 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2983562016 Adult onset basal ganglia disease en Synonym Active Case insensitive SNOMED CT core
2983627019 Neuroferritinopathy (disorder) en Fully specified name Active Case insensitive SNOMED CT core
2983630014 Ferritin related neurodegeneration en Synonym Active Case insensitive SNOMED CT core
2983654016 Neuroferritinopathy en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Neuroferritinopathy Is a Iron overload true Inferred relationship Some
Neuroferritinopathy Is a Disorder of basal ganglia true Inferred relationship Some
Neuroferritinopathy Is a Disorder presenting primarily with chorea true Inferred relationship Some
Neuroferritinopathy Causative agent Iron AND/OR iron compound false Inferred relationship Some
Neuroferritinopathy Finding site Basal ganglion structure true Inferred relationship Some 2
Neuroferritinopathy Causative agent Iron and/or iron compound true Inferred relationship Some 1

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

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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