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699299001: Neuroferritinopathy (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
2983562016 Adult onset basal ganglia disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2983627019 Neuroferritinopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2983630014 Ferritin related neurodegeneration en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2983654016 Neuroferritinopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3659561000052112 neuroferritinopati sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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