699299001: Neuroferritinopathy (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Head finding (finding)\Finding of brain\Disorder of brain (disorder)\Disorder of basal ganglia (disorder)\Neuroferritinopathy (disorder)
\Head finding (finding)\Finding of head region\Disorder of basal ganglia (disorder)\Neuroferritinopathy (disorder)
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain (disorder)\Disorder of basal ganglia (disorder)\Neuroferritinopathy (disorder)

\Central nervous system finding\Finding of brain\Disorder of brain (disorder)\Disorder of basal ganglia (disorder)\Neuroferritinopathy (disorder)
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Disorder of basal ganglia (disorder)\Neuroferritinopathy (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Neuroferritinopathy (disorder)
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder (disorder)\Neuroferritinopathy (disorder)
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Neuroferritinopathy (disorder)
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\Neuroferritinopathy (disorder)
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Disorder of basal ganglia (disorder)\Neuroferritinopathy (disorder)
\Disease\Disorder of head (disorder)\Disorder of brain (disorder)\Disorder of basal ganglia (disorder)\Neuroferritinopathy (disorder)
\Disease\Metabolic disease\Disorder of mineral metabolism\Disorder of iron metabolism\Iron overload\Neuroferritinopathy (disorder)
\Disease\Nutritional disorder\Disorder of hyperalimentation\Excess intake of micronutrients\Mineral excess\Iron overload\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

966601000172114 neuroferritinopathie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

996331000172114 ferritinopathie héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

3381031001000117 Neuroferritinopathie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Neuroferritinopathy (disorder)	Is a	Iron overload	true	Inferred relationship	Some
Neuroferritinopathy (disorder)	Is a	Disorder of basal ganglia (disorder)	true	Inferred relationship	Some
Neuroferritinopathy (disorder)	Is a	trouble présent principalement avec la chorée	false	Inferred relationship	Some
Neuroferritinopathy (disorder)	Causative agent (attribute)	Iron AND/OR iron compound	false	Inferred relationship	Some
Neuroferritinopathy (disorder)	Finding site	Structure of basal nucleus	true	Inferred relationship	Some	2
Neuroferritinopathy (disorder)	Causative agent (attribute)	Iron and/or iron compound	true	Inferred relationship	Some	1
Neuroferritinopathy (disorder)	Is a	Autosomal dominant hereditary disorder (disorder)	true	Inferred relationship	Some
Neuroferritinopathy (disorder)	Is a	Hereditary disorder of nervous system	true	Inferred relationship	Some

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

This concept is not in any reference sets