699299001: Neuroferritinopathy (disorder)

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

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

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

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

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Neuroferritinopathy	Is a	Iron overload (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Neuroferritinopathy	Is a	Disorder of basal ganglia (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Neuroferritinopathy	Is a	trouble présent principalement avec la chorée	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Neuroferritinopathy	Causative agent (attribute)	Iron AND/OR iron compound	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Neuroferritinopathy	Finding site	Basal ganglion structure (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Neuroferritinopathy	Causative agent (attribute)	Iron and/or iron compound (substance)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Neuroferritinopathy	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Neuroferritinopathy	Is a	Hereditary disorder of nervous system (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)

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

This concept is not in any reference sets

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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
2983562016	Adult onset basal ganglia disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
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	Only initial character 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	Only initial character 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	Only initial character 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
3381031001000117	Neuroferritinopathie	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
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
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