699299001: neuroferritinopathie (aandoening)

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\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 (disorder)\Neuroferritinopathy (disorder)
\Disease\Nutritional disorder\Disorder of hyperalimentation\Excess intake of micronutrients\Mineral excess\Iron overload (disorder)\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

2224101000146113 neuroferritinopathie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

2224111000146110 neuroferritinopathie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

2224121000146117 laat optredende basalegangliaziekte nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

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	aandoening met chorea als primaire manifestatie	false	Inferred relationship	Some
Neuroferritinopathy (disorder)	Causative agent	Iron AND/OR iron compound	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
Neuroferritinopathy (disorder)	Is a	Autosomal dominant hereditary 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