1260360005: dystonie door atypische pantothenaatkinasegeassocieerde neurodegeneratie (aandoening)

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

\Head finding (finding)\Finding of brain\Disorder of brain (disorder)\Extrapyramidal disease\Dystonia\Dystonia due to hereditary disease (disorder)\Dystonia due to atypical pantothenate kinase associated neurodegeneration (disorder)
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain (disorder)\Extrapyramidal disease\Dystonia\Dystonia due to hereditary disease (disorder)\Dystonia due to atypical pantothenate kinase associated neurodegeneration (disorder)

\Finding of movement (finding)\Movement disorder\Extrapyramidal disease\Dystonia\Dystonia due to hereditary disease (disorder)\Dystonia due to atypical pantothenate kinase associated neurodegeneration (disorder)

\Central nervous system finding\Finding of brain\Disorder of brain (disorder)\Extrapyramidal disease\Dystonia\Dystonia due to hereditary disease (disorder)\Dystonia due to atypical pantothenate kinase associated neurodegeneration (disorder)
\Central nervous system finding\Disorder of the central nervous system (disorder)\Central nervous system complication\Dystonia due to hereditary disease (disorder)\Dystonia due to atypical pantothenate kinase associated neurodegeneration (disorder)
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Extrapyramidal disease\Dystonia\Dystonia due to hereditary disease (disorder)\Dystonia due to atypical pantothenate kinase associated neurodegeneration (disorder)

\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Central nervous system complication\Dystonia due to hereditary disease (disorder)\Dystonia due to atypical pantothenate kinase associated neurodegeneration (disorder)
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Extrapyramidal disease\Dystonia\Dystonia due to hereditary disease (disorder)\Dystonia due to atypical pantothenate kinase associated neurodegeneration (disorder)
\Disease\Disorder of head (disorder)\Disorder of brain (disorder)\Extrapyramidal disease\Dystonia\Dystonia due to hereditary disease (disorder)\Dystonia due to atypical pantothenate kinase associated neurodegeneration (disorder)
\Disease\Movement disorder\Extrapyramidal disease\Dystonia\Dystonia due to hereditary disease (disorder)\Dystonia due to atypical pantothenate kinase associated neurodegeneration (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2023. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Dystonia due to atypical pantothenate kinase associated neurodegeneration (disorder)	Interprets	Movement	true	Inferred relationship	Some	2
Dystonia due to atypical pantothenate kinase associated neurodegeneration (disorder)	Finding site	Extrapyramidal system structure	true	Inferred relationship	Some	1
Dystonia due to atypical pantothenate kinase associated neurodegeneration (disorder)	Is a	Dystonia due to hereditary disease (disorder)	true	Inferred relationship	Some
Dystonia due to atypical pantothenate kinase associated neurodegeneration (disorder)	Due to	Atypical pantothenate kinase associated neurodegeneration (disorder)	true	Inferred relationship	Some	3

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
5160234013	Dystonia in neurodegeneration with brain iron accumulation type 1	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5160235014	Dystonia due to atypical pantothenate kinase associated neurodegeneration (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5168664010	Dystonia due to atypical pantothenate kinase associated neurodegeneration	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5168665011	Dystonia due to atypical pigmentary pallidal degeneration	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
14276581000146112	dystonie door atypische neurodegeneratie met cerebrale ijzeraccumulatie type 1	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
14276591000146114	dystonie door atypische pantothenaatkinasegeassocieerde neurodegeneratie (aandoening)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
14276601000146116	dystonie door atypische neurodegeneratie met ijzerstapeling in hersenen type 1	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
14276611000146119	dystonie door atypische NBIA 1	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
14276621000146112	dystonie door atypische PKAN	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
14276631000146114	dystonie door atypische pantothenaatkinasegeassocieerde neurodegeneratie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)