1260396009: Dystonia due to hereditary disease (disorder)

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

\Head finding (finding)\Finding of brain\Disorder of brain\Extrapyramidal disease\Dystonia\Dystonia due to hereditary disease (disorder)
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain\Extrapyramidal disease\Dystonia\Dystonia due to hereditary disease (disorder)

\Finding of movement\Movement disorder\Extrapyramidal disease\Dystonia\Dystonia due to hereditary disease (disorder)

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

\Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the central nervous system (disorder)\Central nervous system complication\Dystonia due to hereditary disease (disorder)
\Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain\Extrapyramidal disease\Dystonia\Dystonia due to hereditary disease (disorder)
\Disease\Disorder of head (disorder)\Disorder of brain\Extrapyramidal disease\Dystonia\Dystonia due to hereditary disease (disorder)
\Disease\Movement disorder\Extrapyramidal disease\Dystonia\Dystonia due to hereditary disease (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 hereditary disease (disorder)	Is a	Dystonia	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Dystonia due to hereditary disease (disorder)	Is a	Central nervous system complication	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Dystonia due to hereditary disease (disorder)	Interprets	Movement	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Dystonia due to hereditary disease (disorder)	Due to	Hereditary disease	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Dystonia due to hereditary disease (disorder)	Finding site	Extrapyramidal system structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Dystonia due to hereditary spastic paraplegia	Is a	True	Dystonia due to hereditary disease (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Dystonia due to Leigh syndrome (disorder)	Is a	True	Dystonia due to hereditary disease (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Dystonia due to Lesch Nyhan syndrome	Is a	True	Dystonia due to hereditary disease (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Dystonia due to GM2 gangliosidosis	Is a	True	Dystonia due to hereditary disease (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Dystonia due to Pelizaeus-Merzbacher disease (disorder)	Is a	True	Dystonia due to hereditary disease (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Dystonia due to Niemann-Pick disease type C (disorder)	Is a	True	Dystonia due to hereditary disease (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Dystonia due to atypical pantothenate kinase associated neurodegeneration (disorder)	Is a	True	Dystonia due to hereditary disease (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Dystonia due to ataxia telangiectasia syndrome	Is a	True	Dystonia due to hereditary disease (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Dystonia due to Wilson disease	Is a	True	Dystonia due to hereditary disease (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Dystonia due to metachromatic leucodystrophy (disorder)	Is a	True	Dystonia due to hereditary disease (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Dystonia due to Rett syndrome	Is a	True	Dystonia due to hereditary disease (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
5160314014	Dystonia due to inherited disorder	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5160315010	Dystonia due to hereditary disease (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5160347017	Dystonia due to hereditary disease	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5160314014	Dystonia due to inherited disorder	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5160315010	Dystonia due to hereditary disease (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5160347017	Dystonia due to hereditary disease	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core