720466001: Adult-onset dystonia parkinsonism (disorder)

SNOMED CT Concept\Clinical finding\...

\Finding of movement\Bradykinesia\Parkinsonism\Adult-onset dystonia parkinsonism
\Finding of movement\Movement disorder\Extrapyramidal disease\Parkinsonism\Adult-onset dystonia parkinsonism
\Finding of movement\Movement disorder\Extrapyramidal disease\Dystonia\Adult-onset dystonia parkinsonism

\Central nervous system finding\Finding of brain\Disorder of brain\Extrapyramidal disease\Parkinsonism\Adult-onset dystonia parkinsonism
\Central nervous system finding\Finding of brain\Disorder of brain\Extrapyramidal disease\Dystonia\Adult-onset dystonia parkinsonism
\Central nervous system finding\Finding of brain\Disorder of brain\Disorder of basal ganglia\Parkinsonism\Adult-onset dystonia parkinsonism
\Central nervous system finding\Disorder of the central nervous system\Disorder of brain\Extrapyramidal disease\Parkinsonism\Adult-onset dystonia parkinsonism
\Central nervous system finding\Disorder of the central nervous system\Disorder of brain\Extrapyramidal disease\Dystonia\Adult-onset dystonia parkinsonism
\Central nervous system finding\Disorder of the central nervous system\Disorder of brain\Disorder of basal ganglia\Parkinsonism\Adult-onset dystonia parkinsonism

\Finding of head and neck region\Head finding\...

\Finding of brain\Disorder of brain\...

\Extrapyramidal disease\Parkinsonism\Adult-onset dystonia parkinsonism
\Extrapyramidal disease\Dystonia\Adult-onset dystonia parkinsonism

\Disorder of basal ganglia\Parkinsonism\Adult-onset dystonia parkinsonism

\Finding of head region\Disorder of basal ganglia\Parkinsonism\Adult-onset dystonia parkinsonism

\Disorder of head\Disorder of brain\...

\Extrapyramidal disease\Parkinsonism\Adult-onset dystonia parkinsonism
\Extrapyramidal disease\Dystonia\Adult-onset dystonia parkinsonism

\Disorder of basal ganglia\Parkinsonism\Adult-onset dystonia parkinsonism

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Adult-onset dystonia parkinsonism
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Adult-onset dystonia parkinsonism
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Adult-onset dystonia parkinsonism
\Disease\Disorder of body system\Disorder of nervous system\Hereditary disorder of nervous system\Adult-onset dystonia parkinsonism
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Disorder of brain\Extrapyramidal disease\Parkinsonism\Adult-onset dystonia parkinsonism
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Disorder of brain\Extrapyramidal disease\Dystonia\Adult-onset dystonia parkinsonism
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Disorder of brain\Disorder of basal ganglia\Parkinsonism\Adult-onset dystonia parkinsonism
\Disease\Disorder of head\Disorder of brain\Extrapyramidal disease\Parkinsonism\Adult-onset dystonia parkinsonism
\Disease\Disorder of head\Disorder of brain\Extrapyramidal disease\Dystonia\Adult-onset dystonia parkinsonism
\Disease\Disorder of head\Disorder of brain\Disorder of basal ganglia\Parkinsonism\Adult-onset dystonia parkinsonism
\Disease\Movement disorder\Extrapyramidal disease\Parkinsonism\Adult-onset dystonia parkinsonism
\Disease\Movement disorder\Extrapyramidal disease\Dystonia\Adult-onset dystonia parkinsonism

Status: current, Sufficiently defined by necessary conditions definition status. Date: 30-Sep 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

3320934019 Adult-onset dystonia parkinsonism (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

3320935018 Adult-onset dystonia parkinsonism en Synonym Active Entire term case insensitive SNOMED CT core module

3320936017 Dystonia parkinsonism Paisan-Ruiz type en Synonym Active Only initial character case insensitive SNOMED CT core module

3320937014 PLA2G6 (phospholipase A2 group VI) related dystonia parkinsonism en Synonym Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Adult-onset dystonia parkinsonism	Is a	Dystonia	true	Inferred relationship	Existential restriction modifier
Adult-onset dystonia parkinsonism	Is a	Parkinsonism	true	Inferred relationship	Existential restriction modifier
Adult-onset dystonia parkinsonism	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier
Adult-onset dystonia parkinsonism	Is a	Hereditary disorder of nervous system	true	Inferred relationship	Existential restriction modifier
Adult-onset dystonia parkinsonism	Occurrence	Adulthood	true	Inferred relationship	Existential restriction modifier	1
Adult-onset dystonia parkinsonism	Finding site	Basal ganglion structure	true	Inferred relationship	Existential restriction modifier	2
Adult-onset dystonia parkinsonism	Interprets	Movement	true	Inferred relationship	Existential restriction modifier	4
Adult-onset dystonia parkinsonism	Has interpretation	Slow	true	Inferred relationship	Existential restriction modifier	4

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
3320934019	Adult-onset dystonia parkinsonism (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3320935018	Adult-onset dystonia parkinsonism	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3320936017	Dystonia parkinsonism Paisan-Ruiz type	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3320937014	PLA2G6 (phospholipase A2 group VI) related dystonia parkinsonism	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module