722763000: Infantile dystonia parkinsonism (disorder)

SNOMED CT Concept\Clinical finding\...

\Finding of movement\Bradykinesia\Parkinsonism\Infantile dystonia parkinsonism
\Finding of movement\Movement disorder\Extrapyramidal disease\Parkinsonism\Infantile dystonia parkinsonism
\Finding of movement\Movement disorder\Extrapyramidal disease\Dystonia\Infantile dystonia parkinsonism

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

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

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

\Extrapyramidal disease\Parkinsonism\Infantile dystonia parkinsonism
\Extrapyramidal disease\Dystonia\Infantile dystonia parkinsonism

\Disorder of basal ganglia\Parkinsonism\Infantile dystonia parkinsonism

\Finding of head region\Disorder of basal ganglia\Parkinsonism\Infantile dystonia parkinsonism

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

\Extrapyramidal disease\Parkinsonism\Infantile dystonia parkinsonism
\Extrapyramidal disease\Dystonia\Infantile dystonia parkinsonism

\Disorder of basal ganglia\Parkinsonism\Infantile dystonia parkinsonism

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

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

3333387019 Infantile dystonia parkinsonism (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

3333388012 Dopamine transporter deficiency syndrome en Synonym Active Entire term case insensitive SNOMED CT core module

3333389016 Infantile dystonia parkinsonism en Synonym Active Entire term case insensitive SNOMED CT core module

3333390013 Parkinsonism-dystonia infantile en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Infantile dystonia parkinsonism	Is a	Dystonia	true	Inferred relationship	Existential restriction modifier
Infantile dystonia parkinsonism	Is a	Parkinsonism	true	Inferred relationship	Existential restriction modifier
Infantile dystonia parkinsonism	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier
Infantile dystonia parkinsonism	Is a	Hereditary disorder of nervous system	true	Inferred relationship	Existential restriction modifier
Infantile dystonia parkinsonism	Occurrence	Infancy	true	Inferred relationship	Existential restriction modifier	1
Infantile dystonia parkinsonism	Finding site	Basal ganglion structure	true	Inferred relationship	Existential restriction modifier	1
Infantile dystonia parkinsonism	Interprets	Movement	true	Inferred relationship	Existential restriction modifier	3
Infantile dystonia parkinsonism	Has interpretation	Slow	true	Inferred relationship	Existential restriction modifier	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
3333387019	Infantile dystonia parkinsonism (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3333388012	Dopamine transporter deficiency syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3333389016	Infantile dystonia parkinsonism	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3333390013	Parkinsonism-dystonia infantile	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module