770939009: Huntington disease-like 3 (disorder)

SNOMED CT Concept\Clinical finding\...

\Finding of movement\Movement disorder\Extrapyramidal disease\Huntington disease-like syndrome\Huntington disease-like 3

\Central nervous system finding\Finding of brain\Disorder of brain\Chronic brain syndrome\Huntington disease-like 3
\Central nervous system finding\Finding of brain\Disorder of brain\Extrapyramidal disease\Huntington disease-like syndrome\Huntington disease-like 3
\Central nervous system finding\Finding of brain\Disorder of brain\Disorder of basal ganglia\Huntington disease-like syndrome\Huntington disease-like 3
\Central nervous system finding\Disorder of the central nervous system\Disorder of brain\Chronic brain syndrome\Huntington disease-like 3
\Central nervous system finding\Disorder of the central nervous system\Disorder of brain\Extrapyramidal disease\Huntington disease-like syndrome\Huntington disease-like 3
\Central nervous system finding\Disorder of the central nervous system\Disorder of brain\Disorder of basal ganglia\Huntington disease-like syndrome\Huntington disease-like 3

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

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

\Chronic brain syndrome\Huntington disease-like 3

\Extrapyramidal disease\Huntington disease-like syndrome\Huntington disease-like 3

\Disorder of basal ganglia\Huntington disease-like syndrome\Huntington disease-like 3

\Finding of head region\Disorder of basal ganglia\Huntington disease-like syndrome\Huntington disease-like 3

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

\Chronic brain syndrome\Huntington disease-like 3

\Extrapyramidal disease\Huntington disease-like syndrome\Huntington disease-like 3

\Disorder of basal ganglia\Huntington disease-like syndrome\Huntington disease-like 3

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Huntington disease-like 3
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Huntington disease-like 3
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Huntington disease-like 3
\Disease\Disorder of body system\Disorder of nervous system\Hereditary disorder of nervous system\Huntington disease-like 3
\Disease\Disorder of body system\Disorder of nervous system\System disorder of the nervous system\Disorder presenting primarily with chorea\Huntington disease-like syndrome\Huntington disease-like 3
\Disease\Disorder of body system\Disorder of nervous system\Chronic nervous system disorder\Chronic brain syndrome\Huntington disease-like 3
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Disorder of brain\Chronic brain syndrome\Huntington disease-like 3
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Disorder of brain\Extrapyramidal disease\Huntington disease-like syndrome\Huntington disease-like 3
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Disorder of brain\Disorder of basal ganglia\Huntington disease-like syndrome\Huntington disease-like 3
\Disease\Disorder of head\Disorder of brain\Chronic brain syndrome\Huntington disease-like 3
\Disease\Disorder of head\Disorder of brain\Extrapyramidal disease\Huntington disease-like syndrome\Huntington disease-like 3
\Disease\Disorder of head\Disorder of brain\Disorder of basal ganglia\Huntington disease-like syndrome\Huntington disease-like 3
\Disease\Movement disorder\Extrapyramidal disease\Huntington disease-like syndrome\Huntington disease-like 3
\Disease\Chronic disease\Chronic nervous system disorder\Chronic brain syndrome\Huntington disease-like 3

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

3703531018 Huntington disease-like 3 en Synonym Active Entire term case sensitive SNOMED CT core module

3703532013 Huntington disease-like 3 (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Huntington disease-like 3	Clinical course	Progressive	true	Inferred relationship	Existential restriction modifier	1
Huntington disease-like 3	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier
Huntington disease-like 3	Is a	Hereditary disorder of nervous system	true	Inferred relationship	Existential restriction modifier
Huntington disease-like 3	Is a	Huntington disease-like syndrome	true	Inferred relationship	Existential restriction modifier
Huntington disease-like 3	Is a	Chronic brain syndrome	true	Inferred relationship	Existential restriction modifier
Huntington disease-like 3	Finding site	Basal ganglion structure	true	Inferred relationship	Existential restriction modifier	2
Huntington disease-like 3	Interprets	Movement	true	Inferred relationship	Existential restriction modifier	3

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Chorea due to Huntington disease-like 3	Due to	True	Huntington disease-like 3	Inferred relationship	Existential restriction modifier	2

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
3703531018	Huntington disease-like 3	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3703532013	Huntington disease-like 3 (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module