230306001: Benign hereditary chorea (disorder)

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

\Head finding (finding)\Finding of brain\Disorder of brain\Extrapyramidal disease\Chorea (disorder)\Benign hereditary chorea
\Head finding (finding)\Finding of brain\Disorder of brain\Disorder of basal ganglia (disorder)\Chorea (disorder)\Benign hereditary chorea
\Head finding (finding)\Finding of head region\Disorder of basal ganglia (disorder)\Chorea (disorder)\Benign hereditary chorea
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain\Extrapyramidal disease\Chorea (disorder)\Benign hereditary chorea
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain\Disorder of basal ganglia (disorder)\Chorea (disorder)\Benign hereditary chorea

\Finding of movement\Involuntary movement\Chorea (disorder)\Benign hereditary chorea
\Finding of movement\Movement disorder\Extrapyramidal disease\Chorea (disorder)\Benign hereditary chorea

\Central nervous system finding\Finding of brain\Disorder of brain\Extrapyramidal disease\Chorea (disorder)\Benign hereditary chorea
\Central nervous system finding\Finding of brain\Disorder of brain\Disorder of basal ganglia (disorder)\Chorea (disorder)\Benign hereditary chorea
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain\Extrapyramidal disease\Chorea (disorder)\Benign hereditary chorea
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain\Disorder of basal ganglia (disorder)\Chorea (disorder)\Benign hereditary chorea

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of nervous system (disorder)\Benign hereditary chorea
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of nervous system (disorder)\Benign hereditary chorea
\Disease\Disorder of body system\Disease of nervous system (disorder)\Hereditary disorder of nervous system (disorder)\Benign hereditary chorea
\Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain\Extrapyramidal disease\Chorea (disorder)\Benign hereditary chorea
\Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain\Disorder of basal ganglia (disorder)\Chorea (disorder)\Benign hereditary chorea
\Disease\Disorder of head (disorder)\Disorder of brain\Extrapyramidal disease\Chorea (disorder)\Benign hereditary chorea
\Disease\Disorder of head (disorder)\Disorder of brain\Disorder of basal ganglia (disorder)\Chorea (disorder)\Benign hereditary chorea
\Disease\Movement disorder\Extrapyramidal disease\Chorea (disorder)\Benign hereditary chorea

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Benign hereditary chorea	Is a	trouble présent principalement avec la chorée	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Benign hereditary chorea	Finding site	Nervous system structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Benign hereditary chorea	Is a	Hereditary disorder of nervous system (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Benign hereditary chorea	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Benign hereditary chorea	Is a	Chorea (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Benign hereditary chorea	Finding site	Basal ganglion structure (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Benign hereditary chorea	Interprets	Movement	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Benign hereditary chorea	Interprets	Movement observable	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Childhood-onset benign chorea with striatal involvement	Is a	True	Benign hereditary chorea	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
345132017	Benign hereditary chorea	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
618095015	Benign hereditary chorea (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
345132017	Benign hereditary chorea	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
345132017	Benign hereditary chorea	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
618095015	Benign hereditary chorea (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
618095015	Benign hereditary chorea (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3452811001000111	Chorea, benigne hereditäre	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
946821000172113	chorée bénigne familiale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
974451000172114	chorée bénigne héréditaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
946821000172113	chorée bénigne familiale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
974451000172114	chorée bénigne héréditaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3452811001000111	Chorea, benigne hereditäre	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module