230306001: Benign hereditary chorea (disorder)

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

\Head finding (finding)\Finding of brain\Disorder of brain (disorder)\Extrapyramidal disease\Involuntary movement characterised by brief, unpredictable, irregular, non-stereotyped movements that flow randomly from one body part to another.\Benign hereditary chorea
\Head finding (finding)\Finding of brain\Disorder of brain (disorder)\Disorder of basal ganglia (disorder)\Involuntary movement characterised by brief, unpredictable, irregular, non-stereotyped movements that flow randomly from one body part to another.\Benign hereditary chorea
\Head finding (finding)\Finding of head region\Disorder of basal ganglia (disorder)\Involuntary movement characterised by brief, unpredictable, irregular, non-stereotyped movements that flow randomly from one body part to another.\Benign hereditary chorea
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain (disorder)\Extrapyramidal disease\Involuntary movement characterised by brief, unpredictable, irregular, non-stereotyped movements that flow randomly from one body part to another.\Benign hereditary chorea
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain (disorder)\Disorder of basal ganglia (disorder)\Involuntary movement characterised by brief, unpredictable, irregular, non-stereotyped movements that flow randomly from one body part to another.\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:

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

1773981000005119 benign hereditær chorea da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Benign hereditary chorea	Is a	Sygdom, der primært manifesterer sig ved chorea	false	Inferred relationship	Some
Benign hereditary chorea	Finding site	Structure of nervous system (body structure)	false	Inferred relationship	Some	1
Benign hereditary chorea	Is a	Hereditary disorder of nervous system	true	Inferred relationship	Some
Benign hereditary chorea	Has interpretation	Abnormal	true	Inferred relationship	Some	2
Benign hereditary chorea	Is a	Involuntary movement characterised by brief, unpredictable, irregular, non-stereotyped movements that flow randomly from one body part to another.	true	Inferred relationship	Some
Benign hereditary chorea	Finding site	Basal ganglion structure (body structure)	true	Inferred relationship	Some	1
Benign hereditary chorea	Interprets	Movement	true	Inferred relationship	Some	3
Benign hereditary chorea	Interprets	Movement observable (observable entity)	true	Inferred relationship	Some	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
A rare genetic hyperkinetic movement disorder characterized predominantly by chorea of variable severity, associated with bilateral striatal abnormalities on cerebral MRI. The disease is scarcely progressive, and cognitive performance is preserved in the majority of cases, although mild cognitive delay has also been reported.	Is a	True	Benign hereditary chorea	Inferred relationship	Some

This concept is not in any reference sets