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190823004: Westphal-Strumpell syndrome (disorder)

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

\Viscus structure finding (finding)\Abdominal organ finding\Liver finding\Disease of liver\Metabolic and genetic disorder affecting the liver\Wilson's disease\Westphal-Strumpell syndrome

\Head finding (finding)\Finding of brain\Disorder of brain\Extrapyramidal disease\Chorea (disorder)\Wilson's disease\Westphal-Strumpell syndrome
\Head finding (finding)\Finding of brain\Disorder of brain\Disorder of basal ganglia (disorder)\Chorea (disorder)\Wilson's disease\Westphal-Strumpell syndrome
\Head finding (finding)\Finding of brain\Disorder of brain\Degenerative brain disorder\Wilson's disease\Westphal-Strumpell syndrome
\Head finding (finding)\Finding of head region\Disorder of basal ganglia (disorder)\Chorea (disorder)\Wilson's disease\Westphal-Strumpell syndrome
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain\Extrapyramidal disease\Chorea (disorder)\Wilson's disease\Westphal-Strumpell syndrome
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain\Disorder of basal ganglia (disorder)\Chorea (disorder)\Wilson's disease\Westphal-Strumpell syndrome
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain\Degenerative brain disorder\Wilson's disease\Westphal-Strumpell syndrome

\Digestive system finding (finding)\Liver finding\Disease of liver\Metabolic and genetic disorder affecting the liver\Wilson's disease\Westphal-Strumpell syndrome
\Digestive system finding (finding)\Disease of digestive system (disorder)\Digestive system hereditary disorder\Wilson's disease\Westphal-Strumpell syndrome
\Digestive system finding (finding)\Disease of digestive system (disorder)\Disorder of digestive organ\Disorder of liver and/or biliary tract\Disease of liver\Metabolic and genetic disorder affecting the liver\Wilson's disease\Westphal-Strumpell syndrome

\Finding of movement\Involuntary movement\Chorea (disorder)\Wilson's disease\Westphal-Strumpell syndrome
\Finding of movement\Movement disorder\Extrapyramidal disease\Chorea (disorder)\Wilson's disease\Westphal-Strumpell syndrome

\Central nervous system finding\Finding of brain\Disorder of brain\Extrapyramidal disease\Chorea (disorder)\Wilson's disease\Westphal-Strumpell syndrome
\Central nervous system finding\Finding of brain\Disorder of brain\Disorder of basal ganglia (disorder)\Chorea (disorder)\Wilson's disease\Westphal-Strumpell syndrome
\Central nervous system finding\Finding of brain\Disorder of brain\Degenerative brain disorder\Wilson's disease\Westphal-Strumpell syndrome
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain\Extrapyramidal disease\Chorea (disorder)\Wilson's disease\Westphal-Strumpell syndrome
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain\Disorder of basal ganglia (disorder)\Chorea (disorder)\Wilson's disease\Westphal-Strumpell syndrome
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain\Degenerative brain disorder\Wilson's disease\Westphal-Strumpell syndrome
\Central nervous system finding\Disorder of the central nervous system (disorder)\Degenerative disease of the central nervous system\Hereditary degenerative disease of central nervous system\Wilson's disease\Westphal-Strumpell syndrome
\Central nervous system finding\Disorder of the central nervous system (disorder)\Degenerative disease of the central nervous system\Degenerative brain disorder\Wilson's disease\Westphal-Strumpell syndrome

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of nervous system (disorder)\Hereditary degenerative disease of central nervous system\Wilson's disease\Westphal-Strumpell syndrome
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Digestive system hereditary disorder\Wilson's disease\Westphal-Strumpell syndrome
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Wilson's disease\Westphal-Strumpell syndrome
\Disease\Degenerative disorder\Degenerative disease of the central nervous system\Hereditary degenerative disease of central nervous system\Wilson's disease\Westphal-Strumpell syndrome
\Disease\Degenerative disorder\Degenerative disease of the central nervous system\Degenerative brain disorder\Wilson's disease\Westphal-Strumpell syndrome
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of nervous system (disorder)\Hereditary degenerative disease of central nervous system\Wilson's disease\Westphal-Strumpell syndrome
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Digestive system hereditary disorder\Wilson's disease\Westphal-Strumpell syndrome
\Disease\Disorder of body system\Disease of nervous system (disorder)\Hereditary disorder of nervous system (disorder)\Hereditary degenerative disease of central nervous system\Wilson's disease\Westphal-Strumpell syndrome
\Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain\Extrapyramidal disease\Chorea (disorder)\Wilson's disease\Westphal-Strumpell syndrome
\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)\Wilson's disease\Westphal-Strumpell syndrome
\Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain\Degenerative brain disorder\Wilson's disease\Westphal-Strumpell syndrome
\Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the central nervous system (disorder)\Degenerative disease of the central nervous system\Hereditary degenerative disease of central nervous system\Wilson's disease\Westphal-Strumpell syndrome
\Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the central nervous system (disorder)\Degenerative disease of the central nervous system\Degenerative brain disorder\Wilson's disease\Westphal-Strumpell syndrome
\Disease\Disorder of body system\Disease of digestive system (disorder)\Digestive system hereditary disorder\Wilson's disease\Westphal-Strumpell syndrome
\Disease\Disorder of body system\Disease of digestive system (disorder)\Disorder of digestive organ\Disorder of liver and/or biliary tract\Disease of liver\Metabolic and genetic disorder affecting the liver\Wilson's disease\Westphal-Strumpell syndrome
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Disorder of liver and/or biliary tract\Disease of liver\Metabolic and genetic disorder affecting the liver\Wilson's disease\Westphal-Strumpell syndrome
\Disease\Disorder of head (disorder)\Disorder of brain\Extrapyramidal disease\Chorea (disorder)\Wilson's disease\Westphal-Strumpell syndrome
\Disease\Disorder of head (disorder)\Disorder of brain\Disorder of basal ganglia (disorder)\Chorea (disorder)\Wilson's disease\Westphal-Strumpell syndrome
\Disease\Disorder of head (disorder)\Disorder of brain\Degenerative brain disorder\Wilson's disease\Westphal-Strumpell syndrome
\Disease\Metabolic disease\Metabolic and genetic disorder affecting the liver\Wilson's disease\Westphal-Strumpell syndrome
\Disease\Metabolic disease\Disorder of mineral metabolism\Disorder of copper metabolism\Wilson's disease\Westphal-Strumpell syndrome
\Disease\Movement disorder\Extrapyramidal disease\Chorea (disorder)\Wilson's disease\Westphal-Strumpell syndrome

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
Westphal-Strumpell syndrome	Is a	Autosomal recessive hereditary disorder	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Westphal-Strumpell syndrome	Finding site	Brain tissue structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Westphal-Strumpell syndrome	Associated morphology	Degenerative abnormality (morphologic abnormality)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Westphal-Strumpell syndrome	Associated morphology	Degenerative abnormality (morphologic abnormality)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Westphal-Strumpell syndrome	Associated morphology	Degenerative abnormality (morphologic abnormality)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Westphal-Strumpell syndrome	Finding site	Liver structure (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Westphal-Strumpell syndrome	Finding site	Body tissue structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Westphal-Strumpell syndrome	Is a	Wilson's disease	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Westphal-Strumpell syndrome	Interprets	Movement	true	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Westphal-Strumpell syndrome	Finding site	Basal ganglion structure (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Westphal-Strumpell syndrome	Interprets	Movement observable	true	Inferred relationship	Existential restriction modifier (core metadata concept)	6
Westphal-Strumpell syndrome	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier (core metadata concept)	6
Westphal-Strumpell syndrome	Finding site	Brain structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2

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
293387010	Westphal-Strumpell syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
574452017	Westphal-Strumpell syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4572807010	Westphal-Strumpell cerebral pseudosclerosis	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4572808017	Pseudosclerotic type of Wilson's disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4572809013	Westphal-Strumpell form of Wilson's disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
293387010	Westphal-Strumpell syndrome	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
293387010	Westphal-Strumpell syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
574452017	Westphal-Strumpell syndrome (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
574452017	Westphal-Strumpell syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4572807010	Westphal-Strumpell cerebral pseudosclerosis	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4572808017	Pseudosclerotic type of Wilson's disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4572809013	Westphal-Strumpell form of Wilson's disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
6061701000241112	pseudosclérose de Westphal	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6061711000241114	syndrome de Westphal-Strumpell	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6061701000241112	pseudosclérose de Westphal	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6061711000241114	syndrome de Westphal-Strumpell	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module