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88518009: Wilson's disease (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

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

\Finding of movement\Involuntary movement\Chorea (disorder)\Wilson's disease
\Finding of movement\Movement disorder\Extrapyramidal disease\Chorea (disorder)\Wilson's disease

\Central nervous system finding\Finding of brain\Disorder of brain\Extrapyramidal disease\Chorea (disorder)\Wilson's disease
\Central nervous system finding\Finding of brain\Disorder of brain\Disorder of basal ganglia (disorder)\Chorea (disorder)\Wilson's disease
\Central nervous system finding\Finding of brain\Disorder of brain\Degenerative brain disorder\Wilson's disease
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain\Extrapyramidal disease\Chorea (disorder)\Wilson's disease
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain\Disorder of basal ganglia (disorder)\Chorea (disorder)\Wilson's disease
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain\Degenerative brain disorder\Wilson's disease
\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
\Central nervous system finding\Disorder of the central nervous system (disorder)\Degenerative disease of the central nervous system\Degenerative brain disorder\Wilson's disease

\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
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Digestive system hereditary disorder\Wilson's disease
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Wilson's disease
\Disease\Degenerative disorder\Degenerative disease of the central nervous system\Hereditary degenerative disease of central nervous system\Wilson's disease
\Disease\Degenerative disorder\Degenerative disease of the central nervous system\Degenerative brain disorder\Wilson's disease
\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
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Digestive system hereditary disorder\Wilson's disease
\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
\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
\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
\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
\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
\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
\Disease\Disorder of body system\Disease of digestive system (disorder)\Digestive system hereditary disorder\Wilson's disease
\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
\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
\Disease\Disorder of head (disorder)\Disorder of brain\Extrapyramidal disease\Chorea (disorder)\Wilson's disease
\Disease\Disorder of head (disorder)\Disorder of brain\Disorder of basal ganglia (disorder)\Chorea (disorder)\Wilson's disease
\Disease\Disorder of head (disorder)\Disorder of brain\Degenerative brain disorder\Wilson's disease
\Disease\Metabolic disease\Metabolic and genetic disorder affecting the liver\Wilson's disease
\Disease\Metabolic disease\Disorder of mineral metabolism\Disorder of copper metabolism\Wilson's disease
\Disease\Movement disorder\Extrapyramidal disease\Chorea (disorder)\Wilson's disease

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
Wilson's disease	Is a	trouble présent principalement avec la chorée	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Wilson's disease	Is a	Hereditary disorder of nervous system (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Wilson's disease	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Wilson's disease	Is a	Metabolic and genetic disorder affecting the liver	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Wilson's disease	Is a	Disorder of copper metabolism	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Wilson's disease	Is a	Digestive system hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Wilson's disease	Is a	Degenerative disorder	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Wilson's disease	Associated morphology	dégénérescence	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Wilson's disease	Finding site	Liver structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Wilson's disease	Finding site	Brain tissue structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Wilson's disease	Is a	Degenerative disease of the central nervous system	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Wilson's disease	Is a	Disorder of brain	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Wilson's disease	Is a	Lesion of brain (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Wilson's disease	Is a	Lesion of liver (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Wilson's disease	Is a	Degenerative brain disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Wilson's disease	Finding site	Liver structure (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Wilson's disease	Finding site	Brain tissue structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Wilson's disease	Associated morphology	dégénérescence	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Wilson's disease	Associated morphology	dégénérescence	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Wilson's disease	Finding site	Liver structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Wilson's disease	Associated morphology	dégénérescence	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Wilson's disease	Associated morphology	dégénérescence	false	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Wilson's disease	Finding site	Brain tissue structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Wilson's disease	Finding site	Body tissue structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Wilson's disease	Finding site	Brain tissue structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Wilson's disease	Associated morphology	Degenerative abnormality (morphologic abnormality)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Wilson's disease	Associated morphology	Degenerative abnormality (morphologic abnormality)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Wilson's disease	Associated morphology	Degenerative abnormality (morphologic abnormality)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Wilson's disease	Finding site	Body tissue structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Wilson's disease	Is a	Hereditary degenerative disease of central nervous system	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Wilson's disease	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Wilson's disease	Is a	Chorea (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Wilson's disease	Finding site	Basal ganglion structure (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Wilson's disease	Interprets	Movement	true	Inferred relationship	Existential restriction modifier (core metadata concept)	6
Wilson's disease	Interprets	Movement observable	true	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Wilson's disease	Finding site	Brain structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Chorea co-occurrent and due to Wilson disease (disorder)	Due to	True	Wilson's disease	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Chorea co-occurrent and due to Wilson disease (disorder)	Is a	True	Wilson's disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Westphal-Strumpell syndrome	Is a	True	Wilson's disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Hypoparathyroidism due to Wilson disease	Due to	True	Wilson's disease	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Dementia due to Wilson disease (disorder)	Due to	True	Wilson's disease	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Dystonia due to Wilson disease	Due to	True	Wilson's disease	Inferred relationship	Existential restriction modifier (core metadata concept)	3

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
146760018	Wilson's disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
146761019	Hepatolenticular degeneration syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
146762014	Copper storage disease	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
508067014	Hepatocerebral degeneration	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
508068016	Hepatolenticular degeneration	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
508069012	Kinnier-Wilson disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
508070013	Neurohepatic degeneration	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
508071012	Progressive lenticular degeneration	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
508072017	WD - Wilson's disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
831218010	Wilson's disease (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
2840410019	Wilson disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
146760018	Wilson's disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
146761019	Hepatolenticular degeneration syndrome	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
146761019	Hepatolenticular degeneration syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
146762014	Copper storage disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
146762014	Copper storage disease	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
146763016	Cerebral pseudosclerosis	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
146764010	Westphal-Strümpell syndrome	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
146765011	Westphal-Strumpell syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
508067014	Hepatocerebral degeneration	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
508067014	Hepatocerebral degeneration	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
508068016	Hepatolenticular degeneration	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
508068016	Hepatolenticular degeneration	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
508069012	Kinnier-Wilson disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
508070013	Neurohepatic degeneration	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
508070013	Neurohepatic degeneration	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
508071012	Progressive lenticular degeneration	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
508071012	Progressive lenticular degeneration	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
508072017	WD - Wilson's disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
831218010	Wilson's disease (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
831218010	Wilson's disease (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
2840410019	Wilson disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
424441000274117	Morbus Wilson	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
462161000274113	Kupferspeicherkrankheit	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
864161000195111	Hepatolentikuläre Degeneration	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3429161001000113	Wilson-Krankheit	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
193521000172110	maladie de Wilson	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
193521000172110	maladie de Wilson	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
424441000274117	Morbus Wilson	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
462161000274113	Kupferspeicherkrankheit	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
864161000195111	Hepatolentikuläre Degeneration	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3429161001000113	Wilson-Krankheit	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module