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88518009: Wilson's disease (disorder)

SNOMED CT Concept\Clinical finding\...

\Viscus structure finding\Abdominal organ finding\Liver finding\Liver disease\Metabolic and genetic disorder affecting the liver\Wilson's disease

\Digestive system finding\Liver finding\Liver disease\Metabolic and genetic disorder affecting the liver\Wilson's disease
\Digestive system finding\Disorder of digestive system\Digestive system hereditary disorder\Wilson's disease
\Digestive system finding\Disorder of digestive system\Disorder of digestive organ\Liver disease\Metabolic and genetic disorder affecting the liver\Wilson's disease

\Central nervous system finding\Finding of brain\Encephalopathy\Degenerative brain disorder\Wilson's disease
\Central nervous system finding\Disorder of the central nervous system\Encephalopathy\Degenerative brain disorder\Wilson's disease
\Central nervous system finding\Disorder of the central nervous system\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\Degenerative disease of the central nervous system\Degenerative brain disorder\Wilson's disease

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

\Finding of brain\Encephalopathy\Degenerative brain disorder\Wilson's disease

\Disorder of head\Encephalopathy\Degenerative brain disorder\Wilson's disease

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\Wilson's disease
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\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\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\Wilson's disease
\Disease\Disorder of body system\Hereditary disorder by system\Digestive system hereditary disorder\Wilson's disease
\Disease\Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\Wilson's disease
\Disease\Disorder of body system\Neurological disorder\System disorder of the nervous system\Disorder presenting primarily with chorea\Wilson's disease
\Disease\Disorder of body system\Neurological disorder\Disorder of the central nervous system\Encephalopathy\Degenerative brain disorder\Wilson's disease
\Disease\Disorder of body system\Neurological disorder\Disorder of the central nervous system\Degenerative disease of the central nervous system\Hereditary degenerative disease of central nervous system\Wilson's disease
\Disease\Disorder of body system\Neurological disorder\Disorder of the central nervous system\Degenerative disease of the central nervous system\Degenerative brain disorder\Wilson's disease
\Disease\Disorder of body system\Disorder of digestive system\Digestive system hereditary disorder\Wilson's disease
\Disease\Disorder of body system\Disorder of digestive system\Disorder of digestive organ\Liver disease\Metabolic and genetic disorder affecting the liver\Wilson's disease
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Liver disease\Metabolic and genetic disorder affecting the liver\Wilson's disease
\Disease\Disorder of head\Encephalopathy\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\Copper metabolism disorder\Wilson's disease

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

146760018 Wilson's disease en Synonym Active Case sensitive SNOMED CT core
146761019 Hepatolenticular degeneration syndrome en Synonym Active Case insensitive SNOMED CT core
146762014 Copper storage disease en Synonym Active Case insensitive SNOMED CT core
146763016 Cerebral pseudosclerosis en Synonym Inactive Initial character case insensitive SNOMED CT core
146764010 Westphal-Strümpell syndrome en Synonym Inactive Initial character case insensitive SNOMED CT core
146765011 Westphal-Strumpell syndrome en Synonym Inactive Case sensitive SNOMED CT core
2840410019 Wilson disease en Synonym Active Case sensitive SNOMED CT core
508067014 Hepatocerebral degeneration en Synonym Active Case insensitive SNOMED CT core
508068016 Hepatolenticular degeneration en Synonym Active Case insensitive SNOMED CT core
508069012 Kinnier-Wilson disease en Synonym Active Case sensitive SNOMED CT core
508070013 Neurohepatic degeneration en Synonym Active Case insensitive SNOMED CT core
508071012 Progressive lenticular degeneration en Synonym Active Case insensitive SNOMED CT core
508072017 WD - Wilson's disease en Synonym Active Case sensitive SNOMED CT core
831218010 Wilson's disease (disorder) en Fully specified name Active Case sensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Wilson's disease	Finding site	Brain tissue structure	true	Inferred relationship	Some	2
Wilson's disease	Associated morphology	Degenerative abnormality	true	Inferred relationship	Some	2
Wilson's disease	Associated morphology	Degenerative abnormality	true	Inferred relationship	Some	1
Wilson's disease	Associated morphology	Degenerative abnormality	true	Inferred relationship	Some	3
Wilson's disease	Finding site	Body tissue structure	true	Inferred relationship	Some	3
Wilson's disease	Is a	Hereditary degenerative disease of central nervous system	true	Inferred relationship	Some
Wilson's disease	Is a	Degenerative disease of the central nervous system	false	Inferred relationship	Some
Wilson's disease	Is a	Encephalopathy	false	Inferred relationship	Some
Wilson's disease	Is a	Lesion of brain	false	Inferred relationship	Some
Wilson's disease	Is a	Lesion of liver	false	Inferred relationship	Some
Wilson's disease	Is a	Degenerative brain disorder	true	Inferred relationship	Some
Wilson's disease	Is a	Disorder presenting primarily with chorea	true	Inferred relationship	Some
Wilson's disease	Is a	Hereditary disorder of nervous system	false	Inferred relationship	Some
Wilson's disease	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Wilson's disease	Is a	Metabolic and genetic disorder affecting the liver	true	Inferred relationship	Some
Wilson's disease	Is a	Copper metabolism disorder	true	Inferred relationship	Some
Wilson's disease	Is a	Digestive system hereditary disorder	true	Inferred relationship	Some
Wilson's disease	Is a	Degenerative disorder	false	Inferred relationship	Some
Wilson's disease	Finding site	Liver structure	true	Inferred relationship	Some	1
Wilson's disease	Finding site	Brain tissue structure	false	Inferred relationship	Some	1
Wilson's disease	Associated morphology	Degeneration	false	Inferred relationship	Some	1
Wilson's disease	Associated morphology	Degeneration	false	Inferred relationship	Some	2
Wilson's disease	Finding site	Liver structure	false	Inferred relationship	Some	2
Wilson's disease	Associated morphology	Degeneration	false	Inferred relationship	Some	3
Wilson's disease	Associated morphology	Degeneration	false	Inferred relationship	Some	4
Wilson's disease	Finding site	Brain tissue structure	false	Inferred relationship	Some	3
Wilson's disease	Finding site	Body tissue structure	false	Inferred relationship	Some	4
Wilson's disease	Associated morphology	Degeneration	false	Inferred relationship	Some	1
Wilson's disease	Finding site	Liver structure	false	Inferred relationship	Some	1
Wilson's disease	Finding site	Brain tissue structure	false	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Westphal-Strumpell syndrome	Is a	True	Wilson's disease	Inferred relationship	Some
Hypoparathyroidism due to Wilson disease	Due to	True	Wilson's disease	Inferred relationship	Some	3
Dementia due to Wilson disease	Due to	True	Wilson's disease	Inferred relationship	Some	3
Chorea co-occurrent and due to Wilson disease	Due to	True	Wilson's disease	Inferred relationship	Some	3
Chorea co-occurrent and due to Wilson disease	Is a	True	Wilson's disease	Inferred relationship	Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
146760018	Wilson's disease	en	Synonym	Active	Case sensitive	SNOMED CT core
146761019	Hepatolenticular degeneration syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
146762014	Copper storage disease	en	Synonym	Active	Case insensitive	SNOMED CT core
146763016	Cerebral pseudosclerosis	en	Synonym	Inactive	Initial character case insensitive	SNOMED CT core
146764010	Westphal-Strümpell syndrome	en	Synonym	Inactive	Initial character case insensitive	SNOMED CT core
146765011	Westphal-Strumpell syndrome	en	Synonym	Inactive	Case sensitive	SNOMED CT core
2840410019	Wilson disease	en	Synonym	Active	Case sensitive	SNOMED CT core
508067014	Hepatocerebral degeneration	en	Synonym	Active	Case insensitive	SNOMED CT core
508068016	Hepatolenticular degeneration	en	Synonym	Active	Case insensitive	SNOMED CT core
508069012	Kinnier-Wilson disease	en	Synonym	Active	Case sensitive	SNOMED CT core
508070013	Neurohepatic degeneration	en	Synonym	Active	Case insensitive	SNOMED CT core
508071012	Progressive lenticular degeneration	en	Synonym	Active	Case insensitive	SNOMED CT core
508072017	WD - Wilson's disease	en	Synonym	Active	Case sensitive	SNOMED CT core
831218010	Wilson's disease (disorder)	en	Fully specified name	Active	Case sensitive	SNOMED CT core