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88518009: Wilson's disease (disorder)

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

Descriptions:

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

2 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Wilson's disease Is a Disorder presenting primarily with chorea true Inferred relationship Existential restriction modifier
Wilson's disease Is a Hereditary disorder of nervous system false Inferred relationship Existential restriction modifier
Wilson's disease Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Wilson's disease Is a Metabolic and genetic disorder affecting the liver true Inferred relationship Existential restriction modifier
Wilson's disease Is a Disorder of copper metabolism true Inferred relationship Existential restriction modifier
Wilson's disease Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier
Wilson's disease Is a Degenerative disorder false Inferred relationship Existential restriction modifier
Wilson's disease Associated morphology Degeneration false Inferred relationship Existential restriction modifier 1
Wilson's disease Finding site Liver structure false Inferred relationship Existential restriction modifier 1
Wilson's disease Finding site Brain tissue structure false Inferred relationship Existential restriction modifier 1
Wilson's disease Is a Degenerative disease of the central nervous system false Inferred relationship Existential restriction modifier
Wilson's disease Is a Disorder of brain false Inferred relationship Existential restriction modifier
Wilson's disease Is a Lesion of brain false Inferred relationship Existential restriction modifier
Wilson's disease Is a Lesion of liver false Inferred relationship Existential restriction modifier
Wilson's disease Is a Degenerative brain disorder true Inferred relationship Existential restriction modifier
Wilson's disease Finding site Liver structure true Inferred relationship Existential restriction modifier 1
Wilson's disease Finding site Brain tissue structure false Inferred relationship Existential restriction modifier 1
Wilson's disease Associated morphology Degeneration false Inferred relationship Existential restriction modifier 1
Wilson's disease Associated morphology Degeneration false Inferred relationship Existential restriction modifier 2
Wilson's disease Finding site Liver structure false Inferred relationship Existential restriction modifier 2
Wilson's disease Associated morphology Degeneration false Inferred relationship Existential restriction modifier 3
Wilson's disease Associated morphology Degeneration false Inferred relationship Existential restriction modifier 4
Wilson's disease Finding site Brain tissue structure false Inferred relationship Existential restriction modifier 3
Wilson's disease Finding site Body tissue structure false Inferred relationship Existential restriction modifier 4
Wilson's disease Finding site Brain tissue structure true Inferred relationship Existential restriction modifier 2
Wilson's disease Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 2
Wilson's disease Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 1
Wilson's disease Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 3
Wilson's disease Finding site Body tissue structure true Inferred relationship Existential restriction modifier 3
Wilson's disease Is a Hereditary degenerative disease of central nervous system true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Chorea co-occurrent and due to Wilson disease Due to True Wilson's disease Inferred relationship Existential restriction modifier 3
Chorea co-occurrent and due to Wilson disease Is a True Wilson's disease Inferred relationship Existential restriction modifier
Westphal-Strumpell syndrome Is a True Wilson's disease Inferred relationship Existential restriction modifier
Hypoparathyroidism due to Wilson disease Due to True Wilson's disease Inferred relationship Existential restriction modifier 3
Dementia due to Wilson disease Due to True Wilson's disease Inferred relationship Existential restriction modifier 3

This concept is not in any reference sets

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