88518009: Wilson's disease (disorder)

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

\Viscus structure finding (finding)\Liver finding\Disease of liver\...

\Structural abnormality of liver (disorder)\Wilson's disease

\Metabolic and genetic disorder affecting the liver\Wilson's disease

\Finding of trunk structure\Liver finding\Disease of liver\Structural abnormality of liver (disorder)\Wilson's disease
\Finding of trunk structure\Liver finding\Disease of liver\Metabolic and genetic disorder affecting the liver\Wilson's disease
\Finding of trunk structure\Disorder of trunk (disorder)\Disease of liver\Structural abnormality of liver (disorder)\Wilson's disease
\Finding of trunk structure\Disorder of trunk (disorder)\Disease of liver\Metabolic and genetic disorder affecting the liver\Wilson's disease

\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Wilson's disease
\Disease\Disorder of body system\Chorea\Wilson's disease
\Disease\Disorder of body system\Disease of liver\Structural abnormality of liver (disorder)\Wilson's disease
\Disease\Disorder of body system\Disease of liver\Metabolic and genetic disorder affecting the liver\Wilson's disease
\Disease\Disorder of trunk (disorder)\Disease of liver\Structural abnormality of liver (disorder)\Wilson's disease
\Disease\Disorder of trunk (disorder)\Disease of liver\Metabolic and genetic disorder affecting the liver\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

Status: current. Date: 31-Jan 2002

Descriptions:

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
146763016 Cerebral pseudosclerosis en Synonym (core metadata concept) Inactive Only initial character case insensitive (core metadata concept) SNOMED CT core
146764010 Westphal-Strümpell syndrome en Synonym (core metadata concept) Inactive Only initial character case insensitive (core metadata concept) SNOMED CT core
146765011 Westphal-Strumpell syndrome en Synonym (core metadata concept) Inactive Entire term case sensitive (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

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Wilson's disease	Is a	Metabolic and genetic disorder affecting the liver	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly
Wilson's disease	Is a	Chorea	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly
Wilson's disease	Is a	Disorder of copper metabolism	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly
Wilson's disease	Is a	Autosomal recessive hereditary disorder	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly
Wilson's disease	Is a	Structural abnormality of liver (disorder)	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly
Wilson's disease	Associated morphology	Degenerative abnormality	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	1
Wilson's disease	Finding site	Liver structure	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	1
Wilson's disease	Associated morphology	Degenerative abnormality	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	2
Wilson's disease	Finding site	Brain structure	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	2
Wilson's disease	Associated morphology	Degenerative abnormality	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	3
Wilson's disease	Finding site	Body tissue structure	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	3
Wilson's disease	Has interpretation	Abnormal	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	4
Wilson's disease	Interprets	Movement observable	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	4
Wilson's disease	Finding site	Structure of basal nucleus	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	5

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Chorea co-occurrent and due to Wilson disease (disorder)	Is a	True	Wilson's disease	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly
Chorea co-occurrent and due to Wilson disease (disorder)	Due to	True	Wilson's disease	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	6
Westphal-Strumpell syndrome	Is a	True	Wilson's disease	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly

This concept is not in any reference sets