Autosomal recessive hereditary disorder
Autosomal recessive hereditary disorder
Degenerative brain disorder
Degenerative brain disorder
Digestive system hereditary disorder
Digestive system hereditary disorder
Disorder of copper metabolism
Disorder of copper metabolism
Disorder presenting primarily with chorea
Disorder presenting primarily with chorea
Hereditary degenerative disease of central nervous system
Hereditary metabolic disease
Metabolic and genetic disorder affecting the liver
Metabolic and genetic disorder affecting the liver
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Wilson's disease (disorder)
Wilson's disease
WD - Wilson's disease
Kinnier-Wilson disease
Hepatolenticular degeneration syndrome
Progressive lenticular degeneration
Hepatolenticular degeneration
Neurohepatic degeneration
Wilson disease
Hepatocerebral degeneration
Copper storage disease
ziekte van Wilson
hepatolenticulaire degeneratie
koperstapelingsziekte
ziekte van Wilson
Hierbij is er sprake van een stoornis van de koperstofwisseling.
Id88518009
StatusPrimitive
Associated morphologyDegenerative abnormality
Finding siteLiver structure
Associated morphologyDegenerative abnormality
Finding siteBrain tissue structure
Associated morphologyDegenerative abnormality
Finding siteBody tissue structure
PALGA thesaurus simple reference set for pathology
General Practice / Family Practice reference set
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetE83.0
RuleTRUE
AdviceALWAYS E83.0
CorrelationSNOMED CT source code to target map code correlation not specified
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Chorea co-occurrent and due to Wilson disease
Westphal-Strumpell syndrome