5C64.00 Wilson disease
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
Wilson disease is an autosomal recessive disorder of copper metabolism characterised by the toxic accumulation of copper, mainly in the liver and central nervous system that may present as hepatic, neurologic or psychiatric forms.
postcoordination
Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
Has manifestation - multiple selections are allowed
synonyms
- Wilson disease
- Copper retention
- Copper storage disease
- Hepatocerebral degeneration
- Kinnier-Wilson disease
- Neurohepatic degeneration
- Progressive hepatolenticular degeneration
- lenticular degenerative disease
- Wilson's syndrome
- lenticular syndrome
- Westphal-Strumpell Syndrome
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