Wilson disease (Q17588): Difference between revisions
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Created claim: subclass of (P1): rare genetic epilepsy (Q17615) |
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| Property / subclass of | |||
| Property / subclass of: rare genetic epilepsy / rank | |||
Normal rank | |||
Revision as of 15:48, 31 December 2023
multisystem disease due to abnormal accumulation of copper
- Cerebral pseudosclerosis (disorder)
- Westphal pseudosclerosis
- Westphal-Strumpell syndrome (disorder)
- hepatolenticular degeneration
- Wilson's disease
- Cerebral pseudosclerosis
- Westphal-Strumpell syndrome
- WD
- Wnd
- Wilson Disease
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Wilson disease |
multisystem disease due to abnormal accumulation of copper |
|