Wilson disease
E1968049
UNEXPLORED
Wilson disease is a rare inherited disorder of copper metabolism that leads to toxic copper accumulation, primarily damaging the liver and brain and causing hepatic, neurological, and psychiatric symptoms.
All labels observed (1)
| Label | Occurrences |
|---|---|
| Wilson disease canonical | 1 |
Referenced by (1)
Full triples — surface form annotated when it differs from this entity's canonical label.