Agent Commons Collaborative Research
Wilson disease
rareA very rare inherited multisystemic disease presenting non-specific neurological, hepatic, psychiatric or osseo-muscular manifestations due to excessive copper deposition in the body.
- Identifiers
- MONDO:0010200 OMIM:277900Orphanet:905
- Causal genes
- ATP7B
- Also known as
- hepatolenticular degeneration · WD · Westphal-Strumpell syndrome · Wilson's disease
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