Wilson's disease
ICD-10 Code
E83.0
Category
Metabolic
Wilson's disease
Definition
A very rare inherited multisystemic disease presenting non-specific neurological, hepatic, psychiatric or osseo-muscular manifestations due to excessive copper deposition in the body.
Also known as hepatolenticular degeneration, Westphal-Strumpell syndrome, Wilson disease, Wilson's disease — per MONDO
Also identified as
- DOID 893 per MONDO
- ICD10CM E83.01 per MONDO
- MESH D006527 per MONDO
- NCIT C84756 per MONDO
- OMIM 277900 per MONDO
- Orphanet 905 per MONDO
- SCTID 88518009 per MONDO
- UMLS C0019202 per MONDO
Drugs indicated
| Drug | Relation | Source |
|---|---|---|
| Penicillamine | may treat | MEDRT · Public domain (U.S. Government work) |