| Metadata | |
|---|---|
| ID | DOID:893 |
| Name | Wilson disease |
| Definition | A metal metabolism disease that is characterized by excess copper stored in various body tissues, particularly the liver, brain, and corneas of the eyes. https://pubmed.ncbi.nlm.nih.gov/32279718/, https://www.genome.gov/Genetic-Disorders/Wilson-Disease |
| Xrefs |
SNOMEDCT_US_2023_03_01:88518009 |
| Subsets |
DO_rare_slim NCIthesaurus |
| Synonyms |
Cerebral pseudosclerosis [EXACT] hepatolenticular degeneration [EXACT] Westphal pseudosclerosis [EXACT] Westphal-Strumpell syndrome [EXACT] Wilson's disease [EXACT] |
| Parent Relationships | |
| Subclass Logical Relationships |