loading...| Preferred Name | Wilson disease | |
| Synonyms |
hepatolenticular Degeneration Wnd WD cerebral pseudosclerosis Westphal pseudosclerosis Wilson's disease Westphal-Strumpell syndrome hepatolenticular degeneration Wilson disease |
|
| Definitions |
A very rare inherited multisystemic disease presenting non-specific neurological, hepatic, psychiatric or osseo-muscular manifestations due to excessive copper deposition in the body. |
|
| ID |
http://purl.obolibrary.org/obo/MONDO_0010200 |
|
| altLabel |
hepatolenticular Degeneration Wnd WD cerebral pseudosclerosis Westphal pseudosclerosis Wilson's disease Westphal-Strumpell syndrome hepatolenticular degeneration Wilson 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. |
|
| has characteristic | ||
| has_exact_synonym |
cerebral pseudosclerosis Westphal pseudosclerosis Wilson's disease Westphal-Strumpell syndrome hepatolenticular degeneration Wilson disease |
|
| has_related_synonym |
hepatolenticular Degeneration Wnd WD |
|
| label |
Wilson disease |
|
| prefixIRI |
MONDO:0010200 |
|
| prefLabel |
Wilson disease |
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| seeAlso |
https://rarediseases.info.nih.gov/diseases/7893/wilson-disease |
|
| textual 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. |
|
| subClassOf |