Disease #00020 (WD (WILSON DISEASE), OMIM:277900)
Official abbreviation |
WD |
Name |
WILSON DISEASE |
OMIM ID |
277900 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
ATP7B |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2016-07-08 14:44:00 +00:00 (UTC) |
Date last edited |
2023-06-16 08:38:09 +00:00 (UTC) |
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