Disease #00012 (WD (Hepatolenticular Degeneration), OMIM:277900)
| Official abbreviation |
WD |
| Name |
Hepatolenticular Degeneration |
| OMIM ID |
277900 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
164 |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
ATP7B |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
Individuals
|
|