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
|
|