Disease #00032 (PSP (Progressive Supranuclear Palsy), OMIM:601104)
| Official abbreviation |
PSP |
| Name |
Progressive Supranuclear Palsy |
| OMIM ID |
601104 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
16 |
| Phenotype entries for this disease |
- |
| Associated with 3 genes |
DCTN1, MAPT, PARK2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
Individuals
|
|