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
|
|