Disease #00029 (PD (Parkinson Disease), OMIM:168600)
| Official abbreviation |
PD |
| Name |
Parkinson Disease |
| OMIM ID |
168600 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
558 |
| Phenotype entries for this disease |
1 |
| Associated with 15 genes |
ADORA1, DNAJC13, FBXO7, LRRK2, MAPT, PARK2, PARK7, PINK1, PODXL, PRNP, PTRHD1, RIC3, SNCA, SYNJ1, VPS35 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
Individuals
|