Disease #00031 (PBP (Progressive Bulbar Palsy))
| Official abbreviation |
PBP |
| Name |
Progressive Bulbar Palsy |
| OMIM ID |
- |
| Inheritance |
- |
| Individuals reported having this disease |
3 |
| Phenotype entries for this disease |
- |
| Associated with 2 genes |
SOD1, TTR |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
Individuals
|