Disease #00021 (MSA (Multiple System Atrophy), OMIM:146500)
| Official abbreviation |
MSA |
| Name |
Multiple System Atrophy |
| OMIM ID |
146500 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
26 |
| Phenotype entries for this disease |
- |
| Associated with 2 genes |
COQ2, POLG |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
Individuals
|
|