Disease #05035 (SCA21 (ataxia, spinocerebellar, type 21 (SCA-21)), OMIM:607454)
| Official abbreviation |
SCA21 |
| Name |
ataxia, spinocerebellar, type 21 (SCA-21) |
| OMIM ID |
607454 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
TMEM240 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 11:00:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|