Disease #01564 (SCA6 (ataxia, spinocerebellar, type 6), OMIM:183086)
Official abbreviation |
SCA6 |
Name |
ataxia, spinocerebellar, type 6 |
OMIM ID |
183086 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
4 |
Phenotype entries for this disease |
3 |
Associated with 1 gene |
CACNA1A |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2023-03-22 16:53:30 +01:00 (CET) |
Individuals
|