Disease #02634 (SCA17 (ataxia, spinocerebellar, type 17 (SCA-17)), OMIM:607136)
Official abbreviation |
SCA17 |
Name |
ataxia, spinocerebellar, type 17 (SCA-17) |
OMIM ID |
607136 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
- |
Associated with 1 gene |
TBP |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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