Disease #04529 (SCA15 (ataxia, spinocerebellar, type 15 (SCA-15)), OMIM:606658)
| Official abbreviation |
SCA15 |
| Name |
ataxia, spinocerebellar, type 15 (SCA-15) |
| OMIM ID |
606658 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
ITPR1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:22 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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