Disease #07231 (SPAX10 (ataxia, spastic, type 10), OMIM:620666)
| Official abbreviation |
SPAX10 |
| Name |
ataxia, spastic, type 10 |
| OMIM ID |
620666 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
COQ4 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2026-02-24 15:29:32 +01:00 (CET) |
| Date last edited |
N/A |
|