Disease #03601 (CIAT (cognitive impairment, ataxia, cerebellar (CIAT)), OMIM:614306)
| Official abbreviation |
CIAT |
| Name |
cognitive impairment, ataxia, cerebellar (CIAT) |
| OMIM ID |
614306 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
SCN8A |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2019-10-25 11:02:39 +02:00 (CEST) |
Individuals
|