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
|