Disease #01453 (EA1 (ataxia, episodic, type 1 (EA-1)), OMIM:160120)
Official abbreviation |
EA1 |
Name |
ataxia, episodic, type 1 (EA-1) |
OMIM ID |
160120 |
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 |
KCNA1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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