Disease #03175 (EA6 (ataxia, episodic, type 6 (EA-6)), OMIM:612656)
Official abbreviation |
EA6 |
Name |
ataxia, episodic, type 6 (EA-6) |
OMIM ID |
612656 |
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 |
SLC1A3 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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