Disease #01185 (EA2 (ataxia, episodic, type 2), OMIM:108500)
Official abbreviation |
EA2 |
Name |
ataxia, episodic, type 2 |
OMIM ID |
108500 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
9 |
Phenotype entries for this disease |
4 |
Associated with 1 gene |
CACNA1A |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2023-03-22 16:51:15 +01:00 (CET) |
Individuals
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