| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A hemiplegia characterized by recurrent episodes of temporary weakness or complete paralysis on one or both sides of the body. (Human Disease Ontology, DOID_0050635) |
| External Link | http://www.omim.org/entry/104290 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the alternating hemiplegia of childhood phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| ATP1A2 | ATPase, Na+/K+ transporting, alpha 2 polypeptide |
