| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| 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://ctdbase.org/detail.go?type=disease&acc=MESH:C536589 |
| Similar Terms | |
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2 genes/proteins associated with the disease Alternating hemiplegia of childhood from the curated CTD Gene-Disease Associations dataset.
