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- Ba7f3b42d47c63336dbb57baf8e012bca hasDbXref "Orphanet:25968" @default.
- Ba7f3b42d47c63336dbb57baf8e012bca type Axiom @default.
- Ba7f3b42d47c63336dbb57baf8e012bca annotatedProperty IAO_0000115 @default.
- Ba7f3b42d47c63336dbb57baf8e012bca annotatedSource MONDO_0007558 @default.
- Ba7f3b42d47c63336dbb57baf8e012bca annotatedTarget "Benign occipital epilepsy is a rare, genetic neurological disorder characterized by visual seizures and occipital epileptiform paroxysms reactive to ocular opening which present in infancy to mid-adolescence. Vomiting, tonic eye deviation and impairment of consciousness are typically associated with the Panayiotopoulos type, while visual hallucinations, ictal blindness and post-ictal headache are commonly observed in the Gastaut type. Electroencephalographic findings in both types are similar and include bilateral, synchronous, high voltage spike-wave complexes in a normal background activity located predominantly in the occipital lobes." @default.