Rare disease search prototype built on Orphanet data

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ORPHA:86911

Epilepsy with myoclonic absences

Body system: Neurological diseases
Inheritance pattern: Multigenic/multifactorial
Typical age of onset: Adolescent, Childhood, Infancy
Estimated prevalence: Not documented in Orphadata
Rarity class: Not documented in Orphadata

ORPHA:86911 is classified under "Neurological diseases" in the Orphanet nomenclature.

Common signs