epilepsy with myoclonic absences
MONDO:0019487Mondo
Findings
No curated finding names epilepsy with myoclonic absences yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A rare childhood-onset epilepsy characterized by sudden onset, short lasting absence associated with rhythmical myoclonia of head and shoulders.
Definition from the Mondo Disease Ontology (MONDO:0019487), read 2026-09-29. CC BY 4.0.
Where it sits
Other names
1 name
Resolves to: epilepsy with myoclonic absences
- Also called
- EMA