Epilepsy with myoclonic absences

Orpha code: 86911OMIM code:

Definition

A rare childhood-onset epilepsy characterized by sudden onset, short lasting absence associated with rhythmical myoclonia of head and shoulders.

Disease data
Classification

Disease

ORPHA code
86911
OMIM code
-
ICD10 code
G40.4
ICD11 code
8A61.23

No additional description.

Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl