Definition
A rare, genetic, neurodevelopmental disorder characterized by early-onset of recurrent, transient episodes of hemiplegia (including quadriplegia), which typically disappear upon sleep.
Definition
A rare, genetic, neurodevelopmental disorder characterized by early-onset of recurrent, transient episodes of hemiplegia (including quadriplegia), which typically disappear upon sleep.
Disease data
Classification
Disease
Synonyms
AHC
AHC
ORPHA code
2131
OMIM code
614820
ICD10 code
G98
ICD11 code
MB53.0
No additional description.
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