DISEASES

Disease-gene associations mined from literature

Human genes for alternating hemiplegia of childhood

Alternating hemiplegia of childhood [DOID:0050635]

A hemiplegia characterized by recurrent episodes of temporary weakness or complete paralysis on one or both sides of the body.

Synonyms:  alternating hemiplegia of childhood,  DOID:0050635,  alternating hemiplegia of childhoods,  AHC

Linkouts:  OMIM #1 #2