Xenbase may experience sporadic downtime from September 1st to September 3rd due to scheduled IT maintenance work. We apologize for the inconvenience. Click on this message to dismiss it.
Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (2)
MIM:614820 - ALTERNATING HEMIPLEGIA OF CHILDHOOD 2; AHC2

Xenbase Genes: atp1a3

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013900 - alternating hemiplegia of childhood 2
MONDO:0016241 - alternating hemiplegia of childhood

Disease Ontology (DO):
DOID:0050635 - alternating hemiplegia of childhood