/alternating hemiplegia of childhood 2

alternating hemiplegia of childhood 2

Rare Disease

MONDO:0013900

Also Known As

ATP1A3 alternating hemiplegia of childhoodalternating hemiplegia of childhood 2alternating hemiplegia of childhood caused by mutation in ATP1A3alternating hemiplegia of childhood type 2AHC2

Definition

Any alternating hemiplegia of childhood in which the cause of the disease is a mutation in the ATP1A3 gene.

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Associated Genes

ATP1A3 ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:614820 ↗

GARD

GARD:15845 ↗

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