Alternating hemiplegia of childhood 1

MONDO:0007087

Any alternating hemiplegia of childhood in which the cause of the disease is a mutation in the ATP1A2 gene.

Also known as: ATP1A2 alternating hemiplegia of childhood, alternating hemiplegia of childhood 1, alternating hemiplegia of childhood caused by mutation in ATP1A2, alternating hemiplegia of childhood type 1, AHC1

0 clinical trials for this condition and its sub-types, 0 tagged with Alternating hemiplegia of childhood 1 itself.

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↑ Alternating hemiplegia of childhood (3)

Including sub-types (0) Tagged with Alternating hemiplegia of childhood 1 (0)

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