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

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Broader categories

Disease (680) Nervous system disorder (231) Hereditary disease (176) Hemiplegia (169) Neurodevelopmental disorder (147) Central nervous system disorder (107) Palsy (33) Human disease (14) Hereditary neurological disease (6) Alternating hemiplegia of childhood (3)

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