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Alternating hemiplegia of childhood 1
rareAny alternating hemiplegia of childhood in which the cause of the disease is a mutation in the ATP1A2 gene.
- Identifiers
- MONDO:0007087 OMIM:104290
- Causal genes
- ATP1A2
- Also known as
- AHC1 · alternating hemiplegia of childhood caused by mutation in ATP1A2 · alternating hemiplegia of childhood type 1 · ATP1A2 alternating hemiplegia of childhood
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