RS80356537 ATP1A3
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What This Variant Does
"[OMIM:?]
Associated Conditions
Dystonia 12
Alternating hemiplegia of childhood 2
Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome
Dystonia 12
Inborn genetic diseases
Tetraparesis
Dystonic disorder
Oculogyric crisis
ATP1A3-related disorder
Developmental and epileptic encephalopathy 99
Alternating hemiplegia of childhood 2
Dystonia 12
Alternating hemiplegia of childhood 2
Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome
Dystonia 12
Other Variants in ATP1A3