rs387907281, ATP1A3

N. diseases: 13
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hemiplegia, Crossed
CUI: C0278110
Disease: Hemiplegia, Crossed
0.010 GeneticVariation BEFREE We describe a case of a child suffering from alternating hemiplegia with a heterozygous p. E815K pathogenic variant of ATP1A3. 28637637 2017