Disease #03735 (AHC2 (hemiplegia, alternating, of childhood, type 2 (AHC2)), OMIM:614820)

Official abbreviation AHC2
Name hemiplegia, alternating, of childhood, type 2 (AHC2)
OMIM ID 614820
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene ATP1A3
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Individuals

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00163016 A09803 - - F yes China Chinese 14y 0 - - AHC2 Abnormal eye movement, quadriplegia, dysphagia, and slight developmental delay ATP1A3 ATP1A3 1 1 Xiaoxu Yang
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