Phenotypes for disease #03735 (AHC2 (hemiplegia, alternating, of childhood, type 2 (AHC2)), OMIM:614820)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000129982 Abnormal eye movement, quadriplegia, dysphagia, and slight developmental delay AHC AHC Familial, autosomal dominant 15y 15y 00y01m Abnormal eye movement - Xiaoxu Yang 00163016
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