Global Variome shared LOVD

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Phenotype #0000130098 Individual ID 00164002 Associated disease AHC Diagnosis/Initial AHC Diagnosis/Definite AHC Phenotype details Hemiplegia start at 10m, 2 time/m, abnormal eye movement, dystonia, slight developmental delay (language delay) Inheritance Familial, autosomal dominant Age/Examination 08y (8 years) Age/Diagnosis 08y Age/Onset 00y10m Phenotype/Onset Hemiplegia Protein - Owner name Xiaoxu Yang Database submission license No license selected Created by Xiaoxu Yang Date created 2018-07-02 00:52:40 +02:00 (CEST) Date last edited 2018-07-02 14:01:50 +02:00 (CEST)

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