Global Variome shared LOVD

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Phenotype #0000130094 Individual ID 00163984 Associated disease AHC Diagnosis/Initial AHC Diagnosis/Definite AHC Phenotype details Abnormal eye movement, dystonia, can not walk by himself (4y) Inheritance Familial, autosomal dominant Age/Examination 02y (2 years) Age/Diagnosis 02y Age/Onset 00y03m Phenotype/Onset Abnormal eye movement Protein - Owner name Xiaoxu Yang Database submission license No license selected Created by Xiaoxu Yang Date created 2018-07-02 00:37:36 +02:00 (CEST) Date last edited 2018-07-02 13:59:24 +02:00 (CEST)

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