Global Variome shared LOVD

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Phenotype #0000129983 Individual ID 00163017 Associated disease AHC1 Phenotype details Dystonia, Abnormal eye movement, automatic dysfunction, dysphagia, dysarthria, and slight developmental delay Diagnosis/Initial AHC Inheritance Familial, autosomal dominant Diagnosis/Definite AHC Age/Examination 02y (2 years) Age/Diagnosis 02y Age/Onset 00y02m Phenotype/Onset dystonia Protein - Owner name Xiaoxu Yang Database submission license No license selected Created by Xiaoxu Yang Date created 2018-06-24 19:34:42 +02:00 (CEST) Date last edited 2018-06-26 09:08:02 +02:00 (CEST)

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