Global Variome shared LOVD

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Phenotype #0000129967 Individual ID 00155757 Associated disease AHC1 Phenotype details Abnormal eye movement, quadriplegia, dystonia, ataxia, epilepsy, and developmental delay Diagnosis/Initial AHC Inheritance Familial, autosomal dominant Diagnosis/Definite AHC Age/Examination 03y (3 years) Age/Diagnosis 03y Age/Onset 01y Phenotype/Onset Abnormal eye movement Protein - Owner name Xiaoxu Yang Database submission license No license selected Created by Xiaoxu Yang Date created 2018-06-24 18:48:10 +02:00 (CEST) Date last edited 2018-06-26 09:05:59 +02:00 (CEST)

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