Global Variome shared LOVD

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Phenotype #0000129989 Individual ID 00163023 Associated disease AHC1 Phenotype details Dystonia, quadriplegia, and slight developmental delay. Diagnosis/Initial AHC Inheritance Familial, autosomal dominant Diagnosis/Definite AHC Age/Examination 03y (3 years) Age/Diagnosis 03y Age/Onset 00y08m Phenotype/Onset Dystonia Protein - Owner name Xiaoxu Yang Database submission license No license selected Created by Xiaoxu Yang Date created 2018-06-24 19:52:03 +02:00 (CEST) Date last edited 2018-06-26 09:08:44 +02:00 (CEST)

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