Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000130101 Individual ID 00164005 Associated disease AHC Diagnosis/Initial AHC Diagnosis/Definite AHC Phenotype details Hemiplegia first onset at 18m, 3-5 times/m, dysarthria, language delay Inheritance Familial, autosomal dominant Age/Examination 09y (9 years) Age/Diagnosis 09y Age/Onset 00y18m Phenotype/Onset Hemiplegia Protein - Owner name Xiaoxu Yang Database submission license No license selected Created by Xiaoxu Yang Date created 2018-07-02 01:34:17 +02:00 (CEST) Date last edited 2018-07-02 14:03:35 +02:00 (CEST)

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