Global Variome shared LOVD

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

Phenotype #0000128828 Individual ID 00163692 Associated disease AHC Diagnosis/Initial alternating hemiplegia of childhood (AHC) Diagnosis/Definite AHC-2 Phenotype details - Inheritance Isolated (sporadic) Age/Examination - Age/Diagnosis - Age/Onset 2m Phenotype/Onset abnormal eye movement Protein - Owner name Gao Hua Database submission license No license selected Created by Gao Hua Date created 2013-07-08 11:34:48 +02:00 (CEST) Date last edited N/A

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