Global Variome shared LOVD

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Phenotype #0000367858 Individual ID 00485136 Associated disease SCZD Phenotype details neurovisual disorder, dyspraxia, epilepsy with myoclonus, metabolic syndrome Diagnosis/Initial - Inheritance Isolated (sporadic) Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Camille Verebi Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International Created by Camille Verebi Date created 2026-09-24 17:06:11 +02:00 (CEST) Date last edited 2026-09-24 17:58:20 +02:00 (CEST)

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