Global Variome shared LOVD

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Phenotype #0000283613 Individual ID 00390075 Associated disease MRMV Phenotype details dysplastic corpus callosum, asymmetric ventriculomegaly; mild gross motor delay; regular education; OFC -1 SD; no epilepsy; no cerebellar signs; no dystonia Diagnosis/Initial congenital mirror movement Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination 9m Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2021-11-09 17:45:02 +01:00 (CET) Date last edited N/A

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