Global Variome shared LOVD

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Phenotype #0000331176 Individual ID 00441757 Associated disease ? Diagnosis/Initial neurodevelopmental delay Diagnosis/Definite - Phenotype details see paper; ..., speech delay; motor delay; hyperactivity; dysmorphism; esotropia; mild camptodactyly, pes planus Inheritance Isolated (sporadic) Age/Examination 4y (4 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2023-11-10 18:34:41 +01:00 (CET) Date last edited N/A

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