Global Variome shared LOVD

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Phenotype #0000155722 Individual ID 00207950 Associated disease ? Diagnosis/Initial profound global developmental delay Diagnosis/Definite - Phenotype details HP:0001263 (Global developmental delay), reduced amount of white matter, profound developmental delay Inheritance Unknown Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name Andreas Laner Database submission license Creative Commons Attribution 4.0 International Created by Andreas Laner Date created 2018-12-04 16:43:50 +01:00 (CET) Date last edited 2019-02-18 12:01:29 +01:00 (CET)

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