Global Variome shared LOVD

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Phenotype #0000117197 Individual ID 00144429 Associated disease ? Diagnosis/Initial - Diagnosis/Definite - Phenotype details Encephalopathy (HP:0001298); Epileptic encephalopathy (HP:0200134); Postnatal microcephaly (HP:0005484); Global developmental delay (HP:0001263) Inheritance Unknown Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name IMGAG Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by IMGAG Date created 2017-12-13 15:17:20 +01:00 (CET) Date last edited 2020-04-01 13:57:49 +02:00 (CEST)

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