Global Variome shared LOVD

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Phenotype #0000233453 Individual ID 00308027 Associated disease ? Diagnosis/Initial developmental delay Diagnosis/Definite AGS2 Phenotype details severe global developmental delay, spastic tetraplegic cerebral palsy, microcephaly Inheritance Familial, autosomal recessive Age/Examination - 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 2020-08-25 19:47:51 +02:00 (CEST) Date last edited N/A

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