Global Variome shared LOVD

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Phenotype #0000067657 Individual ID 00088193 Associated disease ID Diagnosis/Initial - Diagnosis/Definite - Inheritance Familial, autosomal recessive Phenotype details severe intellectual disability (HP:0010864); severe global developmental delay (HP:0011344); motor delay (HP:0001270) Age/Examination 00y01m? (approximately 1 month) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Joaquin Brintrup Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Joaquin Brintrup Date created 2016-11-24 16:48:15 +01:00 (CET) Date last edited 2020-05-12 12:33:06 +02:00 (CEST)

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