Global Variome shared LOVD

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Phenotype #0000180305 Individual ID 00240154 Associated disease ID Diagnosis/Initial intellectual disability Diagnosis/Definite MRT71 Inheritance Familial, autosomal recessive Phenotype details see paper; …, intellectual disability (3/3), epilepsy (2/3), global developmental delay (3/3) Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2019-06-11 17:44:39 +02:00 (CEST) Date last edited 2025-11-11 17:12:11 +01:00 (CET)

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