Global Variome shared LOVD

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Phenotype #0000155620 Individual ID 00207836 Associated disease MOPD Diagnosis/Initial - Diagnosis/Definite MOPD-1 Phenotype details see paper; no severe developmental delay, no neurological symptoms, ... Inheritance Familial, autosomal recessive Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2018-12-02 10:28:44 +01:00 (CET) Date last edited 2018-12-02 10:32:56 +01:00 (CET)

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