Global Variome shared LOVD

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Phenotype #0000170832 Individual ID 00225723 Associated disease MKS Diagnosis/Initial Meckel-Gruber syndrome Diagnosis/Definite MKS-1 Phenotype details see paper; ... 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 2019-02-22 23:56:54 +01:00 (CET) Date last edited N/A

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