Global Variome shared LOVD

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Phenotype #0000287990 Individual ID 00394790 Associated disease RRS Phenotype details core nervous system anomalies, seizure, facial dysmorphism Diagnosis/Initial Robinow syndrome Inheritance Familial, autosomal recessive Diagnosis/Definite RRS2 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 2021-12-02 09:15:49 +01:00 (CET) Date last edited N/A

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