Global Variome shared LOVD

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Phenotype #0000334385 Individual ID 00445132 Associated disease ? Diagnosis/Initial congenital Rubella syndrome Diagnosis/Definite - Phenotype details see paper; ..., 5y-deceased; developmental delay, microcephaly, congenital heart disease, microcornea, nystagmus, dense nuclear opacity peripheral cortical opacity lens Inheritance Unknown Age/Examination 11m Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2024-01-03 11:39:20 +01:00 (CET) Date last edited N/A

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