Global Variome shared LOVD

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Phenotype #0000154688 Individual ID 00206896 Associated disease MCSZ;EIEE10 Phenotype details see paper; ... Diagnosis/Initial microcephaly, seizures, developmental delay Inheritance Familial, autosomal recessive Diagnosis/Definite MCSZ 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 2018-11-16 22:08:04 +01:00 (CET) Date last edited N/A

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