Global Variome shared LOVD

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Phenotype #0000210660 Individual ID 00275978 Associated disease PCH Phenotype details - Diagnosis/Initial pontocerebellar hypoplasia Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Onset - Phenotype/Onset - Protein - Owner name Enza Maria Valente Database submission license No license selected Created by Johan den Dunnen Date created 2020-01-21 19:32:30 +01:00 (CET) Date last edited N/A

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