Global Variome shared LOVD

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Phenotype #0000185025 Individual ID 00245067 Associated disease progeroid Diagnosis/Initial - Diagnosis/Definite - Phenotype details progeroid syndrome, neonatal (Wiedemann-Rautenstrauch syndrome) Inheritance Familial, autosomal recessive Age/Examination - Age/Onset - Phenotype/Onset - Protein - Owner name Philippe Campeau Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Philippe Campeau Date created 2019-06-30 23:07:17 +02:00 (CEST) Date last edited 2019-07-05 12:23:50 +02:00 (CEST)

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