Global Variome shared LOVD

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Phenotype #0000344922 Individual ID 00456407 Associated disease MPS Diagnosis/Initial Hunter syndrome Diagnosis/Definite MPS2 Phenotype details severe; coarse facial features, dysostosis multiplex, global developmental delay, hepatomegaly, joint stiffness, splenomegaly, umbilical hernia Inheritance Isolated (sporadic) Age/Examination 4y6m (4 years, 6 months) Age/Diagnosis - Age/Onset - Phenotype/Onset - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2024-10-25 15:49:01 +02:00 (CEST) Date last edited N/A

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