Global Variome shared LOVD

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Phenotype #0000354695 Individual ID 00469542 Associated disease EL Diagnosis/Initial anemia, elliptocytosis Diagnosis/Definite EL3 Phenotype details see paper; ..., hereditary spherocytosis, neonatal hemolytic anemia; mother hereditary spherocytosis, hemolytic anemia Inheritance Familial, autosomal dominant Age/Examination 10y (10 years) 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 2025-11-17 21:44:29 +01:00 (CET) Date last edited N/A

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