Global Variome shared LOVD

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Phenotype #0000352801 Individual ID 00467589 Associated disease HP1 Phenotype details see paper; ... Diagnosis/Initial hyperoxaluria Inheritance Familial, autosomal recessive Diagnosis/Definite HP1 Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Mohamed A. Elmonem Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2025-10-22 10:35:48 +02:00 (CEST) Date last edited N/A

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