Global Variome shared LOVD

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Phenotype #0000290583 Individual ID 00397449 Associated disease HR Diagnosis/Initial hypophosphatemic rickets Diagnosis/Definite XLHR Phenotype details see paper; ... Inheritance Familial, X-linked dominant Age/Examination - 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 2021-12-21 19:44:58 +01:00 (CET) Date last edited N/A

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