Global Variome shared LOVD

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Phenotype #0000288122 Individual ID 00394923 Associated disease XLHR Phenotype details no bone deformities, no active rickets, no longitudinal growth retardation (≤2 SD), no dental problems Diagnosis/Initial hypophosphatemic rickets Inheritance Familial, X-linked dominant Diagnosis/Definite XLHR Age/Examination - Age/Diagnosis 4y Age/Onset - Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2021-12-02 16:30:25 +01:00 (CET) Date last edited N/A

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