Global Variome shared LOVD

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Phenotype #0000294435 Individual ID 00401664 Associated disease hypophosphatemia Diagnosis/Initial mild hypophosphataemic rickets Diagnosis/Definite XLHR Phenotype details see paper; ... cases in general with milder phenotype 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 2022-02-01 16:43:34 +01:00 (CET) Date last edited N/A

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