Global Variome shared LOVD

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Phenotype #0000286507 Individual ID 00393266 Associated disease XLHR Phenotype details see paper; ..., severe bowing, osteotomy, severe dental severity Diagnosis/Initial hypophosphatemic rickets Inheritance Familial, autosomal dominant Diagnosis/Definite XLHR Age/Examination 33y (33 years) Age/Diagnosis 30y Age/Onset <1y 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 2021-11-28 13:11:04 +01:00 (CET) Date last edited N/A

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