Global Variome shared LOVD

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Phenotype #0000285454 Individual ID 00392176 Associated disease XLHRD Phenotype details see paper; ..., S-FGF23 103 pg/ml Diagnosis/Initial hypophosphatemic rickets Inheritance Isolated (sporadic) Diagnosis/Definite XLHR Age/Examination - Age/Diagnosis - 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 2021-11-21 17:33:37 +01:00 (CET) Date last edited N/A

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