Phenotype #0000285766

Individual ID 00392490
Associated disease XLHR
Phenotype details -
Diagnosis/Initial hypophosphatemic rickets
Inheritance Familial, X-linked dominant
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 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2021-11-22 19:38:38 +01:00 (CET)
Date last edited N/A

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