Global Variome shared LOVD

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Phenotype #0000294284 Individual ID 00401265 Associated disease ATS Phenotype details see paper; ..., hematuria, proteinuria, serum creatinine 91 umol/L Diagnosis/Initial Alport syndrome Inheritance Familial, autosomal recessive Diagnosis/Definite ATS2 Age/Examination - Age/Diagnosis - Age/Onset 25y 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 2022-01-30 13:46:00 +01:00 (CET) Date last edited N/A

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