Global Variome shared LOVD

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Phenotype #0000336103 Individual ID 00446899 Associated disease - Phenotype details No microscopic hematuria, no proteinuria, no kidney failure, no reductio of kidney functionality Diagnosis/Initial Alport Syndrome Inheritance Familial, X-linked Diagnosis/Definite Alport Syndrome Age/Examination 6 Age/Diagnosis 06y Age/Onset - Phenotype/Onset - Protein - Owner name Sergio Daga Database submission license Creative Commons Attribution-NonCommercial 4.0 International Created by Sergio Daga Date created 2024-01-25 15:38:00 +01:00 (CET) Date last edited 2024-02-15 12:33:32 +01:00 (CET)

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