Phenotype #0000336103

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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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	No license selected
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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