Phenotype #0000036715

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

Individual ID	00050100
Associated disease	VUR2
Phenotype details	see paper; congenital anomalies kidney and urinary tract incl. vesicoureteral reflux; daugther bilateral VUR, hypoplastic kidneys, nephropathy; mother required ureteral reimplantation for severe VUR; ...
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2015-09-21 20:15:42 +02:00 (CEST)
Date last edited	N/A

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.