Phenotypes for disease #02990

3 entries on 1 page. Showing entries 1 - 3.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000036715 see paper; congenital anomalies kidney and urinary tract incl. vesicoureteral reflux; daugther bilateral VUR, hypoplastic kidneys, nephropathy; mother required ureteral reimplantation for severe VUR; ... - - Familial, autosomal dominant - - - - - Johan den Dunnen 00050100
0000036716 see paper; proband bilateral VUR, right duplex collecting system and kidney; mother and two aunts urinary tract symptoms, ultrasonographical evidence of CAKUT; grandmother unilateral small kidney; ... - - Familial, autosomal dominant - - - - - Johan den Dunnen 00050101
0000036717 see paper; bilateral high-grade VUR, right megaureter at UVJ; 9y-required ureteral reimplantation surgery; wide-open right/left ureteral orifices due to bilateral absence of intravesical ureteral segments, ... - - Isolated (sporadic) - - - - - Johan den Dunnen 00050103
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