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GENATLAS PHENOTYPE

last update : 11-03-2014

Symbol	RADP2
Location	10q24.31
Name	renal adysplasia 2
Corresponding gene	PAX2
Main clinical features	unilateral renal aplasia, renal dysplasia, or renal aplasia with renal dysplasia with frequent Potter syndrome in newborns with bilateral renal agenesis or other kidney abnormalities, including renal aplasia, dysplasia, hypoplasia, or multicystic disease
Genetic determination	autosomal dominant
	other
Function/system disorder	kidney and urinary tract
Type	disease

Remark(s)