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GENATLAS PHENOTYPE

last update : 11-03-2009

Symbol	RADP
Location	10q11.21
Name	renal adysplasia
Corresponding gene	RET
Main clinical features	'Potter syndrome' in newborns with bilateral renal agenesis or other kidney abnormalities, including renal aplasia, dysplasia, hypoplasia, or multicystic disease bilateral renal agenesis, including severe bilateral renal dysplasia, unilateral renal agenesis with contralateral dysplasia (URA/RD) and severe obstructive uropathy
Genetic determination	autosomal recessive
Function/system disorder	kidney and urinary tract
Type	malformation

Remark(s)