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GENATLAS PHENOTYPE
last update : 12-03-2014
Symbol RADP4
Location 22q13.31
Name renal adysplasia 4
Other name(s) renal hypodysplasia/aplasia 4
Corresponding gene UPK3A
Other symbol(s) RHDA4
Main clinical features
  • a spectrum of kidney development defects including renal agenesis, hypoplasia, and (cystic) 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)