GREB1 like retinoic acid receptor coactivator
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Covered on Genetics Home Reference:
From NCBI Gene:
- Renal hypodysplasia/aplasia 3
Renal hypodysplasia/aplasia 3 (RHDA3): A severe, autosomal dominant disease encompassing a spectrum of kidney development defects. Clinical manifestations are highly variable and include bilateral or unilateral renal agenesis, renal aplasia, hypoplasia, (cystic) dysplasia, severe obstructive uropathy, and vesicoureteral reflux. Bilateral renal agenesis is almost invariably fatal in utero or in the perinatal period. Unilateral renal agenesis can lead to future health issues including end-stage renal disease. [MIM:617805]