Renal hypodysplasia/aplasia 2

MONDO:0014319

Any renal agenesis in which the cause of the disease is a mutation in the FGF20 gene.

Also known as: FGF20 renal agenesis (disease), renal agenesis (disease) caused by mutation in FGF20, renal hypodysplasia/aplasia 2, renal hypodysplasia/aplasia type 2, RHDA2

11 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by