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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

1 clinical trial for this condition and its sub-types.

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Broader categories

Disease (717) Kidney disorder (223) Hereditary disease (188) Urinary system disorder (72) Human disease (15) Disease of genetic or genomic mechanism (2) Inherited kidney disorder (1) Renal agenesis (1) Disease by body system or component (0) Disease by developmental or physiological process (0)

Trials to join now! 1

Could a diabetes drug protect kidneys in children with genetic disease?

Disease control Recruiting now

This study tests whether adding dapagliflozin (a diabetes drug) to standard care reduces protein leakage in the urine of children with hereditary kidney diseases. About 44 children will receive either dapagliflozin plus standard care or standard care alone for 12 weeks, then swit…

Phase 3 • Sponsor: Children's Hospital of Fudan University • Aim: Disease control

Last updated Jul 08, 2026 00:00 UTC