Nephronophthisis 19

MONDO:0014537

Any nephronophthisis in which the cause of the disease is a mutation in the DCDC2 gene.

Also known as: DCDC2 nephronophthisis (disease), NPHP19, nephronophthisis (disease) caused by mutation in DCDC2, nephronophthisis 19, nephronophthisis type 19

1 clinical trial for this condition and its sub-types, 0 tagged with Nephronophthisis 19 itself.

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Where it sits in the disease tree

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↑ Nephronophthisis (4)

Including sub-types (1) Tagged with Nephronophthisis 19 (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

Nephronophthisis 19

Where it sits in the disease tree

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