Nephronophthisis 2

MONDO:0011190

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

Also known as: INVS nephronophthisis (disease), NPH2, NPHP2, nephronophthisis (disease) caused by mutation in INVS, nephronophthisis 2, nephronophthisis 2, infantile, nephronophthisis type 2, Nph2

1 clinical trial for this condition and its sub-types, 0 tagged with Nephronophthisis 2 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Nephronophthisis (4)

Including sub-types (1) Tagged with Nephronophthisis 2 (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 2

Where it sits in the disease tree

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