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Senior-Loken syndrome 1

MONDO:0009962

Any Senior-Loken syndrome in which the cause of the disease is a mutation in the NPHP1 gene.

Also known as: NPHP1 Senior-Loken syndrome, Senior-Loken syndrome 1, Senior-Loken syndrome caused by mutation in NPHP1, Senior-Loken syndrome type 1, senior-loken syndrome-1, Loken-Senior syndrome, SENIOR-Loken syndrome 1, SLSN1

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

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Broader categories

Disease (680) Kidney disorder (214) Hereditary disease (176) Urinary system disorder (66) Human disease (14) Autosomal recessive disease (4) Ciliopathy (2) Disease by molecular mechanism (2) Disease of genetic or genomic mechanism (2) Inherited kidney disorder (1)
Trials to join now! 1 Not yet finished but already full! 1
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  • 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: PHASE3 • Sponsor: Children's Hospital of Fudan University • Aim: Disease control

    Last updated Jul 08, 2026 00:00 UTC

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