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Nephronophthisis 20

MONDO:0014997

Any nephronophthisis in which the cause of the disease is a mutation in the MAPKBP1 gene.

Also known as: MAPKBP1 nephronophthisis (disease), NPHP20, nephronophthisis (disease) caused by mutation in MAPKBP1, nephronophthisis 20, nephronophthisis type 20

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

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Broader categories

Disease (618) Kidney disorder (202) Hereditary disease (172) Urinary system disorder (62) Human disease (14) Autosomal recessive disease (4) Nephronophthisis (4) Disease of genetic or genomic mechanism (2) Renal tubule disorder (1) Autosomal genetic disease (0)

Trials to join now! 5 Not yet recruiting 2 Not yet finished but already full! 3 Completed 1

Sweat sensor could replace needles for kidney patients

Diagnosis Completed

This study tested a new wearable patch that collects sweat to measure sodium and creatinine levels, which are important for monitoring kidney health and dehydration. Five adults with kidney disease wore the patch while their sweat was analyzed using a special light-based techniqu…

Phase: NA • Sponsor: Korea University • Aim: Diagnosis

Last updated Jun 27, 2026 08:11 UTC