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Nephronophthisis 11

MONDO:0013302

A nephronophthisis that has material basis in homozygous or compound heterozygous mutation in the TMEM67 gene on chromosome 8q22.1.

Also known as: NPHP11, nephronophthisis 11, nephronophthisis type 11

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