Dent disease
MONDO:0015612Dent disease is a rare genetic renal tubular disease characterized by manifestations of proximal tubule dysfunction.
Also known as: Dent syndrome, X-linked recessive hypercalciuric hypophosphatemic rickets, X-linked recessive hypophosphatemic rickets, X-linked recessive nephrolithiasis, low-molecular-weight proteinuria with hypercalciuria and nephrocalcinosis, renal Fanconi syndrome with nephrocalcinosis and renal stones, Dent disease 1, Dent disease 2
6 clinical trials for this condition and its sub-types, 5 tagged with Dent disease itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Dent disease
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Dent disease type 1 0 trials
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Dent disease type 2 0 trials
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Can blood and urine markers reveal how rare kidney diseases progress?
Knowledge-focused Recruiting nowThis study follows people with rare inherited forms of kidney stones and chronic kidney disease, such as primary hyperoxaluria, cystinuria, and Dent disease, to learn how these conditions develop over time. Researchers will measure markers of inflammation in blood and urine and t…
Sponsor: Mayo Clinic • Aim: Knowledge-focused
Last updated Aug 09, 2026 00:00 UTC
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Could a biobank unlock secrets of rare kidney stone diseases?
Knowledge-focused Recruiting nowThis study creates a biobank of blood, urine, and tissue samples from people with rare kidney stone diseases—primary hyperoxaluria, cystinuria, APRT deficiency, and Dent disease—and their family members. By storing these samples, researchers hope to enable future studies that cou…
Sponsor: Mayo Clinic • Aim: Knowledge-focused
Last updated Jul 24, 2026 00:00 UTC
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Global registry aims to crack the code of rare kidney stone diseases
Knowledge-focused Recruiting nowThis study collects medical information from people around the world who have one of four rare hereditary kidney stone diseases: primary hyperoxaluria, Dent disease, cystinuria, or APRT deficiency. By gathering data from many patients, researchers hope to better understand how th…
Sponsor: Mayo Clinic • Aim: Knowledge-focused
Last updated Jul 12, 2026 00:00 UTC
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Scientists hunt for kidney stone genes in 6,000-Person study
Knowledge-focused Recruiting nowThis study aims to find the specific genes and mutations that cause rare, inherited forms of kidney stone disease. Researchers will analyze DNA from up to 6,000 participants to understand how these genetic changes lead to stones. The goal is to use this knowledge to develop bette…
Sponsor: Mayo Clinic • Aim: Knowledge-focused
Last updated Jun 27, 2026 12:06 UTC