Renal tubule disorder
MONDO:0021568A disease that involves the renal tubule.
Also known as: disease of renal tubule, disease or disorder of renal tubule, disorder of renal tubule, renal tubular disease, renal tubular disorder, renal tubule disease, renal tubule disease or disorder
47 clinical trials for this condition and its sub-types, 1 tagged with Renal tubule disorder itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
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Sub-types of Renal tubule disorder
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Inherited renal tubular disease 0 trials · 40 incl. sub-types
28 sub-types
- Pseudohypoparathyroidism 8 trials · 9 incl. sub-types Sub-types →
- Cystinuria 7 trials Sub-types →
- Dent disease 5 trials Sub-types →
- Familial primary hypomagnesemia 5 trials Sub-types →
- Nephronophthisis 4 trials Sub-types →
- Oculocerebrorenal syndrome 3 trials
- Jeune syndrome 1 trial · 2 incl. sub-types Sub-types →
- Senior-Loken syndrome 1 trial · 2 incl. sub-types Sub-types →
- Hereditary renal hypouricemia 2 trials Sub-types →
- Nephrogenic diabetes insipidus 1 trial · 2 incl. sub-types Sub-types →
- Pseudohypoaldosteronism type 1 1 trial · 2 incl. sub-types Sub-types →
- EAST syndrome 1 trial
- HELIX syndrome 1 trial
- RHYNS syndrome 1 trial
- Nephrogenic syndrome of inappropriate antidiuresis 1 trial
- Bartter syndrome 0 trials Sub-types →
- Gitelman syndrome 0 trials
- Senior-Boichis syndrome 0 trials Sub-types →
- Autosomal dominant proximal renal tubular acidosis 0 trials
- Autosomal recessive proximal renal tubular acidosis 0 trials
- Cranioectodermal dysplasia 0 trials Sub-types →
- Familial juvenile hyperuricemic nephropathy type 2 0 trials
- Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome 0 trials
- Inherited Fanconi renotubular syndrome 0 trials Sub-types →
- Mitochondrial DNA depletion syndrome, hepatocerebrorenal form 0 trials
- Nephrogenic diabetes insipidus-intracranial calcification syndrome 0 trials
- Psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome 0 trials
- Renal tubular acidosis, distal, 3, with or without sensorineural hearing loss 0 trials
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Fanconi renotubular syndrome 4 trials
4 sub-types
- Deal Barratt Dillon syndrome 0 trials
- Acquired Fanconi syndrome 0 trials Sub-types →
- Adult Fanconi syndrome 0 trials
- Inherited Fanconi renotubular syndrome 0 trials Sub-types →
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Renal tubular acidosis 2 trials
5 sub-types
Most studied deeper sub-types
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Slower magnesium drip may help sickest patients hold onto the mineral
Disease control Stopped earlyCritically ill patients often have low magnesium, which can lead to heart rhythm problems and other complications. When magnesium is given through an IV, the body keeps only about half of it. Researchers are testing whether giving the same dose over 8 hours instead of 4 hours hel…
Sponsor: CAMC Health System • Aim: Disease control
Last updated Sep 12, 2026 00:00 UTC
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New drug aims to keep acid in check for rare kidney disorder
Disease control Stopped earlyThis study tested a medicine called ADV7103 in children and adults with distal renal tubular acidosis (dRTA), a rare kidney condition that causes too much acid in the blood. The goal was to see if ADV7103 could prevent dangerous acid buildup better than a placebo. Only 3 people e…
Phase 3 • Sponsor: Advicenne Pharma • Aim: Disease control
Last updated Jun 27, 2026 13:01 UTC
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Why are people with this rare bone disorder prone to diabetes?
Knowledge-focused Stopped earlyThis pilot study aims to understand why people with pseudohypoparathyroidism type 1A (PHP1A) have a higher risk of type 2 diabetes. Researchers will measure insulin sensitivity and beta-cell function in 14 participants with PHP1A or related conditions, comparing them to matched h…
Sponsor: Vanderbilt University Medical Center • Aim: Knowledge-focused
Last updated Jun 27, 2026 12:28 UTC