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href=\"https://medlineplus.gov/genetics/condition/dent-disease\">Dent disease</a></li></ul>","identityNote":"MONDO cross-references identify native condition entries. Ancestor membership does not transfer phenotype values between groups.","importantHtml":""},"sections":[{"bodyHtml":"<p>Changes in the CLCN5 gene cause Dent disease 1, while changes in the OCRL gene cause Dent disease 2. Genetic changes that cause disease are called pathogenic variants. Approximately 60 percent of people with Dent disease have type 1. Another 15 to 20 percent of people with Dent disease have type 2.</p><p>The proteins produced from the CLCN5 and OCRL genes play important roles in normal kidney function, particularly within the proximal tubules. Studies suggest that certain pathogenic variants in the CLCN5 or OCRL genes lead to abnormal protein reabsorption within the proximal tubules. As a result, proteins that should be reabsorbed into the bloodstream are released in the urine. This leads to the kidney problems seen in people with Dent disease.</p><p>Approximately 20 to 25 percent of people with Dent disease do not have an identified variant in the CLCN5 or OCRL genes. The cause of the condition in these cases is not known.</p><p class=\"section-source\"><a href=\"https://medlineplus.gov/genetics/condition/dent-disease/#causes\">MedlinePlus Genetics: Causes</a></p>","key":"forms","title":"What causes Dent disease?"},{"bodyHtml":"<p>The signs and symptoms of Dent disease tend to appear in childhood and worsen over time. However, the features and the severity of Dent disease vary greatly among affected individuals.</p><p>The most frequent sign of Dent disease is the loss of small proteins in the urine (also called low-molecular-weight or LMW proteinuria). Too much calcium in the urine (hypercalciuria) is another common sign of Dent disease. LMW proteinuria and hypercalciuria may be the only signs of Dent disease in affected children.</p><p>Additional signs and symptoms of Dent disease can include calcium deposits in the kidneys (nephrocalcinosis) and kidney stones (nephrolithiasis). Kidney stones can cause abdominal pain and blood in the urine (hematuria). Thirty to 80 percent of people with Dent disease develop kidney failure in early to mid-adulthood. Kidney failure can be life-threatening and occurs when the kidneys are no longer able to effectively filter fluids and waste products from the body.</p><p>In some people with Dent disease, low levels of vitamin D and other factors can cause bones to soften and weaken. This can result in a condition called rickets or a similar condition called osteomalacia. These conditions can cause bone pain and make bones more likely to break. Rickets can also be associated with bowed legs, difficulty walking, and short stature.</p><p>Researchers have described two forms of Dent disease that are caused by changes in different genes: Dent disease 1 and Dent disease 2. Both forms are characterized by the features described above, but Dent disease 2 can also be associated with mild intellectual disabilities and developmental delays. People with Dent disease 2 may also have a clouding of the lens of the eye (cataract) that does not typically cause severe visual impairment. Studies have also suggested that people with Dent disease 2 may be more likely to develop a painful skin condition called hidradenitis suppurativa.</p><p class=\"section-source\">Source: <a href=\"https://medlineplus.gov/genetics/condition/dent-disease\">MedlinePlus Genetics</a></p>","key":"overview","title":"Condition overview"}],"sharedSources":[],"slug":"dent-disease","sourceDocuments":[{"name":"Dent disease","reviewed":"2026-04","sections":{"causes":{"fetchedAt":"2026-10-20T20:20:53.509457+00:00","label":"Causes","pageSha256":"0d8f9f5c2b554a95ae09d09756a6d80e52063bccd8b3c06a85b33d9edc2d964a","sourceUrl":"https://medlineplus.gov/genetics/condition/dent-disease/#causes","status":"available"}},"source_release":"2026-10-01","url":"https://medlineplus.gov/genetics/condition/dent-disease"}],"sourceNote":"MedlinePlus descriptions and Causes; original HPO annotations.","takeawayHtml":"Cause explanations are from MedlinePlus Genetics. Feature values below retain their original sources and patient groups.","title":"Dent disease"},"schemaVersion":1}