Structured Summary
Abstract
X-linked recessive NEPHROLITHIASIS characterized by HYPERCALCIURIA; HYPOPHOSPHATEMIA; NEPHROCALCINOSIS; and PROTEINURIA. It is associated with mutations in the voltage-gated chloride channel, CLC-5 (Dent Disease I). Another group of mutations associated with this disease is in phosphatidylinositol 4,5-bisphosphate-5-phosphatase gene.
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Synonyms
5 entry terms
- Dent's Disease
- Dents Disease
- Disease, Dent
- Disease, Dent's
- Disease, Dents
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Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
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History Note
2011
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References
- National Library of Medicine. Dent Disease. Medical Subject Headings (MeSH). 2026. Unique ID D057973. http://id.nlm.nih.gov/mesh/2026/D057973
- Dent Disease. In: Wikipedia. https://en.wikipedia.org/wiki/Dent%27s_disease
- Dent Disease. In: Wikidata. https://www.wikidata.org/wiki/Q4420121