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Results 1 - 10 of 120 for kidney diseases
  1. ... gene have been identified in people with polycystic kidney disease. These mutations are responsible for about 85 percent of cases of autosomal dominant polycystic kidney disease (ADPKD), which is the most common type of ...
  2. ... gene have been identified in people with polycystic kidney disease. These mutations are responsible for about 15 percent of all cases of autosomal dominant polycystic kidney disease (ADPKD), which is the most common type of ...
  3. ... gene have been identified in people with polycystic kidney disease. These mutations cause autosomal recessive polycystic kidney disease (ARPKD), which is a severe type of the ...
  4. ... gene have been found to cause uromodulin-associated kidney disease. Most of these mutations change single protein building ... destruction (apoptosis) of cells in the kidneys, causing kidney disease. More About This Health Condition Tamm-Horsfall protein ...
  5. ... gene have been found to cause REN-related kidney disease, a condition in which the kidneys become less ... each cell. The mutations involved in REN-related kidney disease either change or remove a protein building block ( ...
  6. ... Mutations in the MUC1 gene cause medullary cystic kidney disease type 1 (MCKD1). This condition is characterized by ... although it is unclear how this change causes kidney disease. Why the effects of MUC1 gene mutations are ...
  7. ... can cause Alport syndrome, a condition characterized by kidney disease, hearing loss, and eye abnormalities. Most of these ... hematuria) but no other signs or symptoms of kidney disease. In the past, this condition was often called ...
  8. ... can cause Alport syndrome, a condition characterized by kidney disease, hearing loss, and eye abnormalities. Most of these ... hematuria) but no other signs or symptoms of kidney disease. In the past, this condition was often called ...
  9. ... microdeletions but not intragenic HNF1B mutations link developmental kidney disease and psychiatric disorder. Kidney Int. 2016 Jul;90( ... JF, Nijenhuis T. Hepatocyte Nuclear Factor 1beta-Associated Kidney Disease: More than Renal Cysts and Diabetes. J Am ...
  10. ... with Mainzer-Saldino syndrome, a disorder characterized by kidney disease, eye problems, and skeletal abnormalities. Mutations in the ... gene IFT140 in skeletal ciliopathies with early progressive kidney Disease. Hum Mutat. 2013 May;34(5):714-24. ...
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