Other Names for this Disease
- Extramembranous glomerulonephritis
- Glomerulonephritis, membranous
- Idiopathic membranous glomerulonephritis
- Idiopathic membranous nephropathy
- Membranous glomerulonephritis
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 When the glomerular basement membrane becomes thickened, it does not work normally, allowing large amounts of protein to be lost in the urine. Symptoms develop gradually and may include swelling, fatigue, weight gain, and high blood pressure. In many cases, the underlying cause of membranous nephropathy is not known. Some cases are associated with other conditions (lupus), infections (hepatitis B and C), cancer or as a side effect of certain medications. The goal of treatment is to reduce symptoms and slow the progression of the disease.Membranous nephropathy is a kidney disease characterized by inflammation of the structures inside the kidney that help filter wastes and fluids.
Last updated: 9/2/2014
- Silberberg C. Membranous nephropathy. MedlinePlus. September 8, 2013; http://www.nlm.nih.gov/medlineplus/ency/article/000472.htm. Accessed 9/2/2014.
- Membranous Nephropathy (MN). Nephrotic Syndrome Study Network (NEPTUNE). http://www.rarediseasesnetwork.org/NEPTUNE/patients/learnmore/MN/. Accessed 9/2/2014.
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- MedlinePlus was designed by the National Library of Medicine to help you research your health questions, and it provides more information about this topic.
- The Nephrotic Syndrome Rare Disease Clinical Research Network (NEPTUNE) has information about Membranous nephropathy for patients and their families.
- The University of North Carolina Kidney Center has a summary of Membranous nephropathy in their Kidney Health Library.
- Medscape Reference provides information on this topic. Click on the link to view this information. You may need to register to view the medical textbook, but registration is free.
- The Merck Manual for health care professionals provides information on Membranous nephropathy.
- Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
- Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.