"Nephritis, Hereditary" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A group of inherited conditions characterized initially by HEMATURIA and slowly progressing to RENAL INSUFFICIENCY. The most common form is the Alport syndrome (hereditary nephritis with HEARING LOSS) which is caused by mutations in genes for TYPE IV COLLAGEN and defective GLOMERULAR BASEMENT MEMBRANE.
| Descriptor ID |
D009394
|
| MeSH Number(s) |
C12.706.742 C12.777.419.570.620 C13.351.875.742 C13.351.968.419.570.620 C16.131.939.742 C17.300.200.517
|
| Concept/Terms |
Nephritis, Hereditary- Nephritis, Hereditary
- Hereditary Nephritis
- Nephritis, Familial
- Familial Nephritis
- Hereditary Interstitial Pyelonephritis
- Pyelonephritis, Hereditary Interstitial
Hemorrhagic Hereditary Nephritis- Hemorrhagic Hereditary Nephritis
- Nephritis, Hemorrhagic Hereditary
- Hemorrhagic Familial Nephritis
- Nephritis, Hemorrhagic Familial
- Hereditary Hematuria Syndrome
- Congenital Hereditary Hematuria
- Hematuria, Congenital Hereditary
- Hematuric Hereditary Nephritis
- Nephritis, Hematuric Hereditary
- Hereditary Familial Congenital Hemorrhagic Nephritis
Alport Syndrome- Alport Syndrome
- Syndrome, Alport
- Hematuria-Nephropathy-Deafness Syndrome
- Hematuria Nephropathy Deafness Syndrome
- Syndrome, Hematuria-Nephropathy-Deafness
- Alport's Syndrome
|
Below are MeSH descriptors whose meaning is more general than "Nephritis, Hereditary".
Below are MeSH descriptors whose meaning is more specific than "Nephritis, Hereditary".
This graph shows the total number of publications written about "Nephritis, Hereditary" by people in this website by year, and whether "Nephritis, Hereditary" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1994 | 3 | 1 | 4 |
| 1995 | 3 | 0 | 3 |
| 1996 | 1 | 0 | 1 |
| 1997 | 1 | 1 | 2 |
| 1998 | 2 | 0 | 2 |
| 1999 | 3 | 1 | 4 |
| 2000 | 3 | 0 | 3 |
| 2002 | 0 | 1 | 1 |
| 2004 | 1 | 0 | 1 |
| 2005 | 2 | 1 | 3 |
| 2006 | 1 | 0 | 1 |
| 2007 | 2 | 0 | 2 |
| 2008 | 2 | 1 | 3 |
| 2009 | 1 | 0 | 1 |
| 2010 | 1 | 1 | 2 |
| 2014 | 1 | 0 | 1 |
| 2022 | 3 | 0 | 3 |
| 2023 | 1 | 0 | 1 |
| 2024 | 1 | 0 | 1 |
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Below are the most recent publications written about "Nephritis, Hereditary" by people in Profiles.
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Genetic reprogramming with stem cells regenerates glomerular epithelial podocytes in Alport syndrome. Life Sci Alliance. 2024 Jun; 7(6).
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Molecular MR Imaging of Renal Fibrogenesis in Mice. J Am Soc Nephrol. 2023 07 01; 34(7):1159-1165.
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Genetic diagnosis and renal biopsy findings in the setting of a renal genetics clinic. Am J Med Genet C Semin Med Genet. 2022 09; 190(3):302-308.
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Variants in genes coding for collagen type IV a-chains are frequent causes of persistent, isolated hematuria during childhood. Pediatr Nephrol. 2023 03; 38(3):687-695.
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Col4a3-/- Mice on Balb/C Background Have Less Severe Cardiorespiratory Phenotype and SGLT2 Over-Expression Compared to 129x1/SvJ and C57Bl/6 Backgrounds. Int J Mol Sci. 2022 Jun 15; 23(12).
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End-stage kidney disease due to Alport syndrome: outcomes in 296 consecutive Australia and New Zealand Dialysis and Transplant Registry cases. Nephrol Dial Transplant. 2014 Dec; 29(12):2277-86.
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Identification of the NC1 domain of {alpha}3 chain as critical for {alpha}3{alpha}4{alpha}5 type IV collagen network assembly. J Biol Chem. 2010 Dec 31; 285(53):41874-85.
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Genotype-phenotype correlation in X-linked Alport syndrome. J Am Soc Nephrol. 2010 May; 21(5):876-83.
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Stem cell therapies benefit Alport syndrome. J Am Soc Nephrol. 2009 Nov; 20(11):2359-70.
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Thrombocytopenia and proteinuria. Nonmuscle myosin heavy-chain-9-related disease ( MYH9 RD) or Epstein syndrome (ES). Pediatr Nephrol. 2009 Mar; 24(3):485-8.