"Kidney Diseases, Cystic" 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 heterogeneous group of hereditary and acquired disorders in which the KIDNEY contains one or more CYSTS unilaterally or bilaterally (KIDNEY, CYSTIC).
| Descriptor ID |
D052177
|
| MeSH Number(s) |
C12.777.419.403 C13.351.968.419.403
|
| Concept/Terms |
Kidney Diseases, Cystic- Kidney Diseases, Cystic
- Cystic Kidney Disease
- Disease, Cystic Kidney
- Diseases, Cystic Kidney
- Kidney Disease, Cystic
- Cystic Kidney Diseases
- Cystic Renal Diseases
- Cystic Renal Disease
- Disease, Cystic Renal
- Diseases, Cystic Renal
- Renal Disease, Cystic
- Renal Diseases, Cystic
Kidney, Cystic- Kidney, Cystic
- Cystic Kidney
- Cystic Kidneys
- Kidneys, Cystic
|
Below are MeSH descriptors whose meaning is more general than "Kidney Diseases, Cystic".
Below are MeSH descriptors whose meaning is more specific than "Kidney Diseases, Cystic".
This graph shows the total number of publications written about "Kidney Diseases, Cystic" by people in this website by year, and whether "Kidney Diseases, Cystic" 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 |
|---|
| 2000 | 2 | 0 | 2 |
| 2001 | 1 | 0 | 1 |
| 2014 | 1 | 0 | 1 |
| 2015 | 1 | 2 | 3 |
| 2018 | 2 | 0 | 2 |
To return to the timeline,
click here.
Below are the most recent publications written about "Kidney Diseases, Cystic" by people in Profiles.
-
Homozygosity for the c.428delG variant in KIAA0586 in a healthy individual: implications for molecular testing in patients with Joubert syndrome. J Med Genet. 2019 04; 56(4):261-264.
-
Clinical and experimental evidence suggest a link between KIF7 and C5orf42-related ciliopathies through Sonic Hedgehog signaling. Eur J Hum Genet. 2018 02; 26(2):197-209.
-
TALPID3 controls centrosome and cell polarity and the human ortholog KIAA0586 is mutated in Joubert syndrome (JBTS23). Elife. 2015 Sep 19; 4.
-
Syndromic ciliopathies: From single gene to multi gene analysis by SNP arrays and next generation sequencing. Mol Cell Probes. 2015 Oct; 29(5):299-307.
-
Non-manifesting AHI1 truncations indicate localized loss-of-function tolerance in a severe Mendelian disease gene. Hum Mol Genet. 2015 May 01; 24(9):2594-603.
-
Mutation of POC1B in a severe syndromic retinal ciliopathy. Hum Mutat. 2014 Oct; 35(10):1153-62.
-
Establishing an algorithm for molecular genetic diagnostics in 127 families with juvenile nephronophthisis. Kidney Int. 2001 Feb; 59(2):434-45.
-
A deletion distinct from the classical homologous recombination of juvenile nephronophthisis type 1 (NPH1) allows exact molecular definition of deletion breakpoints. Hum Mutat. 2000 Sep; 16(3):211-23.
-
Children with ocular motor apraxia type Cogan carry deletions in the gene (NPHP1) for juvenile nephronophthisis. J Pediatr. 2000 Jun; 136(6):828-31.
MeSH information
