"Urogenital Abnormalities" 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.
Congenital structural abnormalities of the UROGENITAL SYSTEM in either the male or the female.
Descriptor ID |
D014564
|
MeSH Number(s) |
C12.706 C13.351.875 C16.131.939
|
Concept/Terms |
Urogenital Abnormalities- Urogenital Abnormalities
- Abnormality, Urogenital
- Urogenital Abnormality
- Genitourinary Abnormalities
- Abnormalities, Genitourinary
- Abnormality, Genitourinary
- Genitourinary Abnormality
- Abnormalities, Urogenital
|
Below are MeSH descriptors whose meaning is more general than "Urogenital Abnormalities".
Below are MeSH descriptors whose meaning is more specific than "Urogenital Abnormalities".
This graph shows the total number of publications written about "Urogenital Abnormalities" by people in this website by year, and whether "Urogenital Abnormalities" 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 |
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1996 | 0 | 1 | 1 |
2001 | 0 | 1 | 1 |
2005 | 1 | 0 | 1 |
2006 | 1 | 0 | 1 |
2010 | 0 | 1 | 1 |
2011 | 2 | 0 | 2 |
2012 | 3 | 0 | 3 |
2013 | 1 | 0 | 1 |
2014 | 6 | 1 | 7 |
2015 | 5 | 1 | 6 |
2016 | 6 | 1 | 7 |
2017 | 4 | 0 | 4 |
2018 | 6 | 1 | 7 |
2019 | 6 | 0 | 6 |
2020 | 12 | 4 | 16 |
2021 | 6 | 2 | 8 |
2022 | 4 | 1 | 5 |
2023 | 4 | 0 | 4 |
2024 | 1 | 0 | 1 |
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Below are the most recent publications written about "Urogenital Abnormalities" by people in Profiles.
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Frequency of Treatment Failure of UTIs in Children With Congenital Urinary Tract Anomalies. Hosp Pediatr. 2024 Mar 01; 14(3):189-196.
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LUMBAR Syndrome and Bladder Exstrophy: A Case Report. Urology. 2024 Jan; 183:212-214.
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Presentation and Management of Uterine Didelphys with Unilateral Cervicovaginal Agenesis/Dysgenesis (CVAD): A Multicenter Case Series. J Pediatr Adolesc Gynecol. 2024 Feb; 37(1):72-77.
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Rare variant enrichment analysis supports GREB1L as a contributory driver gene in the etiology of Mayer-Rokitansky-K?ster-Hauser syndrome. HGG Adv. 2023 07 13; 4(3):100188.
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Genetic Variants in ARHGEF6 Cause Congenital Anomalies of the Kidneys and Urinary Tract in Humans, Mice, and Frogs. J Am Soc Nephrol. 2023 02 01; 34(2):273-290.
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Gene dosage changes in KCTD13 result in penile and testicular anomalies via diminished androgen receptor function. FASEB J. 2022 11; 36(11):e22567.
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An overview and video tutorial to the new interactive website for the American Society for Reproductive Medicine M?llerian Anomalies Classification 2021. Am J Obstet Gynecol. 2022 10; 227(4):644-647.
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Phenotypic and mutational spectrum of ROR2-related Robinow syndrome. Hum Mutat. 2022 07; 43(7):900-918.
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Diagnosis and Management of Mullerian Anomalies Across Differing Resource Settings: Worldwide Adaptations. J Pediatr Adolesc Gynecol. 2022 Oct; 35(5):536-540.
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Biallelic pathogenic variants in roundabout guidance receptor 1 associate with syndromic congenital anomalies of the kidney and urinary tract. Kidney Int. 2022 05; 101(5):1039-1053.