"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 |
|---|
| 2007 | 1 | 0 | 1 |
| 2017 | 3 | 1 | 4 |
| 2018 | 2 | 0 | 2 |
| 2019 | 1 | 1 | 2 |
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Below are the most recent publications written about "Urogenital Abnormalities" by people in Profiles.
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Uric acid and hypertension: a focused review and practical recommendations. J Hypertens. 2019 05; 37(5):878-883.
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A case of 20-week abortion in a rare communicating rudimentary horn of a misinterpreted unicornuate uterus, incorrectly diagnosed as bicornuate: A serious hazard! Eur J Obstet Gynecol Reprod Biol. 2019 Apr; 235:133-135.
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The copy number variation landscape of congenital anomalies of the kidney and urinary tract. Nat Genet. 2019 01; 51(1):117-127.
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Surgical repair in case of covered exstrophy of bladder with complete duplication of lower genitourinary tract and visceral sequestration. Int Braz J Urol. 2018 May-Jun; 44(3):647-648.
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Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations. Am J Hum Genet. 2017 Nov 02; 101(5):789-802.
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The association of Mullerian anomalies and placenta abruption: a meta-analysis. J Matern Fetal Neonatal Med. 2019 Feb; 32(3):512-516.
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Identification of a novel FOXL2 mutation in a single family with both types of blepharophimosis--ptosis-epicanthus inversus syndrome. Mol Med Rep. 2017 Oct; 16(4):5529-5532.
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Ethical Controversy About Hysterectomy for a Minor. Pediatrics. 2017 Jun; 139(6).
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Renal aplastic dysplasia and ipsilateral ectopic ureter obstructing the seminal via: a possible cause of male infertility: Part 2. Eur Urol. 2007 Sep; 52(3):600-1.