Urogenital Abnormalities

"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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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

Below are MeSH descriptors whose meaning is more general than "Urogenital Abnormalities".

Diseases [C]
Male Urogenital Diseases [C12]
Urogenital Abnormalities [C12.706]
Female Urogenital Diseases and Pregnancy Complications [C13]
Female Urogenital Diseases [C13.351]
Urogenital Abnormalities [C13.351.875]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Urogenital Abnormalities [C16.131.939]

Below are MeSH descriptors whose meaning is related to "Urogenital Abnormalities".

Below are MeSH descriptors whose meaning is more specific than "Urogenital Abnormalities".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Urogenital Abnormalities" by people in Harvard Catalyst Profiles by year, and whether "Urogenital Abnormalities" was a major or minor topic of these publication.

Bar chart showing 107 publications over 25 distinct years, with a maximum of 12 publications in 2021

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
1994	1	0	1
1996	1	1	2
1998	0	3	3
2001	0	1	1
2002	1	1	2
2003	0	1	1
2004	0	1	1
2005	1	0	1
2006	2	0	2
2007	1	1	2
2008	2	2	4
2009	1	0	1
2011	1	1	2
2012	4	0	4
2013	1	1	2
2014	6	5	11
2015	2	0	2
2016	5	0	5
2017	5	2	7
2018	6	0	6
2019	6	1	7
2020	7	2	9
2021	10	2	12
2022	7	4	11
2023	8	0	8

Below are the most recent publications written about "Urogenital Abnormalities" by people in Profiles.

Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT). Kidney Int. 2024 Apr; 105(4):844-864.

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Mouse and human studies support DSTYK loss of function as a low-penetrance and variable expressivity risk factor for congenital urinary tract anomalies. Genet Med. 2023 Dec; 25(12):100983.

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Characterization of the prenatal renal phenotype associated with 17q12, HNF1B, microdeletions. Prenat Diagn. 2024 02; 44(2):237-246.

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The genetics and pathogenesis of CAKUT. Nat Rev Nephrol. 2023 11; 19(11):709-720.

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Recessive CHRM5 variant as a potential cause of neurogenic bladder. Am J Med Genet A. 2023 08; 191(8):2083-2091.

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Exome sequencing in individuals with congenital anomalies of the kidney and urinary tract (CAKUT): a single-center experience. Eur J Hum Genet. 2023 06; 31(6):674-680.

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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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A homozygous truncating ETV4 variant in a Nigerian family with congenital anomalies of the kidney and urinary tract. Am J Med Genet A. 2023 05; 191(5):1355-1359.

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Disease mechanisms of monogenic congenital anomalies of the kidney and urinary tract American Journal of Medical Genetics Part C. Am J Med Genet C Semin Med Genet. 2022 09; 190(3):325-343.

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Double Trouble: A Singleton in Each Horn of a Bicornuate Uterus. Neoreviews. 2022 10 01; 23(10):e699-e702.

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