 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.
Congenital structural abnormalities of the UROGENITAL SYSTEM in either the male or the female.
| Descriptor ID |
D014564
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| MeSH Number(s) |
C12.706 C13.351.875 C16.131.939
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| Concept/Terms |
Urogenital Abnormalities- Urogenital Abnormalities
- Abnormality, Urogenital
- Urogenital Abnormality
- Genitourinary Abnormalities
- Abnormalities, Genitourinary
- Abnormality, Genitourinary
- Genitourinary Abnormality
- Abnormalities, Urogenital
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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 |
|---|
| 2015 | 1 | 0 | 1 | | 2017 | 2 | 0 | 2 |
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Below are the most recent publications written about "Urogenital Abnormalities" by people in Profiles.
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Boczek NJ, Kruisselbrink T, Cousin MA, Blackburn PR, Klee EW, Gavrilova RH, Lanpher BC. Multigenerational pedigree with STAR syndrome: A novel FAM58A variant and expansion of the phenotype. Am J Med Genet A. 2017 May; 173(5):1328-1333.
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Hsieh MH, Wood HM, Dicianno BE, Dosa NP, Gomez-Lobo V, Mattoo TK, Misseri R, Norton JM, Sawin KJ, Scal P, Wright JE, Star RA, Bavendam T. Research Needs for Effective Transition in Lifelong Care of Congenital Genitourinary Conditions: A Workshop Sponsored by the National Institute of Diabetes and Digestive and Kidney Diseases. Urology. 2017 May; 103:261-271.
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Solomon BD, Bodian DL, Khromykh A, Mora GG, Lanpher BC, Iyer RK, Baveja R, Vockley JG, Niederhuber JE. Expanding the phenotypic spectrum in EP300-related Rubinstein-Taybi syndrome. Am J Med Genet A. 2015 May; 167A(5):1111-6.
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