 Genitalia, Male
"Genitalia, Male" 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.
The male reproductive organs. They are divided into the external organs (PENIS; SCROTUM;and URETHRA) and the internal organs (TESTIS; EPIDIDYMIS; VAS DEFERENS; SEMINAL VESICLES; EJACULATORY DUCTS; PROSTATE; and BULBOURETHRAL GLANDS).
| Descriptor ID |
D005837
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| MeSH Number(s) |
A05.360.444
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| Concept/Terms |
Genitalia, Male- Genitalia, Male
- Male Genitalia
- Genital Organs, Male
- Male Genital Organs
- Organs, Male Genital
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Below are MeSH descriptors whose meaning is more general than "Genitalia, Male".
Below are MeSH descriptors whose meaning is more specific than "Genitalia, Male".
This graph shows the total number of publications written about "Genitalia, Male" by people in this website by year, and whether "Genitalia, Male" 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 |
|---|
| 2002 | 0 | 1 | 1 | | 2004 | 0 | 1 | 1 | | 2005 | 1 | 0 | 1 | | 2007 | 1 | 0 | 1 |
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Below are the most recent publications written about "Genitalia, Male" by people in Profiles.
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Hsieh MH, Grantham EC, Liu B, Macapagal R, Willingham E, Baskin LS. In utero exposure to benzophenone-2 causes hypospadias through an estrogen receptor dependent mechanism. J Urol. 2007 Oct; 178(4 Pt 2):1637-42.
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Kantaputra PN, Tanpaiboon P. A newly recognized syndrome involving limbs, pelvis, and genital organs or a variant of Al-Awadi/Raas-Rothschild syndrome? Am J Med Genet A. 2005 Jan 01; 132A(1):63-7.
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Kato M, Das S, Petras K, Kitamura K, Morohashi K, Abuelo DN, Barr M, Bonneau D, Brady AF, Carpenter NJ, Cipero KL, Frisone F, Fukuda T, Guerrini R, Iida E, Itoh M, Lewanda AF, Nanba Y, Oka A, Proud VK, Saugier-Veber P, Schelley SL, Selicorni A, Shaner R, Silengo M, Stewart F, Sugiyama N, Toyama J, Toutain A, Vargas AL, Yanazawa M, Zackai EH, Dobyns WB. Mutations of ARX are associated with striking pleiotropy and consistent genotype-phenotype correlation. Hum Mutat. 2004 Feb; 23(2):147-59.
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Macayran JF, Doroshow RW, Phillips J, Sinow RM, Furst BA, Smith LM, Lin HJ. PAGOD syndrome: eighth case and comparison to animal models of congenital vitamin A deficiency. Am J Med Genet. 2002 Mar 15; 108(3):229-34.
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