I can see this term was previously requested here, but I did not see that it was created, so I would like to re-request.
Preferred term label:
Congenital seminal vesicle cyst
Synonyms
Cysts of the seminal vesicles
Cysts involving the seminal vesicles
Seminal vesicle cysts
Seminal vesicular cysts
Definition (free text, please give PubMed ID)
A cystic structure caused by distention of the seminal vesicle due to atresia of the ejaculatory duct. Caused by altered development of the mesonephric duct (AKA Wolffian duct). Two-thirds are associated with abnormal development of other ipsilateral mesonephric derivatives, such as vas deferens, kidney, and ureter. Sometimes considered the male equivalent of Mayer-Rokitansky-Kuster-Hauser syndrome. (PMID: 31024871)
Parent term (use hpo.jax.org/app)
Abnormal male reproductive system physiology HP:0012874
def: A cyst (sac-like mass that may contain serous liquid or semisolid material) caused by distention of the seminal vesicle due to atresia of the ejaculatory duct.
comment: Congenital seminal vesical cysts are caused by altered development of the mesonephric (Wolffian) duct. They are often associated with abnormal development of other ipsilateral mesonephric derivatives, such as vas deferens, kidney, and ureter.
Preferred term label: Congenital seminal vesicle cyst
Synonyms
Definition (free text, please give PubMed ID) A cystic structure caused by distention of the seminal vesicle due to atresia of the ejaculatory duct. Caused by altered development of the mesonephric duct (AKA Wolffian duct). Two-thirds are associated with abnormal development of other ipsilateral mesonephric derivatives, such as vas deferens, kidney, and ureter. Sometimes considered the male equivalent of Mayer-Rokitansky-Kuster-Hauser syndrome. (PMID: 31024871)
Parent term (use hpo.jax.org/app) Abnormal male reproductive system physiology HP:0012874
Diseases characterized by this term? (e.g. Orphanet or OMIM number) Zinner syndrome (no Orphanet or OMIM entry) (Reference: PMID: 34268266) Autosomal dominant polycystic kidney disease (ORPHA:730) (Reference: PMID: 9829485) Renal agenesis (ORPHA:411709)
Your nano-attribution (ORCID) 0000-0001-8481-3559