Müllerian agenesis
congenital atypical development of Müllerian ducts
Facts
9 properties- Instance of
- rare disease, class of disease, intersex condition[2][3]
- Subclass of
- agenesis, uterine malformation, syndrome with 46,XX disorder of sex development, syndrome with disorder of sex development of gynecological interest, partial bilateral aplasia of the mullerian ducts, vaginal aplasia, developmental defect during embryogenesis, disorder of sex development[6][7][8][9][10][11][12][13]
- Facet of
- women's health[14]
- Different from
- gonadal agenesis[17]
- Health specialty
- medical genetics[18]
- On focus list of Wikimedia project
- gender gap on Dutch Wikipedia[20]
🏷️ Also known as
en MRKH
en MRKH syndrome
en Müllerian aplasia and hyperandrogenism
en Mullerian duct failure and hyperandrogenism
en MULLERIAN APLASIA AND HYPERANDROGENISM
en Mayerův-Rokitanského-Küsterův-Hauserův syndrom
en Rokitansky syndrome
en Mayer-Rokitansky-Küster-Hauser syndrome
en Mayer-Rokitansky-Kuster-Hauser syndrome
en WNT4 deficiency
en Müllerian agenesis
en Müllerian duct failure and hyperandrogenism
ar عدم تخلق مولري
cs Mayer-Rokitansky-Kuster-Hauserův syndrom
cs Mayerův-Rokitanského-Küsterův-Hauserův syndrom
cs Syndrom Rokitansky-Küster-Häusner
cs Mayer-Von Rokitansky-Kuster-Hauserův syndrom
da Mayer-Rokitansky-Küster-Hauser syndrom
de Mayer-Rokitansky-Küster-Hauser-Syndrom
de Mayerův-Rokitanského-Küsterův-Hauserův syndrom
🔖 Identifiers · 27
- OpenAlex ID
- C2911074991
- Image (Wikimedia Commons)
- Agenesia de vagina2.png ↗
- DiseasesDB
- 8390
- Exact match
- www.orpha.net, www.orpha.net
- Freebase ID
- /m/04zjnf
- Homosaurus ID (V2)
- MRKH
- Homosaurus ID (V3)
- homoit0002865
- Homosaurus ID (V4)
- homoit0002865
- ICD-10-CM
- Q51.8
- ICD-11 ID (MMS)
- LB44.Y
- ICD-9 ID
- 626.0
Show all 27 identifiers +15
- KEGG ID
- H00600
- MeSH descriptor ID
- C567186
- Microsoft Academic ID (discontinued)
- 2779788458, 2911138178
- Miraheze article ID
- lgbta:Müllerian_Agenesis
- Mondo ID
- MONDO_0017771
- NL CR AUT ID
- ph1133405
- PatientsLikeMe condition ID
- mrkh
- UK Parliament thesaurus ID
- 429448
- UniProt disease ID
- DI-01999
- WikiKids ID
- Syndroom_van_Mayer-Rokitansky-Küster
- WikiProjectMed ID
- Müllerian agenesis
🔗 Connections
Instance of 2
Named after 2
Subclass of 2
Facet of 1
Genetic association 1
Health specialty 1
← Genetic association 1
← Medical condition 1
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Summary
Müllerian agenesis is a rare disease[1].