Type 2 Mayer-Rokitansky-Küster-Hauser syndrome (https://homosaurus.org/v3/homoit0002882)




Identifier
homoit0002882
Preferred Label
Type 2 Mayer-Rokitansky-Küster-Hauser syndrome
English
Alternative Label
Type 2 MRKH
English
Description
People with Type 2 Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome have both the differences associated with MRKH syndrome and additional differences in other parts of their body, such as their fallopian tubes, kidneys, spine, or heart. A specific example of Type 2 MRKH known as Müllerian agenesis, Renal agenesis, Cervicothoracic Somite (MURCS) association, occurs when someone’s kidneys do not develop typically. They may have scoliosis or fused vertebrae in addition to the usual features of MRKH.
English
Contributors
Developed during an extended collaboration with interACT: Advocates for Intersex Youth, 2022-2023.
English
Issued (Created)
2023-06-28 18:43:30 UTC
Modified
2023-06-28 18:43:30 UTC
Broader
Mayer-Rokitansky-Küster-Hauser syndrome [homoit0002865]

Hierarchy Display

Mayer-Rokitansky-Küster-Hauser syndrome
Type 2 Mayer-Rokitansky-Küster-Hauser syndrome


Other formats (including language identifiers): N-Triples, JSON-LD, Extended JSON, TTL, XML, MARC XML


Legacy formats (without language identifiers) N-Triples, JSON-LD, TTL

Homosaurus.org is a linked data service maintained by the Digital Transgender Archive
This vocabulary is made available under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International license (CC BY NC-ND 4.0)