Síndrome de Mayer-Rokitansky-Küster-Hauser tipo 2 (https://es.homosaurus.org/v3/homoit0002882)




Identificador
homoit0002882
Etiqueta preferida
Type 2 Mayer-Rokitansky-Küster-Hauser syndrome
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Etiqueta alternativa
Type 2 MRKH
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Descripción
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.
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Colaboradores
Developed during an extended collaboration with interACT: Advocates for Intersex Youth, 2022-2023.
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Emitido (creado)
2023-06-28 18:43:30 UTC
Modificado
2025-02-23 07:12:59 UTC
Más amplio
Síndrome de Mayer-Rokitansky-Küster-Hauser [homoit0002865]

Visualización de jerarquía

Síndrome de Mayer-Rokitansky-Küster-Hauser
Síndrome de Mayer-Rokitansky-Küster-Hauser tipo 2


Otros formatos (incluidos identificadores de idioma): N-Triples, JSON-LD, Extended JSON, TTL, XML, MARC XML


Formatos heredados (sin identificadores de idioma) N-Triples, JSON-LD, TTL

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