MURCS association (Q46723): Difference between revisions

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A associação MURCS, que significa aplasia do ducto de Müller (MU), displasia renal congênita (R), anomalias do somito cervical (CS), é a forma atípica (ou tipo II) da síndrome de Mayer-Rokitansky-Küster-Hauser, caracterizada por atresia útero-vaginal em mulheres normais, bem como anormalidades renais e esqueléticas associadas e problemas auditivos.
description / endescription / en
 
MURCS association, which stands for Müllerian duct aplasia (MU), congenital renal dysplasia (R), cervical somite anomalies (CS), is the atypical (or type II) form of Mayer-Rokitansky-Küster-Hauser syndrome, characterised by utero-vaginal atresia in otherwise normal females as well associated kidney and skeletal abnormalities and hearing problems.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/1521808255 / rank
 
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Property / CURIE
 
CID11:LD2F.14
Property / CURIE: CID11:LD2F.14 / rank
 
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Property / Canary Token
 
dki-india-LD2F.14
Property / Canary Token: dki-india-LD2F.14 / rank
 
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Property / Verification Status
 
Concluído
Property / Verification Status: Concluído / rank
 
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Property / Knowledge Architect
 
Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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Property / Collection date
 
13 August 2026
Timestamp+2026-08-13T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / Collection date: 13 August 2026 / rank
 
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Property / Linked ICD 10
 
Property / Linked ICD 10: FLAVIA MARIA DOS SANTOS BERGAMI / rank
 
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Latest revision as of 15:31, 13 August 2026

MURCS association, which stands for Müllerian duct aplasia (MU), congenital renal dysplasia (R), cervical somite anomalies (CS), is the atypical (or type II) form of Mayer-Rokitansky-Küster-Hauser syndrome, characterised by utero-vaginal atresia in otherwise normal females as well associated kidney and skeletal abnormalities and hearing problems.
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LD2F.14
    English
    MURCS association
    MURCS association, which stands for Müllerian duct aplasia (MU), congenital renal dysplasia (R), cervical somite anomalies (CS), is the atypical (or type II) form of Mayer-Rokitansky-Küster-Hauser syndrome, characterised by utero-vaginal atresia in otherwise normal females as well associated kidney and skeletal abnormalities and hearing problems.

      Statements

      CID11:LD2F.14
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      dki-india-LD2F.14
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      Concluído
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      13 August 2026
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