Chimaera 46, XX, 46, XY (Q46932): Difference between revisions

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description / pt-brdescription / pt-br
 
Doença causada pela fusão embrionária XX e XY ou dois eventos distintos de perda de um cromossomo sexual de um embrião XXY no início do desenvolvimento. Isso resulta em um subconjunto de células no corpo com um cariótipo XX, enquanto outras células demonstram um cariótipo XY. Esta doença pode se manifestar com desenvolvimento genital anormal.
description / endescription / en
 
A disease caused by XX and XY embryonic fusion or two distinct loss events of a sex chromosome from an XXY embryo early in development. This results in a subset of cells in the body having an XX karyotype, while other cells demonstrate an XY karyotype. This disease may present with abnormal genital development.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/1262245334 / rank
 
Normal rank
Property / CURIE
 
CID11:LD56
Property / CURIE: CID11:LD56 / rank
 
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Property / Canary Token
 
dki-india-LD56
Property / Canary Token: dki-india-LD56 / rank
 
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Property / Verification Status
 
Concluído
Property / Verification Status: Concluído / rank
 
Normal rank
Property / Knowledge Architect
 
Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
Normal rank
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: FRANCISCO MONTEIRO BARUCCO / rank
 
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Latest revision as of 15:50, 13 August 2026

A disease caused by XX and XY embryonic fusion or two distinct loss events of a sex chromosome from an XXY embryo early in development. This results in a subset of cells in the body having an XX karyotype, while other cells demonstrate an XY karyotype. This disease may present with abnormal genital development.
Language Label Description Also known as
default for all languages
LD56
    English
    Chimaera 46, XX, 46, XY
    A disease caused by XX and XY embryonic fusion or two distinct loss events of a sex chromosome from an XXY embryo early in development. This results in a subset of cells in the body having an XX karyotype, while other cells demonstrate an XY karyotype. This disease may present with abnormal genital development.

      Statements

      CID11:LD56
      0 references
      dki-india-LD56
      0 references
      Concluído
      0 references
      13 August 2026
      0 references