Chromosome inversion in normal individual (Q46907): Difference between revisions

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Property / Canonical URI: https://id.who.int/icd/entity/1635052482 / rank
 
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Property / CURIE
 
CID11:LD47.1
Property / CURIE: CID11:LD47.1 / rank
 
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dki-india-LD47.1
Property / Canary Token: dki-india-LD47.1 / rank
 
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Concluído
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Property / Knowledge Architect
 
Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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13 August 2026
Timestamp+2026-08-13T00:00:00Z
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CalendarGregorian
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Property / Collection date: 13 August 2026 / rank
 
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Property / Linked ICD 10: LUIS HENRIQUE PARAVELA PELA / rank
 
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Latest revision as of 15:47, 13 August 2026

Any disease caused by inversion of genetic material on a chromosome, in an individual demonstrating no abnormalities. Confirmation is through observation of a chromosomal inversion by genetic testing.
Language Label Description Also known as
default for all languages
LD47.1
    English
    Chromosome inversion in normal individual
    Any disease caused by inversion of genetic material on a chromosome, in an individual demonstrating no abnormalities. Confirmation is through observation of a chromosomal inversion by genetic testing.

      Statements

      CID11:LD47.1
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      dki-india-LD47.1
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      Concluído
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      13 August 2026
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