MODY 7 syndrome (Q102317): Difference between revisions

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Isso se refere a uma forma hereditária de diabetes causada por mutações em um gene autossômico dominante (independente do sexo, ou seja, herdado de qualquer um dos pais), interrompendo a produção de insulina. KLF11 tem sido descrito associado a forma de diabetes que tem sido caracterizada como ''MODY7'' por OMIM.
description / endescription / en
 
This refers to the hereditary form of diabetes caused by mutations in an autosomal dominant gene (sex independent, i.e. inherited from any of the parents) disrupting insulin production. KLF11 has been associated with a form of diabetes that has been characterised as "MODY7" by OMIM.
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Property / Canonical URI: https://id.who.int/icd/entity/1745614099 / rank
 
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CID11:ID_1745614099
Property / CURIE: CID11:ID_1745614099 / rank
 
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dki-india-ID_1745614099
Property / Canary Token: dki-india-ID_1745614099 / rank
 
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Concluído
Property / Verification Status: Concluído / rank
 
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Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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15 August 2026
Timestamp+2026-08-15T00:00:00Z
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CalendarGregorian
Precision1 day
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Property / Collection date: 15 August 2026 / rank
 
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Latest revision as of 19:15, 16 August 2026

This refers to the hereditary form of diabetes caused by mutations in an autosomal dominant gene (sex independent, i.e. inherited from any of the parents) disrupting insulin production. KLF11 has been associated with a form of diabetes that has been characterised as "MODY7" by OMIM.
Language Label Description Also known as
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ID_1745614099
    English
    MODY 7 syndrome
    This refers to the hereditary form of diabetes caused by mutations in an autosomal dominant gene (sex independent, i.e. inherited from any of the parents) disrupting insulin production. KLF11 has been associated with a form of diabetes that has been characterised as "MODY7" by OMIM.

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      CID11:ID_1745614099
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      dki-india-ID_1745614099
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      Concluído
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      15 August 2026
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