MODY 6 syndrome (Q102318): 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. Mutações do gene para o fator de transcrição conhecido como fator de diferenciação neurogênica 1. Muito raro: 5 famílias relatadas até o momento. | |||
| description / en | description / 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. Mutations of the gene for the transcription factor referred to as neurogenic differentiation 1. Very rare: 5 families reported to date. | |||
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. Mutations of the gene for the transcription factor referred to as neurogenic differentiation 1. Very rare: 5 families reported to date.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2096037122 |
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| English | MODY 6 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. Mutations of the gene for the transcription factor referred to as neurogenic differentiation 1. Very rare: 5 families reported to date. |
