Blau syndrome (Q102968): Difference between revisions
From determinar.ia.br - Determine suas informações
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Changed label, description and/or aliases in pt-br, en |
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| description / pt-br | description / pt-br | ||
A síndrome de Blau é uma doença autoinflamatória monogênica dominante associada a mutações em um gene chamado NOD2 (símbolo anterior CARD15) | |||
| description / en | description / en | ||
Blau syndrome is a monogenic dominant autoinflammatory disease associated with mutations in a gene called NOD2 (previous symbol CARD15) | |||
Revision as of 08:46, 17 August 2026
Blau syndrome is a monogenic dominant autoinflammatory disease associated with mutations in a gene called NOD2 (previous symbol CARD15)
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_382488319 |
||
| English | Blau syndrome |
Blau syndrome is a monogenic dominant autoinflammatory disease associated with mutations in a gene called NOD2 (previous symbol CARD15) |
