Blau syndrome (Q102968): Difference between revisions
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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) |
Statements
CID11:ID_382488319
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