Blau syndrome (Q441077)
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An autosomal dominant disease characterized by familial granulomatous arthritis, uveitis and skin granulomas. It has material basis in mutations in the NOD2/CARD15 genes.
- ARTHROCUTANEOUVEAL GRANULOMATOSIS
- Jabs syndrome
- Granulomatous arthritis of childhood
- Synovitis granulomatous with uveitis and cranial neuropathies
- Granulomatous Inflammatory Arthritis, Dermatitis, and Uveitis, Familial
- ACUG
- Pediatric Granulomatous Arthritis
- Granulomatosis, Familial, Blau Type
- BLAU SYNDROME; BLAUS
- Synovitis, Granulomatous, With Uveitis and Cranial Neuropathies
- BLAUS
- Granulomatosis, Familial Juvenile Systemic
- BLAU SYNDROME
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Blau syndrome |
An autosomal dominant disease characterized by familial granulomatous arthritis, uveitis and skin granulomas. It has material basis in mutations in the NOD2/CARD15 genes. |
|
Statements
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17 May 2019
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714.89
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692.9
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C116794
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Blau syndrome
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Identifiers
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Sitelinks
Wikipedia(9 entries)
- arwiki متلازمة بلاو
- bswiki Blauov sindrom
- cawiki Síndrome de Blau
- dewiki Blau-Syndrom
- enwiki Blau syndrome
- eswiki Síndrome de Blau
- fiwiki Blaun oireyhtymä
- plwiki Zespół Blaua
- ttwiki Нәселле ювениль системалы гранулематоз синдромы
Wikibooks(0 entries)
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Multilingual sites(1 entry)
- commonswiki Category:Blau syndrome