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Blau syndrome
Sign in to saveAlso known as 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
autosomal dominant disease characterized by familial granulomatous arthritis, uveitis and skin granulomas. It has material basis in mutations in the NOD2/CARD15 genes
In the Vinony graph
Within Vinony's link graph, Blau syndrome is referenced by 19 other articles, and connects out to uveitis, International Standard Book Number and digital object identifier.
Vinony files it under Autoinflammatory syndromes and Genodermatoses.
Its subject is documented across 10 Wikipedia language editions.
Wikidata facts
- Subclass of
- syndrome
- Image
- Blau syndrome.jpg
Show 7 more facts
- Commons category
- Blau syndrome
- NCI Thesaurus ID
- C116794
- exact match
- www.orpha.net/ORDO/Orphanet_90340
- ICD-9-CM
- 692.9
- external data available at URL
- www.nanbyou.or.jp/entry/3826
- on focus list of Wikimedia project
- WikiProject Medicine
- health specialty
- dermatology
Sources (7)
via Wikidata · CC0