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Blau syndrome

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EntityQ441077· pop 11· linked from 19 articles

Blau syndrome

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Also 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
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Commons category
Blau syndrome
NCI Thesaurus ID
C116794
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

Available in 10 languages

via Wikidata sitelinks · CC0

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